107例高龄老人头发锰铜锌铬微量元素含量的探讨

对１０７例７０～８０岁高龄老人作头发８种微量元素含量测定，测定结果以Ｍｎ，Ｃｕ，Ｚｎ，Ｃｒ与长寿地区广西巴马县老人作比较，结果表明本组是低Ｍｎ、高Ｃｕ、低Ｚｎ、高Ｃｒ，差异极为显著（Ｐ＜０．００１），符合非长寿地区低Ｍｎ的现状．本组与４５～５９岁，６０～６９岁二个年龄组比较，本组为高Ｍｎ、低Ｃｕ、低Ｚｎ、高Ｃｒ，差异均显著（Ｐ＜０．０５），表明本组微量元素组合优于７０岁前老人．从本组男、女微量元素比较，女性表现为高Ｍｎ、高Ｓｒ、高Ｃａ、低Ｃｒ、低Ｃｕ，说明老年女性在抗衰防衰方面优于老年男性．     

血清中Mo、Se、Mn、Cu、Zn与食管癌的关系探讨

通过对１８例食管癌患者以及８０例对照组血清中Ｍｏ、Ｓｅ、Ｍｎ、Ｃｕ、Ｚｎ的测定分析，发现食管瘤患者血硒含量明显低于对照组，二者之间有极显著性差异（Ｐ＜０．０１）。而血铜、铜／锌比值食管癌组明显高于对照组，差异有显著性（Ｐ＜０．０５）。Ｍｏ、Ｍｎ、Ｚｎ元素的含量在二组之间无显著性差异（Ｐ＞０．０５）．提示血清硒铜与食管癌有关。     

胃癌病人发微量元素测定及其临床意义

对４３例胃癌病人测定了发中Ｚｎ、Ｃｕ、Ｆｅ、Ｍｎ、Ｃａ、Ｍｇ六种元素，结果：胃癌组发中Ｃｕ、Ｆｅｘ±ＳＤ值较健康对照组升高，Ｐ＜０．０５，有显著性差异．Ｚｎ、Ｃａ、Ｍｇｘ±ＳＤ值较健康组降低，Ｐ＜０．０５、＜０．０１、＜０．０１，差异有显著性和高度显著性．ＭＵｘ±ＳＤ值与健康对照组近似，Ｐ＞０．０５，差异无显著性．胃癌组Ｚｎ／Ｃｕ比值较健康对照组降低，Ｐ＜０．０１，差异高度显著性；胃癌组Ｚｎ／Ｆｅ比值与健康组近似，Ｐ＞０．０５，差异无显著性．Ｆｅ升高，Ｍｎ、Ｚｎ降低是胃癌的危险因素，Ｍｎ有抗癌抑癌作用，Ｆｅ、具有强烈催化自由基及过氧化反应的能力．发中微量元素测定可作为临床胃癌病人辅助诊断参考．     

肿瘤和微量元素的关系

采用量子共振检测仪测定了２５例恶性肿瘤患者、２５例良性肿瘤者和２５例无肿瘤人头发中Ｚｎ、Ｃｕ、Ｍｎ、Ｓｅ的含量。结果表明,恶性肿瘤患者头发中的锌含量明显高于良性肿瘤患者（Ｐ〈０．００１）和无肿瘤人（Ｐ〈０．００１）,而Ｓｅ、Ｍｎ、Ｃｕ的含量明显低于良性肿瘤患者和无肿瘤人（Ｐ〈０．００１）。恶性肿瘤患者锌含量过高,而Ｓｅ、Ｍｎ、Ｃｕ含量过低,所以高锌是诱发癌症的危险因素,也是诱发良好肿瘤的因素,而Ｓ     

慢性支气管炎患者头发及血清微量元素的测定

用催化极谱法测定７２例慢性支气管炎患者及５０例健康者人发及血清中锌、铁、铜、锰四种微量元素的含量。结果表明，Ｚｎ、Ｆｅ元素的含量比对照组低，并表现有显著性差异（Ｐ〈０．０１），Ｃｕ、Ｍｎ元素的含量在两组之间无显著性差异（Ｐ〉０．０５）。     

