一种分离抗凝血酶Ⅲ的高效亲和色谱填料的制备及表征

以聚甲基丙烯酸环氧丙酯微球 ( PGMA)为基质 ,利用还原氨化方法将肝素键合在其表面上 ,得到一种以肝素为配基的高效亲和色谱填料 ,该填料对抗凝血酶 的亲和容量为 1 .2 mg/g,对抗凝血酶 和人血清白蛋白的回收率分别为 96.9%和 94 .4 % .利用前沿色谱法测定了肝素与抗凝血酶 之间的表观解离常数为 1 .96× 1 0 - 5mol/L.利用该填料可直接从人血浆中分离出抗凝血酶     

LiAgSO4-Al2O3复合电解质的导电性研究

研究了分散第二相α－Ａｌ２Ｏ３对ＬｉＡｇＳＯ４的离子导电性的影响，发现ＬｉＡｇＳＯ４－Ａｌ２Ｏ３的电导率随ａ－Ａｌ２Ｏ３含量的增加而升高，在３００－５００℃间电导率高于纯ＬｉＡｇＳＯ４，ａ－Ａｌ２Ｏ３含量摩尔比约为４０时最高。ＴＧ－ＤＴＡ和ＸＲＤ分析表明，在高温稳定的体立心ＬｉＡｇＳＯ４降温后以Ａｇ２ＳＯ４的正交β相形式存在，但在Ｈ２Ｏ存在下，生成Ｌｉ２ＳＯ４．Ｈ２Ｏ和Ａｇ２ＳＯ４．ＦＴ－ＩＲ分析     

FTIR－PAS技术在卟啉类化合物中的应用（Ⅲ）──乙酰丙酮－meso－四－（对－氯代）苯基卟啉稀土配合物的红外光声光谱

研究乙酰丙酮－ｍｅｓｏ－四－（对－氯代）苯基卟啉及其Ｎｄ、Ｓｍ、Ｅｕ、Ｇｄ、Ｔｂ、Ｄｙ、Ｈｏ、Ｅｒ、Ｌｕ配合物在３６００～２２０ｃｍ－１范围内的傅立叶变换红外光声光谱，对其主要谱带进行经验归属．实验结果表明，四－（对－氯代）苯基卟啉与稀土乙酰丙酮配合物中的金属离子配位，削弱乙酰丙酮环上的Ｍ－Ｏ键伸缩振动，使该谱带向低波数方向移动．金属敏感带出现在～１５５８、～１４７４、～１４２７、～１２１９、～７９８、～７３３、～２５０ｃｍ－１．     

含氨基酸侧链的有机硅高分子催化剂——聚γ-(色氨酸基)丙基硅氧烷钯催化剂的合成及加氢活性

本世纪60年代以来,Overberser等把存在于酶中的催化基团引入聚合物中,合成了一系列类酶聚合物催化剂。氨基酸是酶分子中的重要组成部分,它们分子中所含的氨基、羧基等均可络合金属离子形成催化剂的活性中心,氨基酸残基又可造成不同的配位环境,因此,用氨基酸作侧链合成类金属酶高分子催化剂有可能提高催化活性和选择性。     

芹菜中黄酮类物质的提取和测定

采用碱溶酸析法，成功地提取了芹菜中黄酮类物质。经HCl-镁粉反应和红外光谱鉴定，提取物为黄酮类物质。另外，利用分光光度法，以芦丁为标准对芹菜的叶和茎中的总黄酮分别进行了测定，其质量分数分别为10．19mg／g，3．064mg／g。同时讨论了时间及色素对测定方法的影响，结果表明，显色时间在40min内稳定，色素引起误差为5％。     

Laser irradiation induced spectral evolution of the Laser irradiation induced spectral evolution of the surface-enhanced Raman scattering(SERS)of 4-tert-butylbenzylmercaptan on gold nanoparticles assembly

The spectral evolution of the surface-enhanced Raman scattering (SERS) of 4-tert-butylbenzylmer-captan(4-tBBM)on gold nanopanlcles assembly under laser irradiation is reported.The reIative intensities of typical peaks in the spectrum of 4-tBBM gradually change with irradiation time.Comparison of the rate of spectral changes under several experimental conditions indicates that the surface plasmon resonance(SPR)induced heat in the gold nanoparticles assembly is the origin of the spectraI evolution.During the process of self-assembly,4-tBBM molecules do not form a compact ordered monolayer because of the spatial hindrance of the 4-tert-butyl end group.The heat induced by laser irradiation drives the 4-tBBM molecules to rearrange to a more stable orientation.     

