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1.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. 63. Preparation and Crystal Structure of Tetramethyltitanium Tetrahydrofuran Me4Ti · 2THF 1 dissoziates partially in n-pentane. The formed Me4Ti · THF 2 could be isolated. According to X-ray structure determination the molecules of 2 have a trigonalbipyramidal shape with the THF molecule in axial position. 相似文献
2.
Karl-Heinz Thiele Harald Windisch Heike Windisch Frank T. Edelmann Ulrike Kilimann Mathias Noltemeyer 《无机化学与普通化学杂志》1996,622(4):713-716
Contributions to the Chemistry of Transition Metal Alkyl Compounds. 64 [1] Preparation and Crystal Structure of Bis[N,N′ -bis(trimethylsilyl)-benzamidinato]dimethyltitanium Tetramethyltitanium reacts with excess N,N′-bis(trimethylsilyl)-benzamidine ( 1 ) to give bis[N,N′-bis(trimethylsilyl)benzamidinato]dimethyl-titanium ( 2 ) via protolysis. This compound was isolated and characterized by X-ray crystal structure analysis. In the crystal, 2 adopts an octahedral coordination with the methyl groups in cis-positions. The monomethyl complexes [PhC(NSiMe3)2]2M(Me)Cl ( 3 : M = Ti, 4 : M = Zr) have been prepared by treatment of the dichloro precursors with one equivalent of methyllithium. 相似文献
3.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XLI. Preparation and Thermolysis Products of Methyl Titanium Halides (CH3)nTiX4 ? n derivatives (X = Cl, Br, I) can be prepared by comproportionation reactions of tetramethyl titanium with titanium tetrahalides at deep temperature. Furthermore, the methyl titanium iodides are formed from tetramethyl titanium and iodine. Thermolysis of CH3TiX3 derivatives yields titanium(III) halides. At decomposition of the (CH3)2TiX2 compounds in ether solution titanium(II) halides are obtained in a fine-distributed, very reactive form. 相似文献
4.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XVIII. On the Preparation and Properties of Tetrabenzyl Vanadium and Benzyl Tantalum Chlorides Pure tetrabenzyl vanadium was isolated and characterized by elementary analyses, EPR and 1H-NMR spectra, by hydrolysis and thermal decomposition. — Experiments for the preparation of tetra or pentabenzyl compounds of niobium and tantalum failed, but we could prepare C6H5CH2TaCl4, (C6H5CH2)2TaCl3, and (C6H5CH2)3TaCl2, the last two in form of bipyridyl complexes. 相似文献
5.
Titanium(IV)chloride and bromide react with zinc dialkyls forming the corresponding titanium trihalides. In detail the preparation and charakterisation of methyltitanium trichloride, methyltitanium tribromide, phenyltitanium trichloride and of complexes of proypl-, pentyl- and phenyltitanium trichloride are described. Furthermore some considerations are made on the stabilities of organotitanium compounds. 相似文献
6.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXVII. Preparation of Titanium Acetates from Tetramethyl and Tetrabenzyl Titanium (CH3)4Ti reacts with CH3COOH at deep temperature to the colourless Ti(OCOCH3)4. Using ClCH2COOH slight violet Ti(OCOCH2Cl)4 is formed containing small amounts of reduction products. A complete reduction occurs in the analogous reaction with CF3COOH yielding dark green Ti(OCOCF3)3. From (C6H5CH2) 4 Ti and CH3COOH a green titanium(III,IV) acetat of the formula 4 Ti(OCOCH3) · Ti(OCOCH3)4 was obtained. – The isolated titanium acetates were characterized by elementary analyses, magnetic moments and i.r. spectra. 相似文献
7.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXIV. Preparation and Properties of Tetrabenzyl Molybdenum and Tetrabenzyl Uranium Tetrabenzyl molybdenum, (C6H5CH2)4Mo, can be obtained by the reaction of MoCl4 · 2 THF with dibenzyl magnesium. The compound forms darkbrown crystals, which are stable at room temperature. The analogous reaction of UCl4 · 3 THF with dibenzyl magnesium yields a reddish brown complex of tetrabenzyl uranium of the formula (C6H5CH2)4U · MgCl2. The synthesized compounds are characterized more in detail. 相似文献
