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Cited by 169

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Controlled Orientation of Cyclodextrin Derivatives Immobilized on Gold Surfaces

Nelles, Gabriele, Weisser, Michael, Back, Roberta, Wohlfart, Peter, Wenz, Gerhard, Mittler-Neher, Silvia·1996·Journal of the American Chemical Society

Abstract

Several different cyclodextrinthiol derivatives have been immobilized on gold surfaces through a chemisorption process to form films which exhibit significantly different features. Three monothiolated cyclodextrin derivatives with different spacers between the cyclodextrin cavity and the thiol group and a mixture of multithiolated cyclodextrins were synthesized and characterized. Chemisorption of these compounds onto gold surfaces gave films which were investigated by Fourier transform infrared (FTIR) spectroscopy, time-of-flight mass spectrometry, contact angle measurements, plasmon surface polariton (PSP) spectroscopy, and cyclic voltammetry. It was found that the chemical structure of each cyclodextrin derivative had a strong influence on the molecular architecture in the resulting films, and in particular on the orientation of the cyclodextrin torus. Models were developed to describe the molecular arrangement in the films.

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Metadata

Authors
Nelles, G., Weisser, M., Back, R., Wohlfart, P., Wenz, G., & Mittler-Neher, S.
Venue
Journal of the American Chemical Society
Published
1996-01-01
Volume
118
Issue
21
Pages
5039-5046
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2052865791
Cited by
169
References
0
FWCI
7.78
Type
journal article
Language
en
Open access
closed

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.