Suppr超能文献

含寡聚(苯乙炔)桥联配体的双钌配合物的电子结构及一些相关的分子结构。

The electronic structures of diruthenium complexes containing an oligo(phenylene ethynylene) bridging ligand, and some related molecular structures.

机构信息

Department of Chemistry, Durham University, South Rd, Durham, UK DH1 3LE.

出版信息

Dalton Trans. 2010 Dec 28;39(48):11605-15. doi: 10.1039/c0dt00809e. Epub 2010 Nov 1.

Abstract

The complexes {Cp'(L(2))Ru}C≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡C{Ru(L(2))Cp'} = (PPh(3))(2), Cp' = Cp; L(2) = dppe, Cp' = Cp*) in which the metal centres are bridged by an oligomeric phenylene ethynylene (OPE) ligand have been prepared and the electronic structure of these representative ruthenium-capped OPEs investigated using a combination of electrochemical, UV-vis-NIR and IR spectroelectrochemical methods, and DFT-based calculations. The diruthenium complexes are oxidised to the thermodynamically stable dications Cp'Ru(L(2))C≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡CRu(L(2))Cp', which on the basis of the spectroelectrochemical and computational results can be described in terms of two non-interacting Ru(C≡CAr)(L(2))Cp' moieties. X-ray structures of the oligophenyleneethynylene HC≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡CH, the bis(gold) complex Ph(3)PAuC≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡CAuPPh(3) and the precursor 1-ethynyl-4-(trimethylsilylethynyl)benzene are also reported.

摘要

{Cp'(L(2))Ru}C≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡C{Ru(L(2))Cp'} = (PPh(3))(2), Cp' = Cp; L(2) = dppe, Cp' = Cp*) 这种复合物中,金属中心由一个聚合的苯乙炔(OPE)配体桥接,使用电化学、紫外可见近红外和红外光谱电化学方法以及基于密度泛函理论的计算相结合,研究了这些具有代表性的钌封端 OPE 的电子结构。二钌配合物被氧化为热力学稳定的二阳离子Cp'Ru(L(2))C≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡CRu(L(2))Cp',根据光谱电化学和计算结果,可以用两个非相互作用的 Ru(C≡CAr)(L(2))Cp' 部分来描述。聚合苯乙炔 HC≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡CH、双(金)配合物 Ph(3)PAuC≡CC(6)H(4)C≡CC(6)H(2)(OMe)(2)C≡CC(6)H(4)C≡CAuPPh(3) 和前体 1-乙炔基-4-(三甲基硅基乙炔基)苯的 X 射线结构也被报道。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验