267221-88-5Relevant articles and documents
Rationalize the roles of electron donating-withdrawing groups in the impacts on solvatochromism, nonlinear optics, and electroluminescence devices
Chen, Chih-Hsien,Luo, Zi-Huan,Huan, I-Hong,Chen, Yu-Han,Lim, Tsong-Shin
, (2020)
The correlation between chemical structure and photophysical behavior is vital for development of luminogens in the application of optoelectronics. Different donor, acceptor and π-bridge were systematically combined to produce a series of D-π-A-π-D chromo
6,6′-Ditriphenylamine-2,2′-bipyridine: Coordination Chemistry and Electrochemical and Photophysical Properties
Cording, Andrew P.,Crowley, James D.,Gordon, Keith C.,Mapley, Joseph I.,McAdam, C. John,Ross, Daniel A. W.,Vasdev, Roan A. S.
, p. 11852 - 11865 (2021)
A 2,2′-bipyridine with bulky triphenylamine substituents in the 6 and 6′ positions of the ligand (6,6′-ditriphenylamine-2,2′-bipyridine, 6,6′-diTPAbpy) was generated. Despite the steric bulk, the ligand readily formed bis(homoleptic) complexes with copper
Decreasing the energy consumption of memory devices by enhancing the conjugation extent of the terminal electron- donating moieties within molecules
Bo, Rongcheng,Liu, Hongzhang,Zhou, Qianhao,Chen, Dongyun,Xu, Qingfeng,Li, Najun,Li, Hua,Lu, Jianmei
, p. 461 - 467 (2015)
Three small organic molecules that contained a phenothiazine backbone and triphenylamine (TPA), carbazole (CZ), or anthracene (AN) as a terminal electron donor were synthesized and fabricated in ITO/organic film/Al sandwiched memory devices. The influence
Multiple Luminescence Responses towards Mechanical Stimulus and Photo-Induction: The Key Role of the Stuck Packing Mode and Tunable Intermolecular Interactions
Dang, Qianxi,Hu, Lanzhen,Wang, Jiaqiang,Zhang, Qunhua,Han, Mengmeng,Luo, Simeng,Gong, Yanbin,Wang, Can,Li, Qianqian,Li, Zhen
, p. 7031 - 7037 (2019)
Organic luminescence with different forms continues to be one of the most active research fields in science and technology. Herein, an ultra-simple organic molecule (TPA-B), which exhibits both mechanoluminescence (ML) and photo-induced room-temperature phosphorescence (RTP) in the crystalline state, provides an opportunity to reveal the internal mechanism of ML and the dynamic process of photo-induced RTP in the same molecule. Through the detailed investigation of photophysical properties together with crystal structures, the key role of molecular packing and intermolecular interactions was highlighted in the luminescence response by mechanical and light stimulus, affording efficient strategies to design potential smart functional materials with multiple luminescence properties.
Charge separation and singlet fission in covalently linked diketopyrrolopyrrole derivatives and triphenylamine triad in solution
Bangal, Prakriti Ranjan,Chakali, Madhu,Dyaga, Bharath,Mandal, Haraprasad,Rao, V. Jayathirtha,Venkatesan, Munisamy
, (2020/11/26)
A covalently linked push-pull type triad containing two unsymmetrical electron donors, triphenylamine (TPA) and benzothiophene (BT), and diketopyrrolopyrrole (DPP), an electron acceptor, through thiophene spacer has been synthesized (BT-DPP-TPA(7)) and ultrafast relaxation dynamics of the triad has been explored in solution phase by various spectroscopic methods. Steady-state and time-resolved emission studies show the efficient fluorescence quenching of the DPP entity of as prepared BT-DPP-TPA(7) triad. The negative free energy values comprising the redox potentials and singlet state energy of BT-DPP-TPA(7) revealed the probability of electron transfer from the singlet ground state of TPA to the excited singlet state of DPP. Femtosecond transient absorption (fsTA) spectroscopic studies confirmed the formation of charge separation state by detecting triphenylamine radical cation as electron-transfer transients. The rate of charge separation, kCS, is (109?108 s?1) observed to be increasing from nonpolar to polar solvents and the rate of charge recombination, kCR, was found to be slower (μs time scale) in polar solvents like DMF and chloroform, than that in hexane, non-polar solvent (ns time scale). This novel aspect could be due to asymmetrically designed push-pull type triad, a feature that was not evident in push-pull triad constructed using symmetric TPA as electron donors. Furthermore, fsTA studies also demonstrate, for the first time, that the DPP derivatives, TDPP(4) and BT-DPP-TPA(7), both undergo singlet fission (SF) event (S→TT) in 100?200 ps time scale in solution phase for the solution of concentration above ~100 μM. These results may pave the new avenue for device design comprising DPP derivatives.
Arylamine-based organic compound and organic electroluminescent device containing same
-
Paragraph 0236-0237; 0239, (2021/09/21)
The invention relates to the technical field of semiconductor materials, in particular to an arylamine organic compound and an organic electroluminescent device containing the same. The structure of the compound is shown in the general formula (I). The ar