Literature DB >> 11192090

4-Oxo-2,3,5,6-tetrafluorocyclohexa-2,5-dienylidene--a highly electrophilic triplet carbene.

W Sander1, R Hübert, E Kraka, J Gräfenstein, D Cremer.   

Abstract

The 4-oxocyclohexa-2,5-dienylidenes are an interesting class of highly electrophilic carbenes. We investigated the reactivity of the 2,3,5,6-tetrafluorinated and -tetrachlorinated derivatives 1b and 1c with small molecules under conditions of matrix isolation. The reactions with molecular oxygen and with carbon monoxide produce the expected carbonyl O-oxides and ketenes, respectively. As a result of the extreme electrophilicity of 1b and c both carbenes insert with no or very small activation barriers into H2 or the CH bonds of hydrocarbons. Obviously, spin restrictions for these formally spin-forbidden reactions do not result in substantial thermal activation barriers.

Entities:  

Year:  2000        PMID: 11192090     DOI: 10.1002/1521-3765(20001215)6:24<4567::aid-chem4567>3.0.co;2-a

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  CO fixation to stable acyclic and cyclic alkyl amino carbenes: stable amino ketenes with a small HOMO-LUMO gap.

Authors:  Vincent Lavallo; Yves Canac; Bruno Donnadieu; Wolfgang W Schoeller; Guy Bertrand
Journal:  Angew Chem Int Ed Engl       Date:  2006-05-19       Impact factor: 15.336

2.  Stable singlet carbenes as mimics for transition metal centers.

Authors:  David Martin; Michele Soleilhavoup; Guy Bertrand
Journal:  Chem Sci       Date:  2011-01-01       Impact factor: 9.825

3.  Aryl-Cl vs heteroatom-Si bond cleavage on the route to the photochemical generation of σ,π-heterodiradicals.

Authors:  Lorenzo Di Terlizzi; Francesca Roncari; Stefano Crespi; Stefano Protti; Maurizio Fagnoni
Journal:  Photochem Photobiol Sci       Date:  2021-11-13       Impact factor: 4.328

  3 in total

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