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Synthesis 2016; 48(15): 2461-2465
DOI: 10.1055/s-0035-1560447
DOI: 10.1055/s-0035-1560447
paper
Oligomerization Reactions of Bis(ethynyl)tetraphenylporphyrin Derivatives by Glaser–Hay Coupling Reaction: Isolation and Characterization of Dimer, Trimer, and Tetramer
Further Information
Publication History
Received: 27 January 2016
Accepted after revision: 07 March 2016
Publication Date:
28 April 2016 (online)
Abstract
The Glaser–Hay coupling reaction of a tetraphenylporphyrin derivative having two acetylenes in the quasi-trans positions was carried out. Although this oxidative coupling reaction has high reactivity and produces various butadiynylene oligomers, the degree of oligomerization was low. A large substrate and/or product might decrease the frequency factor of the Arrhenius equation and the resultant rate constant. This finding is in agreement with that of the one-pot synthesis of structurally well-defined porphyrin oligomers, such as trimers and tetramers, which are used frequently in the field of advanced materials.
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1561427.
- Supporting Information
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