首页> 外文OA文献 >Bimetallic Iridium-Carbene Complexes with Mesoionic Triazolylidene Ligands for Water Oxidation Catalysis
【2h】

Bimetallic Iridium-Carbene Complexes with Mesoionic Triazolylidene Ligands for Water Oxidation Catalysis

机译:介孔三唑基亚配体的双金属铱-碳配合物用于水氧化催化

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Two new diiridium–triazolylidene complexes were prepared as bimetallic analogues of established mononuclear water oxidation catalysts. Both complexes are efficient catalyst precursors in the presence of cerium ammonium nitrate (CAN) as sacrificial oxidant. Up to 20000:1 ratios of CAN/complex, the turnover limitation is the availability of CAN and not the catalyst stability. The water oxidation activity of the bimetallic complexes is not better than the monometallic species at 0.6 mm catalyst concentration. Under dilute conditions (0.03 mm), the bimetallic complexes double their activity, whereas the monometallic complexes show an opposite trend and display markedly reduced rates, thereby suggesting a benefit of the close proximity of two metal centers in this low concentration regime. The high dependence of catalyst activity on reaction conditions indicates that caution is required when catalysts are compared by their turnover frequencies only.
机译:制备了两种新的二铱-三唑基亚烷基配合物,作为已建立的单核水氧化催化剂的双金属类似物。在硝酸铈铵(CAN)作为牺牲氧化剂的情况下,两种络合物都是有效的催化剂前体。高达20000:1的CAN /复合物比率时,周转限制是CAN的可用性而不是催化剂的稳定性。在催化剂浓度为0.6 mm时,双金属配合物的水氧化活性不比单金属物种好。在稀薄条件下(0.03毫米),双金属配合物的活性翻倍,而单金属配合物显示出相反的趋势并显示出明显降低的速率,从而暗示了在这种低浓度条件下两个金属中心的紧密接近所带来的好处。催化剂活性对反应条件的高度依赖性表明,仅通过催化剂的周转频率比较催化剂时需要谨慎。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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