EARLY-TIME DYNAMICS AND REACTIVITY OF POLYOXOMETALATE EXCITED-STATES - IDENTIFICATION OF A SHORT-LIVED LMCT EXCITED-STATE AND A REACTIVE LONG-LIVED CHARGE-TRANSFER INTERMEDIATE FOLLOWING PICOSECOND FLASH EXCITATION OF [W10O32](4-) IN ACETONITRILE

被引:167
作者
DUNCAN, DC
NETZEL, TL
HILL, CL
机构
[1] EMORY UNIV,DEPT CHEM,ATLANTA,GA 30322
[2] GEORGIA STATE UNIV,ATLANTA,GA 30303
关键词
D O I
10.1021/ic00122a021
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
We report here picosecond flash excitation results on [W10O32](4-), 1, which demonstrate that the initially prepared ligand-to-metal charge-transfer (LMCT) excited state decays within similar to 30 ps to a single intermediate, 2, that persists for > 15 ns. Little or no substrate reaction is derived from the short-lived LMCT excited state. Furthermore, the long-lived intermediate, 2, is not the 1-electron-reduced species [W10O32](5-), 3, or one of its protonated derivatives. This long-lived intermediate, 2, is the primary photoreactant and has substantial charge-transfer character itself. Additionally, 2 and 3 are likely to have similar W-orbital electron density; the principal differences in electronic structure derive from the presence of an oxidized oxygen site in 2 which is lacking in
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页码:4640 / 4646
页数:7
相关论文
共 38 条
[1]   WEAK TERNARY CT SALTS FORMED BY ALPHA-KEGGIN POLYANIONS AND TETRAPHENYLPORPHYRINATO ZN(II) IN THE PRESENCE OF HALIDE-IONS [J].
ATTANASIO, D ;
BACHECHI, F .
ADVANCED MATERIALS, 1994, 6 (02) :145-147
[2]   STABILIZATION AND MAGNETIC-RESONANCE CHARACTERIZATION OF THE ONE-ELECTRON HETEROPOLY BLUE DERIVATIVE OF THE MOLYBDOPHOSPHATE [P2MO18O62](6-) - SLOW INTRAMOLECULAR PROTON-EXCHANGE OF THE 2-ELECTRON BLUE IN ACETONITRILE SOLUTION [J].
BARROWS, JN ;
POPE, MT .
INORGANICA CHIMICA ACTA, 1993, 213 (1-2) :91-98
[3]   MAGNETIC-PROPERTIES OF MIXED-VALENCE HETEROPOLY BLUES - INTERACTIONS WITHIN COMPLEXES CONTAINING PARAMAGNETIC ATOMS IN VARIOUS SITES AS WELL AS BLUE ELECTRONS DELOCALIZED OVER POLYTUNGSTATE FRAMEWORKS [J].
CASANPASTOR, N ;
BAKER, LCW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (26) :10384-10394
[4]   ELECTROCHEMICAL AND PHOTOCHEMICAL REDUCTION OF DECATUNGSTATE - A REINVESTIGATION [J].
CHEMSEDDINE, A ;
SANCHEZ, C ;
LIVAGE, J ;
LAUNAY, JP ;
FOURNIER, M .
INORGANIC CHEMISTRY, 1984, 23 (17) :2609-2613
[5]   USE OF EXCITED-STATE AND GROUND-STATE REDOX PROPERTIES OF POLYOXOMETALATES FOR SELECTIVE TRANSFORMATION OF UNACTIVATED CARBON HYDROGEN CENTERS REMOTE FROM THE FUNCTIONAL-GROUP IN KETONES [J].
COMBSWALKER, LA ;
HILL, CL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (03) :938-946
[6]  
DUNCAN DA, UNPUB
[7]   PHOTOACTIVATION OF METAL-OXIDE SURFACES - PHOTOCATALYZED OXIDATION OF ALCOHOLS BY HETEROPOLYTUNGSTATES [J].
FOX, MA ;
CARDONA, R ;
GAILLARD, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (21) :6347-6354
[8]   ELECTRONIC-SPECTRA OF MIXED-VALENCE REDUCED HETEROPOLYANIONS [J].
FRUCHART, JM ;
HERVE, G ;
LAUNAY, JP ;
MASSART, R .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1976, 38 (09) :1627-1634
[9]  
Hill C. L., 1993, PHOTOSENSITIZATION P, P307
[10]   ANAEROBIC FUNCTIONALIZATION OF REMOTE UNACTIVATED CARBON-HYDROGEN BONDS BY POLYOXOMETALATES [J].
HILL, CL ;
RENNEKE, RF ;
COMBS, L .
TETRAHEDRON, 1988, 44 (24) :7499-7507