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Sulfamide chemistry applied to the functionalization of self-assembled monolayers on gold surfaces.
Pantaine, Loïc; Humblot, Vincent; Coeffard, Vincent; Vallée, Anne.
Afiliação
  • Pantaine L; Institut Lavoisier de Versailles, UMR 8180, Université Paris-Saclay, Université de Versailles Saint-Quentin, 45 avenue des Etats-Unis, 78035 Versailles Cedex, France.
  • Humblot V; Sorbonne Universités, UPMC Univ. Paris 06, Laboratoire de Réactivité de Surface, UMR CNRS 7197, 4 place Jussieu, 75005 Paris, France.
  • Coeffard V; Université de Nantes, CNRS, CEISAM, UMR 6230, Faculté des Sciences et des Techniques, rue de la Houssinière, BP 92208, 44322 Nantes Cedex 3, France.
  • Vallée A; Institut Lavoisier de Versailles, UMR 8180, Université Paris-Saclay, Université de Versailles Saint-Quentin, 45 avenue des Etats-Unis, 78035 Versailles Cedex, France.
Beilstein J Org Chem ; 13: 648-658, 2017.
Article em En | MEDLINE | ID: mdl-28487759
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).
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article