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Cover Picture: Inherently Chiral Macrocyclic Oligothiophenes: Easily Accessible Electrosensitive Cavities with Outstanding Enantioselection Performances (Chem. Eur. J. 47/2014).

Authors :
Sannicolò, Francesco
Mussini, Patrizia R.
Benincori, Tiziana
Cirilli, Roberto
Abbate, Sergio
Arnaboldi, Serena
Casolo, Simone
Castiglioni, Ettore
Longhi, Giovanna
Martinazzo, Rocco
Panigati, Monica
Pappini, Marco
Quartapelle Procopio, Elsa
Rizzo, Simona
Source :
Chemistry - A European Journal. Nov2014, Vol. 20 Issue 47, p15257-15257. 1p.
Publication Year :
2014

Abstract

When new topologically appealing molecules are formed, fantasy ‐ assisted cogitation tries to associate their shapes to objects of everyday life: knots, cylinders, pretzels, baskets, ladders, etc. Chirality adds a touch of intelligence to these molecules, which gain the ability to recognize enantiomorphic species. In their Communication on page 15298 ff., F. Sannicolò et al. describe some inherently chiral elliptical and triangular oligothiophene macrocycles which they associate with the pictograms of some more or less mysterious crop circles. Photograph courtesy of Mr. Steve Alexander, www.temporarytemples.co.uk. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09476539
Volume :
20
Issue :
47
Database :
Academic Search Index
Journal :
Chemistry - A European Journal
Publication Type :
Academic Journal
Accession number :
99277097
Full Text :
https://doi.org/10.1002/chem.201490194