α-羟基膦酸酯芳甲酸酯的合成、晶体结构和质谱裂解规律研究

α-羟基膦酸酯与各种取代苯甲酸或吡啶甲酸,通过酰氯或缩合剂的作用,合成了一系列的O,O-二烷基-α-苯基-α-(取代芳基甲酸酯基)-甲基膦酸酯的衍生物.它们的合成收率为61%～84%,这些化合物的结构经过核磁(1HNMR,13CNMR和31PNMR)、红外、质谱、元素分析或高分辨质谱确证,同时化合物C1的结构在晶体结构解析上进一步得到证实.利用多级质谱分析了化合物C2,C5和C8的质谱裂解规律,解释了重排离子的形成机制.     

A cyclopenta-fused dibenzo[b,d]thiophene-co-phenanthrene macrocyclic tetraradicaloid

A cyclopenta-fused macrocyclic tetraradicaloid, MC4-S, containing alternating phenanthrene (Phen) and dibenzo[b,d]thiophene (DBTh) units was synthesized and isolated in single-crystal form. Compared with its all-carbon isoelectronic structure, CPTP-M, the incorporation of two sulfur atoms leads to a smaller radical character and a larger singlet–triplet energy gap. X-ray crystallographic analysis reveals that the spin–spin coupling through the DBTh unit is stronger than that through the Phen moiety. In addition, the electron-rich sulfur atoms also raise the energies of both the HOMO and LUMO in MC4-S, but the overall optical and electronic energy gaps are close to that of the CPTP-M. MC4-S displays global anti-aromaticity according to the NMR measurements and theoretical calculations (NICS, ACID and 2D ICSS), with a 36π ring current circuit along the all-carbon periphery excluding the two sulphur atoms. Its dication becomes globally aromatic due to the existence of a dominant 34π-conjugation pathway. This study sheds some light on the effect of heteroatoms on the electronic properties of open-shell polyradicaloids.

The first member of sulfur-heterocycloarene neutral tetraradicaloids, MC4-S, was synthesized in crystalline form, which displays strong global anti-aromaticity and unique properties.     

对微量元素与恶性肿瘤关系的新认识

微量元素与恶性肿瘤关系是当前十分引人注目的研究课题．MEDLINE数据库显示．近5年中硒、锌、铜与肿瘤关系的文章最多．微量元素与恶性肿瘤相关性有三种可能,即微量元素的丰缺是恶性肿瘤的结果.是肿瘤发生的条件因素或病因．微量元素之间的关系相当复杂．既拮抗。又协同，微量元素的研究刚起步．取样和检测方法等均需标准化．其与恶性肿瘤的发生和发展的机理更需积极研究.     

CaxSr1—xS：Bi,Tm,Cu和CaS：Eu荧光材料的研究

所作的一部分工作是对长余辉的荧光材料ＣａｘＳｒ１－ｘＳＢｉ，Ｔｍ，Ｃｕ（ｘ＝０，０．７５，１）进行了研究．ＣａＳ和ＳｒＳ两种基质材料高温互溶后，因为基质的晶体微结构上的变化引起Ｂｉ３＋离子荧光效应的变化，即发光的发射波数发生改变．另一部分工作是对ＣａＳＥｕ加入陷阱机制后发光效应的研究．新的陷阱机制的引进，使得其余辉效应有较大的延长．     

Layered Double Hydroxide Nanosheets with Multiple Vacancies Obtained by Dry Exfoliation as Highly Efficient Oxygen Evolution Electrocatalysts

Layered double hydroxides (LDHs) with two-dimensional lamellar structures show excellent electrocatalytic properties. However, the catalytic activity of LDHs needs to be further improved as the large lateral size and thickness of the bulk material limit the number of exposed active sites. However, the development of efficient strategies to exfoliate bulk LDHs into stable monolayer LDH nanosheets with more exposed active sites is very challenging. On the other hand, the intrinsic activity of monolayer LDH nanosheets can be tuned by surface engineering. Herein, we have exfoliated bulk CoFe LDHs into ultrathin LDH nanosheets through Ar plasma etching, which also resulted in the formation of multiple vacancies (including O, Co, and Fe vacancies) in the ultrathin 2D nanosheets. Owing to their ultrathin 2D structure, the LDH nanosheets expose a greater number of active sites, and the multiple vacancies significantly improve the intrinsic activity in the oxygen evolution reaction (OER).     

Generation of Quantum States for Atomic Ensemble via Cavity QED

A scheme is proposed for generating quantum states of atomic ensemble. In this scheme, a beam of three-level atoms in the Λ configuration is trapped in a cavity, then squeezed vacuum state and squeezed coherent state of the atomic ensemble are prepared by choosing different initial states of the system. The scheme is based on the off-resonant interaction between the atom and cavities, so the high-level of the atom is eliminated adiabatically.     

圆弧刃刀具刀尖圆弧精密测量

圆弧刃刀具刀尖圆弧参数会影响加工尺寸精度、表面质量和刀刃耐用度,研磨和测量的精度要求已达微米甚至亚微米级别;针对其本底噪声强、圆弧刃直线刃过度不明显等问题,提出结合形态学闭运算、滑动窗口三点定圆和空间矩法,分步实现圆弧初、精定位;实验结果表明,算法具有较强的抗噪能力,可快速对0.2~0.8 mm的刀尖进行直线刃与圆弧刃正确分离,圆弧半径、圆度误差测量精度达亚微米量级,角度测量精度达0.1°。     

Achieving Pure Green Electroluminescence with CIEy of 0.69 and EQE of 28.2% from an Aza‐Fused Multi‐Resonance Emitter

Pure green emitters are essential for realizing an ultrawide color gamut in next‐generation displays. Herein, by fusing the difficult‐to‐access aza‐aromatics onto B (boron)–N (nitrogen) skeleton, a hybridized multi‐resonance and charge transfer (HMCT) molecule AZA‐BN was successfully synthesized through an effective one‐shot multiple cyclization method. AZA‐BN shows pure green fluorescence with photoluminance quantum yield of 99.7 %. The corresponding green device exhibits a maximum external quantum efficiency and power efficiency of 28.2 % and 121.7 lm W^?1, respectively, with a full width half maximum (FWHM) of merely 30 nm and Commission Internationale de l'Eclairage (CIE) coordinate y of 0.69, representing the purest green bottom‐emitting organic light‐emitting diode.