Influence of synthetic pathway, molecular weight and side chains on properties of indacenodithiophene-benzothiadiazole copolymers made by direct arylation polycondensation
Artikel i vetenskaplig tidskrift, 2021

Atom-economic protocols for the synthesis of poly(indacenodithiophene-alt-benzothiadiazole) (PIDTBT) are presented in which all C-C coupling steps are achieved by direct arylation. Using two different synthetic pathways, PIDTBT copolymers with different side chains (hexylphenyl, octylphenyl, dodecyl, methyl/2-octyldodecylphenyl, 2-octyldodecylphenyl/2-octyldodecylphenyl) and molecular weight (MW) are prepared. Route A makes use of direct arylation polycondensation (DAP) of indacenodithiophene (IDT) and 4,7-dibromo-2,1,3-benzothiadiazole (BTBr2) leading to PIDTBT in high yields, with adjustable MW and without indications for structural defects. Route B starts from a polyketone precursor also prepared by DAP following cyclization. While route B allows introduction of asymmetric side chains at the IDT unit, polymer analogous cyclization gives rise to defect formation. The absorption coefficient of PIDTBT with alkylphenyl side chains made by route A increases with MW. Field-effect hole mobilities around similar to 10(-2) cm(2) V-1 s(-1) are molecular weight-independent, which is ascribed to a largely amorphous thin film morphology. PIDTBT with linear dodecyl side (C12) chains exhibits a bathochromic shift (20 nm), in agreement with theory, and more pronounced vibronic contributions to absorption spectra. In comparison to alkylphenyl side chains, C12 side chains allow for increased order in thin films, a weak melting endotherm and lower energetic disorder, which altogether explain substantially higher field-effect hole mobilities of similar to 10(-1) cm(2) V-1 s(-1).

Författare

Desiree Adamczak

Technische Universität Chemnitz

Andrea Perinot

Istituto Italiano di Tecnologia

Hartmut Komber

Leibniz-Institut fur Polymerforschung

Anna Illy

Technische Universität Chemnitz

Sandra Hultmark

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Christian Müller Group

Bianca Passarella

Istituto Italiano di Tecnologia

Politecnico di Milano

Wen Liang Tan

Monash University

Sebastian Hutsch

Technische Universität Dresden

Technische Universität München

David Becker-Koch

Technische Universität Dresden

Charlotte Rapley

Imperial College London

Alberto D. Scaccabarozzi

Istituto Italiano di Tecnologia

Martin Heeney

Imperial College London

Yana Vaynzof

Technische Universität Dresden

Frank Ortmann

Technische Universität München

Technische Universität Dresden

Christopher R. McNeill

Monash University

Christian Müller

Chalmers, Kemi och kemiteknik, Tillämpad kemi, Christian Müller Group

Mario Caironi

Istituto Italiano di Tecnologia

Michael Sommer

Technische Universität Chemnitz

Journal of Materials Chemistry C

2050-7534 (ISSN)

Vol. In Press

Ämneskategorier

Polymerkemi

Teoretisk kemi

Organisk kemi

DOI

10.1039/d1tc00043h

Mer information

Senast uppdaterat

2021-04-08