Self-assembled monolayers (SAMs) of alkanethiols on gold are a commonly used platform for nanotechnology owing to their ease of preparation and high surface coverage. Unfortunately, the gold-sulfur bond is oxidized at ambient conditions which alters the stability and structure of the monolayer. We show using scanning tunneling microscopy and X-ray photoelectron spectroscopy that decanethiolate molecules oxidize into decanesulfonates that organize into a hitherto unknown striped phase. Air-exposed SAMs oxidize, as can be determined by a shift of the S 2p peak and the appearance of O 1s photoelectrons as part of the decanethiol monolayer transforms into a lamellae-like decanesulfonate structure when exposed to air. The herringbone structure of the Au(111) surface is preserved, indicating that the interaction between the molecules and the surface is rather weak as these findings are substantiated by density functional theory calculations.
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http://dx.doi.org/10.1021/acs.jpcc.8b01389 | DOI Listing |
Nanoscale
January 2021
Mathematics, Mechanics, and Materials Unit (MMMU), Okinawa Institute of Science and Technology Graduate University (OIST), 1919-1 Tancha, Onna-son, Kunigami-gun, Okinawa 904-0495, Japan.
Polymer-nanodiamond composites are excellent candidates for the fabrication of multifunctional hybrid materials. They integrate polymer flexibility and exceptional properties of nanodiamonds (NDs), such as biocompatibility, mechanical strength, color centers, and chemically-tailored surfaces. However, their development is hindered by the challenge of ensuring that NDs are homogeneously distributed in the composites.
View Article and Find Full Text PDFJ Phys Chem C Nanomater Interfaces
April 2018
Physics of Interfaces and Nanomaterials, and Molecular Nanofabrication, MESA+ Institute for Nanotechnology, University of Twente, P. O. Box 217, 7500AE Enschede, The Netherlands.
Self-assembled monolayers (SAMs) of alkanethiols on gold are a commonly used platform for nanotechnology owing to their ease of preparation and high surface coverage. Unfortunately, the gold-sulfur bond is oxidized at ambient conditions which alters the stability and structure of the monolayer. We show using scanning tunneling microscopy and X-ray photoelectron spectroscopy that decanethiolate molecules oxidize into decanesulfonates that organize into a hitherto unknown striped phase.
View Article and Find Full Text PDFEnviron Technol
May 2019
a The State Key Laboratory of Chemical Engineering , East China University of Science and Technology, Shanghai , People's Republic of China.
Low-cost activated carbon (KAC) was functionalized by HNO, (NH)SO and air oxidation, respectively, to remove dibenzothiophene (DBT) from model fuel. The changes in physical and chemical properties of these activated carbons were characterized by thermal analysis, elemental analysis, nitrogen adsorption apparatus, Raman spectra, scanning electron microscope and Boehm's titration method. HNO and (NH)SO oxidation result in a significant decrease in pore structure, while air oxidation only causes slight pore reduction due to the re-activation by O.
View Article and Find Full Text PDFJ Bacteriol
September 2011
Department of Chemistry and Biochemistry, Utah State University, 0300 Old Main Hill, Logan, UT 84322, USA.
NADPH:2-ketopropyl-coenzyme M oxidoreductase/carboxylase (2-KPCC), an atypical member of the disulfide oxidoreductase (DSOR) family of enzymes, catalyzes the reductive cleavage and carboxylation of 2-ketopropyl-coenzyme M [2-(2-ketopropylthio)ethanesulfonate; 2-KPC] to form acetoacetate and coenzyme M (CoM) in the bacterial pathway of propylene metabolism. Structural studies of 2-KPCC from Xanthobacter autotrophicus strain Py2 have revealed a distinctive active-site architecture that includes a putative catalytic triad consisting of two histidine residues that are hydrogen bonded to an ordered water molecule proposed to stabilize enolacetone formed from dithiol-mediated 2-KPC thioether bond cleavage. Site-directed mutants of 2-KPCC were constructed to test the tenets of the mechanism proposed from studies of the native enzyme.
View Article and Find Full Text PDFLangmuir
October 2007
School of Materials, Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287, USA.
The movement of a liquid droplet on a flat surface functionalized with a photochromic azobenzene may be driven by the irradiation of spatially distinct areas of the drop with different UV and visible light fluxes to create a gradient in the surface tension. In order to better understand and control this phenomenon, we have measured the wetting characteristics of these surfaces for a variety of liquids after UV and visible light irradiation. The results are used to approximate the components of the azobenzene surface energy under UV and visible light using the van Oss-Chaudhury-Good equation.
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