Ionic, paramagnetic and photophysical properties of a new biohybrid material incorporating copper perchlorate. (10th August 2015)

• Record Type: Journal Article
• Authors: Leones, R.; Donoso, J.P.; Magon, C.J.; Silva, I.D.A.; de Camargo, A.S.S.; Pawlicka, A.; Silva, M.M.
• Is Part Of: Electrochimica acta. Volume 173(2015)
• Page Start: 76
• Page End: 81
• Publication Date: 2015-08-10
• Subjects: Ormolytes -- Electron paramagnetic resonance -- Impedance spectroscopy -- Photoluminescence spectroscopy -- Conductivity; Electrochemistry -- Periodicals; Electrochemistry, Industrial -- Periodicals; 541.37
• DOI: 10.1016/j.electacta.2015.04.158
• Languages: English
• ISSNs: 0013-4686

Abstract

Graphical abstract: Highlights: Poly(ϵ-caprolactone)/siloxane biohybrids electrolytes were prepared by sol-gel method. The polymer electrolytes were doped with copper perchlorate salt. The ionic, paramagnetic and photophysical properties of the samples were evaluated. The samples were analyzed by means of impedance spectroscopy, electron paramagnetic resonance (EPR) and photoluminescence spectroscopy. Abstract: The sol-gel method was employed in the synthesis of di-urethane cross-linked poly(ϵ-caprolactone) (d-PCL(530)/siloxane biohybrid ormolytes incorporating copper perchlorate (Cu(ClO4 )2 ). The highest ionic conductivity of the d-PCL(530)/siloxanen Cu(ClO4 )2 system is that with n = 10 (1.4 × 10 −7 and 1.4 × 10 −5 S cm −1, at 25 and 100 °C, respectively). In an attempt to understand the ionic conductivity/ionic association relationship, we decided to inspect the chemical environment experienced by the Cu 2+ ions in the d-PCL(530)/siloxane medium. The observed EPR spectra are typical of isolated monomeric Cu 2+ ions in axially distorted sites. The molecular orbital coefficients obtained from the EPR spin Hamiltonian parameters and the optical absorption band suggests that bonding between the Cu 2+ and its ligand in the ormolytes are moderately ionic. Investigation by photoluminescence spectroscopy did not evidence or allow selective excitation of transitions corresponding to complexed Cu 2+ species.