A cyclic silylone ("siladicarbene") with an electron-rich silicon(0) atom

Yun Xiong; Shenglai Yao; Shigeyoshi Inoue; Jan Dirk Epping; Matthias Driess

doi:10.1002/anie.201302537

A cyclic silylone ("siladicarbene") with an electron-rich silicon(0) atom

Yun Xiong
, Shenglai Yao
, Shigeyoshi Inoue
, Jan Dirk Epping
, Matthias Driess

Technische Universität Berlin

Research output: Contribution to journal › Article › peer-review

228 Scopus citations

Abstract

King of donor: The chelating bis(carbene) 1 enabled the synthesis of the new silyliumylidene salt 2. This salt can be dechlorinated with sodium naphthalenide to give the first cyclic siladicarbene 3, which bears a single Si⁰ atom with strikingly high basicity. The small C-Si-C angle of 89.1° and the average C-Si distance of 1.869 Å are consistent with results from theoretical calculations, which revealed that 3 is best described as a silylone.

Original language	English
Pages (from-to)	7147-7150
Number of pages	4
Journal	Angewandte Chemie International Edition in English
Volume	52
Issue number	28
DOIs	https://doi.org/10.1002/anie.201302537
State	Published - 8 Jul 2013
Externally published	Yes

Keywords

main-group chemistry
siladicarbenes
silicon
silylenes
silyliumylidenes

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10.1002/anie.201302537

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abstract = "King of donor: The chelating bis(carbene) 1 enabled the synthesis of the new silyliumylidene salt 2. This salt can be dechlorinated with sodium naphthalenide to give the first cyclic siladicarbene 3, which bears a single Si0 atom with strikingly high basicity. The small C-Si-C angle of 89.1° and the average C-Si distance of 1.869 {\AA} are consistent with results from theoretical calculations, which revealed that 3 is best described as a silylone.",

keywords = "main-group chemistry, siladicarbenes, silicon, silylenes, silyliumylidenes",

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year = "2013",

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T1 - A cyclic silylone ("siladicarbene") with an electron-rich silicon(0) atom

AU - Xiong, Yun

AU - Yao, Shenglai

AU - Inoue, Shigeyoshi

AU - Epping, Jan Dirk

AU - Driess, Matthias

PY - 2013/7/8

Y1 - 2013/7/8

N2 - King of donor: The chelating bis(carbene) 1 enabled the synthesis of the new silyliumylidene salt 2. This salt can be dechlorinated with sodium naphthalenide to give the first cyclic siladicarbene 3, which bears a single Si0 atom with strikingly high basicity. The small C-Si-C angle of 89.1° and the average C-Si distance of 1.869 Å are consistent with results from theoretical calculations, which revealed that 3 is best described as a silylone.

AB - King of donor: The chelating bis(carbene) 1 enabled the synthesis of the new silyliumylidene salt 2. This salt can be dechlorinated with sodium naphthalenide to give the first cyclic siladicarbene 3, which bears a single Si0 atom with strikingly high basicity. The small C-Si-C angle of 89.1° and the average C-Si distance of 1.869 Å are consistent with results from theoretical calculations, which revealed that 3 is best described as a silylone.

KW - main-group chemistry

KW - siladicarbenes

KW - silicon

KW - silylenes

KW - silyliumylidenes

UR - https://www.scopus.com/pages/publications/84880140182

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DO - 10.1002/anie.201302537

M3 - Article

AN - SCOPUS:84880140182

SN - 1433-7851

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EP - 7150

JO - Angewandte Chemie International Edition in English

JF - Angewandte Chemie International Edition in English

IS - 28

ER -

A cyclic silylone ("siladicarbene") with an electron-rich silicon(0) atom

Abstract

Keywords

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