8.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXXII. On Benzyl Copper Compounds Benzyl copper is formed reacting copper dichloride or acetylacetonate with dibenzyl zinc complexed by chlorides or acetylacetonates of copper and zinc. The complexes decompose between ?15 and +25°C with separation of copper and benzyl radicals proved by spin trap experiments. The stability of the compound is not influenced remarkably by substituents in o-position but is caused by complex formation with triphenyl phosphine. Pure benzyl copper, obtained by decomposition of BzCu · 0.25 BzZn(acac) · 0.75 Zn(acac)2 by means of diethyl ether, decomposes spontaneously even at a temperature of ?50°C. 相似文献
9.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. 61. Preparation and Crystal Structure of Tetramethyltitanium-1,2-bis(dimethylphosphino)ethane The title complex 1 was synthesized by addition of 1,2-bis(dimethylphosphino)ethane to a solution of tetramethyltitanium in diethylether. The complex was characterized by 1H, 13C and 31P NMR spectra and by X-ray crystal structure analysis. 1 consists of two independent molecules with distorted octahedral structure. 相似文献
10.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XV Preparation and Properties of Phenyl Vanadium Dichloride Vanadium(IV) chloride reacts with diphenyl zinc forming extremely air sensitive, at room temperature stable phenyl vanadium dichloride. The diffuse reflectance spectrum indicates an octahedral structure of the vanadium compound which is to regard as a coordination polymer. – Diethyl ether causes a cleavage of the V – C bond with formation of a vanadium dichloride etherate. 相似文献
11.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XIV. Investigations on Benzyl Tungsten Compounds. – On the Formation and Characterization of Tetrabenzyl Tungsten Unstable benzyl tungsten pentachloride is formed from tribenzyl boron and tungsten hexachloride. Other benzylating agents yield only less defined reduction products. – Reacting WCl4 · 2 THF with dibenzyl magnesium W(CH2C6H5)4 can be obtained. The new compound is stable at room temperature and is thoroughly characterized. 相似文献
12.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXXVIII. Reactions of Dibenzyl Manganese with Oxygene (C6H5CH2)2Mn · C4H8O2 reacts with oxygen forming an unstable deep violet compound which changes in a stable unsoluble yellow peroxide of the formula C6H5CH2MnO? OMnCH2C6 H5. With excess oxygen a polynuclear complex of 3 valent manganese is formed with the composition Mn4O4(OH)4(OCHC6H5)2. The compounds isolated were characterized by the products of hydrolyses and thermolyses, anaerobic reaction with iodine, magnetic moments, i.r. and e.s.r. spectra. 相似文献
13.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. 60 Synthesis and Properties of Zirconocene Dibenzyl Compounds — Molecular Structure of (Me3SiC5H4)2Zr(CH2C6H5)2 It is reported about the synthesis and n.m.r. spectroscopic characterization of zirconocene dibenzyl compounds with substituted cyclopentadienyl rings and the influence of the substituents on the Zr? CH2 bonds. The molecular structure of (Me3SiC5H4)2Zr · (CH2C6H5)2 is reported and discussed. 相似文献
