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Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+)

The design of photoswitchable transition metal complexes with tailored properties is one of the most important challenges in chemistry. Studies explaining the underlying mechanisms are, however, scarce. Herein, the early relaxation dynamics towards NO photoisomerization in trans‐[RuCl(NO)(py)(4)](2+...

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Autores principales: Talotta, Francesco, Boggio‐Pasqua, Martial, González, Leticia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539916/
https://www.ncbi.nlm.nih.gov/pubmed/32281169
http://dx.doi.org/10.1002/chem.202000507
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author Talotta, Francesco
Boggio‐Pasqua, Martial
González, Leticia
author_facet Talotta, Francesco
Boggio‐Pasqua, Martial
González, Leticia
author_sort Talotta, Francesco
collection PubMed
description The design of photoswitchable transition metal complexes with tailored properties is one of the most important challenges in chemistry. Studies explaining the underlying mechanisms are, however, scarce. Herein, the early relaxation dynamics towards NO photoisomerization in trans‐[RuCl(NO)(py)(4)](2+) is elucidated by means of non‐adiabatic dynamics, which provided time‐resolved information and branching ratios. Three deactivation mechanisms (I, II, III) in the ratio 3:2:4 were identified. Pathways I and III involve ultrafast intersystem crossing and internal conversion, whereas pathway II involves only internal conversion.
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spelling pubmed-75399162020-10-09 Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+) Talotta, Francesco Boggio‐Pasqua, Martial González, Leticia Chemistry Full Papers The design of photoswitchable transition metal complexes with tailored properties is one of the most important challenges in chemistry. Studies explaining the underlying mechanisms are, however, scarce. Herein, the early relaxation dynamics towards NO photoisomerization in trans‐[RuCl(NO)(py)(4)](2+) is elucidated by means of non‐adiabatic dynamics, which provided time‐resolved information and branching ratios. Three deactivation mechanisms (I, II, III) in the ratio 3:2:4 were identified. Pathways I and III involve ultrafast intersystem crossing and internal conversion, whereas pathway II involves only internal conversion. John Wiley and Sons Inc. 2020-08-04 2020-09-04 /pmc/articles/PMC7539916/ /pubmed/32281169 http://dx.doi.org/10.1002/chem.202000507 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Talotta, Francesco
Boggio‐Pasqua, Martial
González, Leticia
Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+)
title Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+)
title_full Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+)
title_fullStr Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+)
title_full_unstemmed Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+)
title_short Early Relaxation Dynamics in the Photoswitchable Complex trans‐[RuCl(NO)(py)(4)](2+)
title_sort early relaxation dynamics in the photoswitchable complex trans‐[rucl(no)(py)(4)](2+)
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539916/
https://www.ncbi.nlm.nih.gov/pubmed/32281169
http://dx.doi.org/10.1002/chem.202000507
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