A ligand for a metallocene catalyst used to prepare propylene based polymers, and its preparation method

0001The present invention relates to the ligands useful as intermediates in the synthesis of a class of metal complexes used in a high yield process for producing substantially amorphous propylene-based polymers having high molecular weights.

0002Metallocene compounds are well-known in the state of the art as catalyst components in olefin polymerization reactions, in association with suitable cocatalysts, such as alumoxanes or aluminum derivatives. For instance, <patcit id="pcit0001" dnum="EP0129368A"><text>EP 0 129 368</text></patcit> discloses a catalyst system for the polymerization of olefins comprising a bis-cyclopentadienyl coordination complex with a transition metal, wherein the two cyclopentadienyl groups may be linked by a divalent bridging group, such as an ethylene or a dimethylsilandiyl group.

0003Another class of polymerization catalysts known in the state of the art are the bridged cyclopentadienyl amido catalysts, which usually include monocyclopentadienyl titanium compounds activated by an alumoxane or other suitable cocatalysts (see for instance <patcit id="pcit0002" dnum="EP0416815A"><text>EP 0 416 815</text></patcit> and <patcit id="pcit0003" dnum="EP0420436A"><text>EP 0 420 436</text></patcit>).

0004The <patcit id="pcit0004" dnum="WO9822486A"><text>international patent application WO 98/22486</text></patcit>, in the name of the same Applicant, describes bridged and unbridged metallocenes comprising at least a coordinating group containing a six π electron central radical, directly coordinating a transition metal atom, to which are associated one or more radicals containing at least one non carbon atom selected from B, N, O, Al, Si, P, S, Ga, Ge, As, Se, In, Sn, Sb and Te. Said metallocenes are useful as catalyst components for the production of polyethylene and polypropylene.

0005The <patcit id="pcit0005" dnum="WO9837106A"><text>international patent application WO 98/37106</text></patcit> describes a polymerization catalyst system comprising a catalytic complex formed by activating a transition metal compound which comprises a group 13, 15 or 16 heterocyclic fused cyclopentadienide ligand and a metal selected from the group consisting of Group 3-9 and 10 metals; said heterocyclic fused cyclopentadienide ligand preferably contains, as endocyclic heteroatoms, one or more B, N, P, O or S atoms.

0006The <patcit id="pcit0006" dnum="WO9924446A"><text>international patent application WO 99/24446</text></patcit>, in the name of the same Applicant, describes bridged and unbridged metallocenes comprising at least a heterocyclic cyclopentadienyl group of one of the following formulae: <chemistry id="chem0001" num="0001"><img file="EP1533324B1_D0001.tif" /></chemistry><chemistry id="chem0002" num="0002"><img file="EP1533324B1_D0002.tif" /></chemistry> wherein one of X or Y is a single bond, the other being O, S, NR or PR, R being hydrogen or an hydrocarbon group; R^2, R³ and R⁴ are hydrogen, halogen, -R, -OR, -OCOR, -SR, -NR₂ or -PR₂; a is 0-4. These metallocenes may be used as catalyst components in the polymerization of olefins, particularly in the production of homo and copolymers of ethylene.

0007The <patcit id="pcit0007" dnum="WO9806727A"><text>international applications WO 98/06727</text></patcit> and <patcit id="pcit0008" dnum="WO9806728A"><text>WO 98/06728</text></patcit> describe respectively 3-heteroatom and 2-heteroatom substituted cyclopentadienyl-containing metal complexes, useful as catalysts for olefin polymerization; more specifically, these complexes contain a heteroatom-Cp bond, respectively in the 3-position and 2-position of the Cp, and are used for preparing ethylene/1-octene copolymers.

0008The Applicant has now unexpectedly found ligands useful as intermediates in the synthesis of a class of metallocene compounds useful as catalyst components in propylene polymerization, able to produce high molecular weight substantially amorphous propylene (co)polymers in high yields.

0009The present invention concerns a ligand of formula (II) <chemistry id="chem0003" num="0003"><img file="EP1533324B1_D0003.tif" /></chemistry> wherein <ol id="ol0001" compact="compact"><li>X is a nitrogen or phosphorous atom;</li><li>Z is a C, Si or Ge atom; Y² is selected from the group consisting of CR⁸ or Y¹; and m is 0 or 1; when the group Y² is a CR⁸ group, m is 1 and the 6-membered ring formed is an aromatic benzene ring; when Y² is different from CR⁸, m is 0 and the carbon atom bonding the R⁴ group is directly bonded to the cyclopentadienyl ring and the ring formed is a 5-membered ring; the groups R¹, equal to or different from each other, are selected from the group consisting of hydrogen, linear or branched, saturated or unsaturated C₁-C₂₀ alkyl, C₃-C₂₀ cycloalkyl, C₆-C₂₀ aryl, C₇-C₂₀ alkylaryl and C₇-C₂₀ arylalkyl radical optionally containing Si or heteroatoms belonging to groups 13 or 15-17 of the Periodic Table of the Elements, or two R¹ groups form together a C₄-C₇ ring;</li><li>Y¹ is an atom selected from the group consisting of NR⁷, oxygen (O), PR⁷ or sulfur (S), wherein the group R⁷ is selected from the group consisting of linear or branched, saturated or unsaturated, C₁-C₂₀ alkyl, C₆-C₂₀ aryl and C₇-C₂₀ arylalkyl radical;</li><li>the groups R² and R³ , equal to or different from each other, are selected from the group consisting of hydrogen, halogen, -R, -OR, -OCOR, -OSO₂CF₃, -SR, -NR₂ and -PR₂, wherein R is a linear or branched, saturated or unsaturated C₁-C₂₀ alkyl, C₃-C₂₀ cycloalkyl, C₆-C₂₀ aryl, C₇-C₂₀ alkylaryl or C₇-C₂₀ arylalkyl radical; two R can also form a saturated or unsaturated C₄-C₇ ring, preferably R is methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, phenyl, p-n-butyl-phenyl or benzyl radical, or R² and R³ form a condensed aromatic or aliphatic C₄-C₇ ring that can be substituted with one or more R⁹ groups wherein R⁹ is selected from the group consisting of halogen, -R, -OR, -OCOR, -OSO₂CF₃, -SR, -NR₂ and -PR₂, wherein R has the meaning reported above, or two vicinal R⁹ groups form together a condensed aromatic or aliphatic C₄-C₇ ring;</li><li>the groups R⁸, R⁴ and R⁵, equal to or different from each other, are selected from the group consisting of hydrogen, halogen, -R, -OR, -OCOR, -OSO₂CF₃, -SR, -NR₂ and -PR₂, wherein R has the meaning reported above, or R⁸ and R⁴, R⁴ and R⁵ or R⁵ and R⁸ form together a condensed C₄-C₇ ring that can be substituted with one or more R groups;</li><li>the group R⁶ is selected from the group consisting of a linear or branched, saturated or unsaturated C₁-C₂₀ alkyl, C₆-C₂₀ aryl and C₇-C₂₀ arylalkyl radical, optionally containing heteroatoms belonging to groups 13 or 15-17 of the Periodic Table of the Elements; the above ligands are particularly useful as intermediates in the preparation of the titanium complexes disclosed in <patcit id="pcit0009" dnum="EP1159310A"><text>EP 1 159 310</text></patcit> (patent application).</li></ol>

0010The titanium complex of formula (I) may be suitably used in a complexed form, for example in the presence of a coordination molecules such as Lewis bases.

0011Preferred complexes of formula (I) are those belonging to the following three classes (1), (2) and (3), having respectively formula (III), (IV) and (V).

Class (1)

Titanium complexes belonging to class (1) have the following formula (III)

0012<chemistry id="chem0004" num="0004"><img file="EP1533324B1_D0004.tif" /></chemistry> wherein X, Z, Y¹, L, R¹, R², R³, R⁴, R⁵, R⁶ and R⁸ have the meaning reported above with the proviso that R² and R³ do not form a condensed aromatic or aliphatic C₄-C₇ ring.

0013Preferably in the titanium complexes of formula (III): X is a nitrogen atom; the divalent bridge >ZR¹₂ is preferably selected from the group consisting of dimethylsilyl, diphenylsilyl, diethylsilyl, di-n-propylsilyl, di-isopropylsilyl, di-n-butyl-silyl, di-t-butyl-silyl, di-n-hexylsilyl, ethylmethylsilyl, n-hexylmethylsilyl, cyclopentamethylenesilyl, cyclotetramethylenesilyl, cyclotrimethylenesilyl, methylene, dimethylmethylene and diethylmethylene; even more preferably, it is dimethylsilyl, diphenylsilyl or dimethylmethylene; Y¹ is N-methyl, N-ethyl or N-phenyl; R² and R³ ,equal to or different from each other, are selected from the group consisting of hydrogen, halogen, -R, -OR, -OCOR, -OSO₂CF₃, -SR, -NR₂ and -PR₂; more preferably R² is hydrogen, methyl, ethyl, propyl or phenyl; and R³ is hydrogen, methyl or phenyl; even more preferably R² is hydrogen, or methyl; R⁴ and R⁸ are hydrogen; R⁵ is hydrogen, methoxy or tertbutyl; R⁶ is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, phenyl, p-n-butyl-phenyl, benzyl, cyclohexyl and cyclododecyl; more preferably R⁶ is t-butyl; the substituents L, equal to or different from each other, are preferably halogen atoms, linear or branched, saturated or unsaturated C₇-C₂₀ alkylaryl, C₁-C₆ alkyl groups or OR wherein R is described above; more preferably the substituents L are Cl, CH₂C₆H₅, OCH₃ or CH₃.

0014Examples of complexes of formula (III) are: <chemistry id="chem0005" num="0005"><img file="EP1533324B1_D0005.tif" /></chemistry><chemistry id="chem0006" num="0006"><img file="EP1533324B1_D0006.tif" /></chemistry><chemistry id="chem0007" num="0007"><img file="EP1533324B1_D0007.tif" /></chemistry><chemistry id="chem0008" num="0008"><img file="EP1533324B1_D0008.tif" /></chemistry> and the corresponding titanium dichloride or dimethoxy complexes.

0015The titanium complexes belonging to class (1) can be prepared starting from the ligand of formula (IIIa) <chemistry id="chem0009" num="0009"><img file="EP1533324B1_D0009.tif" /></chemistry> wherein X, Z, Y¹, R¹, R², R³, R⁴, R⁵, R⁶ and R⁸ have the meaning reported above.

Class (2)

Titanium complexes of class (2) have the following formula (IV)

0016<chemistry id="chem0010" num="0010"><img file="EP1533324B1_D0010.tif" /></chemistry> wherein X, Z, Y¹, L, R¹, R⁴, R⁵, R⁶, R⁸, and R⁹ have the meaning reported above and k ranges from 0 to 4.

0017Preferably in the titanium complexes of formula (IV): X is a nitrogen atom; the divalent bridge >ZR¹₂ is selected from the group consisting of dimethylsilyl, diphenylsilyl, diethylsilyl, di-n-propylsilyl, di-isopropylsilyl, di-n-butyl-silyl, di-t-butyl-silyl, di-n-hexylsilyl, ethylmethylsilyl, n-hexylmethylsilyl, cyclopentamethylenesilyl, cyclotetramethylenesilyl, cyclotrimethylenesilyl, methylene, dimethylmethylene and diethylmethylene; even more preferably, it is dimethylsilyl, diphenylsilyl or dimethylmethylene; Y¹ is N-methyl, N-ethyl or N-phenyl; k is 0 or 1 and R⁹ is 2-methyl, 2-isopropyl and 2-<i>tert</i>-butyl; R⁶ is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, phenyl, p-n-butyl-phenyl, benzyl, cyclohexyl and cyclododecyl; more preferably R⁶ is t-butyl; R⁴, R⁵ and R⁸ are hydrogen atoms; the substituents L, equal to or different from each other, are halogen atoms, linear or branched, saturated or unsaturated C₁-C₆ alkyl, C₇-C₂₀ alkylaryl groups or OR wherein R is defined above; more preferably the substituents L are Cl, CH₃, OCH₃ or CH₂C₆H₅.

0018Examples of titanium complexes of formula (IV) are the following: <chemistry id="chem0011" num="0011"><img file="EP1533324B1_D0011.tif" /></chemistry><chemistry id="chem0012" num="0012"><img file="EP1533324B1_D0012.tif" /></chemistry><chemistry id="chem0013" num="0013"><img file="EP1533324B1_D0013.tif" /></chemistry><chemistry id="chem0014" num="0014"><img file="EP1533324B1_D0014.tif" /></chemistry><chemistry id="chem0015" num="0015"><img file="EP1533324B1_D0015.tif" /></chemistry> and the corresponding titanium dimethyl or dimethoxy complexes.

