Синтез, оптические и электрохимические свойства комплексов иридия(III) с 2-арилбензимидазолами (1105740), страница 21
Текст из файла (страница 21)
Grätzel, M.K. Nazeeruddin, Cyclometalated iridium complexes for conversion of light into electricity and electricity into light, J. Organomet.Chem., 2009, V. 694, p. 2661-2670.28. E.I. Mayo, K. Kilsa, T. Tirrell, P.J. Djurovich, H.B. Gray, Cyclometalated iridium(III)sensitized titanium dioxide solar cells, Photochem. Photobiol. Sci., 2006, V. 5, P.
871873.29. C. Teng, X. Yang, S. Li, M. Cheng, A. Hagfeldt, L. Wu, L. Sun, Tuning the HOMO energy levels of organic dyes for dye-sensitized solar cells based on Br-/Br3- electrolytes,Chem. Eur. J., 2010, V. 16, P. 13127-13138.30. E. Baranoff, J.-H. Yum, I. Jung, R. Vulcano, M. Grätzel, M.K. Nazeeruddin, Cyclometalated iridium complexes as sensitizers for dye-sensitized solar cells, Chem. Asian J.,2010, V. 5, P. 496-499.31. Y.-J. Yuan, J.-Y. Zhang, Z.-T. Yu, J.-Y.
Feng, W.-J. Luo, J.-H. Ye, Z.-G. Zou, Impact ofligand modification on hydrogen photogeneration and light-harvesting applications usingcyclometalated iridium complexes, Inorg. Chem. 2012, V. 51, P. 4123−4133.32. C. Dragonetti, A. Valore, A. Colombo, S. Righetto, V. Trifiletti, Simple novel cyclometallated iridium complexes for potential application in dye-sensitized solar cells, Inorg.Chim. Acta 2012, V. 388, P. 163–167.33. Y. Shinpuku, F. Inui, M. Nakai, Y. Nakabayashi, Synthesis and characterization of novelcyclometalated iridium(III) complexes for nanocrystalline TiO2-based dye-sensitized solar cells, J.
Photochem. Photobiol. A: Chemistry, 2011, V. 222, P. 203– 209.10834. Z. Ning, Q. Zhang, W. Wu, H. Tian, Novel iridium complex with carboxyl pyridyl ligandfor dye-sensitized solar cells: high fluorescence intensity, high electron injection efficiency?, J. Organomet. Chem., 2009, V. 694, P.
2705-2711.35. K. Hasan, E. Zysman-Colman, Panchromic cationic iridium(III) complexes, Inorg. Chem.2012, V. 51, P. 12560-12564.36. S. Takizawa, C. Perez-Bolivar, P. Anzenbacher, S. Murata, Cationic iridium complexescoordinated with coumarin dyes – sensitizers for visible-light-driven hydrogen generation, Eur. J. Inorg. Chem. 2012, P. 3975-3979.37. K. Hasan, E. Zysman-Colman, The effect of aryl substitution on the properties of a seriesofhighlyabsorptivecationiciridium(III)complexesbearingancillarybis(arylimino)acenaphthene ligands, Eur. J.
Inorg. Chem. 2013, P. 4421-4429.38. D.R. Whang, K. Sakai, S.Y. Park, Highle efficient catalytic water reduction with robustiridium(III) photosensitizers containing arylsilyl substituents, Angew. Chem. Int. Ed.,2013, V. 52, P. 11612-11615.39. L. Donato, C.E. McCusker, F.N. Castellano, E.
Zysman-Colman, Mono- and dinuclearcationic iridium(III) complexes bearing a 2,5-dipyridylpyrazine (2,5-dpp) ligand, Inorg.Chem. 2013, V. 52, P. 8495-8504.40. V. Bulovic, G. Gu, P.E. Burrows, S.R. Forrest, M.E. Thompson, Transparent lightemitting devices, Nature, 1996, V.
380, P. 29.41. S. Kappaun, C. Slugovc, E.J.W. List, Phosphorescent organic light-emitting devices:working principle and iridium based emitter materials, Int. J. Mol. Sci. 2008, V. 9, P.1527-1547.42. C. Ulbricht, Phosphorescent systems based on iridium(III) complexes, Proefschrift terverkrijging van de graad van doctor aan de Technische Universiteit Eindhoven, Eindhoven, 2009, 207 p.43. E.
Holder, B.M.W. Langeveld, U.S. Schubert, New trends in the use of transition metalligand complexes for applications in electroluminescent devices, Adv. Mater., 2005, V.17, P. 1109-1121.44. Organic light emitting devices. Synthesis, properties and applications, Ed. by K. Müllen,U. Scherf, WILEY-VCH, Weinheim, 2006, 410 p.45. W.-Y. Wong, C.-L. Ho, Heavy metal organometallic electrophosphors derived from multi-component chromophores, Coord. Chem.
Rev., 2009, V. 253, P. 1709-1758.46. R.C. Evans, P. Douglas, C.J. Winscom, Coordination complexes exhibiting roomtemperature phosphorescence: evaluation of their suitability as triplet emitters in organiclight emitting diodes, Coord. Chem. Rev., 2006, V. 250, P. 2093-2126.10947. K.K.-W. Lo, W.-K.
