Mechanism and Origin of CuH-Catalyzed Regio- and Enantioselective Hydrocarboxylation of Allenes

The CuH-catalyzed hydrocarboxylation of allenes is an enantio- and regioselective approach for the synthesis of (S)-carboxyl-containing compounds. With density functional theory (DFT) calculations, we elucidate the reaction mechanism and the origins of the enantioselectivity and regioselectivity. The hydrocarboxylation proceeds through the migratory insertion of allenes on CuH complex, the enantioselective addition of fluoroformate, and the β-fluoride elimination gives the branched carboxylation products. The electron-donating alkyl and phenyl groups in the allene polarize the C=C bond and thus lead to the anti-Markovnikov-selective migratory insertion. In addition, the enantioselective addition of fluoroformate by either (R)- or (S)-addition determines the enantioselectivity. The (S)-addition is more favorable due to the bulky −tBu group of (R)-DTBM-SEGPHOS ligand, which prefers keeping the C=C bond of allene away from the reaction center in six-membered transition state and thus results in (S)-carboxyl-containing products.     

聚多巴胺包埋G-四联体/血红素DNA酶制备过氧化氢生物传感器

利用多巴胺的氧化自聚实现对G-四联体/血红素DNA酶的包埋,成功构建了H2O2电化学生物传感器。DNA和血红素混合得到G-四联体/血红素复合物;DNA酶物理吸附在玻碳电极上后,将10μL 5 g/L多巴胺的磷酸盐缓冲液(pH 8.0)滴在表面,空气中的氧气氧化多巴胺形成聚多巴胺膜,实现DNA酶的固定。考察了不同DNA序列对传感器性能的影响,表明电化学与光学传感过程具有不同序列响应。此传感器对H2O2的检出限为2.2μmol/L;线性范围为0.01～1.5 mmol/L。本研究证实了利用聚多巴胺固定酶和用DNA酶代替天然酶构筑传感器的可行性。     

Liquid heat capacity of the solvent system (piperazine + n-methyldiethanolamine + water)

A new set of values for the heat capacity of aqueous mixtures of piperazine (PZ) and n-methyldiethanolamine (MDEA) at different concentrations and temperatures are reported in this paper. The differential scanning calorimetry technique was used to measure the property over the range T = 303.2 K to T = 353.2 K for mixtures containing 0.60 to 0.90 mole fraction water with 15 different concentrations of the system (PZ + MDEA + H₂O). Heat capacity for four concentrations of the binary system (PZ + MDEA) was also measured. A Redlich–Kister-type equation was adopted to estimate the excess molar heat capacity, which was used to predict the value of the molar heat capacity at a particular concentration and temperature, which would then be compared against the measured value. A total of 165 data points fit into the model resulted in a low overall average absolute deviation of 4.6% and 0.3% for the excess molar heat capacity and molar heat capacity, respectively. Thus, the results presented here are of acceptable accuracy for use in engineering process design.     

Sieve methods in combinatorics

We develop the Turán sieve and a ‘simple sieve’ in the context of bipartite graphs and apply them to various problems in combinatorics. More precisely, we provide applications in the cases of characters of abelian groups, vertex-colourings of graphs, Latin squares, connected graphs, and generators of groups. In addition, we give a spectral interpretation of the Turán sieve.     

Changes of the electron dynamics in hydrogen inductively coupled plasma

Changes of the electron dynamics in hydrogen （H2） radio-frequency （RF） inductively coupled plasmas are investigated using a hairpin probe and an intensified charged coupled device （ICCD）. The electron density, plasma emission intensity, and input current （voltage） are measured during the E to H mode transitions at different pressures. It is found that the electron density, plasma emission intensity, and input current jump up discontinuously, and the input voltage jumps down at the E to H mode transition points. And the threshold power of the E to H mode transition decreases with the increase of the pressure. Moreover, space and phase resolved optical emission spectroscopic measurements reveal that, in the E mode, the RF dynamics is characterized by one dominant excitation per RF cycle, while in the H mode, there are two excitation maxima within one cycle.     

