A Complex between C-Methylcalix[4]resorcinarene and Triethylammonium Nitrate |
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Authors: | Pierre Thuéry Martine Nierlich |
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Affiliation: | CEA/Saclay, SCM (CNRS URA 331) , B[acaron]t. 125, 91191 Gif-sur-Yvette, France |
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Abstract: | Abstract The synthesis and crystal structure of the complex formed by the all-cis epimer of C-methylcalix[4]resorcinarene (1) and triethylammonium nitrate are reported. “1.(HNEt+ 3)4. (NO? 3)4(2)”, crystallizes in the monoclinic space group P21/n, a=25.796(2), b=16.6048(11), c=29.5659(10) Å, β=94.636(4)°, V=12623(2) Å3, Z=8. Refinement led to a final conventional R1 value of 0.128 for 12428 reflections and 1473 parameters. The resorcinarene displays the usual bowl-type shape, with four hydroxyl protons involved in intramolecular hydrogen bonds, whereas the remaining four make hydrogen bonds with four bridging nitrate ions, which results in the formation of infinite chains. Those chains are arranged so as to form layers, between which the triethylammonium ions and the remaining nitrate ions are hydrogen-bonded one to another. |
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Keywords: | Calix[4]resorcinarene hydrogen bonds supramolecular assembly |
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