Australian Nuclear Science and Technology Organisation (ANSTO), Locked Bag 2001, Kirrawee DC NSW 2232, Australia.
Langmuir. 2011 Sep 6;27(17):10753-62. doi: 10.1021/la202359c. Epub 2011 Aug 4.
We have examined the nanoscale adsorption of molecular water under ambient conditions onto a series of well-characterized functionalized surfaces produced by Cu(I)-catalyzed alkyne-azide cycloaddition (CuAAC or "click") reactions on alkyne-terminated self-assembled monolayers on silicon. Water contact angle (CA) measurements reveal a range of macroscopic hydrophilicity that does not correlate with the tendency of these surfaces to adsorb water at the molecular level. X-ray reflectometry has been used to follow the kinetics of water adsorption on these "click"-functionalized surfaces, and also shows that dense continuous molecular water layers are formed over 30 h. For example, a highly hydrophilic surface, functionalized by an oligo(ethylene glycol) moiety (with a CA = 34°) showed 2.9 Å of adsorbed water after 30 h, while the almost hydrophobic underlying alkyne-terminated monolayer (CA = 84°) showed 5.6 Å of adsorbed water over the same period. While this study highlights the capacity of X-ray reflectometry to study the structure of adsorbed water on these surfaces, it should also serve as a warning for those intending to characterize self-assembled monolayers and functionalized surfaces to avoid contamination by even trace amounts of water vapor. Moreover, contact angle measurements alone cannot be relied upon to predict the likely degree of moisture uptake on such surfaces.
我们研究了在环境条件下,分子水在一系列经过炔基-叠氮点击化学反应(CuAAC 或“点击”)修饰的硅基炔基终止自组装单层上的功能化表面的纳米尺度吸附。水接触角(CA)测量揭示了宏观亲水性的范围,但与这些表面在分子水平上吸附水的趋势没有相关性。X 射线反射法已被用于跟踪这些“点击”功能化表面上水的吸附动力学,也表明在 30 小时内形成了密集的连续分子水层。例如,一个高度亲水的表面,通过一个聚(乙二醇)部分(CA = 34°)功能化,在 30 小时后显示出 2.9 Å 的吸附水,而几乎疏水的底层炔基终止单层(CA = 84°)在同一时期显示出 5.6 Å 的吸附水。虽然这项研究强调了 X 射线反射法研究这些表面上吸附水结构的能力,但它也应该对那些打算对自组装单层和功能化表面进行特性化的人起到警示作用,以避免甚至痕量水蒸气的污染。此外,仅凭接触角测量不能预测此类表面吸收水分的可能程度。