Papers by Keyword: Charge Transfer Complex CTC

Abstract: Charge transfer complexes (CTC) can be readily introduced into materials by cohydrolysis-copolymerisation of bis-silylated ter-thiophenes as precursors with TMOS and TEOS in the presence of TCNQ. CTC formation is shown in the visible spectrum of the xerogel by the band at 850 nm characteristic of the TCNQ·- radical anion. Vibrational spectra have shown that strong vibration of C≡N bond at 2184, 2120 and 1595 cm-1 as peaks characteristics of CTC. The CTC bands are weak and the complex is easily destroyed by washing with acetone, which removes the TCNQ. The gelification effect of the charge transfer complexes on the hybrid materials of 2,5’’- bis(trime thoxysilyl)terthiophene/TCNQ/ TMOS showed that the peak with distance of more than 11.68 Å, formed by precursors and matrices, as a lamellar structure. The birefringence of xerogel BTS3T in presence of alkoxysilane showed that the value is near the detection limit of 0.1 – 0.4 x 10-3, which is weaker than BTS3T / THF with the birefringence value of 4.5 x 10-3.

Abstract: Copolymerization of MAn and CHDDVE was conducted by using azobisisobutyronitrile (AIBN) or benzoyl peroxide (BPO) as the initiator, ethyl acetate (EA) or n-butyl acetate (BA) as the solvent, and n-hexane as the precipitator. Effects of several factors on monomer conversion were studied, such as reaction time, reaction temperature, composition of the monomer feed (MAn/CHDDVE) and initiator concentration. Molecular weight and its polydispersity and polymer material morphology were characterized by gel permeation chromatography (GPC) and transmission electron microscope (TEM) technologies, respectively. It was demonstrated that CTC was formed in MAn/CHDDVE system, based on ultraviolet-visible spectroscopy (UV-vis) analysis. The product was alternating copolymer with high crosslinking degree, so it could not be dissolved in common solvents, e.g. water, chloroform, N, N-dimethyl formamide (DMF), tetrahydrofuran (THF) and acetone (Ac).