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Photoreduction of methyl viologen mediated by tris(bipyridyl)ruthenium(II) in inert colloidal suspensions

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100076a024· OSTI ID:6980526
;  [1]
  1. Bowling Green State Univ., OH (United States)
The photoreduction of methyl viologen, covalently attached to a tris(bipyridyl)ruthenium(II) chromophore, in suspensions of positively charged alumina-coated colloidal silica particles, via N-phenylglycine electron donor, is reported. In the tris(bipyridyl)ruthenium(II) complexes, the central metal atom is coordinated to two 4,4[prime]-dicarboxy-2,2[prime]-bipyridine ligands and thus carries a net 2-charge at pH 5.0. Coadsorption of the N-phenylglycine and ruthenium chromophore to the colloidal particles results in rapid production of reduced viologen following visible laser flash excitation of the tris(bipyridyl)ruthenium(II) complex. The yield of the radical was dependent upon the concentration of the electron donor added to the system, but its multiphasic decay was independent of both the N-phenylglycine concentration and the initial concentration of viologen radical cation. Furthermore, both the yield and decay kinetics of the viologen radical cation were relatively independent of the number of intervening methylene units between the ruthenium complex and viologen electron acceptor. 18 refs., 5 figs., 2 tabs.
OSTI ID:
6980526
Journal Information:
Journal of Physical Chemistry; (United States), Journal Name: Journal of Physical Chemistry; (United States) Vol. 98:25; ISSN JPCHAX; ISSN 0022-3654
Country of Publication:
United States
Language:
English

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