Krykunov Mykhaylo, Autschbach Jochen
Department of Chemistry, State University of New York at Buffalo, Buffalo, New York 14260-3000, USA.
J Chem Phys. 2007 Jan 14;126(2):024101. doi: 10.1063/1.2423007.
We report implementations and results of time-dependent density functional calculations (i) of the frequency-dependent magnetic dipole-magnetic dipole polarizability, (ii) of the (observable) translationally invariant linear magnetic response, and (iii) of a linear intensity differential (LID) which includes the dynamic dipole magnetizability. The density functional calculations utilized density fitting. For achieving gauge-origin independence we have employed time-periodic magnetic-field-dependent basis functions as well as the dipole velocity gauge, and have included explicit density-fit related derivatives of the Coulomb potential. We present the results of calculations of static and dynamic magnetic dipole-magnetic dipole polarizabilities for a set of small molecules, the LID for the SF6 molecule, and dispersion curves for M-hexahelicene of the origin invariant linear magnetic response as well as of three dynamic polarizabilities: magnetic dipole-magnetic dipole, electric dipole-electric dipole, and electric dipole-magnetic dipole. We have also performed comparison of the linear magnetic response and magnetic dipole-magnetic dipole polarizability over a wide range of frequencies for H2O and SF6.
(i)频率相关的磁偶极 - 磁偶极极化率;(ii)(可观测的)平移不变线性磁响应;(iii)包含动态偶极磁极化率的线性强度微分(LID)。密度泛函计算采用了密度拟合。为实现规范原点无关性,我们采用了与时间周期磁场相关的基函数以及偶极速度规范,并纳入了库仑势与密度拟合相关的显式导数。我们给出了一组小分子的静态和动态磁偶极 - 磁偶极极化率的计算结果、SF6分子的LID、M - 六螺旋烯的原点不变线性磁响应的色散曲线以及三种动态极化率(磁偶极 - 磁偶极、电偶极 - 电偶极和电偶极 - 磁偶极)的计算结果。我们还对H2O和SF6在很宽频率范围内的线性磁响应和磁偶极 - 磁偶极极化率进行了比较。