Synthesis and characterization of a copolymer involving PVK and MEH-PPV for organic electronic devices

2017 ◽  
Vol 103 ◽  
pp. 142-146 ◽  
Author(s):  
F. Abbassi ◽  
M. Mbarek ◽  
D. Kreher ◽  
K. Alimi
Keyword(s):  
Electronic Devices ◽  
Synthesis And Characterization ◽  
Organic Electronic Devices ◽  
Organic Electronic

Facile synthesis of arylthiophenyl-functionalized diketopyrrolopyrrole derivatives via direct C–H arylation: characterization and utilization in organic electronic devices

2016 ◽  
Vol 40 (1) ◽  
pp. 385-392 ◽  
Author(s):  
Akshaya Kumar Palai ◽  
Amit Kumar ◽  
Kyoseung Sim ◽  
Jaehyuk Kwon ◽  
Tae Joo Shin ◽  
...  
Keyword(s):  
Electronic Devices ◽  
Synthesis And Characterization ◽  
Facile Synthesis ◽  
Organic Electronic Devices ◽  
Organic Electronic ◽  
End Capping

We report the synthesis and characterization of three arylthiophenyl-functionalized diketopyrrolopyrrole derivatives with different end-capping groups via direct C–H arylation.

Synthesis by Stille Cross-Coupling Procedure and Electrochemical Characterization of Branched Polymers Based on Substituted 1,3,5-Triarylbenzenes

2010 ◽  
Vol 663-665 ◽  
pp. 876-879 ◽  
Author(s):  
Krzysztof R. Idzik ◽  
Rainer Beckert ◽  
Eric Tauscher ◽  
Przemyslaw Ledwon ◽  
Sylwia Golba ◽  
...  
Keyword(s):  
Elemental Analysis ◽  
13C Nmr ◽  
Electronic Devices ◽  
Cross Coupling ◽  
Branched Polymers ◽  
Organic Electronic Devices ◽  
Organic Electronic ◽  
Wide Range ◽  
Coupling Procedure

A series of various substituted 1,3,5-triarylbenzenes, 2,4,6-triaryl-1-phenoles, 1,3,5-triaryl-1-methoxybenzenes and 2,4,6-triaryl-1,3,5-trimethoxybenzenes were synthesized by a Stille cross-coupling procedure. Their structures were confirmed by 1H NMR, 13C NMR, and elemental analysis. Containing thienyl, furyl and EDOT groups polymers obtained in the process of electropolymerization could be carefully considered as a building material in a wide range of organic-electronic devices. We compare properties of monomers and related polymers depending on aryls moieties and their influence of hydroxyl and methoxyl groups attached to the central benzene core.

scholarly journals Waiting for Act 2: what lies beyond organic light-emitting diode (OLED) displays for organic electronics?

Nanophotonics ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 31-40
Author(s):  
Stephen R. Forrest
Keyword(s):  
Organic Electronics ◽  
Light Emitting Diode ◽  
Electronic Devices ◽  
Organic Electronic Devices ◽  
Organic Electronic ◽  
Light Emitting ◽  
Organic Light Emitting Diode ◽  
Organic Light ◽  
Semiconductor Thin Films ◽  
Display Technology

AbstractOrganic light-emitting diode (OLED) displays are now poised to be the dominant mobile display technology and are at the heart of the most attractive televisions and electronic tablets on the market today. But this begs the question: what is the next big opportunity that will be addressed by organic electronics? We attempt to answer this question based on the unique attributes of organic electronic devices: their efficient optical absorption and emission properties, their ability to be deposited on ultrathin foldable, moldable and bendable substrates, the diversity of function due to the limitless palette of organic materials and the low environmental impact of the materials and their means of fabrication. With these unique qualities, organic electronics presents opportunities that range from lighting to solar cells to medical sensing. In this paper, we consider the transformative changes to electronic and photonic technologies that might yet be realized using these unconventional, soft semiconductor thin films.

Organic vapor phase deposition for the growth of large area organic electronic devices

2009 ◽  
Vol 95 (23) ◽  
pp. 233305 ◽  
Author(s):  
Richard R. Lunt ◽  
Brian E. Lassiter ◽  
Jay B. Benziger ◽  
Stephen R. Forrest
Keyword(s):  
Vapor Phase ◽  
Electronic Devices ◽  
Large Area ◽  
Organic Electronic Devices ◽  
Organic Electronic ◽  
Organic Vapor ◽  
Vapor Phase Deposition ◽  
Organic Vapor Phase Deposition
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