Asymmetric group 8 (viii) metallocene compounds

Description of equivalent WO 2004041832 A2

ASYMMETRIC GROUP 8 (VIII) METALLOCENE COMPOUNDS

BACKGROUND OF THE INVENTION Chemical vapor deposition (CVD) methods are employed to form films of material on substrates such as wafers or other surfaces during the manufacture or processing of semiconductors. In CVD, a CVD precursor, also known as a CVD chemical compound, is decomposed thermally, chemically, photochemically or by plasma activation, to form a thin film having a desired composition. For instance, a vapor phase CVD precursor can be contacted with a substrate that is heated to a temperature higher than the decomposition temperature of the precursor, to form a metal or metal oxide film on the substrate.

Thin films that include ruthenium (Ru) , ruthenium oxide (Ru0₂) or iron (Fe) have good electrical conductivity, high work function, are chemically and thermally stable, resistant to inter-layer chemical diffusion and are compatible with many dielectric substrate materials. Ru and Ru0₂ films, for instance, have been investigated as film electrode material for semiconductor devices such as DRAM (Dynamic Random Access Memory) devices. Bis (pentaiαaptocyclopentadienyl) ruthenium

(ruthenocene) and the symmetrical, diethyl-substituted ruthenocene (1, 1' -diethylruthenocene) have been investigated as possible precursors for forming ruthenium-based thin films by CVD techniques. These compounds have been prepared by several synthetic routes. One existing method for forming ruthenocene includes the reaction of RuCl₃-XH₂0 with cyclopentadiene, in the presence of Zn, to produce ruthenocene, ZnCl₂ and HCl , as shown in Fig. 1A. A similar approach, using ethyl- substituted cyclopentadiene, has been employed to produce 1, 1' -diethylruthenocene, as shown in Fig. IB. Generally, yields obtained by this method are about 70%.

As shown in Fig. 1C, unsubstituted ruthenocene also has been prepared by the reaction of cyclopentadiene, chloro (cyclopentadienyl) bis (triphenylphosphine) ruthenium( II) and sodium hydride (NaH) in benzene. Chloro (cyclopentadienyl) bis (triphenylphosphine) ruthenium ( II) precursor has been synthesized by reacting ruthenium trichloride and triphenylphosphine in ethanol .

Another method that has been investigated for the synthesis of ruthenocene includes the transmetallation reactions of a bis (alkylcyclopentadienyl) iron compound with RuCl₃-XH₂0 and results in the formation of low yield 1, 1' -dialkylruthenocene, iron trichloride (FeCl₃) and difficult to separate iron species.

As seen in Figs. 1A and IB, these synthetic approaches include a one step addition of both cyclopentadienyl rings and thus are suitable for preparing unsubstituted ruthenocene or the symmetrically substituted 1,1' -diethylruthenocene.

Monosubstituted ruthenocene, e.g., 1 - ethylruthenocene, is formed as an impurity during the synthesis of 1,1' -diethylruthenocene. Another monosubstituted ruthenocene, tert- butyl (cyclopentadienyl) (cyclopentadienyl) ruthenium has been prepared by reacting a heated mixture of bis (cyclopentadienyl) ruthenium, aluminum chloride and polyphosphoric acid, with tert-butyl alcohol, followed by distillation. Both ruthenocene and 1, 1' -diethylruthenocene have relatively low vapor pressure (less than 10 Torr at 100 °C) . At room temperature, ruthenocene is a solid and 1, 1' -diethylruthenocene is a liquid. Generally, more volatile CVD precursors are preferred, as are precursors that are liquid at room temperature, rather than solid. In addition, desired CVD precursors also are heat decomposable and capable of producing uniform films under suitable CVD conditions. Therefore, a need exists for developing new ruthenocenes that are liquid at room temperature and have relatively high vapor pressure and for exploring their potential as CVD precursors for film depositions. A need also exists for developing other Group 8 (VIII) metallocene compounds that can be used as CVD precursors for forming osmium- or iron-based films .

SUMMARY OF THE INVENTION The invention generally is related to asymmetric Group 8 (VIII) metallocenes . More specifically, the invention is directed to a compound of the general formula CpMCp' , where M is a metal selected from the group consisting of Ru, Os and Fe; Cp is a first substituted cyclopentadienyl or indenyl moiety that includes at least one substituent group D_x; and Cp' is a second substituted cyclopentadienyl or indenyl moiety that includes at least one substituent group Di' .

The two groups, D and Di' , are different from each other and are independently selected. Di can be : X; CalHblXcl

C_a2H_b2 c₂ ( C=0 ) CaiHbiXci ; or

C_a2Hb₂Xc2θC_aιH iXci . where

X is a halogen atom or a nitro (N0₂) group; al is an integer from 2 to 8 ; bl is an integer from 0 to 2(al)+l-cl; cl is an integer from 0 to 2(al)+l - bl; bl + cl is at least 1; a2 is an integer from 0 to 8 ; b2 is an integer from 0 to 2(a2) + 1 - c2; c2--is an -integer -from J-l-to .2_(a2_)_+_l_ -_b2... can be: X;

CalHblXcl /"

Ca₂Hb₂Xc₂ ( C=0) CaiHbiXci ; or C_a2Hb₂X OC_aιHbiXci / where

X is a halogen atom or N0₂; al is an integer from 1 to 8 ; bl is an integer from 0 to 2(al)+l-cl; cl is an integer from 0 to 2(al)+l - bl; bl + cl is at least 1; a2 is an integer from 0 to 8 ; b2 is an integer from 0 to 2(a2) + 1 - c2; c2 is an integer from 0 to 2(a2) + 1 - b2. One specific example of a metallocene compound of the invention is 1-methyl-l' -ethylruthenocene .

