Spectral Insights into Microdynamics of Thermoresponsive Polymers from the Perspective of Two-dimensional Correlation Spectroscopy

Generalized two-dimensional correlation spectroscopy （2DCOS） and its derivate technique, perturbation correlation moving window （PCMW）, have found great potential in studying a series of physico-chemical phenomena in stimuli-responsive polymeric systems. By spreading peaks along a second dimension,...

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Bibliographic Details
Published in:Chinese journal of polymer science 2017-06, Vol.35 (6), p.700-712
Main Authors: Sun, Sheng-tong, Wu, Pei-yi
Format: Article
Language:English
Subjects:
Characterization and Evaluation of Materials
Chemistry
Chemistry and Materials Science
Condensed Matter Physics
Correlation
Feature Article
Group dynamics
Industrial Chemistry/Chemical Engineering
Infrared spectroscopy
Liquid crystal polymers
Liquid crystals
Molecular chains
Near infrared radiation
Perturbation
Phase transitions
Polymer Sciences
Polymers
Power spectra
Raman spectroscopy
Spectral resolution
Spectrum analysis
Transition points
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Summary:Generalized two-dimensional correlation spectroscopy （2DCOS） and its derivate technique, perturbation correlation moving window （PCMW）, have found great potential in studying a series of physico-chemical phenomena in stimuli-responsive polymeric systems. By spreading peaks along a second dimension, 2DCOS can significantly enhance spectral resolution and discern the sequence of group dynamics applicable to various external perturbation-induced spectroscopic changes, especially in infrared （IR）, near-infrared （NIR） and Raman spectroscopy. On the basis of 2DCOS synchronous power spectra changing, PCMW proves to be a powerful tool to monitor complicated spectral variations and to find transition points and ranges. This article reviews the recent work of our research group in the application of 2DCOS and PCMW in thermoresponsive polymers, mainly focused on liquid crystalline polymers and lower critical solution temperature （LCST）-type polymers. Details of group motions and chain conformational changes upon temperature perturbation can thus be elucidated at the molecular level, which contribute to the understanding of their phase transition nature.
ISSN:0256-7679
1439-6203
DOI:10.1007/s10118-017-1938-1