0019The titanium complexes belonging to class (2) can be prepared starting from the ligand of formula (IVa) <chemistry id="chem0016" num="0016"><img file="EP1533324B1_D0016.tif" /></chemistry> wherein X, Z,Y¹, R¹, R⁴, R⁵, R⁶, R⁸, R⁹ and k have the meaning reported above.

Class (3)

0020Titanium complexes belonging to class (3) have the following formula (V): <chemistry id="chem0017" num="0017"><img file="EP1533324B1_D0017.tif" /></chemistry> wherein X, Z, L, Y¹, R¹, R², R³, R⁴, R⁵ and R⁶ have the meaning reported above.

0021Preferably in the titanium complexes of formula (IV): X is a nitrogen atom; the divalent bridge >ZR¹₂ is preferably selected from the group consisting of dimethylsilyl, diphenylsilyl, diethylsilyl, di-n-propylsilyl, di-isopropylsilyl, di-n-butyl-silyl, di-t-butyl-silyl, di-n-hexylsilyl, ethylmethylsilyl, n-hexylmethylsilyl, cyclopentamethylenesilyl, cyclotetramethylenesilyl, cyclotrimethylenesilyl, methylene, dimethylmethylene and diethylmethylene; even more preferably, it is dimethylsilyl, diphenylsilyl or dimethylmethylene; two Y¹ are the same group; more preferably they are NR⁷ or S; R² is hydrogen, methyl, ethyl, propyl or phenyl; and R³ is hydrogen or R² and R³ form a condensed benzene ring that can be substituted with one or more R groups; R⁴ is hydrogen and R⁵ is hydrogen, methyl, ethyl, propyl or phenyl or R⁴ and R⁵ form a condensed benzene ring that can be substituted with one or more R groups; R⁶ is preferably selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, phenyl, p-n-butyl-phenyl, benzyl, cyclohexyl and cyclododecyl; more preferably R⁶ is t-butyl; the substituents L, equal to or different from each other, are preferably halogen atoms, linear or branched, saturated or unsaturated C₇-C₂₀ alkylaryl, C₁-C₆ alkyl groups or OR; more preferably the substituents L are Cl, CH₂C₆H₅, OCH₃ or CH₃.

0022Examples of complex of formula (V) are: <chemistry id="chem0018" num="0018"><img file="EP1533324B1_D0018.tif" /></chemistry><chemistry id="chem0019" num="0019"><img file="EP1533324B1_D0019.tif" /></chemistry><chemistry id="chem0020" num="0020"><img file="EP1533324B1_D0020.tif" /></chemistry><chemistry id="chem0021" num="0021"><img file="EP1533324B1_D0021.tif" /></chemistry> and the corresponding titanium dichloride or dimethoxy complexes.

0023The titanium complexes belonging to class (3) can be prepared starting from the ligand of formula (Va) <chemistry id="chem0022" num="0022"><img file="EP1533324B1_D0022.tif" /></chemistry> wherein X, Z, Y¹, R¹, R², R³, R⁴, R⁵ and R⁶ have the meaning reported above.

0024The ligands of formula (II) can be prepared by a process comprising the following steps: <ol id="ol0002" compact="compact"><li>i) reacting a compound of formula (VI): <chemistry id="chem0023" num="0023"><img file="EP1533324B1_D0023.tif" /></chemistry> wherein Y¹, m, Y², R², R³, R⁴, R⁵, and R⁸ have the meaning reported above, with at least one equivalent of a base such as hydroxides and hydrides of alkali metals or alkaline-earth metals, metallic sodium and potassium or organolithium compounds such as buthilithium, methilithium, and then contacting the obtained compound with a compound of formula R¹₂ZY³Y⁴, wherein R¹ and Z have the meaning reported above, Y³ is a halogen atom preferably chlorine and Y⁴ is an halogen atom preferably chlorine or a group R⁶XH wherein R⁶ and X have the meaning reported above and H is hydrogen;</li><li>ii) if Y⁴ is an halogen atom, reacting the obtained product with a compound of formula R⁶XH₂ wherein R⁶ and X have the meaning reported above and H is hydrogen and recovering the product.</li></ol>

0025Compound of formula VI can be prepared according to general procedures known in the state of the art, starting from commercially obtainable products or from derivatives which can be prepared by known methods. Synthesis of compounds of formula (VI) can be found for example in <patcit id="pcit0010" dnum="WO9924446A"><text>WO 99/24446</text></patcit>, <patcit id="pcit0011" dnum="EP99204566A"><text>EP 99204566</text></patcit>, <patcit id="pcit0012" dnum="EP99204565A"><text>EP 99204565</text></patcit> and <patcit id="pcit0013" dnum="WO0147939A"><text>WO 01/47939</text></patcit>.

0026The ligand can be finally purified by general procedures known in the state of the art, such as crystallization or chromatography. All the steps are carried out in an aprotic solvent that can be a polar or apolar solvent. Examples of aprotic polar solvents which can be used in the above process are tetrahydrofurane, dimethoxyethane, diethylether and dichloromethane. Examples of apolar solvents suitable for the above process are toluene, pentane, hexane and benzene. The temperature in the various steps is preferably kept between -180°C and 80°C, and more preferably between -20°C and 40°C.

0027The titanium complexes of formula (I) can be prepared by first reacting a ligand of formula (II), prepared as described above, with a compound able to form a delocalized dianion, such as hydroxides and hydrides of alkali metals or alkaline-earth metals, metallic sodium and potassium or organolithium compounds such as butylithium, methylithium, on the cyclopentadienyl ring and on the group X, and thereafter with a compound of formula TiL'₄, wherein the substituents L' are halogen or -OR, wherein R has the meaning reported above. Examples of compounds of formula TiL'₄ are titanium tetrachloride and titanium tetramethoxy.

0028According to a preferred method, a ligand (II) is dissolved in an aprotic polar solvent and at least two equivalents of an organic lithium compound are added. The thus obtained anionic compound is added to a solution of the compound TiL'₄ in an aprotic solvent. At the end of the reaction, the solid product obtained is separated from the reaction mixture by techniques commonly used in the state of the art. Examples of aprotic polar solvents suitable for the above reported processes are tetrahydrofurane, dimethoxyethane, diethylether and dichloromethane. Examples of apolar solvents suitable for the above process are pentane, hexane and toluene. During the whole process, the temperature is preferably kept between -180°C and 80°C, and more preferably between -20°C and 40°C.

0029All the above processes are carried out in inert atmosphere such as nitrogen.

0030Titanium compounds of formula (I) in which at least one L substituent is different from halogen can be conveniently prepared by methods known in the state of the art for example, such compounds may be obtained by reacting the dihalogenated metallocene with alkylmagnesium halides (Grignard reagents) or with lithiumalkyl compounds.

0031When one or both L substituents are alkyl, the above titanium complexes (I) can be conveniently obtained by reacting directly a ligand of formula (II) with at least one molar equivalent of a compound of formula TiCl₄, in the presence of at least 3 molar equivalents of a suitable alkylating agent; said alkylating agent can be an alkaline or alkaline-earth metal, such as dialkyl-lithium, dialkyl-magnesium or a Grignard reagent, as described in <patcit id="pcit0014" dnum="WO9936427A"><text>WO 99/36427</text></patcit> and <patcit id="pcit0015" dnum="WO0075151A"><text>WO 00/75151</text></patcit>.

0032An alternative process for preparing titanium complex of formula (I) in which both L substituents are OR groups comprises to prepare the titanium complex of formula (I) in which two L groups are R and then contact the obtained complex with oxygen. The resulting derivative having as L substituents two OR groups shows a better stability than the correspondent R substituted complex and therefore they can be stored for a long time without losing activity.

0033Suitable activating cocatalyst according to the process of the invention are alumoxanes or compounds able to form an alkyl metallocene cation.

0034Alumoxane useful as cocatalyst (B) may be linear alumoxanes of the formula (VII): <chemistry id="chem0024" num="0024"><img file="EP1533324B1_D0024.tif" /></chemistry> wherein R¹⁰ is selected from the group consisting of halogen, linear or branched, saturated or unsaturated C₁-C₂₀ alkyl, C₃-C₂₀ cycloalkyl, C₆-C₂₀ aryl, C₇-C₂₀ alkylaryl and C₇-C₂₀ arylalkyl radicals and y ranges from 0 to 40; or cyclic alumoxanes of the formula (VIII): <chemistry id="chem0025" num="0025"><img file="EP1533324B1_D0025.tif" /></chemistry> wherein R¹⁰ has the meaning described above and y is an integer ranging from 2 to 40.

0035The above alumoxanes may be obtained according to procedures known in the state of the art, by reacting water with an organo-aluminum compound of formula AlR¹⁰₃ or Al₂R¹⁰₆, with the condition that at least one R¹⁰ is not halogen. In this case, the molar ratios of Al/water in the reaction is comprised between 1:1 and 100:1. Particularly suitable are the organometallic aluminum compounds of formula (II) described in <patcit id="pcit0016" dnum="EP0575875A"><text>EP 0 575 875</text></patcit> and those of formula (II) described in <patcit id="pcit0017" dnum="WO9602580A"><text>WO 96/02580</text></patcit>. Moreover, suitable cocatalysts are those described in <patcit id="pcit0018" dnum="WO9921899A"><text>WO 99/21899</text></patcit> and in <patcit id="pcit0019" dnum="WO0121674A"><text>WO 01/21674</text></patcit>.

0036The molar ratio between aluminum and the metal of the titanium complex is comprised between 10:1 and 5000:1, and preferably between 100:1 and 4000:1.

0037Examples of alumoxanes suitable as activating cocatalysts in the process of the invention are methylalumoxane (MAO), tetra-isobutyl-alumoxane (TIBAO), tetra-2,4,4-trimethylpentylalumoxane (TIOAO) and tetra-2-methyl-pentylalumoxane. Mixtures of different alumoxanes can also be used.

0038Examples of aluminum compounds of formula AlR¹⁰₃ or Al₂R¹⁰₆ are: <ul id="ul0001" list-style="none" compact="compact"><li>tris(methyl)aluminum, tris(isobutyl)aluminum,</li><li>tris(isooctyl)aluminum, bis(isobutyl)aluminum hydride,</li><li>methyl-bis(isobutyl)aluminum, dimethyl(isobutyl)aluminum,</li><li>tris(isohexyl)aluminum, tris(benzyl)aluminum,</li><li>tris(tolyl)aluminum, tris(2,4,4-trimethylpentyl)aluminum,</li><li>bis(2,4,4-trimethylpentyl)aluminum hydride, isobutyl-bis(2-phenyl-propyl)aluminum,</li><li>diisobutyl-(2-phenyl-propyl)aluminum, isobutyl-bis(2,4,4-trimethyl-pentyl)aluminum,</li><li>diisobutyl-(2,4,4-trimethyl-pentyl)aluminum, tris(2,3 -dimethyl-hexyl)aluminum,</li><li>tris(2,3,3 -trimethyl-butyl)aluminum, tris(2,3-dimethyl-butyl)aluminum,</li><li>tris(2,3-dimethyl-pentyl)aluminum, tris(2-methyl-3-ethyl-pentyl)aluminum,</li><li>tris(2-ethyl-3-methyl-butyl)aluminum, tris(2-ethyl-3-methyl-pentyl)aluminum,</li><li>tris(2-isopropyl-3-methyl-butyl)aluminum and tris(2,4-dimethyl-heptyl)aluminum.</li></ul>

0039Particularly preferred aluminum compounds are trimethylaluminum (TMA), tris(2,4,4-trimethylpentyl) aluminum (TIOA), triisobutylaluminum (TIBA), tris(2,3,3-trimethyl-butyl)aluminum and tris(2,3 -dimethyl-butyl)aluminum.

0040Mixtures of different organometallic aluminum compounds and/or alumoxanes can also be used.

0041In the catalyst system used in the process of the invention, both said titanium complex and said alumoxane can be pre-reacted with an organometallic aluminum compound of formula AlR¹⁰₃ or Al₂R¹⁰₆, wherein R¹⁰ has the meaning reported above. Pre reaction time can vary from 20 seconds to 1 hour, preferably from 1 minute to 20 minutes.

0042Further activating cocatalysts suitable as component (B) in the catalysts of the invention are those compounds capable of forming an alkylmetallocene cation; preferably, said compounds have formula Q⁺W^-, wherein Q⁺ is a Bronsted acid capable of donating a proton and of reacting irreversibly with a substituent L of the compound of formula (I), and W^- is a compatible non-coordinating anion, capable of stabilizing the active catalytic species which result from the reaction of the two compounds, and which is sufficiently labile to be displaceable by an olefinic substrate. Preferably, the W^- anion comprises one or more boron atoms. More preferably, the anion W^- is an anion of formula BAr₄^(-), wherein the Ar substituents, equal to or different from each other, are aryl radicals such as phenyl, pentafluorophenyl, bis(trifluoromethyl)phenyl. Tetrakis-pentafluorophenyl-borate is particularly preferred. Moreover, compounds of formula BAr₃ can be conveniently used.

