Two photochromic diarylethenes blocked by alkyl bridges in an ideal conformation for photocyclization are studied by stationary and femtosecond transient spectroscopy in order to depict the photocyclization processes: the bistable 1,2-dicyano[2.n]metacyclophan-1-ene with n = 2, abbreviated as [2.2], and its non-bistable analogue with n = 4, abbreviated as [2.4]. The data are interpreted in the light of AM1-CIS calculations and state correlation diagrams based on conclusive TD-DFT calculations. For [2.2], a solvent-sensitive excitation wavelength threshold governing the photocyclization yield is clearly evidenced between the S(1) and S(2) singlet states. Excitation above and beyond this threshold induces two distinct photochemical pathways. The S(1) vertical excitation induces direct efficient (phi approximately = 0.9-1), and ultrafast (approximately 120 fs) photocylization from S(1) open form that leads to a ground-state transition structure, probably through a conical intersection, then to a hot cyclized ground state that relaxes by vibrational cooling. Upon higher excitation energy, the system undergoes internal conversion to the hot S(1) state, then evolves toward the cyclized S(1) state and relaxes by ultrafast S(1)-S(0) internal conversion. Alternatively, the possibility for a second conical intersection near hot S(1) state is discussed. This second photoclosure reaction is less efficient and both the photocylization yield and overall kinetics depend on solvent polarity (phi = 0.49, tau = 2.5 ps in nonpolar solvent; phi = 0.7, tau = 1.5 ps in polar solvent). In the case of [2.4], for which the distance between the two reactive carbons is larger, a unique photoclosure mechanism is found and a structural effect is reported. Indeed, this mechanim is similar to the above second reaction of [2.2] but characterized by much slower kinetics ranging from 12 to 20 ps (depending on the excitation wavelength and solvent polarity). All polarity effects are rationalized in terms of stabilization of the transient states of charge-transfer character involved in the photocyclization process.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.