Prof.dr. H. Zuilhof

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Wageningen Universiteit & Researchcentrum (198)

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Biosynthesis of an amphiphilic silk-like polymer (2008)

Auteurs: Werten, M.W.T.; Moers, A.P.H.A.; Vong, T.H.; Zuilhof, H.; Hest, van J.C.M.; Wolf, de F.A.
In: Biomacromolecules, 9(7), 1705 - 1711. ISSN 1525-7797.

Samenvatting:
An amphiphilic silk-like protein polymer was efficiently produced in the yeast Pichia pastoris. The secreted product was fully intact and was purified by solubilization in formic acid and subsequent precipitation of denatured host proteins upon dilution with water. In aqueous alkaline solution, the
One-Step Photochemical Attachment of NHS-Terminated Monolayers onto Silicon Surfaces and Subsequent Functionalization (2008)

Auteurs: Yang, M.; Teeuwen, R.L.M.; Giesbers, M.; Baggerman, J.; Arafat, A.; Wolf, de F.A.; Hest, van J.C.M.; Zuilhof, H.
In: Langmuir, 24(15), 7931 - 7938. ISSN 0743-7463.

Samenvatting:
N-Hydroxysuccinimide (NHS)-ester-terminated monolayers were covalently attached in one step onto silicon using visible light. This mild photochemical attachment, starting from ¿-NHS-functionalized 1-alkenes, yields a clean and flat monolayer-modified silicon surface and allows a mild and rapid funct

Auteurs:	Werten, M.W.T.; Moers, A.P.H.A.; Vong, T.H.; Zuilhof, H.; Hest, van J.C.M.; Wolf, de F.A.
In:	Biomacromolecules, 9(7), 1705 - 1711. ISSN 1525-7797.

Auteurs:	Yang, M.; Teeuwen, R.L.M.; Giesbers, M.; Baggerman, J.; Arafat, A.; Wolf, de F.A.; Hest, van J.C.M.; Zuilhof, H.
In:	Langmuir, 24(15), 7931 - 7938. ISSN 0743-7463.

Complexation of Phenols and Thiophenol by Phosphine Oxides and Phosphates. Extraction, Isothermal Titration Calorimetry, and ab Initio Calculations (2008)

Auteurs:	Cuypers, R.; Burghoff, B.; Marcelis, A.T.M.; Sudhölter, E.J.R.; Haan, de A.B.; Zuilhof, H.
In:	The Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment, & General Theory, 112(46), 11714 - 11723. ISSN 1089-5639.

Samenvatting:

To develop a new solvent-impregnated resin system for the removal of phenols from water the complex formation of triisobutylphosphine sulfide (TIBPS), tributylphosphate (TBP), and tri-n-octylphosphine oxide (TOPO) with a series of phenols (phenol, thiophenol, 3-chlorophenol, 3,5-dichlorophenol, 4-cy

Alkyl-Functionalized Oxide-Free Silicon Nanoparticles: Synthesis and Optical Properties (2008)

Auteurs: Rosso-Vasic, M.; Spruijt, E.; Lagen, van B.; Cola, de L.; Zuilhof, H.
In: Small, 4(10), 1835 - 1841. ISSN 1613-6810.

Samenvatting:
Highly monodisperse silicon nanoparticles (1.57 ± 0.21 nm) are synthesized with a covalently attached alkyl monolayer on a gram scale. Infrared spectroscopy shows that these silicon nanoparticles contain only a few oxygen atoms per nanoparticle. XPS spectra clearly show the presence of unoxidized Si
Divergent synthesis and optoelectronic properties of oligodiacetylene building blocks (2008)

Auteurs: Pilzak, G.S.; Lagen, van B.; Sudhölter, E.J.R.; Zuilhof, H.
In: Tetrahedron Letters, 49(33), 4949 - 4952. ISSN 0040-4039.

