Abstract: A method of forming a film on a substrate using, Group III metal complexes, including Group IIIA metals and Group IIIB metals, which include the lanthanides. The complexes and methods are particularly suitable for the preparation of semiconductor structures using chemical vapor deposition techniques and systems.

Abstract: Improved precursors for use in chemical vapor deposition of thin films of low-valent metals are provided, which are sterically saturated and protected from attack of the coreactant in the gas phase. Specific precursors have the formulae:(L).sub.x M.sup.n+ (N(R.sup.1)(C(R.sup.2 R.sup.3)).sub.y N(R.sup.4 R.sup.5)).sub.z (I)(L).sub.x M.sup.n+ (N(R.sup.1)(C(R.sup.2 R.sup.3)).sub.y O(R.sup.4)).sub.z(II)(L).sub.x M.sup.n+ (N(R.sup.1)(C(R.sup.2 R.sup.3)).sub.y S(R.sup.4)).sub.z(III)wherein L is an auxiliary ligand; x is 0-6; M is a metal of valence 1 to 5; n is the oxidation state of the metal; R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are hydrogen or (C.sub.1 -C.sub.12) alkyl groups; y is 1-5, z is 1-n.

Abstract: This invention provides volatile, intramolecularly coordinated amido/amine alane complexes, H.sub.2 Al{(R.sup.1)(R.sup.2)NC.sub.2 H.sub.4 NR.sup.3 }, wherein R.sup.1, R.sup.2 and R.sup.3 are each independently H or C.sub.1 -C.sub.3 alkyl. These aluminum complexes show extremely high thermal stability and deposit high-quality aluminum films at low temperatures. They are capable of selectively depositing aluminum films on metallic or other electrically conductive substrates with wide process window.

Abstract: Novel organometallic complexes of aluminium, gallium and indium are disclosed, having improved stability and volatility for use in CVD processes. These are donor ligand complexes of the formula MR.sub.2 L where M is the metal, R is an alkyl group and L is a ligand containing an amidine (R'N. . . C(R'). . . NR') group, where R' is H, alkyl etc.

Abstract: Aluminum amidinate compounds of the formula ##STR1## wherein R.sup., R.sup.2, and R.sup.3 are selected from the group consisting of C.sub.1 to C.sub.50 alkyl, aryl, and silyl groups, X is an anionic ligand, preferably a hydrocarbyl, n=0 or 1, L, if present, is a labile Lewis base ligand, preferably having an oxygen, nitrogen, or phosphorus atom donating a lone pair of electrons to the aluminum center, and A.sup.- is an anion which balances the charge of the aluminum cation and only weakly if at all coordinates to the aluminum center and preferably contains boron, are disclosed. These compounds are useful as olefin polymerization catalysts without the need for cocatalysts or transition metal species.

Abstract: There are disclosed bisamido azides of gallium (Ga), aluminum (Al), or Indium (In) which when pyrolized in accordance with the invention, produce metal nitride films on a substrate. A representative example of a bisamido azide is bisdimethylamidogallium azide, (CH.sub.3)N).sub.2 GaN.sub.3.

Abstract: A new class of organometallic complexes with built-in fluorescent dye for use in electroluminescent (EL) devices and a method of preparation are disclosed. An organometallic complex with built-in fluorescent dye as guest dopant is introduced into an organic EL device by thoroughly pre-mixing it with a host organometallic emitter in a certain ratio and co-depositing it from a single source. The organometallic complex with built-in fluorescent dye determines the emission color of the EL device.

Abstract: An aluminate complex represented by formula (I): ##STR1## with the groups in the aluminate complex as defined in the specification, and which is capable of radical generation upon photoexcitation; a photopolymerizable composition comprising an ethylenically unsaturated polymerizable compound and the aluminate complex; and an image-forming material comprising a support, an organoaluminum compound anion represented by formula (I'): ##STR2## with the groups in the organoaluminum compound anion as defined in the specification, and a photobleachable dye; are disclosed.

Abstract: Compositions comprisinga) a functional liquid or an internal combustion engine fuel andb) at least one compound of the general formula I ##STR1## wherein R.sub.1 is --(CH.sub.2 --X).sub.n R, where X=--S-- or --O--, n=0 or 1 to 18 carbon atoms, a phenyl group, a phenyl group which is substituted by at least one C.sub.1 -C.sub.18 alkyl group, a phenyl-C.sub.1 -C.sub.4 alkyl group or a phenyl-C.sub.1 -C.sub.4 alkyl group which is substituted by at least one C.sub.1 -C.sub.4 alkyl group, or R.sub.1 is an alkyl group of 1 to 18 carbon atoms which is substituted by at least one OH group, or R.sub.1 is a ##STR2## group in which the alkyl moiety contains 1 to 18 carbon atoms, and R.sub.2 and R.sub.3 are the same or different and are --H or, independently of R.sub.1, have the same meanings as R.sub.1, and M is B, Al, Fe, Cr, Sb or Bi, or M is a group M'--R' or a group M'--OR", where M' is Ti, Zr or Sn, and R' and R" is C.sub.1 -C.sub.18 alkyl or R' is ##STR3## wherein M' is defined above, and R.sub.1 ', R.sub.

