Excited-state structure and dynamics of keto-amino cytosine: the 1ππ* state is nonplanar and its radiationless decay is not ultrafast

J Phys Chem B. 2013 May 23;117(20):6106-15. doi: 10.1021/jp401881b. Epub 2013 May 14.

Abstract

We have measured the mass- and tautomer-specific S0 → S1 vibronic spectra and S1 state lifetimes of the keto–amino tautomer of cytosine cooled in supersonic jets, using two-color resonant two-photon ionization (R2PI) spectroscopy at 0.05 cm(–1) resolution. The rotational contours of the 0(0)(0) band and nine vibronic bands up to +437 cm(–1) are polarized in the pyrimidinone plane, proving that the electronic excitation is to a 1ππ* state. All vibronic excitations up to +437 cm(–1) are overtone and combination bands of the low-frequency out-of-plane ν1′ (butterfly), ν2′ (boat), and ν3′ (H–N–C6–H twist) vibrations. UV vibronic spectrum simulations based on approximate second-order coupled-cluster (CC2) calculations of the ground and 1ππ* states are in good agreement with the experimental R2PI spectrum, but only if the calculated ν1′ and ν2′ frequencies are reduced by a factor of 4 and anharmonicity is included. Together with the high intensity of the ν1′ and ν2′ overtone vibronic excitations, this implies that the 1ππ* potential energy surface is much softer and much more anharmonic in the out-of-plane directions than predicted by the CC2 method. The 1ππ* state lifetime is determined from the Lorentzian line broadening necessary to reproduce the rotational band contours: at the 0(0)(0) band it is τ = 44 ps, remains at τ = 35–45 ps up to +205 cm(–1), and decreases to 25–30 ps up to +437 cm(–1). These lifetimes are 20–40 times longer than the 0.5–1.5 ps lifetimes previously measured with femtosecond pump–probe techniques at higher vibrational energies (1500–3800 cm(–1)). Thus, the nonradiative relaxation rate of keto–amino cytosine close to the 1ππ* state minimum is k(nr) 2.5 × 10(10) s(–1), much smaller than at higher energies. An additional nonradiative decay channel opens at +500 cm(–1) excess energy. Since high overtone bands of ν1′ and ν2′ are observed in the R2PI spectrum but only a single weak 2ν3′ band, we propose that ν3′ is a promoting mode for nonradiative decay, consistent with the observation that the ν3′ normal-mode eigenvector points toward the “C6-puckered” conical intersection geometry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytosine / chemistry*
  • Isomerism
  • Models, Molecular
  • Molecular Conformation
  • Photons

Substances

  • Cytosine