Ambipolar Transport in Organic Conjugated Materials

2007 ◽  
Vol 19 (14) ◽  
pp. 1791-1799 ◽  
Author(s):  
J. Cornil ◽  
J.-L. Brédas ◽  
J. Zaumseil ◽  
H. Sirringhaus
2020 ◽  
Vol 44 (12) ◽  
pp. 4681-4693 ◽  
Author(s):  
Maryam F. Abdollahi ◽  
Yuming Zhao

This review highlights the recent studies of advanced organic π-conjugated materials that contain 1,4-dithiafulvene (DTF) as a redox-active component.


2000 ◽  
Vol 62 (10) ◽  
pp. 6296-6300 ◽  
Author(s):  
M. Muccini ◽  
M. Schneider ◽  
C. Taliani ◽  
M. Sokolowski ◽  
E. Umbach ◽  
...  

Synlett ◽  
2018 ◽  
Vol 29 (08) ◽  
pp. 993-998 ◽  
Author(s):  
Lei Fang ◽  
Alexander Kalin ◽  
Jongbok Lee

Conjugated ladder-type oligomers are a class of important functional organic materials. They possess intriguing properties stemming from their fully fused aromatic backbones. The construction of the ladder-type backbone relies on a ‘ladderization’ step, which may be accomplished through either kinetically or thermodynamically controlled annulation reactions. The attributes of these reactions are discussed, with relevant recent examples. The development of these reactions is key to continued advances and innovation in the field of organic conjugated materials.1 Introduction2 Kinetic Annulations3 Thermodynamic Annulations4 Future Outlooks and Conclusion


2014 ◽  
Vol 47 (4) ◽  
pp. 1155-1164 ◽  
Author(s):  
Tammie Nelson ◽  
Sebastian Fernandez-Alberti ◽  
Adrian E. Roitberg ◽  
Sergei Tretiak

2021 ◽  
pp. 1521-1532
Author(s):  
Qiang Fu ◽  
Zhiyuan Xu ◽  
Xingchen Tang ◽  
Tingting Liu ◽  
Xiyue Dong ◽  
...  

Polymers ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 75
Author(s):  
Yiqi Fan ◽  
Jinjin Zhang ◽  
Zhouyi Hong ◽  
Huayu Qiu ◽  
Yang Li ◽  
...  

Conjugated polymers generally contain conjugated backbone structures with benzene, heterocycle, double bond, or triple bond, so that they have properties similar to semiconductors and even conductors. Their energy band gap is very small and can be adjusted via chemical doping, allowing for excellent photoelectric properties. To obtain prominent conjugated materials, numerous well-designed polymer backbones have been reported, such as polyphenylenevinylene, polyphenylene acetylene, polycarbazole, and polyfluorene. 4,4′-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY)-based conjugated polymers have also been prepared owing to its conjugated structure and intriguing optical properties, including high absorption coefficients, excellent thermal/photochemical stability, and high quantum yield. Most importantly, the properties of BODIPYs can be easily tuned by chemical modification on the dipyrromethene core, which endows the conjugated polymers with multiple functionalities. In this paper, BODIPY-based conjugated polymers are reviewed, focusing on their structures and applications. The forms of BODIPY-based conjugated polymers include linear, coiled, and porous structures, and their structure–property relationship is explored. Also, typical applications in optoelectronic materials, sensors, gas/energy storage, biotherapy, and bioimaging are presented and discussed in detail. Finally, the review provides an insight into the challenges in the development of BODIPY-based conjugated polymers.


Sign in / Sign up

Export Citation Format

Share Document