Synthesis and Structure Elucidation of Large Phosphorus Macrocycles |
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Authors: | Bernard Tinant Pascale Delangle Jean-Christophe Mulatier Jean-Paul Declercq Jean-Pierre Dutasta |
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Affiliation: | (1) Université Catholique de Louvain, Unité de Chimie Structurale et des Mécanismes Réactionnels, 1 Place Louis Pasteur, B-1348 Louvain-la-Neuve, Belgium;(2) école Normale Supérieure de Lyon, Laboratoire de Chimie, UMR CNRS n° 5182, 46, Allée d’Italie, F-69364 Lyon 07, France;(3) Laboratoire de Reconnaissance Ionique, SCIB, DRFMC, CEA-Grenoble, 17 avenue des Martyrs, 38054 Grenoble cedex 9, France |
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Abstract: | The simple reaction between 1,ω-diamino derivatives and R-bis-(dimethylamino)-phosphane (R = CH3, C6H5), followed by an oxidation step led to the formation of the expected macrocyclic phosphorus compounds. By this way 17- to 27-membered macrocycles were easily obtained. During the synthesis, the formation of dimeric (40- and 52-membered rings) and trimeric (78-membered rings) macrocyclic species were obtained from 3 and 5 and fully characterized by NMR and mass spectrometry. The P(III) phosphorus species exchange in solution and the macrocycle/oligomers ratio is temperature and concentration dependent. The crystal structure analysis of macrocycles 1, 5, 7 and 8 show that voids are minimized in the solid so that the macrocyclic cavity is filled up with part of the molecule itself or with a guest molecule, when the size of the macrocycle does not allow molecular folding for self-filling the cavity. Dedicated to the memory of Prof. Jean-Bernard Robert |
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Keywords: | macrocyclic compounds oligomers phosphoramide phosphorus macrocycles supramolecular chemistry X-ray analysis |
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