Cargando…

ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes

ItBu (ItBu = 1,3-di-tert-butylimidazol-2-ylidene) represents the most important and most versatile N-alkyl N-heterocyclic carbene available in organic synthesis and catalysis. Herein, we report the synthesis, structural characterization and catalytic activity of ItOct (ItOctyl), C(2)-symmetric, high...

Descripción completa

Detalles Bibliográficos
Autores principales: Rahman, Md. Mahbubur, Meng, Guangrong, Bisz, Elwira, Dziuk, Błażej, Lalancette, Roger, Szostak, Roman, Szostak, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189875/
https://www.ncbi.nlm.nih.gov/pubmed/37206400
http://dx.doi.org/10.1039/d3sc01006f
_version_ 1785043176379121664
author Rahman, Md. Mahbubur
Meng, Guangrong
Bisz, Elwira
Dziuk, Błażej
Lalancette, Roger
Szostak, Roman
Szostak, Michal
author_facet Rahman, Md. Mahbubur
Meng, Guangrong
Bisz, Elwira
Dziuk, Błażej
Lalancette, Roger
Szostak, Roman
Szostak, Michal
author_sort Rahman, Md. Mahbubur
collection PubMed
description ItBu (ItBu = 1,3-di-tert-butylimidazol-2-ylidene) represents the most important and most versatile N-alkyl N-heterocyclic carbene available in organic synthesis and catalysis. Herein, we report the synthesis, structural characterization and catalytic activity of ItOct (ItOctyl), C(2)-symmetric, higher homologues of ItBu. The new ligand class, including saturated imidazolin-2-ylidene analogues has been commercialized in collaboration with MilliporeSigma: ItOct, 929 298; SItOct, 929 492 to enable broad access of the academic and industrial researchers within the field of organic and inorganic synthesis. We demonstrate that replacement of the t-Bu side chain with t-Oct results in the highest steric volume of N-alkyl N-heterocyclic carbenes reported to date, while retaining the electronic properties inherent to N-aliphatic ligands, such as extremely strong σ-donation crucial to the reactivity of N-alkyl N-heterocyclic carbenes. An efficient large-scale synthesis of imidazolium ItOct and imidazolinium SItOct carbene precursors is presented. Coordination chemistry to Au(i), Cu(i), Ag(i) and Pd(ii) as well as beneficial effects on catalysis using Au(i), Cu(i), Ag(i) and Pd(ii) complexes are described. Considering the tremendous importance of ItBu in catalysis, synthesis and metal stabilization, we anticipate that the new class of ItOct ligands will find wide application in pushing the boundaries of new and existing approaches in organic and inorganic synthesis.
format Online
Article
Text
id pubmed-10189875
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-101898752023-05-18 ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes Rahman, Md. Mahbubur Meng, Guangrong Bisz, Elwira Dziuk, Błażej Lalancette, Roger Szostak, Roman Szostak, Michal Chem Sci Chemistry ItBu (ItBu = 1,3-di-tert-butylimidazol-2-ylidene) represents the most important and most versatile N-alkyl N-heterocyclic carbene available in organic synthesis and catalysis. Herein, we report the synthesis, structural characterization and catalytic activity of ItOct (ItOctyl), C(2)-symmetric, higher homologues of ItBu. The new ligand class, including saturated imidazolin-2-ylidene analogues has been commercialized in collaboration with MilliporeSigma: ItOct, 929 298; SItOct, 929 492 to enable broad access of the academic and industrial researchers within the field of organic and inorganic synthesis. We demonstrate that replacement of the t-Bu side chain with t-Oct results in the highest steric volume of N-alkyl N-heterocyclic carbenes reported to date, while retaining the electronic properties inherent to N-aliphatic ligands, such as extremely strong σ-donation crucial to the reactivity of N-alkyl N-heterocyclic carbenes. An efficient large-scale synthesis of imidazolium ItOct and imidazolinium SItOct carbene precursors is presented. Coordination chemistry to Au(i), Cu(i), Ag(i) and Pd(ii) as well as beneficial effects on catalysis using Au(i), Cu(i), Ag(i) and Pd(ii) complexes are described. Considering the tremendous importance of ItBu in catalysis, synthesis and metal stabilization, we anticipate that the new class of ItOct ligands will find wide application in pushing the boundaries of new and existing approaches in organic and inorganic synthesis. The Royal Society of Chemistry 2023-04-18 /pmc/articles/PMC10189875/ /pubmed/37206400 http://dx.doi.org/10.1039/d3sc01006f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Rahman, Md. Mahbubur
Meng, Guangrong
Bisz, Elwira
Dziuk, Błażej
Lalancette, Roger
Szostak, Roman
Szostak, Michal
ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes
title ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes
title_full ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes
title_fullStr ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes
title_full_unstemmed ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes
title_short ItOct (ItOctyl) – pushing the limits of ItBu: highly hindered electron-rich N-aliphatic N-heterocyclic carbenes
title_sort itoct (itoctyl) – pushing the limits of itbu: highly hindered electron-rich n-aliphatic n-heterocyclic carbenes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189875/
https://www.ncbi.nlm.nih.gov/pubmed/37206400
http://dx.doi.org/10.1039/d3sc01006f
work_keys_str_mv AT rahmanmdmahbubur itoctitoctylpushingthelimitsofitbuhighlyhinderedelectronrichnaliphaticnheterocycliccarbenes
AT mengguangrong itoctitoctylpushingthelimitsofitbuhighlyhinderedelectronrichnaliphaticnheterocycliccarbenes
AT biszelwira itoctitoctylpushingthelimitsofitbuhighlyhinderedelectronrichnaliphaticnheterocycliccarbenes
AT dziukbłazej itoctitoctylpushingthelimitsofitbuhighlyhinderedelectronrichnaliphaticnheterocycliccarbenes
AT lalancetteroger itoctitoctylpushingthelimitsofitbuhighlyhinderedelectronrichnaliphaticnheterocycliccarbenes
AT szostakroman itoctitoctylpushingthelimitsofitbuhighlyhinderedelectronrichnaliphaticnheterocycliccarbenes
AT szostakmichal itoctitoctylpushingthelimitsofitbuhighlyhinderedelectronrichnaliphaticnheterocycliccarbenes