175845-24-6Relevant articles and documents
Phosphorescent OLEDs assembled using Os(ii) phosphors and a bipolar host material consisting of both carbazole and dibenzophosphole oxide
Lin, Cheng-Huei,Hsu, Che-Wei,Liao, Jia-Ling,Cheng, Yi-Ming,Chi, Yun,Lin, Tsung-Yi,Chung, Min-Wen,Chou, Pi-Tai,Lee, Gene-Hsiang,Chang, Chih-Hao,Shih, Chin-Yao,Ho, Chi-Lung
experimental part, p. 10684 - 10694 (2012/07/31)
We report on the synthesis of a new series of Os(ii) complexes (1-3) functionalized with 2-pyridyl (or 2-isoquinolyl) pyrazole chelates, together with a new diphosphine, 1,2-bis(phospholano)benzene chelate (pp2b). The resulting Os(ii) complexes are fully characterized and their structural versus spectroscopic properties have been comprehended by absorption/emission together with computational approaches. The inherent electron richness, restricted rotational barrier and good steric hindrance of pp2b lead to the production of both orange and red phosphorescence with high quantum efficiency. For exploring these Os(ii) based OLEDs, we also synthesized a bipolar material 5-[4-(carbazo-9-yl)phenyl] dibenzophosphole-5-oxide (CzPhO), possessing both carbazole donor and dibenzophosphole oxide acceptor. Successful fabrication of OLEDs using complexes 1 and 3 as the dopant and either 4,4′-N,N′- dicarbazolebiphenyl (CBP) or CzPhO as host is reported. For comparison, the CBP and CzPhO devices with 1 as the emitter showed peak efficiencies EQE of 10.9%, ηL of 21.7 cd A-1, and ηp of 11.9 lm W-1, and EQE of 14.3%, ηL of 34.8 cd A-1, and ηp of 45.2 lm W-1, respectively. The Royal Society of Chemistry 2012.
Probing the importance of the hemilabile site of bis(phosphine) monoxide ligands in the copper-catalyzed addition of diethylzinc to N-phosphinoylimines: Discovery of new effective chiral ligands
Bonnaventure, Isabelle,Charette, Andre B.
, p. 6330 - 6340 (2008/12/22)
(Chemical Equation Presented) The hemilabile ligand Me-DuPHOS(O) 2 has proven to be a successful ligand for the copper-catalyzed addition of diethylzinc to N-phosphinoylimines. The corresponding α-chiral amines were obtained in high yields (80-98%) and enantiomeric ratios (19.0:1 to 99.0:1 er). Furthermore, this Cu?2 catalytic system has been shown to be effective in the addition of diethylzinc to nitroalkenes and in the reduction of β,β-disubstituted vinyl phenyl sulfones. This paper describes a general structure/selectivity study in which the three ligand subunits (chiral phospholane-linker-labile coordinating group (Z)) are systematically modified and tested in the copper-catalyzed addition of diethylzinc to the N-phosphinoylimine 1 derived from benzaldehyde. This study led to the discovery of a new class of effective chiral ligands that combine a chiral phospholane unit and an achiral phosphine oxide.