首页> 外文期刊>Journal of Organometallic Chemistry >Oligo thiophene-2-yl-vinyl bridged mono-and binuclear ruthenium(II) tris-bipyridine complexes: Synthesis, photophysics, electrochemistry and electrogenerated chemiluminescence
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Oligo thiophene-2-yl-vinyl bridged mono-and binuclear ruthenium(II) tris-bipyridine complexes: Synthesis, photophysics, electrochemistry and electrogenerated chemiluminescence

机译:寡聚噻吩-2-基-乙烯基桥联的单核和双核钌(II)三联吡啶配合物:合成,光物理,电化学和电化学发光

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A series of mono- and binuclear ruthenium(II) tris-bipyridine complexes tethered to oligothienylenevinyleries have been synthesized and characterized by H-1 NMR, C-13 NMR and TOF-MS spectrometry. Photophysics, electrochemistry and electrogenerated chemiluminescence (ECL) properties of these complexes are investigated. The electronic absorption spectra of the mononuclear ruthenium complexes show a significant red shift both at MLCT (metal-to-ligand charge transfer) and pi-pi* transitions of oligothienylenevinylenes with increase in the number of thiophenyl-2-yl-vinyl unit. For the binuclear complexes these two absorption bands are overlapped.) All the metal complexes have very weak emission compared to that of the reference complex Ru(bpy)(3)(2+). The first reduction potentials of all mononuclear ruthenium complexes are less negative than that of Ru(bpy)(3)(2+), due to the moderate electron-withdrawing effect of oligothienylenevinylenes. For binuclear ruthenium complexes, only one Ru(II/III) oxidation peak (E-1/2=0.96V vs. Ag/Ag+) was observed, suggesting a weak interaction between two metal centers. Three successive reduction processes of bipyridine ligands are similar among all ruthenium complexes except for RuTRu, which has a very sharp peak owing to the accumulation of neutral product oil the electrode surface. All these ruthenium complexes exhibited different ECL property in CH3CN solution without any additional reductant or oxidant. For three mononuclear ruthenium complexes, the ECL intensity strengthens with increase in the number of thiophene-2-yl-vinyl unit. However, the ECL efficiency dramatically decreased in the binuclear ruthenium complexes. The ECL efficiencies of all the)2+, reported complexes do not exceed that of Ru(bpy 3 where the ECL efficiency decreases in the order of RuTRu > Ru3T > Ru2T > RuT > Ru2TRu (RuT, bis-2,2'-bipyridyl-(4-metliyl-4'-(2-thienylethenyl)-2,2'-bipyridine) ruthenium dihexafluorophosphate; Ru2T, bis-2,2'-bipyridyl-(4-methyl-4'-{(E) -2-[5-((E) -2-thienylethenyl)-thienylethenyl])-2,2'-bipyridine)ruthenium dihexafluorophosphate; Ru3T, bis-2,2'-bipyridyl-(4-methyl-4'-[(E)-2-{(E)-2-[5-((E)-2-thienylethenyl)-thienylethenyl])}-2,2'-bipyridine) ruthenium dihexafluorophosphate; RuTRu, bis-2,2'-bipyridyl-ruthenium-bis-[2-((E)-4'-methyl-2,2'-bipyridinyl-4)-ethenyl]-thienyl-bis-2,2'-bipyridyl-ruthenium tetrahexafluorophosphate; Ru2TRu, bis-2,2'-bipyridyl-ruthenium-(E)-1,2-bis-{2-[2-((E)-4'-methyl-2,2'-bipyridinyl-4)-ethenyl]-thienyl}ethenyl-bis-2,2'-bipyridyl-ruthenium tetrahexafluorophosphate). (c) 2007 Elsevier B.V. All rights reserved.
机译:合成了一系列与单噻吩乙烯乙烯基化合物拴在一起的单核和双核钌(II)三联吡啶化合物,并通过H-1 NMR,C-13 NMR和TOF-MS光谱进行了表征。研究了这些配合物的光物理,电化学和电化学发光(ECL)性质。单核钌配合物的电子吸收光谱显示,随着硫代苯基-2-基-乙烯基单元数量的增加,低聚亚硫基亚乙烯基乙烯的MLCT(金属至配体电荷转移)和pi-pi *跃迁都显示出明显的红移。对于双核配合物,这两个吸收带是重叠的。)与参考配合物Ru(bpy)(3)(2+)相比,所有金属配合物的发射都非常弱。所有的单核钌配合物的第一还原电位都比Ru(bpy)(3)(2+)的负还原电位小,这是由于低聚噻吩乙烯撑乙烯具有中等的吸电子作用。对于双核钌配合物,仅观察到一个Ru(II / III)氧化峰(E-1 / 2 = 0.96V vs. Ag / Ag +),表明两个金属中心之间的相互作用较弱。在所有钌配合物中,联吡啶配体的三个连续还原过程相似,但RuTRu除外,RuTRu由于中性产物在电极表面的积聚而具有非常尖锐的峰。所有这些钌络合物在CH3CN溶液中均表现出不同的ECL性质,而没有任何其他还原剂或氧化剂。对于三种单核钌配合物,ECL强度随着噻吩-2-基-乙烯基单元数量的增加而增强。但是,双核钌配合物的ECL效率急剧下降。所有报告的2)配合物的ECL效率均不超过Ru(bpy 3),其中ECL效率按RuTRu> Ru3T> Ru2T> RuT> Ru2TRu(RuT,bis-2,2'-bipyridyl -(4-甲基-4'-(2-噻吩基乙烯基)-2,2'-联吡啶)二氟磷酸钌; Ru2T,bis-2,2'-联吡啶-(4-甲基-4'-{(E)-2 -[5-((E)-2-噻吩基乙烯基)-噻吩基乙烯基])-2,2'-联吡啶)六氟磷酸钌; Ru3T,bis-2,2'-联吡啶基-(4-甲基-4'-[[E )-2-{(E)-2- [5-((E)-2-噻吩基乙烯基)-噻吩基乙烯基])-2,2'-联吡啶)六氟磷酸钌; RuTRu,双-2,2'-联吡啶基钌-双-[2-(((E)-4'-甲基-2,2'-联吡啶基-4)-乙烯基]-噻吩基-双-2,2'-联吡啶钌四六氟磷酸盐; Ru2TRu,双-2,2'-联吡啶钌-(E)-1,2-双-{2- [2-(((E)-4'-甲基-2,2'-联吡啶基-4)-乙烯基]-噻吩基}乙烯基-双-2,2'-联吡啶基-钌四六氟磷酸盐)。 (c)2007 Elsevier B.V.保留所有权利。

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