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Click Functionalization of Aromatic Polymers for Organic Electronic Device Applications
Author(s) -
Michinobu Tsuyoshi
Publication year - 2015
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201500086
Subject(s) - click chemistry , tetracyanoethylene , cycloaddition , chromophore , polymer , alkyne , materials science , conjugated system , azide , surface modification , photochemistry , polymer chemistry , electron acceptor , chemistry , combinatorial chemistry , organic chemistry , catalysis
The [2 + 2] cycloaddition–retroelectrocyclization between electron‐rich alkynes and tetracyanoethylene (TCNE)/7,7,8,8‐tetracyanoquinodimethane (TCNQ), yielding the tetracyanated donor–acceptor (D–A) chromophores, is a new class of click chemistry reactions, due to the high efficiencies, no byproducts, and applicability to polymer syntheses. As compared to the conventional click reactions represented by the Cu(I)‐catalyzed azide–alkyne cycloaddition (CuAAC), these new click reactions provide fascinating optoelectronic properties originating from the D–A chromophore structures formed. A series of π‐conjugated aromatic polymers containing electron‐rich alkynes were successfully functionalized by these click reactions, producing novel organic or organometallic materials featuring conducting and photovoltaic properties in thin film electronic devices. This review article describes the recent results of the author's research group. The power of click chemistry is highlighted by the polymer synthesis using CuAAC. This is followed by the alkyne–TCNE/TCNQ postfunctionalization to produce high‐performance aromatic polymers for use as active components in organic electronic devices, such as thin film transistors, organic solar cells and polymer memory devices.