TY - JOUR
T1 - Light induced step-growth polymerization of Donor-Acceptor-Donor (DAD) type monomers based on thiophene – [1,2,5] Chalcogenazolo[3,4-f]-benzo [1,2,3] triazole – Thiophene
AU - Kaya, Kerem
AU - Alkan, Ecem Aydan
AU - Yasa, Mustafa
AU - Süerkan, Ali
AU - Udum, Yasemin Arslan
AU - Toppare, Levent
AU - Yagci, Yusuf
N1 - Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/12/5
Y1 - 2021/12/5
N2 - Two new donor-acceptor-donor(DAD) polymers type near-infrared (NIR) absorbing polymers containining thiophene as the donor and [1,2,5] chalcogenazolo [ 3,4-f]-benzo [1,2,3] triazole (chalcoen = S (P1a) or Se (P1b)) derivatives as the acceptor unit were designed and synthesized via light induced step-growth polymerization. The effect of different acceptor groups on the electrochemical and optical properties of the polymers was investigated. Highest occupied molecular orbital (HOMO) energy levels of the resultant black colored soluble polymers were calculated via cyclic voltammetry (CV) as −5.17 and −5.09 eV for P1a and P1b, respectively. Optical electronic band gaps were calculated as 0.81 and 0.74 eV for P1a and P1b, respectively. Lowest unoccupied molecular orbital (LUMO) energy levels were determined as −4.37 and −4.35 eV for P1a and P1b, respectively. NMR and gel-permeation chromatography (GPC) results supported the formation of high-molecular weight species. Synthesized polymers have promising features for application in various optoelectronic devices.
AB - Two new donor-acceptor-donor(DAD) polymers type near-infrared (NIR) absorbing polymers containining thiophene as the donor and [1,2,5] chalcogenazolo [ 3,4-f]-benzo [1,2,3] triazole (chalcoen = S (P1a) or Se (P1b)) derivatives as the acceptor unit were designed and synthesized via light induced step-growth polymerization. The effect of different acceptor groups on the electrochemical and optical properties of the polymers was investigated. Highest occupied molecular orbital (HOMO) energy levels of the resultant black colored soluble polymers were calculated via cyclic voltammetry (CV) as −5.17 and −5.09 eV for P1a and P1b, respectively. Optical electronic band gaps were calculated as 0.81 and 0.74 eV for P1a and P1b, respectively. Lowest unoccupied molecular orbital (LUMO) energy levels were determined as −4.37 and −4.35 eV for P1a and P1b, respectively. NMR and gel-permeation chromatography (GPC) results supported the formation of high-molecular weight species. Synthesized polymers have promising features for application in various optoelectronic devices.
KW - Conjugated polymers
KW - Donor-acceptor-donor polymers
KW - Light induced polymerization
KW - Step-growth polymerization
UR - http://www.scopus.com/inward/record.url?scp=85117812854&partnerID=8YFLogxK
U2 - 10.1016/j.eurpolymj.2021.110831
DO - 10.1016/j.eurpolymj.2021.110831
M3 - Article
AN - SCOPUS:85117812854
SN - 0014-3057
VL - 161
JO - European Polymer Journal
JF - European Polymer Journal
M1 - 110831
ER -