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Shedding Light on Structure–Property Relationships for Conjugated Microporous Polymers: The Importance of Rings and Strain
Author(s) -
Martijn A. Zwijnenburg,
Ge Cheng,
Tom O. McDonald,
Kim E. Jelfs,
JiaXing Jiang,
Shijie Ren,
Tom Hasell,
Frédéric Blanc,
Andrew I. Cooper,
Dave J. Adams
Publication year - 2013
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/ma401311s
Subject(s) - pyrene , conjugated system , chromophore , microporous material , polymer , conjugated microporous polymer , dendrimer , chemical physics , amorphous solid , materials science , density functional theory , absorption (acoustics) , fluorescence , chemistry , computational chemistry , photochemistry , polymer chemistry , crystallography , organic chemistry , optics , physics , composite material
The photophysical properties of insoluble porous pyrene networks, which are central to their function, differ strongly from those of analogous soluble linear and branched polymers and dendrimers. This can be rationalized by the presence of strained closed rings in the networks. A combined experimental and computational approach was used to obtain atomic scale insight into the structure of amorphous conjugated microporous polymers. The optical absorption and fluorescence spectra of a series of pyrene-based materials were compared with theoretical time-dependent density functional theory predictions for model clusters. Comparison of computation and experiment sheds light on the probable structural chromophores in the various materials.

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