14.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXXVII. About the Existence of 1-Norbornyl Compounds of Tungsten and Molybdenum Reactions of WCl6, WCl4, WO2Cl2, WOCl4, MoCl5, and MoO2(acac)2 with 1-Norbornyl lithium (1-NorLi1)) are described. From WCl6 and WCl4 [(1-Nor)2W]n is formed, whereas in dependence of the solvent WO2Cl2 and WOCl4 are transformed into the complexes Li2[1-NorWOCl4] · THF, Li[WOCl4], Li[WO2Cl2], and Li2[WO2Cl2]. MoCl5 and MoO2(acac)2 are reduced with formation of Li[MoCl5], Li[MoO2(acac)2] and Li2[MoO2(acac)2]. — Stable (1-Nor)4M-derivatives of molybdenum and tungsten, comparable those of 3d-metals (M = Ti? Co) seem not to exist. 相似文献
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Contributions to the Chemistry of Transition Metal Alkyl Compounds. XXXIV. Synthesis and Properties of 3-(N,N-dialkylamino)propyl Manganese Compounds MnCl2 reacts with lithium organyls of the type R2N(CH2)3Li with formation of definite organomanganese complexes. The pure [(CH3)2N(CH2)3]2Mn, [(C2H5)2N(CH2)3]2Mn, [(CH2)5N(CH2)3]2Mn and the complexes [(CH3)2N(CH2)3]2Mn · LiCl and Li{Mn[(CH2)3N(CH3)2]3} · 1,5 THF were isolated. [(CH3)2N(CH2)3]2Mn · 2 Li(acac) was obtained as a result of reactions of Mn(acac)2 and Mn(acac)3 with the corresponding lithium organyl. The σ-organomanganese(II) derivatives were characterized in detail by elementary analysis, molecular weight determination, ESR- and IR-spectra, conductivity measurements and the magnetic moments. 相似文献
16.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XL. About Lithium Alkenylmanganates(II) MnCl2 reacts with vinyl, 2,2-dimethylvinyl, allyl, and methallyl lithium giving rise to alkenyl manganates(II). In a pure state the compounds Li2[Mn(CH?CH2)4] · 1.5 diox, Li2[Mn(CH?C(CH3)2)4] · 1.5 diox, Li2[Mn(CH2? CH?CH2)4] · 2.5 diox and Li3[Mn(CH2? C(CH3)?CH2)5] · 2 diox were isolated. The compounds were characterized by elementary analysis, EPR and IR spectra, magnetic moments, and reactions with iodine. 相似文献
17.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. XLIII. Tetrakis(alkoxycarbonylmethyl)titanium Compounds Organotitanium(IV) compounds of the type (ROCOCH2)4Ti (R ? C2H5, i-C3H7, t-C4H9, C6H5, C6H5CH2) were obtained by reactions of ROCOCH2Li derivatives with TiCl4 at low temperature. The compounds which decompose only above 90°C were characterized by the hydrolysis products, anaerobic reactions with iodine, and the i.r. spectra. The bond conditions are discussed. 相似文献
18.
Contribution to the Chemistry of Transition Metal Alkyl Compounds. XXVIII. Benzylation of the Trivalent Titanium, Vanadium, and Chromium Acetylacetonates BzCr(acac)2, 2Bz(Vacac)2 · Mg(acac)2 and 3BzV(acac)2 · Al(acac)3 were obtained in definite form by reaction of Cr(acac)3 and V(acac)3 with Bz3Al, Bz2Mg, and BzMgCl. Ti(acac)3, reacts with Bz2Mg and BzLi forming deep green Bz3Ti, which could'nt be isolated free of impurities (Bz = C6H5CH2, acacH = acetylacetone). 相似文献
19.
Experiments on alkylation and arylation of titanium trichloride by means of organometallic compounds are reported. The formation of trimethyl titanium and derivates of triphenyl titanium was proved, and diphenyl titanium chloride was isolated in the crystalline state in form of a complex with diethyl ether. 相似文献
20.
Contributions to the Chemistry of Transition Metal Alkyl Compounds. 50. A non-common Organolanthanum Compound Lanthanum reacts with dibenzyl mercury in tetrahydrofuran as a solvent with splitting of solvent molecules and with formation of ethylene and a benzyl hydrido vinyloxide lanthanum complex of the composition C6H5CH2La(H)OCH?CH2 · 2 THF. This complex, primary well soluble in tetrahydrofuran, is extremely sensitive against air and moisture and undergoes a fast coordination polymerisation with a strong decrease of the solubility. The compound was characterized by elementary analysis, the hydrolysis and deuterolysis reaction, and by the i.r. spectra. 相似文献