Anion interaction with ferrocene-functionalised cyclic and open-chain polyaza and aza-oxa cycloalkanes

被引:57
作者
Beer, PD
Cadman, J
Lloris, JM
Martínez-Máñez, R
Soto, J
Pardo, T
Marcos, MD
机构
[1] Univ Oxford, Inorgan Chem Lab, Oxford OX1 3QR, England
[2] Univ Politecn Valencia, Dept Quim, E-46071 Valencia, Spain
[3] Univ Politecn Valencia, ICMUV, Inst Ciencias Mat, E-46071 Valencia, Spain
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 2000年 / 11期
关键词
D O I
10.1039/b000079p
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A family of ferrocene-functionalised receptors of different topologies have been used as receptors for anions. The compounds have been designed to contain both amine nitrogen and ether oxygen atoms and comprises from monoaza to pentaaza derivatives both open-chain (L-1, L-2, L-3) or cyclic (L-4, L-5) and having from one to five ferrocenyl groups. Solution studies directed to determine the protonation constants of L-1, L-2 and L-3 have been carried out in water (0.1 mol dm(-3) KNO3, 25 & emsp14;degrees C) and those of L-4 and L-5 in 1,4-dioxane-water (70:30 v/v, 0.1 mol dm(-3) KNO3, 25 degrees C). The protonation behaviour of the receptors can be explained taking into account electrostatic considerations. Speciation studies in the presence of phosphate have been carried out in water for L-1, L-2 and L-3 and in dioxane-water for L-4 and L-5. Speciation studies have also been performed in the presence of ATP with L-1, L-2 and L-3 in water. Selectivity of a mixture of receptors against a certain anion is discussed in terms of ternary diagrams. The shift of the redox potential of the ferrocenyl groups as a function of the pH has been studied. The difference between the oxidation potentials at basic and acidic pH has been determined experimentally and is compared with that theoretically predicted using an electrostatic model previously reported. The electrochemical shift in the presence of ATP and phosphate has been measured in water for L-1, L-2 and L-3 and in the presence of phosphate and sulfate in 1,4-dioxane-water for L-4 and L-5 as a function of the pH. The electrochemical response found against those anions is quite poor with maximum cathodic shifts of ca. 30-40 mV. The electrochemical response induced by HSO4- and H2PO4- has also been studied in acetonitrile solutions where a large cathodic shift for H2PO4- up to ca. 200 mV was found.
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页码:1805 / 1812
页数:8
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