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41.
42.
The quality of colour changes of the indicators hematoxylin, 4(2-pyridylazo)resorcinol (PAR), xylenol orange, pyrocatechol violet, chromazurolS and eriochrome cyanineR in the complexometric titration of copper(II) with ethylenediaminetetraacetic acid (EDTA) were studied with the help of tristimulus colorimetry, utilising a comparative study of the parameters SCD (specific colour discrimination), CIE La*b* 1976 and LABHNU 1977. Hematoxylin was found to be the best indicator among those studied. A screened indicator, viz. PAR + malachite green (52), was developed to enhance the quality of colour transition at the end-point and the accuracy of the titrimetric determination. 相似文献
43.
Simon G. Bott Duddu Raja Gopal Annavajhula Durga Prasad Alan P. Marchand 《Journal of chemical crystallography》1993,23(12):1013-1017
The structure of a compound derived from a symmetrical cage diketone in which one of the ketone C=O groups has been converted into a ketal is reported. An investigation into reasons for the selective functionalization resulted in the isolation of acis, cisoid, cis linear triquinane derivative in which both ketones are converted to ketals that share a transannular oxygen atom. Crystal data:2, monoclinic,P21/c,a=7.6298(9),b=7.673(3),c=22.125(3)Å,=97.59(1)°,V=1283.9(5)Å3, andR=0.048 (1001 reflections);4, triclinic,P¯1,a=7.3864(9),b=9.6362(9),c=10.3889(9)Å,=75.749(6),=76.300(8), =83.100(8)°,V=694.8(4)Å3, andR=0.088 (1284 reflections). 相似文献
44.
Gabapentin is an anticonvulsant drug used for the treatment of epilepsy. It is not bound to plasma protein and is not metabolized. A high performance liquid chromatography–mass spectrometric micro method is described in this report for its determination from human plasma. Chromatography was performed on a 50 × 4.6 mm, 4 μm nitrile column and the parent ion detected in the positive ionization mode on single quadrupole analyzer (Q1MI) with atmospheric pressure ionization source. Extraction was carried out on C18, 100 mg/3cc cartridge using 10 μL sample volume. The mean extraction recovery was 97% and within batch and between batch coefficients of variation were <9%. Lack of interference from endogenous substances helped in achieving a highly sensitive method without the need for monitoring fragment ions. The lowest concentration injected on column for calibration curve was 195 pg (range 0.5–64 ng). The method was applied for analysis of samples from a cross-over bio-equivalence study comparing two formulations. 相似文献
45.
The phosphorescence spectra of naphthalene-octafluoronaphthalene and durene-octafluoronaphthalene at 4.2 K reveal a localized exciton emission from octafluoronaphthalene, a weak intercomponent triplet-states quasi-resonance and a weak exciton-phonon coupling. 相似文献
46.
47.
K. Nagarajan M. Bhupathy Rajendra Prasad Ziley Singh V. Venugopal D.D. Sood 《Thermochimica Acta》1980,36(1):85-89
The thermal decomposition kinetics of Pr2(SO4)3 to Pr2O2SO4 have been studied by isothermal weight change determination. The reaction was found to obey a linear law up to α = 0.5; beyond α = 0.5 it could be described as a phase-boundary controlled process. A dependence of the activation energy upon the sample weight was observed. The changes in surface area and density which occur during the decomposition are also given. 相似文献
48.
The Raman phonon spectroscopic study shows that the photodimerization of 2,6-dimethyl-p-benzoquinone. In the solid state is initially a homogeneous reaction but later becomes heterogeneous as the product accumulates. The Ion-temperature electronic absorption spectrum reveals that the reaction is phonon assisted by a polaron formed due to a strong electron- phonon coupling in the cxcited 1nπ* state. 相似文献
49.
J. V. N. Vara Prasad 《Journal of heterocyclic chemistry》1996,33(6):1599-1603
A series of 2-aryl-4-hydroxy-5-thio substituted 1,3-thiazin-6-ones were synthesized for human immunodeficiency virus-1 protease inhibition. These compounds were synthesized by the treatment of 4-hydroxy-5-thio substituted-1,3-thiazin-6-ones with the corresponding sulfenyl chlorides. The products were obtained in good isolated yields, inspite of the presence of bulkyl substitutents at the ortho position of phenyl sulfenyl chloride portion. 相似文献
50.
Condensation of azetidinones 2a and 2b with mercaptan 3 gave respectively compound 10 or a 1:1 mixture of 17 and 17 ′. Bromination of 10 , afforded cis and trans-bromohydrins 13a and of 17 and 17 ′ cis and trans-bromohydrins 18a . Acetylation and reduction with zinc and acetic acid of these bromohydrins gave cephems 4a or 4b and 4b ′ respectively. 相似文献