Abstract
The synthesis and characterization of the first rigid fused porphyrin-phthalocyanine hetero-dyad with two different metals is reported; was based on porphyrin’s dienophile features in Diels–Alder reactions. This synthetic procedure represents a new approach for the synthesis of extended systems based on tetrapyrrolic macrocycles.
Keywords: Bimetallic systems, Diels-Alder reactions, Extended heterocyclic systems, Porphyrins, Phthalocyanines.
Current Organic Chemistry
Title:Synthesis of a Rigid Fused Porphyrin-Phthalocyanine Hetero-Dyad with Two Different Metals
Volume: 17 Issue: 10
Author(s): Mario J.F. Calvete, Joao P.C. Tome and Jose A.S. Cavaleiro
Affiliation:
Keywords: Bimetallic systems, Diels-Alder reactions, Extended heterocyclic systems, Porphyrins, Phthalocyanines.
Abstract: The synthesis and characterization of the first rigid fused porphyrin-phthalocyanine hetero-dyad with two different metals is reported; was based on porphyrin’s dienophile features in Diels–Alder reactions. This synthetic procedure represents a new approach for the synthesis of extended systems based on tetrapyrrolic macrocycles.
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Cite this article as:
Calvete Mario J.F., Tome Joao P.C. and Cavaleiro Jose A.S., Synthesis of a Rigid Fused Porphyrin-Phthalocyanine Hetero-Dyad with Two Different Metals, Current Organic Chemistry 2013; 17 (10) . https://dx.doi.org/10.2174/1385272811317100010
DOI https://dx.doi.org/10.2174/1385272811317100010 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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