Benign approaches for the synthesis of bis-imine Schiff bases

Article

van den Ancker, Tania R., Cave, Gareth W. V. and Ralston, Colin L.. 2006. "Benign approaches for the synthesis of bis-imine Schiff bases." Green Chemistry. 8 (1), pp. 50-53. https://doi.org/10.1039/B513289d
Article Title

Benign approaches for the synthesis of bis-imine Schiff bases

ERA Journal ID34334
Article CategoryArticle
Authorsvan den Ancker, Tania R. (Author), Cave, Gareth W. V. (Author) and Ralston, Colin L. (Author)
Journal TitleGreen Chemistry
Journal Citation8 (1), pp. 50-53
Number of Pages4
Year2006
PublisherThe Royal Society of Chemistry
Place of PublicationCambridge, United Kingdom
ISSN1463-9262
1463-9270
Digital Object Identifier (DOI)https://doi.org/10.1039/B513289d
Web Address (URL)http://pubs.rsc.org/en/content/articlepdf/2006/gc/b513289d
Abstract

Pure bis-imine Schiff bases are readily accessible in high yield, typically >95%, when aliphatic diamine/aldehyde condensation reactions are carried out under solvent-free
conditions or in poly(propyleneglycol) (PPG) as a recyclable reaction medium, with negligible waste.

KeywordsSchiff bases; organic synthesis; metal ion; complexation; azomethine; aldimines
ANZSRC Field of Research 2020349999. Other chemical sciences not elsewhere classified
320501. Medical biochemistry - amino acids and metabolites
340504. Organic green chemistry
340503. Organic chemical synthesis
Byline AffiliationsDepartment of Biological and Physical Sciences
Nottingham Trent University, United Kingdom
University of Western Australia
Institution of OriginUniversity of Southern Queensland
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