Theoretical study of the reaction mechanism between triphenylphosphine with dimethyl acetylenedicarboxylates in the presence of 2-mercapto thiazoline

Author:

Zakarianezhad Mohammad1ORCID,Makiabadi Batoul2ORCID,Hosseini Seyede Samira3ORCID,Zeydabadi Elham3ORCID

Affiliation:

1. Payam Noor University

2. Sirjan University of Technology

3. Payame Noor University

Abstract

In this research, the mechanism of the reaction between triphenylphosphine R1 and dimethyl acetylenedicarboxylate R2 was investigated in the presence of NH-acid, such as 2-mercapto thiazoline R3 based on the quantum mechanical calculations. Theoretical studies performed for evaluation of the potential energy surfaces of all structures participated in the reaction mechanism. All structures were optimized at the B3LYP/6-311++g(d,p) levels. The first step of the reaction was recognized as a rate-determining step in the reaction mechanism. To check the effect of solvent on the potential energy surfaces, condensed phase calculations in acetone were carried out with the polarizable continuum model (CPCM). Finally, the natural bond orbital (NBO) method was applied for a better understanding of molecular interaction.

Publisher

Turkish Computational and Theoretical Chemistry

Reference58 articles.

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