Jha Prakash Chandra, Rinkevicius Zilvinas, Agren Hans
Department of Theoretical Chemistry, School of Biotechnology, Royal Institute of Technology, Roslagstullsbacken 15, S-106 91 Stockholm, Sweden.
Chemphyschem. 2009 Mar 23;10(5):817-23. doi: 10.1002/cphc.200800671.
Open-shell spin-restricted time-dependent density functional theory is applied to explore the spin multiplicity dependence of linear and nonlinear optical properties. An open-shell neutral conjugated system, the C(4)H(4)N radical in the doublet X(2)A(2), quartet X(4)A(2), and sextet X(6)A(1) states, is chosen as a model system to illustrate various aspects of the theory. It is found that irrespective of the exchange-correlation functional employed, the components of the polarizability alpha(-omega,omega) and first hyperpolarizability beta(-2 omega,omega,omega) show very different dependency with respect to the multiplicity, with an increasing trend for higher spin states. This is rationalized by the decrease in conjugation and stability of the system with increasing multiplicity, and by the way the interaction between unpaired electrons and the external field is shielded by remaining electrons of the molecule. The study suggests the applicability of open-shell systems for frequency-dependent nonlinear optical properties and for the possibility of spin control for such properties.
开壳层自旋限制时变密度泛函理论被用于探究线性和非线性光学性质对自旋多重性的依赖性。选取一个开壳层中性共轭体系,即处于二重态X(2)A(2)、四重态X(4)A(2)和六重态X(6)A(1)的C(4)H(4)N自由基,作为模型体系来说明该理论的各个方面。结果发现,无论采用何种交换关联泛函,极化率α(-ω,ω)和一阶超极化率β(-2ω,ω,ω)的分量对多重性的依赖性都非常不同,随着自旋态的升高呈增加趋势。这可以通过随着多重性增加体系共轭性和稳定性的降低,以及未成对电子与外场之间的相互作用被分子中其余电子屏蔽的方式来解释。该研究表明开壳层体系在频率相关的非线性光学性质方面的适用性,以及对这类性质进行自旋控制的可能性。