Low-spin signature inversion in the pi h(9/2)circle times nu i(13/2) oblate band

Excited states in Tl-188,Tl-190 have been studied experimentally by means of in-beam gamma spectroscopy techniques, and resulted in the identification of a strongly coupled band based on the pi h(9/2) circle times nu i(13/2) configuration with oblate deformation. The oblate band in doubly odd Tl nuclei shows low-spin signature inversion. It is the first experimental observation of low-spin signature inversion for a band associated with the oblate pi h(9/2) circle times nu i(13/2) configuration.

Observation of a pi h(9/2) circle times nu i(13/2) oblate band in Tl-188

Excited states in Tl-188 have been studied experimentally using the Gd-157(Cl-35;4n) reaction at a beam energy of 170 MeV. A rotational band built on the pi h(9/2) x nu i(13/2) configuration with oblate deformation has been established for Tl-188. Based on the structure systematics of the oblate pi h(9/2) x nu i(13/2) bands in the heavier odd-odd Tl nuclei, we have tentatively proposed spin values for the new band in Tl-188. The pi h(9/2) x nu i(13/2) oblate band in Tl-188 shows low-spin signature inversion, and it can be interpreted qualitatively by the two-quasiparticle plus rotor model including a J-dependent p-n residual interaction.

Properties of the pi h(9/2)circle times nu i(13/2) oblate band in Tl-188

High spin states in Tl-188 have been investigated via the Gd-157(Cl-35,4n) reaction at beam energy of 170 MeV. A rotational band built on the pi h(9/2) circle times nu(13/2) configuration with oblate deformation has been established. Considering the similarity between the band structure observed in odd-odd Tl nuclei, spin values have been tentatively proposed for the new band in Tl-188. The pi h(9/2) circle times nu(13/2) oblate band in Tl-188 shows low-spin signature inversion, and it can be interpreted qualitatively by the two quasiparticle plus rotor model including a J-dependent p-n residual interaction.

Signature inversion in pi h(9/2) circle times nu i(13/2) oblate band of Tl-188

High-spin Level structure of Tl-188 has been studied via Gd-157 (Cl-35,4n) fusion-evaporation reaction at beam energy of 170MeV. A rotational band built on the pi h(9/2) circle times nu i(13/2) configuration with oblate deformation has been established. Spin values have been proposed to the pi h(9/2) circle times nu i(13/2) oblate band based on the similarities between the oblate band of Tl-188 and those in odd-odd Tl190-200. With the spin assignments, the low-spin signature inversion has been revealed for the pi h(9/2) circle times nu i(13/2) oblate band of Tl-188. The low-spin signature inversion can be interpreted qualitatively in the framework of the quasi-particles plus rotor model including a J dependent p-n residual interaction.

Multi-electron processes in C-13(6+) ions with neon collisions in energy region 4.15-11.08 keV/u

The cross-section ratios of double-, triple-, quadruple-, and the total multi-electron processes to the single electron capture process sigma(DE)/sigma(SC), sigma(TE)/sigma(SC), sigma(QE)/sigma(SC) and sigma(ME)/sigma(SC)) as well as the relative ratios among reaction channels in double-electron active, triple-electron active and quadruple- electron active are measured in C-13(6+) -Ne collision in the energy region of 4.15-11.08 keV/u by employing position-sensitive and time-of-flight coincident techniques. It is determined that the cross-section ratios sigma(DE)/sigma(SC), sigma(TE)/sigma(SC), sigma(QE)/sigma(SC) and sigma(ME)/sigma(SC) are approximately the constants of 0.20 +/- 0.03, 0.16 +/- 0.04, 0.06 +/- 0.02 and 0.42 +/- 0.05. These values are obviously smaller than the predictions of the molecular Coulomb over-the-barrier model (MCBM) [J. Phys. B 23 (1990) 4293], the extended classical over-the-barrier model (ECBM) [J. Phys. B 19 (1986) 2925] and the semiempirical scaling laws (SL) [Phys. Rev. A 54 (1996) 4127]. However, the relative ratios among partial processes of DE, TE and QE are found to depend on collision energy, which suggests that the collision dynamics depends on the collision velocity. The limitation of velocity-independent character of ECBM, MCBM and SL is undoubtedly shown.

