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Sulfur phase and sulfur removal in high sulfur-containing bauxite 被引量:15
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作者 胡小莲 陈文汨 谢巧玲 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2011年第7期1641-1647,共7页
The sulfur phase in high sulfur-containing bauxite was studied by an X-ray diffraction analysis and a chemistry quantitative analysis.The methods for the removal of different shaped sulfur were also discussed.The resu... The sulfur phase in high sulfur-containing bauxite was studied by an X-ray diffraction analysis and a chemistry quantitative analysis.The methods for the removal of different shaped sulfur were also discussed.The results show that sulfur phases in high sulfur-containing bauxites exist in the main form of sulfide sulfur (pyrite) or sulfate sulfur,and the main sulfur forms of bauxites from different regions are not the same.Through a combination of an X-ray diffraction analysis and a chemistry quantitative analysis,the sulfur phases of high sulfur-containing bauxite could be accurately investigated.Deciding the main sulfur form of high sulfur-containing bauxite could provide theoretical instruction for choosing methods for the removal of sulfur from bauxite,and an oxidizing-roasting process is an effective way to remove sulfide sulfur from high sulfur-containing bauxite,the content of S^2-in crude ore in the digestion liquor is above 1.7 g/L,but in the roasted ore digestion liquor,it is below 0.18 g/L.Using the sodium carbonate solution washing technology to wash bauxite can effectively remove sulfate sulfur,the content of the total sulfur in ore is lowered to below 0.2% and can meet the production requirements for the sulfur content. 展开更多
关键词 high sulfur-containing bauxite sulfur phase oxidizing-roasting sodium carbonate solution washing technology
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Highly Efficient and Selective Removal of Pb(II) ions by Sulfur-Containing Calcium Phosphate Nanoparticles 被引量:1
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作者 龚成云 耿志刚 +3 位作者 董安乐 叶新新 汪国忠 张云霞 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2016年第5期607-616,I0002,共11页
A facile one-step co-precipitation method was demonstrated to fabricate amorphous sulfurcontaining calcium phosphate (SCP) nanoparticles, in which the sulfur group was in-situ introduced into calcium phosphate. The ... A facile one-step co-precipitation method was demonstrated to fabricate amorphous sulfurcontaining calcium phosphate (SCP) nanoparticles, in which the sulfur group was in-situ introduced into calcium phosphate. The resulting SCP exhibited a noticeable enhanced performance for Pb(II) removal in comparison with hydroxyapatite (HAP), being capable of easily reducing 20 ppm of Pb(II) to below the acceptable standard for drinking water within less than 10 min. Remarkably, the saturated removal capacities of Pb(II) on SCP were as high as 1720.57 mg/g calculated by the Langmuir isotherm model, exceeding largely that of the previously reported absorbents. Significantly, SCP displayed highly selective removal ability toward Pb(II) ions in the presence of the competing metal ions (Ni(II), Co(II), Zn(II), and Cd(II)). Further investigations indicated that such ultra-high removal efficiency and preferable affinity of Pb(II) ions on SCP may be reasonably ascribed to the formation of rodlike hydroxypyromorphite crystals on the surface of SCP via dissolution-precipitation and ion exchange reactions, accompanied by the presence of lead sulfide precipitates. High removal efficiency, fast removal kinetics and excellent selectivity toward Pb(II) made the obtained SCP material an ideal candidate for Pb(II) ions decontamination in practical application. 展开更多
