Design and syntheses of blue luminescent zinc(II) and cadmium(II) complexes with bidentate or tridentate pyridyl-imidazole ligands

被引:102
作者
Yue, SM [1 ]
Xu, HB [1 ]
Ma, JF [1 ]
Su, ZM [1 ]
Kan, YH [1 ]
Zhang, HJ [1 ]
机构
[1] NE Normal Univ, Fac Chem, Inst Funct Mat Chem, Changchun 130024, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
2-(2-pyridyl)-imidazole; 2-(2-pyridyl)-benzimidazole; 2,6-bis(benzimidazol-2yl)-pyridine; complex; luminescence;
D O I
10.1016/j.poly.2005.07.021
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of luminescent Zn(II) and Cd(II) complexes have been prepared based on three different pi-conjugated ligands, 2-(2-pyridyl)-imidazole (HL1), 2-(2-pyridyl)-benzimidazole (HL2) and 2.6-bis(benzimidazol-2yl)-pyridine (H(2)L3). The PL spectra of the ligands exhibit a bathochromic shift in agreement with the extended pi-conjugation of the ligand. The spectra of the complexes with the ligands follow the same rule. The structures of Zn(L2)(2)H2O (5), [Cd(L-2)(2)(H2O)(2)] center dot 2DMSO (6), Zn(HL3)(2) (9) and Cd(HL3)(2) (10) have been established by X-ray crystallography. The structure of 5 can be best described as a square pyramid. The coordination geometries of 6, 9 and 10 can be described as distorted octahedrons. In the solid state and in DMSO, these complexes show emission maxima in the blue region. The complexes have a bathochromic shift of the emission energy in sharp contrast to the free ligands. They display blue luminescence and have high luminescence quantum efficiency. A theoretical study reveals that the emissions are assigned to intraligand transitions of the deprotonated L2 and HL3 ligands, and the metal ions in the complexes play a key role in stabilizing the ligand and promoting the luminescence, which is consistent with the experimental results. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:635 / 644
页数:10
相关论文
共 102 条
[1]   BLUE LIGHT-EMITTING ORGANIC ELECTROLUMINESCENT DEVICES [J].
ADACHI, C ;
TSUTSUI, T ;
SAITO, S .
APPLIED PHYSICS LETTERS, 1990, 56 (09) :799-801
[2]   CONFINEMENT OF CHARGE-CARRIERS AND MOLECULAR EXCITONS WITHIN 5-NM-THICK EMITTER LAYER IN ORGANIC ELECTROLUMINESCENT DEVICES WITH A DOUBLE HETEROSTRUCTURE [J].
ADACHI, C ;
TSUTSUI, T ;
SAITO, S .
APPLIED PHYSICS LETTERS, 1990, 57 (06) :531-533
[3]   SYNTHESIS OF SOME IMIDAZOLE-DERIVED AND PYRAZOLE-DERIVED CHELATING-AGENTS [J].
ADDISON, AW ;
BURKE, PJ .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1981, 18 (04) :803-805
[4]   LIGHT-EMITTING POLYMERS WITH PENDANT CHROMOPHORIC GROUPS .1. POLY(STILBENYL-P-METHOXYSTYRENE) [J].
AGUIAR, M ;
KARASZ, FE ;
AKCELRUD, L .
MACROMOLECULES, 1995, 28 (13) :4598-4602
[5]  
[Anonymous], 1992, INT TABLES XRAY CRYS, VC
[6]  
[Anonymous], 1979, MET IONS BIOL SYST
[7]   Syntheses, structures, solution, and solid-state 27Al NMR studies of blue luminescent mononuclear aluminum complexes:: Al(7-azain)2(7-azain-H)(CH3), Al(7-azain)3(7-azain-H), and Al(7-azain)(7-azain-H) (OCH(CF3)2)2 (7-azain-H=7-azaindole) [J].
Ashenhurst, J ;
Wu, G ;
Wang, SN .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (11) :2541-2547
[8]   High-efficiency fluorescent organic light-emitting devices using a phosphorescent sensitizer [J].
Baldo, MA ;
Thompson, ME ;
Forrest, SR .
NATURE, 2000, 403 (6771) :750-753
[9]   Highly efficient phosphorescent emission from organic electroluminescent devices [J].
Baldo, MA ;
O'Brien, DF ;
You, Y ;
Shoustikov, A ;
Sibley, S ;
Thompson, ME ;
Forrest, SR .
NATURE, 1998, 395 (6698) :151-154
[10]   Stability analysis for solutions of the closed shell Kohn-Sham equation [J].
Bauernschmitt, R ;
Ahlrichs, R .
JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (22) :9047-9052