0043The catalysts system of the present invention can also be supported on an inert carrier (support), by depositing the titanium complex (A), or the reaction product of the titanium complex (A) with the cocatalyst (B), or the cocatalyst (B) and successively the titanium complex (A), on the inert support, such as silica, alumina, magnesium halides, olefin polymers or prepolymers (i.e. polyethylenes, polypropylenes or styrene-divinylbenzene copolymers). The thus obtained supported catalyst system, optionally in the presence of alkylaluminum compounds, either untreated or pre-reacted with water, can be usefully employed in gas-phase polymerization processes. The solid compound so obtained, in combination with further addition of the alkyl aluminum compound as such or prereacted with water, is usefully employed in gas phase polymerization.

0044The polymerization yield depends on the purity of metallocenes in the catalyst; the metallocene according to the present invention may be used as such or may be previously subjected to purification treatments.

0045Catalyst components (A) and (B) may be suitably contacted among them before the polymerization. The contact time may be comprised between 1 and 60 minutes, preferably between 5 and 20 minutes. The pre-contact concentrations for the titanium complex (A) are comprised between 0.1 and 10^-8 mol/l, whereas for the cocatalyst (B) they are comprised between 2 and 10^-8 mol/l. The precontact is generally carried out in the presence of a hydrocarbon solvent and, optionally, of small amounts of monomer.

0046The catalysts then prepared are particularly advantageous in propylene polymerization, wherein they give substantially amorphous propylene polymers with high activities. When in the compounds of formula (I) Y¹ is NR⁷ and preferably the compounds of formula (I) belong to classes (1) and (2), the propylene polymers obtained have predominantly syndiotactic structure. The syndiotacticity of a polyolefins can be conveniently defined by the percent content of rr triads, as described in <nplcit id="ncit0001" npl-type="s"><text>L. Resconi et al, Chemical Reviews, 2000, 100, 1253</text></nplcit>. When in the compounds of formula (I) Y¹ is NR⁷ and preferably the compounds of formula (I) belong to classes (1) and (2), the propylene polymers obtained typically have triad contents in the range 60 - 80 %, more preferably 65 - 75 %. Their syndiotacticity is not high enough to produce substantial crystallinity (as measured by DSC), but it is high enough to generate resiliency in the polypropylene.

0047Being substantially void of crystallinity, their melting enthalpy (ΔH_f) is preferably lower than about 20 J/g and even more preferably lower than about 10 J/g.

0048A further interesting use of these catalysts is directed to the preparation of propylene-based copolymers, wherein suitable comonomers are ethylene, alpha-olefins of formula CH₂=CHR' wherein R' is a linear or branched, C₂-C₁₀ alkyl such as for example 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, non conjugate diolefins containing up to 20 carbon atoms, for examples said diolefins can belong to the formula CH₂=CH-(CR"₂)_h-CR"₂=CR" wherein R" is hydrogen or a linear or branched, C₁-C₁₀ alkyl and h ranges from 1 to 15, such as 1,4-hexadiene, 1,5-hexadiene, 2-methyl-1,5-hexadiene, 7-methyl-1,6-octadiene, 1,7-octadiene, or said olefins can be norbornene or its derivatives such as 5-ethylidene-2-norbornene.

0049The preferred ranges of composition depend on the type of polymer desired, and on the type of polymerization process employed. For example, in the case of amorphous copolymers of propylene with ethylene, such as those described in <patcit id="pcit0020" dnum="EP729984A"><text>EP 729984</text></patcit>, the content of ethylene ranges from 1 to 35% by moles preferably from 5 to 20% by moles. In the case of ethylene/propylene elastomers the content of propylene ranges from 20 to 80 wt %, preferably from 70 to 30 wt %, while in ethylene/propylene/diene elastomers the content of the diene, which preferably is ethylidenenorbomene or 1,4-hexadiene, range from 0.5 to 5 wt %.

0050Moreover, the molecular weight of the polymers can be varied by changing the polymerization temperature or the type or the concentration of the catalyst components, or by using molecular weight regulators, such as hydrogen, as well-known in the state of the art. The molecular weight of the propylene-based polymers may be also easily controlled by copolymerizing small amounts of ethylene.

0051The polymerization process according to the present invention can be carried out in gaseous phase or in liquid phase, optionally in the presence of an inert hydrocarbon solvent either aromatic (such as toluene), or aliphatic (such as propane, hexane, heptane, isobutane and cyclohexane).

0052The polymerization temperature ranges from 0 °C to 180 °C, preferably from 40 °C to 120 °C, more preferably from 60 °C to 90 °C.

0053The molecular weight distribution can be varied by using mixtures of different metallocenes or by carrying out the polymerization in various steps differing in the polymerization temperature and/or in the concentration of the polymerization monomers.

0054The following examples are reported for illustrative purposes.

GENERAL PROCEDURES AND CHARACTERIZATIONS

0055All operations were performed under nitrogen by using conventional Schlenk-line techniques. Solvents were purified by degassing with N₂ and passing over activated (8 hours, N₂ purge, 300 °C) Al₂O₃, and stored under nitrogen. The cocatalyst was a commercial MAO from Witco AG (10 % wt solution in toluene).Me₂Si(Me₄Cp)(NtBu)TiCl₂ was purchased from Witco AG.

¹H-NMR

0056The proton spectra of ligands and metallocenes were obtained using a Bruker DPX 200 spectrometer operating in the Fourier transform mode at room temperature at 200.13 MHz. The samples were dissolved in CDCl₃, CD₂Cl₂, C₆D₆ or C₆D₅CD₃. As a reference, the residual peak of CHCl₃, CHDCl₂, C₆D₅H or C₆D₅CH₃ in the ¹H spectra (7.25 ppm, 5.35 ppm, 7.15 and 2.10 ppm respectively) were used. Proton spectra were acquired with a 15° pulse and 2 seconds of delay between pulses; 32 transients were stored for each spectrum. All NMR solvents were dried over activated molecular sieves, and kept under nitrogen. Preparation of the samples was carried out under nitrogen using standard inert atmosphere techniques.

¹³C-NMR

0057Carbon spectra were obtained using a Bruker DPX-400 spectrometer operating in the Fourier transform mode at 120 °C at 100.61 MHz. The samples were dissolved in C₂D₂Cl₄. The peak of the <i>mmmm</i> pentad in the ¹³C spectra (21.8 ppm) was used as a reference. The carbon spectra were acquired with a 90° pulse and 12 seconds of delay between pulses. About 3000 transients were stored for each spectrum. The ethylene content was determined according to M. Kakugo, Y. Naito, K. Mizunuma, T. Miyatake, Macromolecules 1982, 15, 1150. The 1-butene content was determined from the diad distribution, from the S_αα carbons, as described in <nplcit id="ncit0002" npl-type="s"><text>J.C. Randall, Macromolecules 1978, 11, 592</text></nplcit>.

GC-MS

0058GC-MS analyses were carried out on a HP 5890 - series 2 gas chromatograph and a HP 5989B quadrupole mass spectrometer.

VISCOSITY MEASUREMENTS

0059The intrinsic viscosity (I.V.) was measured in tetrahydronaphtalene (THN) at 135°C.

0060The polymer molecular weights were determined from the viscosity values.

DSC ANALYSIS

0061Melting point and heat of fusion measurements were carried out on a Perkin Elmer DSC 7 instrument by heating the sample from 25 °C to 200 °C at 10 °C/min, holding for 2 min at 200 °C, cooling from 200 °C to 25 °C at 10 °C/min, holding for 2 min at 25 °C, heating from 25 °C to 200 °C at 10 °C/min. The reported values are those determined from the second heating scan.

0062T_g values were determined on a DSC30 Mettler instrument equipped with a cooling device, by heating the sample from 25 °C to 200 °C at 20 °C/min, holding for 10 min at 200 °C, cooling from 200 °C to -140 °C, holding for 2 min at -140 °C, heating from -140 °C to 200 °C at 20 °C/min. The reported values are those determined from the second heating scan.

<u style="single">Example 1:</u>

synthesis of dimethylsilyl(tert-butylamido)(N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl titanium (B-1)

0063<chemistry id="chem0026" num="0026"><img file="EP1533324B1_D0026.tif" /></chemistry>

<i>First Synthetic route</i>

(a) Synthesis of 2-methyl-5,6-dihydroindeno[2,1-b]indole

0064All operations were carried out in air, with out-of-the bottle solvents and reagents: isopropanol, RPE Carlo Erba (99%); 2-indanone, Chemische Fabrik Berg (98%); p-tolyl-hydrazine hydrochloride, Aldrich (98%).

0065In a 1-L jacketed glass reactor (Büchi) with magnetically driven, three blade stirrer, connected to a thermostat for temperature control, were charged 85.0 g of 2-indanone (Mw=132.16, 0.63 mol), 102.0 g of <i>p</i>-M_CC₆H₄NHNH₂·HCl (Mw=158.63, 0.63 mol) and 0.5 L of <i>i</i>-PrOH. The thick suspension was warmed to 80 °C in about 30 minutes and the slurry darkened to dark brown under stirring. The mixture was stirred at 80 °C for 1 hour and then was cooled to room temperature in about 30 minutes.

0066The slurry was siphoned into 1.2 L of water containing 1.5 equivalents of NaHCO₃, thus obtaining a fine dispersion of a dark green product (no heat evolution was observed). The slurry was then filtered on a G3 frit, washed with water, dried in air under moderate vacuum, then in the rotating evaporator at 80°C and finally under high vacuum (mechanical pump).

0067121.2 g of the target product were obtained with a yield of 87.3% (purity of 99.6 % by G.C.)

0068¹H-NMR (CDCl₃, δ, ppm): 2.52 (s, 3H, CH₃); 3.70 (s, 2H, CH₂); 7.01-7.66 (m, 7H, Ar); 8.13 (bs, 1H, <i>N</i>-H).

(b) Synthesis of N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indole

006910.2 g of 2-methyl-5,6-dihydroindeno[2,1-b]indole (Mw=219.28, purity 99.6%, 46.33 mmol), obtained as reported above, were dissolved in 100 mL of 1,3-dioxolane (Aldrich) at room temperature. 5.42 g of <i>tert-</i>BuOK (Fluka, 97%, Mw=112.22, 46.85 mmol) were then added; the solution changed color from green to dark brown and was stirred at room temperature for 10 minutes; then 2.90 mL of MeI (Mw=141.94, d=2.280, 46.58 mmol) were added. After 15 minutes of stirring, a solid started forming. Stirring was continued for 1 hour, then the reaction mixture was poured into water containing 4 g of NH₄Cl. The formed solid was isolated by filtration and dried in vacuo, to obtain 9.5 g of the target product as a microcrystalline brown solid in pure state, with a yield of 86.3% (purity of 98.2% by G.C.). ¹H-NMR (CDCl₃, δ, ppm): 2.52 (s, 3H, CH₃); 3.68 (s, 2H, CH₂); 3.78 (s, 3H, <i>N</i>-CH₃); 7.02-7.64 (m, 7H, Ar).

(c) Synthesis of chlorodimethyl(N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indol-6-yl)silane

00709.5 mL of a 2.5 M solution of <i>n</i>-BuLi in hexane (23.75 mmol) were added dropwise to a solution of 5.1 g of N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indole, obtained as reported above, (purity 98.2%, Mw=233.32, 21.46 mmol; indenoindole: <i>n</i>-BuLi = 1:1.1) in 70 mL of THF, previously cooled to -78°C. At the end of the addition, the brown solution was allowed to warm up to room temperature and stirred for 6 hours. Then it was cooled again to -78°C and added dropwise to a solution of dichlorodimethylsilane (Mw=129.06, d=1.064, 2.6 mL, 21.43 mmol; indenoindole: Me₂SiCl₂ = 1:1) in 20 mL of THF, previously cooled to -78°C. At the end of the addition, the reaction mixture was allowed to warm up to room temperature and stirred overnight. The solvents were evaporated under reduced pressure to give a brown sticky solid, which at the ¹H-NMR analysis resulted to be the target product, with few by-products. The product was used in the subsequent step without further purification. ¹H-NMR (CDCl₃, δ, ppm): - 0.13 (s, 3H, Si-CH₃); 0.48 (s, 3H, Si-CH₃); 2.53 (s, 3H, CH₃); 3.44 (s, 1H, CH); 3.88 (s, 3H, <i>N</i>-CH₃); 6.90-7.71 (m, 7H, Ar).