At least one of Cp or Cp' can include one or more additional substituents, e.g., D₂, D₃, D₄, D₅, D₂' , D₃' , D₄' , and D₅' . The invention has several advantages. The compounds of the invention provide additional options and flexibility to existing methods for producing Ru- , Os-, or Fe-based thin films by CVD. Some of these compounds are liquid at room temperature. In addition, it has been found that 1-methyl-l' -ethylruthenocene has a higher vapor pressure than 1, 1' -diethylruthenocene. Independent functionalization of each of the cyclopentadienyl rings in the compounds of the invention is believed to modify properties such as solubility, vapor pressure, decomposition, combustion and other reaction pathways, reduction/oxidation potentials, geometry, preferred orientations and electron density distribution through modification of the cyclopentadienyl rings. Functionalization of the cyclopentadienyl ring allows tailoring or optimization of the metallocene for a desired application.

BRIEF DESCRIPTION OF THE DRAWINGS

Fig. 1A depicts a prior art synthetic route for forming unsubstituted ruthenocene.

Fig. IB depicts a prior art synthetic route for forming 1, 1' -diethylruthenocene . Fig. 1C depicts another prior art method that has been used to form unsubstituted ruthenocene.

Fig. 2A shows the molecular formula of a metallocene in a staggered conformation.

Fig. 2B shows the molecular formula of a metallocene in an eclipsed conformation.

Fig. 3 shows a structural formula of a disubstituted asymmetric metallocene compound of the invention. Fig. 4 shows a generalized structural formula of a metallocene compound of the invention.

Fig. 5 shows illustrative asymmetric ruthenocene compounds of the invention. Fig. 6 shows a synthetic method that can be employed to form a metallocene compound of the invention.

Fig. 7 shows a synthetic method for forming 1- methyl-1' -ethylruthenocene .

DETAILED DESCRIPTION OF THE INVENTION

The foregoing and other objects, features and advantages of the invention will be apparent -from the following more particular description of preferred embodiments of the invention, as illustrated in the accompanying drawings in which like reference characters refer to the same parts throughout the different views. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the invention. The invention generally relates to Group 8 (VIII) asymmetric metallocenes . As used herein, the term "metallocene" refers to an organometallic coordination compound, having a sandwich-type structure similar to that of ferrocene, in which a transition metal is believed to be π-bonded (electrons are moving in orbitals extending above and below the ring) to cyclic moieties. In the asymmetric metallocenes described herein, the cyclic moieties are cyclopentadienyl or indenyl. If all 5 carbon atoms in the cyclopentadienyl ring are bonding to the transition metal, cyclopentadienyl or indenyl (a cyclopentadienyl ring fused to a phenyl ring) moieties also can be described as η⁵-coordinated moieties. Thus a complete description of ferrocene would be (η⁵-C₅H₅) ₂Fe . Shown in Fig 2A is a staggered conformation of an unsubstituted metallocene, where M is a group 8 (VIII) metal, e.g., ruthenium, osmium or iron. Metallocenes also can have an eclipsed conformation, as shown in Fig. 2B. As used herein, molecular formulae are not intended to depict a particular metallocene conformation.

The invention relates to Group 8 (VIII) asymmetric metallocenes of the general formula CpMCp' , where M is Ru, Os or Fe . Cyclopentadienyl and indenyl moieties are abbreviated- herei-n--as Cp-. -In one example, -both Cp--and Cp' are cyclopentadienyl moieties. In another example, both Cp and Cp' are indenyl moieties. In yet another example, one of Cp and Cp' is cyclopentadienyl, while the other is indenyl .

In each of the Cp and Cp' moiety of the compounds of the invention, at least one hydrogen (H) atom is replaced by a substituent group, e.g. D_x and D_x' . The two groups, Di and Di' , are different from each other and are independently selected. <img file="WO2004041832A2_D0001.tif" /> X;

CalHbl cl ; C_a2H_b2Xo2 ( C=0) CaiHbiXci ; or

C_a2Hb2Xc₂0CalHblX_cl where

X is a halogen atom, e.g., fluorine (F) , chlorine (Cl) , bromine (Br) or iodine (I) ; or N0₂; al is an integer from 2 to 8 ; bl is an integer from 0 to 2(al)+l - cl cl is an integer from 0 to 2(al)+l - bl; bl + cl is at least 1; a2 is an integer from 0 to 8 ; b2 is an integer from 0 to 2(a2) + 1 - c2; c2 is an integer from 0 to 2(a2) + 1 - b2.

