DESIGN AND SYNTHESIS OF A C-4-SYMMETRICAL HARD-SOFT DITOPIC METAL RECEPTOR BY CALIXARENE-PORPHYRIN COUPLING

Citation
T. Nagasaki et al., DESIGN AND SYNTHESIS OF A C-4-SYMMETRICAL HARD-SOFT DITOPIC METAL RECEPTOR BY CALIXARENE-PORPHYRIN COUPLING, Journal of the Chemical Society. Perkin transactions. I, (15), 1995, pp. 1883-1888
Citations number
31
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0300922X
Issue
15
Year of publication
1995
Pages
1883 - 1888
Database
ISI
SICI code
0300-922X(1995):15<1883:DASOAC>2.0.ZU;2-O
Abstract
A tetraphenylporphyrin capped with a calix[4]aryl amide through L-alan ine pillars (compound 1) has been synthesized. Owing to C-4 symmetry i n both the tetraphenylporphyrin and the calix[4]arene this molecule st ill retains C-4 symmetry. As the calix[4]aryl amide moiety can bind al kali metal cations, and the porphyrin moiety can bind transition metal cations, compound 1 acts as a host molecule with a hard-soft ditopic metal-binding site. It was found that the Zn-II complex of 1 (complex 1 . Zn-II) can bind KI very strongly with log K-ass = 5.23 (CHCl3:MeCN = 4:1 v/v; 25 degrees C) whereas KClO4 is scarcely captured by 1 . Zn -II. Absorption and fluorescence spectroscopic studies showed that I- ion is bound to this cavity, interacting with both calix[4]arene-bound K+ through electrostatic attraction and porphyrin-bound Zn-II through coordination as an axial ligand. The results establish that complex 1 . Zn-II acts as a unique ditopic receptor for I- ion.