Samenvatting:
A new and divergent synthetic route to oligodiacetylene (ODA) building blocks has been developed via Sonogashira reactions under a reductive atmosphere. These central building blocks provide a new way for rapid preparation of long ODAs. In addition, we report on their optoelectronic properties which
Formation of organic monolayers onto SixN4 and SiC surfaces for food and biosensor applications (2008)

Auteurs: Rosso, M.; Schroën, C.G.P.H.; Zuilhof, H.; Boom, R.M.
Formation of organic monolayers onto SixN4 and SiC surfaces for food and biosensor applications (2008)Open access

Auteurs: Rosso, M.; Schroën, C.G.P.H.; Zuilhof, H.; Boom, R.M.

Auteurs:	Rosso-Vasic, M.; Spruijt, E.; Lagen, van B.; Cola, de L.; Zuilhof, H.
In:	Small, 4(10), 1835 - 1841. ISSN 1613-6810.

Auteurs:	Pilzak, G.S.; Lagen, van B.; Sudhölter, E.J.R.; Zuilhof, H.
In:	Tetrahedron Letters, 49(33), 4949 - 4952. ISSN 0040-4039.

Auteurs:	Rosso, M.; Schroën, C.G.P.H.; Zuilhof, H.; Boom, R.M.

Auteurs:	Rosso, M.; Schroën, C.G.P.H.; Zuilhof, H.; Boom, R.M.

GM3, GM2 and GM1 mimics designed for biosensing: chemoenzymatic synthesis, target affinities and 900 MHz NMR analysis (2008)

Auteurs:	Pukin, A.V.; Weijers, C.A.G.M.; Lagen, van B.; Wechselberger, R.; Sun, B.; Gilbert, M.; Karwaski, M.F.; Florack, D.E.A.; Jacobs, B.C.; Tio-Gillen, A.P.; Belkum, van A.; Endtz, H.P.; Visser, G.M.; Zuilhof, H.
In:	Carbohydrate Research, 343(4), 636 - 650. ISSN 0008-6215.

Samenvatting:

Undec-10-enyl, undec-10-ynyl and 11-azidoundecyl glycoside analogues corresponding to the oligosaccharides of human gangliosides GM3, GM2 and GM1 were synthesized in high yields using glycosyltransferases from Campylobacter jejuni. Due to poor water solubility of the substrates, the reactions were c

Ureidobenzotriazine Multiple H-Bonding Arrays: The Importance of Geometrical Details on the Stability of H-Bonds (2008)

Auteurs: Ligthart, G.B.W.L.; Guo, D.; Spek, A.L.; Kooijman, H.; Zuilhof, H.; Sijbesma, R.P.
In: Journal of Organic Chemistry, 73(1), 111 - 117. ISSN 0022-3263.

Samenvatting:
A 3-ureidobenzo-1,2,4-triazine 1-N-oxide (1) was synthesized successfully. The derivative displays an acceptor-donor-acceptor-acceptor (ADAA) hydrogen-bonding motif in CDCl3 and DMSO-d6 solution as well as in the solid state. Although moderately strong association of 1 was observed with DAD motifs,

Auteurs:	Ligthart, G.B.W.L.; Guo, D.; Spek, A.L.; Kooijman, H.; Zuilhof, H.; Sijbesma, R.P.
In:	Journal of Organic Chemistry, 73(1), 111 - 117. ISSN 0022-3263.

Femtosecond Time-Resolved Photophysics of 1,4,5,8-Napthalene Diimides (2007)

Auteurs:	Ganesan, P.; Baggerman, J.; Zhang, H.; Sudhölter, E.J.R.; Zuilhof, H.
In:	The Journal of Physical Chemistry Part A: Molecules, Spectroscopy, Kinetics, Environment, & General Theory, 111, 6151 - 6156. ISSN 1089-5639.

Samenvatting:

The photophysical properties of a tetrahedral molecule with naphthalene diimide (NDI) moieties and of two model compounds were investigated. The absorption and fluorescence spectra of dialkyl-substituted NDI are in agreement with literature. While the absorption spectra of phenyl-substituted molecul

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