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11.
Rashid A. Zeineh George Kyriakidis Roger Acey Christopher Smith 《Applied biochemistry and biotechnology》1986,13(2):119-125
Citrus tristeza virus (CTV) extracted from Etrog citron (C.medica L.) was immunoprecipitated. The immunoprecipitate was fractionated by SDS-PAGE and western blotted onto nitrocellulose. The CTV
antigens were determined by immunoblot analysis using rabbit anti-CTV IgG, and the protein-band pattern exhibited on the nitrocellulose
was assessed by soft-laser scanning densitometry. The densitometric tracing revealed the presence of bands that were not visible
to the naked eye. Using the superimposition mode of the instrument, it was also revealed that the protein-band patterns of
different CTV samples were not identical. Computer-aided soft-laser scanning densitometry proved to be a powerful approach
in the detection and assessment of protein bands revealed on nitrocellulose immunoblots, which we were previously unable to
do employing conventional methods. 相似文献
12.
M. H. Hashmi Ahmad Iftikhar Ajmal Abdur Rashid Tehseen Qureshi 《Mikrochimica acta》1969,57(1):100-107
Summary Cupric chloride-triphenylphosphine complex gives red color witho-phenylenediamine having maximum absorption at 505–520 nm and 0.5g/ml as visual limit of identification. The reaction is specific foro-phenylenediamine and obeys Beer's law (1 to 10g/ml). This reaction provides the basis of a new method for the Spectrophotometric determination ofo-phenylenediamine ing quantities.Ruthenium trichloride-triphenylphosphine complex gives blue color withp-phenylenediamine having maximum absorption at 580 nm and 2g/ml as visual limit of identification. On the basis of this color reaction a Spectrophotometric method for the determination ofp-phenylenediamine in hair dyes is described. The recovery of the dye from commercial preparations is better than 97%. Other organic compounds do not interfere.
Zusammenfassung Kupfer(II)chlorid-triphenylphosphin reagiert mito-Phenylendiamin unter Rotfärbung mit maximaler Absorption bei 505 bis 520 nm und 0,5g/ml als Erfassungsgrenze. Die Reaktion ist für o-Phenylendiamin spezifisch und folgt dem Beerschen Gesetz zwischen 1 und 10g/ml. Sie dient als Grundlage für eine neue Methode der spektrophotometrischen Bestimmung von Mikrogrammengen o-Phenylendiamin.Rutheniumtrichlorid-triphenylphosphin reagiert mit p-Phenylendiamin unter Blaufärbung mit maximaler Absorption bei 580 nm und 2g/ml als Erfassungsgrenze. Auf dieser Grundlage läßt sich p-Phenylendiamin in Haarfärbemitteln bestimmen. In handelsüblichen Präparaten werden mehr als 97% des enthaltenen Farbstoffes gefunden. Andere Verbindungen stören nicht.相似文献
13.
In the presence of triethylamine, 2-mercaptobenzoic acid readily adds onto acylhydrazonoyl chlorides (1a-c) (precursors of the reactive nitrile imine 1,3-dipolar species) to afford good yields of the corresponding 2-[(2-oxo-1-arylhydrazonopropan-1-yl)mercapto]benzoic acids (2a-c). The latter acyclic adducts, in THF in the presence of 1,1'-carbonyldiimidazole, undergo intramolecular cyclization involving the activated carboxy and the enol functionality to deliver the respective 2-(N-arylhydrazono)-3-oxobenzothiophenes (3a-c). In the solid state, the latter compounds adopt the (Z)-geometry around the C=N double bond as evidenced by single crystal X-ray structure determination for 3b. 相似文献
14.
Jalal A.?Zahra Bassam Abu?Thaher Mustafa M.?El-Abadelah Hans-Hartwig?OttoEmail author 《Monatshefte für Chemie / Chemical Monthly》2005,136(4):567-570
Summary. Nitrilimines prepared from N-arylhydrazono chlorides reacted with 2-mercaptonicotinic acid yielding the corresponding addition products, 2-[(2-oxo-1-arylhydrazonopropan-1-yl)mercapto] nicotinic acids, which were treated with 1,1-carbonyldiimidazole in THF affording by cyclocondensation the corresponding hitherto unknown 2-arylhydrazono-3-oxothieno[2,3-b]pyridines. 相似文献
15.
Rashid MA Gustafson KR Crouch RC Groweiss A Pannell LK Van QN Boyd MR 《Organic letters》2002,4(19):3293-3296
Poecillastrin A (1), a new polyketide-derived macrolide lactam, was isolated from a deep-water collection of the marine sponge Poecillastra species. The structure of poecillastrin A (1) was assigned using NMR data acquired at 500 MHz with an inverse-detection cryogenic probe and at 800 MHz with a room-temperature probe. 相似文献
16.
As copper(II) is a common ion in a variety of analytical samples, its effect on the stripping response of lead(II) at bismuth film screen-printed carbon electrode (BFSPCE) was investigated. The study was conducted using a screen-printed three-electrode system (working, counter and reference electrodes), with the carbon-working electrode plated in situ with bismuth film. Copper present at significant concentration level in samples was found to affect the sensitivity of the electrode by reducing the constant current stripping chronopotentiometric (CCSCP) response of lead(II). Recovery of the lead stripping response at the BFSPCE in the presence of copper was obtained when 0.1 mM ferricyanide was added to the test solution. The ferricyanide added circumvents the detrimental effect of copper(II) by selectively masking the copper ions by forming a complex. The analytical utility of the procedure is illustrated by the stripping chronopotentiometric determinations of lead(II) in soil extracts. 相似文献
17.