Synthesis and Structural Characterization of a Polyoxomolybdate HNa_7[Mo_(36)O_(112)(H_2O)_(16)]·47H_2O

A new polyoxomolybdate complex HNa7[Mo36O112(H2O)16]·47H2O 1 has been prepared in the beaker solution and characterized by single-crystal X-ray diffraction and elemental analyses. Crystal data: H127Mo36Na7O175, Mr = 6542.79, monoclinic, C2/c, a = 40.891(6), b = 17.900(3), c = 25.580(4) , β = 125.673(2)°, V = 15210(4) 3, Z = 4, Dc = 2.857 g/cm3, F(000) = 12464, μ = 3.013 mm-1, R = 0.0633 and wR = 0.1654 (I > 2σ(I)). With the bridging sodium cations, the [Mo36O112(H2O)16]8- units in compound 1 are linked to form a one-dimensional structure, on the basis of which a three-dimensional architecture is further constructed via other sodium cations and complicated hydrogen bonds.     

Design and Synthesis of Glycosylated Aromatic Nitrogen Mustard Derivatives

Antibody-directed enzyme prodrug therapy(ADEPT) is a new strategy for the treatment of cancer that has arisen in recent twenty years, the main merits of which are that it can improve the selectivity of anticancer drugs and reduce the side effects in remote tissue. In the present study, two prodrugs-glycosylated aromatic nitrogen mustard derivatives were synthesized. Glucose and lactose were converted into glycosyl donors-trichloroacetimidate; the obtained glycosyl donors were glycosylated with p-nitrophenol(glycosyl donors) to form β-glucosyl p-nitrobenzene and β-lactosyl p-nitrobenzene that were protected by acetyl in a stereoselective manner; the two products were reduced by zinc dust and then treated with ethylene oxide, afforded two glycosylated nitrogen mustard derivatives that were protected by acetyl; the last step was to deacetylate and then afforded the two target compounds that could be used as prodrugs of ADEPT for further Anti-tumor research.     

Synthesis, Crystal Structure and Properties of [Co(1,3- bdoaH)_2·4H_2O]·4H_2O with Benzene-1,3-dioxyacetate Ligand

1INTRODUCTIONTheorganicaromaticcarboxylatemetalcom-plexeshavearousedmuchattentionandbeenwidelyinvestigated.However,thestrategyofdesignandsynthesisofthesecomplexesismostlyfocusedonrigidligands,suchasterephthalicacidandbenzenetricarboxylicacid,etc.[1～5].Theassemblyofcom-plexesbyusingflexiblearomaticcarboxylateli-gandsisfarlessdeveloped[6,.Phenylenedioxydia-7]ceticacids(bdoaH2)withbiologicalactivitiesandwideapplicationsinagriculture[8]areafamilyofmultidentateflexibleligandswithversatilebind…     

十二烷基甜菜碱与聚乙烯吡咯烷酮相互作用的研究

通过表面张力测定和13CNMR、ESR波谱研究了十二烷基甜菜碱（C12BE）与聚乙烯吡咯烷酮（PVP）的相互作用．表面张力测定表明,在pH＝6．5及NaCI存在下,C12BE与PVP之间有明显的相互作用,可形成C12BE／PVP复合物,且C12BE－PVP混合溶液的β－lgc曲线出现2个转折点,第一个转折点时C12BE浓度c1（C12BE－PVP开始缔合）低于C12BE的cmc值;而第二个转折点时C12BE浓度c2（C12BE－PVP缔合达饱和）大于cmc值．（c2─c1）与PVP浓度呈线性关系．PVP降低C12BE胶束化标准自由能（△G0）随PVP浓度增加而增大．13CNMR测定表明,PVP骨架上α-CH、β-CH2和吡咯环上与N相连的亚甲基吸附于C12BE胶束表面的碳氢链部位,屏蔽了C12BE胶束表面碳氢链与水的接触．ESR波谱表明,PVP－C12BE聚集体"界面"的粘度高于C12BE胶束"界面"的粘度．