健康老年人与若干常量及微量元素的相关性研究

用原子吸收光谱法测定了７０例健康老年人、３０例健康成年人和３０例老年高血压病人血清中Ｃｕ、Ｚｎ、Ｆｅ、Ｍｎ、Ｃａ、Ｍｇ６种元素的含量．结果表明，健康老年人组与健康成年人组（对照组）相比，除Ｆｅ以外，Ｃｕ、Ｚｎ、Ｍｎ、Ｃａ、Ｍｇ均有显著性差异；与老年高血压病人组相比，除Ｍｇ以外，Ｃｕ、Ｚｎ、Ｆｅ、Ｍｎ、Ｃａ均有显著性差异．我们认为稳定的Ｃｕ／Ｚｎ比值及较高的血Ｍｇ水平是健康老年人未发生心血管疾病及糖尿病的重要原因之一，而高Ｃｕ、高Ｃａ及显著偏高的Ｃｕ／Ｚｎ比值，则是发生高血压的一个重要原因。     

170对新生儿与产妇全血微量元素含量的研究

随机对１７０对产妇及其新生儿全血１４种微量元素（Ｍｇ、Ｍｎ、Ｍｏ、Ｐｂ、Ｓｒ、Ｃｄ、Ｃｒ、Ｃｏ、Ｎｉ、Ｔｉ、Ｚｎ、Ｆｅ、Ｃｕ、Ｃａ）含量进行检测，采用母子配对分析探讨健康人新生儿微量元素的基础水平及母体对子体的影响，结果显示：１）铬、镁、铅３种元素母子间无差异（Ｐ＞０．０５）；２）锰、铁、镉、钴、钼、镍、钛７种元素子体含量高于母体（Ｐ＜０．０５，Ｐ＜０．０１）；３）锌、铜、钙、锶４种元素子体含量低于母体（Ｐ＜０．０１）；新生儿全血１４种元素男、女性别并未见有差异（Ｐ＞０．０５）。新生儿全血锌、铜、钙、锶低于母体为先天发育不足所致，故临床上需注意补充。在哺乳不足或疾病状态下，锌、钙等会进一步降低，及时补充是十分必要的。     

活动性肺结核患者头发微量元素分析

通过ＥＰＭ－８１０Ｑ电子探针扫描分析电镜，对在治疗中５３例结核患者头发Ｍｇ、Ａｌ、Ｃｄ、Ｃａ、Ｃｒ、Ｍｎ、Ｆｅ、Ｃｕ、Ｚｎ、Ｐｂ、Ｓｅ１１种元素含量进行分析，并与健康人头发比较。结果表明：结核组中Ｃａ、Ｚｎ元素含量低于健康组，Ｃｕ、Ｆｅ元素含量高于健康组（Ｐ〈０．０１）。     

肝素和低效阶肝素对兔动脉壁微量元素的影响

给家兔静脉注射不同效阶肝素，并用在子发射光谱仪（ＤＣＰ－ＡＥＳ）测定兔动脉壁中Ｍｏ、Ｚｎ、Ｓｅ、Ｍｎ、Ａｌ、Ｃｄ、Ｆｅ、Ｍｇ、Ｃａ、Ｐｂ、Ｎｉ、Ｔｉ、Ｃｏ、Ｋ、Ｎａ、Ｌｉ、Ｃｒ等元素含量。结果表明，与盐水组比较，商品肝素、低效阶肝素（３８ｕ／ｍｇ）使Ｍｇ、Ｋ明显高于（Ｐ〈０．０５或Ｐ〈０．０１）；低效阶肝素使Ｚｎ显著升高（Ｐ〈０．０５）；而商品肝素使Ｃｏ显著升高，Ａｌ显著降低（Ｐ〈０．０５）；两组     

乙肝患者头发微量元素分析

应用装有ＥＰＭ－８１０Ｑ电子探针扫描分析电镜，对５０例乙肝患者头发中Ｍｇ、Ａｌ、Ｃｄ、Ｃａ、Ｃｒ、Ｍｎ、Ｆｅ、Ｃｕ、Ｚｎ、Ｐｂ、Ｓｅ１１种元素含量进行分析，并与健康人头发进行比较。结果表明：乙肝组中Ｚｎ含量低于健康组，Ｃｕ、Ｃｄ、Ｆｅ含量高于健康组（Ｐ〈０．０１）。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

N-Heterocyclic carbene-palladacyclic complexes: synthesis,characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides

N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.     

Sulfur-directed metal-free and regiospecific methyl C(sp3)–H imidation of thioanisoles

Regiospecific and direct imidation of the methyl C(sp³)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products.