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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >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
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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

机译:多羟甲酸酯激发态的早期动力学和反应性-短暂的LMCT激发态和反应性长寿命电荷转移中间[W10O32](4-)的PICCONFLASH激发的鉴定

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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 [References: 47]
机译:我们在此处报告[W10O32](4-),1上的皮秒闪光激发结果,该结果表明最初制备的配体-金属电荷转移(LMCT)激发态在大约30 ps内衰减到单个中间体2,持续> 15 ns。短寿命LMCT激发态很少或没有底物反应。此外,长寿命中间体2不是1电子还原的物质[W10O32](5-)3或质子化衍生物之一。这种长寿命的中间体2是主要的光反应剂,本身具有大量的电荷转移特性。另外,2和3可能具有相似的W轨道电子密度;电子结构的主要差异源自[2]中缺少的2中存在氧化的氧位。

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