Photoresponsive crown ethers. Part 14. Photoregulated crown-metal complexation by competitive intramolecular tail(ammonium)-biting

Seiji Shinkai, Midori Ishihara, Kaori Ueda, Osamu Manabe

研究成果: ジャーナルへの寄稿記事

65 引用 (Scopus)

抄録

New photoresponsive crown ethers (1H+) having a crown ether ring and an ammoniumalkyl [H3N+-(CH2)n, n = 4,6,10] group attached to the two sides of an azobenzene have been synthesized. These photoresponsive 'tail-biting' crown ethers have been designed so that intramolecular 'biting' of the ammonium group to the crown can only occur upon photoisomerisation to the cis-forms. In the thermal cis-trans isomerisation, the first-order rate constants for cis- (1H+) were smaller by 1.6-2.2-fold than those for (1) (the analogous free amines). Moreover, this rate increased with increasing added K+ concentration. This suggests that the ammonium tail is intramolecularly bound to the crown ether ring in cis-(1H+). This intramolecular 'biting' is further reflected in the relative affinities of (1H+) for alkali-metal cations. The affinities were markedly reduced by u.v.-light irradiation and in particular, cis- (1H+) (n = 6) and cis-(1H+)(n = 10) showed almost no metal-binding ability. This marked difference in the metal-binding ability was used to generate the light-controlled systems for the passive or active ion-transport of ions across a liquid membrane.

元の言語英語
ページ(範囲)511-518
ページ数8
ジャーナルJournal of the Chemical Society, Perkin Transactions 2
発行部数4
出版物ステータス出版済み - 12 1 1985
外部発表Yes

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Crown Ethers
Complexation
Ammonium Compounds
Metals
Ions
Alkali Metals
Photoisomerization
Liquid membranes
Isomerization
Amines
Cations
Rate constants
Irradiation

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

これを引用

Photoresponsive crown ethers. Part 14. Photoregulated crown-metal complexation by competitive intramolecular tail(ammonium)-biting. / Shinkai, Seiji; Ishihara, Midori; Ueda, Kaori; Manabe, Osamu.

:: Journal of the Chemical Society, Perkin Transactions 2, 番号 4, 01.12.1985, p. 511-518.

研究成果: ジャーナルへの寄稿記事

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AU - Ueda, Kaori

AU - Manabe, Osamu

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N2 - New photoresponsive crown ethers (1H+) having a crown ether ring and an ammoniumalkyl [H3N+-(CH2)n, n = 4,6,10] group attached to the two sides of an azobenzene have been synthesized. These photoresponsive 'tail-biting' crown ethers have been designed so that intramolecular 'biting' of the ammonium group to the crown can only occur upon photoisomerisation to the cis-forms. In the thermal cis-trans isomerisation, the first-order rate constants for cis- (1H+) were smaller by 1.6-2.2-fold than those for (1) (the analogous free amines). Moreover, this rate increased with increasing added K+ concentration. This suggests that the ammonium tail is intramolecularly bound to the crown ether ring in cis-(1H+). This intramolecular 'biting' is further reflected in the relative affinities of (1H+) for alkali-metal cations. The affinities were markedly reduced by u.v.-light irradiation and in particular, cis- (1H+) (n = 6) and cis-(1H+)(n = 10) showed almost no metal-binding ability. This marked difference in the metal-binding ability was used to generate the light-controlled systems for the passive or active ion-transport of ions across a liquid membrane.

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