Jump to main content
Jump to site search

Issue 39, 2013
Previous Article Next Article

Synthesis, structure and reactivity of cyclopropenyl-1-ylidene stabilized S(II), Se(II) and Te(II) mono- and dications

Author affiliations

Abstract

The syntheses and structural characterization of carbene-stabilized chalcogen centred mono- and dications employing a reverse electron demand onio-substitutent transfer strategy are reported. The electronic structures of these compounds were determined by density functional calculations and their reactivity towards Pd(0) centres was evaluated.

Graphical abstract: Synthesis, structure and reactivity of cyclopropenyl-1-ylidene stabilized S(ii), Se(ii) and Te(ii) mono- and dications

Back to tab navigation

Supplementary files

Publication details

The article was received on 27 Aug 2012, accepted on 12 Oct 2012 and first published on 29 Oct 2012


Article type: Communication
DOI: 10.1039/C2CC36225B
Citation: Chem. Commun., 2013,49, 4145-4147
  •   Request permissions

    Synthesis, structure and reactivity of cyclopropenyl-1-ylidene stabilized S(II), Se(II) and Te(II) mono- and dications

    Á. Kozma, J. Petuškova, C. W. Lehmann and M. Alcarazo, Chem. Commun., 2013, 49, 4145
    DOI: 10.1039/C2CC36225B

Search articles by author

Spotlight

Advertisements