Di' can be: X;

C_aιHbiX_cι;

C_a2Hb₂Xc2 ( C=0) CaiH iXci ; or Ca2Hb₂Xc2θC_aιHbiXci / where

X is a halogen atom,- e.g., F,--C1-, J3r or_~I; or N0₂; al is an integer from 1 to 8 ; bl is an integer from 0 to 2(al)+l-cl; cl is an integer from 0 to 2(al)+l - bl; bl + cl is at least 1 ; a2 is an integer from 0 to 8 ; b2 is an integer from 0 to 2(a2) + 1 - c2; c2 is an integer from 0 to 2(a2) + 1 - b2.

As used herein, integer ranges are inclusive. Straight as well as branched substituent groups Di and Di' can be employed. For example, Di and/or Di' can be a straight or branched C1-C8 alkyl group. In one embodiment of the invention, D_x is selected from the following: C_aιHbiX_cι;

Ca₂Hb₂Xc2 (C=0) CaiHbiXci ; or C_a2H 2Xc₂OC_aιH iXci i where

X is a halogen atom, e.g., F, Cl, Br or I; al is an integer from 1 to 8; bl is an integer from 0 to 2(al)+l - cl; cl is an integer from 0 to 2(al)+l - bl; bl + cl is equal to or greater than 1; a2 is an integer from 0 to 8 ; b2 is an integer from 0 to 2(a2)+l - c2; c2 is an integer from 0 to 2(a2)+l - b2; b2 + c2 is equal to or greater than 1 ; and Di' is selected from the following:

CalHblXcl / Ca₂H_b2Xc2 (C=0) CaiHbiXci , or

C_a2Hb2 c2θCaiHbi ci ^•where ,

X is a halogen atom, e.g., F, Cl, Br or I ; al is an integer from 1 to 8 ; bl is an integer from 0 to 2(al)+l - cl cl is an integer from 0 to 2(al)+l - bl bl + cl is equal to or greater than 1 a2 is an integer from 0 to 8 b2 is an integer from 0 to 2(a2)+l - c2 c2 is an integer from 0 to 2(a2)+l - b2 b2 + c2 is equal to or greater than 1. In another embodiment, D_x is a halogen atom, X, e.g., F, Cl, Br, I; or N0₂ and D_x' is selected from:

CalHblXcl / Ca₂Hb₂ c2 (C=0) C_aiHbiXci or

C_a2Hb₂Xc2θC_aιHbiXci / where ,

X is a halogen atom, e . g . , F, Cl , Br, I ; or N0₂ ; al is an integer from 2 to 8 ; bl is an integer from 0 to 2 (al ) +l - cl cl is an integer from 0 to 2 (al) +l - bl bl + cl is equal to or greater than 1 a2 is an integer from 0 to 8 b2 is an integer from 0 to 2(a2)+l - c2 c2 is an integer from 0 to 2(a2)+l - b2 b2 + c2 is equal to or greater than 1. One example of the structural formula of a metallocene compound (CpMCp' ) of the invention is shown in Fig 3.

Optionally, either or both Cp and Cp' moieties of the metallocene compounds of the invention further include one or more additional substituent group, D_x. In one example, at least one of Cp and Cp' is a ulti- -substituted cyclopentadienyl or -indenyl—moiet .-

A generalized structural formula of a CpMCp' metallocene compound of the invention is shown in Fig 4. Di and Di' are independently selected as described above. D_2/ D₃, D₄, D₅, D₂' , D₃' , D₄' , and D₅' are independently selected from: X,

CalHblXcl / C_a2H_b2X_c2 ( C=0 ) CaiHbiXci ,

C_a2Hb₂Xc2θCaiHbi cl ,

Ca2Hb2Xc2 ( C=0) OC_aiHbiXci . or

C_a2H 2Xc2θ (C=0) CalHblXcl where , X is a halogen atom, e.g., F, Cl , Br, I; or N0₂; al is an integer from 0 to 8 bl is an integer from 0 to 2(al)+l - cl cl is an integer from 0 to 2(al)+l - bl bl + cl is greater to or equal to 1 a2 is an integer from 0 to 8 b2 is an integer from 0 to 2(a2)+l - c2 c2 is an integer from 0 to 2(a2)+l - b2 b2 + c2 is greater to or equal to 1 Specific examples of ruthenium-based metallocene compounds of the invention are shown in Table 1 and in Fig. 5.

<img file="WO2004041832A2_D0002.tif" />

The metallocene compounds of the invention also include osmium-based and iron-based compounds similar to those shown in Table 1 or Fig. 6. A suitable synthetic method for preparing metallocene compounds of the invention is disclosed in U.S. Patent Application, by David M. Thompson and Cynthia A. Hoover with the title Methods for Making Metallocene Compounds, filed concurrently herewith, under Attorney Docket Number D-21245, the entire teachings of which are incorporated herein by reference .

