An Aminopyridinium Ionic Liquid: A Simple and Effective Bifunctional Organocatalyst for Carbonate Synthesis from Carbon Dioxide and Epoxides.
carbon dioxide
hydrogen-bond donors
ionic liquids
organocatalysis
ring-opening reactions
Journal
ChemPlusChem
ISSN: 2192-6506
Titre abrégé: Chempluschem
Pays: Germany
ID NLM: 101580948
Informations de publication
Date de publication:
07 2020
07 2020
Historique:
received:
11
05
2020
revised:
02
07
2020
entrez:
31
7
2020
pubmed:
31
7
2020
medline:
31
7
2020
Statut:
ppublish
Résumé
An aminopyridinium ionic liquid is presented as a green, tunable, and active metal-free one-component catalytic system for the atom-efficient transformation of oxiranes and CO
Identifiants
pubmed: 32729682
doi: 10.1002/cplu.202000367
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1587-1595Informations de copyright
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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For additional details see the Supporting Information.
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We performed a detailed computational studies for two other possible pathways including i) CO2 activation by the pyridinium amine group and ii) nucleophilic ring-opening of the epoxide by 3 c. In either of these cases the calculated free energy of the first transition states was higher by 12.4 and 8.1 kcal/mol, respectively, (see the Supporting Information;
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