X-ray Photoelectron Spectroscopy Sulfur 2p Study of Organic Thiol and Disulfide Binding Interactions with Gold Surfaces

Langmuir ◽  
1996 ◽  
Vol 12 (21) ◽  
pp. 5083-5086 ◽  
Author(s):  
David G. Castner ◽  
Kenneth Hinds ◽  
David W. Grainger
2017 ◽  
Vol 13 ◽  
pp. 648-658 ◽  
Author(s):  
Loïc Pantaine ◽  
Vincent Humblot ◽  
Vincent Coeffard ◽  
Anne Vallée

Aniline-terminated self-assembled monolayers (SAMs) on gold surfaces have successfully reacted with ArSO2NHOSO2Ar (Ar = 4-MeC6H4 or 4-FC6H4) resulting in monolayers with sulfamide moieties and different end groups. Moreover, the sulfamide groups on the SAMs can be hydrolyzed showing the partial regeneration of the aniline surface. SAMs were characterized by water contact angle (WCA) measurements, Fourier-transform infrared reflection absorption spectroscopy (IRRAS) and X-ray photoelectron spectroscopy (XPS).


2018 ◽  
Vol 96 (10) ◽  
pp. 929-933 ◽  
Author(s):  
Gabrielle C. Hoover ◽  
Jennifer Ham ◽  
Connie Tang ◽  
Elisa I. Carrera ◽  
Dwight S. Seferos

An asymmetric thiol-modified tellurophene was designed and synthesized, and the ability of the compound to form a monolayer on a gold electrode was confirmed. The surface-active tellurophene was synthesized using Cadiot–Chodkiewicz coupling followed by ring closing and thiol modification. The tellurophene compound forms a monolayer on gold surfaces from a concentrated solution within 24 h. The ability of the compound to conjugate to gold is confirmed by X-ray photoelectron spectroscopy (XPS). A surface blocking experiment was used to evaluate the extent of formation of a monolayer on a gold electrode.


1998 ◽  
pp. 1727-1728 ◽  
Author(s):  
Caroline Chavigny ◽  
Franck Le Bideau ◽  
Claire-Marie Pradier ◽  
Gérard Jaouen ◽  
Claire-Marie Pradier ◽  
...  

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