Synthesis and optical properties of light-emitting polyfluorene derivatives

The emitting-polymers, Polyfluorene (PF) and Poly(fluorene- benzothiadiazole-quinoline) [PF-BT-QL], have been synthesized by the Suzuki coupling reactions. The properties of polymers were characterized using UV-Vis spectroscopy, GPC, DSC, TGA, Photoluminescence (PL), Fluoresence (FL), Electrolumines...

Full description

Saved in:
Bibliographic Details
Main Authors: Philaiwan Aiamsen, David L. Carroll, Sukon Phanichphant
Format: Journal
Published: 2018
Subjects:
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79957599394&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/49829
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-49829
record_format dspace
spelling th-cmuir.6653943832-498292018-09-04T04:30:20Z Synthesis and optical properties of light-emitting polyfluorene derivatives Philaiwan Aiamsen David L. Carroll Sukon Phanichphant Chemistry Materials Science Physics and Astronomy The emitting-polymers, Polyfluorene (PF) and Poly(fluorene- benzothiadiazole-quinoline) [PF-BT-QL], have been synthesized by the Suzuki coupling reactions. The properties of polymers were characterized using UV-Vis spectroscopy, GPC, DSC, TGA, Photoluminescence (PL), Fluoresence (FL), Electroluminescence (EL) spectroscopy. The synthetic polymers were soluble in common organic solvents and easily spin-coated onto the indium-tin oxide (ITO)-coated glass substrates. Light-emitting devices (LEDs) with ITO/PEDOT:PSS/polymer/LiF/Al configuration were fabricated, and the devices using copolymers showed red shift EL spectra relative to that of PF. The turns on voltages of copolymers were lower than that of PF. Copyright © Taylor & Francis Group, LLC. 2018-09-04T04:18:46Z 2018-09-04T04:18:46Z 2011-06-01 Journal 15635287 15421406 2-s2.0-79957599394 10.1080/15421406.2011.566065 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79957599394&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/49829
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Chemistry
Materials Science
Physics and Astronomy
spellingShingle Chemistry
Materials Science
Physics and Astronomy
Philaiwan Aiamsen
David L. Carroll
Sukon Phanichphant
Synthesis and optical properties of light-emitting polyfluorene derivatives
description The emitting-polymers, Polyfluorene (PF) and Poly(fluorene- benzothiadiazole-quinoline) [PF-BT-QL], have been synthesized by the Suzuki coupling reactions. The properties of polymers were characterized using UV-Vis spectroscopy, GPC, DSC, TGA, Photoluminescence (PL), Fluoresence (FL), Electroluminescence (EL) spectroscopy. The synthetic polymers were soluble in common organic solvents and easily spin-coated onto the indium-tin oxide (ITO)-coated glass substrates. Light-emitting devices (LEDs) with ITO/PEDOT:PSS/polymer/LiF/Al configuration were fabricated, and the devices using copolymers showed red shift EL spectra relative to that of PF. The turns on voltages of copolymers were lower than that of PF. Copyright © Taylor & Francis Group, LLC.
format Journal
author Philaiwan Aiamsen
David L. Carroll
Sukon Phanichphant
author_facet Philaiwan Aiamsen
David L. Carroll
Sukon Phanichphant
author_sort Philaiwan Aiamsen
title Synthesis and optical properties of light-emitting polyfluorene derivatives
title_short Synthesis and optical properties of light-emitting polyfluorene derivatives
title_full Synthesis and optical properties of light-emitting polyfluorene derivatives
title_fullStr Synthesis and optical properties of light-emitting polyfluorene derivatives
title_full_unstemmed Synthesis and optical properties of light-emitting polyfluorene derivatives
title_sort synthesis and optical properties of light-emitting polyfluorene derivatives
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79957599394&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/49829
_version_ 1681423480469323776