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A Porphyrin with Two Coordination Sites: The Biquinoline Ligand as a New Potential External Chelate

✍ Scribed by Christophe Jeandon; Romain Ruppert


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
190 KB
Volume
2011
Category
Article
ISSN
1434-193X

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✦ Synopsis


A highly symmetrical doubly fused porphyrin was obtained after two successive intramolecular cyclizations. [1] The first supplementary ring was closed by using the Cadogan reaction, involving the generation of an intermediate nitrene from the starting nitro function. By trying to use the same methodology for the second ring closure, we found that the Cadogan reaction could be used but that cyclization yields remained low. We showed, by taking into account unusual

[a] UMR