David N. Reinhoudt
MESA+ Institute for Nanotechnology
1082 Papers
20.9K Citations
David N. Reinhoudt is an academic researcher from MESA+ Institute for Nanotechnology. The author has contributed to research in topics: Chemistry & Membrane. The author has an hindex of 107, co-authored 1082 publications. Previous affiliations of David N. Reinhoudt include University of Modena and Reggio Emilia & University of Mainz.
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Papers
Self-assembled monolayers of heptapodant ß-cyclodextrins on gold
Marcel W. J. Beulen,Jürgen Bügler,B. H. M. Lammerink,Frank A. J. Geurts,Ed M. E. F. Biemond,Kees van Leerdam,Frank C. J. M. van Veggel,Johan F.J. Engbersen,David N. Reinhoudt +8 more
TL;DR: In this paper, a route was developed for the synthesis of three different cyclodextrin adsorbates: heptakis{6-O-[3-(thiomethyl)propionyl)]-2,3-di-O-methyl}-s======-cyclodextrins, heptonakis{ 6-O]-12-(thiododecyl)dodecanoyl]--2.3-dimethyl]-s======]-s-cyclodescopextrin, and Heptakis[6-deoxy
108
syn-1,2-dialkylated calix[4]arenes : general intermediates in the NaH/DMF tetraalkylation of calix[4]arenes
L. C. Groenen,Bianca H.M. Ruel,Alessandro Casnati,Peter Timmerman,Willem Verboom,Sybolt Harkema,A. Pochini,Rocco Ungaro,David N. Reinhoudt +8 more
TL;DR: In this paper, the tetraalkylation of calix[4]arenes 1a and 1b proceeds via the syn-1,2-disubstituted products to the tri-alkylated calix(4)arenes in the cone conformation.
108
Gradient-driven motion of multivalent ligand molecules along a surface functionalized with multiple receptors
András Perl,Alberto Gomez-Casado,Damien Thompson,Henk H. Dam,Pascal Jonkheijm,David N. Reinhoudt,Jurriaan Huskens +6 more
TL;DR: The study shows that the interfacial behaviour of multivalent systems is much more complex than that of monovalent ones, and identifies multiple surface diffusion mechanisms, which are called walking, hopping and flying.
107
Upper rim calixcrowns : elucidation of the mechanism of conformational interconversion of calix[4]arenes by quantitative 2-D EXSY NMR spectroscopy
TL;DR: In this paper, the mechanism of conformational interconversion of calix[4]arenes (4 and 5) was elucidated by quantitative 2-D EXSY NMR spectroscopy.