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Felix Hugo Beijer
Researcher at DSM
Publications - 23
Citations - 3627
Felix Hugo Beijer is an academic researcher from DSM. The author has contributed to research in topics: Hydrogen bond & Supramolecular polymers. The author has an hindex of 10, co-authored 23 publications receiving 3390 citations. Previous affiliations of Felix Hugo Beijer include Eindhoven University of Technology & Millennium Pharmaceuticals.
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Journal ArticleDOI
Reversible Polymers Formed from Self-Complementary Monomers Using Quadruple Hydrogen Bonding
Rint P. Sijbesma,Felix Hugo Beijer,Felix Hugo Beijer,Luc Brunsveld,Luc Brunsveld,B. J. B. Folmer,B. J. B. Folmer,J. H. K. Ky Hirschberg,J. H. K. Ky Hirschberg,Ronald Frans Maria Lange,Ronald Frans Maria Lange,Jimmy K. L. Lowe,Jimmy K. L. Lowe,E. W. Meijer,E. W. Meijer +14 more
TL;DR: 2-ureido-4-pyrimidone that dimerize strongly in a self-complementary array of four cooperative hydrogen bonds were used as the associating end group in reversible self-assembling polymer systems.
Journal ArticleDOI
Strong dimerization of ureidopyrimidones via quadruple hydrogen bonding
TL;DR: In this paper, a donor-donor-acceptor−acceptor −acceptor (DDAA) array of hydrogen bonding sites in the 4[1H]-pyrimidinone tautomer was used to preorganize the molecules for dimerization.
Journal ArticleDOI
Self-Complementarity Achieved through Quadruple Hydrogen Bonding
TL;DR: In this paper, a donor-acceptor-donoracceptor array of four hydrogen-bonding sites is used to pre-organize the molecule for dimerization. But the structure of the compound is unknown.
Journal ArticleDOI
Supramolecular polymers from linear telechelic siloxanes with quadruple- hydrogen- bonded units
J.H.K.K. Hirschberg,Felix Hugo Beijer,H.A.M. van Aert,Pieter C. M. M. Magusin,Rint P. Sijbesma,E. W. Meijer +5 more
TL;DR: In this paper, two ureidopyrimidone (UPy) functional groups are associated via quadruple hydrogen bonds in a donor-donor-acceptor−acceptor −acceptor (DDAA) array.
Journal ArticleDOI
Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities.
Felix Hugo Beijer,Rint P. Sijbesma,Jef A. J. M. Vekemans,E. W. Meijer,Huub Kooijman,Anthony L. Spek +5 more
TL;DR: Repulsive secondary electrostatic interactions between the cis-amide and uracil carbonyl groups are thought to be responsible for the low association constant of complexes of bis(acylamino)triazines with uracils.