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On the Impact of Linear Siloxanated Side Chains on the Molecular Self‐Assembling and Charge Transport Properties of Conjugated Polymers
Author(s) -
Kamatham Narayanaswamy,
Ibraikulov Olzhas A.,
Durand Pablo,
Wang Jing,
Boyron Olivier,
Heinrich Benoît,
Heiser Thomas,
Lévêque Patrick,
Leclerc Nicolas,
Méry Stéphane
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202007734
Subject(s) - polymer , side chain , siloxane , materials science , conjugated system , alkyl , stacking , polymer chemistry , comonomer , chain (unit) , thiophene , crystallography , copolymer , chemistry , organic chemistry , composite material , physics , astronomy
Herein reported is the impact of the functionalization of four different semiconducting polymer structures by a linear siloxane‐terminated side‐chains. The latter is tetrasiloxane (Si 4 ) or trisiloxane (Si 3 ) chains, substituted at their extremity to a pentylene linker. The polymer structure is based on 5,6‐difluorobenzothiadiazole comonomer (PF2), a diketopyrrolopyrrole unit (PDPP‐TT), a naphtalediimide unit (PNDI‐T 2 ), and a poly[bis(thiophen‐2‐yl)thieno[3,2,b]thiophene (PBTTT). The properties of these siloxane‐functionalized polymers are scrutinized and compared with the ones of their alkyl‐substituted polymer analogues. The impact of the alkyl‐to‐siloxane chain substitution clearly depends on the molecular section of the side chains. When a branched 2‐octyldodecyl chain (C 20 ) is replaced by a Si 4 chain of same molecular section, the greatest impact is the strong increase of the π‐stacking overlap of the polymer backbones. This effect leads to a significative enhancement of the charge mobility values of the polymers. As in‐plane and out‐of‐plane mobility are increased simultaneously, this π‐overlap enhancement effect happens to be preponderant over the polymer orientation variations. When a linear tetradecyl chain (C 14 ) is replaced by a linear Si 3 chain of twice larger molecular section, the polymer structure is profoundly affected. While PBTTT‐C 14 is crystalline and purely edge‐on, PBTTT‐Si 3 is mesomorphic and shows a mixed face‐on/edge‐on orientation.