Constraints on the symmetry energy and neutron skins from pygmy resonances in Ni-68 and Sn-132

Correlations between the behavior of the nuclear symmetry energy, the neutron skins, and the percentage of energy-weighted sum rule (EWSR) exhausted by the pygmy dipole resonance (PDR) in Ni-68 and Sn-132 are investigated by using different random phase approximation (RPA) models for the dipole response, based on a representative set of Skyrme effective forces plus meson-exchange effective Lagrangians. A comparison with the experimental data has allowed us to constrain the value of the derivative of the symmetry energy at saturation. The neutron skin radius is deduced under this constraint.

小麦~(13)C分辨率和水分利用效率对氮素与水分的响应

水分利用效率反映了环境养分资源对植物生理状况的影响。在Ｃ3 植物中 ,碳同位素分辨率 (Δ)可用来反映植物水分利用效率 (ＷＵＥ)状况[1,2 ] ,(已被用作衡量Ｃ3 植物叶片气体交换对环境变化的指标 ,如土壤水分亏缺[3 ] 、光辐射[4] 、湿度[5 ] 、高ＣＯ2 [6] 和盐渍[7] 。植物Δ与ＷＵＥ或干物质产量间呈负相关[8] ,但Ｗｒｉｇｈｔｅｔａｌ认为正常水分条件下Δ和ＷＵＥ为负相关 ,而干旱条件下Δ和ＷＵＥ无相关性[9] ,但就Δ和ＷＵＥ关系在氮素和水分互作条件下的变化至今研究较少。由于不同资源胁迫预处理会使植物产生一系列生理适应机制[10 ] ,所以 ,我们对不同氮素溶液下培养的小麦幼苗通过添加不同量ＰＥＧ( 6 0 0 0 )来模拟水分亏缺条件 ,利用稳定性碳同位素技术探讨不同氮素营养和水分亏缺条件下小麦Δ和ＷＵＥ的关系。1　材料与方法小偃 6号小麦 (ＴｒｉｔｉｃｕｍａｅｓｔｉｖｕｍＬ .ｃｖ .ｘｉａｏｙａｎＮｏ .6 )在 2 5℃恒温、黑暗条件下于吸湿滤纸上萌发 5ｄ后 ,选长势均一的幼苗移至装蛭石和炭沙 (1∶1,ｖ/ｖ)的塑料盒中 ,每周用改良的半强度Ｈｏａｇｌａｎｄ营养液灌...

Study on structure and molecular dynamics of starch/poly(sodium acrylate)grafted superabsorbent by C-13 solid state NMR

The domain-structure of samples containing a series of starch/poly(sodium acrylate)-grafted superabsorbents, pure starch, pure poly(sodium acrylate), and blend of starch/poly(sodium acrylate) has been studied by high-resolution solid-state C-13 NMR spectroscopy at room temperature. The result shows that the crystallinity of starch decreases greatly in the grafted and blended samples.

Pr掺杂对Ce_(0.87)Sm_(0.13)O_(2-δ)结构及电性能的影响

采用溶胶-凝胶法合成Ce0.87Sm0.13-xPrxO2-δ(x=0.00,0.01,0.02)氧化物,通过X射线衍射、拉曼光谱、场发射扫描电镜对氧化物进行结构表征,利用交流阻抗谱测试电性能,并讨论了掺杂Pr对Ce0.87Sm0.13O2-δ微观结构和电性能的影响.结果表明,掺入少量Pr3+可减少或消除晶粒表面和晶界处的坑痕或孔隙,增加材料的致密性,从而降低材料的晶界电阻和电极界面电阻以及晶界电阻在总电阻中所占的比例,提高了材料的电导率.

~(13)C-NMR方法研究酚酞聚芳醚酮砜共聚物的序列结构

通过亲核共缩聚合成了一系列酚酞聚芳醚酮砜共聚物和嵌段共聚物 ,并利用1 3C NMR方法研究了共聚物的链结构 ,通过观察酚酞单元中三个位置的季碳原子的化学位移及其相应强度的变化 ,计算共聚物中不同链段的共聚物的组成、平均序列长度和无规度 .结果表明 ,除嵌段共聚物外 ,其它共聚物的无规度均接近 1 ,表明共聚物为无规共聚物 ,而且对三个位置的季碳原子分析均得出了相同的结果.

