Please use this identifier to cite or link to this item: https://doi.org/10.1002/1521-3765(20020104)8:13.0.CO;2-0
Title: The thermal decomposition of thiirane: A mechanistic study by Ab initio MO theory
Authors: Steudel, Y.
Steudel, R.
Wong, M.W. 
Keywords: Ab initio calculations
Desulfurization
Episulfide
Radicals
Reaction mechanisms
Issue Date: 4-Jan-2002
Source: Steudel, Y.,Steudel, R.,Wong, M.W. (2002-01-04). The thermal decomposition of thiirane: A mechanistic study by Ab initio MO theory. Chemistry - A European Journal 8 (1) : 217-228. ScholarBank@NUS Repository. https://doi.org/10.1002/1521-3765(20020104)8:13.0.CO;2-0
Abstract: Using high-level ab initio MO methods, we have identified two reaction pathways with different thermodynamic and kinetic properties for the thermal decomposition of the three-membered heterocycle thiirane (C2H4S) and related derivatives. A homolytic ring opening, followed by attack of the generated diradical on another thiirane molecule, and subsequent elimination of ethene in a fast radical chain reaction results in the formation of disulfur molecules in their triplet ground state (3S2) and requires activation enthalpies of ΔH298 # = 222 kJ mol-1 and ΔG298 # = 212 kJ mol-1. This reaction mechanism would result in a first-order rate law in agreement with one reported gas-phase experiment but does neither match the experimental activation energy nor does it explain the observed retention of the stereochemical configuration in the thermal decomposition of certain substituted thiiranes. Alternatively, sulfur atoms can be transferred from one thiirane molecule to another with the intermediate formation of thiirane 1-sulfide (C2H4S2). This molecule can either decompose unimolecularly to ethene and disulfur in its excited singlet state (1S2) or, by means of spin crossover, S2 in its triplet ground state may be formed. On the other hand, the thiirane 1-sulfide may react with itself and transfer one sulfur atom from one molecule to another with formation of thiirane 1,1-disulfide (C2H4S3), which is an analogue of thiirane sulfone; thiirane is formed as the second product. The 1,1-disulfide may then decompose to ethene and S3. In still another bimolecular reaction, the thiirane 1-sulfide may react with itself in a strongly exothermic reaction to give S4 and two equivalents of ethene. This series of reactions results in a second-order rate law and requires activation enthalpies of ΔH298 # = 109 kJ mol-1 and ΔG298 # = 144 kJ mol-1 for the formation of thiirane 1-sulfide, while the consecutive reactions require less activation enthalpy. Elemental sulfur (S8) is eventually formed by oligomerization of either S2, S3, or S4 in spin-allowed reactions. These findings are in agreement with most experimental data on the thermal desulfurization of thiirane and its substituted derivatives. Thiirane 1-persulfide (C2H4S3) with a linear arrangement of the three sulfur atoms as well as zwitterions and radicals derived from thiirane are not likely to be intermediates in the thermal decomposition of episulfides.
Source Title: Chemistry - A European Journal
URI: http://scholarbank.nus.edu.sg/handle/10635/95269
ISSN: 09476539
DOI: 10.1002/1521-3765(20020104)8:13.0.CO;2-0
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Page view(s)

33
checked on Jan 14, 2018

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.