(d) Synthesis of 6-[dimethylsilyl(tert-butylamino)]N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indole

00713.96 g of chlorodimethyl(N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indol-6-yl)silane (Mw=325.92, 12.15 mmol), obtained as described above, were dissolved in 50 mL of toluene and added at -78°C to a solution of <i>t</i>-BuNH₂ (3.0 mL, Mw=73.14, d= 0.696, 28.55 mmol) in 20 mL of toluene. At the end of the addition, the reaction mixture was allowed to warm up to room temperature and stirred for 2 days to give a black suspension, which was filtered to remove the ammonium salt formed. The filtrate was concentrated under vacuum, obtaining 3.49 g of the target product, as a black sticky solid (raw yield = 79.2%). ¹H-NMR (CDCl₃, δ, ppm): - 0.15 (s, 3H, Si-CH₃); - 0.04 (s, 3H, Si-CH₃); 1.23 (s, 9H, <i>t</i>-Bu); 2.52 (s, 3H, CH₃); 3.44 (s, 1H, CH); 3.86 (s, 3H, <i>N</i>-CH₃); 6.90-7.71 (m, 7H, Ar).

(e) Synthesis of dimethylsilyl(tert-butylamido)(N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl titanium

007225.3 mL of a 1.6 M solution of MeLi in diethylether (40.48 mmol) were added dropwise at room temperature to a solution of 3.49 g of 6-[dimethylsilyl(<i>tert</i>-butylamino)]N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indole (Mw=362.60, 9.62 mmol), obtained as reported above, in 45 mL of Et₂O. The reaction mixture was stirred overnight: an increasing turbidity developed with final formation of a black suspension. Then 1.05 mL of TiCl₄ (Mw 189.71, d=1.730, 9.62 mmol) in 40 mL of pentane were slowly added at room temperature, and the resulting mixture was stirred overnight. The solvents were removed under reduced pressure to give a black sticky solid, which was extracted with 50 mL of toluene. The extract was then concentrated, yielding 3.02 g of the desired compound as a black powder (raw yield = 71.6%). ¹H-NMR (C₆D₆, δ, ppm): - 0.02 (s, 3H, Ti-CH₃); 0.07 (s, 3H, Ti-CH₃); 0.56 (s, 3H, Si-CH₃); 0.74 (s, 3H, Si-CH₃); 1.41 (s, 9H, <i>t</i>-Bu); 2.45 (s, 3H, CH₃); 3.12 (s, 3H, <i>N</i>-CH₃); 6.90-7.94 (m, 7H, Ar).

<i>Second Synthetic route</i>

(a) Synthesis of N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indole

007322.37 g of 2-methyl-5,6-dihydroindeno[2,1-b]indole (99.6% by G.C., Mw = 219.28, 101.6 mmol) were dissolved into 220 mL of 1,3-dioxolane (Aldrich) at room temperature and added of 11.46 g of <i>t</i>-BuOK (Aldrich, Mw = 112.22, 101.6 mmol). The solution changed colour from green to dark brown and was stirred at room temperature for 10 minutes; then 6.33 mL of MeI (Acros, Mw = 141.94, d = 2.280, 101.6 mmol) were added. After 15 minutes stirring, a solid started forming. Stirring was continued for 1 hour, then the reaction mixture was poured into water containing 8 g of NH₄Cl (Carlo Erba RPE, purity 99.5%). After two hours stirring, the formed solid was isolated by filtration and dried in vacuo to give 23.2 g of a brown powder, which was analysed by NMR spectroscopy and GC-MS. The GC-MS analysis showed a purity in the desired product of 91.5% (yield = 89.5%). 2-methyl-5,6-dihydroindeno[2,1-b]indole and N-methyl-2,6-dimethyl-5,6-hydroindeno[2,1-b] indole were also present, in percentage of 2.6% and 3.7%, respectively.

0074An aliquot of the product (9.98 g) was suspended in 150 mL of MeOH (Carlo Erba RPE, purity 99.9%, b.p.= 64.6°C). After 30 min stirring at room temperature, a dark brown microcrystalline powder was isolated by filtration (9.18 g). The GC-MS analysis showed a higher purity (99.0%) in the desired product. ¹H NMR (CDCl₃, δ, ppm): 2.53 (s, 3H, CH₃); 3.65 (s, 2H, CH₂); 3.76 (s, 3H, <i>N</i>-CH₃); 7.00-7.60 (m, 7H, Ar). ¹³C NMR (CDCl₃, δ, ppm): 21.52 (CH₃); 29.98 (CH₂); 31.08 (N-CH₃); 109.38; 118.11; 119.13; 121.83; 122.14; 122.26; 124.62; 126.95; 129.11 (2C); 139.59; 140.50; 142.14; 148.87. m/z (%): 233 (100) [M⁺]; 218 (35).

(b) Synthesis of (<i>tert</i>-butylamino)dimethylchlorosilane

007515.7 mL of Me₂SiCl₂ (Mw = 129.06, d = 1.07, 130.21 mmol) in 20 mL of Et₂O were added dropwise at 0°C to a solution of 20.0 g of <i>t</i>-BuNH₂ (Mw = 73.14, d = 0.696, 273.44 mmol, <i>t</i>-BuNH₂: Me₂SiCl₂ = 2.1:1) in 40 mL of Et₂O. The resulting solution was allowed to warm up to room temperature and stirred for 1.5 hours. It was observed a colour change from yellow to light yellow with final formation of a white milky suspension. The latter was filtered and the filtrate concentrated in vacuo to give 18.93 g of a light yellow oil, which by ¹H-NMR analysis appeared to be mainly the target product, together with a by-product, identified as di(<i>t</i>-butylamino)dimethylsilane. The silylamine was used in the subsequent step without further purification. Yield 65.8% (purity by ¹H NMR = 75.0% mol.) ¹H-NMR (CD₂Cl₂, δ, ppm): 0.48 (s, 6H, Si-CH₃); 1.26 (s, 9H, <i>t</i>-Bu); 1.42 (bs, 1H, NH).

(c) Synthesis of 6-[dimethylsilyl(<i>tert</i>-butylamino)]N-methyl-2-methyl-5,6-dihydro indeno [2,1-b]indole

00766.66 mL of <i>n</i>-BuLi 2.5 M in hexane (16.65 mmol) were added dropwise at 0°C to a solution of 3.53 g of N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indole (Mw = 233.32, purity 99.0%, 15.13 mmol) in Et₂O. At the end of the addition, the reaction mixture was allowed to warm up to room temperature and stirred for two hours. Subsequently, 3.34 g of <i>(tert</i>-butylamino)dimethylchlorosilane (Mw = 165.74, purity 75.0% mol., d = 0.887, 20.17 mmol) were added at 0°C to the Li salt suspension and the resulting mixture was allowed to warm up to room temperature. After three hours stirring, the solvents were evaporated under reduced pressure and the residue was dissolved in 50 mL of toluene, obtaining a dark brown suspension, which was filtered. The filtrate was evaporated to dryness under reduced pressure, obtaining 5.86 g of a dark brown oil, which resulted to be 86.5% wt. pure (calculated by ¹H-NMR). Yield = 92.4%. ¹H-NMR (C₆D₆, δ, ppm): - 0.14 (s, 3H, Si-CH₃); - 0.13 (s, 3H, Si-CH₃); 0.99 (s, 9H, <i>t</i>-Bu); 2.54 (s, 3H, CH₃); 3.27 (s, 3H, <i>N</i>-CH₃); 3.40 (s, 1H, CH); 7.10-7.90 (m, 7H, Ar). m/z (%): 362 (39) [M⁺]; 232 (16); 130 (100); 74 (18).

(d) Synthesis of dimethylsilyl(tert-butylamido)(N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl titanium

007719.14 mL of a 1.6 M solution of MeLi in diethylether (30.63 mmol) were added dropwise at 0°C to a solution of 2.76 g of 6-[dimethylsilyl(<i>tert</i>-butylamino)]N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indole (Mw=362.60, 7.62 mmol), obtained as reported above, in 40 mL of Et₂O. The resulting dark brown solution was allowed to warm up to room temperature and stirred for 1.5 hours. Then 0.84 mL of TiCl₄ (Mw 189.71, d=1.730, 7.63 mmol) in 4 mL of pentane were slowly added at room temperature and the resulting black suspension stirred for 1.5 hours. The solvents were removed under reduced pressure and the residue was extracted with 50 mL of toluene. The extract (3.07 g) was added of 70 mL of pentane, the resulting dark brown suspension stirred for 30 min at room temperature and filtered, giving as residue a light brown powder, which was dried and analysed by ¹H-NMR. The ¹H-NMR analysis showed a purity of 97.0% wt. in the desired catalyst together with a 3.0% wt. of starting ligand. Yield = 64.4% (2.22g). ¹H-NMR (C₆D₆, δ, ppm): -0.02 (q, 3H, Ti-CH₃, J= 0.36 Hz); 0.07 (q, 3H, Ti-CH₃, J= 0.36 Hz); 0.55 (s, 3H, Si-CH₃); 0.74 (s, 3H, Si-CH₃); 1.39 (s, 9H, <i>t</i>-Bu); 2.43 (s, 3H, CH₃); 3.10 (s, 3H, <i>N</i>-CH₃); 6.91 (d, 1H, J=8.31 Hz); 7.02 (ddd, 1H, J=8.61, 6.87, 1.17 Hz); 7.13 (dq, 1H, J=8.31, 1.57, 0.59 Hz); 7.31 (ddd, 1H, J=8.26, 6.87, 0.96 Hz); 7.80 (dt, 1H, J=8.61, 0.96 Hz); 7.77-7.79 (m, 1H, Ar); 7.92 (dt, 1H, J=8.26, 1.17 Hz). ¹³C-NMR (C₆D₆, δ, ppm): 6.91 (<i>C</i>-Si); 7.37 (<i>C</i>-Si); 21.66 (CH₃); 33.01 (<i>N</i>-CH₃); 34.62 (<i>t</i> -Bu); 55.56 (<i>C</i>-Ti); 57.24 (<i>C</i>-Ti); 68.74 (<i>C</i>- <i>t</i>-Bu); 109.43 (<i>C</i>H); 120.76 (<i>C</i>H); 124.17 (<i>C</i>H); 124.27 (<i>C</i>H); 125.22 (<i>C</i>H); 125.76 (<i>C</i>H); 128.44 (<i>C</i>H). m/z (%) by "direct insertion probe" technique: 439 (32) [M⁺ + 1]; 422 (100); 407 (26).

<u style="single">Example 2:</u>

Synthesis of dimethylsilyl(tert-butylamido)(N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl titanium (B-2)

0078<chemistry id="chem0027" num="0027"><img file="EP1533324B1_D0027.tif" /></chemistry>

(a) Synthesis of 2-methoxy-5,6-dihydroindeno[2,1-b]indole

00798.21 g of 2-indanone (Aldrich, 98%, Mw=132.16, 60.88 mmol), 40 mL of isopropanol, 10.84 g of p-methoxyphenylhydrazin hydrochloride (Aldrich, 98%, Mw=174.63, 60.83 mmol) were charged at room temperature in a 250 mL flask equipped with magnetic stirrer. The slurry was brought to reflux (82°C), (a black slurry was obtained), and kept at reflux for 1 hour. The dark brown viscous suspension was then cooled to room temperature; 200 mL of water saturated with NaHCO₃ were added into the reactor (final pH ca. 7.5-8), the resulting mixture was filtered and the residue washed with plenty of water. The dark green solid on the filter was dried in vacuo at 70 °C for 4 hours (14 g, 98.9 % pure by GC, 96.7 % yield of pure product). ¹H-NMR (CDCl₃, δ, ppm): 3.69 (s, 2H, CH₂); 3.93 (s, 3H, <i>O</i>-CH₃); 6.83-7.64 (m, 7H, Ar); 8.14 (bs, 1H, <i>N</i>-H).

(b) Synthesis of N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indole

00807.53 g of 2-methoxy-5,6-dihydroindeno[2,1-b]indole, obtained as reported above, (Mw=235.29, purity of 98.9%, 31.65 mmol) were dissolved in 60 mL of 1,3-dioxolane (Aldrich) at room temperature. 3.6 g of <i>tert</i>-BuOK (Fluka, Mw=112.22, 31.90 mmol) were added: the solution changed color from green to dark brown, and was stirred at room temperature for 10 min. Then 1.96 mL of MeI (Mw 141.94, d = 2.280, 31.50 mmol) were added. After 10 min of stirring, a solid started forming. Stirring was continued for 1 hour, then the mixture was poured into water containing 5 g of NH₄Cl. The formed solid was isolated by filtration, the brown residue was dried in vacuo to obtain 7.85 g of microcrystalline brown solid: GC purity 85.8%, 85.2 % yield of pure product. ¹H-NMR (CDCl₃, δ, ppm): 3.65 (s, 2H, CH₂); 3.75 (s, 3H, <i>N</i>-CH₃); 3.93 (s, 3H, <i>O</i>-CH₃); 6.85-7.61 (m, 7H, Ar).

