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61.
E.p.r. spectra of [Cu(et2dtc)2], Na[Cu(asp/glut)(et2dtc)] and Na2[Cu(asp/glut)(et2dtc)2] in the polycrystalline state have
been recorded and discussed. The complexes display an antiferromagnetic exchange interaction, increasing in the order: Na2[Cu(asp/glut)(et2dtc)2]
< Na[Cu(asp/glut)(et2dtc)] < [Cu(et2dtc)2]
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
62.
63.
64.
Summary Triisopropoxy bis(O,O-dialkyl dithiophosphates), (i-PrO)3M[S2P(OR)2]2 (M = Nbv, Tav; R = n-Pr, i-Pr, i-Bu and Ph) have been prepared by reacting the appropriate triisopropoxymetal(V)dichloride, (i-PrO)3MCl2 (1 mol) with sodium/ammonium dialkyl dithiophosphates (2 mols)in THF. The monomeric products which are viscous liquids, soluble in common organic solvents and highly susceptible to hydrolysis, were characterized by i.r. and n.m.r. spectra which indicate a bidentate mode of attachment of dithiophosphato groups to the metal. 相似文献
65.
Ghanshyam Pandey 《Tetrahedron letters》2005,46(12):2137-2140
The reactions of alkyl nitriles, acetyl chloride, aldehydes and β-ketoesters or simple ketones was studied for the one-pot synthesis of β-acetamido carbonyl compounds. It was observed that the reaction proceeds in the absence of Lewis acids. However, a Lewis acid catalyzes the reaction and several were tested. It was found that whereas Cu(OTf)2 is suitable for the coupling of β-ketoesters with aldehydes, Sc(OTf)3 is the best for ketones. A possible mechanism is proposed based on the isolation and characterization of an intermediate. 相似文献
66.
B. Pandey M. P. Mahajan R. K. Tikare M. Muneer N. P. Rath P. V. Kamat M. V. George 《Research on Chemical Intermediates》1991,15(3):271-291
The reaction of tetracyclone (1) with potassium in THF gave a mixture of benzoic acid (4), tetraphenylfuran (5) and cis-1,2-dibenzoylstilbene (6). The reaction of 1 with potassium in oxygen-saturated THF gave a mixture of 2-hydroxy-2,4,5-triphenyl-3(2H)furanone (3), 4, 5 and 6, whereas the reaction of 1 with potassium superoxide gave a moderate yield of 3,4,5,6-tetraphenyl-2-pyrartone (7), besides 3, 4, 5, and 6. The reaction of tetraphenylfuran (5) itself with potassium in THF gave a mixture of 6, 1,2,3,4-tetraphenylbutan-1-one (9), 2,3-diphenyl-1-indenone (10) and 2,3-epoxy-4-hydroxy-2,3,4-tnphenyltetralone-l (11), whereas practically no reaction occurred on treatment of 5 with potassium superoxide. Treatment of 10 with potassium in THF, however, gave a mixture of 4, dibenzo[a,c]-13-fluorenone (13), 2,3-diphenyl-2-hydroxyl-1-indanone (14) and 2,3-diphenylbenzofuran (15). A similar mixture of products consisting of 4, 13, 14 and 15 was obtained when the reaction of 10 with potassium was carried out in oxygen-saturated THF or when 10 was treated with potassium superoxide. Treatment of 2,3-diphenyl-2,3-epoxy-1-indanone (16) with potassium on the other hand, gave 10 in excellent yield. Cyclic voltammetric studies have been carried out to measure the reduction potentials of 1, 5, 10 and 16 in the generation of their radical anions. The radical anions of 1, 5, 10 and 16 were also generated pulse radiolytically in methanol and their spectra showed absorption maxima in the region 320–380 nm. 相似文献
67.
