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41.
Mohamed Mongi Ftini Mohamed Krifa Haddad Amor 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(8):i106-i108
The title compounds, potassium pentamolybdenum oxide, KMo5O13, and potassium niobate antimonate or potassium niobium antimony oxide (1/1.76/3.24), KNb1.76Sb3.24O13, were synthesized by solid‐state reactions and are isomorphous in space group Cmcm. The structure of the Mo complex has three unique Mo atoms and consists of MoO6 octahedra sharing edges to form Mo2O6 pairs and Mo3O9 triplets, which, in turn, form layers by sharing corners. These layers are linked together in the [100] direction, yielding a three‐dimensional network similar to that of KSb5O13. This framework delimits interconnected tunnels, running approximately along the [110] and [10] directions, in which K+ ions are located. In the isomorphous KNb1.76Sb3.24O13 structure, one of the Mo sites in KMo5O13 is replaced by Sb and the other two Mo sites have been replaced by Nb/Sb. 相似文献
42.
43.
Mohamed E. Khalifa 《合成通讯》2020,50(17):2590-2616
Abstract Thiophenes are a highly important group of heterocycles and have been of great interest to researchers due to their various reactivities. Many synthetic strategies are used to generate functionalized thiophene derivatives. Several reactions are described, depending on the reactivity of the substituents attached to the thiophene nucleus toward different nucleophiles to yield the versatile thiophene products. Many diverse applications have been utilized for thiophenes from medicinal chemistry to material science. 相似文献
44.
Mohamed Brakta Denis Sinou Michel Becchi Joseph Banoub 《Journal of mass spectrometry : JMS》1992,27(5):621-624
A series of anomeric unsaturated C-glycosides were studied by negative ion mass spectrometry following keV ion bombardment The compounds bearing an acidic hydrogen show a prominent [M ? H]? peak; in the other cases, the [M ? H]? peak is of very low intensity. A retro-Diels–Alder fragmentation and the abstraction of a hydrogen atom from the aglycon residue are observed in all cases. 相似文献
45.
N. A. Mohamed Farook 《Journal of solution chemistry》2007,36(3):345-356
The oxidation kinetics of substituted and unsubstituted 4-oxoacids (S) by N-chlorosaccharin (NCSA) have been studied in aqueous acetic acid media. The reaction follows first-order kinetics in each
of the 4-oxoacids, NCSA and H+. The effect of changes in the electronic nature of the substrate reveals that positive charge develops in the transition
state. Based on the kinetic results and product analysis, a suitable mechanism has been proposed for the reaction of NCSA
with 4-oxoacids. 相似文献
46.
Pierre Netchitaïlo Mohamed Othman Bernard Decroix 《Journal of heterocyclic chemistry》1997,34(1):321-324
2-Thienylthiomethylphthalimides 3a,b were synthesized by action of Chloromethylphthalimide on 2-or 3-mercaptothiophene. Reduction of 3a,b and Wittig reaction using carbethoxycarbonyltriphenyl-phosphorane gave the corresponding acetic acids 5a,b which cyclized under Friedel and Crafts conditions to lead the thienothiazocinoisoindolediones 6a,b. Thienothiazinoisoindolones 7a,b were obtained from hydroxyisoindolones derivatives 4a,b in acid conditions via an acyliminium ion. 相似文献
47.
Nonribosomal peptide synthetases (NRPS) are multimodular biocatalysts that bacteria and fungi use to assemble many complex peptides with broad biological activities. The same modular enzymatic assembly line principles are found in fatty acid synthases (FAS), polyketide synthases (PKS), and most recently in hybrid NRPS/PKS multienzymes. FAS as well as PKS are known to function as homodimeric enzyme complexes, raising the question of whether NRPS may also act as homodimers. To test this hypothesis, biophysical methods (size exclusion chromatography, analytical equilibrium ultracentrifugation, and chemical crosslinking) and biochemical methods (two-affinity-tag-system and complementation studies with enzymes being inactivated in different catalytic domains) were applied to NRPS subunits from the gramicidin S (GrsA-ATE), tyrocidine (TycB(1)-CAT and TycB(2-3)-AT.CATE), and enterobactin (EntF-CATTe) biosynthetic systems. These methods had revealed the dimeric structure of FAS and PKS previously, but all three NRPS systems investigated are functionally active as monomers. 相似文献
48.
Mohamed Brakta Paul Lhoste Denis Sinou Joseph Banoub 《Journal of mass spectrometry : JMS》1991,26(2):85-88
Electron impact mass spectra at 70 eV electron energy and chemical ionization mass spectra with ammonia as the reagent gas are reported for certain unsaturated C-glycosides. Comparisons are made between the mass spectra of anomeric pairs of these glycosides. 相似文献
49.
Ahmed A. El-Asmy Yehia M. Shaibi Abdallah S. Babaqi Mohamed Mounir Salah A. Ashour 《Transition Metal Chemistry》1988,13(5):332-335
Summary The interaction of 1-benzoin-4-phenylthiosemicarbazone (H2 BPS) with some transition metal ions has been investigated. The ligand can function as a tridentate chelating agent, giving M(HBPS)2 and M(BPS). Potentiometric studies proved that the mechanism of chelation is based on hydrogen ion liberation. Spectral studies in solution show that the ligand could be used for the microdetermination of CuIIions. On the basis of magnetic and spectral data, an octahedral structure is proposed for the CoII and NiII complexes and a square-planar structure for the CuII complex. The corrosion inhibition of aluminium in Cl3CCO2H using H2BPS is studied. The electrical conductivity of H2BPS and of its complexes have been measured. The ligand shows an activation energy in the range of semiconducting materials. The antimicrobial activity of all compounds has also been demonstrated. 相似文献
50.
Mohamed Zaki Barakat Mohamed Fathy Abdel-Wahab 《Monatshefte für Chemie / Chemical Monthly》1961,92(5):1061-1065
Zusammenfassung Die Reaktionen von Natrium-1,2-naphthochino-4-sulfonat mit -Aminosäuren, primären aliphatischen Aminen, Dicarbonsäuren, aliphatischen -Hydroxysäuren und primären Alkoholen werden beschrieben. In allen diesen Fällen reagiert Natrium-1,2-naphtochinon-4-sulfonat als Oxydationsmittel und wird zu dem entsprechenden Diphenol reduziert. 相似文献