关键词 sulfur-containing calcium phosphate Pb(II) ions Selective removal
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A review of gold extraction using noncyanide lixiviants: Fundamentals, advancements, and challenges toward alkaline sulfur-containing leaching agents 被引量:12
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作者 Chun-bao Sun Xiao-liang Zhang +1 位作者 Jue Kou Yi Xing 《International Journal of Minerals,Metallurgy and Materials》 SCIE EI CAS CSCD 2020年第4期417-431,共15页
Alkaline sulfur-containing lixiviants,including thiosulfate,polysulfides,and alkaline sulfide solutions,stand out as a promising class of alternatives to cyanide because of their low toxicity,high efficiency,and stron... Alkaline sulfur-containing lixiviants,including thiosulfate,polysulfides,and alkaline sulfide solutions,stand out as a promising class of alternatives to cyanide because of their low toxicity,high efficiency,and strong adaptability.In this paper,we summarized the research progress and remaining challenges in gold extraction using these noncyanide reagents.After a brief introduction to the preparation method,the transformation process of various sulfur-containing species in alkaline solutions was discussed.Thereafter,some insights into the mechanism of gold leaching in alkaline sulfur-containing solutions were presented from different aspects,including thermodynamics analysis,electrochemical dissolution,and leaching kinetics.Moreover,recent progress in in-situ generation of sulfur-containing anions from gold-bearing sulfide minerals was outlined as well.Gold passivation caused by sulfur species was discussed in particular because it is considered the greatest challenge facing sulfur-containing leaching systems.Alkaline sulfur-containing lixiviants are expected to serve as alternatives in industrial applications of gold extraction,particularly for refractory gold ores containing copper and carbonaceous matter. 展开更多
关键词 GOLD extraction sulfur-containing lixiviants degradation in-situ generation PASSIVATION
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pH variation mechanism of high sulfur-containing bauxite 被引量:2
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作者 陈兴华 胡岳华 +2 位作者 李旺兴 陈湘清 曹学锋 《Journal of Central South University》 SCIE EI CAS CSCD 2015年第8期2909-2913,共5页
In order to fundamentally solve the acidification problem of high sulfur-containing bauxite during storage, by simulating the environment of minerals storage in laboratory, the acidification mechanism and influencing ... In order to fundamentally solve the acidification problem of high sulfur-containing bauxite during storage, by simulating the environment of minerals storage in laboratory, the acidification mechanism and influencing factors of high sulfur-containing bauxite were studied and confirmed using the single variable method to control the atmosphere, water and other variables. The results show that the acidification is