Thiophene‐Based Double Helices: Radical Cations with SOMO‐HOMO Energy Level Inversion

Author(s):  
Andrzej Rajca ◽  
Chan Shu ◽  
Hui Zhang ◽  
Sheng Zhang ◽  
Hua Wang ◽  
...  
2016 ◽  
Vol 138 (23) ◽  
pp. 7298-7304 ◽  
Author(s):  
Ying Wang ◽  
Hui Zhang ◽  
Maren Pink ◽  
Arnon Olankitwanit ◽  
Suchada Rajca ◽  
...  

Polymer ◽  
2016 ◽  
Vol 102 ◽  
pp. 84-91 ◽  
Author(s):  
Juae Kim ◽  
Nam Hee Kim ◽  
Seyeong Song ◽  
Song Yi Park ◽  
Sangmin Chae ◽  
...  

2012 ◽  
Vol 22 (29) ◽  
pp. 14645 ◽  
Author(s):  
Elena Poverenov ◽  
Yana Sheynin ◽  
Natalia Zamoshchik ◽  
Asit Patra ◽  
Gregory Leitus ◽  
...  

2019 ◽  
Vol 7 (24) ◽  
pp. 14473-14477 ◽  
Author(s):  
Liren Zhang ◽  
Jionghua Wu ◽  
Dongmei Li ◽  
Wenhua Li ◽  
Qingbo Meng ◽  
...  

Intramolecular S–O interactions were adopted for designing HTMs with high hole mobility and a suitable HOMO energy level in PVSK.


2017 ◽  
Vol 53 (1) ◽  
pp. 180-183 ◽  
Author(s):  
Yang Wang ◽  
Shumeng Wang ◽  
Junqiao Ding ◽  
Lixiang Wang ◽  
Xiabin Jing ◽  
...  

Low-voltage-driving and power-efficient nondoped electrophosphorescent devices have been realized by increasing the dendron's HOMO energy level to favor effective hole injection and promote exciton formation.


2018 ◽  
Vol 3 (1) ◽  
pp. 131-141 ◽  
Author(s):  
Yan Zou ◽  
Yue Wu ◽  
Hang Yang ◽  
Yingying Dong ◽  
Chaohua Cui ◽  
...  

The engineering of alkylthio side chains in the molecular conjugated backbone of small molecules is in favor of achieving a linear molecular backbone conformation, slightly red-shifting the absorption spectrum, and down-shifting the HOMO energy level of the resulting molecule.


2018 ◽  
Vol 22 (01n03) ◽  
pp. 32-45 ◽  
Author(s):  
Masashi Yatabe ◽  
Akio Kajitani ◽  
Mikio Yasutake ◽  
Kazuchika Ohta

We have synthesized a series of novel phthalocyaninato copper(II) (abbreviated as PcCu) compounds, 1,4,8,11,15,18,22,25-octakisalkoxy-2,3,9,10,16,17,23,24-octachloro-phthalocyaninato copper(II) (abbreviated as ([Formula: see text]-C[Formula: see text]O)[Formula: see text]-Cl)[Formula: see text]PcCu (4a–4d): [Formula: see text] 6 (a), 8 (b), 10 (c) and 12 (d)) and, for comparison, another series of PcCu compounds, 1,4,8,11,15,18,22,25-octakisalkoxyphthalocyaninato copper(II) (abbreviated as ([Formula: see text]-C[Formula: see text]O)[Formula: see text]PcCu (1a–1d)). The PcCu derivatives 1a–1d are substituted by alkoxy chains only at the [Formula: see text] positions (1,4,8,11,15,18,22,25). On the other hand, the PcCu derivatives 4a–4d are substituted by alkoxy chains at the [Formula: see text] positions and chlorine atoms at the [Formula: see text] positions (2,3,9,10,16,17,23,24). We have investigated the influence of chlorine atoms substituted at the [Formula: see text] positions of the Pc ring on mesomorphism, spectroscopic and electronic properties for these two series of PcCu derivatives 1 and 4 by using a polarizing optical microscope, DSC, temperature-variable small angle X-ray diffractometer, a UV-Vis spectrophotometer and cyclic voltammetry. Each of the derivatives 1a–1d is crystalline without showing mesomorphism. On the other hand, each of the chlorine-substituted PcCu derivatives 4a–4d shows plural phase transitions, and the longer chain-substituted PcCu derivatives 4c–4d show a rectangular ordered columnar [Col[Formula: see text](P2m)] mesophase. Furthermore, we have revealed that each of the PcCu derivatives 4a–4d shows a Q-band in the near-infrared region and a lower HOMO energy level than conventional phthalocyanine derivatives.


2010 ◽  
Vol 122 (3) ◽  
pp. 539-541 ◽  
Author(s):  
Tetsuro Kusamoto ◽  
Shoko Kume ◽  
Hiroshi Nishihara

2012 ◽  
Vol 3 (12) ◽  
pp. 3276 ◽  
Author(s):  
Jonggi Kim ◽  
Myoung Hee Yun ◽  
Gi-Hwan Kim ◽  
Jin Young Kim ◽  
Changduk Yang

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