The method includes the steps of combining a metal salt compound, a ligand (L) compound and a first Cp compound, for example a substituted cyclopentadiene (HCp) , to form an intermediate compound; and reacting the intermediate compound with a second (Cp' ) compound, for instance, a compound including a cyclopentadienyl anion, such as a cyclopentadienide salt, to form CpMCp' . The metal salt can be a metal (III) salt, such as, for example, a metal halide (e.g., chloride, bromide, iodide, fluoride), a metal nitrate and other suitable metal salts. M is a Group 8 (VIII) metal, e.g., Ru, Os or Fe . Generally, the metal salt is abbreviated as MX_n. As used herein, the abbreviation MX_n does not exclude metal salt compounds that include water of hydration and that, as known in the art, can be more specifically represented by the formula MX_nQDH₂0, D being other than 0. Thus in specific examples, the abbreviation FeX₃ used herein includes anhydrous as well as hydrated iron salts that can be employed to form ferrocenes or ferrocene-like compounds.

Ligand (L) generally is an electron pair donor compound. A neutral electron pair donor, such as, for example, triphenylphosphine (PPh₃) is employed in one example . Tricyclohexylphosphine and other phosphines of the general formula PR₃, as well as phosphite triesters, P(OR)₃, where R is phenyl, cyclohexyl, alkyl or branched alkyl, e.g., t-butyl, group, also can be employed. Other suitable electron pair donors include amines, phosphates, carbonyl compounds, olefins, polyolefins, chelating phosphines, chelating amines and others.

The Cp compound is a precursor of the Cp moiety in the CpMCp' compound described above. Preferably the Cp compound is HCp, e.g., cyclopentadiene or indene . The Cp compound^" also^""can ^"Be^" a^~saT.Tt^~"of^~'a^"~cγclopeϊfiadi^nyl^~ r indenyl anion, e.g., potassium cyclopentadienyl (KCp) , sodium cyclopentadienyl (NaCp) , lithium cyclopentadienyl (LiCp) and others. Suitable cations for use with a cyclopentadienyl anion in the synthetic method described herein include trimethylsilyl (TMS) , Na, Li, K, Mg, Ca and Tl.

At least one hydrogen atom in the Cp moiety is replaced by a group Di, as described above. Specific examples of HCp include, methylcyclopentadiene, ethylcyclopentadiene, n-propyl- or isopropylcyclopentadiene, n-butyl-, sec-butyl- or tert- butylcyclopentadiene, halo-cyclopentadiene and others.

The Cp compound also can be di- or multi-substituted, e.g., it can be a di-, tri-, tetra- and penta-substituted- cyclopentadiene . Specific examples of substituent groups D₂, D₃, D₄ and D₅ are described above.

Each of the MX_n, L and HCp components can be provided in neat form or can optionally include a suitable solvent. Preferred solvents that can be employed in the method of the invention include alcohols, such as, for instance, ethanol, methanol, isopropanol and other alcohols. Ethyl acetate, tetrahydrofuran (THF) , saturated or unsaturated hydrocarbons, aromatic heterocycles, alkyl halides, silylated hydrocarbons, ethers, polyethers thioethers, esters, lactones, amides, amines, polyamines, nitriles, silicone oils and other aprotic solvents also can be employed. Combinations of solvents also can be employed. Generally, concentrations of MX_n, L and Cp are selected as^"~kήown ^"in ^"the^" a t^". ^{~ ~}For example-, ^" the molar ^"cόncent ationT of MX_n in a suitable solvent can be in the range of from about 0.1 M to neat. That of L in a suitable solvent can be in the range of from about 0.1 M to neat . The molar concentration of Cp in a suitable solvent can be in the range of from about 0.1 to neat. If neat phosphine is employed it is believed that the reaction would be highly exothermic. Methods and systems for dissipating substantial amounts of heat of reaction per unit volume are known in the art .

The three components can be combined in any order. In one example, the metal component and the HCp component are added concurrently to the L component . In another embodiment, the metal component and the HCp component are combined to form a mixture and then the mixture is combined with the L component, for instance by adding the L component to the mixture. In yet another embodiment, all components are combined at the same time. Typically the molar ratio of HCp to MX_n used is in the range from about 50 to about 1, preferably from about 12 to about 2 and most preferably in the range from about 7 to about 5. Typically, the molar ratio of L to MX_n is in the range of from about 8 to about 0 , preferably from about 6 to about 2 and most preferably from about 5 to about 3.5. If a large excess amount of HCp component is employed, the reaction is driven to forming (Cp) ₂M product.

The reaction temperature preferably is around the boiling point of the solvent employed or the boiling point of the^{^ ~}±eactTon ^"mixture . Ot^"her^~~suita^"ble^~tempe^:ratTures^~"can^" be determined by routine experimentation. Generally, the reaction can be conducted at a temperature that is in the range of from above the freezing point to about the boiling point of the reaction composition. For instance, the reaction can be conducted at a temperature in the range of from about -100DC to about 150DC.

The time of reaction generally depends on temperature, and concentration of the various reactants, and can range, for example, from about 5 minutes to about 96 hours.

