Siewertsen, R., Schonborn, J. B., Hartke, B., Renth, F. and Temps, F. (2011) Superior Z-->E and E-->Z photoswitching dynamics of dihydrodibenzodiazocine, a bridged azobenzene, by S1(npi*) excitation at lambda = 387 and 490 nm. Phys Chem Chem Phys, 13 (3). pp. 1054-63. DOI 10.1039/c0cp01148g.

Abstract

The ultrafast Z-->E and E-->Z photoisomerisation dynamics of 5,6-dihydrodibenzoc,g1,2diazocine (1), the parent compound of a class of bridged azobenzene-based photochromic molecular switches with a severely constrained eight-membered heterocyclic ring as central unit, have been studied by femtosecond time-resolved spectroscopy in n-hexane as solvent and by quantum chemical calculations. The diazocine contrasts with azobenzene (AB) in that its Z rather than E isomer is the energetically more stable form. Moreover, it stands out compared to AB for the spectrally well separated S(1)(npi*) absorption bands of its two isomers. The Z isomer absorbs at around lambda = 404 nm, the E form has its absorption maximum around lambda = 490 nm. The observed transient spectra following S(1)(npi*) photoexcitation show ultrafast excited-state decays with time constants tau(1) = 70 fs for the Z and <50 fs for the E isomer reflecting very fast departures of the excited wave packets from the S(1) Franck-Condon regions and tau(2) = 270 fs (320 fs) related to the Z-->E (resp. E-->Z) isomerisations. Slower transient absorption changes on the time scale of tau(3) = 5 ps are due to vibrational cooling of the reaction products. The results show that the unique steric constraints in the diazocine do not hinder, but accelerate the molecular isomerisation dynamics and increase the photoswitching efficiencies, contrary to chemical intuition. The observed isomerisation times and quantum yields are rationalised on the basis of CASPT2//CASSCF calculations by a S(1)/S(0) conical intersection seam at a CNNC dihedral angle of approximately 96 degrees involving twisting and torsion of the central CNNC moiety. With improved photochromism, high quantum yields, short reaction times and good photostability, diazocine 1 and its derivatives constitute outstanding candidates for photoswitchable molecular tweezers and other applications.

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