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Coordination chemistry of pyridines of Ni(100)

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00329a027· OSTI ID:6462614
The coordination chemistry of methyl-substituted pyridine molecules on Ni(100) is described. The position of methyl substitution had a profound effect upon pyridine surface chemistry. 4-Methylpyridine behaved analogously to pyridine and showed extensive molecular desorption. The decomposition of this pyridine yielded H/sub 2/ in three different maxima: the data suggest that the first step yields ..cap alpha.. pyridyl and that CH/sub 3/ C-H bonds are now cleaved at low temperatures (as is the case for 3,5-dimethylpyridine). In contrast, both 2-methylpyridine and 2,6-dimethylpyridine show CH/sub 3/ C-H bond breaking at low temperatures. These results are discussed in terms of C/sub 5/N ring orientation with respect to the Ni(100) plane for this methylpyridine chemistry. 25 references, 4 figures, 1 table.
Research Organization:
Lawrence Berkeley Lab., CA
DOE Contract Number:
AC03-76SF00098
OSTI ID:
6462614
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 106:17; ISSN JACSA
Country of Publication:
United States
Language:
English