Theoretical investigation of the reactivity of copper atoms with carbon disulfide

Yana Dobrogorskaya, Joëlle Mascetti, Imre Pápai, Alexander Nemukhin, Yacine Hannachi

Research output: Contribution to journalArticle

13 Citations (Scopus)


The mechanism of the Cu + CS2 reaction has been investigated using density functional and coupled cluster calculations. The lowest energy route on the potential energy surface corresponds to the insertion product SCuCS via the formation of intermediate coordination complexes: η1 s and η2 cs, which all lie below the energy of the reactants. Another path corresponding to the formation of a cyclic C2v compound η2 ss leads to the same insertion product, but it involves a higher energy barrier (34.7 kcal/mol vs 26.9 kcal/mol with respect to the reactants at the CCSD(T) level). The dissociation of the insertion product SCuCS into the CuS and CS fragments is found to be endothermic by 43 kcal/mol (CCSD(T) level). Our results are related to experimental data obtained in low-temperature rare gas matrixes and in the gas phase.

Original languageEnglish
Pages (from-to)2711-2715
Number of pages5
JournalJournal of Physical Chemistry A
Issue number15
Publication statusPublished - Apr 17 2003

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Fingerprint Dive into the research topics of 'Theoretical investigation of the reactivity of copper atoms with carbon disulfide'. Together they form a unique fingerprint.

  • Cite this