scispace - formally typeset
H

Hans G. Börner

Researcher at Humboldt University of Berlin

Publications -  195
Citations -  8897

Hans G. Börner is an academic researcher from Humboldt University of Berlin. The author has contributed to research in topics: Polymer & Polymerization. The author has an hindex of 47, co-authored 195 publications receiving 8435 citations. Previous affiliations of Hans G. Börner include University of North Carolina at Chapel Hill & Max Planck Society.

Papers
More filters
Journal ArticleDOI

Quantum states of neutrons in the Earth's gravitational field

TL;DR: In this article, it was shown that the falling neutrons do not move continuously along the vertical direction, but rather jump from one height to another, as predicted by quantum theory, and the particles are allowed to fall towards a horizontal mirror which, together with the Earth's gravitational field, provides the necessary confining potential well.
Journal ArticleDOI

Modern trends in polymer bioconjugates design

TL;DR: This review describes recent changes and progress in the field of polymer bioconjugation, i.e. covalent attachment of synthetic polymers to biological entities such as nucleic acids, oligopeptides, proteins, enzymes, carbohydrates, viruses or cells.
Journal ArticleDOI

Synthesis of Molecular Brushes with Block Copolymer Side Chains Using Atom Transfer Radical Polymerization

TL;DR: In this article, the molecular weights of the resulting polymers were characterized by gel permeation chromatography (GPC) using refractive index and multiangle light scattering detection, confirming the synthesis of well-defined copolymer brushes.
Journal ArticleDOI

Combining Atom Transfer Radical Polymerization and Click Chemistry: A Versatile Method for the Preparation of End-Functional Polymers

TL;DR: In this paper, the bromine chain ends of polystyrene were successfully transformed into various functional end groups (ω-hydroxy, ω-carboxyl and ω -methyl-vinyl) by a two-step pathway: (1) substitution of the brome terminal atom by an azide function and (2) 1,3-dipolar cycloaddition of the terminal azide and functional alkynes (propargyl alcohol, propiolic acid and 2-methyl-1-buten-3-yne).