Titlebook: Be Organoberyllium Compounds; Part 1 Hubert Schmidbaur,Aflons Kubny,Marlis Mirbach,Adol Book 1987Latest edition Springer-Verlag Berlin Heid

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Lecture Notes in Computer ScienceTo 1,2-C.B.H. in C.H. is added an equimolar amount of Be(C.H.).∙3.30(C.H.).. C.H. is evolved, and a white precipitate is formed in a small yield. The precipitate is separated by filtration, washed with C.H., and dried at 50°C.

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Compounds with Ligands Bonded by Two or Three Carbon Atoms (Beryllocarbaboranes),To 1,2-C.B.H. in C.H. is added an equimolar amount of Be(C.H.).∙3.30(C.H.).. C.H. is evolved, and a white precipitate is formed in a small yield. The precipitate is separated by filtration, washed with C.H., and dried at 50°C.

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Gmelin Handbook of Inorganic and Organometallic Chemistry - 8th editionhttp://image.papertrans.cn/b/image/181897.jpg

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Zygmunt Vetulani,Joseph Mariani,Marek Kubison Be.R.H. (R = CH., C.H.) or Be.(C.H.).H [1 to 5]. There is little evidence about their constitution. Whereas the latter example is discussed as a single compound in the literature [4, 5], solutions of Be.R.H. may contain many species in complex equilibria [2]. Mainly on the basis of their reaction

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Roman Grundkiewicz,Marcin Junczys-Dowmuntcal compounds are included in this volume in deviation from the Gmelin practice, since extensive theoretical calculations exist, whereas the experimental work on organoberyllium compounds has become extremely scarce because of the toxicity.

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