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101.
M. V. Leena Chandra S. Karthikeyan S. Selvasekarapandian D. Vinoth Pandi S. Monisha S. Arulmozhi Packiaseeli 《Ionics》2016,22(12):2409-2420
A solid polymer blend electrolyte is prepared using poly(vinyl acetate) (PVAc) and poly(methyl methacrylate) (PMMA) polymers with different molecular weight percentage (wt%) of ammonium thiocyanate (NH4SCN) by solution casting technique with tetrahydrofuran (THF) as a solvent. The structural, morphological, vibrational, thermal and electrical properties of the prepared polymer blend electrolytes have been studied. The incorporation of NH4SCN into the polymeric matrix causes decrease in the degree of crystallinity of the samples. The complex formation between the polymer and salt has been confirmed by FTIR technique. The increase in T g with increase in salt concentration has been investigated. The maximum conductivity of 3.684?×?10?3 S cm?1 has been observed for the composition of 70PVAc/30PMMA/30 wt% of NH4SCN at 303 K. This value of ionic conductivity is five orders of magnitude greater than that of 70PVAc/30PMMA polymer membrane. Dielectric and transport studies have been done. The highest conducting polymer electrolyte is used to fabricate proton battery with the configuration Zn/ZnSO4·7H2O (anode) ||polymer electrolyte||PbO2/V2O5 (cathode). The open circuit voltage of the fabricated battery is 1.83 V, and its performance has been studied. 相似文献
102.
S. Sikkanthar S. Karthikeyan S. Selvasekarapandian Dorai Arunkumar Hellar Nithya Kawamura Junichi 《Ionics》2016,22(7):1085-1094
Poly (acrylonitrile) (PAN) and ammonium chloride (NH4Cl)-based proton conducting polymer electrolytes with different compositions have been prepared by solution casting technique. The amorphous nature of the polymer electrolytes has been confirmed by XRD analysis. The FTIR analysis confirms the complex formation of the host polymer (PAN) with the salt (NH4Cl). DSC measurements show a decrease in Tg with the increase in salt concentration. The conductivity analysis shows that the 25 mol% ammonium chloride doped polymer electrolyte has a maximum ionic conductivity, and it has been found to be 6.4 × 10?3 Scm?1, at room temperature. The temperature dependence of conductivity of the polymer electrolyte complexes appears to obey the Arrhenius nature. The activation energy (Ea = 0.23 eV) has been found to be low for 25 mol% salt doped polymer electrolyte. The dielectric behavior has been analyzed using dielectric permittivity (ε*), and the relaxation frequency (τ) has been calculated from the loss tangent spectra (tan δ). Using this maximum ionic conducting polymer electrolyte, the primary proton conducting battery with configuration Zn + ZnSO4·7H2O/75 PAN:25 NH4Cl/PbO2 + V2O5 has been fabricated and their discharge characteristics have been studied. 相似文献
103.
Balakrishnan Karthikeyan 《Journal of Sol-Gel Science and Technology》2008,45(1):79-82
Surface enhanced Raman scattering (SERS) studies have been undertaken on Ag doped sol–gel derived film with 7-azaindole (7-AI)
used as the reference compound. The enhancement factor in the film is comparable with the result of the chloride aggregated
silver citrate sol. Along with the spectral observation and assignments of the frequencies, the significance of colloidal
sol–gel film in which the size of the metal is in the dimensions of nanometers have been discussed. 相似文献
104.
