Literature DB >> 21638401

Microwave-assisted one-pot synthesis of hyperbranched epoxide-amine adducts.

Julia Theis1, Helmut Ritter, Joachim E Klee.   

Abstract

Hyperbranched epoxide-amine adducts were synthesized by a one-pot microwave (MW) assisted reaction. 4-(2,3-epoxypropyl-1-oxy)benzonitrile was hydrogenated using Pd/C under microwave conditions, forming the AB(2) monomer 1-aminomethyl-4-(2,3-epoxypropyl-1-oxy)benzene. Depending on the reaction temperature this monomer immediately reacts to give hyperbranched epoxide-amine adducts. Mass spectrometric investigations proved the formation of a homologous series of oligomers containing up to six repeating units. Due to the complexing properties of the poly(amino alcohol) moieties in the presence of Cu(2+) ions, large aggregates were formed.
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2009        PMID: 21638401     DOI: 10.1002/marc.200900157

Source DB:  PubMed          Journal:  Macromol Rapid Commun        ISSN: 1022-1336            Impact factor:   5.734


  2 in total

1.  Formation of epoxide-amine oligo-adducts as OH-functionalized initiators for the ring-opening polymerization of ε-caprolactone.

Authors:  Julia Theis; Helmut Ritter
Journal:  Beilstein J Org Chem       Date:  2010-10-01       Impact factor: 2.883

2.  Polymerization of novel methacrylated anthraquinone dyes.

Authors:  Christian Dollendorf; Susanne Katharina Kreth; Soo Whan Choi; Helmut Ritter
Journal:  Beilstein J Org Chem       Date:  2013-02-28       Impact factor: 2.883

  2 in total

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