(c) Synthesis of chlorodimethyl(N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)silane

00813.4 mL of a 2.5 M solution of <i>n</i>-BuLi in hexane (8.50 mmol) were added dropwise to a solution of 2.22 g of N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indole, obtained as reported above, (Mw=249.32, purity 85.8%, 7.64 mmol; indenoindole: <i>n</i>-BuLi = 1:1.1) in 50 mL of THF, previously cooled to -78°C. At the end of the addition, the brown solution was allowed to warm up to room temperature and stirred for 5 hours. Then it was cooled again to -78°C and added dropwise to a solution of dichlorodimethylsilane (Mw=129.06, d=1.064, 0.92 mL, 7.64 mmol; indenoindole: Me₂SiCl₂ = 1:1) in 20 mL of THF, previously cooled to -78°C. At the end of the addition, the dark brown solution was allowed to warm up to room temperature and stirred overnight. The solvents were evaporated under reduced pressure to give the desired product, containing few by-products, in the form of a brown sticky solid; this product was used in the following step without further purification.

d) Synthesis of 6-[dimethylsilyl(tert-butylamino)]N-methyl-2-methoxy 5,6-dihydro indeno [2,1-b]indole

00823.25 g of crude chlorodimethyl(N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)silane (Mw=341.91, 9.50 mmol), obtained as reported above, were dissolved in 50 mL of toluene and added at -78°C to a solution of <i>t</i>-BuNH₂ (2.3 mL, Mw=73.14, d= 0.696, 21.89 mmol) in 20 mL of toluene. At the end of the addition, the reaction mixture was allowed to warm up to room temperature and stirred overnight to give a brown suspension, which was filtered to remove the ammonium salt formed. The filtrate was concentrated under vacuum to give 2.18 g of the desired product as a brown sticky solid (raw yield = 60.6%). This product was used in the next step without further purification. ¹H-NMR (CDCl₃, δ, ppm): -0.14 (s, 3H, Si-CH₃); -0.02 (s, 3H, Si-CH₃); 1.23 (s, 9H, <i>t</i>-Bu); 3.86 (s, 3H, <i>N</i>-CH₃); 3.926 (s, 1H, CH); 3.934 (s, 3H, <i>O</i>-CH₃); 6.80-7.70 (m, 7H, Ar).

0083The fraction insoluble in toluene was extracted with 30 mL of CH₂Cl₂ and 0.58 g of the by-product bis(N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl silane, formed in the previous step, were isolated as a light brown powder (13.7% yield towards starting N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indole). ¹H-NMR (CDCl₃, δ, ppm): - 0. 23 (s, 6H, Si-CH₃); 3.35 (s, 6H, <i>N</i>-CH₃); 3.91 (s, 6H, <i>O</i>-CH₃); 3.93 (s, 2H, CH); 6.82-7.63 (m, 14H, Ar).

(e) Synthesis of dimethylsilyl(tert-butylamido)(N-methyl-2-methoxy 5,6-dihydroindeno[2,1-b]indol-6-yl) dimethyl titanium

008415.6 mL of a 1.6 M solution of MeLi in diethylether (24.96 mmol) were added dropwise at room temperature to a solution of 2.18 g of 6-[dimethylsilyl(tert-butylamino)]N-methyl-2-methoxy-5,6-dihydroindeno[2,1-b]indole (Mw=378.58, 5.76 mmol), obtained as reported above, in 45 mL of Et₂O. The reaction mixture was stirred for 5 hours at room temperature with final formation of a dark brown suspension. Then 0.65 mL of TiCl₄ (Mw=189.71, d=1.730, 5.93 mmol) in 20 mL of pentane were slowly added at room temperature, and the resulting mixture was stirred overnight. The solvents were removed under reduced pressure to give a black solid, which was extracted with 35 mL of toluene. The extract was concentrated yielding 1.16 g of the target product as a brown powder (raw yield = 44.3%). ¹H-NMR (C₆D₆, δ, ppm): - 0.01 (s, 3H, Ti-CH₃); 0.04 (s, 3H, Ti-CH₃); 0.55 (s, 3H, Si-CH₃); 0.74 (s, 3H, Si-CH₃); 1.40 (s, 9H, <i>t</i>-Bu); 3.09 (s, 3H, <i>N</i>-CH₃); 3.55 (s, 3H, <i>O</i>-CH₃); 6.82-7.92 (m, 7H, Ar).

<u style="single">Example 3:</u>

synthesis of dimethylsilyl(tert-butylamido)(N-methyl-2-methyl-1,8-dihydroindeno[2,1-b]pyrrol-6-yl)dimethyl titanium (B-3)

0085<chemistry id="chem0028" num="0028"><img file="EP1533324B1_D0028.tif" /></chemistry><ol id="ol0003" compact="compact"><li>(a) N-methyl-2-methyl-1,8-dihydroindeno[2,1-b]pyrrole was prepared according to the protocol described in <patcit id="pcit0021" dnum="WO9924446A"><text>Patent Application WO 99/24446</text></patcit>.</li><li><b>(b) Synthesis of 8-[dimethylsilyl(<i>tert</i>-butylamino)]N-methyl-2-methyl-1,8-dihydroindeno [2,1-b]pyrrole</b></li></ol>

008618 mL of 1.6 M solution of BuLi (28.8 mmol) in hexane was added dropwise to a solution of 3.5 g of <i>N</i>-Me-2-Me-indenopyrrole (19 mmol) in 60mL of ether at -30 °C. At the end of the addition the solution was allowed to warm up to room temperature and stirred for 4 hours. Then it was cooled again to -30 °C and treated with 5 mL of Me₂SiCl₂ (42 mmol) in 5 mL of ether. The mixture was allowed to warm up to room temperature and stirred overnight. The resulting suspension was filtered, the solvent was evaporated in vacuum. The crude product was dissolved in 50 mL of ether and then was treated dropwise with 17.5 mL (167 mmol) of <i>t</i>-butylamine at -20 °C. The resulting mixture was allowed to warm up to room temperature and then stirred overnight. The solution was isolated by filtration and the solvent was evaporated to give the silyl-amine as a reddish-brown oil. Yield 4.67 g (83 %). ¹H NMR (toluene-d⁸): 7.48 (d, 1H); 7.44 (d, 1H); 7.23 (t, 1H); 7.05(t, 1H); 6.18 (1H); 3.12 (s, 3H); 2.15 (s, 3H); 1.02 (s, 9H); -0.11 (s, 3H); -0.12 (s, 3H).

(c) Synthesis of dimethylsilyl(tert-butylamido)(N-methyl-2-methyl-1,8-dihydroindeno[2,1-b]pyrrol-6-yl) dimethyl titanium

008749 mL of a 1.33 M solution of MeLi in diethyl ether (65.2 mmol) were added dropwise at -20 °C to a solution of 4.15 g of 8-[dimethylsilyl(tert-butylamino)]-N-methyl-2-methyl-indenopyrrole (14 mmol) in 60 mL of ether. The reaction mixture was stirred overnight and then was cooled to -30 °C and was treated with 1.54 mL of TiCl₄ (14 mmol) in 60 mL of hexane. The resulting black mixture was stirred overnight, then it was evaporated and added with 60 mL of toluene. Then the reaction mixture was evaporated and the residue was extracted twice with 50 mL of toluene. The resulting solution was evaporated to a volume of 15 mL and kept at room temperature for 15 hours. Red crystals were isolated, washed twice with 10 mL of cooled pentane and dried. Yield 2.1 g. ¹H NMR (toluene-d⁸): 7.68 (d, 1H); 7.61 (d, 1H); 7.20 (dd, 1H); 6.94 (dd, 1H); 6.13 (s, 1H); 2.88 (s, 3H); 1.98 (s, 3H); 1.41 (s, 9H); 0.73 (s, 3H); 0.51 (s, 3H); 0.05 (s, 3H); -0.04 (s, 3H)

<u style="single">Example 4:</u>

synthesis of dimethylsilyl(<i>tert</i>-butylamido)(N-ethyl-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl titanium (B-4)

0088<chemistry id="chem0029" num="0029"><img file="EP1533324B1_D0029.tif" /></chemistry>

(a) Synthesis of 5,6-dihydroindeno[2,1-b]indole

0089In a 1-L flask were charged 36.55 g of 2-indanone (Aldrich, Mw=132.16, 276.6 mmol), 40.00 g of phenyl-hydrazine hydrochloride (Aldrich, 99%, Mw=144.61, 276.6 mmol) and 0.3 L of <i>i</i>-PrOH. The suspension was warmed to 80 °C in about 30 minutes and the slurry changed colour from yellow to dark brown under stirring. The reaction mixture was stirred at 80 °C for 1.5 hours and then was cooled to room temperature in about 30 minutes. The slurry was siphoned into 1.0 L of water containing 34.85 g of NaHCO₃, thus obtaining a fine dispersion of a green product (no heat evolution was observed). The slurry was then filtered on a G4 frit, washed with water, dried in air under moderate vacuum for 24 h until to achieve constant weight. 52.81 g of the target product as a green powder were obtained with a yield of 92.8% (purity of 99.8 % by G.C.) ¹H-NMR (CDCl₃, δ, ppm): 3.72 (s, 2H, CH₂); 7.12 (td, 1H, H8, J=7.48, 1.17 Hz); 7.16-7.29 (m, 2H, H2, H3); 7.31-7.39 (m, 2H, H1, H9); 7.42 (dt, 1H, H7, J=7.24 Hz); 7.66 (dt, 1H, H10, J=7.48 Hz); 7.85-7.89 (m, 1H, H4); 8.26 (bs, 1H, <i>N</i>-H). ¹³C-NMR (CDCl₃, δ, ppm): 31.51 (<i>C</i>H₂); 112.18 (<i>C</i>-H1); 118.77 (<i>C</i>-H10); 119.56 (<i>C</i>-H4); 120.73, 121.84 (<i>C</i>-H2, <i>C</i>-H3); 122.47 (<i>C</i>10c); 122.91 (<i>C</i>-H8); 125.05 (<i>C</i>-H7); 127.38 (<i>C</i>-H9); 140.32 (<i>C</i>10b); 140.93 (<i>C</i>4a); 142.88 (<i>C</i>6a,10a); 146.44 (<i>C</i>5a).

(b) Synthesis of N-ethyl-5,6-dihydroindeno[2,1-b]indole

009015.00 g of 5,6-dihydroindeno[2,1-b]indole (99.8% by G.C., Mw = 205.26, 73.1 mmol) were dissolved into 200 mL of 1,3-dioxolane (Aldrich) at room temperature in a 0.5-L flask. 8.28 g of <i>t</i>-BuOK (Fluka, 99%, Mw = 112.22, 73.1 mmol) were added and the reaction mixture turned from a green suspension to a brown solution. After 30 min stirring at room temperature, 5.51 mL of EtBr (Fluka, 99%, Mw = 108.97, d = 1.46, 73.1 mmol) were added, obtaining a brown suspension. Stirring was continued for 2 hours, then the reaction mixture was poured into water containing 8 g of NH₄Cl (Carlo Erba RPE, purity 99.5%). After two hours stirring, the green-brown suspension was filtered on a G4 frit, the solid dried in air under moderate vacuum to give a green powder (8.98 g), which was analysed by ¹H NMR. Purity 98.9% wt. by ¹H NMR (yield = 52.1%). ¹H-NMR (CDCl₃, δ, ppm): 1.48 (t, 3H, CH₃, J=7.26 Hz); 3.73 (s, 2H, CH₂); 4.24 (q, 2H, CH₂, J=7.26 Hz); 7.04-7.90 (m, 8H, Ar).

(c) Synthesis of (<i>tert</i>-butylamino)dimethylchlorosilane

009115.95 mL of Me₂SiCl₂ (Mw = 129.06, 99%, d = 1.064, 130.21 mmol) in 20 mL of Et₂O were added dropwise at 0°C to a solution of 20.41 g of <i>t</i>-BuNH₂ (Mw = 73.14, 98%, d = 0.696, 273.45 mmol, <i>t</i>-BuNHz: Me₂SiCl₂ = 2.1:1) in 40 mL of Et₂O. The resulting milky suspension was allowed to warm up to room temperature and stirred for 30 min. The solvent was removed and the residue extracted with 50 mL of pentane, to give 13.76 g of a colourless oil, which by ¹H-NMR analysis appeared to be the target product 83.7% wt. pure, together with 16.3% wt. of di(<i>t</i>-butylamino)dimethylsilane. The silylamine was used in the subsequent step without further purification. Yield 53.4%. ¹H-NMR (CDCl₃, δ, ppm): 0.44 (s, 6H, Si-CH₃); 1.21 (s, 9H, <i>t</i>-Bu).

