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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1523-1529 
    ISSN: 1434-1948
    Keywords: Boron ; Iron ; Ruthenium ; Boryl Complexes ; Borylene Complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactivity of aminodihaloboranes R2NBX2 (R = Me, SiMe3; × = Cl, Br) towards transition metal complexes of the type Na[(η5-C5R′5)M(CO)2)] (M = Fe, Ru; R′ = H, Me) was investigated. In the case of Me2NBBr2 and M = Fe the borylcomplexes [(η5-C5R′5)(CO)2Fe{BBr(NMe2)}] (C5R′5 = C5H59a; C5R′5 = C5H4Me 9b; C5R′5 = C5Me510) were obtained. The compounds 9aand 9bwere formed together with the corresponding bridged borylene complexes [μ-BNMe2(μ-CO){(η5-C5R′5)Fe(CO)}2] (C5R′5 = C5H511a; C5R′5 = C5H4Me 11b) in a 1:1 ratio, the latter, however, could be isolated from these mixtures as pure materials. In addition the novel boryl and borylene ruthenium complexes [(η5-C5H5)(CO)2Ru{BX(NMe2)}] (X = Cl 12a; × = Br 12b), [(η5-C5H5)(CO)2Ru{BCl{NSiMe3{BClN(SiMe3)2}}}] (13) and [μ-BN(SiMe3)2(μ-CO){(η5-C5H5)Ru(CO)}2] (14) were obtained by similar methods. All compounds were characterized by multinuclear NMR and IR spectroscopy. The structure of 13 in the solid state was determined by a single-crystal X-ray diffraction study.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 1418-1431 
    ISSN: 0947-6539
    Keywords: ab initio calculations ; alkali metals ; Si ligands ; silicon ; structure elucidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transmetalation reactions between bis(hypersilyl)zinc Zn[Si(SiMe3)3]2 and alkali metals have already been established as a facile route to powders of the solvent-free potassium, rubidium, and cesium derivatives of tris(trimethylsilyl)-silane (hypersilane, (Me3Si)3SiH).[1,2] By the use of boiling n-heptane as the solvent, the hitherto unknown NaSi(SiMe3)3 (1) along with the previously synthesized KSi(SiMe3)3 (2) have now been obtained as colorless crystalline materials. Information from NMR and Raman spectra in conjunction with the acute Si-Si-Si angles found in their molecular structures indicate mainly ionic bonding. This was verified by population analyses of suitable model systems. Both hypersilanides[2] consist of cyclic dimers [MSi(SiMe3)3]2 (1a, M = Na; 2a, M = K) with almost planar M2Si2 rings (Na-Si = 299 pm (av); K-Si = 339 pm (av)), which are linked up into coordination polymers. In a similar manner to the related rubidium and cesium derivatives, a pentane suspension of the potassium compound afforded a yellow solution on addition of benzene, from which the crystalline, bright yellow tris(benzene) solvate 2·(benzene)3 (2b) was isolated. Complex 2b consists of monomers containing short K-Si bonds (332-334 pm) and three η6-bonded benzene molecules. No solvate of 1 was obtained under these conditions. However, on crystallization from pure benzene, crystals of (1)2·benzene (1b) were isolated (Na-Si = 302 pm (av)). Benzene was found to be intercalated between rods of coordination polymers of (1)2. In addition, the influence of π or s̰ donors on the molecular and crystal structures of hypersilylrubidium (3) and cesium (4) was investigated. The structures of the tetrahydrofuran solvate (4)2·THF (4c), the biphenylene/pentane complex (4)2·biphen·(pentane)0.5 (4b) along with the known toluene solvates (3)27dot;toluene (3a) and (4)2·(toluene)3 (4a)[1a] are compared. Finally, an example is presented of how the alkali metal hypersilanides could be utilized in preparing extremely bulky stannanide anions.
    Additional Material: 20 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 579-582 
    ISSN: 1434-1948
    Keywords: Lead ; Plumbylenes ; Plumbanediyles ; Diplumbene ; Plumbylene dimers ; Double-bond systems ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of the diarylplumbylene R2Pb: (R = 2,4,6-iPr3C6H2) with the disilylplumbylene R′2Pb: [R′ = Si(SiMe3)3] furnishes the heteroleptic plumbylene RR′Pb: which exists as the diplumbene RR′Pb=PbRR′ (7) in the solid state. The X-ray structure analysis of 7 reveals a trans-bent angle of 42.7° and a Pb-Pb bond length of 298.99(5) pm, the shortest observed so far for diplumbenes with a lead-lead double bond. Reaction of mesitylmagnesium bromide with PbCl2 yielded black crystals of an MgBr2 stabilized dimesitylplumbylene dimer with a large trans-bent angle of 71°, a lead-lead separation of 335.49(6) pm, and long Pb···Br contacts of 315.71(8) pm.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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