Abstract: This invention provides a process for manufacturing aluminum-nitrogen polymers (i.e., polymers having a backbone of alternating aluminum and nitrogen atoms) in which portions of the polymer have an organic substituent on each aluminum and nitrogen atom. The novel polymers so produced are useful for making green shapes pyrolyzable to AlN articles suitable for high performance applications. The process generally comprises reacting an organic nitrile having the formula R.sup.1 CN with a trialkylaluminum compound having the formula R.sup.2 R.sup.3 R.sup.4 Al, and optionally heating the reaction product, to form an organoaluminum imine, and heating the organoaluminum imine to a temperature of at least 300.degree. C. and less than 600.degree. C. for at least two hours to form an aluminum-nitrogen polymer. The polymer or the imine can be pyrolyzed to form an aluminum nitride ceramic article. In the foregoing formulae, R.sup.

Abstract: Novel tertiary amine-aluminoxane halide derivatives are disclosed along with olefin polymerization catalyst and polymerization processes using such derivatives in combination with metallocenes.

Abstract: Novel primary and secondary amino-aluminoxane derivatives are prepared by reacting an aluminoxane and a primary or secondary amine in an organic solvent, heating the reaction mixture to form a homogeneous solution and filtering the solution.

Abstract: Neutral single-source molecular organic precursors containing tetradentate tripodal chelating ligands are provided that are useful for the preparation of films using chemical vapor deposition. These complexes can be generally represented by the formula ##STR1## wherein "M" is selected from the group consisting of a lanthanide, an actinide, a Group IIIA metal, a Group IIIA metalloid, a Group IVA metal, a Group IVA metalloid, a Group VA metal, a Group VA metalloid, a Group IIIB metal, a Group IVB metal, a Group VB metal, a Group VIB metal, a Group VIIB metal, and a Group VIIIB metal. The ligand "Z" can be present or absent, i.e., k=0-1, and is selected from the group consisting of hydrogen, halide, and a group bonded to "M" through N, O, P, S, As, Si, or C. In the tetradentate tripodal chelating ligand "E.sub.c " is N, P, or As, and m=0-1. When "E.sub.t " is N, P, or As, m=1, and when "E.sub.t " is O, S, or Se, m=0. Each "R.sup.1 " is independently selected from the group consisting of hydrogen, (C.sub.1 -C.

Abstract: Organic-solvent soluble magnesium hydrides or formulas ##STR1## are prepared by catalytically hydrogenating finely powdered magnesium, optionally in the presence of a magnesium halide, in an organic solvent in the presence of their MgH.sub.2 -free counterparts in whichQ is an alkyl, alkenyl, alkoxy, dialkylamino, aralkyl, aryl or diarylamino group, each with up to 18 carbon atoms,R is an alkenyl, aralkyl or aryl group, each with up to 18 carbon atoms,X is chlorine, bromine, or iodine, ##STR2## is a chelating ligand, E is --CH.sub.2, --N(R)-- or --O--,is an alkylene radical of the formula --(CH.sub.2).sub.p,D is a dialkylamino, diarylamino or alkoxy group, each with up to 18 carbon atoms,M is aluminum or boron,m is 1, 2, or 3, and1<n.ltoreq.50.

Abstract: This invention provides essentially pure dimethylethylamine alane, which is useful for the chemical vapor deposition of thin films of aluminum.

Abstract: Methods are described for preparing aluminum nitride of controllable morphology for ceramic and heat conduction applications. The methods comprise forming spherical particles or flakes of an intermediate, RAlNH, followed by heating the spheres or flakes of RAlNH at elevated temperatures to produce high purity aluminum nitride of corresponding morphology. Spheres of RAlNH are formed by (i) freezing a suspension of RAlNH in a liquid medium and thawing, by (ii) aging the suspension, or by (iii) dissolving RAlNH in a liquid medium and precipitating it. Flakes are formed by freezing a suspension of RAlNH in a liquid medium and removing frozen medium from the frozen suspension.

