977 resultados para radical scavenger hydroxyl radical, 1,2 selenazoles, COX, LOX


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用固相反应法合成了三个新的交生相氧化物:Sm_2SrCo_2O_7,Gd_2SrCO_2O_7和Sm_2BaCo_2O_7.它们均具有Sr_3Ti_2O_7型的结构,其中Sm_2BaCo_2O_7属于正交晶系,其它属于四方晶系.与LnSrCoO_4相比,Ln_2SrCo_2O_7(Ln=Sm,Gd)中CoO_2平面上的Co-O键缩短,电子离域化趋势增强,导电能力提高.在300~1100K之间,电阻率与温度关系表明,五个氧化物均表现弱定域系统的特性. 300~1100K之间的磁化率与温度关系表明,在较低温度下,GdSrCoO_4和Gd_2SrCo_2O_7符合Curie-Weiss定律,但前者的CoO_2平面上的磁交换作用是反铁磁性的,而后者是铁磁性的;含Sm~(3+)的三个氧化物表现出较为复杂的磁性质,这可能与Sm~(3+)离子磁性质的复杂性有关.

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Electrochemical catalytic reactions of tetraphenylporphinatocobalt were studied in DMF and EtCl2 solutions in the presence of 1,2-dibromoethane and 1, 2-dichloroethane utilizing cyclic voltammetry, thin-layer electrochemistry, in situ UV-visible spectroel

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1990年,Schumann,H.等报道了用双(环戊=烯基)稀土甲基化物与二苯胺进行交换反应制得了[Li(THF)_4][Cp_2Sm(NPh_2)_2],并测定了相应配合物镥的结构。但是,到目前为止,类似的轻稀土配合物尚未报道。这里,我们以双(叔丁基环戊二烯基)氯化钛为前体,与等当量的二苯胺基锂反应,制得了阴离子型配合物[Li(DME)_3][(t—BUCP)_2Nd(NPh_2)_2]·1/2DME,并测定了其单晶结构。

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A method for the specific determination of cobalt based on reversed-phase liquid chromatography with amperometric detection via on-column complex formation has been developed. A water-soluble chelating agent, 1-(2-pyridylazo)-2-naphthol-6-sulphonic acid (PAN-6S), is added to the mobile phase and aqueous cobalt solutions are injected directly into the column to form in situ the cobalt-PAN-6S chelate, which is then separated from other metal PAN-6S chelates and subjected to reductive amperometric detection at a moderate potential of -0.3 V. Because the procedure eliminates the interference of oxygen and depresses the electrochemical reduction of the mobile phase-containing ligand PAN-6S, by virtue of the quasi:reversible electrode process of the cobalt-PAN-6S complex, a low detection limit of 0.06 ng can be readily obtained. Interference effects were examined for sixteen common metal species, and at a 5- to 8000-fold excess by mass no obvious interference was observed. The feasibility of the method as an approach to the specific analysis of cobalt in a hair sample has been demonstrated.

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钼体系1,2-PB橡胶屈服强度随1,2-链节含量增加而上升,过屈服后,伸长率相同,1,2-链节含量高的其强度大([η]相近的橡胶)。1,2-链节含量与T’_(11)转变温度呈线性关系,方程为:T’_(11)=1.804W—67(W为1,2-含量),当W趋于零时,T’_(11)=67℃,即为顺丁橡胶的T’_(11)转变温度。1,2-PB的T_g受其1,2-链节含量和间同立构含量的影响,当1,2-链节含量相近时,间同含量高,T_g亦高。在DSC和扭辫动态力学图谱上,存在两个结晶峰。

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应用EI质谱和联动扫描技术研究了13个有机磷杂环化合物,讨论了主要离子的形成过程,分子离子在EI条件下的各种重排反应和取代基对不同解离反应产物离子相对强度的影响。

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本文报道了1:12-磷铜杂多酸(PMo_(12)薄膜修饰碳纤维(CF)微电极的制备及其电化学性质。采用简单,快速的浸渍吸附制备的PMo_(12)薄膜修饰CF电极在酸性介质中具有很高的稳定性和氧化还原活性,电解质溶液的pH值和扫描电位范围对PMo_(12)膜的稳定性和电化学性质产生较大的影响。另一方面,PMo_(12)薄膜修饰CF微电极对酸性水溶液中的PMo_(12)和氯酸根离子(ClO)_3~-)的电催化还原作用也进行了描述。

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1,2-链节含量分别为89.5%(mol)和30%~53%及顺式-1,4含量98%的聚丁二烯(PB)及其三烷基硅氢加成物的热分析研究表明,侧链乙烯基(外双键)热氧化温度与活化能高于主链双健(内双键),热交联温度则与此相反;PB经硅氢加成后,热氧化温度及热交联温度均随加成率的增加而明显提高。加成产物热分解后有较多残重,并与双键加成率有关。加成产物的流动温度T_(?)有较大提高。PB及其硅氢加成产物经完全氢化后,高1,4-链节PB及其硅氢加成产物室温为结晶状态,而高1,2-链节PB及其硅氢加成物则是非晶态的。

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In chain molecules of 1, 2-PBD, there are two kinds of gauche arrangements, which is the cause of making the spectrum of the secondary carbon in main chain of the polymer split. In such a complex system, the gauche arrangements of the secondary carbon and the tertiary carbon occupy an important position. Hence, the contribution of the tertiary carbon to the chemical shifts of the secondary carbon has a decisive effect on the sequence structure distribution. In comparison the contribution of vinyl groups is ...

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本文采用Cole-Cole,Fuoss-Kirkwood经验相关时间分布模型和构象跳跃,高聚物局部主链运动阻尼取向扩散分子模型,对1,2-聚丁二烯在溶液中的~(13)C-NMR自旋-晶格弛豫时间nT_1和核Overhauser效应(NOE)值进行了数值拟合。用拟合所得分子运动参数讨论了1,2-聚丁二烯微观分子运动对链结构和温度的依赖性。

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利用测得(?)和[η]数据,由Stockmayer-Fixman-Burchard、Stockmayer-Kurata-Roig和Inagaki-Suzuki-Kurata方程外推,估算了塑炼过程中不同1,2-链节含量的1,2-聚丁二烯(1,2-PB)的无扰尺寸变化规律。1,2-链节含量分别为40%和87.2%时,随薄通次数的增加,无扰尺寸降低;但前者薄通50次后变化很小,后者薄通100次后仍有波动。1,2-链节含量为87.2%的1,2-PB,薄通后放置30d,其无扰尺寸随薄通次数的增加而降低的程度,均大于当日测定的结果。

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采用GPC法与[η]测定相结合的方法,研究了1,2-PB在薄通过程中分子量和分子量分布的变化。结果表明,同一类型的1,2-PB,当[η]>200mL/g时,随薄通次数的增加[η]下降,分子量分布向低分子量方向移动。[η]降到200mL/g左右时,尽管成倍增加薄通次数,[η]降低缓慢,並趋于稳定,[η]≈200mL/g时,在薄通过程中[η]变化极小。比较当日和放置30d后测定的薄通样品,结果表明,薄通样品在放置过程中会产生自由基结合,生成支链结构,致使流体力学体积降低。

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本工作发现钼体系1,2-聚丁二烯橡胶的屈服强度(σy)与其[η]呈线性关系,方程式为:[η]=Kσy+C(未加分子量调节剂时为[η]=0.46σy+1.39)。方程式的斜率K随温度降低由正值变为负值。该胶料的T_g和应力-应变受分子量调节剂的影响,且后者影响明显。分子量调节剂用量一般控制在0.25—0.75质量份。