[1] Xu H, Chen R,Sun Q. Recent progress in metal-organic complexes for optoelectronic applications[J]. Chemical Society Reviews, 2014,43(10):3259-3302.
[2] Volz D,Wallesch M, Fléchon C. From iridium and platinum to copper and carbon:new avenues for more sustainability in organic light-emitting diodes[J]. Green Chemistry, 2015,17(4):1988-2011.
[3] Chi Y, Tong B, Chou P T. Metal complexes with pyridylazolates:design, preparation and applications[J]. Coordination Chemistry Reviews, 2014,281(1):1-25.
[4] Ma Y, Che C M, Chao H Y, Zhou X, Chan W H, Shen J. High luminescence gold(Ⅰ) and copper(Ⅰ) complexes with a triplet excited state for use in light-emitting diodes[J]. Advanced Materials, 1999,11(10):852-857.
[5] Cuttell D G, Kuang S M, Fanwick P E. Simple Cu(Ⅰ) complexes with unprecedented excited-state lifetimes[J]. Journal of the American Chemical Society, 2002,124(1):6-7.
[6] Zhang Q, Zhou Q, Cheng Y, Wang L, Ma D, Jing X. Highly efficient green phosphorescent organic light-emitting diodes based on CuI complexes[J]. Advanced Materials, 2004,16(5):432-436.
[7] Vorontsov Ⅱ, Graber T, Kovalevsky A Y. Capturing and analyzing the excited-state structure of a Cu(Ⅰ) phenanthroline complex by time-resolved diffraction and theoretical calculations[J]. Journal of the American Chemical Society, 2009,131(18):6566-6573.
[8] Wada A, Zhang Q, Yasuda T. Efficient luminescence from a copper(Ⅰ) complex doped in organic light-emitting diodes by suppressing C-H vibrational quenching[J]. Chemical Communications, 2012,48(43):5340-5342.
[9] Hsu C W, Lin C C, Chung M W. Systematic investigation of the metal-structure-photophysics relationship of emissive d10-complexes of group 11 elements:the prospect of application in organic light emitting devices[J]. Journal of the American Chemical Society, 2011,133(31):12085-12099.
[10] Hashimoto M, Igawa S, Yashima M. Highly efficient green organic light-emitting diodes containing luminescent three-coordinate copper(Ⅰ) complexes[J]. Journal of the American Chemical Society, 2011,133(27):10348-10351.
[11] Gneuß T, Leitl M J, Finger L H, Rau N. A new class of luminescent Cu(Ⅰ) complexes with tripodal ligands-TADF emitters for the yellow to red color range[J]. Dalton Transactions, 2015,44(18):8506-8520.
[12] Leitl M J, Krylova V A, Djurovich P I, Thompson M E,Yersin H. Phosphorescence versus thermally activated delayed fluorescence. Controlling singlet-triplet splitting in brightly emitting and sublimable Cu(Ⅰ) compounds[J]. Journal of the American Chemical Society, 2014,136(45):16032-16038.
[13] Hofbeck T, Monkowius U, Yersin H. Highly efficient luminescence of Cu(Ⅰ) compounds:thermally activated delayed fluorescence combined with short-lived phosphorescence[J]. Journal of the American Chemical Society, 2015,137(1):399-404.
[14] Deaton J C, Switalski S C, Kondakov D Y. E-type delayed fluorescence of a phosphine-supported Cu2(μ-NAr2)2 diamond core:harvesting singlet and triplet excitons in OLEDs[J]. Journal of the American Chemical Society, 2010,132(27):9499-9508.
[15] Gneuß T, Leitl M J, Finger L H, Yersin H, Sundermeyer J. A new class of deep-blue emitting Cu(Ⅰ) compounds-effects of counter ions on the emission behavior[J]. Dalton Transactions, 2015,44(46):20045-20055.
[16] Coppens P, Sokolow J, Trzop E. On the biexponential decay of the photoluminescence of the two crystallographically-independent molecules in crystals of[Cu(Ⅰ)(phen)(PPh3)2] [BF4] [J]. Journal of Physics Chemistry Letters, 2013,4(4):579-582.
[17] Wang Z, Zheng C, Wang W, Xu C, Ji B, Zhang X. Synthesis, structure, and photophysical properties of two four-coordinate CuI-NHC complexes with efficient delayed fluorescence[J]. Inorganic Chemistry, 2016,55(5):2157-2164.
[18] Liang D, Chen X L, Liao J Z, Hu J Y, Jia J H, Lu C Z. Highly efficient cuprous complexes with thermally activated delayed fluorescence for solution-processed organic light-emitting devices[J]. Inorganic Chemistry, 2016,55(15):7467-7475.
[19] Elie M, Sguerra F, Meo F D. Designing NHC-copper(Ⅰ) dipyridylamine complexes for blue light-emitting electrochemical cells[J]. ACS Applied Materials & Interfaces, 2016,8(23):14678-14691.
[20] Chai W, Hong M, Song L. Three reversible polymorphic copper(Ⅰ) complexes triggered by ligand conformation:insights into polymorphic crystal habit and luminescent properties[J]. Inorganic Chemistry, 2015,54(9):4200-4207.
