首页> 外文OA文献 >Lattice Imaging of Self-Assembled Monolayers of Partially Fluorinated Disulfides and Thiols on Sputtered Gold by Atomic Force Microscopy
【2h】

Lattice Imaging of Self-Assembled Monolayers of Partially Fluorinated Disulfides and Thiols on Sputtered Gold by Atomic Force Microscopy

机译:原子力显微镜在溅射金上自组装的部分氟化二硫和硫醇单分子层的晶格成像

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The structure of self-assembled monolayers (SAMs) of various fluorinated disulfides, perfluoroalkylamide thiols, and a mixed alkyl perfluoroalkylamide disulfide on sputtered gold was studied by atomic force microscopy (AFM). AFM, performed both in air and in ethanol, revealed the monolayer structure with molecular resolution on the polycrystalline gold substrates. For all partially fluorinated disulfides containing ester groups, a hexagonal lattice with a lattice constant of 5.8-5.9 Å was found. A mixed alkyl perfluoroalkylamide disulfide formed a hexagonal lattice of a slightly larger lattice constant (6.1 Å), whereas the lattice observed for fluorinated thiols containing an amide group was either hexagonal (5.7-5.8 Å) or distorted hexatic (5.6, 6.2, 5.6 Å), depending on the length of the perfluoroalkane segment and the imaging force. The observed deviation from hexagonal symmetry is attributed to the distorting effect of hydrogen bonding between neighboring amide groups within the monolayer. For short perfluoroalkane segments the distortion is observed at low imaging forces, whereas for long perfluoroalkane segments significantly higher imaging forces are necessary in order to observe the distortion. The force dependence of the measured lattice symmetries for different chain lengths suggests that the AFM tip penetrates into the SAM and probes at least partially the interior of the SAM.
机译:通过原子力显微镜(AFM)研究了各种氟化二硫化物,全氟烷基酰胺硫醇和混合的烷基全氟烷基酰胺二硫化​​物在溅射金上的自组装单层结构。在空气和乙醇中进行的AFM揭示了在多晶金基底上具有分子分辨率的单层结构。对于所有含酯基的部分氟化的二硫化物,发现其晶格常数为5.8-5.9的六边形晶格。混合的烷基全氟烷基酰胺二硫化​​物形成了一个稍大的晶格常数(6.1Å)的六边形晶格,而观察到的含酰胺基团的氟化硫醇的晶格是六边形(5.7-5.8Å)或扭曲的六价酸(5.6,6.2,5.6Å) ),取决于全氟烷烃链段的长度和成像力。所观察到的偏离六边形对称性的原因归因于单层内相邻酰胺基之间氢键的扭曲作用。对于短的全氟烷烃链段,在低成像力下会观察到畸变,而对于较长的全氟烷烃链段,则需要较高的显像力才能观察到畸变。对于不同的链长,测得的晶格对称性与力的相关性表明,AFM尖端会穿透SAM,并至少部分探测SAM内部。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号