Issue 3, 1990

Retinylidene Schiff-base protonation in surfactant-solubilized water pools in heptane

Abstract

All-trans-N-retinylidene-n-butylamine (4) and its 3-chloropropionic acid (CPA) protonated analogue (5) remained stable in sodium bis(2-ethylhexyl) sulphosuccinate, reversed-micelle-solubilized water pools in heptane, and the extent to which (4) protonated depended on the [CPA] to [(4)] ratio and on the amount of solubilized water; hence, this system mimicked the behaviour of rhodopsins.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 233-234

Retinylidene Schiff-base protonation in surfactant-solubilized water pools in heptane

A. K. Singh, C. Sandorfy and J. H. Fendler, J. Chem. Soc., Chem. Commun., 1990, 233 DOI: 10.1039/C39900000233

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