Effective PET and ICT switching of boradiazaindacene emission: a unimolecular, emission-mode, molecular half-subtractor with reconfigurable logic gates

[reaction, structure: see text] We report a unimolecular system functioning as a combinatorial logic circuit for half-subtractor. The emission characteristics can be modulated by chemical inputs, and when followed at two different wavelengths, two functionally integrated logic gates XOR and INHIBIT are obtained. Both logic gates function in the emission mode, and with very large differences in the signal intensity allowing unequivocal assignment of logic-0 and logic-1.     

Ion sensing coupled to resonance energy transfer: a highly selective and sensitive ratiometric fluorescent chemosensor for Ag(I) by a modular approach

We report a novel dimeric boradiazaindacene dye which can be converted in one step to an efficient resonance energy transfer (RET) dyad. In addition, if this modification is done with appropriate ligands, RET can be coupled to ion sensing. The utility of this approach is demonstrated in a highly selective, emission ratiometric chemosensor for Ag(I).     

The effects of polyelectrolytes on the inhibition and aggregation of calcium oxalate crystallization

The influence of polyelectrolytes with different architecture on spontaneous batch crystallization of calcium oxalate was investigated. A series of acidic acrylate block copolymers were been made, by radical polymerization, with defined molecular weight and structure. Radical polymerization of acrylic acid (AA) was carried out in the presence of α‐thiopolyethylene glycol monomethylether as a chain transfer agent to produce poly(ethylene glycolblockacrylic acid) copolymers. Poly(ethylene glycol) (PEG) block length in the copolymers was controlled by using three different molecular weight chain transfer agents (M_n = 350, 750 and 2000 g/mol). The presence of copolymers inhibited the crystal growth of calcium oxalate possibly through adsorption onto the active growth sites for crystal growth due to the charge and hydrophilic effects. Copyright © 2006 John Wiley & Sons, Ltd.     

Investigation of proton conductivity of anhydrous proton exchange membranes prepared via grafting vinyltriazole onto alkaline‐treated PVDF

This work uses a simple “grafting through” approach in the preparation of anhydrous poly(vinylidene fluoride) (PVDF)‐g‐PVTri polymer electrolyte membranes (PEMs). Alkaline‐treated PVDF was used as a macromolecule in conjunction with vinyltriazole in the graft copolymerization. The obtained polymer was subsequently doped with triflic acid (TA) at different stoichiometric ratios with respect to triazole units and the anhydrous PEMs (PVDF‐g‐PVTri‐(TA)_x) were prepared. All samples were characterized by FTIR and ¹H NMR. The composition of PVDF‐g‐PVTri was determined by energy dispersive spectroscopy. Thermal properties of the membranes were examined by thermogravimetric analysis and differential scanning calorimetry. The surface roughness and morphology of the membranes were studied using atomic force microscopy, X‐ray diffraction, and scanning electron microscopy. PVDF‐g‐PVTri‐(TA)₃ (C3‐TA₃) with a degree of grafting of 47.22% showed a maximum proton conductivity of 0.09 S cm^?1 at 150 °C and anhydrous conditions. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 1885–1897     

Exact inversion of decomposable interval type-2 fuzzy logic systems

It has been demonstrated that type-2 fuzzy logic systems are much more powerful tools than ordinary (type-1) fuzzy logic systems to represent highly nonlinear and/or uncertain systems. As a consequence, type-2 fuzzy logic systems have been applied in various areas especially in control system design and modelling. In this study, an exact inversion methodology is developed for decomposable interval type-2 fuzzy logic system. In this context, the decomposition property is extended and generalized to interval type-2 fuzzy logic sets. Based on this property, the interval type-2 fuzzy logic system is decomposed into several interval type-2 fuzzy logic subsystems under a certain condition on the input space of the fuzzy logic system. Then, the analytical formulation of the inverse interval type-2 fuzzy logic subsystem output is explicitly driven for certain switching points of the Karnik–Mendel type reduction method. The proposed exact inversion methodology driven for the interval type-2 fuzzy logic subsystem is generalized to the overall interval type-2 fuzzy logic system via the decomposition property. In order to demonstrate the feasibility of the proposed methodology, a simulation study is given where the beneficial sides of the proposed exact inversion methodology are shown clearly.     

