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Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid.


ABSTRACT: In order to have access to chiral gels, a series of salts derived from (1R,3S)-(+)-camphoric acid and various secondary amines were prepared based on supramolecular synthon rationale. Out of seven salts prepared, two showed moderate gelation abilities. The gels were characterized by differential scanning calorimetry, table top rheology, scanning electron microscopy, single crystal and powder X-ray diffraction. Structure property correlation based on X-ray diffraction techniques remain inconclusive indicating that some of the integrated part associated with the gelation phenomena requires a better understanding.

SUBMITTER: Adalder TK 

PROVIDER: S-EPMC2956458 | biostudies-literature | 2010 Sep

REPOSITORIES: biostudies-literature

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Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid.

Adalder Tapas Kumar TK   Adarsh N N NN   Sankolli Ravish R   Dastidar Parthasarathi P  

Beilstein journal of organic chemistry 20100921


In order to have access to chiral gels, a series of salts derived from (1R,3S)-(+)-camphoric acid and various secondary amines were prepared based on supramolecular synthon rationale. Out of seven salts prepared, two showed moderate gelation abilities. The gels were characterized by differential scanning calorimetry, table top rheology, scanning electron microscopy, single crystal and powder X-ray diffraction. Structure property correlation based on X-ray diffraction techniques remain inconclusi  ...[more]

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