Über polygermane: XI. Funktionalisierung von hexaphenyldigerman
D Simon, K Häberle, M Dräger
Index: Simon, Dietolf; Haeberle, Karl; Draeger, Martin Journal of Organometallic Chemistry, 1984 , vol. 267, # 2 p. 133 - 142
Full Text: HTML
Citation Number: 29
Abstract
Abstract The optimum conditions for selectively cleaving off two phenyl groups in Ge 2 Ph 6 by trichloroacetic acid have been determined. Neither trihaloacetic acids nor HCl/AlCl 3 nor reactive tetrahalides MCl 4 are suitable reagents for cleaving one phenyl group alone. The 13 C NMR chemical shifts of functional phenyl-mono-and-digermanes are given. The crystal structure of 1, 2-bis (trichloroacetate) tetraphenyldigermane has been determined and ...
Related Articles:
[Amadoruge, Monika L.; Short, Erin K.; Moore, Curtis; Rheingold, Arnold L.; Weinert, Charles S. Journal of Organometallic Chemistry, 2010 , vol. 695, # 14 p. 1813 - 1823]