Jiao J Kanellopoulos J Wang W Ray SS Foerster H Freude D Hunger M 《Physical chemistry chemical physics : PCCP》2005,7(17):3221-3226
27Al spin-echo, high-speed MAS (nu(rot) = 30 kHz), and MQMAS NMR spectroscopy in magnetic fields of B0 = 9.4, 14.1, and 17.6 T were applied for the study of aluminum species at framework and extra-framework positions in non-hydrated zeolites Y. Non-hydrated gamma-Al2O3 and non-hydrated aluminum-exchanged zeolite Y (Al,Na-Y) and zeolite H,Na-Y were utilized as reference materials. The solid-state 27Al NMR spectra of steamed zeolite deH,Na-Y/81.5 were found to consist of four signals. The broad low-field signal is caused by a superposition of the signals of framework aluminum atoms in the vicinity of bridging hydroxyl protons and framework aluminum atoms compensated in their negative charge by aluminum cations (delta(iso) = 70 +/- 10 ppm, C(QCC) = 15.0 +/- 1.0 MHz). The second signal is due to a superposition of the signals of framework aluminum atoms compensated by sodium cations and tetrahedrally coordinated aluminum atoms in neutral extra-framework aluminum oxide clusters (delta(iso) = 65 +/- 5 ppm, C(QCC) = 8.0 +/- 0.5 MHz). The residual two signals were attributed to aluminum cations (delta(iso) = 35 +/- 5 ppm, C(QCC) = 7.5 +/- 0.5 MHz) and octahedrally coordinated aluminum atoms in neutral extra-framework aluminum oxide clusters (delta(iso) = 10 +/- 5 ppm, C(QCC) = 5.0 +/- 0.5 MHz). By chemical analysis and evaluating the relative solid-state 27Al NMR intensities of the different signals of aluminum species occurring in zeolite deH,Na-Y/81.5 in the non-hydrated state, the aluminum distribution in this material was determined. 相似文献
68.
B. N. Pandey 《Annals of the Institute of Statistical Mathematics》1979,31(1):225-233
Summary Consider a normal population with mean μ and variance σ2. We are interested in the estimation of population variance with the help of guess value σ
0
2
and a sample of observations. In this paper, a double stage shrinkage estimator
based on the shrinkage estimatorks
1
2
+(1-k)σ
0
2
ifs
1
2
∈R and the usual estimator
ifs
1
2
∋R, whereR is some specified region, have been proposed. The expressions for bias and mean squared error have been obtained. Comparison
with the usual estimators
2 have been made. It was found that though the largest gain is obtained fork=0, we can use
with 0≦k≦1/2 even when σ2 is very close to σ
0
2 相似文献
69.
Rina Chun Saegun Kim Sang Hoon Han Ashok Kumar Pandey Neeraj Kumar Mishra In Su Kim 《Tetrahedron letters》2018,59(43):3848-3852
The site-selective C–H nitration reaction of 7-azaindoles with t-butyl nitrite under palladium catalysis is described. This protocol provides an efficient method for the construction of ortho-nitrated N-aryl-7-azaindoles with excellent site-selectivity and functional group compatibility. The formed 7-azaindole derivatives can be readily transformed into 7-azaindoles containing an aniline functional group under palladium-catalyzed hydrogenation conditions. 相似文献
70.
A highly selective and sensitive electrochemical sensor has been developed by modification of a glassy carbon electrode (GCE) with graphene (GRP) for quantification of Rizatriptan. The significant increase of the peak current and the improvement of the oxidation peak potential indicate that the electrochemical sensor facilitates the electron transfer of Rizatriptan. The oxidation peak current was proportional to the Rizatriptan concentration in the range from 100 to 600 µg/mL with detection (LOD) and quantification limit (LOQ) of 36.52 and 121.73 µg/mL, respectively. The developed method was successfully employed for quantification of Rizatriptan in pharmaceutical formulations. The sensor shows great promise for simple, sensitive and quantitative detection of Rizatriptan. 相似文献