Collins K D, Washabaugh M W
Q Rev Biophys. 1985 Nov;18(4):323-422. doi: 10.1017/s0033583500005369.
Starting from known properties of non-specific salt effects on the surface tension at an air-water interface, we propose the first general, detailed qualitative molecular mechanism for the origins of ion-specific (Hofmeister) effects on the surface potential difference at an air-water interface; this mechanism suggests a simple model for the behaviour of water at all interfaces (including water-solute interfaces), regardless of whether the non-aqueous component is neutral or charged, polar or non-polar. Specifically, water near an isolated interface is conceptually divided into three layers, each layer being I water-molecule thick. We propose that the solute determines the behaviour of the adjacent first interfacial water layer (I1); that the bulk solution determines the behaviour of the third interfacial water layer (I3), and that both I1 and I3 compete for hydrogen-bonding interactions with the intervening water layer (I2), which can be thought of as a transition layer. The model requires that a polar kosmotrope (polar water-structure maker) interact with I1 more strongly than would bulk water in its place; that a chaotrope (water-structure breaker) interact with I1 somewhat less strongly than would bulk water in its place; and that a non-polar kosmotrope (non-polar water-structure maker) interact with I1 much less strongly than would bulk water in its place. We introduce two simple new postulates to describe the behaviour of I1 water molecules in aqueous solution. The first, the 'relative competition' postulate, states that an I1 water molecule, in maximizing its free energy (--delta G), will favour those of its highly directional polar (hydrogen-bonding) interactions with its immediate neighbours for which the maximum pairwise enthalpy of interaction (--delta H) is greatest; that is, it will favour the strongest interactions. We describe such behaviour as 'compliant', since an I1 water molecule will continually adjust its position to maximize these strong interactions. Its behaviour towards its remaining immediate neighbours, with whom it interacts relatively weakly (but still favourably), we describe as 'recalcitrant', since it will be unable to adjust its position to maximize simultaneously these interactions.(ABSTRACT TRUNCATED AT 400 WORDS)
从非特异性盐对气-水界面表面张力影响的已知性质出发,我们提出了首个关于离子特异性(霍夫迈斯特)对气-水界面表面电势差影响起源的通用、详细的定性分子机制;该机制为所有界面(包括水-溶质界面)的水行为提出了一个简单模型,无论非水成分是中性还是带电、极性还是非极性。具体而言,孤立界面附近的水在概念上被分为三层,每层厚度为一个水分子。我们提出溶质决定相邻的第一界面水层(I1)的行为;本体溶液决定第三界面水层(I3)的行为,并且I1和I3都竞争与中间水层(I2)的氢键相互作用,I2可被视为过渡层。该模型要求极性促溶剂(极性水结构形成剂)与I1的相互作用比其在本体水中时更强;离液剂(水结构破坏剂)与I1的相互作用比其在本体水中时稍弱;非极性促溶剂(非极性水结构形成剂)与I1的相互作用比其在本体水中时弱得多。我们引入两个简单的新假设来描述I1水分子在水溶液中的行为。第一个假设是“相对竞争”假设,即I1水分子在最大化其自由能(-ΔG)时,会倾向于与紧邻邻居的那些具有最大成对相互作用焓(-ΔH)的高度定向极性(氢键)相互作用;也就是说,它会倾向于最强的相互作用。我们将这种行为描述为“顺应性的”,因为I1水分子会不断调整其位置以最大化这些强相互作用。它对其余紧邻邻居的行为,即与其相互作用相对较弱(但仍有利)的邻居,我们描述为“固执的”,因为它无法调整其位置以同时最大化这些相互作用。(摘要截选至400字)