Search results for "RCA"
showing 10 items of 3171 documents
Laponite clay in homopolymer and tri-block copolymer matrices
2007
Macromolecule/laponite nanomaterials were studied by DSC and X-ray diffraction techniques. The matrices are poly(ethylene) glycols at various molecular masses and poly(ethylene oxides)-poly(propylene oxides)-poly(ethylene oxides) tri-block copolymers. The latter were tuned by modulating the molecular masses, at constant hydrophilic/hydrophobic ratio, and the hydrophilicity. For all the investigated systems, the enthalpy of melting (ΔH m) is nearly constant up to a given composition thereafter it increases monotonically reaching the value of the pure macromolecule. We proposed a model to interpret the DSC data. Briefly, it was invoked a mechanism of interaction following which some segments …
Effect of the orientation and rheological behaviour of biodegradable polymer nanocomposites
2014
Abstract The recent increasing interest towards biodegradable polymers has favoured the investigation on these systems, showing also their limits. On the other hand, the success achieved by nanocomposites has fostered the search for new systems where the polymer matrix is biodegradable. The final properties can depend on a number of factors, including the biodegradable polymer used as well as the nanosized filler, their mutual compatibility, the filler dispersion and the processing conditions. In this work, nanocomposites based on a starch-derived matrix and three different lamellar silicates were prepared, and the effects of the elongational flow on the dispersion, the improvement of inter…
Photoinduced and Self‐Activated Nuclease Activity of Copper(II) Complexes with N ‐(Quinolin‐8‐yl)quinolin‐8‐sulfonamide – DNA and Bovine Serum Album…
2016
Two CuII complexes with a new quinoline sulfonamide derivative and phenanthroline (phen), [Cu(QSQ)(phen)]ClO4·0.5H2O (1) and [Cu(QSQ)(phen)(H2O)]ClO4 (2) [HQSQ = N-(quinolin-8-yl)quinolin-8-sulfonamide], have been synthesized and physicochemically characterized. Single-crystal X-ray diffraction studies have revealed a highly distorted trigonal-bipyramidal structure for 1 (τ = 0.68) and an almost perfect trigonal-bipyramidal geometry for 2 (τ = 0.92). DNA binding studies, which were performed by thermal denaturation, viscometry, fluorescence spectroscopy, and cyclic voltammetry, indicated a partial intercalation of 1 with Kapp = 2.45 × 106 M–1. The nuclease activity of 1 was investigated upo…
Electrochemical monitoring of ROS generation by anticancer agents: the case of chartreusin
2017
Solution phase and solid-sate electrochemical techniques centered in the voltammetry of microparticles approach are applied for testing the cytotoxic activity of anticancer drugs. The possibility of electrochemical generation of reactive oxygen species (ROS) is exploited for evaluating their contribution to cellular damage. The described methodology is applied to the case of chartreusin (Ch) whose electrochemistry in non-aqueous solutions and in the solid state in contact with aqueous electrolytes is described in the absence (experimental data were confirmed by theoretical calculations) and in the presence of double-stranded DNA (dsDNA). In parallel, scanning electrochemical microscopy (SEC…
NonclassicalPschorr andSandmeyer Reactions in Pyrazole Series
2005
The diazonium salt derived from 4-amino-N,1,3-trimethyl-N-(3-methyl-1-phenyl-1H-pyrazol-5-yl)-1H-pyrazole-5-carboxamide (14) was reacted with a mixture of CuSO4 and NaCl, with ascorbic acid as an initiator to afford the planar derivative 4,6-dihydro-1,4,6,8-tetramethyl-3-phenyldipyrazolo[3,4-b:4′,3′-d]pyridin-5(3H)-one (16) and its unexpected isomer 4,6-dihydro-3,4,6,8-tetramethyl-1-phenyldipyrazolo[4,3-b:4′,3′-d]pyridin-5(1H)-one (17), as well as the epimers (3S,4S)- (or (3S,4R)-) and (3S,4R)- (or (3S,4S)-) 4-chloro-2,4-dihydro-1′,3′,5,5′-tetramethyl-2-phenylspiro[pyrazole-3,4′(1′H)-pyrrolo[3,4-c]pyrazol]-6′(5′H)-one (18a and b, respectively). Epimers 18a and b were converted under basic c…
Modulation of the Electronic Properties in Polydithienotiiophene Materials
1997
AbstractConjugated polymers with narrow band gap are promising candidates for symmetric electrochemical devices, such as electrochromics and redox supercapacitors, which involve the pand n-doped state of the polymer. Polydithienothiophene materials which are prepared from isomer monomers show this characteristic. The copolymerisation of two dithienothiophene isomers leads to materials whose electronic properties depend on the monomer ratio. Optical and electrochemical characterizations of different copolymers are reported and discussed.
