ESR studies of γ-irradiated histone octamer and the histone H3

ESR spectrum of neat histone H3 γ-irradiated and observed at 77 K with low microwave power and modulation amplitude showed multiple resolved structure depicting nonequivalent interaction of the unpaired electron located at amido-carbonyl radical anion [– )NH–] of the peptide backbone with adjacent –NH– group and the β-proton of –CH group. The predominance of amido-carbonyl radical anion is in good accord with the expected partition of secondary electrons amongst the various electrophilic groups including peptide carbonyl and aromatic acid residues. Following a gradual rise of annealing temperature to room temperature, a double splitting spectrum from the well known -carbon amido radical was evolved.     

Synthesis of triphenylene derivatives by Pd-catalyzed Suzuki coupling/intramolecular CH activation between arylboronic acids and dibromobiphenyls

An efficient and regioselective synthesis of functionalized triphenylenes via palladium-catalyzed Suzuki-Miyaura coupling and subsequent intramolecular CH activation between arylboronic acids and dibromobiphenyls was developed. This methodology showed excellent atomic economy and regiospecificity as well as synthetic feasibility of unsymmetrical triphenylenes.     

含硒杂环化合物的合成和对超氧阴离子作用的ESR研究

引言硒作为人体必需的微量元素,其主要生化作用与谷胱甘肽过氧化物酶密切相关.在体内,该酶可以催化许多过氧化物的分解,并且与谷胱甘肽一起组成一个强有力的细胞防御体系,发挥其抗氧化作用.近几年来,人们发现了一种小分子有机硒化物2-苯基-1,2-苯并异硒唑酮-3(简称Ebselen)具有类似谷胱甘肽过氧化物酶的活性.它能有效地抑制活性氧自由基的产生而引起的细胞损伤,具有良好的抗炎活性,且毒性极低(大鼠LD_(50)>6180mg/os).因而,普遍认为Ebselen及其类似物是一类具有广谱抗炎活性的潜在药物,在医药领域具有广阔的应用前景.     

四（2,4—二叔戊基苯氧基）酞菁铜（Ⅱ）的合成及其LB膜

合成了标题酞菁铜衍生物,并通过元素分析,高压液相色谱,紫外光谱,红外光谱,核磁共振谱,电镜,顺磁共振谱及质谱加以确认。该化合物在稀氯仿溶液和LB膜中各以单,双分子缔合的形式存在。Z型沉积形成的单层LB膜对氨气有很高的灵敏度和选择性。     

Progressive studies on the novel samarium-catalyzed diastereoselective tandem semipinacol rearrangement/Tishchenko reduction of secondary alpha-hydroxy epoxides

A novel and highly diastereoselective samarium-catalyzed tandem rearrangement/reduction of secondary alpha-hydroxy epoxides, which involves a C1 to C3 carbon migration rearrangement and a very interesting hetero-Tishchenko reduction of the intermediate aldehyde and the reductant aldehyde, has been reported. This reaction could be developed to provide a facile and stereoselective construction of 2-quarternary 1,3-diol units with an hydroxymethyl moiety attached to the diastereogenic quaternary carbon center. Detailed investigations have been carried out concerning the screening of the aldehydes as a reductant, the optimization of reaction conditions, and the substrate scope of this tandem reaction. A catalytic cycle for this reaction, the electronic and steric effects of the reductant aldehydes, and the mechanism for the acyl migration of 1,3-diol monoesters are proposed.     

可逆反应的热静力学研究法

化学反应的焓变△H和平衡常数K的测定是热静力学研究的重要任务。通常用量热法可以此较准确地测定△H,但要从量热数据直接得到K则是在六十年代初才开始有所探索。在达方面,Drago和Christensen的工作是值得借鉴的。本文建立了一种中性配位体与一价金属离子络合反应体系的热静力学研究法,并用这种方法研究了二苯并18-冠-6与Na~+的络合反应,同时得到了反应的△H和平衡常数K。实验值与文献值符合。     

高频超声中带退化记忆项的MGT方程解的衰减估计北大核心CSCD

研究了高频超声应用中带无穷退化记忆项的Moore-Gibson-Thompson方程τu_(ttt)+α(x)u_(tt)-c^(2)Δu-bΔu_(t)+∫^(∞)_(0)g(s)div[a(x)▽u(t-s)]ds=0解的适定性和衰减速率,其中非负函数a(x)和α(x)是可退化的并满足a(x)+α(x)≥δ>0.该系统是由黏性热松弛流体中波传播模型的线性化而得到的.通过使用Faedo-Galerkin逼近和能量估计,证明了解的适定性.在适当的假设下,通过构造适当的李雅普诺夫泛函,建立了能量的指数或一般衰减结果.     

Dynamical intricacy and average sample complexity of amenable group actions

In 2018, Petersen and Wilson introduced the notion of dynamical intricacy and average sample complexity for dynamical systems of ?-action, based on the past works on the notion of intricacy in the research of brain network and probability theory. If one wants to take into account underlying system geometry in applications, more general group actions may need to be taken into consideration. In this paper, we consider this notion in the case of amenable group actions. We show that many basic properties in the ?-action case remain true. We also show that their suprema over covers or partitions are equal to the amenable topological entropy and the measure entropy, using the quasitiling technique in the theory of the amenable group.

     

Comparative voltammetric study of 2,4-dinitrophenol (DNP), albumin and DNP-albumin as an analytical approach to the use of DNP as a universal label in immunoelectrochemical assays

A comparative electrochemical study of 2,4-dinitrophenol (DNP), albumin and DNP-albumin has been carried out at a hanging mercury drop electrode, in order to use DNP as a universal label in immunoelectrical assays. Several electrochemical techniques have been used. Differential pulse voltammetry has proved to be the most suitable. Wide dynamic linear ranges (more than three orders of magnitude for DNP-albumin) and low detection limits have been achieved (5 x 10(-10)M, 2 x 10(-10)M, 3 x 10(-12)M for DNP, albumin and DNP-albumin, respectively). Good reproducibility has been obtained in all cases (R.S.D. < 2.2%).