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171.
James P. Kutney Eugene Dimitriadis Gary M. Hewitt Philip J. Salisbury Mahatam Singh James A. Servizi Dennis W. Martens Robert W. Gordon 《Helvetica chimica acta》1982,65(5):1343-1350
One of the fish-toxic chlorinated resin acids, 14-chlorodehydroabietic acid ( 5 ), found in kraft mill effluent is examined. When exposed to the fungus Mortierella isabellina, 5 is converted into a number of hydroxylated derivatives which show low levels of toxicity to fish. These biotransformation products were isolated and characterized. 相似文献
172.
The effect of buoyancy force on laminar boundary layer in two dimensional flow and heat transfer along a semi-infinite vertical surface, when the velocity of the on-coming stream oscillates in magnitude about a steady mean, is analysed. Two separate solutions valid for low and high frequency ranges are developed. It is found that for low frequency oscillations the phase angles of oscillatory components of skin friction and the rate of heat transfer increase as the Grashof number increases. For very high frequencies, the velocity field is of shear-wave type unaffected by the mean flow; the phase lead in the skin friction is, then, /4 and the rate of heat transfer fluctuation indicates a phase lag of /2 over that of the free stream oscillations.The authors are thankful to referee for many useful suggestions. 相似文献
173.
Virendra Singh Anita Rampal S. N. Biswas K. Datta 《Letters in Mathematical Physics》1980,4(2):131-134
The solution of a difference equation in the form of an infinite continued fraction is used to obtain a class of exact solutions for the eigenfunctions and eigenvalues of doubly anharmonic oscillators described by potentials of the type (1/2)2x2+(1/4)x4+(1/6)x6, n>0, provided certain constraints on the couplings are satisfied. The class is denumerably infinite but not complete. 相似文献
174.
Summary Amperometric ascorbimetric determinations of cerium(IV) and ferric iron have been carried out at 50°C with two polarized electrodes at 200 and 100 mV respectively. The results obtained are fairly accurate and precise within ±1.0 per cent. A simple method for successive determination of cerium and iron has been developed; and conditions for such estimations have been established. At an acidity of 2.5 M with respect to sulphuric acid, it is possible to ward off the reduction of ferric iron and thereby cerium(IV) is successfully titrated with ascorbic acid in this medium. After completion of the reaction and then lowering the acid concentration to pH 1.5 with aid of ammonium hydroxide, FeIII is titrated with standard ascorbic acid yielding good results. 相似文献
175.
S. P. Singh R. K. Vaid P. Dinakar Lukhvinder Singh 《Journal of mass spectrometry : JMS》1988,23(2):140-144
The fragmentation of 1-phenyl-, l-(2′-pyridyl)- and 1-(4′-methyl-2′-quinolyl)-4-acetoacetyI-3-methyIpyrazol-5-ols (compounds 1, 2 and 3, respectively) on electron impact has been studied and the major processes interpreted. The common feature in the mass spectra of these compounds is the loss of ketene, acetonyl radical, acetone and two molecules of ketene from the molecular ion. Whereas the ion generated after the last process, which corresponds to 1-substituted-3-methyIpyrazol-5-ols, loses methyl cyanide in the case of 1, similar ions in the case of 2 and 3 lose ?2HO moiety, necessitating an intramolecular hydrogen transfer followed by ring fission and subsequent loss of methyl cyanide. All these and other related processes have been substantiated with the help of accurate mass measurements of the fragment ions and B/E linked-scan spectra. 相似文献
176.
Summary Novel bimetallic alkoxides of copper(II) of the type Cu[M(OPr-i)6]2 (M = Nb or Ta) have been synthesised by the interaction of CuCl2 (1 mol) with K[M(OPr-i)6] (2 mol). These bimetallic isopropoxides undergo facile alcohol interchange with primary alcohols such as MeOH, EtOH,n-PrOH andn-BuOH. However, witht-BuOH, the reaction cannot be driven to completion even under prolonged continuous azeotropic fractionation of the liberatedi-PrOH and the final product corresponded in analysis to Cu[Ta(OPr-i)2(OBu-t)4]2.I.r., electronic and electron spin resonance spectral and magnetic susceptibility measurements indicate a distorted octahedralD
4h geometry for copper(II) in these bimetallic alkoxides. 相似文献
177.
N. S. B. Singh S. V. Mohan G. R. Balasubramanian 《Journal of Radioanalytical and Nuclear Chemistry》1979,52(2):319-327
A very sensitive extraction spectrophotometric method for the analysis of uranium based on the extraction of a uranium—benzoate—crystal
violet complex by a mixture of xylene and benzene is described. The absorbance maximum is at 606 nm and molar absorptivity
is 4.28·104 l·mol−1·cm−1. The interference due to a number of anions and cations studied without any pre-extraction was found to be within permissible
limits. The method has been used for determining uranium in a synthetic solution, i.e., uranium in the presence of various
other ions. The interference due to some cations was eliminated by the use of a masking agent (boric acid). 相似文献
178.
A silver selective electrode based on TEPQA‐MCM‐41 material was developed and used for the selective determination of Ag+ ion in various samples. The effect of various plasticizers i. e. dimethyl phthalate (DMP), Tris(ethylhexyl)phosphate (TEP), bis‐(2‐ethylhexyl)sebacate (BEHS), bis‐(2‐ethylhexyl)adipate (BEHA) was investigated. The electrode of the composition of 2 : 1 : 77 : 12 : 8 (w/w, %) of TEPQA‐MCM‐41 : NaTPB : Graphite powder : paraffin oil : DMP respectively, works satisfactorily in a wide concentration range of 1.3×10?9 M–1.0×10?1 M for Ag+ ion with a lower detection limit (LOD) of 1.0×10?9 M and has Nernstian slope of 63.4 1 mV/decay. The electrode can be used in a pH range of 2.3 to 6.7 for a period of 3 months without any divergence in potential response. The selectivity coefficient calculated by fixed interference method indicates the high selectivity of the electrode towards Ag+ ion over other tested cations. 相似文献
179.
Singh MK 《Photochemistry and photobiology》2000,72(4):438-443
Rotational reorientation times of a polar molecule neutral red (NR) have been measured in n-alkanes using steady-state fluorescence depolarization technique. The rotational dynamics of NR in alkanes is described by the Stokes-Einstein-Debye hydrodynamic theory with slip boundary condition. However, we have observed that as the size of the solvent molecule becomes bigger than the size of the solute molecule, the probe molecule experiences reduced friction and the experimentally measured reorientation times are shorter than those predicted by the hydrodynamic theory. These size effects have been analyzed using quasihydrodynamic theories. 相似文献
180.
Diastereoisomers (1S,2R,3S)-, (1R,2R,3S)-, (1R,2S,3S)- and (1S,2S,3S)-2-methyl-1-phenyl-1,3-butanediols were prepared by simple and convenient strategies using two different chemo-enzymatic approaches for the reduction of racemic 2-methyl-1-phenyl-1,3-butanedione, both involving in situ racemization. The first method comprised a one-pot microbial reduction coupled with a chemical reduction, while in the second method, stepwise chemo-enzymatic reductions were performed. 相似文献