Аннотация:
Novel heteroleptic cyclometallated 1,2,3-triazol-5-ylidene IrIII complexes with 2-(5-trifluoromethyl-2H-1,2,4-triazol-3-yl)pyridine or 2-(1H-tetrazol-5-yl)pyridine as the ancillary ligands demonstrate photoluminescence in green (520nm) and blue (450–480nm) regions.
Образец цитирования:
M. A. Topchiy, S. A. Rzhevskiy, A. A. Ageshina, N. Yu. Kirilenko, G. K. Sterligov, D. Yu. Mladentsev, D. Yu. Parashchuk, S. N. Osipov, M. S. Nechaev, A. F. Asachenko, “Deep blue luminescent cyclometallated 1,2,3-triazol-5-ylidene iridium(iii) complexes”, Mendeleev Commun., 30:6 (2020), 717–718
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1302
https://www.mathnet.ru/rus/mendc/v30/i6/p717
Эта публикация цитируется в следующих 10 статьяx:
Jie Yan, Yangyang Xin, Yi Pan, Guowei Ni, Shek-Man Yiu, Yun Chi, Lian Duan, Kai Chung Lau, “Blue hyperphosphorescence based on green Ir(III) sensitizer with dual CF3 substituted imidazo[4,5-c]pyridin-2-ylidene cyclometalates”, Synthetic Metals, 308 (2024), 117734
Corinne Vanucci-Bacqué, Mariusz Wolff, Béatrice Delavaux-Nicot, Abanoub Mosaad Abdallah, Sonia Mallet-Ladeira, Charles-Louis Serpentini, Florence Bedos-Belval, Kar Wai Fong, Xiao Ying Ng, May Lee Low, Eric Benoist, Suzanne Fery-Forgues, “1,2,3-Triazol-5-ylidene- vs. 1,2,3-triazole-based tricarbonylrhenium(i) complexes: influence of a mesoionic carbene ligand on the electronic and biological properties”, Dalton Trans., 53:27 (2024), 11276
M. A. Topchiy, A. A. Ageshina, S. A. Rzhevskiy, L. I. Minaeva, M. S. Nechaev, A. F. Asachenko, “Solvent-free telomerization of isoprene with alcohols catalyzed by palladium(ɪɪ) carbene complexes”, Russ Chem Bull, 71:5 (2022), 940
Ramananda Maity, Biprajit Sarkar, “Chemistry of Compounds Based on 1,2,3-Triazolylidene-Type Mesoionic Carbenes”, JACS Au, 2:1 (2022), 22
G. T. Sukhanov, Yu. V. Filippova, Yu. V. Gatilov, A. G. Sukhanova, K. K. Bosov, I. A. Krupnova, E. V. Pivovarova, “Acidic N-dealkylation in nitrotriazolium salts”, Mendeleev Commun., 32:2 (2022), 215–217
O. V. Shurupova, G. K. Sterligov, M. A. Rasskazova, E. A. Drokin, A. N. Lysenko, S. A. Rzhevskiy, L. I. Minaeva, M. A. Topchiy, A. F. Asachenko, “One-pot two step synthesis of unsymmetrically substituted indenes from 3,4-diarylbutadiene sulfones”, Mendeleev Commun., 32:4 (2022), 446–448
Felix Stein, Marius Kirsch, Julia Beerhues, Uta Albold, Biprajit Sarkar, “Mono‐ and Di‐Mesoionic Carbene‐Boranes: Synthesis, Structures and Utility as Reducing Agents”, Eur J Inorg Chem, 2021:24 (2021), 2417
Pit Boden, Patrick Di Martino‐Fumo, Tobias Bens, Sophie Steiger, Uta Albold, Gereon Niedner‐Schatteburg, Markus Gerhards, Biprajit Sarkar, “NIR‐Emissive Chromium(0), Molybdenum(0), and Tungsten(0) Complexes in the Solid State at Room Temperature”, Chemistry A European J, 27:51 (2021), 12959
Caifa You, Xue-Qi Wang, Xiuwen Zhou, Yi Yuan, Liang-Sheng Liao, Yu-Chan Liao, Pi-Tai Chou, Yun Chi, “Homoleptic Ir(III) Phosphors with 2-Phenyl-1,2,4-triazol-3-ylidene Chelates for Efficient Blue Organic Light-Emitting Diodes”, ACS Appl. Mater. Interfaces, 13:49 (2021), 59023
S. A. Rzhevskiy, V. N. Bogachev, L. I. Minaeva, G. K. Sterligov, M. S. Nechaev, M. A. Topchiy, A. F. Asachenko, “Efficient synthesis of 3-arylbutadiene sulfones using the Heck–Matsuda reaction”, Mendeleev Commun., 31:4 (2021), 548–549