The dipole polarizability(α) and second dipole hyperpolarizability(γ) tensors are calculated, by finite-field methods, for the ground states of butadiyne, hexatriyne, and octatetrayne. The effects of varying one-particle basis sets and molecular geometry, and the effects of including electron correlation at the fourth-order many-body perturbation theory level, are examined for butadiyne. The hyperpolarizabilities are more sensitive to geometry changes than to electron correlation. Coupled self-consistent-field calculations on hexatriyne and octatetrayne indicate that the longitudinal components αzz and γzzzz, grow as n1.5 and n3.0, respectively, and that the mean values ᾱ and γ̄ grow as n1.2 and n2, respectively, as the chain length increases in the C2nH2 series.
No takes yet. Share an insight, caveat, or question.
Maroulis et al. (1991) studied this question.