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Main Author: Jesús Campos
Format: Artículo científico
Language:en
Published: Sociedad Química de México 2017
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Online Access:https://www.redalyc.org/articulo.oa?id=47552182002
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author Jesús Campos
author_facet Jesús Campos
contents Synthesis and Reactivity Studies of Cationic Ir(III) Alkylidines. a-Hydride Abstraction Reactions Jesús Campos Ernesto Carmona Multidisciplinaria (Ciencias Naturales y Exactas) iridium Alkylidene C coupling metalacycle hydride abstraction The chemistry of late transition metal alkylidenes [M=CR2], where R is H a hydrocarbyl group, have attracted widespread attention although mainly with reference to complexes of metals in low oxidation state. We focus in this paper on reactions based on electrophilic attacks by Ph3C+ that allow either isolation of stable cationic Ir(III) alkylidenes, considerably more attractive than well-known Ir(I) counterparts, or the generation of very reactive variants that experience fast migratory insertion into existing Ir-C and Ir-H sigma bonds. The present studies are based on (η5-C5Me5)Ir(III) complexes that bear a cyclometalated PMeXyl2 ligand (Xyl = 2,6-Me2C6H3). The contribution of different monoanionic ligands (chloride, alkyl or hydride) to either stabilize the Ir=CR2 linkage or provide facile reactivity routes has been investigated, including the use of various deuterium isotopologues of the iridium complex precursors. 2017 artículo científico 1870-249X https://www.redalyc.org/articulo.oa?id=47552182002 en http://www.redalyc.org/revista.oa?id=475 Journal of the Mexican Chemical Society application/pdf Sociedad Química de México Journal of the Mexican Chemical Society (México) Num.2 Vol.61
format Artículo científico
id redalyc_47552182002
language en
publishDate 2017
publisher Sociedad Química de México
spellingShingle Synthesis and Reactivity Studies of Cationic Ir(III) Alkylidines. a-Hydride Abstraction Reactions
Jesús Campos
Multidisciplinaria (Ciencias Naturales y Exactas)
iridium
Alkylidene
C coupling
metalacycle
hydride abstraction
Synthesis and Reactivity Studies of Cationic Ir(III) Alkylidines. a-Hydride Abstraction Reactions Jesús Campos Ernesto Carmona Multidisciplinaria (Ciencias Naturales y Exactas) iridium Alkylidene C coupling metalacycle hydride abstraction The chemistry of late transition metal alkylidenes [M=CR2], where R is H a hydrocarbyl group, have attracted widespread attention although mainly with reference to complexes of metals in low oxidation state. We focus in this paper on reactions based on electrophilic attacks by Ph3C+ that allow either isolation of stable cationic Ir(III) alkylidenes, considerably more attractive than well-known Ir(I) counterparts, or the generation of very reactive variants that experience fast migratory insertion into existing Ir-C and Ir-H sigma bonds. The present studies are based on (η5-C5Me5)Ir(III) complexes that bear a cyclometalated PMeXyl2 ligand (Xyl = 2,6-Me2C6H3). The contribution of different monoanionic ligands (chloride, alkyl or hydride) to either stabilize the Ir=CR2 linkage or provide facile reactivity routes has been investigated, including the use of various deuterium isotopologues of the iridium complex precursors. 2017 artículo científico 1870-249X https://www.redalyc.org/articulo.oa?id=47552182002 en http://www.redalyc.org/revista.oa?id=475 Journal of the Mexican Chemical Society application/pdf Sociedad Química de México Journal of the Mexican Chemical Society (México) Num.2 Vol.61
title Synthesis and Reactivity Studies of Cationic Ir(III) Alkylidines. a-Hydride Abstraction Reactions
topic Multidisciplinaria (Ciencias Naturales y Exactas)
iridium
Alkylidene
C coupling
metalacycle
hydride abstraction
url https://www.redalyc.org/articulo.oa?id=47552182002