...
【24h】

Synthesis, structure, and reactivity of new tetranuclear Ru-Hbpp-based water-oxidation catalysts

机译:新型四核Ru-Hbpp基水氧化催化剂的合成,结构和反应活性

获取原文
获取原文并翻译 | 示例
           

摘要

The preparation of three new octadentate tetranucleating ligands made out of two Ru-Hbpp-based units [where Hbpp is 3, 5(bispyridyl)pyrazole], linked by a xylyl group attached at the pyrazolate moiety, of general formula (Hbpp) _2-u-xyl (u = p, m, or o) is reported, together with its dinucleating counterpart substituted at the same position with a benzyl group, Hbpp-bz. All of these ligands have been characterized with the usual analytical and spectroscopic techniques. The corresponding tetranuclear ruthenium complexes of general formula {[Ru_2(trpy)_2(L)]_2(μ-(bpp) _2-u-xyl)}~(n+) [L = Cl or OAc, n = 4; L = (H _2O)_2, n = 6] and their dinuclear homologues {[Ru _2(trpy)_2(L)](μ-bpp-bz)}~(n+) [L = Cl or OAc, n = 2; L = (H_2O)_2, n = 3] have also been prepared and thoroughly characterized both in solution and in the solid state. In solution, all of the complexes have been characterized spectroscopically by UV-vis and NMR and their redox properties investigated by means of cyclic voltammetry techniques. In the solid state, monocrystal X-ray diffraction analysis has been carried out for two dinuclear complexes {[Ru_2(trpy) _2(L)](μ-bpp-bz)}~(2+) (L = Cl and OAc) and for the tetranuclear complex {[Ru_2(trpy)_2(μ-OAc)] _2(μ-(bpp)_2-m-xyl)}~(4+). The capacity of the tetranuclear aqua complexes {[Ru_2(trpy)_2(H _2O)_2]_2(μ-(bpp)_2-u-xyl)} ~(6+) and the dinuclear homologue {[Ru_2(trpy) _2(H_2O)_2](μ-bpp-bz)}~(3+) to act as water-oxidation catalysts has been evaluated using cerium(IV) as the chemical oxidant in pH = 1.0 triflic acid solutions. It is found that these complexes, besides generating significant amounts of dioxygen, also generate carbon dioxide. The relative ratio of [O_2]/[CO_2] is dependent not only on para, meta, or ortho substitution of the xylylic group but also on the concentration of the starting materials. With regard to the tetranuclear complexes, the one that contains the more sterically constrained ortho-substituted ligand generates the highest [O_2]/[CO_2] ratio.
机译:由两个基于Ru-Hbpp的单元[其中Hbpp是3,5(双吡啶基)吡唑]组成的三个新的八齿四核配体的制备,这些单元通过连接在吡唑酸酯部分的二甲苯基连接,通式为(Hbpp)_2-报告了u-xyl(u = p,m或o),以及在相同位置被苄基Hbpp-bz取代的双核对应物。所有这些配体均已通过常规分析和光谱技术进行了表征。相应的通式为{[Ru_2(trpy)_2(L)] _ 2(μ-(bpp)_2-u-xyl)}〜(n +)的四核钌配合物[L = Cl或OAc,n = 4; L =(H _2O)_2,n = 6]及其双核同系物{[Ru _2(trpy)_2(L)](μ-bpp-bz)}〜(n +)[L = Cl或OAc,n = 2 ;还制备了L =(H_2O)_2,n = 3],并在溶液和固态下进行了彻底表征。在溶液中,所有配合物均已通过紫外可见和NMR光谱表征,并通过循环伏安法研究了它们的氧化还原特性。在固态下,已经对两种双核配合物{[Ru_2(trpy)_2(L)](μ-bpp-bz)}〜(2 +)(L = Cl和OAc)进行了单晶X射线衍射分析。对于四核配合物{[Ru_2(trpy)_2(μ-OAc)] _2(μ-(bpp)_2-m-xyl)}〜(4+)。四核水配合物{[Ru_2(trpy)_2(H _2O)_2] _2(μ-(bpp)_2-u-xyl)}〜(6+)和双核同系物{[Ru_2(trpy)_2在pH = 1.0的三氟甲磺酸溶液中,使用铈(IV)作为化学氧化剂,对用作水氧化催化剂的(H_2O)_2](μ-bpp-bz)}〜(3+)进行了评估。发现这些配合物除了产生大量的双氧以外,还产生二氧化碳。 [O_2] / [CO_2]的相对比例不仅取决于木基的对位,间位或邻位取代,而且还取决于起始原料的浓度。关于四核配合物,包含更受空间约束的邻位取代的配体的化合物产生最高的[O_2] / [CO_2]比。

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