2020
DOI: 10.1002/chem.202004579
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Germaborenes: Borylene Transfer Agents for the Synthesis of Iminoboranes

Abstract: Halide and phenyl substituted germaborenes were shown to react with azides at room temperature and transfer a borylene moiety to give iminoboranes. This iminoborane synthesis based on a borylene transfer route was investigated computationally in the case of the phenyl substituted germaborene.

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Cited by 15 publications
(17 citation statements)
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“…13 Besides the formation of G, phosphine-stabilized germaborenes were also synthesized. 7,14,15 In this publication, we report on the synthesis and reactivity of the phosphine-stabilized germasilenylidene 4 (Scheme 1), a derivative of B.…”
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“…13 Besides the formation of G, phosphine-stabilized germaborenes were also synthesized. 7,14,15 In this publication, we report on the synthesis and reactivity of the phosphine-stabilized germasilenylidene 4 (Scheme 1), a derivative of B.…”
mentioning
confidence: 99%
“…61−65 Obviously, stabilization of the low-valent species by the chelating germylene−phosphine is weak enough to allow for transfer of a germanium atom, borylene units, and a silicon atom. 7,14,15 After storage of a benzene solution of 4 at room temperature for several days, the red color of the solution turns a deeper red to give a burgundy-red solid after evaporation of the solvent. Single crystals suitable for X-ray diffraction were obtained from benzene/pentane and are of purple color.…”
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