| Literature DB >> 28718926 |
Silvia Díaz1,2, Mateusz Z Brela1, Soledad Gutiérrez-Oliva2, Alejandro Toro-Labbé2,3, Artur Michalak1.
Abstract
The partitioning of the reaction force based on the extended-transition-state natural orbital for chemical valence (ETS-NOCV) scheme has been proposed. This approach, together with the analysis of reaction electronic flux (REF), has been applied in a description of the changes in the electronic structure along the IRC pathway for the HCN/CNH isomerization reaction assisted by water. Two complementary ways of partitioning the system into molecular fragments have been considered ("reactant perspective" and "product perspective"). The results show that the ETS-NOCV picture is fully consistent with REF and bond-order changes. In addition, proposed ETS-NOCV decomposition of the reaction force allows for the quantitative assessment of the influence of the observed bond-breaking and bond-formation processes, providing detailed information about the reaction-driving and reaction-retarding force components within the assumed partitioning scheme.Entities:
Keywords: ETS-NOCV; HCN-NCH isomerization; energy decomposition analysis; natural orbitals of chemical valence; reaction electronic flux; reaction force decomposition scheme
Year: 2017 PMID: 28718926 DOI: 10.1002/jcc.24856
Source DB: PubMed Journal: J Comput Chem ISSN: 0192-8651 Impact factor: 3.376