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Closing and coupling: metal linked biliazine dimers

delete2026-05-08
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PRE
AI
J
Jeaydi, Towhidi Illius
C
Chen, Wei-Yuan
T
Tedesco, Michael D.
B
Briana R. Schrage
V
Victor N. Nemykin
Z
Ziegler, Christopher J. *
DOI:10.1039/d6ra01668edelete
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Abstract

Abstract

En 中文
Biliazines, tetradentate chelates similar to the bilin class of heme metabolites, are ring open phthalocyanine analogs where the chelate ring is closed by a hydrogen bond. Linked dimers of biliazines, incorporating both pyrazole and indazole units, can be produced via a self-assembly reaction between the diiminoisoindoline-pyrazole and indazole chelate precursors and zinc ion in a 4 : 3 ratio. The dimers are comprised of zinc metalated biliazines linked by a third tetrahedral zinc metal ion. The closure of the ring with zinc ion does not induce the formation of an aromatic ring current in either the pyrazole or indazole-based dimers.
Keywords:
ISOINDOLINE
PHTHALOCYANINES
ANALOG

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RSC Advances cover
RSC Advances
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4.6
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University System of Ohio
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