(d) Synthesis of 6-[dimethylsilyl(<i>tert</i>-butylamino)]N-ethyl-5,6-dihydro indeno[2,1-b]indole

00928.02 mL of <i>n</i>-BuLi 2.5 M in hexane (20.04 mmol) were added dropwise at 0°C to a solution of 4.30 g of N-ethyl-5,6-dihydroindeno[2,1-b]indole (Mw = 233.31, purity 98.9%, 18.22 mmol) in Et₂O. At the end of the addition, the reaction mixture was allowed to warm up to room temperature and stirred for two hours. The dark brown solution obtained was added at 0°C to a solution of 4.32 g of (<i>tert</i>-butylamino)dimethylchlorosilane (Mw = 165.74, purity 83.7 % wt., d = 0.887, 21.86 mmol) in Et₂O. The final mixture was allowed to warm up to room temperature and stirred for three hours. Then the solvents were evaporated under reduced pressure to give a residue (8.73 g) which was extracted with 50 mL of toluene. The extract, a sticky brown solid (7.48 g), was washed with pentane obtaining 4.32 g of a light brown powder, which was analysed by ¹H-NMR. The ¹H-NMR analysis showed a purity of 96.6% wt. in the desired ligand together with a 3.4% wt. of starting N-ethyl-5,6-dihydroindeno [2, 1 -b] indole. Yield = 63.1%. ¹H-NMR (C₆D₆, δ, ppm): -0.23 (s, 3H, Si-CH₃); -0.01 (s, 3H, Si-CH₃); 0.41 (bs, 1H, NH); 0.99 (s + t, 12H, <i>t</i>-Bu + CH₃); 3.56 (s, 1H, CH); 4.07 (m, 2H, CH₂); 7.15-8.07 (m, 8H, Ar). ¹H-NMR (CDCl₃, δ, ppm): -0.13 (s, 3H, Si-CH₃); 0.03 (s, 3H, Si-CH₃); 0.75 (bs, 1H, NH); 1.26 (s, 9H, <i>t</i>-Bu); 1.37 (t, 3H, CH₃, J = 7.14 Hz); 3.84 (s, 1H, CH); 4.50 (m, 2H, CH₂); 6.90-8.00 (m, 8H, Ar).

(e) Synthesis of dimethylsilyl(tert-butylamido)(N-ethyl-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl titanium

009316.13 mL of a 1.6 M solution of MeLi in diethylether (25.80 mmol) were added dropwise at 0°C to a solution of 2.30 g of 6-[dimethylsilyl(<i>tert</i>-butylamino)]N-ethyl-5,6-dihydroindeno[2,1-b]indole (Mw=362.60, 6.34 mmol), obtained as reported above, in 40 mL of Et₂O. The resulting dark brown suspension was allowed to warm up to room temperature and stirred for 3 hours. Then 0.70 mL of TiCl₄ (Mw 189.71, d=1.730, 6.34 mmol) in 4 mL of pentane were slowly added at room temperature and the resulting dark brown suspension stirred for 1 hour. The solvents were removed under reduced pressure and the residue (4.63 g) was extracted with 50 mL of toluene. The extract (2.27 g of a sticky dark brown powder) was washed with pentane and the residue dried giving a brown powder (1.7 g), which was analysed by ¹H-NMR. The ¹H-NMR analysis showed a purity of 97.6% wt. in the desired catalyst together with a 2.4% wt. of starting ligand. Yield = 79.7%. ¹H-NMR (C₆D₆, δ, ppm): -0.002 (q, 3H, Ti-CH₃, J= 0.41 Hz); 0.09 (q, 3H, Ti-CH₃, J= 0.41 Hz); 0.61 (s, 3H, Si-CH₃); 0.73 (s, 3H, Si-CH₃); 1.05 (t, 3H, CH₃, J=7.26); 1.41 (s, 9H, <i>t</i>-Bu); 3.78 (q, 2H, CH₂, J=7.26 Hz); 6.98-7.06 (m, 2H, H3, H8); 7.24-7.33 (m, 3H, H1, H4 and H9); 7.80 (dt, 1H, J = 8.67 Hz, H7); 7.88-7.93 (m, 2H, H2, H10). ¹³C-NMR (C₆D₆, δ, ppm): 6.62 (Si-<i>C</i>H₃); 7.63 (Si-<i>C</i>H₃); 14.48 (<i>C</i>H₃); 34.51 (<i>t</i>-Bu); 40.00 (CH₂); 56.90 (Ti-<i>C</i>H₃); 57.01 (Ti-<i>C</i>H₃); 57.81 (<i>C</i>-<i>t</i>-Bu); 67.98 (<i>C</i>-Si); 109.81 (<i>C</i>-H3); 114.56 (<i>C</i>-H10c); 120.48 (<i>C</i>-H1); 120.59 (<i>C</i>-H2); 123.67 (<i>C</i>-10a); 124.08 (<i>C</i>-H10); 124.32 (<i>C</i>-H8); 124.49 (<i>C</i>-H4); 125.27 (<i>C</i>-H9); 128.62 (<i>C</i>-H7); 134.89 (<i>C</i>6a); 145.50 (<i>C</i>4a); 147.34 (<i>C</i>5a).

<u style="single">Example 5:</u>

Synthesis of dimethylsilyl(tert-butylamido)(2,5-dimethyl-7H-thieno[3',2':3,4]cyclopenta[1,2-<i>b</i>]thiophen-7-yl) dimethyl titanium (A-1).

0094<chemistry id="chem0030" num="0030"><img file="EP1533324B1_D0030.tif" /></chemistry>

a) Chloro(2,5-dimethyl-7<i>H</i> thieno[3',2':3,4]cyclopenta[1,2-<i>b</i>]thiophen-7-yl)dimethylsilane.

0095A suspension of 4.13 g (20 mmol) 2,5-dimethyl-7H-cyclopenta[1,2-b:4,3-b']-dithiophene in 80 ml ether was treated dropwise with 15 ml (24 mmol, 20% excess) 1.6M BuLi in hexane at -40 °C under stirring. The mixture was stirred for 3 h, and then treated with 4.82 ml (40 mmol) Me₂SiCl₂ in 10 ml Et₂O. The precipitate was filtered and used without further purification. Yield 4,84 g (81 %), taking into consideration the presence of LiCl (1,02 g, 24 mmol). ¹H NMR (CDCl₃, 30°C) δ: 6.85 (q, 2H), 3.93 (s, 1H), 2.57 (bs, 6H), 0.25 (s, 6H).

<i>b) N-</i>(<i>tert</i>-Butyl)(2,5-dimethyl-7<i>H</i>-thieno[3',2':3,4]cyclopenta[1,2-b]thiophen-7-yl) dimethylsilanamine.

0096A solution of 2.12 ml (20 mmol) <i>tert</i>-butylamine in 70 ml ether was treated dropwise with 12.5 ml (20 mmol) 1.6M BuLi in hexane at -30 °C. The reaction mixture was stirred at r. t. for 3 h and the resulting suspension was treated with a solution of 4.84 g (16.2 mmol) chloro(2,5-dimethyl-7<i>H</i>-thieno[3',2':3,4]cyclopenta[1,2-<i>b</i>]thiophen-7-yl)dimethylsilane in 30 ml ether at -70°C. The resulting suspension was allowed to warm to r.t. and was stirred overnight. The solution was separated from LiC1 and evaporated. Yield 4.47 g (82%) of brown solid that was used without further purification. ¹H NMR (CDCl₃, 30°C) δ: 6.85 (q, 2H), 3.80 (s, 1H), 2.58 (bs, 6H), 1.31 (s,9H), 0.05 (s, 6H).

c) Me₂Si(<i>t</i>-BuN)(2,5-dimethyl-7<i>H</i> thieno[3',2':3,4]cyclopenta[1,2-<i>b</i>]thiophen-7-yl) TiMe₂.

0097To a solution of 1.93 g (5.7 mmol) <i>N</i>-(<i>tert</i>-butyl)(2,5-dimethyl-7<i>H</i>-thieno[3',2':3,4]cyclopenta[1,2-<i>b</i>]thiophen-7-yl)dimethylsilanamine in 30 ml ether 23 ml (28.7 mmol) 1.2M MeLi in ether was added at -40°C under stirring. Then the reaction mixture was stirred under reflux for 3 h. The resulting mixture was cooled to -60°C and the solution of 0.63 ml (5.7 mmol) TiCl₄ in 30 ml hexane was added. The mixture was allowed to warm and was stirred overnight. The resulting mixture was evaporated, the residue was extracted with hexane (3 times with 50 ml). The hexane solution was concentrated to a volume of 10 ml and kept for 10 hours at r.t. The crystalline product was separated from the mother solution, washed twice with cold pentane and dried. Yield 0.27 g (11%) of dark red crystals. ¹H NMR (C₇D₈ ,30°C) δ: 6.76 (q, 2H), 2.20 (d, 6H), 1.49 (s, 9H), 0.56 (s, 6H), 0.36 (s, 6H). ¹³C NMR (C₇D₈, 30°C) δ: 146.51, 139.67, 133.08, 116.65, 78.16, 58.00, 56.82, 34.56,16.29 3.21.

<u style="single">Comparative Example 6:</u>

Synthesis of dimethylsilyl(<i>tert</i>-butylamido)(indenyl)dimethyl titanium (C-3)

0098<chemistry id="chem0031" num="0031"><img file="EP1533324B1_D0031.tif" /></chemistry>

009911.3 mL of a 1.6 M solution of methyllithium in diethyl ether (18.04 mmoles) were slowly added at -78°C to a solution of 1.08 gram (4.40 mmoles) of IndMe₂SiNH<i>^t</i>Bu in 23 mL of diethyl ether. During the addition an increasing turbidity develops with final formation of a yellow suspension. This mixture was allowed to warm to room temperature and stirred for two hours. 0.5 mL of TiCl₄ (4,40 mmoles) were diluted in 23 mL of pentane. This solution was added very slowly and cautiously to the Li salt suspension in diethyl ether at room temperature. The resulting dark suspension was stirred at room temperature overnight. The reaction mixture was then brought to dryness under reduced pressure. The dark solid was extracted with 60 mL of toluene and then the filtrate was evaporated to dryness under reduced pressure to give 0.99 g (70 % yield) of a gray-black solid. ¹H NMR confirms formation of [Me₂Si(Ind)(<i>t</i>-BuN)]TiMe₂. ¹H NMR (C₆D₆, δ, ppm): -0.15 (q, J = 0.48 Hz, 3H, Ti-CH₃), 0.36 (s, 3H, Si-CH₃), 0.53 (s, 3H, Si-CH₃), 0.82 (q, J = 0.48 Hz, 3H, Ti-CH₃), 1.44 (s, 9H, <i>t</i>-Bu); 6.05 (d, J = 3.21 Hz, 1H, Cp-H2); 6.88 (ddd, J = 8.50, 6.64, 1.04 Hz, 1H, Ar-H6); 7.01 (dd, J = 3.21, 0.83 Hz, 1H, Cp-H3); 7.07 (ddd, J = 8.50, 6.64, 1.04 Hz, 1H, Ar-H5); 7.46 (dq, J = 8.50, 1.04 Hz, 1H, Ar-H7); 7.48 (dt, J = 8.50, 1.04 Hz, 1H, Ar-H4).

<u style="single">Comparative Example 7:</u>

synthesis of dimethylsilyl(tert-butylamido)(2-methyl-indenyl)dimethyl titanium (C-4)

0100<chemistry id="chem0032" num="0032"><img file="EP1533324B1_D0032.tif" /></chemistry>

0101The complex dimethylsilyl(<i>tert</i>-butylamido)(2-methyl-1-indenyl) dimethyl titanium was prepared from the corresponding ligand in 71 %, by using the same procedure.