Proton NMR was used to study the complexation reaction between silver ion and hexathia-18-crown-6 in a number of binary mixed solvents of dimethyl sulfoxide with acetonitrile and methanol. Formation constants for the resulting 1:1 complexes in different solvent mixtures were determined by computer fitting of the chemical shift-mole ratio data. The influence of solvent composition on the stability of the resulting complex is discussed. The exchange kinetics of Ag+-hexathia-18-crown-6 in 70-30 wt.% dimethyl sulfoxide-acetonitrile and 75-25 wt.% dimethyl sulfoxide-methanol were studied by proton NMR line-shape analysis. In both solvent mixtures, the exchange of thiacrown ether between the free and complexed sites was found to proceed via a dissociative pathway. The exchange rates and the activation parameters E
a, H
, S, and G for the ligand exchange were determined and the influence of solvent properties on these parameters discussed. 相似文献
18.
The present paper describes the synthesis of 5‐azido‐6‐ketones (14) and 6‐hydroxy‐5‐ketone (20) from Hajos Wiechert ketone as chiral building blocks for cephalostatin analogues. The synthesis of symmetric cephalostatin analogue from 6‐hydroxy‐5‐ketone has also been reported. The characterization of the each synthesized compounds was carried out by IR, 1H‐NMR, 13C‐NMR and High resolution Mass Spectrometry. 相似文献
19.
Summary Isonicotinic acid hydrazide reacts with 2,3,5-triphenyltetrazolium chloride in acidic medium in presence of excess of thallium(III) to give a pink-coloured formazan having maximum absorption at 480 nm. This colour reaction is used to determine isonicotinic acid hydrazide in urine and blood. The reaction is specific for isonicotinic acid hydrazide, and the visual limit of identification is1
g per ml.
Zusammenfassung Isonikotinsäurehydrazid reagiert mit 2,3,5-Triphenyltetrazoliumchlorid in saurem Milieu bei Gegenwart von überschüssigem Thallium(III) unter Bildung eines rosa gefärbten Formazans mit dem Absorptionsmaximum bei 480 nm. Diese Farbreaktion wird zur Bestimmung von Isonikotinsäurehydrazid in Harn und Blut verwendet. Sie ist spezifisch. Ihre Erfassungsgrenze beträgt 1g/ml.
Résumé L'hydrazide de l'acide isonicotinique réagit avec le chlorure de triphényl-2,3,5 tétrazolium, en milieu acide en présence d'un excès de thallium-III, en donnant un formazan coloré en rose dont le maximum d'absorption se situe à 480 nm. On utilise cette réaction colorée pour doser l'hydrazide de l'acide isonicotinique dans l'urine et dans le sang. La réaction est spécifique et la limite d'identification visuelle est de 1g par ml.相似文献
20.
Kazi A. Azam Rahima Dilshad Shariff E. Kabir Rashid Miah Mohammad Shahiduzzaman Edward Rosenberg Kenneth I. Hardcastle Michael B. Hursthouse K. M. Abdul Malik 《Journal of Cluster Science》1996,7(1):49-70
The reaction of [Os3(CO)12] with tetramethylthiourea in the presence of a methanolic solution of Me3NO·2H2O at 60° yields the compounds [Os3(CO)11{η 1-SC(NMe2)2}] (1) in 56% yield and [Os3(CO)9(μ-OH)(μ-MeOCO){η 1-SC(NMe2)2}] (2) in 10% yield in which the tetramethylthiourea ligand is coordinatedvia the sulfur atom at an equatorial position. Compound2 is a 50 e? cluster with two metal-metal bonds and the hydroxy and methoxycarbonyl ligands bridging the open metal-metal edge. In contrast, the analogous reaction of [Os3(CO)12] with thiourea gives the compounts [(μ-H)Os3(CO)10{μ-NHC(S)NH2}] (3) in 8% yield and [(μ-H)Os3(CO)9{3-NHC(S)NH2}] (4) in 30% yield. In3, the thioureato ligand bridges two osmium atomsvia the sulfur atom, whereas in4 in addition to the sulfur bridge, one of the nitrogen atoms of thioureato moiety bonds to the remaining osmium atom. The decacarbonyl compounds 3 can also be obtained in 50% yield from the reaction of [Os3(CO)10(MeCN)2] with thiourea at ambient temperature. Compound3 converts to4 (65%) photochemically. Compound1 reacts with PPh3 and acetonitrile at ambient temperature to give the simple substitution products [Os3(CO)11(PPh3)] and [Os3(CO)11(MeCN)], respectively, while with pyridine, the oxidative addition product [(μ-H)Os3(CO)10(μ-NC5H4] is formed at 80°C. All the new compounds are characterized by IR,1-H-NMR and elemental analysis together with the X-ray crystal structures of1,2 and4. Compound1 crystallizes in the triclinic space group P $P\bar 1$ with unit cell parametersa = 8.626(3) Å,b = 11.639(3) Å,c = 12.568(3_ Å,α = 84.67(2)°,β = 75.36(2)°,γ = 79.49(3)°,V = 1199(1) Å3, andZ = 2. Least-squares refinement of 4585 reflections gave a final agreement factor ofR = 0.0766 (R w = 0.0823). Compound2 crystallizes in the monoclinic space group P21/n with unit cell parametersa = 9.149(5) Å,b = 17.483(5) Å,c = 15.094(4) Å,β = 91.75(2)°,V = 2413(2) Å3, andZ = 4. Least-squares refinement of 3632 reflections gave a final agreement factor ofR = 0.0603 (R w = 0.0802). Compound4 crystallizes in the monoclinic space group C2/c with unit cell parametersa = 13.915(7) Å,b = 14.718(6) Å,c = 17.109(6) Å,β = 100.44(3)°,V = 3446(5) Å3, andZ = 8. Least-squares refinement of 2910 reflections gave a final agreement factor ofR = 0.0763 (R w = 0.0863). 相似文献