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1.
Beeranahally H Doreswamy Madegowda Mahendra Hirihally C Devarajegowda Venkatesh B Devaru Sridhar M Anandalwar Javaregowda S Prasad 《Analytical sciences》2004,20(2):407-408
The title compound was extracted from a natural product and its structure was characterized by an X-ray diffraction method. It crystallizes in the tetragonal space group P41 with cell parameters a = 15.832(10)A, c = 11.622(10)A, Z = 4; the final residual factor is R1 = 0.0769. The structure has both intra and intermolecular hydrogen bonds. 相似文献
2.
Yiming Huai Mahendra PakalaZhitao Diao Dmytro ApalkovYunfei Ding Alex Panchula 《Journal of magnetism and magnetic materials》2006
Spin-transfer driven switching was observed in MgO based magnetic tunnelling junctions (MTJ) with tunnelling magnetoresistance ratio of up to 160% and the average intrinsic switching current density (Jc0) down to 2 MA/cm2, which are the best known results reported in spin-transfer switched MTJ nanostructures. Based on a comparison of results both from MgO and AlOx MTJs, further switching current decrease via MgO dual structures with two pinned layers is discussed. 相似文献
3.
Summary The kinetics of reduction of ruthenium(III) by sodium tetrahydroborate in aqueous acidic medium have been studied. The effect of variation in the concentration of substrate (RuCl3·3H2O), pH, and reductant (BH4
–1) has been studied. The activation parameters were evaluated. Based on a one-electron transfer, the mechanism involves the reduction of ruthenium(III) by hydrogen. 相似文献
4.
The effect of solar features on geospheric conditions leading to geomagnetic storms (GMSs) with planetary index,A
P ≥ 20 and the range of horizontal component of the Earth’s magnetic fieldH such that 250γ <H < 400γ has been investigated using interplanetary magnetic field (IMF), solar wind plasma (SWP) and solar geophysical data
(SGD) during the period 1978–99. Statistically, it is observed that maximum number of GMSs have occurred during the maximum
solar activity years of 21st and 22nd solar cycles. A peculiar result has been observed during the years 1982, 1994 when sunspot
numbers (SSNs) decrease very rapidly while numbers of GMSs increase. No distinct association between yearly occurrence of
disturbed days and SSNs is observed. Maximum number of disturbed days have occurred during spring and rainy seasons showing
a seasonal variation of disturbed days. No significant correlation between magnitude (intensity) of GMSs and importance ofH
α
, X-ray solar flares has been observed. Maximum number of GMSs is associated with solar flares of lower importance, i.e.,
SF during the period 1978-93.H
α
, X-ray solar flares occurred within lower helio-latitudes, i.e., (0–30)°N to (0–30)°S are associated with GMSs. NoH
α
, X-ray solar flares have occurred beyond 40°N or 40°S in association with GMSs. In helio-latitude range (10–40)°N to (10–40)°S,
the 89.5% concentration of active prominences and disappearing filaments (APDFs) are associated with GMSs. Maximum number
of GMSs are associated with solar flares. Coronal mass ejections (CMEs) are related with eruptive prominences, solar flares,
type IV radio burst and they occur at low helio-latitude. It is observed that CMEs related GMS events are not always associated
with high speed solar wind streams (HSSWSs). In many individual events, the travel time between the explosion on the Sun and
maximum activity lies between 58 and 118 h causing GMSs at the Earth. 相似文献
5.
Summary Reactions of titanium(IV) isopropoxide with ethyl 1-hydroxycyclohexylacetate, ethyl 2-hydroxy-2-arylpropionate, ethyl 2-hydroxy-2-arylbutyrate and ethyl 2-hydroxy-2-arylhydrocinnamate have been studied in dry benzene in different molar ratios under strictly anhydrous conditions. The Ti(OPr-i)4-nLn type compounds, where L = hydroxy ester and n = 1 to 4, have been isolated and characterised by elemental analysis, molecular weight, i.r. and n.m.r. spectral studies. These products may be distilled unchanged under reduced pressure.Reprints of this are not available. 相似文献
6.
