Synthesis and Characterization of Model Complexes of Catechol Dioxygenases Supported by the Anionic Hydrotris-3,5-dimethyl-pyrazolylborate Ligand

An iron(Ⅲ) complex [FeIII(TpzMe2)(HpzMe2)Cl2](1) has been synthesized at a low temperature,which contains tripodal ligand,namely,the anionic hydrotris-3,5-dimethyl-pyrazolylborate(TpzMe2). A series of iron(Ⅲ) catecholate complexes 2―5 has been obtained via the reaction of compound 1 with catecholate or substituted catecho-lates. These complexes were characterized by X-ray crystallographic analysis,mass spectrometry and elemental analysis,and the results show that TpzMe2 ligand has the beneficial effect on t...     

方波激发下Er~(3+)上转换红光激发机理的研究

用方波电源驱动808 nm激光二极管(LD)激发Er3+掺杂的亚碲酸盐氟氧化物玻璃,测量4F9/2能级上转换发光的上升和衰减,根据上升的时间常数确定中间能级的寿命,从而确定4F9/2能级粒子数积累的过程。通过建立速率方程模型分析4F9/2能级的上升和衰减特性与中间能级的关系,确定808 nm LD激发下上转换红光的激发机理,同时提供了一种通过上转换发光,用光电倍增管测量红外能级寿命的方法。     

Phase Transfer Catalyzed Synthesis under Ultrasonic Irradiation and Bioactivity of N''''-(4,6-Disubstituted-pyrimidin-2-yl)-N-(5-aryl-2-furoyl) Thiourea Derivatives

Acylthiourea derivatives are useful as pesticides, herbicides, fungicides and regulator for plant growth, and also as important intermediates in the organic synthesis. In recent years, phase transfer catalysis reaction technique has been widely recognized as an efficient synthetic tool and attracted much attention. In view of these observations, a series of 5-aryl-2-furoyl thioureas containing substituted pyrimidine ring were synthesized using PEG-400 as solid-liquid phase transfer catalyst under ultrasonic irradiation. All of the new compounds have been exactly determined by IR, 1H NMRand elemental analysis.     

电感耦合等离子体发射光谱法测定钇铝石榴石中掺杂Yb(Ⅲ)离子

采用碳酸钠-硼砂(质量比1：1)做熔剂分解钇铝石榴石,并确定了熔剂的最优化条件．以电感耦合等离子体光谱法对样品中掺杂Yb(Ⅲ)离子作了定量检测考察了样品和熔剂中单个基体和混合基体对分析结果的影响．发现单个基体Y对Yb的测定有增强效应．基体A1对Yb的测定有一定的抑制作用;基体对Yb测定的干扰可通过基体匹配进行消除元素的俭出限为2μg／L,标准加入回收率为88％～100％实际样品7次检测的RSD为2．1％。本方法可以较好地满足实际样品分析的需要。     

新型杯[4]冠醚衍生物聚合单体的合成

从对叔丁基杯[4]芳烃出发,对其下沿的酚羟基进行修饰,先后在1,3-和2-酚羟基位点引入冠醚环和乙基;最后在NaH/THF中与3-溴丙烯酸丙酯反应制得聚合单体——新型杯[4]冠醚衍生物,其结构经1H NMR和MS表征。     

1,3-二(4-吡啶)丙烷-Cd(II)手性配合物的合成与晶体结构

利用室温挥发方法合成了手性化合物[Cd(bbp)2(H2O)2]·bbp·2NO3·H2O(bpp=1,3-二(4-吡啶基)丙烷);利用X射线单晶衍射分析了产物的分子结构,并测定了其荧光光谱和固体圆二色光谱.结果表明,合成产物具有含一维手性链[Cd(bbp)2(H2O)2]n的手性超分子结构;其在室温下表现出中等强度的倍频效应,其二阶非线性极化率为尿素的0.4倍,是潜在的二阶非线性光学材料.此外,合成的手性化合物呈现弱的荧光,其固体圆二色光谱则呈现正的Cotton效应.     

Synthesis,Crystal Structure,and Biological Activity of 4-Chlorobenzaldehyde (2-trifluoromethylTrifluoromethyl-5,6,7,8-tetrahydrobenzo[4 ,5]-thieno[2,3-d]pyrimidin-4-yl)hydrazone Monohydrate