The intermediate component formed by the reaction of the metal salt (MX_n) component, ligand (L) component and HCp can be represented by the formula CpML_fX, where f = 1 or 2. In one example, CpML_fX is isolated, e.g., as a solid, by methods known in the art, such as filtration, centrifugation or recrystallization. Intermediate compound, CpML_fX, is then reacted with a Cp' compound, preferably in the presence of a solvent. Cp' preferably is an anion of the Cp' moiety in the compounds of the invention described above. Counterions can include trimethylsilyl (TMS), Na, Li, K, Mg, Ca, Tl . Specific examples of cyclopentadienyl compounds that can be used include, but are not limited to sodium or lithium ethylcyclopentadienide, sodium or lithium methylcyclopentadienide, sodium or lithium isopropylcyclopentadienide and others. Di- or multi- substituted anions of the Cp' moiety also can be employed (e.g., di-, tri-, tetra- or penta-substituted cyclόpenta^'dienyl anions) . ^"Anions^" o^"f unsubstϊtuT-Ted indenes also can be employed, as described above.

In a specific example, the intermediate compound is CpRu(PPh₃) ₂C1. It is reacted with a salt of Cp' . Recommended salts of Cp' include NaCp' , LiCp' , (Cp')₂Mg, TMS(Cp') and (Cp')Tl.

Examples of suitable solvents include benzene, toluene, xylenes, pentanes, hexanes, petroleum ether, aromatic heterocycles, saturated or unsaturated hydrocarbons, alkyl halides, silylated hydrocarbons, ethers, polyethers, thioethers, esters, lactones, amides, amines, polyamines, nitriles, silicones, and others.

Generally, the molar concentrations of the Cp' component in a solvent can be in the range of from about 0.1 M to about 3.5 M, preferably in the range of from about 0.5 M to about 2.5 M and most preferably in the range of from about 1.4 to about 1.8 M.

Typically, the molar ratio of Cp' relative to the CpML_fX is in the range from about 50 to about 1, preferably from about 6 to about 1 and most preferably from about 1.6 to about 1.2.

In another example the intermediate CpML_fX component is not isolated. Following its formation in solution, a Cp' compound, such as described above, is added to the solution that includes CpML_fX.

The reaction between Cp' and the intermediate CpML_fX (whether isolated or not) is conducted at a temperature such as generally described above and results in the formation of CpMCp' product.

The time of reaction generally depends ^~oΗ^~t^"e^~mperature, and concentration of the various reactants, and can range from about 15 minutes to about 6 days.

The product of the reaction, CpMCp' , can be isolated and/or or purified by methods known in the art, such as, for example, solvent, e.g., hexane, extraction followed by distillation, sublimation or chromatography or directly by distillation, sublimation or chromatography. Recrystallization, ultracentrifugation and other techniques also can be employed. Alternatively, the product can be further employed in the reaction mixture, without further isolation and or purification.

A method for forming the compounds of the invention is described by the chemical reaction shown in Fig. 6. In the method depicted in Fig. 6, MC1₃D XH₂0, triphenylphosphine and a cyclopentadiene react in ethanol, under reflux, to form intermediate compound CpM (PPh₃) ₂C1, which then reacts with a sodium ethylcyclopentadienide to form CpMCp' .

Either or both Cp and/or Cp' can include additional substituent groups, D_x, such as, for instance, groups described above. Thus either or both Cp and/or Cp' can be a di-, tri-, tetra- or penta-substituted cyclopentadiene moiety. In general, asymmetric ruthenocenes can be prepared by first preparing an intermediate of CpRu (PPh₃) ₂C1 , followed by the reaction of this intermediate with a salt of Cp' . The most highly recommended salts of Cp' include NaCp' , LiCp', (Cp')₂Mg, TMS(Cp') and (Cp')Tl. When trying to synthesize structures of the type CpRuCp' and when one of ^"Cp or ^'Cp' colϊtains a ke^'tone^", es^~te^"r^"~or ether^" functionaTity" it is preferred that the ring with the greater number of ketones, esters or ethers is identified as the Cp' ring, and that it is added to the intermediate as a TMS salt . A synthetic scheme that can be employed to form a specific di-substituted asymmetric ruthenocene, i.e., 1- methyl, 1' -ethylruthenocene or (methyl- cycplopentadienyl) (ethylcyclopentadienyl) ruthenium, is shown in Fig. 7. As shown in Fig. 7, RuCl₃DXH₂0, triphenylphosphine and methylcyclopentadiene react in ethanol, under reflux, to form intermediate compound chloro (methylcyclopentadienyl) bis (triphenylphosphine) ruthen ium(II) or (η⁵-C₅H₄C₂H₅) Ru (PPh₃) ₂C1, which then reacts with a sodium ethylcyclopentadienide to form l-methyl,l'- ethylruthenocene .

Examples of techniques that can be employed to characterize the compounds formed by the synthetic methods described above include, but are not limited to, analytical gas chromatography, nuclear magnetic resonance (NMR) , thermogravimetric analysis (TGA) , inductively coupled plasma mass spectrometry (ICPMS) , vapor pressure and viscosity measurements.

Without being held to a particular mechanism to interpret the invention, it is believed that specific functionalization of each of the Cp and Cp' rings modifies properties such as solubility, vapor pressure, decomposition, combustion and other reaction pathways, reduction/oxidation potentials, geometry, preferred orientations and electron density distribution. For

^"example^", iύ^""is believed-tha ^" larger substituent D^~and/or Di' contribute to an increase in molecular entropy and that metallocene compounds of the invention are more likely to be liquid at room temperature in comparison to previously disclosed compounds.

