首页> 外文学位 >Theoretical spectra of floppy molecules.
【24h】

Theoretical spectra of floppy molecules.

机译:软盘分子的理论光谱。

获取原文
获取原文并翻译 | 示例

摘要

Detailed studies of the vibrational dynamics of floppy molecules are presented.;Six-D bound-state calculations of the vibrations of rigid water dimer based on several anisotropic site potentials (ASP) are presented. A new sequential diagonalization truncation approach was used to diagonalize the angular part of the Hamiltonian. Symmetrized angular basis and a potential optimized discrete variable representation for intermonomer distance coordinate were used in the calculations. The converged results differ significantly from the results presented by Leforestier et al. [J. Chem. Phys. 106 , 8527 (1997)]. It was demonstrated that ASP-S potential yields more accurate tunneling splittings than other ASP potentials used.;Fully coupled 4D quantum mechanical calculations were performed for carbon dioxide dimer using the potential energy surface given by Bukowski et al [J. Chem. Phys., 110, 3785 (1999)]. The intermolecular vibrational frequencies and symmetry adapted force constants were estimated and compared with experiments. The inter-conversion tunneling dynamics was studied using the calculated virtual tunneling splittings.;Symmetrized Radau coordinates and the sequential diagonalization truncation approach were formulated for acetylene. A 6D calculation was performed with 5 DVR points for each stretch coordinate, and an angular basis that is capable of converging the angular part of the Hamiltonian to 30 cm−1 for internal energies up to 14000 cm−1. The probability at vinylidene configuration were evaluated. It was found that the eigenstates begin to extend to vinylidene configuration from about 10000 cm−1, and the ra, coordinate is closely related to the vibrational dynamics at high energy.;Finally, a direct product DVR was defined for coupled angular momentum operators, and the SDT approach were formulated. They were applied in solving the angular part of the Hamiltonian for carbon dioxide dimer problem. The results show the method is capable of giving very accurate results with less memory.
机译:给出了对软盘分子振动动力学的详细研究。提出了基于几个各向异性位势(ASP)的刚性水二聚体振动的六维结合态计算。一种新的顺序对角线化截断方法用于对角线化哈密顿量。计算中使用对称角基和对单体间距离坐标的潜在优化离散变量表示。收敛的结果与Leforestier等人的结果有很大不同。 [J.化学物理106,8527(1997)]。证明了ASP-S势能比使用的其他ASP势能产生更精确的隧穿裂隙。利用Bukowski等人给出的势能面对二氧化碳二聚体进行了完全耦合的4D量子力学计算。化学Phys。,110,3785(1999)]。估计分子间的振动频率和对称的力常数,并与实验进行比较。利用计算得到的虚拟隧穿裂隙研究了转换间的隧穿动力学。拟定了对称的Radau坐标和顺序对角化截断方法。对于每个拉伸坐标,使用5个DVR点进行了6D计算,并且对于内部能量高达14000 cm-1的角度,该角度能够将哈密顿量的角部分收敛到30 cm-1。评估了亚乙烯基构型的可能性。发现本征态从大约10000 cm-1开始扩展为亚乙烯基构型,并且ra坐标与高能下的振动动力学密切相关;最后,为耦合角动量算符定义了直接乘积DVR,并制定了SDT方法。它们被用于解决二氧化碳二聚体问题的哈密顿量的角部分。结果表明,该方法能够以更少的内存给出非常准确的结果。

著录项

  • 作者

    Chen, Hua.;

  • 作者单位

    The University of Chicago.;

  • 授予单位 The University of Chicago.;
  • 学科 Chemistry Physical.;Physics Molecular.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 57 p.
  • 总页数 57
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 宗教;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号