(a) Synthesis of (2-Me-Ind)SiMe₂(<i>^t</i>BuNH)

01025.02 g of (2-Me Ind)SiMe₂Cl (25.53 mmol) in Et₂O were added at 0°C to a solution of <i>^t</i>BuNH₂ (56.16 mmol) to give a yellow slurry. The mixture was stirred at room temperature for 16 h. The solvents were evaporated under reduced pressure, and the product extracted with toluene to give, after filtration and evaporation of the solvent, 5.52 g of an orange oil. ¹H NMR analysis shows the presence of the two isomers (allilic, 60 %, vinylic, 40 %). Yield 83.4 %. ¹H-NMR (C₆D₆, δ, ppm), allylic isomer: -0.09 (s, 3H, Si-CH₃); 0.11 (s, 3H, Si-CH₃); 1.02 (s, 9H, <i>^t</i>Bu); 2.14 (s, 3H, CH₃); 3.21 (s, 1H, C-H); 6.52 (s, 1H, C-H); vinylic isomer: 0.46 (s, 6H, Si-CH₃); 1.1 (s, 9H, <i>^t</i>Bu); 2.06 (s, 3H, CH₃); 3.05 (s, 2H, CH₂); both isomers: 6.98-7.82 (m, 8H, Ar);

(b) Synthesis of Me₂Si(2-Me-Ind)(<i>^t</i>BuN)TiMe₂

010325 mL of MeLi 1.6 M in Et₂O (40 mmol) were added at 0 °C to a solution of 2.53 g of (2-Me Ind)SiMe₂(<i>^t</i>BuNH) (9.75 mmol), after 1.5 h stirring at room temperature were added 1.07 mL of TiCl₄ in pentane (9.75 mmol). After 2 h the solvents were removed under reduced pressure, the mixture taken up in 50 mL of toluene, stirred 30 min, and filtered to give, after evaporation of the solvent, 2.68 g of dark brown powder. The powder was taken up in pentane, filtered, and the filtrated brought to dryness under reduced pressure to give 2.31 g of ochra powder. Yield 70.6 %. ¹H-NMR (C₆D₆, δ, ppm): -0.11 (q, 3H, J=0.48 Hz, Ti-CH₃); 0.46 (bs, 3H, Si-CH₃); 0.56 (bs, 3H, Si-CH₃); 0.85 (q, 3H, J=0.48 Hz, Ti-CH₃); 1.47 (s, 9H, <i>^t</i>Bu); 1.99 (s, 3H, CH₃); 6.76 (bs, 1H, H3); 6.89 (ddd, 1H, H6, J=8.41, 6.77, 1.08 Hz); 7.07 (ddd, 1H, H5, J=8.41, 6.77, 1.08 Hz); 7.44 (dt, 1H, H4, J=8.41, 1.08 Hz); 7.51 (dq, 1H, H7, J=8.41, 1.08 Hz). ¹³C-NMR (C₆D₆, δ, ppm): 5.30 (C-Si); 5.55 (C-Si); 17.98 (CH₃); 33.85 ((CH₃)₃); 50.82 (C-Ti); 56.57 (C-Ti); 57.55 (<i>C-^t</i>Bu); 115.64 (C-H3); 124.72 (C-H6); 124.9 (C-H4); 125.17 (C-H5); 127.81 (C-H7); 131.57 (C-C3a); 133.82 (C-C7a); 140.97 (C-CH₃).

<u style="single">Example 8:</u>

Preparation of the supported catalyst

0104Polyethylene (PE) used as carrier has particles diameter of 250-300 µm, porosity measured with Mercury porosimeter technique (MA 17302) is about 50 % V/V, the surface area is 5.6 m²/g and the average diameter of pores is 8923 Å.

Impregnation

0105The apparatus used for the supportation is a glass cylindrical vessel, equipped with a vacuum pump, a dosing pump for the feeding of the catalytic solution on the carrier and a stirrer to allow a good mixing during the impregnation step. The preparation of the supported catalysts is carried out under nitrogen flow at room temperature. 5 g of the PE carrier described above is loaded into the vessel and mechanically stirred under nitrogen flow, 3 ml of a MAO solution (Witco, 100 g /l in toluene) is dosed in a single addition step on the prepolymer to scavenge residual impurities, in order to reach the incipient wetness. The solvent is then evaporated under vacuum.

0106The catalytic solution is prepared by dissolving 17 mg of B-4 in 9 ml of the same MAO solution, with the aim of achieving an Al/Ti = 400 mol/mol. After stirring for 15 minutes, this solution is added to the carrier in 3 aliquots; after each addition, once reached the incipient wetness, the solvent is evaporated under vacuum.

0107The analysis of the obtained supported catalysts are Al = 7.3 %, Ti = 0.03 %.

POLYMERIZATION TESTS

0108Batch polymerizations were carried out in a 1-L or 4.25-L stainless-steel stirred reactor. The reactor was purified by washing with a hexane solution of TIBA (Al(<i>i</i>-Bu)₃), and then dried by purging with propylene at 80 °C for one hour. The catalyst/cocatalyst mixture was prepared by dissolving the Ti complex in the required amount of MAO/toluene solution, and aged 10 min.

<u style="single">Examples 9-11:</u>

Propylene polymerization

0109MAO (commercial product by Witco, 10 % w/w in toluene, 1.7 M in Al) was used as received. The catalyst system was prepared by dissolving the amount of dimethylsilyl(tert-butylamido)(N-methyl-2-methyl-5,6-dihydroindeno[2,1-b]indol-6-yl)dimethyl titanium (B-1) prepared according example 1, first synthetic route, as reported in Table I, with the amount of MAO reported in Table I; the obtained solution was stirred for 10 minutes at room temperature, before being injected into the autoclave.

01101 mmol of Al(<i>i</i>-Bu)₃ (TIBA) (as a 1 M solution in hexane) and 300 g of propylene were charged, at room temperature, in a 1-L jacketed stainless-steel autoclave, equipped with magnetically driven stirrer and a 35-mL stainless-steel vial, connected to a thermostat for temperature control, previously purified by washing with an Al(<i>i</i>-Bu)₃ solution in hexane and dried at 50°C in a stream of propylene. The autoclave was then thermostatted at 2 °C below the polymerization temperature and the catalyst system, prepared as reported above, was injected in the autoclave by means of nitrogen pressure through the stainless-steel vial. The temperature was rapidly raised to the polymerization temperature, as indicated in Table I, and the polymerization was carried out at constant temperature, for the time reported in Table I.

0111After venting the unreacted monomer and cooling the reactor to room temperature, the polymer was dried under reduced pressure, at 60 °C.

0112The polymerization data and the characterization data of the obtained polymers are reported in Table I.

0113The obtained results demonstrate that the titanium complexes based on the ligands of the invention may give high molecular weight amorphous polypropylene.

<u style="single">Example 12:</u>

Propylene polymerization

0114Propylene polymerization was carried out according to the procedure reported in Examples 9-11, with the difference that B-1 obtained according example 1, second synthetic route, was used as catalyst.

0115Polymerization data, yields and characteristics of the obtained polymer are reported in Table I.

<u style="single">Example 13:</u>

Influence of hydrogen

0116In order to evaluate the influence of hydrogen on the molecular weight of the obtained polymers, propylene polymerization was carried out according to the procedure reported in Examples 9-11, with the only difference of introducing 100 mL hydrogen before adding propylene. Polymerization data are reported in Table I.

0117The obtained results confirm that the titanium complexes based on the ligands of the invention are sensitive to hydrogen as a molecular weight regulator.

<u style="single">Example 14:</u>

Propylene/ethylene copolymerization

0118Propylene polymerization was carried out according to the procedure reported in Examples 9-11, with the only difference that, before charging the amount of propylene reported in Table I, 4.1 g of ethylene were charged in the autoclave.

0119The resulting copolymer has an ethylene content of 0.8 %wt (¹³C NMR), the other polymerization data, yields and characteristics of the obtained copolymer are reported in Table I.

0120The obtained results demonstrate a good activity of the titanium complexes based on the ligands of the invention in propylene/ethylene copolymerization; the insertion of small amounts of ethylene in propylene polymers may serve to regulate the molecular weight of the final polymers, at the same time without negatively affecting intrinsic viscosity values and the yield of the process. The use of low amounts of ethylene in propylene polymerization process makes it possible to regulate the molecular weight of the obtained polymers.

<u style="single">Example 15:</u>

Propylene homopolymerization.

01211200 g of liquid propylene were loaded into a 4.25-L stainless-steel stirred reactor at 30 °C, followed by 1 mmol of TIBA in hexane used as a scavenger. The temperature of the reactor was then raised up to 60 °C.

0122The polymerization was started by injecting 2.1 mL of a toluene solution of MAO (ca. 6 mmol of Al) containing 1.4 mg of the B-3 into the autoclave at 60 °C, by means of nitrogen overpressure, then the temperature was maintained at 60 °C for 37 min. The polymerization was stopped by venting and cooling the reactor.

0123The soft, non-sticky, amorphous product obtained was 530 g, corresponding to a yield of about 600 kg/(g_cat×h). The properties of the polymer are: I.V. = 3.65 dL/g, no melting point (DSC), rr = 72.16, rrrr = 51.7 (¹³C NMR).

0124Polymerization data, yields and characteristics of the obtained polymer are summarized in

Table I

<u style="single">Example 16:</u>

Propylene homopolymerization.

01252 mL of a hexane solution of TIBA (1 mmol of TIBA in used as a scavenger), 271 g of liquid propylene were loaded into a 1-L stainless-steel stirred reactor at 30 °C. The temperature of the reactor was then raised up to 70 °C.

0126The polymerization was started by injecting 3 mL of a toluene solution of MAO (0.64 mmol of Al, MAO/Zr = 500) containing 0.5 mg of B-3 into the autoclave at 70 °C, by means of nitrogen overpressure, then the temperature was maintained at 70 °C for 60 min. The polymerization was stopped by pressurizing CO, venting and cooling the reactor.

0127The soft, non-sticky, amorphous product obtained was 53 g, corresponding to a yield of about 106 kg/(g_cat×h). The properties of the polymer are: I.V. = 4.92 dL/g, no melting point (DSC). Polymerization data, yields and characteristics of the obtained polymer are summarized in Table I.

<u style="single">Example 17:</u>

Propylene/ethylene copolymerization.

01282 L of hexane were loaded into a 4.25-L stainless-steel stirred reactor at 30 °C, followed by 2 mmol of TIBA in hexane used as a scavenger. 397 g of propylene and 38 g of ethylene were then pressurized into the reactor, and the temperature of the reactor was then raised up to 50 °C, resulting in a pressure of 9.3 bar-g.

0129The polymerization was started by injecting 4.3 mL of a toluene solution containing MAO (1.29 mmol of Al) and 0.5 mg of B-3 into the autoclave at 50 °C, by means of nitrogen overpressure, then the temperature was maintained at 50 °C and ethylene was continuously fed into the reactor in order to maintain a constant pressure. After 7 g of ethylene were added in 23 min, the polymerization was stopped by pressurizing 1.5 L of CO into the reactor, venting and cooling the reactor. The propylene/ethylene copolymer was recovered from the hexane solution by precipitation in acetone, followed by drying under reduced atmosphere at 70 °C for 4 hours.

0130104 g of non-sticky, amorphous copolymer were obtained, corresponding to a yield of about 540 kg/(g_cat×h). The copolymer contains 20 % by weight of ethylene (¹H NMR analysis), is fully amorphous with T_g = -26 °C, and has an intrinsic viscosity of 6.65 dL/g.

<u style="single">Example 18:</u>

Propylene/butene copolymerization.

01312 mL of a hexane solution of TIBA (1 mmol of TIBA in used as a scavenger), 158 g of propylene and 154 g of 1-butene were loaded into a 1-L stainless-steel stirred reactor at 30 °C. The temperature of the reactor was then raised up to 60 °C (15 bar-g).

0132The polymerization was started by injecting 3 mL of a toluene solution of MAO (ca. 2.6 mmol of Al) containing 1 mg of the B-3 into the autoclave at 60 °C, by means of nitrogen overpressure, then the temperature was maintained at 60 °C for 60 min. The polymerization was stopped by pressurizing Co, venting and cooling the reactor.

0133The soft, non-sticky, amorphous product obtained was 13 g. The properties of the polymer are: I.V. = 0.9 dL/g, no melting point and T_g = -7 °C, (DSC), butene = 47 wt % (measured by ¹³C NMR).

<u style="single">Example 19:</u>

Propylene/butene copolymerization

0134Example 18 was repeated at an Al/Zr ratio of 500, obtaining a copolymer with I.V. = 2.11 dL/g.

<u style="single">Example 20:</u>

Propylene polymerizations at 80°C

0135Following the usual procedure, 1 mmol of TIBA and 585 g of propylene were charged in a 2 L reactor, then heated to 80 °C. 1 mg of B-3 was dissolved with 1.07 mL of a 10 % MAO solution (1.82 mmol Al) in toluene and then diluted with toluene (total volume 3 mL), aged 10 min and injected into the reactor. The polymerization is stopped with CO after 60 min at 80 °C. The results of polymer analysis are shown in Table I.

<u style="single">Example 21:</u>

Propylene polymerizations at 80

°C

0136Following the usual procedure, 1 mmol of TIBA and 585 g of propylene were charged in a 2 L reactor, then heated to 80 °C. 0.5 mg of B-3 was dissolved with 1.07 mL of a 10 % MAO solution (1.82 mmol Al) in toluene and then diluted with toluene (total volume 3 mL), aged 10 min and injected into the reactor. The polymerization is stopped with CO after 60 min at 80 °C. The results of polymer analysis are shown in Table I.

<u style="single">Examples 22-23</u>

0137Propylene polymerization was carried out according to the procedure reported in Examples 9-11, with the difference that B-4 was used as catalyst instead of B-1

0138Polymerization data, yields and characteristics of the obtained polymer are reported in Table I.

