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Charge-transfer interaction mediated organogels from 18?-glycyrrhetinic acid appended pyrene.


ABSTRACT: We describe herein the two-component charge-transfer (CT) interaction induced organogel formation with 18?-glycyrrhetinic acid appended pyrene (GA-pyrene, 3) as the donor, and 2,4,7-trinitrofluorenone (TNF, 4) as the acceptor. The use of TNF (4) as a versatile electron acceptor in the formation of CT gels is demonstrated through the formation of gels in a variety of solvents. Thermal stability, stoichiometry, scanning electron microscopy (SEM), optical micrographs, and circular dichroism (CD) are performed on these CT gels to investigate their thermal and assembly properties. UV-vis, fluorescence, mass spectrometric as well as variable-temperature (1)H NMR experiments on these gels suggest that the CT interaction is one of the major driving forces for the formation of these organogels.

SUBMITTER: Hu J 

PROVIDER: S-EPMC3869347 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Charge-transfer interaction mediated organogels from 18β-glycyrrhetinic acid appended pyrene.

Hu Jun J   Wu Jindan J   Wang Qian Q   Ju Yong Y  

Beilstein journal of organic chemistry 20131216


We describe herein the two-component charge-transfer (CT) interaction induced organogel formation with 18β-glycyrrhetinic acid appended pyrene (GA-pyrene, 3) as the donor, and 2,4,7-trinitrofluorenone (TNF, 4) as the acceptor. The use of TNF (4) as a versatile electron acceptor in the formation of CT gels is demonstrated through the formation of gels in a variety of solvents. Thermal stability, stoichiometry, scanning electron microscopy (SEM), optical micrographs, and circular dichroism (CD) ar  ...[more]

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