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Langmuir, 29, 12176–12182: Single-Chain Mechanics of Poly(N,N-diethylacrylamide) and Poly(N-isopropylacrylamide): Comparative Study Reveals the Effect of Hydrogen Bond Donors
來源:崔樹勛教授個人網(wǎng)站 發(fā)布日期:2015-04-01
作者:Xiangchao Pang, Shuxun Cui*
關(guān)鍵字:Poly(N,N-diethylacrylamide), Poly(N-isopropylacrylamide)
論文來源:期刊
具體來源:Langmuir, 29, 12176–12182.
發(fā)表時間:2013年

The single-chain mechanics of two similar thermosensitive polymers, poly(N,N-diethyl-acrylamide) (PDEAM) and poly(N-isopropyl-acrylamide) (PNIPAM), have been studied by atomic force microscopy-based single-molecule force spectroscopy (SMFS). In a typical nonpolar organic solvent, octane, both the two polymers show the same inherent elasticity, although they have different substitutional groups. However, the mechanics of the two polymers present large differences in water. The energies needed for the changes of the bound water during elongation at room temperature are estimated by the SMFS method at the single-chain level, which is ~1.13 ± 0.10 and ~5.19 ± 0.10 kJ/mol for PDEAM and PNIPAM, respectively. In addition, PNIPAM shows a temperature-dependent single-chain mechanics when the temperature is increased across the lower critical solution temperature (LCST), while PDEAM does not. These differences observed in aqueous solution originate from the different structures of the two polymers. With a hydrogen bond donor in the amide group, PNIPAM will be more hydrated when T < LCST. When T > LCST, PNIPAM will have a larger change in both conformation and hydration. These findings also suggest that PNIPAM is a good candidate for thermo-driven single-molecule motor, while PDEAM is not.

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