共查询到20条相似文献,搜索用时 62 毫秒
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以苯磺酰肼为原料,在低温下滴加苯甲酰氯,方便地合成了7个1-苯甲酰-2-苯磺酰肼类化合物,收率40.3%~75.8%。其结构经1H NMR表征。 相似文献
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合成了11种未见文献报道的含苯乙腈母体的新型酰替芳胺类化合物,其结构经IR、^1HMR、元素等证实,并进行了室内平板杀菌活性试验。 相似文献
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XiaoLiang Wang LiYong Yuan YanFei Wang ZiJie Li JianHui Lan YaLan Liu YiXiao Feng YuLiang Zhao ZhiFang Chai WeiQun Shi 《中国科学:化学(英文版)》2012,55(9):1705-1711
Mesoporous silicas have a very attractive ability of sorption and enrichment of metal ions due to their huge surface area and facile functionalization by organic ligands.In this work,phosphonate-amino bifunctionalized mesoporous silica SBA-15(PA-SBA-15) as U(VI) sorbent was fabricated through post-grafting method.The obtained mesoporous silica was characterized by SEM,XRD,NMR and nitrogen sorption/desorption experiments,which revealed the existence of ordered mesoporous structure with uniform pore diameter and large surface area.The adsorptivity of PA-SBA-15 for U(VI) from aqueous solution was investigated using batch sorption technique under different experimental conditions.The preliminary results show that the U(VI) sorption by PA-SBA-15 is very quick with equilibrium time of less than 1 h,and the U(VI) uptake is as large as 373 mg/g at pH 5.5 under 95 ℃.The sorption isotherm has been successfully modeled by the Langmuir isotherm,suggesting a monolayer homogeneous sorption of U(VI) in PA-SBA-15.The sorption is pH-dependent due to the pH-dependent charge of sorbent in the aqueous solution.The thermodynamics research shows that the sorption is a feasible and endothermic process.Based on these results,PA-SBA-15 could be a promising solid phase sorbent for highly-efficient removal of U(VI) ions from waste water and enrichment of U(VI) from a solution at a very low level. 相似文献
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Fanbo SongJing Zhang Quanbin CuiTing Wang Wenbin ChenLuyuan Li Zhen Xi 《Tetrahedron letters》2012,53(9):1102-1104
Inositol phosphates regulate important biological functions in intracellular signal transduction events. Phosphonates, because of the stability towards the action of phosphatases, were extensively used to replace phosphates. We herein reported the synthesis of inositol phosphonate analogues using myo-inositol as the starting material, and found that two of phosphonate analogues exhibited relative good cytotoxic activity against non-small cell lung cancer (NSCLC) cell line A549. 相似文献
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Poly(styrene-co-diethyl vinylphosphonate) copolymers were synthesized by free radical copolymerization. The ester groups of the copolymers were hydrolyzed to phosphonic acid groups, and the sodium and zinc salts ionomers were obtained by neutralization. The structure and the thermal and viscoelastic properties of the copolymers and ionomers were characterized by nuclear magnetic resonance, Fourier transform infrared spectroscopy, differential scanning calorimetry, dynamic mechanical analysis, and small-angle X-ray scattering. The phosphonate ester lowered the glass transition temperature (Tg) of polystyrene. The free acid derivatives and metal phosphonates increased Tg and produced a rubbery plateau region in the viscoelastic properties due to the formation of a physical network. The acid and salt ionomers exhibited microphase-separated morphologies and were thermorheologically complex. The phosphonic acid derivatives absorbed relatively little water, even for materials with ion-exchange capacities greater than 1.0 mEq/g, and were not conductive, which made them unsuitable for application as proton exchange membranes. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3628–3641, 2004 相似文献
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When N-cyanoimido-( O,O-diethyl)phosphonyl/S-methyl thiocarbonate (1) was treated with o-phenylenediamine in the presence of Et3N in ethanol,diethyl benzimidazole-2-yl phos-phonate (2) was obtained and hydrolyzed during the recrys-tallization in MeOH/H2O,generating ethyl benzimidazole-2-yl phosphonate (3).Hie crystal structure of compound 3 was determined by X-ray diffraction method.The crystals belong to monoclinic,space group C2/c,a = 1.78408(18) ,6 = 0.83725(9),c= 1.67401(18) nm,β= 118.997(2),V = 2.1870(4) nm3,Z = 8,Dc=1.374 g/cm3,F(000)=944.The final R and wR are 0.0499 and 0.1436,respectively.The mechanism of the above reaction is also discussed. 相似文献
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Najmedin AziziMohammad R. Saidi 《Tetrahedron》2003,59(28):5329-5332
A very mild, efficient and simple method for the synthesis of tertiary α-amino phosphonates is reported by reaction of an aldehyde, a secondary amine and trialkylphosphite in ethereal solution of lithium perchlorate, LPDE, at ambient temperature with high yields. 相似文献
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Francis Ignatious Arjen Sein Israel Cabasso Johannes Smid 《Journal of polymer science. Part A, Polymer chemistry》1993,31(1):239-247
Carbamoyl phosphonate derivatives of methacrylic acid and α-methyl styrene were synthesized in good yield by reacting dimethyl and diethylphosphite with isocyanato ethylmethacrylate (IEM) or with meta-isopropenyl-α,α-dimethylbenzylisocyanate (m-TMI). The IEM derivatives yield soluble homopolymers with common radical initiators. The m-TMI carbamoyl phosphonates were copolymerized with styrene and with acrylates yielding soluble materials with better than 50 mol % incorporation of the phosphonate monomer. The side chain carbamoyl phosphonate group drastically lowers the Tg relative to those of the parent polymers. Thermogravimetric studies suggest the NHC(O)? P(O)(OR)2 bond to be stable to about 225°C. The radiopacifying salt UO2(NO3)26 H2O yields transparent films with the phosphonate-containing polymers. The Tg increases with uranyl content. © 1993 John Wiley & Sons, Inc. 相似文献
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