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231224s2015 xx |||||o 00| ||eng c |
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|a 10.1021/acs.langmuir.5b00177
|2 doi
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|a DE-627
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|a eng
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|a Fontanesi, Claudio
|e verfasserin
|4 aut
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|a New one-step thiol functionalization procedure for Ni by self-assembled monolayers
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|c 2015
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
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|a Date Completed 14.05.2015
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|a Date Revised 24.03.2015
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|a published: Print-Electronic
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|a Citation Status PubMed-not-MEDLINE
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|a This article reports on a facile and fast strategy for the self-assembled monolayer (SAM) functionalization of nickel surfaces, employing cyclic voltammetry (CV) cycling of a suitable tailored solution containing the species to be adsorbed. Results are presented for ultrathin films formed on Ni by 1-hexadecanethiol (C16), L-cysteine (L-cys), and the poly{methyl (2R)-3-(2,2'-bithiophen-4-ylsulfanyl)-2-[(tert-butoxycarbonyl)amino]propanoate} (PCT-L) thiophene-based chiral polymer. The effective formation of high-quality ultrathin organic films on the nickel was verified both electrochemically and by exploiting typical surface characterization techniques such as contact angle, ellipsometry, atomic force microscopy (AFM), polarization modulation-infrared reflection-absorption spectroscopy (PM-IRRAS), and X-ray photoelectron spectroscopy (XPS)
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|a Journal Article
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|a Tassinari, Francesco
|e verfasserin
|4 aut
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|a Parenti, Francesca
|e verfasserin
|4 aut
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|a Cohen, Hagai
|e verfasserin
|4 aut
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|a Mondal, Prakash Chandra
|e verfasserin
|4 aut
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|a Kiran, Vankayala
|e verfasserin
|4 aut
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|a Giglia, Angelo
|e verfasserin
|4 aut
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|a Pasquali, Luca
|e verfasserin
|4 aut
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|a Naaman, Ron
|e verfasserin
|4 aut
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|i Enthalten in
|t Langmuir : the ACS journal of surfaces and colloids
|d 1992
|g 31(2015), 11 vom: 24. März, Seite 3546-52
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|x 1520-5827
|7 nnns
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|g volume:31
|g year:2015
|g number:11
|g day:24
|g month:03
|g pages:3546-52
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|u http://dx.doi.org/10.1021/acs.langmuir.5b00177
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