Abstract
In this study, a comprehensive structural analysis of the linear redox-active ferrocenyl-containing polysiloxanes (FPSs) was performed by the liquid-state 1H, 13C, and 29Si nuclear magnetic resonance (NMR) spectroscopy, gel permeation chromatography (GPC), and cyclic voltammetry. FPSs with tunable Fc unit content ranging from 20 to 100 mol% were obtained by anionic ring-opening polymerization (AROP). The 29Si NMR spectroscopy indicates the successful anionic homopolymerization of the mono- and tetraferrocenyl-substituted cyclotetrasiloxanes (Fc4D4 and Fc1D4) by appearance of new signals of Si atoms corresponding to a polymer backbone. An analysis of pentad assignments in 29Si NMR determined the anionic copolymerization of Fc4D4 with D4 by indicating signals of neighboring Si atoms from different types of polymer units (DF and D), which differ from the signals of homopolymers. The Mayo-Lewis copolymerization constants of Fc4D4 and D4 were determined by the Fineman–Ross method. The molecular masses and unimodal molecular weight distribution of FPSs were estimated by using GPC. FPSs possess redox-activity. Thus, the proposed comprehensive approach analyzes structural features of the functional silicones with enhanced redox properties, which can be applied in (opto)electronics, coatings, and biomedicine.
Sign-in/Register to access full text options 
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.