The molybdenum complexes of Schiff base ligands viz. [MoO2LH2O] where L1 = tris(hydroxymethyl)(salicylide-neamino)methane, L2 = tris(hydroxymethyl)(2,3-dihydroxybenzylideneamino)methane and L3 = tris(hydroxymethyl)(2,3,4-trihydroxybenzylideneamino)methane have been synthesized and characterized by spectroscopic and electrochemical techniques. The X-ray crystal structure of the complex [MoO2L1H2O] reveals a distorted octahedral geometry with one ligand and a water molecule coordinated to the MoO2 center. No previous complex of this type contains a coordinated water molecule. The complex undergoes an oxotransfer in the presence of Bu3P to form a -oxobridged molybdenum(V,V) dimer. This rules out Mo—S coordination as a prerequisite for oxotransfer in such molybdenum(VI) complexes. 相似文献
7.
Patra S Sarkar B Ghumaan S Patil MP Mobin SM Sunoj RB Kaim W Lahiri GK 《Dalton transactions (Cambridge, England : 2003)》2005,(7):1188-1194
The isomeric title complexes were obtained in almost equimolar ratio from the reaction of Ru(trpy)Cl3 and L. Crystal structure analyses of the perchlorate hemihydrates, electrochemical and spectroscopic (NMR, UV/VIS, EPR) studies, supported by DFT calculations, reveal distinct differences between the isomeric redox series [1]n+(tetrazine-Nt trans to Cl) and [2]n+(pyrazolyl-Np trans to Cl; n= 0, 1, 2). The latter system with the pi acceptors trpy and tetrazine in the equatorial plane and the pyrazolyl and chloride donors in the axial positions exhibits facilitated oxidation, lower energy MLCT transitions, more balanced chelate coordination, and a higher g anisotropy in the oxidised (RuIII) state. According to partially resolved EPR spectra of one-electron reduced neutral compounds and they have the unpaired electron predominantly in the tetrazine ring of L. 相似文献
8.
Malcolm B. Polk Mahendra Nandu Metha Phingbodhipakkiya 《Journal of polymer science. Part A, Polymer chemistry》1986,24(8):1923-1931
The syntheses and characterizations of poly(oxy-trans-1,4-cyclohexyleneoxycarbonyl-1,4-bicyclo[2.2.2]octylenecarbonyl) (I) and poly(oxy-trans-1,4-cyclohexyleneoxycarbonyl-1,4-bicyclo[2.2.2]octylenecarbonyl-co-oxy-trans-1,4-cyclohexyleneoxysebacoyl) (II) are described. The polymer systems were characterized by infrared spectroscopy, proton magnetic resonance spectroscopy, solution viscosity, and differential scanning calorimetry. The random copolyester prepared from 1:0.65:0.35 mol of trans-1,4-cyclohexanediol, bicyclo[2.2.2]octane-1,4-dicarbonyl chloride, and sebacoyl chloride, respectively, formed a birefringent fluid state in the melt. 相似文献
9.
Summary 2-Aminopyridine reacts with acetylacetone in the presence of VOII, MnII, FeII, CoII, NiII, and CuII metal salts to give complexes of the type [VO(Ap2ac)2X]X and [M(Ap2ac)2X2] where (Ap2ac) is the ligand formedin situ. The complexes are characterised as distorted octahedral by analyses, conductance, molecular weight, magnetic, electronic and i.r. spectral studies. The i.r. studies reveal that two molecules of aminopyridine are joined by a molecule of acetylacetone through a three carbon atom bridge and that the ligand coordinates through the azomethine and imino nitrogen atoms, whereas pyridine does not take part in coordination. The electronic spectra have been interpreted and tentative assignments are made. In the far i.r. spectra, various metal ligand vibrations are observed and discussed. Attempts to carry out electrophilic substitutions in the complexes failed. 相似文献
10.
The viscosity deviation (Δη), the excess molar volume (V
E) and the ultrasonic speed (u) have been investigated from viscosity (η) and density (ρ ) measurements of binary liquid mixtures of 1,2-dimethyoxyethane with methanol, ethanol, propan-1-ol, butan-1-ol,
pentan-1-ol, hexan-1-ol or octan-1-ol over the entire range of composition at 298.15 K. The excess volumes are negative over
the entire range of composition for all of the mixtures with the exception of hexan-1-ol and octan-1-ol. The excess isentropic
compressibilities (K
S
E) and viscosity deviations are negative for all of the mixtures. The magnitudes of the negative values of V
E decrease with the number of carbon atoms of the alkan-1-ol. The trend of increasing K
S
E values with the chain length of the alkanol is similar to that observed in the case of V
E. Graphs of V
E, Δ η, K
S
E, Δ u, L
f
E and Z
E against composition are presented as a basis for a qualitative discussion of the results. 相似文献