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981.
982.
二水·2-羰基丙酸水杨酰腙合铜(Ⅱ)配合物的晶体结构及生物活性 总被引:4,自引:0,他引:4
在水中,以2-羰基丙酸水杨酰腙与硫酸铜反应,制得新配合物Cu(C10H8N2O4)(H2O)2(C10H8N2O42-为2-羰基丙酸水杨酰腙负离子),并以水为溶剂培养了单晶,测试了晶体结构,该单晶为深绿色,属单斜晶系,空间群为C2/c,晶胞参数a=1.1297(1)nm,b=0.9824(8)nm,c=2.1973(3)nm,β=91.91(8)°,V=2.43749(8)nm3,Z=8,μ=1.817mm-1,Dc=1.743Mg·m-3,F(000)=1304,R=0.0264,wR=0.0654,GOF=1.052。其测试结果表明在配合物中Cu2+处于五配位的四方锥配位环境,配位原子分别来自1个三齿配体2-羰基丙酸水杨酰腙负二价离子的2个O原子和1个N原子,2个水分子中的O原子,其中1个水分子的O原子处于四方锥的锥顶,锥底的配位原子基本处于同一平面上。对该配合物所作的皿内抑菌试验和盆栽活体实验表明,配合物对小麦条锈病、白菜黑斑病及辣椒疫霉菌等分别有96%、89%、100%的抑制率,且有一定的助长作用。 相似文献
983.
G. Meissner Kari Hartonen M.-L. Riekkola 《Fresenius' Journal of Analytical Chemistry》1998,360(5):618-621
A method is developed for the determination of β-blockers in serum and urine at levels of 0.5 μg/mL. The technique uses a
combination of solid phase extraction (SPE) with in situ derivatization and supercritical fluid extraction (SFE) with subsequent
gas chromatography mass spectrometry. The optimization of the SFE step shows that a static extraction period can be eliminated.
The method gives good linearity (r = 0.991–0.999) and repeatability in the concentration range of 0.5 to 5 μg/mL. Relative
standard deviations for oxprenolol, propanolol and metoprolol were less than 5% in serum and 5–11% in urine.
Received: 23 May 1997 / Revised: 28 July 1997 / Accepted: 5 August 1997 相似文献
984.
Effects of sugar inhibition on cellulases and β-glucosidase during enzymatic hydrolysis of softwood substrates 总被引:1,自引:0,他引:1
Zhizhuang Xiao Xiao Zhang David J. Gregg John N. Saddler 《Applied biochemistry and biotechnology》2004,115(1-3):1115-1126
A quantitative approach was taken to determine the inhibition effects of glucose and other sugar monomers during cellulase
and β-Glucosidase hydrolysis of two types of cellulosic material: Avicel and acetic acid-pretreated softwood. The increased
glucose content in the hydrolysate resulted in a dramatic increase in the degrees of inhibition on both β-Glucosidase and
cellulase activities. Supplementation of mannose, xylose, and galactose during cellobiose hydrolysis did not show any inhibitory
effects on β-Glucosidase activity. However, these sugars were shown to have significant inhibitory effects on cellulase activity
during cellulose hydrolysis. Our study suggests that high-substrate consistency hydrolysis with supplementation of hemicellulose
is likely to be a practical solution to minimizing end-product inhibition effects while producing hydrolysate with high glucose
concentration. 相似文献
985.
Fabrication of hexaphenylsilole nanowires and their morphology-tunable photoluminescence. 总被引:1,自引:0,他引:1
Liping Heng Jin Zhai Anjun Qin Yuqi Zhang Yongqiang Dong Ben Zhong Tang Lei Jiang 《Chemphyschem》2007,8(10):1513-1518
Immersion of nanoporous alumina membranes into saturated solutions of hexaphenylsilole with subsequent solvent evaporation affords aligned organic nanowires. The luminescent properties of the hexaphenylsilole nanowires can be manipulated by varying their morphologies, which were controlled by changing the channel sizes of the alumina templates. 相似文献
986.
S. L. Reindl G. M. Pastor 《Zeitschrift für Physik D Atoms, Molecules and Clusters》1993,26(Z1):171-173
The low-energy excitation spectra of metal dimers are determined by solving exactly a realistic many-body Hamiltonian with inter- and intra-atomic Coulomb interactions. Our results for Cu2 and Ag2 are in very good agreement with the excitation energies derived from recent photodetachment experiments. The characteristics of the many-body excited states in these clusters are briefly discussed. 相似文献
987.
988.
Urea can be sorbed by coordination (or complexation)with transitional metalpolyacrylic acid complex and transitional metal-polyacrylamide containing polyethylenepolyamine ligand complexes. The experimental results indicate that the sorbents can sorb about 60mg urea per gram of sorbent at 37℃ and the concentration of urea was 1300.0rag/1 in NaH_2PO_4 and Na_2HPO_4 buffer solution (pH=7.0) and the urea sorption capacity was affected by many factors such as other competive ligands, sorption time, pH and the concentration of urea. 相似文献
989.
990.
八配位钇(Ⅲ)-反式-1,2-环己二胺四乙酸配合物NH4[Y(trans-CYDTA)(H2O)2]·4.5H2O的合成及分子结构 总被引:10,自引:0,他引:10
In this paper, the molecular and crystal structures of the NH4[Y(trans CYDTA)(H2O)2]·4.5 H2O(trans-CYDTA=trans 1,2-cyclohexanediaminetetraacetic acid) are reported. The crystal data are as follows: Triclinic system, P1space group,a=0.8599(6)nm,b=1.0021(7)nm,c=1.4370(9)nm,α =88.095(13)°,β =75.559(1)°,γ =88.344(12)°,V=1.1981(14)nm3,Z=2, M=708.68,Dc=1.570g· cm-3, μ =2.506mm-1 and F(000)=590. The final R1 and wR2 are 0.0571 and 0.1350 for 4205 [I >2.0σ (I)] unique reflections and 0.1007 and 0.1615 for all 4981 reflections, respectively. In the title complex, the anion [Y(trans-CYDTA)(H2O)2]- has an eight coordination structure with distorted square antiprism. The trans CYDTA which acts as a hexadentate ligand with four Oatoms and two Natoms and two H2O molecules directly coordinate to central metal Y(Ⅲ) ion. It can be known that the Y(Ⅲ) ion can form an eight coordinate compound with aminopolycarboxylic acid ligands in addition nine coordination structure. 相似文献