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Issue 22, 1989
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Synthesis of a cyclic porphyrin trimer with a semi-rigid cavity

Abstract

A cyclic trinuclear porphyrin host has been synthesised; its binding properties show that it has a spacious cavity which prefers an open conformation but which can close around small bidentate ligands such as 4,4′-bipyridyl.

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Article type: Paper
DOI: 10.1039/C39890001714
Citation: J. Chem. Soc., Chem. Commun., 1989,0, 1714-1715
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    Synthesis of a cyclic porphyrin trimer with a semi-rigid cavity

    H. L. Anderson and J. K. M. Sanders, J. Chem. Soc., Chem. Commun., 1989, 0, 1714
    DOI: 10.1039/C39890001714

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