The asymmetric metallocenes of the invention are believed to be useful in scientific research, for example, in the study and understanding of organometallic chemistry of ferrocene and ferrocene-like molecules and in chemical reactions.

It is believed that the compounds of the invention also can be employed as combustion modifiers for solid propellants. In some cases, functionalization of the parent ferrocene may prevent migration of the ferrocene from the rubber like binder matrix of the solid propel1ant into the surrounding insulation material .

The metallocene compounds of the invention may find uses as catalysis, for instance, in zeolite-impregnated metallocene catalysts for the reduction of nitrogen oxides or as catalysts in chiral organic synthesis.

It is believed that the compounds of the invention may also find uses as iron deficiency supplements for animals and plants; antioxidants and antiknock agents; additives for motor fuels and oils; color pigments; radiation absorberes; and as insecticides and fungicides.

The asymmetric metallocenes of the invention are particularly useful as precursors in processes for forming films, coatings or powders, particularly in film deposition ^~ processes^", ^" sύch^""as^~CVD^" processesT^" Such^" processes^~a"re described in the U.S. Patent Application by David M. Thompson and Cynthia A. Hoover, John Peck and Mike Litwin, entitled Deposition Processes Using Group 8 (VIII) Metallocene Precursors , filed concurrently herewith, under Attorney Docket No. D-21267, the entire teachings of which are incorporated herein by reference.

EXEMPLIFICATION EXAMPLE 1 STEP A

A 5 L five-necked round bottomed flask was equipped with a mechanical stirring paddle through the central neck. It was then charged with ethanol (2.0 L) and PPh3 (420 g, 1.6 mol) . Two 500 mL three necked flasks, were connected to two necks of the 5 L four-necked flask via Teflon^® (perfluorinated polymer, DuPont Corp.) tubing through positive displacement pumps. The remaining neck of the 5 L flask was equipped with a condenser. A heating mantle was placed beneath the 5 L flask and the solution was stired and heated to reflux. At reflux all of the triphenylphosphine dissolved in the ethanol . The system was purged with nitrogen for 30 minutes while at reflux. While this was taking place one of the 500 mL round- bottomed flasks was charged with RuCl₃'XH₂0 (100 g, 0.40 mol) , ethanol (300 mL) and a Teflon^® (perfluorinated polymer, DuPont Corp.) coated magnetic stirring bar. The ethanolic solution immediately developed a brown/orange colour. To dissolve all of the RuCl₃"XH₂0 it was necessary to heat the solution. This solution was sparged with nitrogen for 30 minutes by inserting a needle connected to a 1-2 pounds per square inch gauge (psig) nitrogen source through the septum and into the solution and by piercing the septum with another needle to allow for relief of excess pressure.

An acetonitrile/dry ice bath was made up and the other 500 mL flask was immersed into this bath. Freshly distilled methylcyclopentadiene (190 g, 270 mL, 2.4 mol, freshly distilled under a nitrogen atmosphere) was then cannulated into the cooled flask.

After the nitrogen sparging of the ethanolic solutions of triphenylphosphine and ruthenium trichloride had completed, the contents of the two 500 mL flasks were pumped into the 5.0 L flask by positive displacement pumps at independent rates so that both additions completed after 5 minutes. To accomplish this the ethylcyclopentadiene was pumped in at a rate of 45 mL/min and the ethanolic ruthenium trichloride was pumped in at a rate of 50 mL/min .

After the addition had been completed the solution was left to reflux for an additional 2 hours. During this time small orange crystals could be seen accumulating above the meniscus of the solution on the walls of the 2 L flask.

STEP B

The two positive displacement pumps and Teflon⁰ (perfluorinated polymer, DuPont Corp.) lines were disconnected from the 5 L flask after the 2 hours of

^"stiffing": "^' A^~ distillation "sid'earπv was -connected one of the necks of the flask and approximately 1 L of ethanol was removed via distillation. Mechanical stirring was discontinued and the orange crystals settled to the bottom of the flask. The solution cooled to room temperature over 3 hours. The solution was then removed from the flask by inserting a piece of glass tubing with a coarse frit attached to the end of it and using reduced pressure to draw the solution through the frit and out of the flask. The crystals were washed with heptane (300 mL) and the heptane was removed in a similar fashion. The washing was carried out three times.

STEP C

All of the open ports to the flask were sealed with rubber septa and the flask was evacuated and refilled with nitrogen three times. THF (500 mL, anhydrous) was cannulated into the flask and mechanical stirring was initiated. A THF solution of lithium ethylcyclopentadiene (500 mL, 1.2 M, 0.60 mol) was then cannnulated into the 5 L flask. The contents were heated to reflux and stirred for 4 hours .

After the 4 hours of reflux, stirring was discontinued and the solution was transferred to a 2 L one necked round bottomed flask. This solution was concentrated to a volume of approximately 200 mL on a rotary evaporator. The viscous liquid was then transferred to a 250 mL round bottomed flask.

