Abstract
Selective complex formation in Langmuir dicetyl cyclene monolayers on the surface of aqueous solutions of Cu(II), Ni(II), and Zn(II) salts and their mixtures was studied. The effect of selectivity “inversion” of diphilic cyclene immobilized in monolayers on the surface of solutions of a mixture of copper(II) and nickel(II) salts was observed; the inversion was induced by a change in subphase pH. An analysis of the isotherms of monolayer compression and X-ray fluorescence spectra of the corresponding Langmuir-Blodgett films showed that subphase acidification caused a gradual transition from the selective formation of copper-containing macrocyclic complexes to selective complex formation between the ligand and nickel ions. The effect observed was not characteristic of complex formation with similar unsubstituted tetraamines in bulk solution. The phenomenon was interpreted from the point of view of specific conformational transitions of the diphilic macroring in the two-dimensional system organized at the interphase boundary.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
