Design and Synthesis of Heteroleptic Cyclometalated Iridium(III) Complexes Containing Quinoline-Type Ligands that Exhibit Dual Phosphorescence

被引:59
作者
Kumar, Sarvendra [1 ]
Hisamatsu, Yosuke [1 ]
Tamaki, Yusuke [3 ]
Ishitani, Osamu [3 ]
Aoki, Shin [1 ,2 ]
机构
[1] Tokyo Univ Sci, Fac Pharmaceut Sci, 2641 Yamazaki, Noda, Chiba 2788510, Japan
[2] Tokyo Univ Sci, Res Inst Sci & Technol, Imaging Frontier Canc, 2641 Yamazaki, Noda, Chiba 2788510, Japan
[3] Tokyo Inst Technol, Grad Sch Sci & Engn, Dept Chem, Meguro Ku, 2-12-1-NE-1 O Okayama, Tokyo 1528550, Japan
关键词
LIGHT-EMITTING DEVICES; INTERLIGAND ENERGY-TRANSFER; SINGLET OXYGEN SENSITIZERS; IR(III) COMPLEXES; 8-HYDROXYQUINOLINE DERIVATIVES; PHOTODYNAMIC THERAPY; EXCITED-STATES; CELL-DEATH; PHOTOCHEMICAL REACTIVATION; ELECTROCHEMICAL PROPERTIES;
D O I
10.1021/acs.inorgchem.5b02872
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The design and synthesis of some cyclometalated iridium(III) complexes containing quinoline-type ligands as ancillary ligands are reported. The emission spectra of Ir(III) complexes Containing a quinolinolate (6, 8, 10) moiety exhibit a single emission peak at ca. 590 nm, resulting in, a red colored emission. However, Ir(III) complexes containing 8-sulfonamidoquinoline ligands (11, 13-21) exhibit two different emission peaks (dual emission) at ca. 500 nm and ca. 600 nm upon excitation at 366 run, resulting in a red colored emission for 11 and a pale yellow-colored emission for 14-18 at 298 K. Especially, a white emission was observed for 19 at 298 and 77 K in dimethyl sulfoxide. The mechanistic studies based on time-dependent density functional theory, calculations and time-resolved emission spectroscopy suggest that this dual emission originates from two independent emission states.
引用
收藏
页码:3829 / 3843
页数:15
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