Abstract
Amphiphilic meso-aryl-substituted porphyrins containing an amino group and long-chain hydrophobic substituents were synthesized. Two strategies of the synthesis of asymmetric amino-containing porphyrins using p-acetamidobenzaldehyde and p-nitrobenzaldehyde were developed and investigated. A series of new substituted porphyrin-containing closo-decaborates were prepared based on the synthesized porphyrins and nitrilium derivatives of the closo-decaborate anion [B10H10]2−.
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Dedicated to Academician of the Russian Academy of Sciences A. I. Konovalov on the occasion of his 80th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 0194–0200, January, 2014.
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Zhdanova, K.A., Zhdanov, A.P., Ezhov, A.V. et al. Synthesis of amino-containing meso-aryl-substituted porphyrins and their conjugates with the closo-decaborate anion. Russ Chem Bull 63, 194–200 (2014). https://doi.org/10.1007/s11172-014-0413-1
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DOI: https://doi.org/10.1007/s11172-014-0413-1