Pentagon Identities Arising in Supersymmetric Gauge Theory Computations

Theoretical and Mathematical Physics - The partition functions of three-dimensional N=2 supersymmetric gauge theories on different manifolds can be expressed as q-hypergeometric integrals....     

N,S-Substituted Dienes from Mono(arylthio)substituted- and S-, S,S-Substituted Dienes

Mono(thio)substituted dienes 1a-1b gave compounds 3a-c and 5d-g with piperazine and piperidine derivatives in dichloromethane. Compounds 8 , 9 , and 10 were obtained from the reactions of perchlorobutadiene ( 6 ) with 1,4-butanedithiol ( 7 ) in ethanol in the presence of sodium hydroxide. Compounds 12a-b , 13a-b were obtained from the reactions of perchlorobutadiene ( 6 ) with allylmercaptan (CH 2 =CH--CH 2 --SH) and mercaptoethanol (HO--CH 2 --CH 2 --SH).     

Novel anhydrous proton conducting copolymers of 1‐vinyl‐1,2,4‐triazole and diisopropyl‐p‐vinylbenzyl phosphonate

Phosphonic acid functional polymers are currently of interest because of their high proton conductivity in humidified and anhydrous systems. In addition, heterocyclic compounds are used in anhydrous proton conducting polymer membranes. In that study, a new copolymer based on 1‐vinyl‐1,2,4‐triazole (VTri) and diisopropyl‐p‐vinylbenzyl phosphonate (VBP) was synthesized, and their thermal, chemical, and proton conducting properties were investigated. The copolymers were synthesized by free radical copolymerization of the corresponding monomers at several monomer feed ratios to obtain P(VTri‐co‐VBP) copolymers. The copolymer samples were then hydrolyzed to produce poly(vinyl triazole‐co‐vinyl phosphonic acid) copolymers. The composition of the copolymers was determined by elemental analysis. The copolymerization and hydrolysis reactions were verified by Fourier transform infrared spectroscopy and ion exchange capacity measurements. Thermogravimetry analysis indicates that the copolymers are thermally stable up to 300°C. In order to increase the proton conductivity, the copolymers were doped with H₃PO₄ at several stoichometric ratios. The proton conductivity increases with triazole and phosphoric acid content. In the absence of humidity, the copolymer electrolyte, P(VTri‐co‐VBPA)1:0.5 X = 2, showed a proton conductivity of 0.005 S/cm at 150°C. Copyright © 2013 John Wiley & Sons, Ltd.     

Potassium Sensing by Using a Newly Synthesized Squaraine Dye in Sol-Gel Matrix

Squaraines are a group of fluorescent dyes and pigments derived from squaric acid and dialkylanilines well known in applications such as photoreceptors, organic solar cells, optical recording media, and non-linear optics. Their very promising spectral properties, long wavelength absorption and emission, and high absorptivity and quantum yields have not been exploited so far in relation to optical sensor design. They exhibit excellent solubility in sol-gel matrices, and the ligand is an integral part of the fluorophore system, which makes the molecule a fluoroionophore. In this work, potassium-sensing agent, bis[4-N-(1-aza-4,7,10,13,16-pentaox acyclooctadecyl)-3,5-dihydroxyphenyl] squaraine has been used for potassium sensing in a sol-gel matrix. The spectrofluorimetric response of dye-doped tetraethyl ortosilicate (TEOS) film after exposure to certain concentrations of K⁺ has been investigated, and 62% of relative signal change was achieved. The dynamic working range of the sensor membrane has been found between 10^–9 and 10^–6 M K⁺, in other terms from nanomolar to micromolar levels, which is an advantage over flame emission spectroscopy, in view of detection limit. The sensor is fully reversible within the dynamic range and the response time (₉₀) is found to be 2 min under batch conditions. The cross-sensitivity of the molecule to Na⁺, Ba²⁺, Ca²⁺, and NH⁺ ₄ was also tested in separate solutions.