Novel poly(phenylene ethynylene)-type conjugated polymers containing diketopyrrolopyrrole or triphenylpyrazoline units in the main chain: synthesis, characterization and photophysical properties

2009 ◽  
Vol 58 (6) ◽  
pp. 665-673 ◽  
Author(s):  
Guoqiang Zhang ◽  
Kuan Liu ◽  
Yang Li ◽  
Mujie Yang
2012 ◽  
Vol 442 (2) ◽  
pp. 50-56 ◽  
Author(s):  
M. L. Keshtov ◽  
S. I. Pozin ◽  
D. V. Marochkin ◽  
V. P. Perevalov ◽  
P. V. Petrovskii ◽  
...  

2014 ◽  
Vol 2 (35) ◽  
pp. 7336-7347 ◽  
Author(s):  
Chao Zheng ◽  
Zhongfu An ◽  
Yosuke Nakai ◽  
Taiju Tsuboi ◽  
Yang Wang ◽  
...  

The different effects of binaphthyl enantiomers on the photophysical properties of chiral conjugated polymers were observed and analyzed for chiro-optic investigations.


Materials ◽  
2021 ◽  
Vol 14 (5) ◽  
pp. 1098
Author(s):  
Agata Blacha-Grzechnik

For many years, the research on conjugated polymers (CPs) has been mainly focused on their application in organic electronics. Recent works, however, show that due to the unique optical and photophysical properties of CPs, such as high absorption in UV–Vis or even near-infrared (NIR) region and efficient intra-/intermolecular energy transfer, which can be relatively easily optimized, CPs can be considered as an effective light-activated source of versatile and highly reactive singlet oxygen for medical or catalytic use. The aim of this short review is to present the novel possibilities that lie dormant in those exceptional polymers with the extended system of π-conjugated bonds.


2019 ◽  
Vol 17 (10) ◽  
pp. 2635-2639 ◽  
Author(s):  
Yu Chen ◽  
Ying Tan ◽  
Chunyan Tan ◽  
Yunpeng Lu ◽  
Yuzong Chen ◽  
...  

Different polymer chain configurations along the main chains of poly(naphthalimide and phenylene ethynylene)s lead to dramatic differences in polymer conformations and photophysical properties.


2006 ◽  
Vol 78 (10) ◽  
pp. 1803-1822 ◽  
Author(s):  
Wenping Hu ◽  
Hiroshi Nakashima ◽  
Erjing Wang ◽  
Kazuaki Furukawa ◽  
Hongxiang Li ◽  
...  

In this article, we review the possibility of combining conjugated polymers with nanometer-scale devices (nanodevices), in order to introduce the properties associated with conjugated polymers into such nanodevices. This approach envisages combining the highly topical disciplines of polymer electronics and nanoelectronics to engender a new subdirection of polymer nanoelectronics, which can serve as a tool to probe the behavior of polymer molecules at the nanometer/molecular level, and contribute to clarifying transport mechanisms in conjugated polymers. In this study, we exemplify this combination, using a family of linear and conjugated polymers, poly(p-phenylene-ethynylene)s (PPEs) with thiolacetate-functionalized end groups.


1996 ◽  
Vol 29 (15) ◽  
pp. 5083-5090 ◽  
Author(s):  
Liang Ma ◽  
Qiao-Sheng Hu ◽  
Kwon Yon Musick ◽  
Dilrukshi Vitharana ◽  
Chi Wu ◽  
...  

Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 348 ◽  
Author(s):  
Masashi Otaki ◽  
Reiji Kumai ◽  
Hajime Sagayama ◽  
Hiromasa Goto

While only a few studies have investigated the synthesis of main chain-type polyazobenzenes, they continue to draw an increasing amount of attention owing to their industrial applications in holography, dyes, and functional adhesives. In this study, dibromoazobenzene was prepared as a monomer for constructing azo-based π-conjugated polymers. Miyaura–Suzuki cross-coupling polymerization was conducted to develop copolymers containing an azobenzene unit as a photoisomerization block and a pyrimidine-based liquid crystal generator block. The prepared polymers exhibited thermotropic liquid crystallinity and underwent cis and trans photoisomerization upon irradiation with ultraviolet and visible light. Furthermore, the photoisomerization behavior was examined using optical absorption spectroscopy and synchrotron X-ray diffraction spectrometry.


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