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61.
Abdullah A. Al‐Karim Al‐Shara'ey 《中国化学会会志》2004,51(3):547-552
6‐Aryl‐5‐cyano‐4‐pyrimidinone‐2‐thion derivatives 1a‐c reacted with methyl iodide (1:2) to give the corresponding 2‐S,N‐dimethyl pyrimidine‐4‐one derivatives 2a‐c . Compounds 2a‐c were in turn, reacted with hydrazine hydrate to give the sulfur free reaction products 3a‐c . These reaction products were taken as the starting materials for the synthesis of several new heterocyclic derivatives. Reaction of 3a‐c with acetic anhydride and formic acid gave pyrimido triazines 4a‐c and 7a‐c , respectively. Their reactions with active methylene containing reagents gave the corresponding 2‐(1‐pyrazonyl)‐N‐methyl pyrimidine derivatives 9a‐c and 10a‐c , respectively. Their reactions with aromatic aldehydes afforded the corresponding 2‐hydrazono pyrimidine derivatives 11a‐c . The structure of these reactions products were established based on both elemental analysis and spectral data studies. 相似文献
62.
This work is a part of the systematic study of the ternary based chalcogenides systems. The aim is to determine the phase
equilibrium, and to determine the limits of the phase area. This is done in view to perfecting knowledge of elaboration conditions
for new materials and to study of their physical properties.
Few works have been devoted to the study of the ternary system Se-Te-Sn, only the cross section SnSe-SnTe has been studied
[1] and [2].
The experimental study by DTA, DSC and X-ray diffraction on powder performed at room temperature, exhibits a miscibility gap
in the liquid state which narrows as it goes through the Sn-Se binary system.
Three cross sections behave as ‘quasi-binary‘ system and six ternary invariants have been exhibited: three ternary eutectics
and three ternary quasi-peritectics.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
63.
Contreras Ricardo R. Fontal Bernardo Bahsas Alí Suárez Trino Reyes Marisela Bellandi Fernando Nava Flor Cancines Pedro 《Transition Metal Chemistry》2004,29(1):51-55
The synthesis of [benzyl-N,N-alkylbis(2-amino-1-cyclopentencarbodithioate)]MII [alkyl = ethene (L2) and propene, (L3) and M = Cu, Ni and Co] complexes and their characterization (u.v.–vis., FT-IR, 1H-n.m.r., mass spectra and cyclic voltametry) are reported. 相似文献
64.
E. D. Totchasov M. Yu. Nikiforov O. V. Eliseeva G. A. Al’per 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2006,80(10):1676-1679
This work presents the results obtained in measurements of the kinematic viscosity and density of the methanol-n-nonane, ethanol-n-nonane, and ethanol-n-decane systems at various temperatures and low n-alkane concentrations (within the concentration range of miscibility). The dynamic viscosities of these systems at 298.15 K were calculated according to free volume theory. The results substantiated the existence of an anomaly in the behavior of viscosity of the methanol-n-nonane system (positive Δlnη values) and its absence for the ethanol-n-alkane systems. 相似文献
65.
L. García Rodenas S. P. Alí S. J. Liberman 《Journal of Radioanalytical and Nuclear Chemistry》1990,141(2):289-294
The hydrogen isotope radiolytic yields, G(H2), G(HD) and G(D2) were determined in H2O/D2O mixtures under chemical conditions close to a LOCA in a PHWR like Atucha I Nuclear Station, that is 2·10–3 MH3BO3 and p(H+D)=8.5±0.2. The total hydrogen radiolytic yield G(H2+HD+D2) as a function of the deuterium atom fraction goes through a flat maximum at about 0.58. This result in dicates that the 4% flammability limit for hydrogen in the reactor's containment with be reached sooner than what is expected assuming a linear combination of pure H2 and D2 radiolytic yields. Hydrogen radiolytic production in 10–3 M KBr in H2O/D2O mixtures gives the same results as in the boric solutions suggesting a bimolecular B(OH)
4
–
+OH reaction. Identical isotope concentration factors were calculated for both solutions. 相似文献
66.
Mohammad Reza Ganjali Morteza HosseiniFatemeh Basiripour Mehran JavanbakhtOmid Reza Hashemi Majid Faal RastegarMojtaba Shamsipur Gerald.W Buchanen 《Analytica chimica acta》2002,464(2):181-186
A novel selective membrane electrode for determination of ultra-trace amount of lead was prepared. The PVC membrane containing N,N′-dimethylcyanodiaza-18-cown-6 (DMCDA18C6) directly coated on a graphite electrode, exhibits a Nernstian response for Pb2+ ions over a very wide concentration range (from 1.0×10−2 to 1.0×10−7 M) with a limit of detection of 7.0×10−8 M (∼14.5 ppb). It has a fast response time of ∼10 s and can be used for at least 2 months without any major deviation in potential. The electrode revealed very good selectivity with respect to all common alkali, alkaline earth, transition and heavy metal ions. The proposed sensor was used as an indicator electrode in potentiometric titration of lead ions and in determination of lead in edible oil, human hair and water samples. The proposed sensor was found to be superior to the best Pb2+-selective electrodes reported in terms of detection limit and selectivity coefficient. 相似文献
67.
The ion exchange between60Co2+ ions contained in residual radioactive water and zeolites of the NaA, NaX and CaA types was studied. The more advanced retaining of60Co2+ ions occurs for the NaA zeolite with the higher exchange capacity, as compared to NaX. With the CaA zeolite, a very weak ion exchange with60Co2+ ions was observed. 相似文献
68.
Fatemeh F. Bamoharram Majid M. Heravi Mina Roshani Ali Gharib Manouchehr Jahangir 《中国化学会会志》2007,54(4):1017-1020
Synthesis of aspirin at room temperature via O‐acetylation of salicylic acid in the presence of Preyssler type heteropolyacids has been investigated in order to contribute toward clean technology, which is the most important need of the society. All of the catalysts are recyclable and reusable. 相似文献
69.
Scheuermann JE Sibbons KF Benoit DM Motevalli M Watkinson M 《Organic & biomolecular chemistry》2004,2(18):2664-2670
A number of chiral unsymmetrically N-substituted 1,4,7-triazacyclononane ligands have been prepared by modular methods. The key step in the synthesis centres on the macrocyclisation of three tertiary amide precursors under standard Richman-Atkins conditions which allows for subsequent N-functionalisation. 相似文献
70.
Garcia Ruano JL Alemparte C Martin Castro AM Adams H Rodriguez Ramos JH 《The Journal of organic chemistry》2000,65(23):7938-7943
The behavior of (Z)-3-p-tolylsulfinylacrylonitrile (1) as a chiral dienophile has been evaluated from its reactions with furan and acyclic dienes. Electrostatic interactions of the cyano group with the sulfinyl one restrict the conformational mobility around the C-S bond, thus controlling the pi-facial selectivity, which is almost complete in all cases, the approach of the diene from the less-hindered face of the dienophile (that bearing the lone electron pair) in the predominant rotamer being the favored one. The regioselectivity is also completely controlled by the cyano group. Additionally, the reactivity of compound 1 as well as its endo-selectivity are both higher than those observed for the corresponding (Z)-3-sulfinylacrylates, thus proving the potential of sulfinylnitriles as chiral dienophiles. 相似文献