Structural Dynamics of Neighboring Water Molecules of N-Isopropylacrylamide Pentamer

Kenee Kaiser S Custodio; Gil C Claudio; Ricky B Nellas

doi:10.1021/acsomega.9b02898

Structural Dynamics of Neighboring Water Molecules of N-Isopropylacrylamide Pentamer

ACS Omega. 2020 Jan 10;5(3):1408-1413. doi: 10.1021/acsomega.9b02898. eCollection 2020 Jan 28.

Authors

Kenee Kaiser S Custodio¹, Gil C Claudio¹, Ricky B Nellas¹

Affiliation

¹ Institute of Chemistry, University of the Philippines Diliman, Quezon City 1101, Philippines.

Abstract

Poly(N-isopropylacrylamide) (PNIPAM) is a popular polymer widely used in smart hydrogel synthesis due to its thermo-responsive behavior in aqueous medium. Aqueous PNIPAM hydrogels can reversibly swell and collapse below and above their lower critical solution temperature (LCST), respectively. The present work used molecular dynamics simulations to explore the behavior of water molecules surrounding the side chains of a NIPAM pentamer in response to temperature changes (273-353 K range) near its experimental LCST (305 K). Results suggest a strong inverse correlation of temperature with water density and hydrophobic hydration character of the first coordination shell around the isopropyl groups. Integrity of the first and second coordination shells is further characterized by polygon ring analysis. Predominant occurrence of pentagons suggests clathrate-like behavior of both shells at lower temperatures. This predominance is eventually overtaken by 4-membered rings as temperature is increased beyond 303 and 293 K for the first and second coordination shells, respectively, losing their clathrate-like property. It is surmised that this temperature-dependent stability of the coordination shells is one of the important factors that controls the reversible swell-collapse mechanism of PNIPAM hydrogels.