Chapter 9: Fused (Hetero)Cyclic Polymers Synthesized by Alkyne-Based Polymerizations

Research output: Chapter in Book/Conference Proceeding/ReportBook Chapterpeer-review

Abstract

Fused (hetero)cyclic polymers are an important group of functional materials with unique electrochemical and photophysical properties. They are in great demand in high-tech applications such as organic electronics and advanced optical devices. Alkyne-based polymerizations have been found to be a powerful tool for the synthesis of fused (hetero)cyclic polymers. The fused (hetero)cyclic units can form in situ in the polymer backbones during the polymerizations. In this chapter, the progress in the synthesis of fused (hetero)cyclic polymers by alkyne-based polymerizations will be summarized, including the homopolymerizations of acetylenic monomers, stoichiometric polyannulations of internal diynes and aromatics, non-stoichiometric polyannulations of internal diynes and monofunctional aromatics, and multicomponent acetylenic polymerizations. Meanwhile, the properties and functionalities of the produced fused (hetero)cyclic polymers, such as thermal and morphological stability, light refraction and chromatic dispersion, photoluminescent properties, fluorescent chemosensor, external stimuli-responsive materials, etc., will also be discussed.

Original languageEnglish
Title of host publicationSynthetic Polymer Chemistry
Subtitle of host publicationInnovations and Outlook
EditorsZheng Zhao, Rong Hu, Anjun Qin, Ben Zhong Tang
PublisherRoyal Society of Chemistry
Pages264-306
Number of pages43
Edition32
ISBN (Electronic)9781788015233
DOIs
Publication statusPublished - 2020

Publication series

NameRSC Polymer Chemistry Series
Number32
Volume2020-January
ISSN (Print)2044-0790
ISSN (Electronic)2044-0804

Bibliographical note

Publisher Copyright:
© 2020 The Royal Society of Chemistry.

Fingerprint

Dive into the research topics of 'Chapter 9: Fused (Hetero)Cyclic Polymers Synthesized by Alkyne-Based Polymerizations'. Together they form a unique fingerprint.

Cite this