Titlebook: Ga Organogallium Compounds; Part 1 Jean-Claude Maire,Ulrich Krüerke,Christa Siebert,U Book 1986Latest edition Springer-Verlag Berlin Heidel

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Book 1986Latest editiontely.to the end of 1984 and includes many references to the literature up to the end of 1985. The organic chemistry of gallium is largely dominated by compounds of the types GaR3 (Chapter 1), GaR X _ (Chapters 2 to 12), and M[GaRnX4_nl (M = cation, Chapter 13), where X n 3 n stands for a non-carbon

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Virginia Woolf and D.H. Lawrence,(No. 11 in Table 73) was also described but only characterized by IR spectroscopy. Incorporation of N-bases (C.H.N, tetramethylethylenediamine, 2,2′-bipyridyl) causes the molecule to monomerize to give compounds of Formula V, containing a formally “subvalent” Ga atom.

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Organogallium-Transition Metal Compounds,(No. 11 in Table 73) was also described but only characterized by IR spectroscopy. Incorporation of N-bases (C.H.N, tetramethylethylenediamine, 2,2′-bipyridyl) causes the molecule to monomerize to give compounds of Formula V, containing a formally “subvalent” Ga atom.

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A Revolution in Economic Theoryliquid (condensing at -15°C in a vacuum system) did not correspond in its properties to those reported for Ga(CH.).H and yielded on pyrolysis only ~43% of the expected amount of Ga(CH.). and H. [5]. Ga(CH.).H was mentioned as a decomposition product of unstable Ga(CH.).GeH. but neither compound was isolated in a pure form and characterized [6].