Ammasai Karthikeyan Matthias Zeller Packianathan Thomas Muthiah 《Acta Crystallographica. Section C, Structural Chemistry》2016,72(4):337-340
Zinc thiocyanate complexes have been found to be biologically active compounds. Zinc is also an essential element for the normal function of most organisms and is the main constituent in a number of metalloenzyme proteins. Pyrimidine and aminopyrimidine derivatives are biologically very important as they are components of nucleic acids. Thiocyanate ions can bridge metal ions by employing both their N and S atoms for coordination. They can play an important role in assembling different coordination structures and yield an interesting variety of one‐, two‐ and three‐dimensional polymeric metal–thiocyanate supramolecular frameworks. The structure of a new zinc thiocyanate–aminopyrimidine organic–inorganic compound, (C6H9ClN3)2[Zn(NCS)4]·2C6H8ClN3·2H2O, is reported. The asymmetric unit consist of half a tetrathiocyanatozinc(II) dianion, an uncoordinated 4‐amino‐5‐chloro‐2,6‐dimethylpyrimidinium cation, a 4‐amino‐5‐chloro‐2,6‐dimethylpyrimidine molecule and a water molecule. The ZnII atom adopts a distorted tetrahedral coordination geometry and is coordinated by four N atoms from the thiocyanate anions. The ZnII atom is located on a special position (twofold axis of symmetry). The pyrimidinium cation and the pyrimidine molecule are not coordinated to the ZnII atom, but are hydrogen bonded to the uncoordinated water molecules and the metal‐coordinated thiocyanate ligands. The pyrimidine molecules and pyrimidinium cations also form base‐pair‐like structures with an R22(8) ring motif via N—H…N hydrogen bonds. The crystal structure is further stabilized by intermolecular N—H…O, O—H…S, N—H…S and O—H…N hydrogen bonds, by intramolecular N—H…Cl and C—H…Cl hydrogen bonds, and also by π–π stacking interactions. 相似文献
105.
Ti-loaded ZnO and Ti-loaded ZnO/ZnO nanoparticles have been synthesized by sol–gel method and analyzed for photocatalyst application. The phase confirmation was analyzed by powder XRD and surface morphology with HR-SEM and EDAX spectrum. The particle size measured using HR-TEM and SAED pattern confirms the crystalline nature of Ti-loaded ZnO and Ti-loaded ZnO/ZnO nanoparticles. The optical properties were studied with UV–visible diffuse reflectance spectra. The DRS of Ti-loaded ZnO/ZnO nanoparticles are similar to those of pristine ZnO nanoparticles. The KM plots show both the synthesized Ti-loaded ZnO/ZnO and Ti-loaded ZnO exhibit in UV-A region. The electric properties are studied with impedance analyzer, and the results show the charge-transfer resistance of Ti-loaded ZnO/ZnO is larger than that of Ti-loaded ZnO nanoparticles. The photocatalytic activity was studied with methylene blue dye and phenol degradation by Ti-loaded ZnO/ZnO, Ti-loaded ZnO, TiO2 and ZnO nanoparticles. The photocatalytic activity of Ti-loaded ZnO/ZnO nanospheres is slightly higher than that of other nanoparticles, which shows that they have excellent application as photocatalyst. 相似文献
106.
The aim of this study was to evaluate the gastroprotective efficacy of andrographolide isolated from Andrographis paniculata in rats induced with duodenal ulcers. Duodenal ulcers were induced by cysteamine administration in rats pretreated with 3?mg?kg?1 BW?day?1 of andrographolide for 30 days. Ulcer score, myeloperoxidase activity, TBARS level, GSH/GSSG ratio and enzyme antioxidants were measured in the duodenal tissue. Brush border and basolateral membranes were isolated to assay sucrase, maltase, alkaline phosphatase and total ATPases. Ulcer score was significantly minimised in rats pretreated with andrographolide. Elevation in myeloperoxidase and TBARS levels were found to be minimised significantly due to andrographolide treatment. Membrane-bound enzyme activities and the thiol redox status of glutathione were significantly maintained in duodenal mucosa of rats that received andrographolide. This study reveals that the major component of A. paniculata, andrographolide, has potent antiulcer properties that are most likely caused by minimising inflammatory changes, counteracting free radical formation and maintaining the thiol redox status in the duodenum. 相似文献
107.
