Synthesis, spectroscopy and electrochemistry of 2-(mercapto/hydroxyl)pyridine-bis-{1-(alkyl)-2-(arylazo) imidazole}ruthenium(II)

Byabartta Prithwiraj
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Abstract

Ruthenium–pyridine complexes incorporating azoimidazole ligands, L, of the type [RuII(RaaiR´)2-(X-pyridine)] 1–6 [RaaiR/ = p-R-C6H4-N=N-C3H2-NN-1-R/, (1-6), abbreviated as N,N/-chelator, where N(imidazole) and N(azo) represent N and N/, respectively; R=H (a), Me (b), Cl (c) and R/ = Me (1,4), CH2CH3 (2,5), Bz(3,6), X=S, 2-mercaptopyridine(1-3), X=O, 2-hydroxy-pyridine(4-6)] have been synthesized and their spectroelectrochemical aspects investigated. The complexes show intense charge-transfer bands in the UV-visible region which have been found to be reasonably blue shifted. The complexes systematically exhibit two oxidation processes and two successive one-electron reductions.   Key words: Ruthenium (II), arylazoimidazole, Infrared spectroscopy (IR), Nuclear magnetic resonance (NMR), Electrospray Ionization Mass Spectrometry (ESIMS), Cyclic Voltammetry  (CV).
2-(巯基/羟基)吡啶-双-{1-(烷基)-2-(芳偶氮)咪唑}钌(II)的合成、光谱学和电化学
含有偶氮咪唑配体L型[RuII(RaaiR´)2-(x -吡啶)]1-6 [RaaiR/ = p-R-C6H4-N=N- c3h2 - nn -1- r /,(1-6)]的钌吡啶配合物,缩写为N,N/-螯合剂,其中N(咪唑)和N(偶氮)分别代表N和N/;合成了R=H (a), Me (b), Cl (c)和R/ = Me (1,4), CH2CH3 (2,5), Bz(3,6), X=S, 2-巯基吡啶(1-3),X=O, 2-羟基吡啶(4-6)],并研究了它们的光谱电化学性质。该配合物在紫外可见区显示出强烈的电荷转移带,并被发现有合理的蓝移。配合物系统地表现出两个氧化过程和两个连续的单电子还原。关键词:钌(II),芳唑咪唑,红外光谱,核磁共振,电喷雾电离质谱,循环伏安法
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