Different synthetic procedures for water soluble polythiophenes and their applications in sensing, detection of biomolecules and optoelectronic devices are discussed.

A new and facile approach for synthesizing graphene quantum dots (GQDs) using sono-Fenton reaction in an aqueous dispersion of graphene oxide (GO) is reported. The transmission electron microscopy (TEM) micrographs of GQDs indicate its average diameter as ∼5.6 ± 1.4 nm having a lattice parameter of 0.24 nm. GQDs are used to fabricate composites (PG) with a water-soluble polymer, polythiophene-g-poly[(diethylene glycol methyl ether methacrylate)-co-poly(N,N-dimethylaminoethyl methacrylate)] [PT-g-P(MeO2MA-co-DMAEMA), P]. TEM micrographs indicate that both P and PG possess distinct core-shell morphology and the average particle size of P (0.16 ± 0.08 μm) increases in PG (0.95 ± 0.45 μm). Fourier transform infrared and X-ray photoelectron spectrometry spectra suggest an interaction between -OH and -COOH groups of GQDs and -NMe2 groups of P. A decrease of the intensity ratio of Raman D and G bands (ID/IG) is noticed during GQD and PG formation. In contrast to GO, GQDs do not exhibit any absorption peak for its smaller-sized sp(2) domain, and in PG, the π-π* absorption of polythiophene (430 nm) of P disappears. The photoluminescence (PL) peak of GQD shifts from 450 to 580 nm upon a change in excitation from 270 to 540 nm. PL emission of PG at 537 nm is quenched, and it shifts toward lower wavelength (∼430 nm) with increasing aging time for energy transfer from P to GQDs followed by up-converted emission of GQDs. Both P and PG exhibit semiconducting behavior, and PG produces an almost reproducible photocurrent. Dye-sensitized solar cells (DSSCs) fabricated with an indium-titanium oxide/PG/graphite device using the N719 dye exhibit a short-circuit current (Jsc) of 4.36 mA/cm(2), an open-circuit voltage (Voc) of 0.78 V, a fill factor of 0.52, and a power conversion efficiency (PCE, η) of 1.76%. Extending the use of GQDs to fabricate DSSCs with polypyrrole, both Voc and Jsc increase with increasing GQD concentration, showing a maximum PCE of 2.09%. The PG composite exhibits better cell viability than the components.

Diethyleneglycol methylethermethacrylate(MeO2MA) and oligoethylene glycol methylethermethacrylate(OEGMA) are polymerized on polythiophene(PT) backbone to produce water‐soluble PT‐g‐PMeO2MA(PTD) and PT‐g‐P(MeO2MA‐co‐OEGMA)(PTDO) using atom transfer radical polymerization. They are characterized by 1H NMR and GPC techniques. TEM micrographs indicate that PT‐chains self‐organize as nanospheres, and atomic force micrographs suggest that aggregated PT‐chains are present at the centre surrounded by dispersed PMeO2MA fibers producing miceller‐type aggregates. Dynamic light scattering study indicates an initial decrease followed by sharp increase of Z‐average particle size of PTD with temperature for attaining lower critical solution temperature (LCST) at 20 °C. The LCST increases with OEGMA concentration in PTDO. The temperature dependent PL emission of PTD shows a minimum at 19 °C, followed by a sharp increase till 21 °C, and in the cooling cycle, it shows a complete reversibility. In the PTDO copolymers, the PL intensity shows the hike at progressively higher temperatures due to the increase of LCST with increasing OEGMA concentration. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013

A polythiophene based water soluble thermo and pH responsive graft copolymer is prepared by anchoring the initiator moiety (2-bromoisobutyryl bromide) on 3-thiophene ethanol and polymerizing using ferric chloride to produce the 2,5-poly(3-[1-ethyl-2-(2-bromoisobutyrate)]) thiophene macroinitiator (PTI), followed by polymerization with a mixture of varying composition of diethyleneglycol methylether methacrylate (MeO 2 MA) and N,N-dimethyl aminoethyl methacrylate (DMAEMA) at 30 uC using copper based atom transfer radical polymerization (ATRP). The polymers are characterized by gel permeation chromatography (GPC) and by 1 H NMR spectroscopy. Polythiophene-g-P(MeO 2 MA-co-DMAEMA) (PTDM) exhibits considerable water solubility but due to the lower critical solution temperature (LCST) of aqueous PMeO 2 MA at y26 uC the particle sizes observed by dynamic light scattering (DLS) show a sharp increase in the region 25-30 uC only for a pH value of 9.2. However, at lower pH values (pH 4 or 7), in the LCST region of PMeO 2 MA there is no increase of particle size. The TEM micrographs of PTDM indicate core-shell morphology at pH4 and pH7 with a gradual decreasing of the size (with PT at the core and P(MeO 2 MA-co-DMAEMA) at the shell), and at pH 9.2 no core-shell morphology is observed due to the absence of protonation at the -NMe 2 groups of the PDMAEMA segments. The fluorescence intensity of the PTDM solution at pH 9.2 also shows a sharp increase in the temperature range 22-29 uC, but remains almost without change at pH 4 and 7. Using the pH and temperature as inputs and the fluorescence intensity as an output, the system functions as a fully polymeric AND logic gate, and this is the first report using polythiophene as the fluorescence probe. Also PTDM in the solid/solution state exhibits considerable quenching of fluorescence intensities in the presence of nitroaromatics such as picric acid, dinitro phenol, etc. and may be used for sensing nitroaromatics.

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