Journal
JOURNAL OF MOLECULAR GRAPHICS & MODELLING
Volume 90, Issue -, Pages 51-58Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jmgm.2019.04.004
Keywords
Stimuli-responsive polymer; Thermoresponsive polymer; poly(N-vinylcaprolactam); PVCL; Lower critical solution temperature; LCST; Molecular dynamics simulation
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Funding
- Ministry of Education and Science of Ukraine [0119U002536]
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Thermoresponsive poly(N-vinylcaprolactam) (PVCL) has received growing interest due to a temperaturei-nduced phase transition, which switches its solubility in aqueous solutions. However, the lower critical solution temperature (LCST) of PVCL is greatly influenced by the molecular weight, morphology and the environment. Therefore, despite of numerous experimental studies of the thermal response of PVCL, a driving force and a molecular origin of conformation transitions in solution remain far less studied. To get a better understanding of the coil-to-globule conformation transition of PVCL in aqueous solution, we examined the structure and conformation dynamics of a single-chain PVCL30 in a temperature range of 280-360 K by using atomistic molecular dynamics (MD) simulations. The united-atom GROMOS G53a6 force field was re-parameterized and fine-tuned by DFT calculations to reproduce the experimental LCST transition of PVCL. Our MD model reproduces the LCST transition of PVCL30 to occur within a temperature range of 34.6-38.5 degrees. MD simulation results suggest a significant difference between the hydration state of the carbonyl group of PVCL below and above the LCST threshold. The analysis of the number of hydrogen bonds of PVCL with water molecules demonstrates that dehydration of the polymer plays an important role and drives the temperature-induced polymer collapse. Finally, the developed MD model and FF parameters were successfully tested for large-scale systems, such as mixture PVCL30 oligomer and single-chain PVCL816 polymer, respectively. (C) 2019 Elsevier Inc. All rights reserved.
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