Peer-Reviewed Journal Details
Mandatory Fields
Walsh, JJ;Zhu, J;Zeng, Q;Forster, RJ;Keyes, TE
2012
January
Dalton Transactions
Self assembled composites of luminescent Ru(II) metallopolymers and the Dawson polyoxometalate alpha-[Mo18O54(SO4)(2)](4-)
Published
()
Optional Fields
MULTILAYER FILMS CHARGE-TRANSFER ELECTROCHEMICAL CHARACTERIZATION BIFUNCTIONAL ELECTROCATALYST ELECTRON-TRANSFER RUTHENIUM COMPLEXES ANIONS SERIES LAYER
41
9928
9937
The interaction of two luminescent metallopolymers; [Ru(bpy)(2)(PVP)(10)](2+) and [Ru(bpy)(2)(CAIP)co-poly(7)](+), where bpy is 2,2'-bipyridyl, PVP is polyvinylpyridine, and (CAIP)co-poly(7) is poly(styrene(6)-co-p-(aminomethyl)styrene) amide linked to 2-(4-carboxyphenyl)imidazo[4,5-f] [1,10]phenanthroline, with the Dawson polyoxomolybdate alpha-[Mo18O54(SO4)(2)](4-) is described. Both metallopolymers undergo electrostatic association with the polyoxometalate. From both electronic and luminescence spectroscopy the thermodynamic products were determined to be {[Ru(bpy)(2)(PVP)(10)](4.5)[Mo18O54(SO4)(2)]}(5+) and {[Ru(bpy)(2)(CAIP)co-poly(7)](5)[Mo18O54(SO4)(2)]}(+), i.e. in both instances, the number of ruthenium centres in the cluster exceeds the number required for charge neutralization of the molybdate centre. Association quenches the luminescence of the metallopolymer although, consistent with the excess of Ru(II) present in the associated composites, emission is not completely extinguished even when a large excess of [Mo18O54(SO4)(2)](4-) is present. The observed emission lifetime was not affected by [Mo18O54(SO4)(2)](4-) therefore quenching was deemed static. The luminescent intensity data was found to fit best to a (sphere of action) Perrin model from which the radii of the quenching were calculated as 4.6 angstrom and 5.8 angstrom for [Ru(bpy)(2)(PVP)(10)](2+) and [Ru(bpy)(2)(CAIPco-poly)(7)](+) respectively. Both UV/Vis and resonance Raman data indicate the presence of a new optical transition centered around 490 nm for the composite, {[Ru(bpy)(2)(PVP)(10)](4.5)[Mo18O54(SO4)(2)]}(5+) but not for {[Ru(bpy)(2)(CAIP)co-poly(7)](5)[Mo18O54(SO4)(2)]}(+). This indicates strong electronic interaction between the metal centres in the former composite, which despite good thermodynamic analogy, is not observed for {[Ru(bpy)(2)(CAIP)co-poly(7)](5)[Mo18O54(SO4)(2)]}(+). These results are consistent with photoelectrochemical studies of layer by layer assemblies of these films which indicate that the ruthenium centre sensitizes polyoxometalate photo-oxidation of benzyl alcohol in {[Ru-(bpy)(2)(PVP)(10)](4.5)[Mo18O54(SO4)(2)]}(5+) but not in {[Ru(bpy)(2)(CAIP)co-poly(7)](5)[Mo18O54(SO4)(2)]}(+).
CAMBRIDGE
1477-9226
10.1039/c2dt30503h
Grant Details