## Abstract For Abstract see ChemInform Abstract in Full Text.
Supramolecular exciton chirality of carotenoid aggregates
✍ Scribed by Miklós Simonyi; Zsolt Bikádi; Ferenc Zsila; József Deli
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 905 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0899-0042
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📜 SIMILAR VOLUMES
The aggregation behaviour of a series of chiral amide-containing surfactants 1 ± 5 is studied in order to assess the structural requirements for the generation of supramolecular chirality. It is found that the presence of hydrogenbonding moieties (i.e., amide groups) in the molecules alone is not su
Bilirubin, the yellow pigment of jaundice, is a bichromophoric tetrapyrrole that readily adopts either of two enantiomeric, folded conformations shaped like ridge-tiles and stabilized by a network of six intramolecular hydrogen bonds. Interconversion of these M and P helical chirality conformational