Functional organic gels Chirality induction through formation of highly-oriented structure
- 1 January 1995
- journal article
- research article
- Published by Taylor & Francis in Liquid Crystals
- Vol. 18 (1) , 97-99
- https://doi.org/10.1080/02678299508036596
Abstract
An L-glutamate derivative having one carboxylic and two dodecylamide groups form highly-oriented aggregates in benzene, which interact with a cationic achiral dye to produce extremely strong exciton coupling around the absorption band of the dye.Keywords
This publication has 19 references indexed in Scilit:
- Evaluation of Selective Binding Ability in Chiral Supramolecules Using Induced ChiralityAnalytical Sciences, 1993
- Effect of photopolymerization on the morphology of helical supramolecular assembliesLangmuir, 1992
- Sol-Gel Phase Transition of Switch-Functionalized Cholesterols as Detected by Circular DichroismChemistry Letters, 1992
- New cholesterol-based gelators with light- and metal-responsive functionsJournal of the Chemical Society, Chemical Communications, 1991
- Self-assembly of bilayer membranes in organic solvents by novel amphiphilic compoundsJournal of the American Chemical Society, 1989
- Self-Organization of Solvophobic, Double-Chained Fluorocarbon Derivatives in Organic MediaChemistry Letters, 1989
- Liquid-crystalline solvents as mechanistic probes. Part 37. Novel family of gelators of organic fluids and the structure of their gelsJournal of the American Chemical Society, 1989
- Specific bindings of methyl orange to chiral bilayer membranes with β-alanyl-L-glutamoyl head groups [1]Liquid Crystals, 1987
- ENHANCED CIRCULAR DICHROISM AND FLUIDITY OF DISK-LIKE AGGREGATES OF A CHIRAL, SINGLE-CHAIN AMPHIPHILEChemistry Letters, 1980
- Unique properties of chromophore-containing bilayer aggregates: enhanced chirality and photochemically induced morphological changeJournal of the American Chemical Society, 1980