Effect of the Donor Units on the Properties of Fluorinated Acceptor Based Systems
Loading...

Date
2021
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier Sci Ltd
Open Access Color
Green Open Access
No
OpenAIRE Downloads
OpenAIRE Views
Publicly Funded
No
Abstract
A new series of monomers in the donor-acceptor-donor array, namely 5-fluoro-4,7-di(furan-2-yl)benzo[c][1,2,5] thiadiazole (F2BT-F), and 5-fluoro-4,7-di(selenophen-2-yl)benzo[c][1,2,5] thiadiazole (S2BT-F), bearing 5-fluorobenzo[c][1,2,5]-thiadiazole as the acceptor moiety and furan and selenophene as the electron donating groups was synthesized and polymerized electrochemically. To compare heteroatom effect, thiophene analogue of newly synthesized (FBT)-B-2-F and S2BT-F namely, (5-fluoro-4,7-di(thiophen-2-yl)benzo[c][1,2,5] thiadiazole (T2BT-F)) and its corresponding polymer were also synthesized. Effect of donor units on the electrochemical and optical properties of fluorinated acceptor based systems was investigated in terms of the effect of different sized heteroatoms in five-membered rings on the dihedral angle and planarity. Theoretical calculations also suggested a deviation from planarity upon fluorination. Moreover, electrochemically obtained polymers possess low bandgap values (1.62 eV-1.68 eV for PF2BT-F and PS2BT-F, respectively) and exhibited electrochromic properties with relatively low switching times.
Description
Onal, ahmet muhtar/0000-0003-0644-7180; Çakal, Deniz/0000-0003-1656-2430; Akdag, Akin/0000-0002-0058-905X
Keywords
Electropolymerization, Electrochromism, Dihedral angle, Benzothiadiazole, Furan, Thiophene, Selenophene
Fields of Science
02 engineering and technology, 0210 nano-technology, 01 natural sciences, 0104 chemical sciences
Citation
WoS Q
Q1
Scopus Q
Q2

OpenCitations Citation Count
12
Source
Dyes and Pigments
Volume
185
Issue
Start Page
108955
End Page
PlumX Metrics
Citations
CrossRef : 13
Scopus : 12
Captures
Mendeley Readers : 6
Google Scholar™


