Author:
Biesen Lukas,Hartmann Yannic,Müller Thomas J. J.
Abstract
AbstractAlkynylated aroyl-S,N-ketene acetals are readily synthesized in mostly excellent yields by a Sonogashira reaction resulting in a substance library of more than 20 examples. Upon expansion of the reaction sequence by deprotection and concatenating of the copper-click reaction in a one-pot fashion, a library of 11 triazole-ligated aroyl-S,N-ketene acetals is readily accessible. All derivatives show pronounced solid-state emission and aggregation-induced emission properties depending on the nature of the alkynyl or the triazole substituents.
Funder
Deutsche Forschungsgemeinschaft
Fonds der Chemischen Industrie
Heinrich-Heine-Universität Düsseldorf
Publisher
Springer Science and Business Media LLC
Cited by
2 articles.
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