Stabilization of crown-based organogelators by charge-transfer interaction

Jong Hwa Jung; Soo Jin Lee; Jeong Ah Rim; Haeseong Lee; Tae Sung Bae; Shim Sung Lee; Seiji Shinkai

doi:10.1021/cm048643r

Stabilization of crown-based organogelators by charge-transfer interaction

Jong Hwa Jung, Soo Jin Lee, Jeong Ah Rim, Haeseong Lee, Tae Sung Bae, Shim Sung Lee, Seiji Shinkai

Institute for Advanced Study

Research output: Contribution to journal › Article › peer-review

21 Citations (Scopus)

Abstract

Crown-based organogelators 1 and 2 bearing long alkyl chains were synthesized. Their gelation abilities were drastically enhanced by addition of bypyridinium-based ion (3²⁺), suggesting the bridging effect of the bipyridinium-based ion could be the primary driving force for the stabilization of organogel systems due to the intermolecular charge-transfer interaction with the 1:2 stoichiometry.

Original language	English
Pages (from-to)	459-462
Number of pages	4
Journal	Chemistry of Materials
Volume	17
Issue number	3
DOIs	https://doi.org/10.1021/cm048643r
Publication status	Published - Feb 8 2005

All Science Journal Classification (ASJC) codes

Chemistry(all)
Chemical Engineering(all)
Materials Chemistry

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10.1021/cm048643r

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abstract = "Crown-based organogelators 1 and 2 bearing long alkyl chains were synthesized. Their gelation abilities were drastically enhanced by addition of bypyridinium-based ion (32+), suggesting the bridging effect of the bipyridinium-based ion could be the primary driving force for the stabilization of organogel systems due to the intermolecular charge-transfer interaction with the 1:2 stoichiometry.",

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AU - Jung, Jong Hwa

AU - Lee, Soo Jin

AU - Rim, Jeong Ah

AU - Lee, Haeseong

AU - Bae, Tae Sung

AU - Lee, Shim Sung

AU - Shinkai, Seiji

PY - 2005/2/8

Y1 - 2005/2/8

N2 - Crown-based organogelators 1 and 2 bearing long alkyl chains were synthesized. Their gelation abilities were drastically enhanced by addition of bypyridinium-based ion (32+), suggesting the bridging effect of the bipyridinium-based ion could be the primary driving force for the stabilization of organogel systems due to the intermolecular charge-transfer interaction with the 1:2 stoichiometry.

AB - Crown-based organogelators 1 and 2 bearing long alkyl chains were synthesized. Their gelation abilities were drastically enhanced by addition of bypyridinium-based ion (32+), suggesting the bridging effect of the bipyridinium-based ion could be the primary driving force for the stabilization of organogel systems due to the intermolecular charge-transfer interaction with the 1:2 stoichiometry.

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Stabilization of crown-based organogelators by charge-transfer interaction

Abstract

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