Inherently Chiral Macrocyclic Oligothiophenes: Easily Accessible Electrosensitive Cavities with Outstanding Enantioselection Performances

Inherently Chiral Macrocyclic Oligothiophenes: Easily Accessible Electrosensitive Cavities with Outstanding Enantioselection Performances

Invited for the cover of this issue is Francesco Sannicolò and co‐workers at different Italian institutions, who all contributed to the different specific areas of this multidisciplinary work. The image depicts inherently chiral elliptical and triangular oligothiophene macrocycles and their symmetri...

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Veröffentlicht in:Chemistry : a European journal 2014-11, Vol.20 (47), p.15261-15261
Hauptverfasser: 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
Format: Artikel
Sprache:eng
Schlagworte:
Accessibility
Chemistry
Chirality
Crops
Holes
Macrocyclic compounds
Multidisciplinary
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Zusammenfassung:Invited for the cover of this issue is Francesco Sannicolò and co‐workers at different Italian institutions, who all contributed to the different specific areas of this multidisciplinary work. The image depicts inherently chiral elliptical and triangular oligothiophene macrocycles and their symmetrical resemblance to mysterious crop circles. Read the full text of the article at 10.1002/chem.201404331. “Chirality plays a great aesthetic and fascinating role.” Read more about the story behind the cover in the Cover Profile and about the research itself on page 15298 ff. (DOI: 10.1002/chem.201404331).
ISSN:0947-6539
1521-3765
DOI:10.1002/chem.201405372