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排序方式: 共有412条查询结果,搜索用时 15 毫秒
1.
Cyclic voltammetric studies of certain industrially potential iron chelate catalysts 总被引:1,自引:0,他引:1
For the analysis of infrared spectroscopic bands and complex patterns partial cross correlation functions of a sample spectrum
with reference spectra are calculated. The chosen ranges of the spectra are based on empirical knowledge of infrared spectrum
structure correlations. The normalised maxima of the partial cross correlation functions are interpreted as fuzzy truth values
and are combined by fuzzy logical operators. By application of that procedure larger common substructures will be derived
from the reference spectra than by a maximum common substructure search based on the complete spectra.
Received: 30 October 1996/Revised: 24 February 1997/Accepted: 26 February 1997 相似文献
2.
Basheer C Jayaraman A Kee MK Valiyaveettil S Lee HK 《Journal of chromatography. A》2005,1100(2):137-143
A novel sorbent, dihydroxylated polymethylmethacrylate (DHPMM), coated on hollow-fiber membrane, is used for the polymer-coated hollow-fiber microextraction of trace amounts of natural and synthetic estrogens, such as diethylstilbestrol, estrone, 17beta-estradiol and 17alpha-ethynylestradiol, in aqueous samples. In this procedure, estrogens were extracted using the functionalized polar DHPMM polymer with derivatization using N-methyl-N-(trimethylsilyl)trifluoroacetamide followed by gas chromatography-mass spectrometric analysis. The detection limits for estrogens in aqueous sample were between 0.03 and 0.8 ng l(-1) and the calibration curves were linear over the concentration range 0.05-10 microgl(-1) and had correlation coefficients of >0.994. The relative standard deviations (RSDs) were <15% (n = 3). This simple, accurate, sensitive and selective analytical method is applicable to the determination of trace amounts of estrogens in reservoir and potable water samples. 相似文献
3.
Cheung E Chong KC Jayaraman S Ramamurthy V Scheffer JR Trotter J 《Organic letters》2000,2(18):2801-2804
[reaction: see text] Four methods of asymmetric induction in the cis, trans-photoisomerization of 2beta, 3beta-diphenylcyclopropane-1alpha-carboxylic acid derivatives were studied. Best results (ca. 80% de) were obtained by irradiation of chiral esters, amides, and salts in NaY and LiY zeolites and in the pure crystalline state. 相似文献
4.
5.
Jayaraman Chandrasekhar Eluvathingal D. Jemmis Paul von Ragué Schleyer 《Tetrahedron letters》1979,20(39):3707-3710
The 3,5-dehydrophenyl cation (I), which may represent the structure of C6H3 ions observed mass spectroscopically, illustrates : two different aromatic systems in orthogonal planes. 相似文献
6.
Poly(alkyl aryl ether) dendrimers of up to four generations composed of a phloroglucinol core, branching components, and pentamethylene spacers are synthesized by a divergent growth methodology. A repetitive synthetic sequence of phenolic O-alkylation and O-benzyl deprotection reactions are adopted for the synthesis of these dendrimers. The peripheries of the dendrimers contain 6, 12, 24, and 48 phenolic hydroxyl groups, either in the protected or unprotected form, for the first, second, third, and fourth generations, respectively. Because of the presence of hydrophilic exterior and relatively hydrophobic interior regions, alkaline aqueous solutions of these dendrimers are able to solubilize an otherwise insoluble pyrene molecule and these supramolecular complexes precipitate upon neutralization of the aqueous solutions. 相似文献
7.
Ashton PR Balzani V Clemente-León M Colonna B Credi A Jayaraman N Raymo FM Stoddart JF Venturi M 《Chemistry (Weinheim an der Bergstrasse, Germany)》2002,8(3):673-684
Aliphatic amines, incorporating one or three (branched) acylated beta-D-glucopyranosyl residues, were coupled with the acid chloride of ferrocenecarboxylic acid and with the diacid chloride of 1,1'-ferrocenedicarboxylic acid to afford four dendrimer-type, carbohydrate-coated ferrocene derivatives in good yields (54-92%). Deprotection of the peracylated beta-D-glucopyranosyl residues was achieved quantitatively by using Zemplén conditions, affording four water-soluble ferrocene derivatives. When only one of the two cyclopentadienyl rings of the ferrocene unit is substituted, strong complexes are formed with beta-cyclodextrin in H2O, as demonstrated by liquid secondary ion mass spectrometry (LSIMS), 1H NMR spectroscopy, electrochemical measurements, and circular dichroism spectroscopy. Molecular dynamics calculations showed that the unsubstituted cyclopentadienyl ring is inserted through the cavity of the toroidal host in these complexes. The electrochemical behavior of the protected and deprotected ferrocene-containing dendrimers was investigated in acetonitrile and water, respectively. The diffusion coefficient decreases with increasing molecular weight of the compound. The potential for oxidation of the ferrocene core, the rate constant of heterogeneous electron transfer, and the rate constant for the energy-transfer reaction with the luminescent excited state of the [Ru(bpy)3]2+ complex (bpy = 2,2'-bipyridine) are strongly affected by the number (one or two) of substituents and by the number (one or three) of carbohydrate branches present in the substituents. These effects are assigned to shielding of the ferrocene core by the dendritic branches. Electrochemical evidence for the existence of different conformers for one of the dendrimers in aqueous solution was obtained. 相似文献
8.
In this work we investigate how a pattern imposed in a copolymer film at a certain distance from the surface propagates through the film onto an adsorbing heterogeneous surface. We bias the copolymer film to adopt a specified target pattern and then use simulation to design a surface pattern that helps the adsorbed film to maintain that target pattern. We examine the effect of varying the copolymer chain length, the size of the target pattern, and the distance from the surface where the target pattern is applied, z', on the extent of pattern transfer. For each chain length, target pattern, and z' we compare the energy of the system when a pattern is applied in the bulk to the energy when no pattern is applied in order to understand why a certain pattern size is transferred to the surface with higher fidelity than the others. At constant chain length, pattern transfer is best when the pattern size brings the energy of the system close to the energy when no pattern is applied. At constant pattern size, pattern transfer is best in the systems with longer chains. This is because longer chains are more likely to adsorb as brushes and loops which then helps transfer the pattern through the adsorbed film down to the surface. 相似文献
9.
Nithyanandhan J Jayaraman N Davis R Das S 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(3):689-698
A series of azobenzene-functionalized poly(alkyl aryl ether) dendrimers have been synthesized and their photochemical and photophysical properties in solution and as thin films have been investigated. Although the photochemical behavior of the azodendrimers in solution indicated that the azobenzene units behave independently, very similar to the constituent monomer azobenzene unit, the properties of thin solid films of the dendrimers were distinctly different. The azodendrimers, AzoG1, AzoG2, and AzoG3 were observed to form stable supercooled glasses, which showed long-wavelength absorption and red emission characteristics of J-aggregates of the azobenzene chromophores. Reversible photoinduced isomerization of the azodendrimers in the glassy state is described. 相似文献
10.
A new and highly efficient method for the C–N bond formation using molecular iodine-catalyzed N-alkylation reaction of tosylhydrazones with benzylic/benzhydryl alcohols at room temperature in methylene chloride is described. A variety of tosylhydrazones reacted readily with various substituted benzylic alcohols in presence of 20 mol % iodine under mild reaction conditions to produce the corresponding biologically active N-alkylated compounds in good to excellent yields. 相似文献