Dumbbell-Shaped Dinuclear Iridium Complexes and Their Application to Light-Emitting Electrochemical Cells

被引:53
作者
Costa, Ruben D. [2 ]
Fernandez, Gustavo [1 ]
Sanchez, Luis [1 ]
Martin, Nazario [1 ]
Orti, Enrique [2 ]
Bolink, Henk J. [2 ]
机构
[1] Univ Complutense, Dept Quim Organ, Fac Ciencias Quim, E-28040 Madrid, Spain
[2] Univ Valencia, ICMol, Valencia 46071, Spain
关键词
electroluminescence; iridium; light-emitting electrochemical cells; quenching pathways; CHELATED RUTHENIUM(II) COMPLEX; FUNCTIONAL RESPONSE THEORY; ELECTROLUMINESCENT DEVICES; EXCITATION-ENERGIES; HIGH-EFFICIENCY; SINGLE-LAYER; STATE; BLUE; GREEN; LIGAND;
D O I
10.1002/chem.201000600
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel family of dumbbell-shaped dinuclear complexes in which an oligophenyleneethynylene spacer is linked to two heteroleptic iridium(III) complexes is presented. The synthesis. as well as the electrochemical and photophysical characterization of the new complexes. is reported The experimental results are interpreted with the help of density functional theory calculations From these studies we conclude that the lowest triplet excited state corresponds to a (3)pi-pi* state located on the conjugated spacer The presence of this state below the (MLCT)-M-3/(LLCT)-L-3 emitting states of the end-capping Ir-III complexes explains the low quantum yields observed for the dinuclear complexes (one order-of-magnitude less) with respect to the mononuclear complexes The potential application of the novel dinuclear complexes in optoelectronic devices has been tested by using them as the primary active component in double-layer hat-emitting electrochemical cells (LECs) Although the luminance levels are low, the external quantum efficiency suggests that a near-quantitative internal electron-to-photon conversion occurs in the device This indicates that the emission inside the device is highly optimized and that the self-quenching associated with the high concentration of the complex in the active layer is minimized
引用
收藏
页码:9855 / 9863
页数:9
相关论文
共 56 条
[1]   Connecting two C60 stoppers to molecular wires:: ultrafast intramolecular deactivation reactions [J].
Atienza, C ;
Insuasty, B ;
Seoane, C ;
Martín, N ;
Ramey, J ;
Rahman, GMA ;
Guldi, DM .
JOURNAL OF MATERIALS CHEMISTRY, 2005, 15 (01) :124-132
[2]  
Balzani V, 2007, TOP CURR CHEM, V280, P1, DOI 10.1007/978-3-540-73347-8
[3]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[4]   A MULTICENTER NUMERICAL-INTEGRATION SCHEME FOR POLYATOMIC-MOLECULES [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1988, 88 (04) :2547-2553
[5]   Long-Living Light-Emitting Electrochemical Cells - Control through Supramolecular Interactions [J].
Bolink, Henk J. ;
Coronado, Eugenio ;
Costa, Ruben D. ;
Orti, Enrique ;
Sessolo, Michele ;
Graber, Stefan ;
Doyle, Kevin ;
Neuburger, Markus ;
Housecroft, Catherine E. ;
Constable, Edwin C. .
ADVANCED MATERIALS, 2008, 20 (20) :3910-+
[6]   Origin of the large spectral shift in electroluminescence in a blue light emitting cationic iridium(III) complex [J].
Bolink, Henk J. ;
Cappelli, Luca ;
Cheylan, Stephanie ;
Coronado, Eugenio ;
Costa, Ruben D. ;
Lardies, Nora ;
Nazeeruddin, Md. K. ;
Orti, Enrique .
JOURNAL OF MATERIALS CHEMISTRY, 2007, 17 (48) :5032-5041
[7]  
Brabec CJ, 2001, ADV FUNCT MATER, V11, P15, DOI 10.1002/1616-3028(200102)11:1<15::AID-ADFM15>3.0.CO
[8]  
2-A
[9]   Molecular excitation energies to high-lying bound states from time-dependent density-functional response theory: Characterization and correction of the time-dependent local density approximation ionization threshold [J].
Casida, ME ;
Jamorski, C ;
Casida, KC ;
Salahub, DR .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (11) :4439-4449
[10]   Phosphorescent dyes for organic light-emitting diodes [J].
Chou, Pi-Tai ;
Chi, Yun .
CHEMISTRY-A EUROPEAN JOURNAL, 2007, 13 (02) :380-395