The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water

The iridium complexes Cp*Ir(CO)(Cl)(CH2R), which do not contain any β-hydrogen atoms, react with water to form aldehydes. This reaction was found to be photochemically activated, and a possible pathway involving radical intermediates has been proposed and studied experimentally and computationally.

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Main Authors: Lee, Jia Ying, Fan, Wai Yip, Mak, Garvin Kar Hang, Leong, Weng Kee
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/99564
http://hdl.handle.net/10220/17390
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-995642023-02-28T20:03:00Z The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water Lee, Jia Ying Fan, Wai Yip Mak, Garvin Kar Hang Leong, Weng Kee School of Physical and Mathematical Sciences The iridium complexes Cp*Ir(CO)(Cl)(CH2R), which do not contain any β-hydrogen atoms, react with water to form aldehydes. This reaction was found to be photochemically activated, and a possible pathway involving radical intermediates has been proposed and studied experimentally and computationally. MOE (Min. of Education, S’pore) Accepted version 2013-11-07T07:11:54Z 2019-12-06T20:08:57Z 2013-11-07T07:11:54Z 2019-12-06T20:08:57Z 2012 2012 Journal Article Lee, J. Y., Fan, W. Y., Mak, K. H. G., & Leong, W. K. (2013). The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water. Journal of Organometallic Chemistry, 724, 275-280. 0022-328X https://hdl.handle.net/10356/99564 http://hdl.handle.net/10220/17390 10.1016/j.jorganchem.2012.11.030 en Journal of organometallic chemistry © 2012 Elsevier B.V. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of organometallic chemistry, Elsevier B.V. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1016/j.jorganchem.2012.11.030]. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
description The iridium complexes Cp*Ir(CO)(Cl)(CH2R), which do not contain any β-hydrogen atoms, react with water to form aldehydes. This reaction was found to be photochemically activated, and a possible pathway involving radical intermediates has been proposed and studied experimentally and computationally.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Lee, Jia Ying
Fan, Wai Yip
Mak, Garvin Kar Hang
Leong, Weng Kee
format Article
author Lee, Jia Ying
Fan, Wai Yip
Mak, Garvin Kar Hang
Leong, Weng Kee
spellingShingle Lee, Jia Ying
Fan, Wai Yip
Mak, Garvin Kar Hang
Leong, Weng Kee
The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water
author_sort Lee, Jia Ying
title The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water
title_short The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water
title_full The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water
title_fullStr The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water
title_full_unstemmed The formation of aldehydes from the photochemically activated reaction of Cp*Ir(CO)(Cl)(CH2R) complexes with water
title_sort formation of aldehydes from the photochemically activated reaction of cp*ir(co)(cl)(ch2r) complexes with water
publishDate 2013
url https://hdl.handle.net/10356/99564
http://hdl.handle.net/10220/17390
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