mostly caused by the oxidation of sulfur-containing bauxite, which is mainly the natural oxidation of Pyrite(Fe S2), then the alkaline minerals dissolute in the presence of water, leading to the acidification phenomenon, which is influenced by moisture and air flow. Finally, more acid-producing substances are formed, resulting in the acidification of high sulfur-containing bauxite. The acidification of high sulfur-containing bauxite results from the combined effect of the oxygen in the air and water, which can be significantly alleviated by controlling the diffusion of the oxygen in air. 展开更多
关键词 high sulfur-containing bauxite PYRITE acidification mechanism
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Synthesis and Characterization of New Schiff Bases Formed by Condensation of 2,9-Phenathroline-1,10-dialdehyde with Sulfur-Containing Amines 被引量:2
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作者 Md. Arifuzzaman Mohammad R. Karim +2 位作者 Tasneem A. Siddiquee Aminul H. Mirza Mohamad A. Ali 《International Journal of Organic Chemistry》 2013年第1期81-86,共6页
Four new Schiff bases of 1,10-phenanthroline-2,9-dicarboxaldehyde with sulfur-containing amines such as 2-mercaptoaniline, S-alkyl/aryl dithiocarbazates and thiosemicarbazide have been synthesized and characterized by... Four new Schiff bases of 1,10-phenanthroline-2,9-dicarboxaldehyde with sulfur-containing amines such as 2-mercaptoaniline, S-alkyl/aryl dithiocarbazates and thiosemicarbazide have been synthesized and characterized by spectroscopic and X-ray crystallographic techniques. A comparative study of the methods of synthesis has been made using both traditional and microwave techniques. A significant reduction in reaction time has been observed when the microwave method was used. In some of the reactions, the yields also increased significantly. 展开更多
关键词 PHENANTHROLINE SCHIFF Base Dithiocarbazide sulfur-containing Antibaterial
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QSPR Study on the Boiling Points of Some Oxygenand Sulfur-containing Organic Compounds 被引量:1
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作者 陈建挺 刘红玲 +2 位作者 王甫洋 于红霞 李定龙 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第12期1561-1568,共8页
Structural and thermodynamic parameters of 56 oxygen-containing and 56 sulfur- containing organic compounds were computed at the B3LPY/6-311G** level using density functional theory (DFT) method. Furthermore,the d... Structural and thermodynamic parameters of 56 oxygen-containing and 56 sulfur- containing organic compounds were computed at the B3LPY/6-311G** level using density functional theory (DFT) method. Furthermore,the dependent equations between the experimental data of boiling points (Tb) and theoretical parameters were proposed with SPSS12.0 for windows software,whose correlation coefficients R2 are 0.933 and 0.945. These dependent equations were validated by cross-validation method (q2 are 0.923 and 0.929,respectively). VIF (variance inflation factors) and t-value methods were also used to verify the significance and self-correlationship of each variable. Results indicate that our dependent equation exhibits good prediction ability,and molecular polarizability (α) is the main factor affecting the Tb of oxygen- and sulfur-containing organic compounds. To our interest,obvious dependence could also be found among the oxygen- and sulfur-containing organic compounds' experimental data of boiling points (Tb) with R^2 of 0.857. 展开更多