Abstract: Organic-solvent soluble magnesium hydrides of the formulas(MgH.sub.2).sub.n. MgQ.sub.2 (II)(MgH.sub.2).sub.n. RMgX (III) ##STR1## are prepared by catalytically hydrogenating finely powdered magnesium, optionally in the presence of a magnesium halide, in an organic solvent in the presence of their MgH.sub.2 -free counterparts in whichQ is an alkyl, alkenyl, alkoxy, dialkylamino, aralkyl, aryl or diarylamino group, each with up to 18 carbon atoms,R is an alkenyl, aralkyl or aryl group, each with up to 18 carbon atoms,X is chlorine, bromine, or iodine,--E D.fwdarw. is a chelating ligand,E is --CH.sub.2, --N(R)-- or --O--,is an alkylene radical of the formula --(CH.sub.2).sub.p,D is a dialkylamino, diarylamino or alkoxy group, each with up to 19 carbon atoms,M is aluminum or boron,m is 1, 2, or 3, and1<n.ltoreq.50.

Abstract: Tertiary amine alanes are produced by reacting sodium aluminum hydride and magnesium dichloride. A tertiary amine is admixed to extract the tertiary amine alane. Stoichiometric ratios of sodium aluminum hydride to magnesium dichloride can be varied to effect the magnesium compound by-product produced.

Abstract: Organic-solvent soluble magnesium hydrides of the formulas ##STR1## are prepared by catalytically hydrogenating finely powdered magnesium, optionally in the presence of a magnesium halide, in an organic solvent in the presence of their MgH.sub.2 -free counterparts in whichQ is an alkyl, alkenyl, alkoxy, dialkylamide, aralkyl, aryl or diarylamide group, each with up to 18 carbon atoms,R is an alkenyl, aralkyl or aryl group, each with up to 18 carbon atoms,X is chlorine, bromine, or iodine,--E D.fwdarw. is a chelating ligand,E is --CH.sub.2, --N(R)-- or --O--,is an alkylene radical of the formula --(CH.sub.2).sub.p,D is a dialkylamide, diarylamide or alkoxy group, each with up to 18 carbon atoms,M is aluminum or boron,m is 1, 2, or 3, and1<n.ltoreq.50.

Abstract: Preparation of the novel monomeric compounds of the formula (t-Bu).sub.2 t-Bu).sub.2, where M is Ga, Al, or In and E is As, P, Sb, or N, by reaction of (t-Bu).sub.2 MCl and LiE(t-Bu).sub.2. The resulting product (t-Bu).sub.2 ME(t-Bu).sub.2 can be pyrolyzed to form crystalline films of the metallic material, ME.

Abstract: Preparation of the novel monomeric compounds of the formula (t-Bu).sub.2 t-Bu).sub.2, where M is Ga, Al, or In and E is As, P, Sb, or N, by reaction of (t-Bu).sub.2 MCl and LiE(t-Bu).sub.2. The resulting product (t-Bu).sub.2 ME(t-Bu).sub.2 can be pyrolyzed to form crystalline films of the metallic material, ME.

Abstract: Preparation of the novel monomeric compounds of the formula (t-Bu).sub.2 ME(t-Bu).sub.2, where M is Ga, Al, or In and E is As, P, Sb, or N, by reaction of (t-Bu).sub.2 MCl and LiE(t-Bu).sub.2. The resulting product (t-Bu).sub.2 ME(t-Bu).sub.2 can be pyrolyzed to form crystalline films of the metallic material, ME.

Abstract: A process for making ammonolytic precursors to nitride and carbonitride ceramics. Extreme reaction conditions are not required and the precursor is a powder-like substance that produces ceramics of improved purity and morphology upon pyrolysis.

Abstract: Cyclopentadienyl compounds of aluminum, gallium and indium which when reacted at low temperature with amines, phosphines and arsines form compounds which are potential precursors to ceramic materials and semiconductors.

Abstract: Species-linked diamine triacetic acids of the formula ##STR1## wherein T is an organic species containing at least one amine, hydroxyl, or thiol functional group, L is the residue of at least one of those functional groups and R is a two or more atom long covalent bridge, are disclosed. Methods for their preparation, for the preparation of metal chelates from them and for the use of the chelates are also disclosed. In a preferred embodiment, the metal ions employed in the formation of the chelates are rare earth metal ions capable of forming fluorescent chelates which can in turn be employed in fluoroassay techniques.

Abstract: Lithium aluminum hydride reacts with a tertiary amine to produce an amine alane and Li.sub.3 AlH.sub.6. Lithium values are recycled by reacting Li.sub.3 AlH.sub.6 with aluminum and hydrogen to produce LiAlH.sub.4. Since no metal halide by-product is produced in the first step, it has an advantage over other routes. The amine alane can react with SiF.sub.4 to produce silane and AlF.sub.3.