The 250 mL round-bottomed flask was fitted with a short path distillation adapter with vigreux indentations aricTaT ΪOO^'TαT storage^{"" "}flask ^"feceptacle . ^"" The liquid was distilled under vacuum and a clear yellow liquid, 1-methyl, 1 ' -ethylruthenocene containing some triphenylphosphine (determined by GCMS) . Spinning band distillation of the yellow liquid afforded 84.6 g (82% yield) of triphenylphosphine free 1-methyl, 1 ' -ethylruthenocene in &gt;99% purity (GCMS, IH NMR) , with the remaining impurities being attributable to 1, 1 ' -dimethylruthenocene and 1,1'- diethylruthenocene . TGA studies showed that this liquid had less than 0.01% nonvolatile residue. EXAMPLE 2

A 2 L three-necked round bottomed flask was charged with a Teflon^® (perfluorinated polymer, DuPont Corp.) stirring bar, ethanol (1.0 L) and PPh₃ (263 g, 1.0 mol, 5 eq) . A 250 mL dropping funnel, a 150 mL bath-jacketed dropping funnel, and a condenser were attached to the three necks of the 2L flask. It is important to note that both dropping funnels were equipped with Teflon (perfluorinated polymer, DuPont Corp.) valves that permitted their isolation from the atmosphere of the round-bottomed flask. A rubber septum was connected to the top of the 150 mL bath-jacketed dropping funnel. The top of the condenser was fitted with an T junction adapter and connected to an inert atmosphere. A heating mantle was placed beneath the 2 L three-necked round-bottomed flask and the solution was stirred and heated to reflux. At reflux all of the triphenylphosphine dissolved in the ethanol. The system was purged with nitrogen for 3 hours while at reflux. While this was taking place a 500 mL Erlenmyer flask was charged with RuCl₃-XH₂0 (50 g, 0.20 mol), ethanol (150 mL, 1 eq) and a Teflon" (perfluorinated polymer, DuPont Corp.) coated magnetic stirring bar. The ethanolic solution immediately developed a brown/orange colour. To dissolve all of the RuCl₃-XH₂0 it was necessary to gently heat the solution. This solution was poured into the 250 mL dropping funnel and the dropping funnel was fitted with a rubber septum. This solution was sparged with nitrogen for 30 minutes by inserting a needle connected to a 1-2 psig nitrogen source through the septum and into the solution and by piercing the septum with another needle to allow for relief of excess pressure.

A methanol/dry ice bath was made up in the 150 mL bath-jacketed dropping funnel. The interior of this droppping funnel was purged with nitrogen for 30 minutes in a similar fashion to which the other dropping funnel was sparged. Methylcyclopentadiene (96.2 g, 1.2 mol, 6 eq, doubly distilled under a nitrogen atmosphere) was then cannulated into the cooled dropping funnel through the rubber septum.

After the 3 hours of purging the 2 L-round bottomed flask had elapsed, the Teflon^® (perfluorinated polymer, DuPont Corp.) valves isolating the dropping funnels from the rest of the system were both opened and dropwise addition of the two solutions commenced simultaneously. Over the course of 20 minutes the two solutions were both added to the ethanolic PPh₃ solution. During this entire time the solution was at reflux. The solution quickly developed a deep orange brown color. After ^"the "addition had been completed the solution was left to reflux for an additional 2 hours. During this time small orange crystals of CpRu(PPh₃) ₂C1 could be seen accumulating above the meniscus of the solution on the walls of the 2 L flask.

A piece of tubing with a coarse porous frit attached to one end was attached to a positive displacement pump. The fritted end of the tubing was immersed in the reactor and all of the liquids were pumped out of the 2 L round- bottomed flask. At this stage the dropping funnels were removed from the reactor. One side was fitted with a K- Head distillation adapter and the other side was fitted with a rubber septum. The flask was evacuated and refilled with nitrogen three times. Working under nitrogen, anhydrous toluene (1.0 L) was cannulated into the 5 L flask through the rubber septum. The dark opaque solution was heated to reflux and the K-head distillation adapter was opened to distill off a fraction of the solvent . Distillate was collected until the head temperature reached 109 °C (It is important to note that in different experiments this consumes different volumes of solvent - typically 400-600 mL of liquid) . The solution was then cooled to below reflux. The flask was then charged with additional toluene to obtain a volume of approximately 600 mL toluene. A lithium ethylcyclopentadienide slurry of toluene (35 g, 0.35 mol, 400 mL) was then cannulated into the reaction pot. Following this addition the solution was stirred for 4 hours at 80 °C. At this stage the flask was removed from the glovebox and the majority of toluene^{" "}was removed using a K-head distillation adapter.

The remaining liquid (approximately 400 mL) was decanted into a 1.0 L round-bottomed flask. This round- bottomed flask was fitted with a short path distillation adapter with vigreux indentations and distilled. The liquid collected from the vigreux column was distilled again using spinning band distillation under vacuum and 44 g of a clear yellow liquid, 1-methyl, 1' -ethylruthenocene was obtained in &gt;99% purity (GCMS) . TGA studies showed that this liquid had less than 0.01% nonvolatile residue.

