共查询到20条相似文献,搜索用时 0 毫秒
1.
2.
3.
4.
以3-甲基-4-对溴苯基-5-(2-吡啶基)-1,2,4-三氮唑作为配体(L),合成了1个新的锰配合物[MnL2(NCS)2],对其进行了红外、电喷雾质谱和单晶结构表征,该配合物属于单斜晶系,空间群P21/n,a=1.6480(2)nm,b=0.90707(13)nm,c=2.1919(3)nm,β=97.454(2)°,V=3.248 8(8)nm3,Z=4,R1=0.043 9。单晶结构表明,锰离子处于1个扭曲的八面体配位环境中,2个硫氰根离子呈顺式配位,每个配体L通过三氮唑上1个氮原子和吡啶上1个氮原子参与配位。 相似文献
5.
Niraj K. Ladani Manish P. Patel Ranjan G. Patel 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):658-662
A series of 3-(2-phenyl-6-(2-thienyl)-4-pyridyl)hydroquinolin-2-ones 4a–o were synthesized in high yields by a one–pot cyclocondensation reaction under Kröhnke's reaction conditions using 2-chloro-3-formyl quinoline 1a–c, 2-acetyl thiophene 2, and various N-phenacylpyridinium bromides 3a–e in a mixture of ammonium acetate and acetic acid by microwave irradiation. All the compounds have been characterized by elemental analysis, FT-IR, 1H NMR, and 13C NMR spectral analysis. These compounds have been screened for their antimicrobial activities. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献
6.
7.
8.
Adel A.-H. Abdel-Rahman Ahmed E.-S. Abdel-Megied Mohamed A. M. Hawata Eman R. Kasem Mohamed T. Shabaan 《Monatshefte für Chemie / Chemical Monthly》2007,16(6):889-897
Chalcones were synthesized by a base catalyzed Claisen-Schmidt condensation reaction. Bromination of chalcones afforded the dibromo derivatives. Monobromo derivatives could be obtained
by treating the corresponding dibromochalcones with dry benzene in the presence of triethylamine. Pyrazole derivatives were
obtained by refluxing of dibromochalcones with phenylhydrazine or 2,4-dinitrophenylhydrazine in dry pyridine. Chalcones were
treated with hydrazine hydrate or phenyl hydrazine in ethanol to afford Δ
2-pyrazolines and N-phenyl-Δ
2-pyrazolines. Condensation of chalcones with hydroxylamine hydrochloride or thiourea in ethanolic sodium hydroxide solution
gave 4,5-dihydroisoxazoles and 5,6-dihydropyrimidine-2-(1H)-thiones. The prepared compounds were tested for antimicrobial activity against four different bacterial species displaying
different degrees of antibacterial activities or inhibitory actions. 相似文献
9.
Gein V. L. Rubtsova D. D. Bobyleva A. A. Ryabova O. V. Novikova V. V. Kasimova N. N. Yankin A. N. 《Russian Journal of General Chemistry》2020,90(7):1222-1228
Russian Journal of General Chemistry - A series of novel 5-(het)aryl-3-hydroxy-1-hydroxyethyl-4-(thienyl-2-carbonyl)-3-pyrrolin-2-ones was synthesized by reacting methyl thienyl-2-carbonylpyruvate... 相似文献
10.
A Schiff base was synthesized by 3-methyl-4-amino-5-ethoxycarbonyl-methylsulfanyl-1,2,4-triazole with 3-nitrobenzaldehyde. The structure was confirmed by 1H NMR, IR, H RMS, TGA techniques and X-ray diffraction. The crystal belongs to monoclinic system, space group P21/c, with a = 8.965(2), b = 21.903(5), c = 9.197(2) A, β = 114.011(4)°, C14H15N5O4 S, Mr = 349.08, V = 1649.7(6) A3, Dc = 1.407 g·cm-3, Z = 4, F(000) = 728, μ = 0.226 mm-1, the final R = 0.0574 and wR = 0.1336 for 2932 unique reflections with I 2σ(I). Furthermore, the biological activity to four vegetable pathogens has been tested. The title compound exhibits better biological activity to four vegetable pathogens compared to the Schiff base without 5-ethoxycarbonyl and to Gibberlla saubinetti in EC95 compared with triadimefon. 相似文献
11.