关键词 boiling points oxygen-containing organic compounds sulfur-containing organic compounds quantitative structure-property relationship (QSPR) DFT
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Catalytic kinetics of dimethyl ether one-step synthesis over CeO_2–CaO–Pd/HZSM-5 catalyst in sulfur-containing syngas process 被引量:1
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作者 Ruizhi Chu Wenxin Hou +4 位作者 Xianliang Meng Tingting Xu Zhenyong Miao Guoguang Wu Lei Bai 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2016年第12期1735-1741,共7页
CeO_2–CaO–Pd/HZSM-5 catalyst was prepared for the dimethyl ether(DME) one-step synthesis in a continuous fixed-bed micro-reactor from the sulfur-containing syngas. The catalytic stability over hybrid catalyst of Ce... CeO_2–CaO–Pd/HZSM-5 catalyst was prepared for the dimethyl ether(DME) one-step synthesis in a continuous fixed-bed micro-reactor from the sulfur-containing syngas. The catalytic stability over hybrid catalyst of CeO_2–CaO–Pd/HZSM-5 was investigated to ensure that the kinetics experimental results were not significantly influenced by induction period and catalytic deactivation. A large number of kinetic data points(40 sets) were obtained over a range of temperature(240–300 °C), pressure(3–4 MPa), gas hourly space velocity(GHSV)(2000–3000 L·kg^(-1)·h^(-1)) and H_2/CO mole ratio(2–3). Kinetic model for the methanol synthesis reaction and the dehydration of methanol were obtained separately according to reaction mechanism and Langmuir–Hinshelwood mechanism. Regression parameters were investigated by the method combining the simplex method and Runge–Kutta method. The model calculations were in appropriate accordance with the experimental data. 展开更多
关键词 CeO_2–CaO –Pd/HZSM-5 catalyst DME One-step synthesis Catalytic kinetics sulfur-containing syngas
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An Innovative Method for the Determination of Sulfur-containing Compounds by Vapor Molecular Absorption Spectrometry
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作者 Duan Yixiang, Zhang Hanqi, Liu Xinwei, Wang Lishuang and Jin Qinhan (Department of Chemistry, Jilin University, Changchun) 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 1991年第4期245-246,共2页
Since the most sensitive resonance lines of nonmetallic elements are situated in vacuum ultraviolet region (below 190 nm), they can not be directly determined with a common AAS instrument covering the spectral range... Since the most sensitive resonance lines of nonmetallic elements are situated in vacuum ultraviolet region (below 190 nm), they can not be directly determined with a common AAS instrument covering the spectral range from 190 to 700 nm. The molecular absorption spectrometry is often used for the determination of nonmetallic elements. Syty et al. used vapor molecular absorption spectrometry(VMAS) to determine the sulfur dioxide and sulfide, in which a hydrogen hollow cathode lamp was used as a continuum source to determine SO;at 210 nm and a deuterium arc 展开更多
关键词 Molecular absorption SPECTROMETRY sulfur-containing compound
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The Synthesis of New Sulfur-containing Chiral Macrocyclic Ligands