Hui, C.-K. Chung, K.H.-K. Tsang, T.K.-M. Lee, Luminescent transition metal complex biotin conjugates, Coord. Chem. Rev., 2006, V. 250, P. 1724-1736.48. K.K.-W. Lo, K.H.-K. Tsang, K.-S. Sze, C.-K. Chung, T.K.-M. Lee, K.Y. Zhang, W.-K.Hui, C.-K. Li, J.S.-Y. Lau, D.C.-M. Ng, N. Zhu, Non-covalent binding of luminescenttransition metal polypyridine complexes to avidin, indole-binding proteins and estrogenreceptors, Coord. Chem. Rev., 2007, V.
251, P. 2292-2310.49. G. Di Marco, M. Lanza, A. Mamo, I. Stefio, C. Di Pietro, G. Romeo, S. Campagna, Luminescent mononuclear and dinuclear iridium(III) cyclometalated complexes immobilized in a polymeric matrix as solid-state oxygen sensors, Anal. Chem., 1998, V. 70, P.5019–502350. M.E. Kӧse, R.J. Crutchley, M.C. DeRosa, J.R. Reynolds, K.S.
Schanze, Morphology andoxygen sensor response of luminescent Ir-labeled poly(dimethylsiloxane)/polystyrenepolymer blend films, Langmuir, 2005, V. 21, P. 8255–8262.51. M.M.-S. Toro, J.F. Fernandez-Sanchez, E. Baranoff, M. Gratzel, M.K. Nazeeruddin, A.Fernandez-Gutierrez, Novel luminescent Ir(III) dyes for developing highly sensitive oxygen sensing film, Talanta, 2010, V.
82, P. 620-626.52. J.I. Goldsmith, W.R. Hudson, M.S. Lowry, T.H. Anderson, S. Bernhard, Discovery andhigh-throughput screening of heteroleptic iridium complexes for photoinduced hydrogenproduction, J. Am. Chem. Soc., 2005, V. 127, P. 7502–751053. E.D. Cline, S.E. Adamson, S.Bernhard, Homogeneous catalytic system for photoinducedhydrogen production utilizing iridium and rhodium complexes, Inorg.
Chem., 2008, V.47, P. 10378–10388.54. Z. Ning, Q. Zhang, W. Wu, H. Tian, Novel iridium complex with carboxyl pyridyl ligandfor dye-sensitized solar cells: high fluorescence intensity, high electron injection efficiency?, J. Organomet. Chem., 2009, V. 694, P. 2705-2711.55.
E. Baranoff, J.-H. Yum, M. Gratzel, M.K. Nazeeruddin, Cyclometalated iridium complexes for conversion of light into electricity and electricity into light, J. Organomet.Chem., 2009, V. 694, P. 2661-2670.56. E. Baranoff, J.-H. Yum, I. Jung, R. Vulcano, M. Gratzel, M.K. Nazeeruddin, Cyclometalated iridium complexes as sensitizers for dye-sensitized solar cells, Chem. Asian J.,2010, V. 5, P.
496-499.57. E.I. Mayo, K. Kilsa, T. Tirrell, P.J. Djurovich, H.B. Gray, Cyclometalated iridium(III)sensitized titanium dioxide solar cells, Photochem. Photobiol. Sci., 2006, V. 5, P. 871873.11058. Iridium complexes in organic synthesis, Ed. by L.A. Oro, C. Claver, WILEY-VCH,Weinheim, 2009, 396 p.59. T. Suzuki, Organic synthesis involving iridium-catalyzed oxidation, Chem.
Rev., 2011,V. 111, P. 1825–1845.60. J.-H. Xie, S.-F. Zhu, Q.-L. Zhou, Transition metal-catalyzed enantioselective hydrogenation of enamines and imines, Chem. Rev., 2011, V. 111, P. 1713–1760.61. Синтез органических препаратов, сб. 2, 1949, с. 517.62. C. Liu, W. Yang, A fast and oxygen-promoted protocol for the ligand-free Suzuki reaction of 2-halogenated pyridines in aqueous media, Chem. Commun., 2009, P.
6267-6269.63. C. Liu, N. Han, X. Song, J. Qio, A general and highly efficient method for the construction of aryl-substituted N-heteroarenes, Eur. J. Org. Chem., 2010, P. 5548-5551.64. C.M. So, C.C. Yeung, C.P. Lau, F.Y. Kwong, A new family of tunable indolylphosphineligands by one-pot assembly and their applications in Suzuki-Miyaura coupling of arylchlorides, J.
Org. Chem., 2008, V. 73, P. 7803-7806.65. T. Leermann, F.R. Leroux, F. Colobert, Highly efficient one-pot access to functionalizedarylboronic acids via noncryogenic bromine/magnesium exchanges, Org. Lett., 2011, V.13, P. 4479-4481.66. K.L. Billingsley, S.L. Buchwald, An improved system for the palladium-catalyzedBorylation of aryl halides with pinacol borane, J.
Org. Chem., 2008, V. 73, P. 5589-5591.67. A.R. Katritzky, M. Kingsland, The kinetics and mechanism of the electrophilic substitution of heteroaromatic compounds. Part XIII. The mononitration of 2-phenylpyridine andits N-oxide, J. Chem. Soc. B, 1968, P. 862-864.68.
H.-J. Cristau, P.P. Cellier, J.-F. Spindler, M. Taillefer, Mild conditions for coppercatalysed N-arylation of pyrazoles, Eur. J. Org. Chem. 2004, P. 695-709.69. V.I. Sorokin, Copper (I) catalyzed N-arylation of azoles, the recent developments, MiniRev.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
