Two neutral macrobicyclic anion receptors 4 and 6, containing a calix[4]arene in the cone conformation, two l-alanine units, and a 2,6-diacylpyridine or a phthaloyl bridge, are described. The x-ray crystal structure of the acetone complexes of the pyridine containing macrocycle 6 shows the four amide NH groups to be in close proximity to the chiral pocket delimited by the pyridine and one aroma...

The Cover Feature illustrates the C−N coupling of aniline and aryl bromide in cavity a supramolecular copper phenanthroline calix[8]arene catalyst. In their Research Article, R. A. Talmazan, J. Refugio Monroy co-workers showed how encapsulation an otherwise poor Cu(I) catalyst by enhances catalytic activity for between amines halides. Yields up to 92% were achieved with low loadings (2.5% mol)....

In this study, we examine macrocyclic compounds to determine whether they can provide a safer replacement and stable complex for BPA in thermochromic dyes. To achieve objective, series of compounds, Methyl-N-benzylhexahomotriazacalix[3]arene (MeAC3), p-Chloro-N-benzylhexahomo-triazacalix[3]arene (ClAC3), ?-Cyclodexdrin (?-CD), ?-Cyclodexdrin (?-CD), p-tert-Butylthiacalix[4]arene (TC4), Calix[4]...

Abstract Supramolecular chemistry is one of the current strategies for producing advanced materials. With aim to develop new Thin-Films with antibacterial activity, we embedded an amphiphilic choline-calix[4]arene possessing properties in polymeric based on polyether-co-amide matrix (Pebax ® 2533). The loading calix[4]arene derivative film was performed by solution casting. amount calixarene ad...

A recently developed efficient method for intramolecular direct arylation is employed on a doubly functionalized calix[4]arene fixed in the cone conformation. The reaction takes place in high yield leading to meta substituted calix[4]arenes. The functionalities are located at two opposite aromatic rings and the two possible diastereomers are obtained in a 1:1 ratio. Full sets of data including ...

A chiral calix[4]arene bearing l-2,3-dibenzoyltartaric acid groups at the lower rim was synthesized and could enantioselectively self-assemble to result in a gel or suspension only with one enantiomer of chiral amines; as revealed by electron microscopy, the resultant gel was of nanofibers with a high aspect ratio but the suspension was composed of nanospheres.

A water-soluble, chiral calix[4]arene has been found to form hydrogels when triggered by the presence of specific anions, with efficacy linked to the Hofmeister series; the gel properties are modified by the associated cations, and gelation can be reversibly switched off by increasing pH.

The title calix[4]arene, C(44)H(52)Cl(4)O(4), displays the 1,3-alternate conformation with crystallographically imposed twofold symmetry. Four phenolic rings of the calixarene backbone are tilted into the calix cavity, making dihedral angles of 77.42 (2) and 77.71 (2)° with the plane of the four bridging methyl-ene C atoms. Pairs of opposite aromatic rings make dihedral angles of 25.16 (3) and ...