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Treatment of 4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2,3-triazole-4-yl)-1,3,4-thiadiazoles with benzaldehyde,acetone and ω-bromoacetophenone was tested and compared.The title compounds Schiff bases,amides,imidazolo [2,1-b]-1,3,4-thiadiazoles and 7H-s-triazolo[3,4-b]-1,3,4-thiadiazines have been confirmed by elemental analyses,^1H NMR,IR and MS spectra.All the compounds have also been screened for their antibacterial activities against B.subtilis,S.aureus and E.coli. 相似文献
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标题化合物C23H26O4是水杨醛与5,6-二甲基-1,3-环己二酮在N,N-二甲基甲酰胺中反应而得。结果通过单晶X-射线衍射法确定,其晶体属于单斜晶系,空间群P21/c,a=7.056,b=20.263,c=13.665A,β=93.32,V=1950.7A^3,Mr=366.46,Dc=1.248g/cm^3,Z=4,μ(MOKα)=0.84cm^-1,F(000)=784。晶体结构用直接法解 相似文献
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3,4-反-4,5-反-2-氨基-3-氰基-1,3-二乙氧羰基-4,5-二(4-氯苯基)环戊烯 相似文献
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The novel structures of organometallic compounds 3-biaryl-1-ferrocenyl-2-propene-1-ones 5 were synthesized for nonlinear optical chromophores by Suzuki cross-coupling reaction.Their structures were determined with elemental analyses,^1H NMR spectra and ^13C NMR spectra. 相似文献
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4—取代苯基—6—甲基—5—硫代—1,2,4—三嗪—3—酮的合成 总被引:3,自引:0,他引:3
合成了一系列新的4,6-二取代-5-硫代-1,2,4-三嗪-3-酮类化合物,并用元素分析、IR、^1H NMR及MS对其结构进行了表征。 相似文献
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手性二噁唑啉吡啶铁和镍配合物的制备与表征 总被引:1,自引:0,他引:1
Tridentate bis(oxazolinylpyridine)(1) reacted with nickel chloride or ferrous chloride in anhydrous ethanol to form bis(oxazolinylpyridine) Nickel(Ⅱ) and Iron(Ⅱ) complexes. The stable solid complexes were characterized with IR, UV, MS, XPS and elemental analysis. No stable complexes were formed with bidentate bis(oxazoline)(2) ins- tead of bis(oxazolinylpyridine). 相似文献
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Synthesis of Mono- and Bis(silyl)hydroxylamines Silylamines reacts with hydroxylaminehydrochlorid to give the monosilylhydroxylamines: R2FSiONH2 (R = CMe3 1 ), R2R′SiONH2 (R = CMe3, R′ = Me 2 ), R2(NH2)SiONH2 (R = CMe3 3 ). The reaction of 1 in the present of HCl-acceptors or the reaction of lithiated 1 with Me3SiCl or F2Si(CMe3)2 leads to the formation of bis(silyl)hydroxylamines, (Me3C)2FSiONHSiMe3 4 , and (Me3C)2FSiONHSiF(CMe3)2 5 . The lithium derivatives of Me3SiONH2 and 2 react with fluorosilanes to the bis(silyl)hydroxylamines: Me3SiONHSiFRR′ (R = R′ = CMe3, 6 , R = CMe3, R′ = F 7 , R = R′ = NMeSiMe3 8 ), (Me3C)2MeSiNHOSiFRR′ (R = CMe3, R′ = F 9 , R = (Me3C)3C6H2, R′ = F 10 , R = R′ = CMe3 11 , R = R′ = CHMe2 12 ). The bis(silyl)hydroxylamines 4 and 6 are structure isomers. 相似文献
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以醋酸酐为溶剂, 将9, 9-二(4-羟基苯基)呫吨与浓硝酸在15 ℃左右发生硝化反应1.5 h, 形成中间体-9, 9-二(3-硝基-4-羟基苯基)呫吨, 产率为88.5%;继而以Pd/C 为催化剂, 80%的水合肼为还原剂, 在乙醇和1, 4-二氧六环混合溶剂中, 于70 ℃将中间体进行还原反应10 h, 得到目标产物9, 9-二(3-氨基-4-羟基苯基)呫吨, 产率为90.8%, 两步反应总收率为80.4%。 中间体与目标化合物经NMR、FTIR和元素分析等确定了它们的结构。 相似文献
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Molecular and Crystal Structure of the dimeric Magnesium bis[bis(trimethylsilyl)-amide] The magnesium bis[bis(trimethylsilyl)amide] crystallizes as a dimeric molecule in the space group C2/c with {a = 1821.0(4); b = 1494.4(4); c = 1859.6(6) pm; β = 121.10(2)°; Z = 4 dimers}. The cyclic planar Mg2N2 moiety shows endocyclic NMgN angles of 95.8°. The bond lengths within this ring system to the four-coordinate, bridging nitrogen atoms Nb are 215 pm, whereas the distances between the magnesium atom and the terminal, three-coordinate nitrogen atom Nt display values of approximately 198 pm. These different coordination numbers of the nitrogen atoms affect the NSi bond length (NtSi 171, NbSi 177 pm). 相似文献
