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Persistent Digermenes with Acyl and α‐Chlorosilyl Functionalities

We report the preparation of α‐chlorosilyl‐ and acyl‐substituted digermenes. Unlike the corresponding transient disilenes, these species with a Ge=Ge double bond show an unexpectedly low tendency for cyclization, but in turn are prone to thermal Ge=Ge bond cleavage. Triphenylsilyldigermene has been...

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Detalles Bibliográficos
Autores principales: Klemmer, Lukas, Kaiser, Yvonne, Huch, Volker, Zimmer, Michael, Scheschkewitz, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852044/
https://www.ncbi.nlm.nih.gov/pubmed/31306508
http://dx.doi.org/10.1002/chem.201902553
Descripción
Sumario:We report the preparation of α‐chlorosilyl‐ and acyl‐substituted digermenes. Unlike the corresponding transient disilenes, these species with a Ge=Ge double bond show an unexpectedly low tendency for cyclization, but in turn are prone to thermal Ge=Ge bond cleavage. Triphenylsilyldigermene has been isolated as a crystalline model compound, and is the first fully characterized example of a neutral digermene with an A(2)GeGeAB substitution pattern. Spectroscopic and computational evidence prove the constitution of 1‐adamantoyldigermene as a first persistent species with a heavy double bond conjugated with a carbonyl moiety.