Triptycene-terminated thiolate and selenolate monolayers on Au(111)

Beilstein J Nanotechnol. 2017 Apr 20:8:892-905. doi: 10.3762/bjnano.8.91. eCollection 2017.

Abstract

To study the implications of highly space-demanding organic moieties on the properties of self-assembled monolayers (SAMs), triptycyl thiolates and selenolates with and without methylene spacers on Au(111) surfaces were comprehensively studied using ultra-high vacuum infrared reflection absorption spectroscopy, X-ray photoelectron spectroscopy, near-edge X-ray absorption fine structure spectroscopy and thermal desorption spectroscopy. Due to packing effects, the molecules in all monolayers are substantially tilted. In the presence of a methylene spacer the tilt is slightly less pronounced. The selenolate monolayers exhibit smaller defect densities and therefore are more densely packed than their thiolate analogues. The Se-Au binding energy in the investigated SAMs was found to be higher than the S-Au binding energy.

Keywords: organic thin films; selenolates; self-assembled monolayers; thiolates; triptycene.