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作者 Xiao Ling ZHANG Jing Song YOU +1 位作者 Xing Shu LI Ru Gang XIE(Department of Chemistry, Sichuan Union University, Chengdu 610064) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第10期853-854,共2页
Five new chiral sulfur-containing macrocyclic ligands which can be used in chiral recognition to guests have been synthesized and characterized
关键词 OCH LI CL The Synthesis of New sulfur-containing Chiral Macrocyclic Ligands
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“一锅法”光控开环聚合原位调控聚类肽分子量及分子量分布
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作者 王煜璐 张佳辰 +3 位作者 隆佳颐 廖明臻 宣孙婷 张正彪 《功能高分子学报》 CAS CSCD 北大核心 2024年第4期287-294,共8页
设计和合成了光敏性休眠引发剂2-硝基-4,5-二甲氧基苄基环己胺基甲酸酯,用于氮-丁基-氮-羧酸内酸酐(^(Bu)N-NCA)的可控开环聚合。该光敏性引发剂在紫外光(360 nm)下释放环己胺引发剂。通过改变紫外光的照射时长可控制环己胺引发剂的释放... 设计和合成了光敏性休眠引发剂2-硝基-4,5-二甲氧基苄基环己胺基甲酸酯,用于氮-丁基-氮-羧酸内酸酐(^(Bu)N-NCA)的可控开环聚合。该光敏性引发剂在紫外光(360 nm)下释放环己胺引发剂。通过改变紫外光的照射时长可控制环己胺引发剂的释放量,从而调控聚类肽的分子量。随着照射时长从1 h增至4 h,聚类肽的数均分子量从9.6×10^(3)降至4.6×10^(3)。通过调控紫外光的照射间隔控制环己胺引发剂的释放速率。先释放的引发剂先引发单体,后释放的引发剂后引发单体,形成链长不均一的聚合物。通过光控实现了“一锅法”原位调控聚类肽的分子量及分子量分布,为聚类肽分子量分布宽度及分布形状更精准的调控提供了可能,也为研究聚类肽分子量分布和性能间的关系奠定了基础。 展开更多
关键词 光敏性引发剂 聚类肽 分子量分布调控 开环聚合 氮-取代-氮-羧酸内酸酐
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Comparison of the capacity of biological desulfurization of Thiobacillus ferrooxidans from different sulfur-containing substrates with or without additional ferrous iron
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作者 Yanjin Wang Xiaopeng Chang +2 位作者 Hongge Tao Zhenfeng Wang Quanguo Zhang 《International Journal of Agricultural and Biological Engineering》 SCIE 2024年第3期140-143,共4页
Thiobacillus ferrooxidans,abbreviated as T.ferrooxidans is one of the important microorganisms in the field of biological desulfurization.Effects of ferrous iron and sulfur-containing substrates on biological desulfur... Thiobacillus ferrooxidans,abbreviated as T.ferrooxidans is one of the important microorganisms in the field of biological desulfurization.Effects of ferrous iron and sulfur-containing substrates on biological desulfurization of T.ferrooxidans were studied.Results show that in the absence of Fe^(2+),T.ferrooxidans can utilize three kinds of sulfur-containing substrates of Na_(2)S_(2)O_(3),elemental S and Na_(2)SO_(3) for growth and metabolism.For utilization complexity,Na_(2)S_(2)O_(3) was easiest to use,next was elemental S,and Na_(2)SO_(3) was the worst for use.During the utilization of ferrous iron and sulfur-containing substrates by T.ferrooxidans,the iron oxidation system was first started.With the decrease of the Fe^(2+)concentration,the sulfur oxidation system was started,and then the two systems synergistically acted.The presence of three sulfur-containing substrates had different effects on Fe^(2+)oxidation,and elemental S did not inhibit the oxidation of Fe^(2+),while Na_(2)S_(2)O_(3) and Na_(2)SO_(3) had some inhibition on the oxidation of Fe^(2+),especially the inhibition of Na_(2)SO_(3) was significant,and complete oxidation of ferrous iron needed more time.The isolated T.ferrooxidans is applied to the removal of H2S gas,aiming to provide a new technological approach for biological removal of H2S. 展开更多
关键词 Thiobacillus ferrooxidans ferrous iron sulfur-containing substrate biological desulfurization