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N. N. Aleinikov S. A. Kashtanov I. A. Pomytkin A. M. Sipyagin 《Russian Chemical Bulletin》1995,44(1):180-181
Bis(tetramethylammonium), bis(tetrabutylammonium), and bis(tetraphenylarsonium) dihydrohexaoxoxenonates(VIII) were obtained in an aqueous solution and in acetonitriie. The rate constants of their decomposition were determined.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 184–185, January, 1995.This work was carried out with financial support from the International Scientific Foundation (Grant REI 000). 相似文献
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Mats J. Sundell Esko O. Pajunen Osmo O. E. Hormi Jan H. Nsman 《Journal of polymer science. Part A, Polymer chemistry》1993,31(9):2305-2311
The synthesis of some divinyl monomers—bis(vinylphenyl)ethane ( 2 ), bis(vinylbenzyloxy)hexane ( 3a ), and bis(vinylbenzyloxy)dodecane ( 3b ) is reported. Copolymers of the new monomers and styrene were evaluated as an alternative to divinylbenzene-crosslinked polymers for use as matrices and absorbents. The mechanical properties and the amount of residual double bonds in the copolymers were compared. It was found that the new copolymers, unlike the divinylbenzene-crosslinked polymers, retained their mechanical strength even at high crosslinking degrees. Stress at break values of 79, 68, and 18 N/mm2 were found for the polymers crosslinked with 20 mol % of 3a, 2 , and divinylbenzene; 5, 25 and 45% of the divinyl units in these polymers were left as pendant double bonds. Porous styrene– 2 copolymers were synthesized and shown to have lower surface areas than the corresponding divinylbenzene-crosslinked polymers. The pore size distribution showed that this was due to the absence of the smallest pores which are found in the divinylbenzene-crosslinked polymers in between heavily crosslinked nodules. © 1993 John Wiley & Sons, Inc. 相似文献
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1 INTRODUCTION The coordination chemistry of the nitrogen-contai- ning diphosphine ligand bis(diphenylphosphino)ami- ne (Ph2PNHPPh2) has recently received much atten- tion because the P atoms can bridge metal centers in μ-bonding mode to form bi- or polynuclear complex- es[1~10]. It has been shown that the acidity of N–H proton would promote functionalization on the ligand backbone[4, 5, 11]. Although a few complexes contain- ing deprotonated tridentate Ph2PNPPh2 have been synthesi… 相似文献
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V. Percec M. Grigoras R. S. Clough J. Fanjul 《Journal of polymer science. Part A, Polymer chemistry》1995,33(2):331-344
The ability to achieve high molecular weight poly(ether ketone)s from the polycondensation of bis(aryl chloride)s with bis(phenolate)s has been consistently demonstrated. The polymerizations presented here help to delineate for specific bis(aryl chloride)/bisphenolate pairs the reaction conditions required to obtain high molecular weight polymers. Polycondensation of 1,3-bis(4-chlorobenzoyl)-5-tert-butylbenzene ( 6 ) and 2,2′-bis(4-chlorobenzoyl)-biphenyl ( 15 ) with various bisphenolates as well as of 2,2′-bis(4-hydroxyphenoxy)biphenyl ( 33 ) with 4,4′-dichlorobenzophenone ( 41 ) and 1,3-bis(4-chlorobenzoyl)benzene ( 43 ) were used as representative model systems to select reaction conditions that led to high molecular weight polymers. © 1995 John Wiley & Sons, Inc. 相似文献