Fundamental Studies on Discrimination of Organic/Inorganic Guests at Membrane Interface by Calix[6]arenes and Their Analogues.

Accession number;01A0228954
Title;Fundamental Studies on Discrimination of Organic/Inorganic Guests at Membrane Interface by Calix[6]arenes and Their Analogues.
Author; ODASHIMA KAZUNORI (Nagoya City Univ., Fac. of Pharm. Sci.) MIYAKE JUNKO (Nagoya City Univ., Fac. of Pharm. Sci.) MURAKAMI YUKA (Nagoya City Univ., Fac. of Pharm. Sci.) SHIRAI NAOHIRO (Nagoya City Univ., Fac. of Pharm. Sci.) OZAKU KOJI (Univ. of Tokyo, Grad. Sch.) AMEMIYA SHIGERU (Univ. of Tokyo, Grad. Sch.)
Journal Title;Abstracts. Symposium on Biofunctional Chemistry
Journal Code:L0836A
ISSN:
VOL.15th;NO.;PAGE.24-25(2000)
Figure&Table&Reference;TBL.1, REF.7
Pub. Country;Japan
Language;Japanese
Abstract;Investigations on the potentiometric selectivities of calix[6]arene hexaesters and related hosts revealed that a high dopamine selectivity could be attained by the tri-O-butyl and tri-O-acetic acid ester derivatives of hexahomotrioxacalix[3]arene incorporated in PVC liquid membranes. In addition to structural studies by 1H-NMR and calculation (Hartree-Fock/3-21G*), investigations to understand the reason of potentiometric selectivities were carried out by separating the lipophilicity and complexation factors. It was found that the high dopamine/K+ ion selectivity stemmed from highly selective complexation of dopamine by the host. (author abst.)