溴化苄及其阳离子红外光谱的理论研究

利用密度泛函理论（DFT）在B3LYP/6-311G++（d,p）水平上对溴化苄分子进行了结构优化和频率计算,得到了该分子的稳定构型和全部振动模式。计算得到的几何参数通过与苯分子的实验值相比,发现理论值与其相吻合;理论计算和实验测得的红外光谱数据的比较分析表明,理论计算与实验测量结果符合得较好,并对其振动模式进行了归属。最后,在B3LYP/6-311G++（d,p）水平上计算得到了溴化苄阳离子的红外光谱,并与溴化苄进行了比较,计算表明电离对振动偶极距产生了较大影响。     

偶极子声源在径向厚度有限的模拟地层井孔中激发的声场

利用实轴积分法对偶极子声源在径向厚度有限的模拟地层井孔中激发的声场进行了数值模拟,考察了不同声源、源距、模拟地层半径和最外层吸声介质对井内声场的影响。数值计算结果表明:对于偶极子声源,如果模拟地层为声速较低的泥岩,无论最外层吸声介质为流体还是固体,在源距为3.0～4.064 m时,模拟地层半径为1.2 m就能保证刻度井中的"初至波"不受模拟地层外边界的影响;若要使声波全波列的主要部分不受该界面的影响,则模拟地层的半径需要更大;如果模拟地层为声速很高的白云岩,最外层吸声材料宜使用声阻抗合适的固体介质,即使这样,模拟地层半径还需达到2.6 m。这些结果可为模块地层声速刻度井的构建提供理论参考。     

强外电场作用下二甲基硅酮的分子结构和激发态

采用密度泛函(DFT)方法B3P86在6 311++G(d,p)基组水平上优化得到了分子轴方向不同电偶极 场(-0.04～0.04a.u.)作用下,二甲基硅酮的基态电子状态、几何结构、电偶极矩和分子总能量.在优化构型下 用同样的基组采用杂化CIS DFT方法(CIS B3P86)研究了同样外电场条件下对二甲基硅酮的激发能和振子强度 的影响.计算结果表明,分子几何构型与电场大小和方向呈现强烈的依赖,正向电场下基态偶极矩随电场强度线 性增加,分子总能量降低,当反向电场大于0.03a.u.时,偶极距方向改变,总能量增加;激发能随电场增加急剧减 小,且对电场方向的依赖呈现出不对称性,满足Grozema关系.电场对振子强度的影响比较复杂,但仍满足跃迁选 择定则.     

Development of the Hamiltonian and transition moment operators of symmetric top molecules using the O (3) ⊃ C∞v ⊃ C3v group chain

We present a development of the Hamiltonian, dipole moment, and polarizability operators for XY₃Z molecules. These rovibrational operators are written with the aid of a tensorial formalism derived from the one already used in Dijon and adapted to the XY₃Z symmetric tops in a recent paper [A. El Hilali, V. Boudon, M. Loëte, J. Mol. Spectrosc. 234 (2005) 166-174]. We use the O (3) ⊃ C_∞v ⊃ C_3v group chain. Expressions for the matrix elements are derived for these operators.     

The permanent electric dipole moment of holmium monoxide, HoO

The high resolution molecular beam laser-induced fluorescence (LIF) spectrum of the (0, 0) band of the [17.6]7.5-X₁8.5 system of holmium monoxide, HoO, has been recorded field free and in the presence of a variable static electric field. The rotational constant, B₀, and magnetic hyperfine structure constant, h, for the v = 0 levels of the [17.6]7.5 and X₁8.5 states were obtained by assigning and fitting the field-free spectral features. The Stark shifts and splittings in the LIF spectra were analyzed to produce values for the magnitude of the permanent electric dipole moments, |μ|, of 3.96(6) and 4.80(5) D for [17.6]7.5, v = 0 and X₁8.5, v = 0, respectively.     

Some rules forS(-2k) dipole sums?

Stieltjes conditions and the ratio test provide necessary but not sufficient conditions onS(-2k) dipole sums. If the dipole sums are accurate the associated [n, n –1] Padé approximant provides a better representation of (), the frequency-dependent dipole polarizability, than a truncated series expression and, in addition, should bound () below. It is shown how constraints on the dipole sums effect the form of the [2,1] Padé approximant and an additional constraint is derived that ensures the analyticity of the approximant on 0 < ₁. There then follows a discussion of the reliability of available literature dipole sum values for small molecules containing H, C, N and O.     

Liquid chromatography of benzene derivatives on a porous methacrylate copolymer containing epoxy groups

Summary The retention of benzene derivatives with nonpolar and polar substituents on a porous methacrylate copolymer containing epoxy groups using both nonpolar and polar eluents was investigated. When n-hexane is used as the eluent, the retention of n-alkylbenzenes and polymethylbenzenes is weaker than that of benzene. In the case of benzene derivatives containing polar functional groups their capacity ratios (k) on this porous polymer increases approximately linearly with the increase of the adsorbate molecules dipole moment. The retention characteristics of the methacrylate copolymer were compared with that of a styrene-divinylbenzene copolymer and silica gels with a hydroxylated surface and with a surface modified by chemically bonded alkylsilyl groups.     

1,2-聚丁二烯介电松弛的复平面分析

本文对1,2-聚丁二烯的介电松弛进行了复平面分析.结果表明,在1,2-聚丁二烯的玻璃化转变过程中,ε″(ω)与ε＇(ω)的关系满足Havriliak-Negami方程.由复平面图求出了样品的静态和光频下的介电系数,平均松弛时间和松弛时间分布参数.利用所得数据讨论了1,2-聚丁二烯在玻璃化转变过程中的构象变化、松弛时间分布和平均偶极矩等问题.     

The complete multi-ζ electric dipole moment matrix of π-(C6H6) Cr(CO)3 and tests of semi-empirical MO models

First, we evaluated the complete electric dipole moment matrixeZ using a multi- AO basis on Cr, C, and O centers fortheimportant, parent organometallic molecule -C₆H₆Cr(CO)₃. Second, we generated ground state LCAO-MO eigenvectors employing five commonly used semi-empirical procedures for molecules of this size which contain transition metals. Transformation of operator matrixeZ into the MO space of each of the five methods then leads us to conclude that the empirical input of Basch, Viste and Gray is most suitable. Finally, we compare the merits of several single- basis orbitals with the multi- metal orbitals.[/p]