A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide

This study describes the use of a silicon(II) complex, namely, the NHC-silyliumylidene cation complex [(I ) SiH]I (1, I =:C{N(Me)C(Me)} ), to catalyze the chemoselective N-formylation of primary and secondary amines using CO and PhSiH under mild conditions to afford the corresponding formamides a...

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Main Authors: Leong, Bi-Xiang, Teo, Yeow-Chuan, Condamines, Cloé, Yang, Ming-Chung, Su, Ming-Der, So, Cheuk-Wai
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2021
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Online Access:https://hdl.handle.net/10356/149731
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1497312023-02-28T19:57:06Z A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide Leong, Bi-Xiang Teo, Yeow-Chuan Condamines, Cloé Yang, Ming-Chung Su, Ming-Der So, Cheuk-Wai School of Physical and Mathematical Sciences Science::Chemistry::Organic chemistry Mixtures Catalysts This study describes the use of a silicon(II) complex, namely, the NHC-silyliumylidene cation complex [(I ) SiH]I (1, I =:C{N(Me)C(Me)} ), to catalyze the chemoselective N-formylation of primary and secondary amines using CO and PhSiH under mild conditions to afford the corresponding formamides as a sole product (average reaction time: 4.5 h; primary amines, average yield: 95%, average TOF: 8 h ; secondary amines, average yield: 98%, average TOF: 17 h ). The activity of 1 and product yields outperform the currently available non-transition-metal catalysts used for this catalysis. Mechanistic studies show that the silicon(II) center in complex 1 catalyzes the C−N bond formation via a different pathway in comparison with non-transition-metal catalysts. It sequentially activates CO , PhSiH , and amines, which proceeds via a dihydrogen elimination mechanism, to form formamides, siloxanes, and dihydrogen gas. Ministry of Education (MOE) National Research Foundation (NRF) Accepted version 2021-05-24T15:02:47Z 2021-05-24T15:02:47Z 2020 Journal Article Leong, B., Teo, Y., Condamines, C., Yang, M., Su, M. & So, C. (2020). A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide. ACS Catalysis, 10(24), 14824-14833. https://dx.doi.org/10.1021/acscatal.0c03795 2155-5435 0000-0003-4816-9801 https://hdl.handle.net/10356/149731 10.1021/acscatal.0c03795 2-s2.0-85097733521 24 10 14824 14833 en ACS Catalysis This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Catalysis, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acscatal.0c03795 application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry::Organic chemistry
Mixtures
Catalysts
spellingShingle Science::Chemistry::Organic chemistry
Mixtures
Catalysts
Leong, Bi-Xiang
Teo, Yeow-Chuan
Condamines, Cloé
Yang, Ming-Chung
Su, Ming-Der
So, Cheuk-Wai
A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide
description This study describes the use of a silicon(II) complex, namely, the NHC-silyliumylidene cation complex [(I ) SiH]I (1, I =:C{N(Me)C(Me)} ), to catalyze the chemoselective N-formylation of primary and secondary amines using CO and PhSiH under mild conditions to afford the corresponding formamides as a sole product (average reaction time: 4.5 h; primary amines, average yield: 95%, average TOF: 8 h ; secondary amines, average yield: 98%, average TOF: 17 h ). The activity of 1 and product yields outperform the currently available non-transition-metal catalysts used for this catalysis. Mechanistic studies show that the silicon(II) center in complex 1 catalyzes the C−N bond formation via a different pathway in comparison with non-transition-metal catalysts. It sequentially activates CO , PhSiH , and amines, which proceeds via a dihydrogen elimination mechanism, to form formamides, siloxanes, and dihydrogen gas.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Leong, Bi-Xiang
Teo, Yeow-Chuan
Condamines, Cloé
Yang, Ming-Chung
Su, Ming-Der
So, Cheuk-Wai
format Article
author Leong, Bi-Xiang
Teo, Yeow-Chuan
Condamines, Cloé
Yang, Ming-Chung
Su, Ming-Der
So, Cheuk-Wai
author_sort Leong, Bi-Xiang
title A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide
title_short A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide
title_full A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide
title_fullStr A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide
title_full_unstemmed A NHC-silyliumylidene cation for catalytic N‑formylation of amines using carbon dioxide
title_sort nhc-silyliumylidene cation for catalytic n‑formylation of amines using carbon dioxide
publishDate 2021
url https://hdl.handle.net/10356/149731
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