Abstract: A process is provided wherein tertiary ammonium trichlorosilyl, a complexing tertiary amine, and an alkali metal aluminum tetrahydride are reacted together in molar proportion of about 1:2:3, such that silane and tertiary amine alane are produced. Tertiary ammonium trichlorosilyl may be pre-formed or formed in situ by the reaction of trichlorosilane and tertiary amine. Yields are dramatically higher when the process is conducted in the presence of a tris(polyalkoxyalkyl)amine phase transfer catalyst.A sequential process is also provided for the preparation of silane and aluminum trifluoride. In the first part of this sequence, silane and tertiary amine alane are produced as described above. In the second part of the sequence, silicon tetrafluoride is reacted with the amine alane, producing additional silane and aluminum trifluoride.

Abstract: Methods are described for preparing aluminum nitride of controllable morphology for ceramic and heat conduction applications. The methods comprise forming spherical particles or flakes of an intermediate, RA1NH, followed by heating the spheres or flakes of RA1NH at elevated temperatures to produce high purity aluminum nitride of corresponding morphology. Spheres of RA1NH are formed by (i) freezing a suspension of RA1NH in a liquid medium and thawing, by (ii) aging the suspension, or by (iii) dissolving RA1NH in a liquid medium and precipitating it. Flakes are formed by freezing a suspension of RAINH in a liquid medium and removing frozen medium from the frozen suspension.

Abstract: A process for the preparation of an amine complex of an aluminum trihalide which comprises reacting aluminum with an amine hydrohalide. The process can be extended to the use of other metals besides aluminum, e.g. magnesium, zinc, or iron.

Abstract: Admixing an aluminum alkyl, and optionally a boron compound, with a hydride of nitrogen in the gas phase and maintaining a gas phase temperature, optionally in the presence of a carrier gas, and producing aluminum nitride alone or in admixture with a precursor thereof or boron nitride or both.

Abstract: The present invention relates to aluminate coupling agents, their synthesis and applications. Metallic aluminum is reacted with lower alcohols, then reacted with selected longer chain alcohols, phenols, carboxylic acids etc., satisfied the coordination number of aluminum to give aluminate coupling agents having good hydrolytic stability and lower associativity. They can be used directly as typical coupling agents in processing of composition products such as plastics, rubber, coatings and laminates etc., and as adhesive promoter or primer to treat fillers, pigments and various materials in order to improve the processing and the quality of products, to increase the dosage of filler, to develop new products, to reduce energy consuming and cost of products.

Abstract: The arylaminoaluminums, well adopted as catalysts for the ortho-alkylation of aromatic amines with an olefin, are facilely prepared by reacting at least one aromatic amine with metallic aluminum in the presence of a catalytically effective amount of iodine, or precursor compound thereof which generates elemental iodine under the conditions of reaction.

Abstract: Process for the preparation of silane and a tertiary amine alane, said process comprising reacting:(a) an alkali metal aluminum tetrahydride having the formula MAlH.sub.4, wherein M is an alkali metal selected from the class consisting of lithium, sodium and potassium,(b) silicon tetrachloride, and(c) a complexing tertiary amine, such that the molar proportion of (a) to (b) to (c) is about 4:1:4.In this process, NaAlH.sub.4 and triethylamine are preferred reactants. The amine alane product can be reacted with additional silicon halide to prepare additional silane. This step can be conducted utilizing amine alane in the reaction mixture produced by the process above, and is preferably conducted using SiF.sub.4 as the silicon tetrahalide to produce AlF.sub.3 as a co-product. Both AlF.sub.3 and silane are valuable articles of commerce.

Abstract: Process for the preparation of silane and a tertiary amine alane, said process comprising reacting about equimolar amounts of:(a) an alkali metal aluminum tetrahydride having the formula MAlH.sub.4, wherein M is an alkali metal selected from the class consisting of lithium, sodium and potassium,(b) a hydrogen halide, and(c) a complexing tertiary amine.In this process, NaAlH.sub.4, HCl, and (C.sub.2 H.sub.5).sub.3 N are preferred reactants. The amine alane product can be reacted with a silicon halide to prepare silane.

Abstract: A process for making ammonolytic precursors to nitride and carbonitride ceramics. Extreme reaction conditions are not required and the precursor is a powder-like substance that produces ceramics of improved purity and morphology upon pyrolysis.

Abstract: A process for producing complexes of alane and tertiary amines. Sodium aluminum tetrahydride is reacted with sodium aluminum tetrachloride in the presence of a tertiary amine in an aromatic hydrocarbon reaction medium that is not a solvent for either of the reactants. The tertiary amine alane reaction products are typically soluble in the hydrocarbon reaction medium and readily recoverable.