Sakpal Sushil S, Deshmukh Samadhan H, Chatterjee Srijan, Ghosh Deborin, Bagchi Sayan
Physical and Materials Chemistry Division, National Chemical Laboratory (CSIR-NCL), Dr.Homi Bhabha Road, Pune 411008, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
J Phys Chem Lett. 2021 Sep 16;12(36):8784-8789. doi: 10.1021/acs.jpclett.1c02118. Epub 2021 Sep 7.
Disruption of the deep eutectic solvent (DES) nanostructure around the dissolved solute upon addition of water is investigated by polarization-selective two-dimensional infrared spectroscopy and molecular dynamics simulations. The heterogeneous DES nanostructure around the solute is partially retained up to 41 wt % of added water, although water molecules are gradually incorporated in the solute's solvation shell even at lower hydration levels. Beyond 41 wt %, the solute is observed to be preferentially solvated by water. This composition denotes the upper hydration limit of the deep eutectic solvent above which the solute senses an aqueous solvation environment. Interestingly, our results indicate that the transition from a deep eutectic solvation environment to an aqueous one around the dissolved solute can happen at a hydration level lower than that reported for the "water in DES" to "DES in water" transition.
通过偏振选择性二维红外光谱和分子动力学模拟,研究了加水后溶解溶质周围的低共熔溶剂(DES)纳米结构的破坏情况。尽管即使在较低水合水平下,水分子也会逐渐融入溶质的溶剂化壳层,但溶质周围的非均相DES纳米结构在添加高达41 wt%的水时仍会部分保留。超过41 wt%时,观察到溶质优先被水溶剂化。该组成表示低共熔溶剂的最高水合限度,超过此限度溶质会感知到水相溶剂化环境。有趣的是,我们的结果表明,溶解溶质周围从低共熔溶剂化环境到水相环境的转变可能发生在低于报道的“DES中的水”到“水中的DES”转变的水合水平。