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91.
92.
Hamideh Ahankar Ali Ramazani Issa Amini Yavar Ahmadi Ali Souldozi 《Heteroatom Chemistry》2011,22(5):612-616
The reaction of (E)‐3‐aryl‐2‐propenoic acid derivatives with (N‐isocyanimino) triphenylphosphorane proceeds smoothly at room temperature to afford the corresponding 2‐[(E)‐2‐aryl‐1‐ethenyl]‐1,3,4‐oxadiazole via an intramolecular aza‐Wittig reaction in good yields under neutral conditions. The structures of the products were deduced from their IR, 1H NMR, and 13C NMR spectra and mass spectrometry. © 2011 Wiley Periodicals, Inc. Heteroatom Chem 22:612–616, 2011; View this article online at wileyonlinelibrary.com . DOI 10.1002/hc.20701 相似文献
93.
Davarani SS Najafi NM Ramyar S Masoumi L Shamsipur M 《Chemical & pharmaceutical bulletin》2006,54(7):959-962
Electrochemical oxidation of catechol and some 3-substituted catechols (1a--c) has been studied in the presence of 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (1a--c) participate in a Michael addition reaction with 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3) with consumption of only two electrons per molecule of (1a--c) to from the corresponding benzoforans (10a--c). The electrochemical synthesis of benzofurans has been successfully performed at a carbon rod electrode and in an undivided cell with high yields and purity. 相似文献
94.
Tarlani A Abedini M Nemati A Khabaz M Amini MM 《Journal of colloid and interface science》2006,303(1):32-38
The Keggin and Preyssler tungsten heteropolyacids, H3PW12O40 and H15P5W30O110, have been immobilized on the inner surface of mesoporous MCM-41, fume silica and silica-gel by means of chemical bonding to aminosilane groups. The materials were characterized by FT-IR spectroscopy, low-angle XRD and BET surface area analysis. The tendencies of heteropolyacids adsorption in solution on functionalized silicas have been investigated by UV-vis. Among the functionalized silica materials, MCM-41 showed the largest amine to silica and the least heteropolyacid to silica ratios. The BET surface area revealed that in all three cases the surface area decreased after grafting amine group and anchoring of the HPAs clusters. Low-angle XRD analysis showed that by introducing HPA into functionalized MCM-41 the intensity of the main reflection decreased significantly. 相似文献
95.
In continuation of our investigation of characteristics and thermodynamic properties of the i‐motif 5′‐d[(CCCTAA)3CCCT)] upon insertion of intercalating nucleotides into the cytosine‐rich oligonucleotide, this article evaluates the stabilities of i‐motif oligonucleotides upon insertion of naphthalimide (1H‐benzo[de]isoquinoline‐1,3(2H)‐dione) as the intercalating nucleic acid. The stabilities of i‐motif structures with inserted naphthalimide intercalating nucleotides were studied using UV melting temperatures (Tm) and circular dichroism spectra at different pH values and conditions (crowding and non‐crowding). This study indicated a positive effect of the naphthalimide intercalating nucleotides on the stabilities of the i‐motif structures compared to the wild‐type structure which is in contrast to a previous observation for a pyrene‐intercalating nucleotide showing a decrease in Tm values. 相似文献
96.
In this paper we introduce the notion of module character amenable Banach algebras and show that they possess module character virtual (approximate) diagonals. As a basic example, we show that for an inverse semigroup S with the set of idempotents E, the semigroup algebra ? 1(S) is module character amenable as an ? 1(E)-module if only if S is amenable. 相似文献
97.
S. Masoud Nabavizadeh Hashem Amini Fatemeh Jame Sedigheh Khosraviolya Hamid R. Shahsavari Fatemeh Niroomand Hosseini Mehdi Rashidi 《Journal of organometallic chemistry》2012
New cyclometalated platinum(II) complexes [PtMe(C^N)L], 1, in which C^N = deprotonated 2-phenylpyridine (ppy), benzo[h]quinoline (bhq) or 2-(p-tolyl)pyridine (tpy) and L = PPh3 or PMePh2, were synthesized by the reaction of [PtMe(C^N)(SMe2)] with 1 equiv of L. The reaction of complexes 1 with MeI gave the cyclometalated Pt(IV) complexes [PtMe2I(C^N)L], 3. On the basis of kinetic studies, using Uv–visible spectroscopy, it was suggested that the latter oxidative addition reactions were proceeded by an SN2 mechanism. The rates of the reactions at different temperatures were measured and consistent with the proposed mechanism, large negative ΔS3 values were found for each reaction. Besides, rate of reactions (in CHCl3) involving the PPh3 complexes [PtMe(C^N)(PPh3)], were almost 3–5 times slower than those involving the PMePh2 complexes [PtMe(C^N)(PMePh2)]. This was attributed to the electronic and steric effects of PPh3 ligand as compared with that of PMePh2 ligand which was further confirmed using density functional theory (DFT) calculations through finding approximate structures for the described complexes. 相似文献
98.
Nasir Iravani Jalal Albadi Somaieh Varnaseri Zahra Jaberi Nahid Karami Marzieh Khadamati 《中国化学会会志》2012,59(12):1567-1570
A simple and efficient one‐pot synthesis of alkyl 2‐(alkyl)‐4‐methyl‐2‐thioxo‐2,3‐dihydrothiazole‐5‐carboxylates from the reaction of primary alkylamines and carbon disulfide in the presence of 2‐chloro‐1,3‐dicarbonyl compounds is described. This new protocol has several advantages such as lack of necessity of the catalyst, good yields, mild conditions and short times for reaction. 相似文献
99.
100.
Masoud Salavati-Niasari Mahnaz Dadkhah Mohammad Reza Nourani Alireza Amini Fazl 《Journal of Cluster Science》2012,23(4):1011-1017
A simple thermal decomposition route has been developed to prepare single-phase cubic ZrO2 nanospheres by [Zr(sal)3(H2O)2](NO3) as the new precursor. The ZrO2 nanocrystals have been prepared by bis-aqua, tris-salicylaldehydato zirconium(IV) nitrate; [Zr(sal)3(H2O)2](NO3), as precursor in oleylamine (C18H37N) and triphenylphosphine (C18H15P). To control the particle size, combination of C18H37N and C18H15P were applied as surfactants. The C18H37N and C18H15P play an important role in preventing aggregation of ZrO2 nanocrystals. The products were characterized by X-ray diffraction, transmission electron microscopy, photoluminescence spectroscopy, and Fourier transform infrared (FT-IR) spectroscopy to depict the phase and morphology. The FT-IR spectrum showed the purity of obtained ZrO2 nanocrystals with cubic phase. 相似文献