Browse by author
Lookup NU author(s): Professor Christopher Dennison, Emeritus Prof Alfred Sykes
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Reaction of Scenedesmus obliquus plastocyanin with excess [Ru(trpy)(L)(H2O)]2+ (trpy = 2,2': 6',2''-terpyridine; L = 2,2'-bipyridine, 4,4'-(CH3)2-2,2'-bipyridine, 4,5,4',5'-(CH3)4-2,2'-bipyridine) affords Ru-(trpy)(L)(His59)Pc as the main product. These RuPc derivatives are luminescent with λ(max)(emission) ~ 650 nm and lifetimes of (Cu+) in the range 110-140 ns. Photogenerated *RU2+PcCu2+ is quenched by *Ru2+ → Cu2+ electron transfer (ET) to produce RU3+pcCu+; intramolecular ET was monitored by transient absorption at 590 (Cu+ → Cu2+) and 424 nm (RU3+ → Ru2+). The Cu+ to Ru3+ ET rate constants (k(ET)) are as follows: 2.9(2) x 107 s-1 (L = bpy); 2.3(2) x 107 s-1 (L = dmbpy); and 1.9(2) x 107 s-1 (L = tmbpy). Activationless rates (- ΔG°~ λ ~ 0.70-0.75 eV) are consistent with coupling-limited tunneling through a β sheet at an estimated Cu-Ru distance of 15.6 Å (calcd k(ET) = 107 s-1 for a tunneling decay constant of 1.1 Å-1). Biphasic Cu+ → Ru3+ ET kinetics (k(ET) > 107 and ~ 104 s-1) were observed after flash-quench generation of Ru3+ PcCu+ in acidic solutions. The slow phase kinetics are markedly temperature and pH dependent: the activation parameters (ΔH@= = 43.1 kJ/mol; ΔSα= = -17 J/(K · mol) for L = bpy) suggest that the trigonal low-pH form of Cu+ reorganizes to the tetrahedral form prior to oxidation to the blue CU2+ state.
Author(s): Di Bilio AJ, Dennison C, Gray HB, Ramirez BE, Sykes AG, Winkler JR
Publication type: Article
Publication status: Published
Journal: Journal of the American Chemical Society
Year: 1998
Volume: 120
Issue: 30
Pages: 7551-7556
Print publication date: 21/07/1998
ISSN (print): 0002-7863
ISSN (electronic): 1520-5126
Publisher: American Chemical Society
URL: http://dx.doi.org/10.1021/ja972625b
DOI: 10.1021/ja972625b
Altmetrics provided by Altmetric