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Ring size and strain as a control of reaction selectivity: ethylene sulfide on Mo(110)

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00259a058· OSTI ID:6975111
The adsorption and reaction of sulfur-containing organic on single-crystal transition-metal surfaces form a subject of current to the authors and others. The primary focus of their work is an investigation of how thermodynamic properties of adsorbate molecules affect the mechanism(s) by which they react. To this end, they have studied the reactions of two saturated cyclic sulfides-trimethylene sulfide (c-C/sub 3/H/sub 6/S) and tetrahydrothiophene (c-C/sub 4/H/sub 8/S)--on Mo(110). On the basis of these studies they proposed that ring strain in the cyclic sulfide controls reaction selectivity on Mo(110). This work concerns the reactions of a third cyclic sulfide, ethylene sulfide (c-C/sub 2/H/sub 4/S), on Mo(110). The results presented here demonstrate that ring size as well as ring strain determines the reaction selectivity of cyclic sulfides on Mo(110).
Research Organization:
Harvard Univ., Cambridge, MA (USA)
DOE Contract Number:
FG02-84ER13289
OSTI ID:
6975111
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 109:25; ISSN JACSA
Country of Publication:
United States
Language:
English