A time-dependent density functional theory investigation on the nature of the electronic transitions involved in the nonlinear optical response of [Ru(CF3CO2)(3)T] (T=4 '-(C6H4-p-NBu2)-2,2 ': 6 ',2 ''-terpyridine)

作者：De Angelis F^*; Fantacci S; Sgamelotti A; Cariati F; Roberto D; Tessore F; Ugo R

来源：Dalton Transactions, 2006, (6): 852-859.

DOI：10.1039/b509123c

We report a theoretical study based on density functional theory (DFT) and time-dependent DFT (TDDFT) calculations on the nature and role of the absorption bands involved in the nonlinear optical response of the complexes [Ru(CF3Co2)(3)T] (T - T1, T2; T1 = 4'-(C6H,-p-NBu2)-2,2':6',2"-terpyridine, T2 = 4'-(C6H4-p-NMe2)-2,2':6',2"-terpyridine). Geometry optimizations, performed without any symmetry constraints, confirm a twisting of the -C6H4-p-NBu2 moiety with respect to the plane of the chelated terpyridine. Despite this lack of strong pi interaction, TDDFT excited states calculations of the electronic spectrum in solution provide evidence of a relevant role of the NBu2 donor group in the low-energy LMCT band at 911 rim. Calculations also show that the two bands at higher energy (508 and 455 nm) are not attributable only to LMCT and ILCT transitions but to a mixing of 1LCT/MLCT and ILCT/pi-pi* transitions, respectively. The 911 nm LMCT band, appearing at lower wavelength of the second harmonic (670 nm) of the EFISH experiment, controls the negative value of the second-order NLO response. This is confirmed by our calculations of the static component beta(0)(zzz) of the quadratic hyperpolarizability tensor, showing a large positive value. In addition we have found that the increase of the dipole moment upon excitation occurs, in all the characterized transitions, along the dipole moment axis, thus explaining why the EFISH and solvatochromic experimental values of the quadratic hyperpolarizability agree as sign and value.

• 出版日期2006-2-14