Donor–Acceptor Polymers for Electrochemical Supercapacitors: Synthesis, Testing, and Theory
2014
Donor–acceptor polymers can store both a positive and negative charge allowing them to function as both the positive and negative charge storage material in a supercapacitor device, however few have been explored for this application. Here, we describe the synthesis of several donor–acceptor polymers and their electrodeposited polymer electrodes. We use differing molecular structures to examine the effect of electron acceptor concentration and show that device stability can be improved significantly by increasing the acceptor concentration. Further, we provide computational insight into the important chemical requirements for achieving even higher performance supercapacitors based on donor–…
A High‐Capacity Negative Electrode for Asymmetric Supercapacitors Based on a PMo 12 Coordination Polymer with Novel Water‐Assisted Proton Channels
2020
The development of a negative electrode for supercapacitors is a critical challenge for the next-generation of energy-storage devices. Herein, two new electrodes formed by the coordination polymers [Ni(itmb)4 (HPMo12 O40 )]·2H2 O (1) and [Zn(itmb)3 (H2 O)(HPMo12 O40 )]·4H2 O (2) (itmb = 1-(imidazo-1-ly)-4-(1,2,4-triazol-1-ylmethyl)benzene), synthesized by a simple hydrothermal method, are described. Compounds 1 and 2 show high capacitances of 477.9 and 890.2 F g-1 , respectively. An asymmetric supercapacitor device assembled using 2 which has novel water-assisted proton channels as negative electrode and active carbon as positive electrode shows ultrahigh energy density and power density of…
Lithium intercalation chemistry, microstructure and superconductivity in zirconium and hafnium nitride halides
2000
Abstract Lithium intercalation in β-MNX (M=Zr, Hf; X=Cl, Br) leads to superconducting compounds with critical temperatures between 12 and 24 K. The lithium uptakes after treatment of the host materials with n-butyllithium/hexane solutions are ca. 0.2 atoms per formula for β-ZrNCl and β-ZrNBr, and between 0.07 and 0.67 for β-HfNCl. Electrochemical lithiation experiments agree with the results obtained with chemical methods, as samples with larger capacity on discharge are also those having larger lithium contents after chemical lithiation. Variations exist in the electrochemical profiles of different batches for the three compounds indicating differences in the intercalation reaction pathway…
<title>Cerium-containing counter electrodes for transparent electrochromic devices</title>
1997
Films of Me-Ce oxide (Me: Ti, Zr, Sn, W) and of Ni-Ce hydroxide were produced by reactive magnetron co-sputtering. Li intercalation in Me-Ce oxide, and H exchange in Ni-Ce hydroxide, were accomplished electrochemically. Electrochromism was quenched in proportion with the Ce content in Me-Ce oxide. Films of Zr-Ce (and to some extent Ti-Ce) oxide were able to serve as fully transparent counter electrodes, of much interest for transparent electrochromic devices. In Ni-Ce hydroxide, the Ce addition enhanced the capacity for charge exchange.