ABSTRACT
[structure: see text] A new liquid crystalline material having an ethylenedioxythiophene-pyridazine-ethylenedioxythiophene (EDOT-PDZ-EDOT) core with two peripheral long alkyl chains was prepared. The designated donor-acceptor-donor (D-A-D)-type core structure induced a distinct smectic liquid crystalline phase due to the strong intermolecular interaction. The photophysical property and the layer structure of the liquid crystal were investigated by differential scanning calorimetry, polarized light microscopy, X-ray diffraction, and cyclic voltammetry.
ABSTRACT
Perylenetetracarboxylic diimide (PDI) derivatives bearing two or four peripheral pyrrole pendants (PDI-nPy, n=2 or 4) are cross-linkable materials by electro/phototreatment. In this paper, we introduce a new posttreatment technique to produce an insoluble film. Unlike the common solution-phase electrochemical deposition, we first spin-coated PDI-nPy on an electrode and then electrotreated the coated surface in a monomer-free electrolyte solution. This method gives the film a smooth surface with no granules, while the common method induces a rough film with a lot of granules. The post electrochemical treatment also provides a merit of higher resolution in a patterning process on a specific metal electrode. As one of the applications, we carried out an electrochromic study on the posttreated PDI-4Py film. It turned purple (lambdamax=590 nm) and sky blue (lambdamax=797 nm) at 0 and -1.9 V vs Ag/Ag+, respectively. We believe this method will broaden the patterning concept with the desired film morphology and resolution using PDI on a specific electrode.
Subject(s)
Imides/chemistry , Perylene/analogs & derivatives , Electrochemistry , Microscopy, Atomic Force , Microscopy, Electron, Scanning , Molecular Structure , Perylene/chemistry , Spectrum AnalysisABSTRACT
Perylenetetracarboxylic diimide derivatives bearing 2- or 4-peripheral pyrrole pendants could be efficiently crosslinked to form an insoluble film either by electropolymerization or visible light induced oxidative photopolymerization of the pyrrole units.
