Femtosecond Excited-State Dynamics and Nitric Oxide Photorelease in a Prototypical Ruthenium Nitrosyl Complex
journal contributionposted on 01.06.2020, 17:38 by Vasily Vorobyev, Darya S. Budkina, Alexander N. Tarnovsky
Excited-state relaxation of a prototypical ruthenium nitrosyl complex (pentachloronitrosylruthenate) in water is studied by means of ultrafast dispersed, broadband transient absorption spectroscopy. Excitation pulses (duration, 40–70 fs) utilized at seven different wavelengths in the range from 675 to 335 nm populated excited electronic states of different orbital nature. The second excited singlet state of πNO* nature relaxes into the lowest triplet 3πNO* state in 100 fs via the 1d–d intermediate (lowest excited singlet) state with ca. 80 fs lifetime. The 3πNO* lifetime is 3.2 ps, and all three states are inert toward NO release, which happens in less than 200 fs from higher excited states. The vibrational coherences observed are attributed to the Jahn–Teller effect in the 1πNO* state and nitric oxide loss and provide important insights into the nature of the reaction coordinate in the course of the ultrafast excited-state relaxation dynamics.
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100 fstriplet 3 πNitric Oxide Photoreleaseultrafast excited-state relaxation dynamicsabsorption spectroscopy200 fsnitric oxide lossPrototypical Ruthenium Nitrosyl Complex Excited-state relaxationFemtosecond Excited-State Dynamicsruthenium nitrosylExcitation pulses1 πsinglet statenaturevibrational coherences3.2 ps80 fs lifetime3 π335 nm