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rdf:type
lifeskim:mentions
pubmed:issue
23
pubmed:dateCreated
2011-5-20
pubmed:abstractText
The mechanism of irreversible carbon dioxide binding with a Lewis pair Mes(3)P:AlCl(3) (Mes=2,4,6-C(6)H(2)Me(3)) is computationally investigated to reveal that the steric congestion is not the driving force for the activation of CO(2). Instead, we find that the specific solute-solvent interaction between the Lewis acid and a bromobenzene molecule lowers the effective binding energy of the Lewis pair. This solvation effect affects the reaction in a similar manner to the steric encumbering of conventional frustrated Lewis pairs. Additionally, the transition state toward the CO(2) binding becomes extraordinarily flexible upon solvation. This flexibility encourages the adduct formation entropically and thus lowers the free-energy barrier of the reaction. We conclude that this combination of energy-barrier lowering through solvent-assisted frustration and the entropic encouragement generates a feasible activation route for CO(2) under mild conditions.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
May
pubmed:issn
1521-3765
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
pubmed:issnType
Electronic
pubmed:day
27
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6501-7
pubmed:year
2011
pubmed:articleTitle
On the mechanism of irreversible carbon dioxide binding with a frustrated lewis pair: solvent-assisted frustration and transition-state entropic encouragement.
pubmed:affiliation
Institute of Theoretical and Computational Chemistry, Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang 790-784, Korea.
pubmed:publicationType
Journal Article