New organic gelalors bearing a porphyrin group: A new strategy to create ordered porphyrin assemblies

Hong Jian Tian, Kazuhiko Inoue, Kenji Yoza, Tsutomu Ishi-I, Seiji Shinkai

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Cholesterol-based gelators 1 bearing a porphyrin moiety were synthesized. (S)-1 with a natural C-3 configuration could gelatinize a few solvents whereas (R)-1 with an inverted C-3 configuration could not gelatinize any solvent. The absorption and CD spectra for less cohesive (R)-1 were changed only to a smaller extent at 10-5∼10-2 mol dm-3 whereas more cohesive (S)-1 gave a new λmax at 444 nm and its corresponding CD band only in the gel phase. The results indicate that "gelation" is a new strategy to create ordered porphyrin assemblies.

Original languageEnglish
Pages (from-to)871-872
Number of pages2
JournalChemistry Letters
Issue number9
DOIs
Publication statusPublished - Jan 1 1998
Externally publishedYes

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Bearings (structural)
Porphyrins
Gelation
Gels
Cholesterol

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

New organic gelalors bearing a porphyrin group : A new strategy to create ordered porphyrin assemblies. / Tian, Hong Jian; Inoue, Kazuhiko; Yoza, Kenji; Ishi-I, Tsutomu; Shinkai, Seiji.

In: Chemistry Letters, No. 9, 01.01.1998, p. 871-872.

Research output: Contribution to journalArticle

Tian, Hong Jian ; Inoue, Kazuhiko ; Yoza, Kenji ; Ishi-I, Tsutomu ; Shinkai, Seiji. / New organic gelalors bearing a porphyrin group : A new strategy to create ordered porphyrin assemblies. In: Chemistry Letters. 1998 ; No. 9. pp. 871-872.
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