Effect of alkyl group length on the conductivity in the 2,3,7,8,12,13,17,18-octakis(alkyl-thio)tetraazaporphyrins and redox properties of the metallooctakis(hexyl-thio)tetraazaporphyrins

A series of 2,3,7,8,12,13,17,18-octakis(alkyl-thio)tetraazaporphyrins (H(2)OATTAP) with different alkyl chain lengths have been synthesized. Cyclic voltammetry and differential pulse voltammetry have been used to investigate the effect of the controlled lengths of the eight peripheral thioether tails on the redox behavior of the molecules. The electrochemical reduction of octakis(hexyl-thio)tetraazaporphyrins, MOHTTAP (where M = Cu, Ni), was studied in 1,2-dichloroethane at a platinum electrode. The Cu derivative was oxidized in one single-electron-transfer step to yield a pi-cation radical and reduced in three single-electron-transfer steps to yield a pi-anion radical, dianion and trianion, respectively. For the Ni derivative, electron transfer reactions involving both the central metal atom and the macrocyclic ring were observed. Electron transfer pathways are proposed based upon voltammetric and in situ spectroelectrochemical results.

Zn_4B_6O_(13)∶Ce~(3+),Tb~(3+)的合成与发光

高温固相扩散方法首次合成了Zn4 B6 O1 3:Ce3+ ,Tb3+ 光致发光材料。通过XRD分析获得晶胞参数 :a =0 7472nm ,V =0 .4172nm3,为立方晶系。研究Ce3+ 和Ce3+ ,Tb3+ 在Zn4 B6 O1 3中的激发和发射光谱 ,发现Ce3+ 在Zn4 B6 O1 3中的激发和发射带比Ce3+ 在其他基质中红移2 3 8～ 4.94KK ,Ce3+ 的发射带与Tb3+ 的 7F6 → 5G2 ,5D1 ,5H7吸收带有很好的重叠 ,使Ce3+ 对Tb3+ 有良好的敏化作用。Ce3+ ,Tb3+ 在基质中的能量传递机理为 :Ce3+ →Ce3+ 和Ce3+ →Tb3+ 之间的偶极子—偶极子的电多级相互作用的共振传递机理。色坐标为 :x =0 2 81,y =0 .619。SEM摄取产物的晶貌 ,颗粒均匀 ,平均粒度为 0 .2 3 μm ,接近纳米级。

双-Keggin型四元杂多化合物[Nd(SiMo_7W_4O_(39))_2]~(13-)多层膜在化学修饰玻碳电极上的组装及电催化

报道双－Ｋｅｇｇｉｎ型四元杂多化合物Ｋ１０Ｈ３［Ｎｄ（ＳｉＭｏ７Ｗ４Ｏ３９）２］ＸＨ２Ｏ（简称［Ｎｄ（ＳｉＭｏ７Ｗ４）２］１３－）聚合物的交替组装多层膜在４－氨基苯甲酸修饰玻碳电极上的制备及其电化学特性。各层的循环伏安行为证明膜的均匀增长，峰电流随层数的增加而增加。与溶液中的电化学行为相比，位于多层膜中的杂多化合物的氧化还原特征峰随着多层膜层数的增加，具有一定程度的形变。该电极具有较高的稳定性。并讨论了ｐＨ对其氧化还原行为的影响，考察了该多层膜修饰电极对ＢｒＯ３－、ＨＮＯ２和Ｈ２Ｏ２等的电催化性能。

C-13 NMR study of ethylene/propylene/octene-1 terpolymers synthesized with TiCl4/MgCl2/i-Bu3Al as the catalyst

The theory of chemical shift effect of substituent was applied to the assignment of the C-13 NMR spectra of the ethylene/propylene and ethylene/octene-1 copolymers. Using the parameters derived above and the DEFT technique, we then entirely assigned the C-13 NMR spectra of the ethylene/propylene/octene(-1) terpolymers synthesized in the presence of the same heterogeneous supported Ziegler-Natta catalyst, TiCl4/MgCl2/i-Bu3Al. The present paper also covers the terpolymer composition and the monomer sequence distributions of a series of ethylene/propylene/octene-1 terpolymers.

Carbon-13 nuclear magnetic resonance spectrum simulation of pyridines and quinolines

Artificial neural network (ANN) and multiple linear regression (MLR) were used for the simulation of C-13 NMR chemical shifts of 118 central carbon atoms in 18 pyridines and quinolines. The electronic and geometric features were calculated to describe the environments of the central carbon atom. The results provided by ANN method were better than that achieved by MLR.