Preparation of new robust organic gels by in situ cross-link of a bis(diacetylene) gelator

Kazuhiko Inoue; Yoshiyuki Ono; Yasumasa Kanekiyo; Kenji Hanabusa; Seiji Shinkai

doi:10.1246/cl.1999.429

Preparation of new robust organic gels by in situ cross-link of a bis(diacetylene) gelator

Kazuhiko Inoue, Yoshiyuki Ono, Yasumasa Kanekiyo, Kenji Hanabusa, Seiji Shinkai

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

51 Citations (Scopus)

Abstract

Polymerizable gelator 1 which has two diacetylene groups as well as two amide groups showed an excellent gelation ability for many organic solvents. Photoirradiation readily induced polymerization in the gel phase but the polymerization results were dependent upon the gelation solvent. It was shown that the three-dimensional cross-link of these organic gels resulted in new robust gels, retaining their gel fiber super-structure.

Original language	English
Pages (from-to)	429-430
Number of pages	2
Journal	Chemistry Letters
Issue number	5
DOIs	https://doi.org/10.1246/cl.1999.429
Publication status	Published - Jan 1 1999
Externally published	Yes

All Science Journal Classification (ASJC) codes

Chemistry(all)

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10.1246/cl.1999.429

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abstract = "Polymerizable gelator 1 which has two diacetylene groups as well as two amide groups showed an excellent gelation ability for many organic solvents. Photoirradiation readily induced polymerization in the gel phase but the polymerization results were dependent upon the gelation solvent. It was shown that the three-dimensional cross-link of these organic gels resulted in new robust gels, retaining their gel fiber super-structure.",

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AU - Inoue, Kazuhiko

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AU - Hanabusa, Kenji

AU - Shinkai, Seiji

PY - 1999/1/1

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N2 - Polymerizable gelator 1 which has two diacetylene groups as well as two amide groups showed an excellent gelation ability for many organic solvents. Photoirradiation readily induced polymerization in the gel phase but the polymerization results were dependent upon the gelation solvent. It was shown that the three-dimensional cross-link of these organic gels resulted in new robust gels, retaining their gel fiber super-structure.

AB - Polymerizable gelator 1 which has two diacetylene groups as well as two amide groups showed an excellent gelation ability for many organic solvents. Photoirradiation readily induced polymerization in the gel phase but the polymerization results were dependent upon the gelation solvent. It was shown that the three-dimensional cross-link of these organic gels resulted in new robust gels, retaining their gel fiber super-structure.

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Preparation of new robust organic gels by in situ cross-link of a bis(diacetylene) gelator

Abstract

All Science Journal Classification (ASJC) codes

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