The novel title compound 4-chlorobenzaldehyde (2-trifluoromethyl-5,6,7,8- tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-4-yl)hydrazone monohydrate (C18H14ClF3N4SH2O, Mr = 428.86) has been synthesized by a condensation reaction of 4-chlorobenzaldehyde with (2-trifluoromethyl-5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-4-yl)hydrazine, and its crystal structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/c with a = 7.4252(7), b = 26.344(2), c = 10.3095(9) , = 109.407(2)°, V = 1902.0(3) 3 , Z = 4, Dc = 1.498 g/cm3 , μ = 0.356 mm-1 , F(000) = 880, the final R = 0.0564 and wR = 0.1681 for 2343 observed reflections with I > 2 (I). X-ray diffraction analysis reveals that the title hydrazone molecule is nearly planar except for the cyclohexene and trifluoromethyl moieties. In the crystal packing, the molecules form stacks by a three-dimensional framework, which results from intermolecular N(3)-H(3)···O(1), O(1)-H(1B)···N(2), O(1)- H(1B)···N(4) and O(1)-H(1A)···F(1) hydrogen bonds via water molecules together with π-π stacking interactions. Molecular geometry of the title compound in the ground state optimized by B3LYP functional with 6-311G** basis sets indicates that the calculations are in agreement with the experimental data. The preliminary bioassay suggested that the title compound exhibits relatively good fungicidal activity against Fusarium oxysporium f.sp.vasinfectum and Dothiorella gregaria.     

Ti接枝MCM-41催化剂的结构设计及化学亲和选择性研究

 用二氯化钛茂作为活性物种的来源，利用Si－MCM－41催化剂表面羟基的反应性，得到了Ti接枝MCM－41催化剂的两种结构模型．结构表征结果表明，Ti接枝MCM－41催化剂不仅长程结构好，孔径分布均一，而且催化剂表面活性中心含量高．两种结构模型催化剂上芳烃羟化反应性能表明，Ti接枝MCM－41催化剂表面的亲水／憎水性可以在较宽的范围内调变，从而可实现控制芳烃羟化的化学亲和选择性．另外，研究结果还表明，Ti接枝MCM－41催化剂具有很好的活性稳定性．     

新型蒈酸基双酰肼化合物的合成及其生物活性

先将3-蒈烯分子中的碳碳双键氧化开环制得蒈酮酸，再将羰基还原成亚甲基得到蒈酸，酰氯化后与系列酰肼发生N-酰化反应合成了14个新型蒈酸基双酰肼化合物(5a～5n)，其结构经UV-Vis、¹H NMR、¹³C NMR、 FT-IR和MS(ESI)表征，并测试了目标化合物的抑菌和除草活性。结果显示：在用药量为50 μg·mL^-1时，目标化合物对花生褐斑病菌、小麦赤霉病菌、黄瓜枯萎病菌、苹果轮纹病菌、番茄早疫病菌、玉米小斑病菌、西瓜炭疽病菌以及水稻纹枯病菌等8种植物病原菌具有一定的抑制活性，其中化合物蒈酸基α-噻吩甲酰肼5f（R=α-thiophene）对苹果轮纹病菌的抑制率达85.0%，优于阳性对照百菌清。在用药量为100 μg·mL^-1时，化合物蒈酸基3′,4′-二甲氧基苯甲酰肼5j(R=3′,4′-OMe-Ph)、蒈酸基-m-甲氧基苯甲酰肼5d(R=m-OMe-Ph)、蒈酸基-m-甲基苯甲酰肼5b(R=m-Me-Ph)和蒈酸基苯甲酰肼5a(R=Ph)对油菜胚根生长的抑制率分别为88.5%、 86.1%、 85.1%和82.6%（均为A级活性水平），优于阳性对照丙炔氟草胺。     

超声引导椎旁神经阻滞治疗带状疱疹后遗神经痛的疗效及可行性分析

本文对超声引导椎旁神经阻滞治疗带状疱疹后遗神经痛（post-herpetic neuralgia，PHN）的疗效及可行性进行了分析。研究对象为2015年12月~2017年12月于我院就诊的94例PHN患者，按就诊顺序随机均分为两组，对照组给予普瑞巴林常规治疗，观察组在此基础上联合超声引导椎旁神经阻滞治疗，连续治疗4周。本文比较了治疗前、治疗1周、2周、4周后的匹兹堡睡眠质量指数（PSQI）评分、疼痛视觉模拟（VAS）评分，并评价了治疗后的综合疗效，记录了治疗期间发生不良反应情况。结果显示，较治疗前，治疗1周、2周、4周后两组VAS评分均逐渐降低，且观察组治疗后各时间点的VAS评分显著低于对照组，差异具有统计学意义（P<0.05）；较治疗前，两组治疗1周、2周、4周后PSQI评分均逐渐降低，且观察组治疗后各时间点的PSQI评分显著低于对照组，差异具有统计学意义（P<0.05）；观察组治疗总有效率为89.36%，对照组为78.72%，观察组显著高于对照组，差异具有统计学意义（P<0.05）；两组治疗期间各项不良反应发生率差异无统计学意义（P>0.05）。本文证实了超声引导椎旁神经阻滞治疗PHN能显著改善患者神经疼痛症状，提升睡眠质量，同时具有安全性保障。