热处理温度对La-Y-Ni合金相结构和电化学性能的影响

采用磁悬浮感应熔炼法制备了组分为LaY_2Ni_(9.7)Mn_(0.5)Al_(0.3)的合金,在不同温度(1 073～1 373 K)下对合金进行热处理,利用X射线衍射法(XRD)、电子探针(EPMA)和电化学性能测试等方法,系统地研究了热处理温度对合金相结构和电化学性能的影响。结果表明,热处理可以显著提高合金的相均匀度,随着热处理温度的升高合金中的主相Ce_2Ni_7相先增加后减少。电化学研究表明,合金电极的最大放电容量、倍率性能和循环稳定性随着热处理温度的升高均呈现先升高后降低的趋势,与Ce_2Ni_7相含量的变化一致。电化学压力-组成-温度(P-C-T)测试表明,合金具有2个放氢平台,且随着热处理温度的升高合金的放氢坪台压增加。当热处理温度为1 273 K时,合金的Ce_2Ni_7相含量最高为86.53%(w/w),电化学性能最佳,最大放电容量为386.80 mAh·g~(-1)(60mA·g~(-1)),在电流密度为900 mA·g~(-1)时的高倍率性能HRD_(900)=89.45%,循环300周后的容量保持率S_(300)=72.18%(300 mA·g~(-1))。     

相位角对容性耦合电非对称放电特性的影响

电非对称效应作为一种新兴技术,被广泛用于对离子能量和离子通量的独立调控.此外,在改善等离子体的径向均匀性方面,电非对称效应也发挥了重要作用.本文采用二维流体力学模型,并耦合麦克斯韦方程组,系统地研究了容性耦合氢等离子体中当放电由多谐波叠加驱动时,不同谐波阶数k下的电非对称效应,重点观察了相位角θ_n对自偏压以及等离子体径向均匀性的影响.模拟结果表明：在同一谐波阶数下,自偏压随相位角θ_n的变化趋势不尽相同,且当k增大（k>3）时,自偏压随最高频相位角θ_k的变化范围逐渐减小.此外,通过调节相位角θ_n,可以改变轴向功率密度和径向功率密度的相对关系,进而实现对等离子体径向均匀性的调节.研究结果对于利用电非对称效应优化等离子体工艺过程具有一定的指导意义.     

Prime Divisors of the Number of Rational Points on Elliptic Curves with Complex Multiplication

Let E/Q be an elliptic curve. For a prime p of good reduction,let E(F_p) be the set of rational points defined over the finitefield F_p. Denote by (#E(F_p)) the number of distinct prime divisorsof #E(F_p). For an elliptic curve with complex multiplication,the normal order of (#E(F_p)) is shown to be log log p. The normalorder of the number of distinct prime factors of the exponentof E(F_p) is also studied. 2000 Mathematics Subject Classification11N37, 11G20.     

Generalization of preinvex and B-vex fuzzy mappings

A class of fuzzy mappings, called B-preinvex, and strictly B-preinvex fuzzy mappings, is introduced by relaxing the definition of preinvexity of a fuzzy mapping. Similarly, based on a notion of differentiability of fuzzy mappings different from the usual one, the class of pseudo-B-vex, B-invex, and pseudo-B-invex fuzzy mappings is defined as a generalization of pseudo-convex, invex, and pseudo-invex fuzzy mappings. We prove that a strictly B-vex, or B-preinvex fuzzy mapping has at most one global minimum point, and that the class of B-vex fuzzy mappings forms a subset of the class of quasi-convex fuzzy mappings. B-vex (resp. B-preinvex) fuzzy mappings satisfy most of the basic properties of convex (resp. preinvex) fuzzy mappings. In addition characterizations and sufficient optimality conditions are obtained for B-vex and B-preinvex fuzzy mappings.     

Cationic IrIII Emitters with Near-Infrared Emission Beyond 800 nm and Their Use in Light-Emitting Electrochemical Cells

Solid-state near-infrared (NIR) light-emitting devices have recently received considerable attention as NIR light sources that can penetrate deep into human tissue and are suitable for bioimaging and labeling. In addition, solid-state NIR light-emitting electrochemical cells (LECs) have shown several promising advantages over NIR organic light-emitting devices (OLEDs). However, among the reported NIR LECs based on ionic transition-metal complexes (iTMCs), there is currently no iridium-based LEC that displays NIR electroluminescence (EL) peaks near to or above 800 nm. In this report we demonstrate a simple method for adjusting the energy gap between the highest-occupied molecular orbital (HOMO) and the lowest-unoccupied molecular orbital (LUMO) of iridium-based iTMCs to generate NIR emission. We describe a series of novel ionic iridium complexes with very small energy gaps, namely NIR1 – NIR6 , in which 2,3-diphenylbenzo[g]quinoxaline moieties mainly take charge of the HOMO energy levels and 2,2′-biquinoline, 2-(quinolin-2-yl)quinazoline, and 2,2′-bibenzo[d]thiazole moieties mainly control the LUMO energy levels. All the complexes exhibited NIR phosphorescence, with emission maxima up to 850 nm, and have been applied as components in LECs, showing a maximum external quantum efficiency (EQE) of 0.05 % in the EL devices. By using a host–guest emissive system, with the iridium complex RED as the host and the complex NIR3 or NIR6 as guest, the highest EQE of the LECs can be further enhanced to above 0.1 %.