...
首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Charge-transfer processes in (4-nitrobenzoate)Re(CO)(3)(azine)(2) complexes. Competitive reductions of 4-nitrobenzoate and azine in thermally and photochemically induced redox processes
【24h】

Charge-transfer processes in (4-nitrobenzoate)Re(CO)(3)(azine)(2) complexes. Competitive reductions of 4-nitrobenzoate and azine in thermally and photochemically induced redox processes

机译:(4-硝基苯甲酸酯)Re(CO)(3)(嗪)(2)配合物中的电荷转移过程。热和光化学诱导的氧化还原过程中4-硝基苯甲酸酯和嗪的竞争性还原

获取原文
获取原文并翻译 | 示例
           

摘要

The photochemically and thermally induced redox reactions of the (4-nitrobenzoate)Re(CO)(3) (azine) (azine = 1,10-phenanthroline, 2,2'-bipyridine, and (4-phenylpyridine)(2)) were investigated by flash photolysis and pulse radiolysis. Processes characterized as intramolecular charge transfers from coordinated azine radicals to the 4-nitrobenzoate ligand and vice versa were observed in a 1-100 mu s time scale by pulse radiolysis. In photochemical experiments, the conversion among metal to Ligand charge-transfer excited states, i.e., from the Re to azine to the Re to 4-nitrobenzoate charge-transfer excited stale, involves intermediates with Lives of picoseconds. A mechanism for the conversions that incorporates intraligand excited states is discussed. [References: 19]
机译:(4-硝基苯甲酸酯)Re(CO)(3)(嗪)的光化学和热诱导的氧化还原反应(嗪= 1,10-菲咯啉,2,2'-联吡啶和(4-苯基吡啶)(2))用闪光光解法和脉冲辐射法研究。通过脉冲辐照在1-100毫秒的时间范围内观察到表征为分子内电荷从配位嗪基转移到4-硝基苯甲酸酯配体,反之亦然的过程。在光化学实验中,金属向配体的电荷转移激发态之间的转换,即从Re到嗪,再到Re到4-硝基苯甲酸酯电荷转移的激发态之间的转换,涉及具有皮秒活度的中间体。讨论了一种包含配体​​内激发态的转换机制。 [参考:19]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号