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Dive into the research topics where Armin Burgath is active.

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Featured researches published by Armin Burgath.


Macromolecular Chemistry and Physics | 2000

Multi-arm star block copolymers based on ɛ-caprolactone with hyperbranched polyglycerol core

Armin Burgath; Alexander Sunder; Ingo T. Neuner; Rolf Mülhaupt; Holger Frey

Multi-arm star block copolymers based on e-caprolactone have been prepared by a core-first approach using propoxylated hyperbranched polyglycerol P(G52PO3) as a polyfunctional initiator. Various monomer/initiator ratios were employed in the Sn-catalyzed polymerization in order to vary the length of the caprolactone arms (DPn(arm) = 10 to 50). The molecular weights of the block copolymers were in good aggreement with the calculated values. Careful NMR analysis revealed that the monomer/initiator ratio not only controls the arm length, but also influences the degree of functionalization. Poly(e-CL) stars with 52 arms and absolute molecular weights between 69 200 and 360 400 g/mol have been prepared. SEC measurements showed that the narrow polydispersity of the core molecule (Mw/Mn = 1.24) could be maintained upon block copolymerization. The resulting star polymers exhibited polydispersities between 1.21 and 1.33.


Chemistry: A European Journal | 1999

A Novel Phenol for Use in Convergent and Divergent Dendrimer Synthesis: Access to Core Functionalisable Trifurcate Carbosilane Dendrimers—The X-ray Crystal Structure of [1,3,5-Tris{4-(triallylsilyl)phenylester}benzene]

Robert A. Gossage; Elena Muñoz-Martínez; Holger Frey; Armin Burgath; Martin Lutz; Anthony L. Spek; Gerard van Koten

A new organosilane, 4-(triallylsilyl)phenol, was prepared in high yield and utilised in the divergent and convergent synthesis of dendrimeric molecules. Novel bifurcate carbosilane dendrimers 1 were prepared by divergent synthesis up to the second generation. This phenol was also used for the convergent synthesis of the dendron [1,3,5-tris{4-(triallylsilyl)phenylester}benzene] (2). The X-ray structure of 2 revealed that the three terminal aromatic rings are almost perpendicular to the central phenyl ring.


Macromolecular Chemistry and Physics | 2000

Role of cyclization in the synthesis of hyperbranched aliphatic polyesters

Armin Burgath; Alexander Sunder; Holger Frey


Macromolecules | 2001

Synthesis of Hyperbranched Aromatic Homo- and Copolyesters via the Slow Monomer Addition Method

Andreas Möck; Armin Burgath; Ralf Hanselmann; Holger Frey


Archive | 2004

Low shrinking polymerizable dental material

Joachim E. Klee; Uwe Walz; Dirk Holter; Armin Burgath; Holger Erey; Rolf Mülhaupt


Archive | 2002

Verfahren zur Herstellung von dentalen Formteilen A process for the production of dental shaped parts

Norbert Moszner; Armin Burgath; Rolf Muelhaupt; Ulrich Salz; Volker Rheinberger; Ruediger Landers


Archive | 2001

Thermo Chromer dental material

Peter Burtscher; Armin Burgath; Ulrich Salz; Volker Rheinberger


Archive | 2001

Desktop-Verfahren zur Herstellung von Dentalprodukten unter Verwendung des 3D-Plottings Desktop process for the preparation of dental products using the 3D-dimensional plotting

Armin Burgath; Rüdiger Landers; Norbert Moszner; Rolf Mülhaupt; Volker Rheinberger; Ulrich Salz


Archive | 2001

Thermochromer Dentalwerkstoff Thermo Chromer dental material

Peter Burtscher; Armin Burgath; Ulrich Salz; Volker Rheinberger


Archive | 2001

Desktop process for the preparation of dental products using the 3D-dimensional plotting

Armin Burgath; Rüdiger Landers; Norbert Moszner; Rolf Mülhaupt; Volker Rheinberger; Ulrich Salz

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