{"title":"Quantitative evaluation of the ion-binding characteristics of poly(4′-vinylbenzo-18-crown-6)","authors":"Cindy C. Chen, Thomas W. Smith","doi":"10.1002/polc.5070740116","DOIUrl":null,"url":null,"abstract":"<p>We have carried out an in-depth study of the alkali metal ion binding characteristics of a model ionophoric macromolecule, poly(4′-vinylbenzo 18-crown-6), P18C6. Ion selective electrode potentiometry has been utilized to determine stability constants for complexstion of K<sup>+</sup>, Na<sup>+</sup>, and Cs<sup>+</sup> to P18C6 in methanol/water (80/20)<sub>w</sub>. Our results show that (he intrinsic binding constants, K<sub>n</sub>, of P18C6 towards K<sup>+</sup>C1<sup>−</sup> and Na<sup>+</sup>Cl<sup>−</sup> are identical to that of the monomeric analog, benzo-18-crown-6.</p><p>In the absence of supporting electrolyte, the apparent binding constant of benzo-18-crown-6 is greater than (hat of P18C6. At low tonic strength the binding of K<sup>+</sup> to P18C6 depends strongly on the fraction of crown moieties bound. P18C6 binds K<sup>+</sup>C1<sup>−</sup> and Na<sup>+</sup>Cl<sup>−</sup> with a stoichiometry of 2 mol of crown per mole of M<sup>+</sup> . This binding, however, is not sandwich mode. The binding of K<sup>+</sup>Cl<sup>−</sup>, K<sup>+</sup>NO<sub>3</sub> and K<sup>+</sup>ClO<sub>4</sub><sup>−</sup> to P18C6 in methanol/water differs significantly, with <i>K</i><sub>N</sub>(K<sup>+</sup>ClO<sub>4</sub><sup>−</sup>1 being nearly an order of magnitude greater than <i>K</i><sub>N</sub>(K<sup>+</sup>Cl<sup>−</sup>). Cs<sup>+</sup> is bound to P1SC6 with a stoichiometry of ∼3 mol of crown per mole of Cs<sup>+</sup>, and the ion is bound cooperatively in a sandwich geometry.</p>","PeriodicalId":16867,"journal":{"name":"Journal of Polymer Science: Polymer Symposia","volume":"74 1","pages":"171-185"},"PeriodicalIF":0.0000,"publicationDate":"1986-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/polc.5070740116","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Science: Polymer Symposia","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/polc.5070740116","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
We have carried out an in-depth study of the alkali metal ion binding characteristics of a model ionophoric macromolecule, poly(4′-vinylbenzo 18-crown-6), P18C6. Ion selective electrode potentiometry has been utilized to determine stability constants for complexstion of K+, Na+, and Cs+ to P18C6 in methanol/water (80/20)w. Our results show that (he intrinsic binding constants, Kn, of P18C6 towards K+C1− and Na+Cl− are identical to that of the monomeric analog, benzo-18-crown-6.
In the absence of supporting electrolyte, the apparent binding constant of benzo-18-crown-6 is greater than (hat of P18C6. At low tonic strength the binding of K+ to P18C6 depends strongly on the fraction of crown moieties bound. P18C6 binds K+C1− and Na+Cl− with a stoichiometry of 2 mol of crown per mole of M+ . This binding, however, is not sandwich mode. The binding of K+Cl−, K+NO3 and K+ClO4− to P18C6 in methanol/water differs significantly, with KN(K+ClO4−1 being nearly an order of magnitude greater than KN(K+Cl−). Cs+ is bound to P1SC6 with a stoichiometry of ∼3 mol of crown per mole of Cs+, and the ion is bound cooperatively in a sandwich geometry.