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Surface chemistry of alkyl amines. 1. Ethylamine and triethylamine on W(100), W(100)-(5 x 1)-C, and W(100)-(2 x 1)-O

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00279a029· OSTI ID:5344862
The chemistry associated with ethyl- and triethylamine adsorbed on W(100), W(100)-(5 x 1)-C, and W(100)-(2 x 1)-O surfaces has been investigated with use of temperature-programmed reaction spectroscopy and isotopic labeling methods. The reactivity and selectivity for C-C and C-N vs. C-H bond activation is altered on W(100) by the presence of the carbide and oxide overlayers and the extent of amine substitution. Irreversible decomposition predominates on W(100) at low exposures for both amines. Large ethylamine exposures yield trace quantities of CH/sub 4/ and NH/sub 3/ but no C/sub 2/-hydrocarbons on W(100). Triethylamine undergoes C-N and C-C bond cleavage reactions to produce small amounts of ethylene and methane, respectively, on W(100) at high exposure. In contrast, no C-C bond scission products are observed from (C/sub 2/H/sub 5/)/sub 3/N on W(100)-(5 x 1)-C: ethylene and acetonitrile are produced. As on clean W(100), ethylamine does not yield C/sub 2/-hydrocarbons resulting from C-N bond scission on the -(5 x 1)-C: acetonitrile is the major product from ethylamine reaction on this surface. The W(100)-(2 x 1)-O surface is inert with respect to C-H, C-N, or N-H bond scission, resulting primarily in molecular ethylamine desorption up to 550 K corresponding to a desorption energy of 33 kcal/mol.
Research Organization:
Harvard Univ., Cambridge, MA
DOE Contract Number:
FG02-84ER13289
OSTI ID:
5344862
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 108:19; ISSN JACSA
Country of Publication:
United States
Language:
English