255829-43-7Relevant articles and documents
Pt(II) diimine complexes bearing varied alkyl chains: Synthesis, tunable photophysical properties and aggregation-induced optical power limiting enhancement
Chen, Zhiyuan,Hu, Lai,Liu, Rui,Wang, Hongzhi,Zhu, Hongjun,Zhu, Senqiang
, (2021/11/30)
A series of Pt(II) diimine complexes with varied alkyl chains on 2,2′- dipyridyl ligands (Pt-C1–Pt-C3) have been synthesized and characterized. The photophysical properties and nonlinear absorption properties were elucidated using UV–vis absorption, emission and transient absorption spectroscopy, density functional theory (DFT) calculations and electrochemical experiments. It was found that increasing the alkyl chain led to regular changes in the photophysical properties of Pt-C1–Pt-C3. The original conjugated skeleton of the Pt(II) complexes were affected when the alkyl chain was introduced and extended. All complexes exhibited an obvious aggregation-induced phosphorescence emission (AIPE) in a mixed solution comprised of tetrahydrofuran/water. The formation of nanoparticles in the aggregated state induced these complexes to exhibit different excited state properties. When the water content increased, the emission intensity increases 3 ～ 13-flod and the excited state lifetime increased 98-flod due to the formation of Pt(II) complex nanoparticles. As a result, the optical power limiting (OPL) performance of these complexes was greatly improved. Based on the systematical investigation of nonlinear optical complexes in aggregated state, this work provided a theoretical basis for the development of new OPL materials. Furthermore, the Pt(II) complex nanoparticles will be more conducive to the potential application of OPL devices.
Easily oxidizable triarylamine materials with naphthalene and binaphthalene core: structure–properties relationship
Kerner, Luká?,Gmucová, Katarína,Ko?í?ek, Jozef,Pet?í?ek, Václav,Putala, Martin
, p. 7081 - 7092 (2016/10/14)
We devised and synthesized a series of electron-rich compounds featuring diphenylamine, carbazole or dibenzo[c,g]carbazole connected via phenylacetylene linkers to an aromatic central unit. The key synthetic step was a high yielding cross coupling reaction between halogenated (bi)naphthalene and organometallic reagents prepared in situ from terminal alkynes (side-arms). By masking one of the iodo functions with a diethyltriazenyl group in the side-arm precursors, we efficiently circumvented the formation of doubly aminated by-products. Although one step longer, this approach led to higher yields of terminal alkynes than the direct coupling route. Spectroscopic and electrochemical measurements supported by computational evidence revealed that conjugation in the 1,4-disubstituted naphthalene backbone is superior to the 1,5 or 2,6 substituted cores. The diphenylamine derivative gets oxidized more readily when compared to its carbazole analogs. Expanding the core to binaphthalene did not alter electronic properties, but influenced the physical characteristics significantly.
Highly-efficient hybrid white organic light-emitting diodes based on a high radiative exciton ratio deep-blue emitter with improved concentration of phosphorescent dopant
Ouyang, Xinhua,Li, Xiang-Long,Bai, Yongqi,Mi, Dongbo,Ge, Ziyi,Su, Shi-Jian
, p. 32298 - 32306 (2015/04/27)
An improved concentration of phosphorescent dopant for highly-efficient hybrid white organic light-emitting diodes based on a high radiative exciton ratio (80%) deep-blue emitter has been developed. The high radiative exciton ratio for the deep-blue emitter was found to be the transfer from the higher triplet (T5) to the lowest singlet state (S1) by a "hot-exciton" process. Notably, when the concentration of Ir(2-phq)3 is up to 0.9 wt%, the OLED still exhibited white emission with a maximum total EQE, CE and PE of 22.3%, 53.7 cd A-1 and 60.2 lm W-1, respectively. The exciton transfer mechanism in a high concentration of phosphorescent dopant was also discussed. The studies provide a way to obtain high performance F/P hybrid WOLEDs with a simple architecture and improved doping concentration. This journal is