[21] Marion R, Sguerra F, Meo F D. NHC copper(Ⅰ) complexes bearing dipyridylamine ligands:synthesis, structural, and photoluminescent studies[J]. Inorganic Chemistry, 2014,53(17):9181-9191.
[22] Femoni C, Muzzioli S, Palazzi A. New tetrazole-based Cu(Ⅰ) homo-and heteroleptic complexes with various P∧P ligands:synthesis, characterization, redox and photophysical properties[J]. Dalton Transactions, 2013,42(4):997-1010.
[23] Czerwieniec R, Kowalski K, Yersin H. Highly efficient thermally activated fluorescence of a new rigid Cu(Ⅰ) complex[Cu(dmp)(phanephos)]+[J]. Dalton Transactions, 2013,42(27):9826-9830.
[24] Krylova V A, Djurovich P I, Whited M T, Thompson M E. Synthesis and characterization of phosphorescent three-coordinate Cu(Ⅰ)-NHC complexes[J]. Chemical Communications, 2010,46(36):6696-6698.
[25] Krylova V A, Djurovich P I, Aronson J W. Structural and photophysical studies of phosphorescent three-coordinate copper(Ⅰ) complexes supported by an N-heterocyclic carbene ligand[J]. Organometallics, 2012,31(22):7983-7993.
[26] Krylova V A, Djurovich P I, Conley B L. Control of emission colour with N-heterocyclic carbene (NHC) ligands in phosphorescent three-coordinate Cu(Ⅰ) complexes[J]. Chemical Communications, 2014,50(54):7176-7179.
[27] Kang L, Chen J, Teng T, Chen X L,Yu R, Lu C Z. Experimental and theoretical studies of highly emissive dinuclear Cu(Ⅰ) halide complexes with delayed fluorescence[J]. Dalton Transactions, 2015,44(30):11649-11659.
[28] Okano Y, Ohara H, Kobayashi A, Yoshida M, Kato M. Systematic introduction of aromatic rings to diphosphine ligands for emission color tuning of dinuclear copper(Ⅰ) iodide complexes[J]. Inorganic Chemistry, 2016,55(11):5227-5236.
[29] Czerwieniec R, Yersin H. Diversity of copper(Ⅰ) complexes showing thermally activated delayed fluorescence:basic photophysical analysis[J]. Inorganic Chemistry, 2015,54(9):4322-4327.
[30] Igawa S, Hashimoto M, Kawata I. Highly efficient green organic light-emitting diodes containing luminescent tetrahedral copper(Ⅰ) complexes[J]. Journal of Materials Chemistry C, 2013,1(3):542-551.
[31] Zhang L, Li B, Su Z. Realization of high-energy emission from[Cu(N-N)(P-P)]+ complexes for organic light-emitting diode applications[J]. The Journal of Physical Che-mistry C, 2009,113(31):13968-13973.
[32] Jia W L, McCormick T, Tao Y, Lu J P, Wang S. New phosphorescent polynuclear Cu(Ⅰ) compounds based on linearand star-shaped 2-(2'-Pyridyl)benzimidazolyl derivatives:syntheses, structures, luminescence, and electroluminescence[J]. Inorganic Chemistry, 2005,44(16):5706-5712.
[33] Si Z, Li J, Li B, Liu S, Li W. High light electroluminescence of novel Cu(Ⅰ) complexes[J]. Journal of Luminescence, 2009,129(3):181-186.
[34] Zhang D. Novel green-emitting copper(Ⅰ) complexes with electron donors incorporated ligands:synthesis, photophysical properties, and electroluminescence performances[J]. Journal of Luminescence, 2010,130(8):1419-1424.
[35] Min J, Zhang Q, Sun W, Cheng Y, Wang L. Neutral copper(Ⅰ) phosphorescent complexes from their ionic counterparts with 2-(2'-quinolyl)benzimidazole and phosphine mixed ligands[J]. Dalton Transactions, 2011,40(3):686-693.
[36] Bergmann L, Friendrichs J, Mydlak M. Outstanding luminescence from neutral copper(Ⅰ) complexes with pyridyl-tetrazolate and phosphine ligands[J]. Chemical Communications, 2013,49(58):6501-6503.
[37] Wang R, Xiao J C, Twamley B, Shreeve J M. Efficient heck reactions catalyzed by a highly recyclable palladium(Ⅱ) complex of a pyridyl-functionalized imidazolium-based ionic liquid[J]. Organic & Biomolecular Chemistry, 2007,5(4) 671-678.
[38] Scaltrito D V, Thompson D W, O'Callaghan J A, Meyer G J. MLCT excited states of cuprous bis-phenanthroline coordination compounds[J]. Coordination Chemistry Reviews, 2000,208(1):243-266.
[39] Armaroli N. Photoactive mono-and polynuclear Cu(Ⅰ)-phenanthrolines. A viable alternative to Ru(Ⅱ)-polypyridines[J]. Chemical Society Reviews, 2001,30(2):113-124. |