Kankate Laxman, Turchanin Andrey, Gölzhäuser Armin
Physics of Supramolecular Systems, University of Bielefeld, 33615 Bielefeld, Germany.
Langmuir. 2009 Sep 15;25(18):10435-8. doi: 10.1021/la902168u.
When thiol self-assembled monolayers (SAMs) form on gold surfaces, it is widely believed that, upon adsorption, the thiol molecules dissociate via S-H bond scission. This mechanism is hard to verify since hydrogen is difficult to detect during this process. Hence, other reaction schemes such as nondissociative thiol adsorption have also been proposed. Here we present experimental evidence that clearly shows that hydrogen is released during dissociative thiol adsorption and interacts with the monolayer terminus. Vacuum vapor deposition was used to form SAMs of 4-nitrophenylthiol, 4'-nitro-1,1'-biphenyl-4-thiol, and bis-(4,4'-nitrophenyl)-disulfide on gold surfaces. X-ray photoelectron spectroscopy shows that the nitro groups of the thiol SAMs are partly reduced to amino groups, while those of the disulfide SAMs are not. The reduction is attributed to hydrogen released in the dissociation of S-H bonds during thiol adsorption. Possible pathways for the interaction of hydrogen with the nitro groups are discussed.
当硫醇自组装单分子层(SAMs)在金表面形成时,人们普遍认为,在吸附过程中,硫醇分子通过S-H键断裂而解离。由于在此过程中氢难以检测,这种机制很难得到验证。因此,也有人提出了其他反应方案,如非解离性硫醇吸附。在此,我们提供了实验证据,清楚地表明在解离性硫醇吸附过程中会释放氢,并且氢会与单分子层末端相互作用。采用真空气相沉积法在金表面形成4-硝基苯硫醇、4'-硝基-1,1'-联苯-4-硫醇和双(4,4'-硝基苯基)二硫化物的SAMs。X射线光电子能谱表明,硫醇SAMs的硝基部分还原为氨基,而二硫化物SAMs的硝基则没有。这种还原归因于硫醇吸附过程中S-H键解离所释放的氢。文中还讨论了氢与硝基相互作用的可能途径。