The self-assembly properties in the solid state of tectons derived from the reaction of calix[4]arene aminomethyl derivatives with a carboxylic acid or a protected amino acid are described, along with their conformational properties in solution. The X-ray crystal structures show that these compounds self-assemble in the lattice through a network of hydrogen-bonds between the amide groups, which overall results in infinite nanotubes formed by the calixarene aromatic cavities. Small changes in the upper rim substituents do not disturb the basic self-assembly motif which appears general and quite useful for controlling crystal growth by design and obtaining novel nanoporous crystalline materials.
Designing nanoporous crystalline materials by self-assembly: 2D hydrogen-bonded networks from upper rim calix[4]arene diamide derivatives / Baldini, Laura; Sansone, Francesco; Massera, Chiara; Casnati, Alessandro; Ugozzoli, Franco; Ungaro, Rocco. - In: INORGANICA CHIMICA ACTA. - ISSN 0020-1693. - 360:(2007), pp. 970-980. [10.1016/j.ica.2006.07.023]
Designing nanoporous crystalline materials by self-assembly: 2D hydrogen-bonded networks from upper rim calix[4]arene diamide derivatives
BALDINI, Laura;SANSONE, Francesco;MASSERA, Chiara;CASNATI, Alessandro;UGOZZOLI, Franco;UNGARO, Rocco
2007-01-01
Abstract
The self-assembly properties in the solid state of tectons derived from the reaction of calix[4]arene aminomethyl derivatives with a carboxylic acid or a protected amino acid are described, along with their conformational properties in solution. The X-ray crystal structures show that these compounds self-assemble in the lattice through a network of hydrogen-bonds between the amide groups, which overall results in infinite nanotubes formed by the calixarene aromatic cavities. Small changes in the upper rim substituents do not disturb the basic self-assembly motif which appears general and quite useful for controlling crystal growth by design and obtaining novel nanoporous crystalline materials.File | Dimensione | Formato | |
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