首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Ruthenium(II/III)-bipyridine complexes with four-membered sulphur donor co-ligands: synthesis, metal valence preference, spectroscopic and electron-transfer properties
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Ruthenium(II/III)-bipyridine complexes with four-membered sulphur donor co-ligands: synthesis, metal valence preference, spectroscopic and electron-transfer properties

机译:具有四元硫供体共配体的钌(II / III)-联吡啶配合物:合成,金属化合价,光谱和电子转移性质

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A group of stable ruthenium(II) and (III) mixed-ligand tris-chelaled complexes of the type [Run+(bpy)(L)(2)](z+) (1-8. n=2, Z=0; 9, n=3, Z=1) have been synthesized and characterized (bpy=2,2'-bipvridine; L = anionic form of the ligands, ROC(S)SK, (R=Me, Et, Pr-n, Pr-i, Bu-n, Bu-i, CH2-Ph) or (EtO)(2)P(S)SNH4 or (Et)(2)NC(S)SNa). The complexes 1-8 are diamagnetic and electrically neutral and the complex 9 is one-electron paramagnetic and behaves as 1:1 electrolyte in acetonitrile solvent. The complexes. 1-8 and 9 display two MLCT transitions near 530, 370 nm and 663, 438 nm respectively. Intra-ligand bipyridine based pi-pi* transition is observed near 300 nm. The complexes 1-8 exhibit room-temperature emission from the highest energy MLCT band (similar to 370 nm). At room temperature the lifetime of the excited states for the complexes 2 and 8 are found to be 90 and 95 ns respectively. In acetonitrile solution the complexes 1-9 show a reversible ruthenium(III)ruthenium(II) couple in the ranee - 0.08 --> 0.40 V and irreversible ruthenium(III)-ruthenium(IV) oxidation in the ranee 1.19-1.45 V vs Ag/AgCl. One reversible bipyridine reduction is observed For each complex in the range -1.70 --> -1.85 V vs Ag/AgCl. The presence of trivalent ruthenium in the oxidized solution for one complex 1 is evidenced by the axial EPR spectrum at 77 K, The isolated trivalent complex 9 also exhibits an axial EPR spectrum at 77 K. The EPR spectra of the trivalent ruthenium complexes (1(+) and 9) have been analyzed to finish values of distortion parameters (Delta(cm(-1))-->1(+), 3689; 9. 3699) and energies of the two expected ligand field transitions (v(1)(cm(-1))-->1(+), 3489; 9, 3497 and v(2)(cm(-1))-->1(+), 4339; 9, 4348) within the t(2) shell, One of the ligand field transitions has been experimentally observed at 4673 cm(-1) for complex 9 and which close to the computed v(2) value (4348 cm(-1)).(C) 1998 Elsevier Science Ltd. All rights reserved. [References: 60]
机译:[Run +(bpy)(L)(2)](z +)类型的一组稳定的钌(II)和(III)混合配体三螯合物(1-8。n = 2,Z = 0; 9,n = 3,Z = 1)已经合成并表征(bpy = 2,2'-bipvridine; L =阴离子形式的配体ROC(S)SK,(R = Me,Et,Pr-n, Pr-i,Bu-n,Bu-i,CH2-Ph)或(EtO)(2)P(S)SNH4或(Et)(2)NC(S)SNa)。配合物1-8是抗磁性的并且是电中性的,而配合物9是单电子顺磁性的,并且在乙腈溶剂中表现为1:1的电解质。复合体。 1-8和9显示分别在530、370 nm和663,438 nm附近的两个MLCT跃迁。在300 nm附近观察到基于配体内联吡啶的pi-pi *跃迁。配合物1-8表现出从最高能量MLCT带(类似于370 nm)发出的室温辐射。在室温下,发现配合物2和8的激发态寿命分别为90和95 ns。在乙腈溶液中,配合物1-9在ra中显示可逆的钌(III)钌(II)对-0.08-> 0.40 V,并且在nee中显示不可逆的钌(III)-钌(IV)氧化1.19-1.45 V vs Ag / AgCl。相对于Ag / AgCl,对于每种络合物,观察到一种可逆的联吡啶还原,其范围为-1.70-> -1.85V。一种配合物1的氧化溶液中三价钌的存在通过77 K的轴向EPR光谱证明。分离出的三价配合物9在77 K时也显示轴向EPR光谱。三价钌配合物的EPR光谱(1( +)和9)已被分析以完成畸变参数(Delta(cm(-1))-> 1(+),3689; 9. 3699)和两个预期配体场跃迁的能量(v(1 )(cm(-1))-> 1(+),3489; 9,3497和v(2)(cm(-1))-> 1(+),4339; 9,4348) (2)壳层,已在实验中观察到配体9在4673 cm(-1)处的一个配体场跃迁,该跃迁接近于计算出的v(2)值(4348 cm(-1))。(C)1998 Elsevier科学有限公司。保留所有权利。 [参考:60]

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