Through-bond communication between polymer-bound phosphinic acid ligands and trivalent metal ions probed with FTIR spectroscopy

被引:14
作者
Alexandratos, Spiro D. [1 ,2 ]
Zhu, Xiaoping [1 ,2 ]
机构
[1] CUNY Hunter Coll, Dept Chem, 695 Pk Ave, New York, NY 10065 USA
[2] CUNY, Grad Ctr, New York, NY 10016 USA
关键词
Ion exchange; Polymer; Phosphinic; Ligand; FTIR; TRANSFORM INFRARED-SPECTROSCOPY; EXCHANGE COORDINATION RESINS; AQUEOUS-SOLUTIONS; IMMOBILIZED LIGANDS; CHELATING RESINS; AUXILIARY GROUPS; PHOSPHORIC-ACID; EXTRACTION; COMPLEXES; MECHANISM;
D O I
10.1016/j.vibspec.2018.01.007
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The binding of trivalent metal ions to immobilized ligands is analyzed to determine the principal type of interaction, the extent of ion exchange, and changes due to through-bond communication. FTIR spectroscopy is found to be a readily accessible means of determining through-bond communication and spectra provide support for a molecular level interpretation of the interaction. The affinity of the phosphinic acid ligand for Al(III), La(III), Lu(III), Fe(III), and In(III) is quantified with distribution coefficients from 0.01-6 M nitric acid solutions. High affinities are evident with In(III) > Fe(III) > Lu(III) > La(III) > Al(III). The affinities correlate with the softness parameter and thus the polarizability of the metal ion. The FTIR spectrum of the phosphinic acid has two incompletely separated bands at 1168/1126 cm(-1) associated with the P=O bond and two similar bands at 967/951 cm(-1) due to the P-O (H) bond. The bands at 1168/951 and 1126/967 cm(-1) are assigned to different hydrogen bonded conformers within the metal-free polymer. Through-bond communication is evident as the extent of metal ion binding increases: the P=O and P-O bands at 1168 and 951 cm(-1), respectively, collapse into a single band between 1040 and 1080 cm(-1) representative of PO2(M) while hydrogen bonding among unexchanged -P(O)OH ligands gives the bands at 1133 and 981 cm(-1). (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:80 / 89
页数:11
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