Cyclometalated rhodium and iridium complexes with imidazole containing Schiff bases: Synthesis, structure and cellular imaging

被引:21
|
作者
Mandal, Soumik [1 ]
Poria, Dipak K. [2 ]
Seth, Dipravath K. [3 ]
Ray, Partho Sarothi [2 ]
Gupta, Parna [1 ]
机构
[1] Indian Inst Sci Educ & Res IISER Kolkata, Dept Chem Sci, Nadia 741252, W Bengal, India
[2] Indian Inst Sci Educ & Res IISER Kolkata, Dept Biol Sci, Nadia 741252, W Bengal, India
[3] Jadavpur Univ, Dept Chem, Inorgan Chem Sect, Jadavpur 700032, India
基金
英国惠康基金;
关键词
Rhodium; Iridium; Schiff base; Fluorescence; Cellular imaging; TRANSITION-METAL-COMPLEXES; SWITCH-ON PROBE; POLYPYRIDINE COMPLEXES; LIVING CELLS; ORGANIC-SYNTHESIS; EXCITED-STATES; LUMINESCENT; LIGANDS; DEVICES; PHOTOPHYSICS;
D O I
10.1016/j.poly.2014.01.033
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Cyclometalated rhodium(III) and iridium(III) complexes (1-4) of two Schiff base ligands L1 and L2 with the general formula [M(ppy)(2)(Ln)]Cl {M = Rh, Ir; ppy = 2-phenylpyridine; n = 1,2; L = Schiff base ligand} have been synthesized. The new ligands and the complexes have been characterized with spectroscopic techniques. Electrochemistry of the complexes revealed anodic behavior, corresponding to an M(III) to M(IV) oxidation. The X-ray crystal structures of complexes 2 and 4 have also been determined to interpret the coordination behavior of the complexes. Photophysical study shows that all the complexes display fluorescence at room temperature with quantum yield of about 3 x 10(-2) to 5 x 10(-2). The electronic absorption spectra of all the complexes fit well with the computational studies. Cellular imaging studies were done with the newly synthesized complexes. To the best of our knowledge, this is the first report of organometallic complexes of rhodium(III) and iridium(III) with Schiff base ligands explored for cellular imaging. Emphasis of this work lies on the structural features, photophysical behavior, cellular uptake and imaging of the fluorescent transition metal complexes. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:12 / 21
页数:10
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