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Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies

Herein we demonstrate a synthetic protocol for the regioselective thiocyanation of corroles. To the best of our knowledge, thiocyanato appended corrole has never been reported earlier. The resulting thiocyanato appended corrole turned out to be a good corrole based precursor for the facile synthesis...

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Detalles Bibliográficos
Autores principales: Sahu, Kasturi, Mondal, Sruti, Patra, Bratati, Pain, Tanmoy, Patra, Sajal Kumar, Dosche, Carsten, Kar, Sanjib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419656/
https://www.ncbi.nlm.nih.gov/pubmed/36134003
http://dx.doi.org/10.1039/c9na00671k
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author Sahu, Kasturi
Mondal, Sruti
Patra, Bratati
Pain, Tanmoy
Patra, Sajal Kumar
Dosche, Carsten
Kar, Sanjib
author_facet Sahu, Kasturi
Mondal, Sruti
Patra, Bratati
Pain, Tanmoy
Patra, Sajal Kumar
Dosche, Carsten
Kar, Sanjib
author_sort Sahu, Kasturi
collection PubMed
description Herein we demonstrate a synthetic protocol for the regioselective thiocyanation of corroles. To the best of our knowledge, thiocyanato appended corrole has never been reported earlier. The resulting thiocyanato appended corrole turned out to be a good corrole based precursor for the facile synthesis of thiol protected gold nanoparticles (Au NPs). The ligand system acts as a good bidentate framework and passivates the gold surface. A strong electronic interaction between the corrole and the gold nanoparticles is manifested by their unique photo physical properties and it also confirms that the binding through β-substitutions has a more pronounced effect even though the corrole rings are face-off to the gold surface.
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spelling pubmed-94196562022-09-20 Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies Sahu, Kasturi Mondal, Sruti Patra, Bratati Pain, Tanmoy Patra, Sajal Kumar Dosche, Carsten Kar, Sanjib Nanoscale Adv Chemistry Herein we demonstrate a synthetic protocol for the regioselective thiocyanation of corroles. To the best of our knowledge, thiocyanato appended corrole has never been reported earlier. The resulting thiocyanato appended corrole turned out to be a good corrole based precursor for the facile synthesis of thiol protected gold nanoparticles (Au NPs). The ligand system acts as a good bidentate framework and passivates the gold surface. A strong electronic interaction between the corrole and the gold nanoparticles is manifested by their unique photo physical properties and it also confirms that the binding through β-substitutions has a more pronounced effect even though the corrole rings are face-off to the gold surface. RSC 2019-11-21 /pmc/articles/PMC9419656/ /pubmed/36134003 http://dx.doi.org/10.1039/c9na00671k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Sahu, Kasturi
Mondal, Sruti
Patra, Bratati
Pain, Tanmoy
Patra, Sajal Kumar
Dosche, Carsten
Kar, Sanjib
Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies
title Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies
title_full Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies
title_fullStr Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies
title_full_unstemmed Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies
title_short Regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies
title_sort regioselective thiocyanation of corroles and the synthesis of gold nanoparticle–corrole assemblies
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419656/
https://www.ncbi.nlm.nih.gov/pubmed/36134003
http://dx.doi.org/10.1039/c9na00671k
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