Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines

The reaction of a terminal alkyne (RCCH) and 2- aminopyridine (R′C5NH3NH2) with the dinuclear species [Cp*IrCl2]2 afforded the cationic aminocarbene derivatives Cp*Ir(Cl)[ C- (CH2R)NHC5NH3R′] via a hydroamination and a ligand substitution. The reaction pathway has been examined through computat...

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Main Authors: Kumaran, Elumalai, How, Kai Tong Sonia, Ganguly, Rakesh, Li, Yongxin, Leong, Weng Kee
Other Authors: School of Physical and Mathematical Sciences
Format: Journal Article
Language:English
Published: 2014
Subjects:
Online Access:https://hdl.handle.net/10356/101625
http://hdl.handle.net/10220/18657
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author Kumaran, Elumalai
How, Kai Tong Sonia
Ganguly, Rakesh
Li, Yongxin
Leong, Weng Kee
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Kumaran, Elumalai
How, Kai Tong Sonia
Ganguly, Rakesh
Li, Yongxin
Leong, Weng Kee
author_sort Kumaran, Elumalai
collection NTU
description The reaction of a terminal alkyne (RCCH) and 2- aminopyridine (R′C5NH3NH2) with the dinuclear species [Cp*IrCl2]2 afforded the cationic aminocarbene derivatives Cp*Ir(Cl)[ C- (CH2R)NHC5NH3R′] via a hydroamination and a ligand substitution. The reaction pathway has been examined through computational studies.
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spelling ntu-10356/1016252023-02-28T19:42:20Z Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines Kumaran, Elumalai How, Kai Tong Sonia Ganguly, Rakesh Li, Yongxin Leong, Weng Kee School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds The reaction of a terminal alkyne (RCCH) and 2- aminopyridine (R′C5NH3NH2) with the dinuclear species [Cp*IrCl2]2 afforded the cationic aminocarbene derivatives Cp*Ir(Cl)[ C- (CH2R)NHC5NH3R′] via a hydroamination and a ligand substitution. The reaction pathway has been examined through computational studies. MOE (Min. of Education, S’pore) Accepted version 2014-01-21T08:19:58Z 2019-12-06T20:41:41Z 2014-01-21T08:19:58Z 2019-12-06T20:41:41Z 2013 2013 Journal Article Kumaran, E., How, K. T. S., Ganguly, R., Li, Y., & Leong, W. K. (2013). Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines. Organometallics, 32(15), 4149-4152. https://hdl.handle.net/10356/101625 http://hdl.handle.net/10220/18657 10.1021/om400326c en Organometallics © 2013 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Organometallics, American Chemical Society. 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/10.1021/om400326c]. 4p. application/pdf
spellingShingle DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds
Kumaran, Elumalai
How, Kai Tong Sonia
Ganguly, Rakesh
Li, Yongxin
Leong, Weng Kee
Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines
title Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines
title_full Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines
title_fullStr Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines
title_full_unstemmed Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines
title_short Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines
title_sort synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2 aminopyridines
topic DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds
url https://hdl.handle.net/10356/101625
http://hdl.handle.net/10220/18657
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