Resonance Raman spectroscopy and theoretical study on the photodissociation dynamics of diuron in S₂ state

Abstract

Resonance Raman spectra (RRs) and quantum chemical calculations were used to investigate the photodissociation dynamics of diuron in S2 state. The RRs indicate that the photorelaxation dynamics for the S0 → S2 excited state is predominantly along nine motions: the ring C = C stretch vibration ν12 (1593 cm−1), Ph–N–H wag ν14 (1517 cm−1), CO–N(CH3)2 stretch ν23 (1365 cm−1), CCH wag in plane/ring C = C stretch ν24 (1297 cm−1), ring CH rock in plane/ring deformation ν27 (1233 cm−1), CCH wag in plane ν29 (1151 cm−1), Ph–Cl (para) stretch ν35 (1028 cm−1), Ph–N–H wag ν37 (913 cm−1) and ring breath ν44 (685 cm−1). Dissociation by Ph–Cl (para) cleavage at S2 state directly or relaxation to T2 state by internal conversion (S2 → S1) and intersystem crossing (S1/T2) is expected by ~250 nm irradiation based on the RRS, complete active space self‐consistent field, configuration interaction singles and time‐dependent density functional theory calculations. Copyright © 2012 John Wiley & Sons, Ltd.

Recent advances in linear and nonlinear Raman spectroscopy. Part VII

“…used RR spectroscopy and theoretical analysis to examine the photodissociation dynamics of diuron in the S 2 state. The RR spectra indicate that the photorelaxation dynamics from the excited state is predominantly along nine internal coordinate motions . Wang and co‐workers examined the excited state dynamics of di‐2‐pyridylketone in the A‐band and B‐band absorptions by using RR spectroscopy, IR, and UV‐visible spectroscopy.…”