The use of multi-dimensional “chemistry spaces” to represent large compound collections has become widespread in pharmaceutical
research. In such spaces compounds are treated as points. Points in close proximity represent similar compounds, while distant
points represent dissimilar compounds. Assessing the diversity of a compound collection, thus, is tantamount to characterizing
the distribution of points in chemistry space. To facilitate many procedures such as selecting subsets of compounds for screening,
for compound acquisition and designing combinatorial libraries, chemistry spaces have been partitioned into sets of non-overlapping,
multi-dimensional cells, which are generated by dividing each axis into a number of equal-sized bins. This leads to a lattice
of (Nbins)Ndim{(N_{bins})^{N_{\rm dim}}} cells, where N
bins
is the number of bins on each axis and N
dim is the dimensionality of the space. One diversity measure that is typically used in cell-based chemistry spaces is identical
in form to Shannon entropy, DNcpdcpd{D_{N_{cpd}}^{cpd}} A normalized measure of this Shannon entropy given by, Drelcpd{D_{rel}^{cpd}} enables comparison between compound collections that occupy different number of occupied cells. Although Drelcpd{D_{rel}^{cpd}} characterizes the uniformity and “spreadout” of the corresponding compound collection, it treats cells as positionally independent. Some of the positional information lost can be recaptured by another diversity measure, which is also related in form to
Shannon entropy. This new measure DNbincell (l){D_{N_{bin}}^{cell} (\lambda)} characterizes the distribution of occupied cells along each axis of chemistry space. The normalized measure
á Drelcell
ñ{\left\langle {D_{rel}^{cell}}\right\rangle} over all axes is given then by the average. Examples illustrating the applicability of these two Shannon-like measures to
compound collections are presented. 相似文献
108.
Weak, medium, and strong charge-transfer (CT) complexes containing various electron donors (C(2)H(4), C(2)H(2), NH(3), NMe(3), HCN, H(2)O) and acceptors (F(2), Cl(2), BH(3), SO(2)) were investigated at the CCSD(T)/complete basis set (CBS) limit. The nature of the stabilization for these CT complexes was evaluated on the basis of perturbative NBO calculations and DFT-SAPT/CBS calculations. The structure of all of the complexes was determined by the counterpoise-corrected gradient optimization performed at the MP2/cc-pVTZ level, and most of complexes possess a linear-like contact structure. The total stabilization energies lie between 1 and 55 kcal/mol and the strongest complexes contain BH(3) as an electron acceptor. When ordering the electron donors and electron acceptors on the basis of these energies, we obtain the same order as that based on the perturbative E2 charge-transfer energies, which provides evidence that the charge-transfer term is the dominant energy contribution. The CCSD(T) correction term, defined as the difference between the CCSD(T) and MP2 interaction energies, is mostly small, which allows the investigation of the CT complexes of this type at the "cheap" MP2/CBS level. In the case of weak and medium CT complexes (with stabilization energy smaller than about 15 kcal/mol), the dominant stabilization originates in the electrostatic term; the dispersion as well as induction and δ(HF) terms covering the CT energy contribution are, however, important as well. For strong CT complexes, induction energy is the second (after electrostatic) most important energy term. The role of the induction and δ(HF) terms is unique and characteristic for CT complexes. For all CT complexes, the CCSD(T)/CBS and DFT-SAPT/CBS stabilization energies are comparable, and surprisingly, it is true even for very strong CT complexes with stabilization energy close to 50 kcal/mol characteristic by substantial charge transfer (more than 0.3 e). It is thus possible to conclude that perturbative DFT-SAPT analysis is robust enough to be applied even for dative-like complexes with substantial charge transfer. 相似文献
109.
Karthikeyan B Pandiyarajan T Mangaiyarkarasi K 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2011,82(1):97-101
Optical properties of Ca doped ZnO nanoparticles prepared at room temperature through wet chemical method have been investigated. X-ray diffraction studies show that particles are crystalline in nature and doping did not induce impurity phases. Optical absorption measurements show an absorption peak at ∼372 nm which is due to excitonic absorption of the ZnO. Photoluminescence studies reveal a broad emission at an excitation wavelength of 335 nm and the bands are attributed to near band edge emission, oxygen vacancies, surface dangling bonds and zinc interstitials. Incorporating Ca2+ induces reduction in near band edge emission and there is an enhancement in the oxygen vacancy peaks which are attributed to the shape changes in the nanoparticles. 相似文献