Cargando…

Cationic nickel porphyrinoids with unexpected reactivity

Cationic nickel(ii) complexes of two ring-contracted porphyrinoid ligands distantly related to the corrins were prepared by metal templated macrocyclisation. The compounds show reversible electron transfer processes and were found to be the first porphyrinoid-based catalysts for C–C cross-coupling....

Descripción completa

Detalles Bibliográficos
Autores principales: Wicht, Richard, Bahnmüller, Stefanie, Brandhorst, Kai, Schweyen, Peter, Bröring, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952870/
https://www.ncbi.nlm.nih.gov/pubmed/29896348
http://dx.doi.org/10.1039/c5sc03663a
_version_ 1783323276485853184
author Wicht, Richard
Bahnmüller, Stefanie
Brandhorst, Kai
Schweyen, Peter
Bröring, Martin
author_facet Wicht, Richard
Bahnmüller, Stefanie
Brandhorst, Kai
Schweyen, Peter
Bröring, Martin
author_sort Wicht, Richard
collection PubMed
description Cationic nickel(ii) complexes of two ring-contracted porphyrinoid ligands distantly related to the corrins were prepared by metal templated macrocyclisation. The compounds show reversible electron transfer processes and were found to be the first porphyrinoid-based catalysts for C–C cross-coupling.
format Online
Article
Text
id pubmed-5952870
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-59528702018-06-12 Cationic nickel porphyrinoids with unexpected reactivity Wicht, Richard Bahnmüller, Stefanie Brandhorst, Kai Schweyen, Peter Bröring, Martin Chem Sci Chemistry Cationic nickel(ii) complexes of two ring-contracted porphyrinoid ligands distantly related to the corrins were prepared by metal templated macrocyclisation. The compounds show reversible electron transfer processes and were found to be the first porphyrinoid-based catalysts for C–C cross-coupling. Royal Society of Chemistry 2016-01-01 2015-10-16 /pmc/articles/PMC5952870/ /pubmed/29896348 http://dx.doi.org/10.1039/c5sc03663a Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Wicht, Richard
Bahnmüller, Stefanie
Brandhorst, Kai
Schweyen, Peter
Bröring, Martin
Cationic nickel porphyrinoids with unexpected reactivity
title Cationic nickel porphyrinoids with unexpected reactivity
title_full Cationic nickel porphyrinoids with unexpected reactivity
title_fullStr Cationic nickel porphyrinoids with unexpected reactivity
title_full_unstemmed Cationic nickel porphyrinoids with unexpected reactivity
title_short Cationic nickel porphyrinoids with unexpected reactivity
title_sort cationic nickel porphyrinoids with unexpected reactivity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952870/
https://www.ncbi.nlm.nih.gov/pubmed/29896348
http://dx.doi.org/10.1039/c5sc03663a
work_keys_str_mv AT wichtrichard cationicnickelporphyrinoidswithunexpectedreactivity
AT bahnmullerstefanie cationicnickelporphyrinoidswithunexpectedreactivity
AT brandhorstkai cationicnickelporphyrinoidswithunexpectedreactivity
AT schweyenpeter cationicnickelporphyrinoidswithunexpectedreactivity
AT broringmartin cationicnickelporphyrinoidswithunexpectedreactivity