1] EaStCHEM School of Chemistry, University of Edinburgh, King's Buildings, West Mains Road, Edinburgh EH9 3JJ, UK [2].
Nat Chem. 2013 Dec;5(12):1006-10. doi: 10.1038/nchem.1779. Epub 2013 Oct 20.
The emergent properties that arise from self-assembly and molecular recognition phenomena are a direct consequence of non-covalent interactions. Gas-phase measurements and computational methods point to the dominance of dispersion forces in molecular association, but solvent effects complicate the unambiguous quantification of these forces in solution. Here, we have used synthetic molecular balances to measure interactions between apolar alkyl chains in 31 organic, fluorous and aqueous solvent environments. The experimental interaction energies are an order of magnitude smaller than estimates of dispersion forces between alkyl chains that have been derived from vaporization enthalpies and dispersion-corrected calculations. Instead, it was found that cohesive solvent-solvent interactions are the major driving force behind apolar association in solution. The results suggest that theoretical models that implicate important roles for dispersion forces in molecular recognition events should be interpreted with caution in solvent-accessible systems.
自组装和分子识别现象产生的涌现特性是 非共价相互作用的直接结果。气相测量和计算方法表明,在分子缔合中,色散力占主导地位,但溶剂效应对这些力在溶液中的明确量化变得复杂。在这里,我们使用合成分子天平测量了 31 种有机、全氟和水溶剂环境中非极性烷基链之间的相互作用。实验相互作用能比从汽化焓和色散校正计算得出的烷基链之间的色散力估计值小一个数量级。相反,发现溶剂-溶剂的内聚相互作用是溶液中非极性缔合的主要驱动力。结果表明,在可及溶剂系统中,暗示色散力在分子识别事件中起重要作用的理论模型应谨慎解释。