Enantioselective recognition of dicarboxylic acid guests based on an allosteric effect of a chiral double-decker porphyrin which changes the stoichiometry upon the guest binding

Tomohiro Ikeda, Kazuki Sada, Seiji Shinkai, Masayuki Takeuchi

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

A double-decker porphyrin 1R bearing one chiral substituent per porphyrin ring was synthesised. The host 1R showed highly cooperative binding towards chiral guest 2R with stoichiometry of the complex (1:2) and its stepwise association constants (K1 and K2) were evaluated to be log K1 = 1.6 and log K2 = 4.1, respectively. 1R also recognised 2S cooperatively and formed into a 1:3 complex in log K1 =1.9, log K2 = 1.2 and log K3 = 3.8. When we use racemic 2, 1R exhibits unconventional enantioselectivity only towards 2R in a specific concentration region. It not only showed a chiral screening but also changed the stoichiometry depending on the guest chirality. These high enantioselectivity and stoichiometric modulation are effected by proper incorporation of the structural information of two enantiomers into the host and utilisation of multiple equilibrium characteristic of positive allosterism.

Original languageEnglish
Pages (from-to)59-64
Number of pages6
JournalSupramolecular Chemistry
Volume23
Issue number1-2
DOIs
Publication statusPublished - Jan 1 2011

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Dicarboxylic Acids
Enantioselectivity
Porphyrins
Stoichiometry
Bearings (structural)
Enantiomers
Chirality
Screening
Modulation
Association reactions

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Enantioselective recognition of dicarboxylic acid guests based on an allosteric effect of a chiral double-decker porphyrin which changes the stoichiometry upon the guest binding. / Ikeda, Tomohiro; Sada, Kazuki; Shinkai, Seiji; Takeuchi, Masayuki.

In: Supramolecular Chemistry, Vol. 23, No. 1-2, 01.01.2011, p. 59-64.

Research output: Contribution to journalArticle

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