Solvent Effects on the Stability and Delocalization of Aryl Dicyanomethyl Radicals: The Captodative Effect Revisited

dc.contributor.author Peterson, Joshua
dc.contributor.author Winter, Arthur
dc.contributor.department Chemistry
dc.date 2020-01-02T21:19:33.000
dc.date.accessioned 2020-06-30T01:16:54Z
dc.date.available 2020-06-30T01:16:54Z
dc.date.copyright Tue Jan 01 00:00:00 UTC 2019
dc.date.issued 2019-07-28
dc.description.abstract <p>The captodative effect postulates that radicals substituted with both electron donating and accepting groups enjoy a special enhanced stabilization, a model given theoretical support by simple MO and resonance arguments. A key prediction from theory is that captodative stabilization of radicals is larger in polar solvents than in nonpolar solvents or the gas phase, which can be viewed in the resonance model as solvent stabilization of charge-separated resonance forms. Yet, several experimental studies have failed to observe a solvent effect on radical stability, casting doubt on key aspects of the captodative effect. Here, we examine in detail the effect of solvent on the stability of structurally related captodative aryl dicyanomethyl radicals. An attractive feature of these radicals is that they exist as stable steady state populations of radicals in equilibrium with their dimers, allowing us to directly characterize from experiment their thermodynamic stabilities and spin delocalization in solvents of varying polarity. In contrast to the prior studies, we find that captodative radicals are indeed stabilized by polar solvents, as measured by a shift in the radical–dimer association constants by up to 100-fold toward the radical upon going from nonpolar toluene to more polar DMF. Moreover, in polar solvents, the spin is shifted onto the donor substituent and away from the benzylic carbon. Within the resonance model, these results can be explained by the increased contributions of the zwitterionic resonance structures to the overall hybrid. These results provide experimental support to a key prediction from theory that had previously been dismissed.</p>
dc.description.comments <p>This document is the unedited Author’s version of a Submitted Work that was subsequently accepted for publication in <em>Journal of the American Chemical Society</em>, copyright © American Chemical Society after peer review. To access the final edited and published work see DOI: <a href="http://dx.doi.org/10.1021/jacs.9b06576" target="_blank">10.1021/jacs.9b06576</a>. Posted with permission.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/chem_pubs/1137/
dc.identifier.articleid 2140
dc.identifier.contextkey 15081019
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath chem_pubs/1137
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/14442
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/chem_pubs/1137/2019_WinterArthur_SolventEffects.pdf|||Fri Jan 14 18:48:31 UTC 2022
dc.source.uri 10.1021/jacs.9b06576
dc.subject.disciplines Chemistry
dc.title Solvent Effects on the Stability and Delocalization of Aryl Dicyanomethyl Radicals: The Captodative Effect Revisited
dc.type article
dc.type.genre article
dspace.entity.type Publication
relation.isAuthorOfPublication a2121da6-c591-494f-b9a9-595265e46ff9
relation.isOrgUnitOfPublication 42864f6e-7a3d-4be3-8b5a-0ae3c3830a11
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