Luminescent bis-tridentate ruthenium(II) and osmium(II) complexes based on terpyridyl-imidazole ligand: synthesis, structural characterization, photophysical, electrochemical, and solvent dependence studies

被引:36
|
作者
Bhaumik, Chanchal [1 ]
Das, Shyamal [1 ]
Maity, Dinesh [1 ]
Baitalik, Sujoy [1 ]
机构
[1] Jadavpur Univ, Inorgan Chem Sect, Dept Chem, Kolkata 700032, India
关键词
ROOM-TEMPERATURE LUMINESCENCE; TRANSITION-METAL-COMPLEXES; RU(II) COMPLEXES; BRIDGING LIGAND; EXCITED-STATES; ARTIFICIAL PHOTOSYNTHESIS; ABSORPTION-SPECTRA; ENERGY-TRANSFER; LIFETIMES; BEHAVIOR;
D O I
10.1039/c1dt11645b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Homo- and heteroleptic bis-tridentate ruthenium(II) and osmium(II) complexes of compositions [(tpy-PhCH3)Ru(tpy-HImzPh(3))](ClO4)(2) (1), [(H(2)pbbzim) Ru(tpy-HImzPh(3))] (ClO4)(2) (2) and [M(tpy-HImzPh(3))(2)](ClO4)(2) [M = Ru-II (3) and Os-II (4)], where tpy-PhCH3 = p-methylphenyl terpyridine, H(2)pbbzim = 2,6-bis(benzimidazole-2-yl)pyridine and tpy-HImzPh(3) = 4'-[4-(4,5-diphenyl-1H-imidazol-2-yl)-phenyl]-[2,2':6',2 '']terpyridine, have been synthesized and characterized by using standard analytical and spectroscopic techniques. These compounds were designed to increase the room temperature excited-state lifetimes of bisterpyridine-type ruthenium(II) and osmium(II) complexes. The X-ray crystal structures of two homoleptic complexes 3 and 4 have been determined and show that both the compounds crystallized in orthorhombic form with space group Fddd. The photophysical and redox properties of the complexes have been thoroughly investigated. All the complexes display moderately strong luminescence at room temperature with lifetimes in the range of 6-35 ns. The complexes are found to undergo one reversible oxidation in the positive potential window (0 to + 1.6 V) and one irreversible and two successive quasi-reversible reductions in the negative potential window (0 to -2.0 V). The influence of solvents on the photophysical properties of the complexes has also been investigated in detail.
引用
收藏
页码:2427 / 2438
页数:12
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