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81.
Jolly Andrews Vincent Mathew 《Physica C: Superconductivity and its Applications》2011,471(11-12):338-343
A high transition temperature superconducting microstrip structure is modeled using the theoretical approach developed by Coffey and Clem for elucidating the vortex effects in propagation. Impedance type Green’s functions are derived for the electric field around the strip and the propagation characteristics are computed for a wide range of applied field, reduced temperature and superconducting strip thickness in a Galerkin procedure. The increase of static field and temperature result in increased vortex motion, which in turn, causes a corresponding change in the propagation characteristics of the transmission line. Numerical results are presented for propagation parameters and quality factor. 相似文献
82.
Abstract Application of the method of orthogonal collocation to boundary value problems in structural and applied mechanics is investigated. Typical boundary value problems, such as the torsion of rectangular bars and the bending of plates, are employed as illustrative examples. Simplicity in application and good accuracy of orthogonal collocation are demonstrated by the solution of such complex problems as the large deflection analysis of rectangular isotropic, orthotropic, and sandwich plates. Results are compared wherever possible with existing solutions based on much more laborious and lengthy methods of computation. Excellent agreements are obtained. 相似文献
83.
Mathew W.C. Robinson 《Tetrahedron》2010,66(43):8377-8382
Epoxides undergo a highly efficient Meinwald rearrangement in the presence of catalytic quantities of copper(II) tetrafluoroborate to give carbonyl compounds in high yields and with excellent selectivity. The low toxicity and ease of handling of this reagent make it an attractive alternative to the more corrosive or costly Lewis acids frequently employed. 相似文献
84.
Thomas Mathew C. P. Joshua 《Journal of photochemistry and photobiology. A, Chemistry》1991,60(3):319-324
The photolysis of 2,2′-dinitrodiphenylmethylbenzoates (1a–1d) in 2-propanol gives dibenzo-[c, f]-[1,2]diazepin-11-one-oxides (5a–5d) as the major product. Dibenzo[c, f]-[1,2]diazepin-11-ones (2a–2d), 2,2′-dinitrobenzophenones (3a–3d), 2-amino-2′-nitrobenzophenones (4a–4d) and N-hydroxyacridones (6a–6d) are also formed in the reaction. When the irradiation is carried out in benzene, 3-(2′-nitrophenyl)-2,1-benzisoxazoles (7a–7d) are also obtained together with the above products. 相似文献
85.
86.
K. M. Mathew S. Ravi D. Padmanabhan 《Journal of Radioanalytical and Nuclear Chemistry》2005,265(3):505-506
Summary 4,6-dimethoxy-2-methylsulphonylpyrimidine is a key intermediate for the synthesis of pyrithiobac-sodium, a selective herbicide for cotton plant. 14C labeled pyrithiobac-sodium is required for studying the translocation and metabolism in cotton plants. It was prepared by oxidation of 4,6-dimethoxy-[2-14C]-2-methylmercaptopyrimidine with H5IO6/CrO3 in ethyl acetate at room temperature to give 4,6-dimethoxy-[2-14C]-2-methylsulphonylpyrimidine in high yields. 相似文献
87.
Mathew W.C. Robinson 《Tetrahedron letters》2006,47(33):5919-5921
Epoxides undergo a highly efficient and selective rearrangement in the presence of catalytic quantities of copper tetrafluoroborate to give carbonyl compounds in excellent yields. The low toxicity and ease of handling of this reagent make it an attractive alternative to the more corrosive Lewis acids frequently employed. 相似文献
88.
Lewis Acid Catalyzed Condensation–Cyclization Cascade: Direct Synthesis of Di/Trifluoromethyl‐1,2,3,4‐tetrahydroquinazolines 下载免费PDF全文
Prof. Dr. G. K. Surya Prakash Dr. Attila Papp Socrates B. Munoz Nathan May John‐Paul Jones Prof. Dr. Ralf Haiges Prof. Dr. Pierre Mothé Esteves Dr. Thomas Mathew 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(28):10170-10178
Condensed heterocycles such as quinazolines constitute the framework of many promising drugs. The great impact of the dramatic fluorine effect in pharmaceuticals prompted a great surge in the quest for fluorinated drug design resulting in over 20 % fluorine‐containing drugs in the market today. Therefore, finding an efficient and cost‐effective method for the direct synthesis of fluorine‐tagged quinazoline systems is of great significance in the pharmaceutical arena. For the first time, a one‐pot sequential condensation–cyclization reaction to form selectively the difluoro/trifluoromethylated tetrahydroquinazolines from simple components difluoro/trifluoroacetaldehyde hemiacetal and aromatic amines is reported. Our recent studies using difluoro/trifluoroacetaldehyde hemiacetal as simple and elegant difluoro/trifluoromethyl synthons and metal triflates such as gallium triflate as safe and stable Lewis acid catalysts led us to this direct synthesis protocol for the expedient and convenient synthesis of fluorinated quinazolines. DFT calculations at PCM/B3LYP/6‐31++G** were carried out for evaluating a possible reaction mechanism for this cyclization. According to the DFT calculations, product stereochemistry is thermodynamically driven, favoring the cis isomer as the major product, which is also confirmed experimentally. 相似文献
89.
Rory Campbell Dr. Martin F. Davis Mathew Fazakerley Dr. Peter Portius 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(51):18690-18698
The first charge‐neutral Lewis base adducts of tin(IV) tetraazide, [Sn(N3)4(bpy)], [Sn(N3)4(phen)] and [Sn(N3)4(py)2], and the salt bis{bis(triphenylphosphine)iminium} hexa(azido)stannate [(PPN)2Sn(N3)6] (bpy = 2,2′‐bipyridine; phen = 1,10‐phenanthroline; py = pyridine; PPN = N(PPh3)2) have been prepared using covalent or ionic azide‐transfer reagents and ligand‐exchange reactions. The azides were isolated on the 0.3 to 1 g scale and characterized by IR and NMR spectroscopies, microanalytical and thermal methods and their molecular structures determined by single‐crystal XRD. All complexes have a distorted octahedral Sn[N]6 coordination geometry and possess greater thermal stability than their Si and Ge homologues. The nitrogen content of the adducts of up to 44 % exceed any SnIV compound known hitherto. 相似文献