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Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene

The reaction between allenylpyridine (L1) and (Me(2)S)AuCl resulted in the quantitative formation of the (Indolizy)gold chloride complex 1 (Indolizy = indolizin-2-ylidene). The reaction of 1 with carbazole in the presence of KO(t)Bu affords the corresponding (Indolizy)Au(Cz) complex 2. Both compound...

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Autores principales: Romanov, Alexander S., Linnolahti, Mikko, Bochmann, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631002/
https://www.ncbi.nlm.nih.gov/pubmed/34781337
http://dx.doi.org/10.1039/d1dt03393j
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author Romanov, Alexander S.
Linnolahti, Mikko
Bochmann, Manfred
author_facet Romanov, Alexander S.
Linnolahti, Mikko
Bochmann, Manfred
author_sort Romanov, Alexander S.
collection PubMed
description The reaction between allenylpyridine (L1) and (Me(2)S)AuCl resulted in the quantitative formation of the (Indolizy)gold chloride complex 1 (Indolizy = indolizin-2-ylidene). The reaction of 1 with carbazole in the presence of KO(t)Bu affords the corresponding (Indolizy)Au(Cz) complex 2. Both compounds show high air- and temperature stability. The crystal structure of 2 confirmed the linear co-planar geometry. Complex 1 shows an intense low energy absorption of mixed character in the UV-vis spectrum, ascribed to intraligand and (M + Hal)L charge transfer processes, and exhibits bright yellow phosphorescence with an excited state lifetime of 62.8 μs in the crystal and a luminescence quantum yield up to 65%. On the other hand, the carbazolate complex 2 in a polystyrene matrix shows bright red delayed fluorescence at 617 nm with a sub-microsecond excited state lifetime and a quantum yield of 21.6%.
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spelling pubmed-86310022021-12-13 Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene Romanov, Alexander S. Linnolahti, Mikko Bochmann, Manfred Dalton Trans Chemistry The reaction between allenylpyridine (L1) and (Me(2)S)AuCl resulted in the quantitative formation of the (Indolizy)gold chloride complex 1 (Indolizy = indolizin-2-ylidene). The reaction of 1 with carbazole in the presence of KO(t)Bu affords the corresponding (Indolizy)Au(Cz) complex 2. Both compounds show high air- and temperature stability. The crystal structure of 2 confirmed the linear co-planar geometry. Complex 1 shows an intense low energy absorption of mixed character in the UV-vis spectrum, ascribed to intraligand and (M + Hal)L charge transfer processes, and exhibits bright yellow phosphorescence with an excited state lifetime of 62.8 μs in the crystal and a luminescence quantum yield up to 65%. On the other hand, the carbazolate complex 2 in a polystyrene matrix shows bright red delayed fluorescence at 617 nm with a sub-microsecond excited state lifetime and a quantum yield of 21.6%. The Royal Society of Chemistry 2021-11-08 /pmc/articles/PMC8631002/ /pubmed/34781337 http://dx.doi.org/10.1039/d1dt03393j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Romanov, Alexander S.
Linnolahti, Mikko
Bochmann, Manfred
Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene
title Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene
title_full Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene
title_fullStr Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene
title_full_unstemmed Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene
title_short Synthesis and photophysical properties of linear gold(i) complexes based on a CCC carbene
title_sort synthesis and photophysical properties of linear gold(i) complexes based on a ccc carbene
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631002/
https://www.ncbi.nlm.nih.gov/pubmed/34781337
http://dx.doi.org/10.1039/d1dt03393j
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