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Nickel(Ⅱ)-Catalyzed Reductive Coupling of Xanthate Esters with Sulfur-Containing and Selenium-Containing Compounds:Synthesis of Unsymmetric Sulfides and Selenides
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作者 Jia-Hui Han Daopeng Sheng +4 位作者 Yi-Rong Chen Xiao-Yue Shuai Weidong Rao Shu-Su Shen Shun-Yi Wang 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2024年第20期2453-2458,共6页
Unsymmetric sulfides and selenides have great applications in the pharmaceutical field.Herein,we describe the reductive coupling reaction of xanthate esters with sulfur-containing and selenium-containing compounds(thi... Unsymmetric sulfides and selenides have great applications in the pharmaceutical field.Herein,we describe the reductive coupling reaction of xanthate esters with sulfur-containing and selenium-containing compounds(thio(seleno)sulfonates and disulfides(selenides))under the nickel-catalyzed condition.It provides a mild and effective method for the synthesis of unsymmetric sulfides and selenides which has the advantages of mild reaction conditions,high yields and a wide range of substrates. 展开更多
关键词 sulfur-containing and selenium-containing compounds Sulfides and selenides Xanthate esters Nickel Radical Synthetic methods
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基于开环聚合的聚氨基酸合成的研究进展
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作者 张宝忠 《精细石油化工》 CAS 2024年第6期77-80,共4页
综述了近年来开环聚合法制备聚氨基酸的研究进展,主要包括聚氨基酸开环聚合的反应机理、功能化环状聚合单体的制备、高效快速的聚合体系设计与开发等,展望了基于开环聚合的聚氨基酸合成的未来发展方向。
关键词 聚氨基酸 开环聚合 氨基酸 N-羧酸酐
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N-甲酰-L-甲硫氨酰-L-亮氨酰-L-苯丙氨酸(fMLP)三肽的合成
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作者 廖一静 杨康辉 +2 位作者 王举涛 张瑞环 徐文方 《中国药物化学杂志》 CAS CSCD 2007年第5期299-301,共3页
目的合成N-甲酰-L-甲硫氨酰-L-亮氨酰-L-苯丙氨酸三肽(fMLP)。方法以L-亮氨酸、L-苯丙氨酸为原料,采用环酸酐法(NCA)合成二肽L-亮氨酰-L-苯丙氨酸;又以DCC、HOBT为偶联剂,与N-甲酰-L-甲硫氨酸进行偶联,在0.5mol.L-1的NaOH溶液中水解得到... 目的合成N-甲酰-L-甲硫氨酰-L-亮氨酰-L-苯丙氨酸三肽(fMLP)。方法以L-亮氨酸、L-苯丙氨酸为原料,采用环酸酐法(NCA)合成二肽L-亮氨酰-L-苯丙氨酸;又以DCC、HOBT为偶联剂,与N-甲酰-L-甲硫氨酸进行偶联,在0.5mol.L-1的NaOH溶液中水解得到fMLP三肽。结果与结论合成的三肽fMLP总收率为44.0%。其结构经IR、1H-NMR、MS确证。 展开更多
关键词 三肽 合成 N-甲酰-L-甲硫氨酰-L-亮氨酰-L-苯丙氨酸(fMLP) 环酸酐(NCA)法
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L-丙氨酸-N-羧基-环内酸酐的合成及其聚合研究
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作者 王庭慰 李素文 《精细化工》 EI CAS CSCD 北大核心 2004年第12期953-956,共4页
丙氨酸的四氢呋喃悬浮液在0℃下缓慢通入过量的干燥光气后升温至30℃合成得到了L 丙氨酸 N 羧基 环内酸酐(L Ala NCAn),研究了L Ala NCAn的开环聚合反应以及反应过程中溶剂、温度、引发剂及用量对聚合物特性黏度的影响。利用红外光谱确... 丙氨酸的四氢呋喃悬浮液在0℃下缓慢通入过量的干燥光气后升温至30℃合成得到了L 丙氨酸 N 羧基 环内酸酐(L Ala NCAn),研究了L Ala NCAn的开环聚合反应以及反应过程中溶剂、温度、引发剂及用量对聚合物特性黏度的影响。利用红外光谱确认了所得单体和聚合产物。用硝基苯作溶剂,三乙胺作引发剂,所得聚合物特性黏度为[η]=0 83dL/g。考虑到强酸对生物高分子的降解作用,实验中测定了二氯乙酸(DCA)对聚合物特性黏度的影响,结果发现二氯乙酸对聚丙氨酸特性黏度无影响。 展开更多
关键词 L-丙氨酸 聚丙氨酸 L-丙氨酸-N-羧基-环内酸酐 开环聚合
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聚丙烯酸苄酯/聚谷氨酸苄酯嵌段共聚物的合成与表征
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作者 曹田 任琳 《合肥工业大学学报(自然科学版)》 CAS CSCD 北大核心 2008年第8期1267-1269,共3页
通过自由基聚合制备了氨基封端的聚丙烯酸苄基酯(PBzA-NH2);用PBzA-NH2作为大分子引发剂,引发L-谷氨酸-N-羧酸酐(BLG-NCA)开环聚合,得到聚丙烯酸苄基酯/聚L-谷氨酸苄基酯两嵌段共聚物。用1H-NMR、GPC、元素分析等对聚合物的结构进行表征... 通过自由基聚合制备了氨基封端的聚丙烯酸苄基酯(PBzA-NH2);用PBzA-NH2作为大分子引发剂,引发L-谷氨酸-N-羧酸酐(BLG-NCA)开环聚合,得到聚丙烯酸苄基酯/聚L-谷氨酸苄基酯两嵌段共聚物。用1H-NMR、GPC、元素分析等对聚合物的结构进行表征,结果表明,PBzA-NH2能够引发BLG-NCA开环聚合制备嵌段共聚物,且分子量可控。 展开更多
关键词 聚丙烯酸苄基酯 谷氨酸 L-谷氨酸-N-羧酸酐 聚L-谷氨酸苄基酯
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聚(L-γ-氯乙基谷氨酸酯)的合成与构象 被引量:3
