Pyrolysis of (thio)carbonates via computation analysis

Author:

Xia Jingjing1,Asiri Abdullah M.2,Alamry Khalid A.2,Wu Ping3,Huang Zhihao4

Affiliation:

1. Key Laboratory of Functional Molecule Design and Interface Process, Anhui Jianzhu University, Hefei, Anhui 230601, P. R. China

2. Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia

3. Key Laboratory of Coordination Chemistry and Functional Materials in Universities of Shandong, Dezhou College, Dezhou, Shandong 253023, P. R. China

4. Department of Chemistry, School of Science, Massachusetts Institute of Technology, Cambridge, MA 02139, USA

Abstract

The regioselective production of alkenes from (thio)carbonates was calculated by MP2/6-31G(d) method via pyrolysis processes. Four (thio)carbonates were calculated in this paper. They are S-sec-butyl O-methyl thiocarbonate (I), O-sec-butyl S-methyl thiocarbonate (II), sec-butyl methyl thioncarbonate (III), and sec-butyl methyl dithiocarbonate (IV). Thirteen potential thermolysis routes were revealed for the pyrolysis of each substance, including nine routes to produce regioselective alkenes and four rearrangement/decompose alternatives. Among nine alkene generation routes, six-membered ring transition states via a two-step mechanism required the lowest energy, while the other routes exhibited higher energy barriers. The calculation results demonstrated an alkene distribution hierarchy of 1-butene [Formula: see text] E-butene [Formula: see text] Z-butene for substances I and II, and an order of E-butene [Formula: see text] 1-butene [Formula: see text] Z-butene for substances III and IV.

Funder

National Science Foundation of Anhui Province

Publisher

World Scientific Pub Co Pte Lt

Subject

Computational Theory and Mathematics,Physical and Theoretical Chemistry,Computer Science Applications

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