<u style="single">Examples 24</u>

Polymerization with supported catalysts

01391200 g of liquid propylene were loaded into a 4.25-L stainless-steel stirred reactor at 30 °C, followed by 1 mmol of TIBA in hexane used as a scavenger. 200 mL of hydrogen were added before the catalyst. 650 mg of the solid catalyst prepared in example 8 was then injected into the reactor by means of nitrogen overpressure through a stainless-steel vial, and then the temperature of the reactor was raised up to the polymerization temperature in 15 min.

0140After one hour, the polymerization was stopped by venting and cooling the reactor, and the amorphous product collected and dried.

0141Polymerization data, yields and characteristics of the obtained polymers are summarized in Table I.

<u style="single">Examples 25</u>

Propylene polymerizations at 80 °C

0142Following the usual procedure, 1 mmol of TIBA and 585 g of propylene were charged in a 2 L reactor, then heated to 80 °C. 1.5 mg of A-1 was dissolved with 1.07 mL of a 10 % MAO solution (1.82 mmol Al) in toluene and then diluted with toluene (total volume 3 mL), aged 10 min and injected into the reactor. The polymerization is stopped with CO after 60 min at 80 °C. 85 g of rubbery, amorphous polypropylene were recovered, corresponding to a catalyst activity of 56.6 kgpp/(g_cat×h). The results of polymer analysis are shown in Table 1

<u style="single">Comparative examples 26-28</u>

0143Propylene polymerization was carried out according to the procedure reported in Examples 9-11, with the difference that dimethylsilyl(tert-butylamido)(tetramethylcyclopentadienyl) titanium dichloride was used as catalyst instead of the titanium complex based on the ligands of the invention. Polymerization data, yields and characteristics of the obtained polymer are reported in Table I. The obtained result demonstrates that these titanium complexes are able to exert polymerization activities superior to the one of constrained geometry catalysts known in the state of the art.

<u style="single">Comparative example 29</u>

0144Propylene polymerization was carried out according to the procedure reported in Example 9 with the difference that dimethylsilyl(tert-butylamido)(tetramethylcyclopentadienyl) titanium dichloride was used as catalyst instead of the titanium complex based on the ligand of the invention. mixture. Polymerization data are reported in Table I.

<u style="single">Comparative example 30</u>

0145Propylene/ethylene copolymerization was carried out according to the procedure reported in Example 9 with the difference that 4.5 g of ethylene were added to the reactor before adding 288 g of propylene, dimethylsilyl(tert-butylamido)(tetramethylcyclopentadienyl) titanium dichloride (obtained by Witco) was used as catalyst instead of the titanium complex based on the ligand of the invention, and 15.7 g of ethylene were fed into the reactor over the polymerization time of 1 hour in order to maintain a constant pressure of 25.6 bar-g (of which 0.3 bar are due to nitrogen). The resulting copolymer has an ethylene content of 4.5 %wt (¹³C NMR), the other polymerization data are reported in Table I.

<u style="single">Comparative examples 31-32</u>

0146Propylene polymerization was carried out according to the procedure reported in Examples 9-11, with the difference that dimethylsilyl(tert-butylamido)(indenyl) titanium dimethyl was used as catalyst instead of the titanium complex based on the ligand of the invention.

0147Polymerization data, yields and characteristics of the obtained polymer are reported in Table I. The obtained result demonstrates that the titanium complexes based on the ligands of the invention are able to exert polymerization activities superior to the one of constrained geometry catalysts known in the state of the art.

<u style="single">Comparative example 33</u>

0148Propylene polymerization was carried out according to the procedure reported in Examples 9-11, with the difference that dimethylsilyl(tert-butylamido)(2-methyl-indenyl) titanium dimethyl was used as catalyst instead of the titanium complex based on the ligand of the invention.

0149Polymerization data, yields and characteristics of the obtained polymer are reported in Table I. The obtained result demonstrates that the titanium complexes based on the ligands of the invention are able to exert polymerization activities superior to the one of constrained geometry catalysts known in the state of the art. <tables id="tabl0001" num="0001"><table frame="all"><title>Table I</title><tgroup cols="11"><colspec colnum="1" colname="col1" colwidth="12mm" /><colspec colnum="2" colname="col2" colwidth="17mm" /><colspec colnum="3" colname="col3" colwidth="17mm" /><colspec colnum="4" colname="col4" colwidth="18mm" /><colspec colnum="5" colname="col5" colwidth="16mm" /><colspec colnum="6" colname="col6" colwidth="18mm" /><colspec colnum="7" colname="col7" colwidth="19mm" /><colspec colnum="8" colname="col8" colwidth="17mm" /><colspec colnum="9" colname="col9" colwidth="12mm" /><colspec colnum="10" colname="col10" colwidth="13mm" /><colspec colnum="11" colname="col11" colwidth="12mm" /><thead valign="top"><row><entry rowsep="0" align="center">Ex.</entry><entry rowsep="0" align="center">Ti complex</entry><entry rowsep="0" align="center">mg of complex</entry><entry rowsep="0" align="center">MAO/Ti Molar ratio</entry><entry rowsep="0" align="center">T_POL °C</entry><entry rowsep="0" align="center">Time min</entry><entry rowsep="0" align="center">Activity Kg_PP/g_cat</entry><entry rowsep="0" align="center">I.V. dL/g</entry><entry namest="col9" nameend="col11" align="center">tacticity (%)</entry></row><row><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry align="center"><i>rr</i></entry><entry align="center"><i>rrrr</i></entry><entry align="center">2.1</entry></row></thead><tbody><row><entry align="center">9</entry><entry align="center">B-1</entry><entry align="center">1</entry><entry align="center">500</entry><entry align="center">50</entry><entry align="center">60</entry><entry align="center">41.6</entry><entry align="char" char="." charoff="11">5.97</entry><entry align="center">73.8</entry><entry align="center">57.5</entry><entry align="center">&lt;0.5</entry></row><row><entry align="center">10</entry><entry align="center">B-1</entry><entry align="center">1</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">30</entry><entry align="center">49.4</entry><entry align="char" char="." charoff="11">3.14</entry><entry align="center">72.4</entry><entry align="center">53.3</entry><entry align="center">&lt;0.5</entry></row><row><entry align="center">11</entry><entry align="center">B-1</entry><entry align="center">0.7</entry><entry align="center">1000</entry><entry align="center">70</entry><entry align="center">60</entry><entry align="center">26.9</entry><entry align="char" char="." charoff="11">3.06</entry><entry align="center">69.2</entry><entry align="center">48.4</entry><entry align="center">&lt;0.5</entry></row><row><entry align="center">12</entry><entry align="center">B-1</entry><entry align="center">1</entry><entry align="center">500</entry><entry align="center">70</entry><entry align="center">60</entry><entry align="center">37.9</entry><entry align="char" char="." charoff="11">4.69</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">13^a)</entry><entry align="center">B-1</entry><entry align="center">1</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">60</entry><entry align="center">12.2</entry><entry align="char" char="." charoff="11">1.84</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">14^b)</entry><entry align="center">B-1</entry><entry align="center">1</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">30</entry><entry align="center">81.7</entry><entry align="char" char="." charoff="11">2.41</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">15^c)</entry><entry align="center">B-3</entry><entry align="center">1.4</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">37</entry><entry align="center">530</entry><entry align="char" char="." charoff="11">3.65</entry><entry align="center">72.2</entry><entry align="center">51.7</entry><entry align="center">0</entry></row><row><entry align="center">16</entry><entry align="center">B-3</entry><entry align="center">0.5</entry><entry align="center">500</entry><entry align="center">70</entry><entry align="center">60</entry><entry align="center">106</entry><entry align="char" char="." charoff="11">4.92</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">20</entry><entry align="center">B-3</entry><entry align="center">1</entry><entry align="center">500</entry><entry align="center">80</entry><entry align="center">60</entry><entry align="center">288</entry><entry align="char" char="." charoff="11">4.16</entry><entry align="center">68.9</entry><entry align="center">48.1</entry><entry align="center">0</entry></row><row><entry align="center">21</entry><entry align="center">B-3</entry><entry align="center">0.5</entry><entry align="center">500</entry><entry align="center">80</entry><entry align="center">60</entry><entry align="center">320</entry><entry align="char" char="." charoff="11">5.01</entry><entry align="center">70.2</entry><entry align="center">50.69</entry><entry align="center">0</entry></row><row><entry align="center">22</entry><entry align="center">B-4</entry><entry align="center">0.3</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">60</entry><entry align="center">113</entry><entry align="char" char="." charoff="11">7.89</entry><entry align="center">73.0</entry><entry align="center">57.1</entry><entry align="center">0.3</entry></row><row><entry align="center">23</entry><entry align="center">B-4</entry><entry align="center">0.5</entry><entry align="center">1000</entry><entry align="center">70</entry><entry align="center">60</entry><entry align="center">106</entry><entry align="char" char="." charoff="11">5.96</entry><entry align="center">72.8</entry><entry align="center">54.1</entry><entry align="center">0</entry></row><row><entry align="center">24^c)</entry><entry align="center">B-4</entry><entry align="center">610 ^f)</entry><entry /><entry align="center">60</entry><entry align="center">60</entry><entry align="center">0.28^g)</entry><entry align="char" char="." charoff="11">5.85</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">25</entry><entry align="center">A-1</entry><entry align="center">1.5</entry><entry align="center">500</entry><entry align="center">80</entry><entry align="center">60</entry><entry align="center">56.7</entry><entry align="char" char="." charoff="11">4.25</entry><entry align="center">33.4</entry><entry align="center">10.6</entry><entry align="center">0.5</entry></row><row><entry align="center">26*</entry><entry align="center">C-1^e)</entry><entry align="center">2</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">60</entry><entry align="center">29.5</entry><entry align="char" char="." charoff="11">3.56</entry><entry align="center">50.2</entry><entry align="center">25.3</entry><entry align="center">1.3</entry></row><row><entry align="center">27*</entry><entry align="center">C-1 ^e)</entry><entry align="center">2</entry><entry align="center">1000</entry><entry align="center">70</entry><entry align="center">60</entry><entry align="center">31.5</entry><entry align="char" char="." charoff="11">2.58</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">28*</entry><entry align="center">C-1 ^e)</entry><entry align="center">2</entry><entry align="center">500</entry><entry align="center">70</entry><entry align="center">60</entry><entry align="center">25.8</entry><entry align="char" char="." charoff="11">2.70</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">29^*a)</entry><entry align="center">C-1 ^e)</entry><entry align="center">2</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">60</entry><entry align="center">23.8</entry><entry align="char" char="." charoff="11">2.42</entry><entry align="center">52.1</entry><entry align="center">25.4</entry><entry align="center">1.5</entry></row><row><entry align="center">30^*d)</entry><entry align="center">C-1 ^e)</entry><entry align="center">2</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">60</entry><entry align="center">32.3</entry><entry align="char" char="." charoff="11">4.84</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">31*</entry><entry align="center">C-3</entry><entry align="center">2</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">60</entry><entry align="center">12.7</entry><entry align="char" char="." charoff="11">1.12</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">32*</entry><entry align="center">C-3</entry><entry align="center">2</entry><entry align="center">500</entry><entry align="center">70</entry><entry align="center">60</entry><entry align="center">7.1</entry><entry align="char" char="." charoff="11">0.92</entry><entry align="center">-</entry><entry align="center">-</entry><entry align="center">-</entry></row><row><entry align="center">33*</entry><entry align="center">C-4</entry><entry align="center">1</entry><entry align="center">1000</entry><entry align="center">60</entry><entry align="center">60</entry><entry align="center">18.3</entry><entry align="char" char="." charoff="11">3.15</entry><entry align="center">51.4</entry><entry align="center">28.3</entry><entry align="center">0.6</entry></row></tbody></tgroup><tgroup cols="11" rowsep="0"><colspec colnum="1" colname="col1" colwidth="12mm" /><colspec colnum="2" colname="col2" colwidth="17mm" /><colspec colnum="3" colname="col3" colwidth="17mm" /><colspec colnum="4" colname="col4" colwidth="18mm" /><colspec colnum="5" colname="col5" colwidth="16mm" /><colspec colnum="6" colname="col6" colwidth="18mm" /><colspec colnum="7" colname="col7" colwidth="19mm" /><colspec colnum="8" colname="col8" colwidth="17mm" /><colspec colnum="9" colname="col9" colwidth="12mm" /><colspec colnum="10" colname="col10" colwidth="13mm" /><colspec colnum="11" colname="col11" colwidth="12mm" /><tbody><row><entry namest="col1" nameend="col11" align="justify">a) H₂ = 100 mL; b) C ₂^- = 4,1 g; c) 4.25 L reactor; d) C₂^- = 17 g; e) dimethylsilyl(tert-butylamido)(tetramethylcyclopentadienyl) titanium dichloride (Witco); f) mg of supported catalyst; g) Kg_pol/g_suport. *comparative.</entry></row></tbody></tgroup></table></tables>