12.
13.
Miguel F. Braa Jos M. Castellano Maria J. R. Yunta 《Journal of heterocyclic chemistry》1983,20(5):1403-1405
The title oxadiazoles were formed in the reaction of N-(4-pyridylmethyl)arylamides with nitrosyl chloride in low yields. 相似文献
14.
The title compound 2-(3-methyl-5-(methylthio)-4H-1,2,4-triazol-4-yl)isoindoline-1,3-dione(C12H10N4O2S, Mr = 274.30) has been synthesized by a three-step procedure including the cyclization, hydrazinolysis and substitution reactions, and its crystal structure was determined by X-ray single-crystal diffraction. The crystal belongs to the monoclinic system, space group P21/c with a = 12.264(3), b = 14.646(3), c = 14.349(4) , β = 91.69(3)°, μ = 0.255 mm-1, Mr = 274.30, V = 2576.2(10) 3, Z = 8, Dc = 1.414 g/cm3, F(000) = 1136, R = 0.0487 and w R = 0.1329 for 4048 observed reflections with Ⅰ 2σ(Ⅰ). In addition, the preliminary bioassay suggested that the title compound 6 exhibits relatively good antitumor activity against HT-29 and MCF-7. 相似文献
15.
2-(4-Pyridyl)-1,3,5-triazine, 2-(4-pyridyl)-4-methyl-1,3,5-triazine, 2-(4-pyridyl)-4,6-dimethyl-1,3,5-triazine and 2-(4-pyridyl)pyrimidine have been prepared by modification of established triazine and pyrimidine syntheses. These compounds and some of their relatives have been converted to quaternary pyridinium salts. The polarographic reduction potentials of the salts in aqueous solution are pH dependent. The activity of the salts as post-emergent herbicides is reported. 相似文献
16.
D. A. Tatarinov N. V. Terekhova A. D. Voloshina A. S. Sapunova A. P. Lyubina V. F. Mironov 《Russian Journal of General Chemistry》2018,88(9):1800-1805
New dialkyl(diaryl)-2-(5-chloro-2-hydroxyphenyl)-2-(phenylethenyl)pentylphosphonium salts bearing various substituents at the phosphorus atom were synthesized. Antimicrobial activity of the salts obtained was estimated. Derivatives with 2-methoxyphenyl substituents at the phosphorus atom are most active against grampositive bacteria. Herewith, dibenzyl-substituted phosphonium derivatives possess the best antifungal activity. 相似文献
17.
18.
The target compound(Z)-4-[3-(4-methyl-1,2,3-thiadiazol-5-yl)-3-(4-trifluoromethylphenyl)acryloyl]morpholine was synthesized by the nucleophilic substitution,Horner-Emmons reaction,ester hydrolysis,and condensation.Its structure was characterized by NMR,H RMS and single-crystal X-ray diffraction.The crystal of the target compound belongs to monoclinic system,space group P21 with a=11.5058(15),b=6.6626(10),c=23.184(3)?,V=1777.3(4)?3,Z=8,Dc=1.496 Mg/m3,F(000)=792 andμ=0.229 mm–1.X-ray analysis indicated C–H....O intermolecular H-bonds in this crystal structure.The target compound exhibited 53%curative activity against TMV. 相似文献
19.
Corts C. Eduardo Corts R. Eduardo Roberto Martínez Gustavo Avila Arturo Sandoval 《Journal of heterocyclic chemistry》1989,26(6):1561-1562
The preparation of several 5,4-disubstituted 3-methylisoxazoles is described. The structure of all products was corroborated by ir, 1H-nmr and mass spectrometry. 相似文献