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作者 林恒 邵正中 +2 位作者 周平 高勤卫 于同隐 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2000年第5期819-821,共3页
Triphosgene was used to react with γ-chloroethyl glutamate, which was synthesized from 2-ethylene chlorohydrin and L-glutamic acid, to give γ-chloroethyl glutamate N-carboxyan.hydride (NCA). Thus, poly(γ-chloroethy... Triphosgene was used to react with γ-chloroethyl glutamate, which was synthesized from 2-ethylene chlorohydrin and L-glutamic acid, to give γ-chloroethyl glutamate N-carboxyan.hydride (NCA). Thus, poly(γ-chloroethyl glutamate), a new poly (amino acid) with reactive chloride, was obtained from the NCA by using triethylamine as the initiator which can lead to intrinsic viscosity of polypeptide, [η], over 50 mL/g. NCA and polymer were characterized by IR, 1H NMR and 13C NMR. Oligomer of γ-chloroethyl glutamate was also obtained while NCA was initiated by moisture in air. The conforma- tions of oligomer and polymer of γ-chloroethyl glutamate were observed by IR and CD spectroscopy. The results suggested that the conformation of oligomer mainly be β-sheet, while the polymer be α-helix. 展开更多
关键词 构象 聚(L-γ-氯乙基谷氨酸酯) 合成
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氨基酸N-羧酸内酸酐与胺反应的位阻效应 被引量:1
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作者 黄世俊 黄种宾 +2 位作者 张方建 郑剑峰 靳立人 《厦门大学学报(自然科学版)》 CAS CSCD 北大核心 2005年第4期511-514,共4页
研究了α-氨基酸的N-羧酸内酸酐(4-烷基-2,5-二氧代噁唑啉)与胺缩合反应.用L-苯丙氨酸,L-缬氨酸,L-亮氨酸制得相应的N-羧酸内酸酐,并分别与二乙胺,叔丁胺,异丙胺,正丁胺反应.正丁胺与N-羧酸内酸酐仅分离得到酰胺,而叔丁胺或异丙胺得到... 研究了α-氨基酸的N-羧酸内酸酐(4-烷基-2,5-二氧代噁唑啉)与胺缩合反应.用L-苯丙氨酸,L-缬氨酸,L-亮氨酸制得相应的N-羧酸内酸酐,并分别与二乙胺,叔丁胺,异丙胺,正丁胺反应.正丁胺与N-羧酸内酸酐仅分离得到酰胺,而叔丁胺或异丙胺得到的是脲酸和酰胺的混合物.二乙胺与N-羧酸内酸酐反应则仅得到脲酸衍生物,产率大于80%,具有制备价值.发现N-羧酸内酸酐4位取代基的位阻效应对反应的区域选择性具有一定的导向作用,大位阻基团导致产物中脲衍生物比例增加. 展开更多
关键词 位阻效应 氨基酸 酸酐 羧酸 L-苯丙氨酸 L-缬氨酸 L-亮氨酸 区域选择性 缩合反应 脲衍生物 导向作用 正丁胺 异丙胺 叔丁胺 二乙胺 噁唑啉 二氧代 混合物 取代基 酰胺 分离 产物
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基于多肽和温敏聚合物的光交联囊泡的制备及表征(英文) 被引量:4
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作者 袁康 周雪 杜建忠 《物理化学学报》 SCIE CAS CSCD 北大核心 2017年第4期656-660,共5页
解决聚合物囊泡降解性和稳定性的矛盾是一个重要问题。本文通过可逆加成断裂链转移(RAFT)聚合和开环聚合(ROP)合成了一种聚[(N-异丙基丙烯酰胺-无规-7-(2-甲基丙烯酰氧基乙氧基)-4-甲基香豆素)-嵌段-(L-谷氨酸)][P(NIPAM_(45)-stat-CMA_... 解决聚合物囊泡降解性和稳定性的矛盾是一个重要问题。本文通过可逆加成断裂链转移(RAFT)聚合和开环聚合(ROP)合成了一种聚[(N-异丙基丙烯酰胺-无规-7-(2-甲基丙烯酰氧基乙氧基)-4-甲基香豆素)-嵌段-(L-谷氨酸)][P(NIPAM_(45)-stat-CMA_5)-b-PGA_(42)]的两亲嵌段共聚物。囊泡膜由温敏性的聚N-异丙基丙烯酰胺(PNIPAM)和可光交联聚7-(2-甲基丙烯酰氧基乙氧基)-4-甲基香豆素(PCMA)组成。由囊泡膜向内外舒展的聚谷氨酸(PGA)链使囊泡稳定分散在水中,并且可进一步官能化。透射电子显微镜(TEM)和动态光散射(DLS)表征证实了囊泡的形貌和尺寸分布。本研究为制备基于多肽共聚物的可降解温敏囊泡提供了一个范例,并有望在纳米生物医药领域得到应用。 展开更多
关键词 囊泡 多肽 胶囊 可逆加成断裂链转移聚合 N-羧基酸酐(NCA)
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L-谷氨酸苄酯-NCA与L-丙氨酸-NCA共聚物的合成研究 被引量:2
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作者 姚凯 王庭慰 《合成纤维工业》 CAS CSCD 北大核心 2006年第1期24-27,共4页
以L-谷氨酸、L-丙氨酸为原料,利用硫酸催化-真空脱水制备了L-谷氨酸γ-苄酯(BLG);BLG和L -丙氨酸在四氢呋喃中分别与光气反应合成了L-谷氨酸γ-苄酯羧酸酐(BLG-NCA)和L-丙氨酸羧酸酐(Ala- NCA);BLG-NCA与ALa-NCA在三乙胺的引发下,共聚... 以L-谷氨酸、L-丙氨酸为原料,利用硫酸催化-真空脱水制备了L-谷氨酸γ-苄酯(BLG);BLG和L -丙氨酸在四氢呋喃中分别与光气反应合成了L-谷氨酸γ-苄酯羧酸酐(BLG-NCA)和L-丙氨酸羧酸酐(Ala- NCA);BLG-NCA与ALa-NCA在三乙胺的引发下,共聚反应制得了BLG-NCA与ALa-NCA的共聚物。结果表明:合成BLG,BLG-NCA,ALa-NCA的产率分别为40.25%,88%,61.8%,熔程分别为171-173℃,91-93℃, 90-91℃。红外光谱也验证了所合成产物。BLG-NCA与ALa-NCA(摩尔比为8.194:1)的共聚产物在30℃下,其特性粘数为0.547 dL/g,核磁共振光谱确定了其结构特征,DSC分析证明了该共聚物为单一的共聚产物。 展开更多
关键词 L-谷氨酸 L-谷氨酸γ-苄酯羧酸酐 L-丙氨酸 L-阿氨酸羧酸酐 共聚反应 共聚物
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