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Electrophilicity of Hoveyda‐Grubbs Olefin Metathesis Catalysts as the Driving Force that Controls Initiation Rates

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cris.lastimport.scopus2024-02-12T20:17:58Z
dc.abstract.enThe dissociative mechanism of initiation for a series of Hoveyda-Grubbs type metathesis catalysts modified at the para and meta positions in the isopropoxybenzylidene ligand is investigated by means of DFT calculations. The electron donating/withdrawing capacity of the ligand was screened through the incorporation of various substituents such as halogens, nitro, alkoxides, ketones, esters, amines, and amides. Variations in structural parameters, energy barriers for the Ru−O bond dissociation, and Ru−O bond strength were examined as a function of the Hammett constant. It was found that electronic properties of the catalysts such as chemical potential, hardness, and electrophilicity correlate linearly with the dissociative energy barriers. These findings enable a systematic rationalization and prediction of rate of precatalyst initiation through the calculation of only the HOMO-LUMO gap of catalysts, as the faster the initiation, the more electrophilic the catalyst.
dc.affiliationUniwersytet Warszawski
dc.contributor.authorLopez, Juan Pablo Martinez
dc.contributor.authorTrzaskowski, Bartosz
dc.date.accessioned2024-01-24T22:46:07Z
dc.date.available2024-01-24T22:46:07Z
dc.date.issued2022
dc.description.financeNie dotyczy
dc.description.number23
dc.description.volume23
dc.identifier.doi10.1002/CPHC.202200580
dc.identifier.issn1439-4235
dc.identifier.urihttps://repozytorium.uw.edu.pl//handle/item/106021
dc.identifier.weblinkhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/cphc.202200580
dc.languageeng
dc.pbn.affiliationchemical sciences
dc.relation.ispartofChemPhysChem
dc.rightsClosedAccess
dc.sciencecloudnosend
dc.titleElectrophilicity of Hoveyda‐Grubbs Olefin Metathesis Catalysts as the Driving Force that Controls Initiation Rates
dc.typeJournalArticle
dspace.entity.typePublication