Crystal Structure of [PrAl(CF3COO)(2)(CF3CHOO)(C2H5)(2)(C4H8O)(2)](2)

[PrAl (CF3COO)(2) (CF3CHOO) (C2H5)(2) (C4H8O)(2)](2) M-r = 1420. 56, monoclinic, P2(1)/n, a = 10. 651 (6) , b = 24. 276(9), c = 11. 110(5) Angstrom, beta = 107. 650 (4)degrees , V = 2737. 4(1) Angstrom (3) , Z = 2, D-c = 3. 45 g/cm(3) , F(000) = 2816 , T = 233K, MoK alpha radiation (lambda= 0. 71069 Angstrom), mu(MoK alpha) = 38. 017 cm(-1) , R = 0. 048 for 2847 observed reflections (I greater than or equal to 3 sigma(I)). It is isostructural with [LnAl (CF3COO)(2) (CF3CHOO) -R-2 (C4H8O)(2)](2) (Ln = Ho, R = Et; Ln = Ndt Y, R = Bu-1). Pr3+ is coordinated by eight oxygen atoms from five bridging ligands and two THF forming a distorted bicap-prism.

大功率650 nm 波段AlGaInP/GaInP 应变量子阱半导体激光器的研究

Submitted by zhangdi (zhangdi@red.semi.ac.cn) on 2009-04-13T11:45:31Z

Photostability of single-photon emission from a single quantum dot in the 650-nm wavelength band at room temperature

The photoluminescence correlation from a single CdSe nanocrystal under pulsed excitation is studied, and a single photon is realized at wavelength 655 nm at room temperature. The single colloidal CdSe quantum dot is prepared on a SiO2/silicon surface by a drop-and-drag technique. The long-term stability of the single-photon source is investigated; it is found that the antibunching effect weakens with excitation time, and the reason for the weakening is attributed to photobleaching. The lifetimes of photoluminescence from a single quantum dot are analyzed at different excitation times. By analyzing the probability distribution of on and off times of photoluminescence, the Auger assisted tunneling and Auger assisted photobleaching models are applied to explain the antibunching phenomenon.

利用α关联衰变链鉴别新同位素_(107)~(265)Bh

主要介绍了合成和鉴别107号元素的新同位素265Bh的实验装置、实验方法以及实验结果.目标核265Bh是由能量为135MeV的26Mg离子轰击243Am靶,通过融合蒸发反应而产生.反应产物首先由He jet系统传输到装有数个探测器对的转轮收集测量系统,然后依靠母子核遗传关系通过观察新同位素和它们已知子核261Db和257Lr之间的α衰变的关联,来实现对新核素的鉴别.实验测得265Bh的α衰变能量为(9.24±0.05)MeV, 半衰期为0.94+0.70-0.31s.从该实验得出的265Bh的α衰变能量和半寿命能够与理论预言一致.

新同位素~(265)Bh(Z=107)的合成证据

利用兰州重离子加速器提供的26Mg离子束轰击243Am靶, 产生了新同位素265Bh. 实验中用氦喷技术对产物进行传输, 并用一套具有数对探测器组的转轮收集探测系统对产物进行收集和测量. 通过观测265Bh与它的衰变子核261Db及257Lr之间的α衰变的关联, 实现了对新核素的鉴别. 实验测得265Bh的α衰变能量为(9. 24±0. 05)MeV, 半衰期为 0. 94+0. 70 0. 31 s.

~(265)Bh(Z=107)同位素的首次观测

在兰州的重离子加速器上用 2 6Mg离子束轰击 2 43 Am靶 ,产生了新同位素 2 65Bh .通过观测新同位素 2 65Bh和它的已知子核 2 61Db和 2 57Lr之间的α衰变的关联 ,实现了对新核素的鉴别 .实验中使用了一套新建立的具有数个探测器对的转轮收集探测系统 .将该系统用于特殊的母 -子核搜索模式 ,从而大大减少了本底 .共测得了 8个 2 65Bh的α衰变关联事件 ;同时 4个已知核 2 64Bh的衰变关联事件也被鉴别出来 .实验测得 2 65Bh的α衰变能量为 (9.2 4± 0 .0 5 )MeV ,半衰期为 0 .94 + 0 .70-0 .3 1s .

Grimm1．107颗粒物分析仪和rp2000气溶胶采样仪在北京城区的测试对比

IEECAS SKLLQG

北京城区grimm1.107和rp2000仪器测试对比

IEECAS SKLLQG

Hydrothermal syntheses and crystal structures of bimetallic cluster complexes [{Cd(phen)(2)}(2)V4O12]center dot 5H(2)O and [Ni(phen)(3)](2)[V4O12]center dot 17.5H(2)O

The hydrothermal reactions of vanadium oxide starting materials with divalent transition metal cations in the presence of nitrogen donor chelating ligands yield the bimetallic cluster complexes with the formulae [{Cd(phen(2))(2)V4O12].5H(2)O (1) and [Ni(phen)(3)](2)[V4O12] . 17.5H(2)O (2). Crystal data: C48H52Cd2N8O22V4 (1), triclinic. P (1) over bar, a = 10.3366(10), b = 11.320(3), c = 13.268(3) Angstrom, alpha = 103.888(17)degrees, beta = 92.256(15)degrees, gamma = 107.444(14)degrees, Z = 1; C72H131N12Ni2O29.5V4 (2), triclinic. P (1) over bar, a = 12.305(3), b = 13.172(6), c = 15.133(4), alpha = 79.05(3)degrees, beta = 76.09(2)degrees, gamma = 74.66(3)degrees, Z = 1. Data were collected on a Siemens P4 four-circle diffractometer at 293 K in the range 1.59degrees < theta < 26.02degrees and 2.01degrees < 0 < 25.01degrees using the omega-scan technique, respectively. The structure of 1 consists of a [V4O12](4-) cluster covalently attached to two {Cd(phen)(2)}(2+) fragments, in which the [V4O12](4-) cluster adopts a chair-like configuration. In the structure of 2, the [V4O12](4-) cluster is isolated. And the complex formed a layer structure via hydrogen bonds between the V4O12](4-) unit and crystallization water molecules.