EXAMPLE 3 Lithium(ethylcyclopentadienide) was produced as follows. A 2 L three-necked jacketed round bottomed flask was charged with a Teflon" (perfluorinated polymer, DuPont Corp.) stirring bar. A stopcock adapter, a thermowell adapter with thermowell and a rubber septum were fitted to the three necks of the flask. A nitrogen/vacuum manifold was connected to the stopcock adapater and the flask was evacuated and refilled with nitrogen 3 times. Anhydrous toluene (1.0 L) was then cannulated into the flask through the rubber septum and stirring was initiated. A cold fluid circulator was connected to the outer jacket of the jacketed flask with nalgene tubing and a cold fluid (-15 °C) was circulated through the outside wall of the jacketed flask. Once the toluene reached -10 °C, freshly distilled ethylcyclopentadiene (middle cut distilled on a vigreux column) was cannulated into the flask (127 g, 1.35 mol) . While stirring, n-butyllithium (800 mL, 1.6 M in hexanes, 1.28 mol) was slowly cannulated at a rate that kept the temperature below 0 °C (approximately 2 hours) . During the addition of the n-butyllithium a fine white precipitate (lithium ethylcyclopentadienide) became evident in the solution.

This material could be used as a suspension or isolated as a solid via filtration and removal of solvent.

EXAMPLE 4

In a nitrogen glovebox, a 250 mL flask was charged with THF (50 mL, anhydrous, inhibitor free) , chloro (ethylcyclopentadienyl) bis (triphenylphosphine) rutheni urn (II) (3.22 g, 0.004 mol, 1 equivalent) and a Teflon^®

(perfluorinated polymer, DuPont Corp.) stirring bar. The solution was stirred and a burgundy colored THF solution of sodium isopropylcyclopentadienide was slowly added (0.20 M, 30 mL, 1.5 equivalents) . Following the addition the solution developed a deep red color. Within 30 minutes, the meniscus appeared yellow in color. The solution was stirred overnight.

An aliquot (1.0 mL) was taken from the solution and was analyzed by GC/MS . A peak with a mass of 301 g/mol was observed consistent with the 1-ethyl-l'- isopropylruthenocene . Other peaks with masses consistent with the presence of alkylcyclopentadiene di ers, 1,1'- diethylruthenocene, 1, 1' -diisopropylruthenocene and triphenylphosphine were also observed.

The THF solvent was then removed from the flask under reduced pressure. The 250 mL flask was fitted with a vacuum jacketed short path distillation adapter and the contents of the flask were distilled under reduced pressure (~ 0.1 torr) . A pale yellow liquid was collected (0.72 g) . This liquid was then purified via chromatography. A silica gel in pentane solution was used. The column had a diameter of 0.75" and a 6" length. 0.53 g of 99+% pure 1-ethyl-l' -isopropylruthenocene were isolated via chromatography (41% yield) .

EXAMPLE 5

In a nitrogen glovebox, a 250 mL flask was charged with THF (50 mL, anhydrous, inhibitor free) , chloro (methylcyclopentadienyl) bis (triphenylphosphine) ruthen ium(II) (5.02 g, 0.007 mol, 1 equivalent) and a Teflon^® (perfluorinated polymer, DuPont Corp.) stirring bar. The solution was stirred and a burgundy colored THF solution of sodium isopropylcyclopentadienide was slowly added (0.20 M, 50 mL, 1.5 equivalents). Following the addition the solution developed a deep red color. Within 30 minutes, the meniscus appeared yellow in color. The solution was stirred overnight. An aliquot (1.0 mL) was taken from the solution and was analyzed by GC/MS. A peak with a mass of 287 g/mol was observed consistent with 1-methyl-l' -isopropylruthenocene . Other peaks with masses consistent with the presence of alkylcyclopentadiene dimers, 1, 1' -dimethylruthenocene, 1, 1' -diisopropylruthenocene and triphenylphosphine were also observed.

The THF solvent was then removed from the flask under reduced pressure. The 250 mL flask was fitted with a vacuum jacketed short path distillation adapter and the contents of the flask were distilled under reduced pressure (~ 0.1 torr) . A pale yellow liquid was collected ( 1.78 g) . This liquid was then purified via chromatography. A silica gel in pentane solution was used. The column had a diameter of 0.75" and a 6" length. 1.03 g of 98+% pure 1- methyl-1' -isopropylruthenocene were obtained after chromatography (53% yield) .

EXAMPLE 6

In a nitrogen glovebox, a 250 mL flask was charged with bis (propylcyclopentadienyl) magnesium (5.15 g, 0.02 mol, 1 equivalent) , chloro (methylcyclopentadienyl) bis (triphenylphosphine) ruthen ium(II) (5.02 g, 0.007 mol, 1 equivalent) and a Teflon^® (perfluorinated polymer, DuPont Corp.) stirring bar. Toluene (120 mL, anhydrous, inhibitor free) was cannulated into the 250 mL round-bottomed flask and the contents were stirred. Following the addition of solvent the solution developed a deep red color. The toluene solvent was then removed from the flask under reduced pressure . The toluene solvent was removed under reduced pressure and the flask was fitted with a short path distillation adapter. The distillate was collected and the GC/MS revealed that the main cut from the short path distillation was 88.7% pure 1-propyl-l'- ethylruthenocene . ^' ' -

EQUIVALENTS

While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims .