Literature DB >> 15307747

Reactivity and structure of the 5-dehydro-m-xylylene anion.

Tamara E Munsch1, Lyudmila V Slipchenko, Anna I Krylov, Paul G Wenthold.   

Abstract

The electronic structure of dehydro-m-xylylene anion (DMX-) has been investigated by using chemical reactivity studies and electronic structure calculations. DMX- has been generated in the gas phase via the sequential reaction of trimethyl-3,5-bis(trimethylsilylmethyl)phenylsilane with F- and two molecules of F2. Reactivity and thermochemical properties of the ion indicate a phenyl-like anion (1a), consistent with theoretical predictions. Density functional calculations predict a nonplanar triplet anion, with an allenic singlet anion slightly higher in energy. The driving force for the out-of-plane distortion is more efficient charge delocalization that is achieved at lower symmetry. Copyright 2004 American Chemical Society

Entities:  

Year:  2004        PMID: 15307747     DOI: 10.1021/jo049555t

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Fluorotrimethylsilane affinities of anionic nucleophiles: a study of fluoride-induced desilylation.

Authors:  Ian H Krouse; Paul G Wenthold
Journal:  J Am Soc Mass Spectrom       Date:  2005-05       Impact factor: 3.109

Review 2.  Properties and reactivity of gaseous distonic radical ions with aryl radical sites.

Authors:  Peggy E Williams; Bartłomiej J Jankiewicz; Linan Yang; Hilkka I Kenttämaa
Journal:  Chem Rev       Date:  2013-08-29       Impact factor: 60.622

Review 3.  Theory and practice of uncommon molecular electronic configurations.

Authors:  Ganna Gryn'ova; Michelle L Coote; Clemence Corminboeuf
Journal:  Wiley Interdiscip Rev Comput Mol Sci       Date:  2015-10-26
  3 in total

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