Issue 37, 2011
From the journal:

Chemical Communications

Molecular-shape selectivity by molecular gel-forming compounds: bioactive and shape-constrained isomers through the integration and orientation of weak interaction sites†

Abul K. Mallik,a   Hongdeng Qiu,a   Tsuyoshi Sawada,a   Makoto Takafujia  and  Hirotaka Ihara*a  

* Corresponding authors

a Department of Applied Chemistry and Biochemistry, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555, Japan
E-mail: ihara@kumamoto-u.ac.jp
Fax: +81 96-342-3662
Tel: +81 96-342-3662

Abstract

A molecular gel system was assembled on carrier particles and the integrated effect of weak interaction sites enabled highly efficient separation of the bioactive and shape-constrained isomers of tocopherols, β-carotene, and polycyclic aromatic hydrocarbons (PAHs) by multiple interaction mechanisms.

Graphical abstract: Molecular-shape selectivity by molecular gel-forming compounds: bioactive and shape-constrained isomers through the integration and orientation of weak interaction sites

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Article information

DOI
https://doi.org/10.1039/C1CC13397G
Article type
Communication
Submitted
08 Jun 2011
Accepted
03 Aug 2011
First published
19 Aug 2011

Chem. Commun., 2011,47, 10341-10343

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Molecular-shape selectivity by molecular gel-forming compounds: bioactive and shape-constrained isomers through the integration and orientation of weak interaction sites

A. K. Mallik, H. Qiu, T. Sawada, M. Takafuji and H. Ihara, Chem. Commun., 2011, 47, 10341 DOI: 10.1039/C1CC13397G

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