Issue 0, 1974
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Preparation of a conjugated tautomer of 1,14:7,8-diethenotetrapyrido-[2,1,6-de:2′,1′,6′-gh:2″,1″,6″-kl:2‴,1‴,6‴na][1,3,5,8,10,12]hexa-azacyclotetradecine and its metal derivatives

Shojiro Ogawa,   Tomonobu Yamaguchi  and  (the late)Nobuyuki Gotoh  

Abstract

A hexa-aza-macrocyclic compound of high thermal stability is readily obtained from 2,9-diamino-1,10-phenanthroline by its thermolysis or by its condensation with 2,9-dihalogeno-1,10-phenanthroline. The structure of this macrocycle has been established as a conjugated system of a novel type, related to some extent to porphin and phthalocyanin. The macrocyclic compound forms copper, cobalt, and nickel complexes.

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Article information

DOI
https://doi.org/10.1039/P19740000976
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 976-978

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Preparation of a conjugated tautomer of 1,14:7,8-diethenotetrapyrido-[2,1,6-de:2′,1′,6′-gh:2″,1″,6″-kl:2‴,1‴,6‴na][1,3,5,8,10,12]hexa-azacyclotetradecine and its metal derivatives

S. Ogawa, T. Yamaguchi and N. Gotoh, J. Chem. Soc., Perkin Trans. 1, 1974, 976 DOI: 10.1039/P19740000976

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