Ederth T., Tamada K., Claesson P. M., Valiokas R., Colorado R., Graupe M., Shmakova O. E., Lee T. R.
Department of Chemistry, Surface Chemistry, Royal Institute of Technology, Stockholm, SE-100 44, Sweden
J Colloid Interface Sci. 2001 Mar 15;235(2):391-397. doi: 10.1006/jcis.2000.7318.
Long-range interactions between self-assembled monolayers (SAMs) of semifluorinated alkanethiols have been studied by direct force measurements in water and aqueous NaCl solutions. SAMs prepared from three different thiols, with identical fluorinated head groups but varying hydrocarbon spacer lengths, were investigated: CF(3)(CF(2))(9)(CH(2))(x)SH, where x=2, 11, or 17. Force measurements show that the interactions in water and electrolyte solutions are composed of both double-layer interactions emerging from what appears to be charges adsorbed onto the surfaces and long-range "hydrophobic" attractions, in excess of the expected van der Waals forces. The three investigated thiols produce similar results in force measurements, though the contact angles with water are slightly different. The "hydrophobic" attraction has the form of step-like attractive discontinuities in the force profiles at separations ranging from 20 to 40 nm, caused by bridging of microscopic bubbles residing at the surfaces. The shape or range of these discontinuities are not significantly affected by replacement of the water with either 1 mM or 1 M NaCl solutions. The origin of the charges causing the electrostatic double-layer interaction is unclear, but some possible causes are discussed. Copyright 2001 Academic Press.
通过在水和NaCl水溶液中进行直接力测量,研究了半氟化链烷硫醇自组装单分子层(SAMs)之间的长程相互作用。研究了由三种不同硫醇制备的SAMs,它们具有相同的氟化头基,但碳氢间隔长度不同:CF(3)(CF(2))(9)(CH(2))(x)SH,其中x = 2、11或17。力测量表明,水和电解质溶液中的相互作用由似乎吸附在表面的电荷产生的双层相互作用以及超出预期范德华力的长程“疏水”吸引力组成。尽管与水的接触角略有不同,但所研究的三种硫醇在力测量中产生了相似的结果。“疏水”吸引力在20至40 nm的分离距离处表现为在力曲线中呈阶梯状的吸引性不连续,这是由驻留在表面的微观气泡的桥接引起的。用1 mM或1 M NaCl溶液代替水不会显著影响这些不连续的形状或范围。导致静电双层相互作用的电荷来源尚不清楚,但讨论了一些可能的原因。版权所有2001年学术出版社。