Cyclobutane thymine dimerization is the most prominent DNA photoinduced damage. While the ultrafast mechanism that proceeds in the singlet manifold is nowadays well established, the triplet-state pathway is not completely understood. Here we report the underlying mechanism of the photosensitized dimerization process in the triplet state. Quantum chemical calculations, combined with wavefunction analysis, and nonadiabatic molecular dynamics simulations demonstrate that this is a stepwise reaction, traversing a long-lived triplet biradical intermediate, which is characterized as a Frenkel exciton with very small charge-transfer character. The low yield of the reaction is regulated by two factors: (i) a relatively large energy barrier that needs to be overcome to form the exciton intermediate, and (ii) a bifurcation of the ground-state potential-energy surface that mostly leads back to the Franck–Condon region because dimerization requires a very restricted combination of coordinates and velocities at the event of non-radiative decay to the ground state.
The formation of cyclobutane thymine T〈〉T dimers between two adjacent thymine bases is the most frequent DNA damage under UV radiation . This photolesion, which can take place in both the singlet and triplet manifolds, has been extensively investigated spectroscopically [2,3,4,5,6,7] and computationally [8,9,10,11,12,13,14,15]. The triplet pathway is a much slower process  and exhibits a smaller yield [6, 16] than the singlet mechanism due to inefficient intersystem crossing. As a consequence, this pathway yields very weak spectroscopic signals that preclude unambiguous statements regarding the mechanism [5,6,7]. In order to enhance the triplet signals, photosensitization is commonly used, increasing the T〈〉T dimerization yield [5, 17,18,19]. This enhancement can also play a role with photosensitizers acting as phototoxic drugs . Photosensitization involves intersystem crossing of a photosensitizer after excitation, transferring its electronic energy to a neighboring thymine, which is then promoted to the lowest triplet state.
Using the photosensitizer 2′-methoxyacetophenone and the dinucleotide TpT, stationary and time-resolved experiments provided two time constants, 22.5 and 62 ns, for the decay of the TpT in the triplet manifold . These constants have been related to a local triplet state (3L, see Fig. 1a, c), which is populated after triplet–triplet energy transfer (TTET) from the photosensitizer, and a biradical triplet state (3BR, see Fig. 1b, d, e), which can be formed from 3L. Quantum chemical calculations  suggested that the T〈〉T dimerization is triggered by the formation of the biradical intermediate, but the barrierless pathway calculated for the transition from 3L to 3BR is in conflict with the experimental lifetime of 22.5 ns assigned to the 3L species. This conflict is likely caused by the use in the theoretical study of a perfectly stacked geometrical configuration with C s symmetry, which is hardly achieved in a DNA strand or in a TpT dimer due to the geometrical constraints of the sugar-phosphate backbone. Recent quantum mechanics/molecular mechanics (QM/MM) calculations have found a small barrier of 0.15 eV separating the 3L and 3BR minima, in better agreement with the experimental lifetime of 22.5 ns assigned to the 3L species .
An intriguing question in the dimerization process is the character of the 3BR state. Calculations showed that the excited electronic density of 3BR is distributed over the two thymine units  and spectroscopic measurements suggested that dimerization involves the participation of delocalized triplet states . However, electronic delocalization over the two monomers can correspond to two different electronic states: (i) a Frenkel exciton, in which two local excitations are coupled (Fig. 1d), or a charge-resonance state, in which two charge-transfer states with charge flow in opposite directions are combined (Fig. 1e) . It has been speculated that the triplet state involved in dimerization could be a charge-transfer state , as theoretically predicted for the thymine–thymine 6-4 adduct formation . However, evidence of charge-transfer states for the T〈〉T dimerization has never been reported. An additional unsolved mechanistic feature is the reason behind the very low yield of dimerization even when the triplet manifold is forced to be populated after triplet–triplet energy transfer from a photosensitizer.
In this paper, we use quantum chemical calculations, wavefunction analysis, and nonadiabatic surface-hopping molecular dynamics simulations to provide a clear-cut mechanism for the photosensitized thymine dimerization. We study the formation of the 3BR precursor electronic triplet state from the 3L state and identify the nature of these species in terms of electronic delocalization and charge-transfer character. Furthermore, we offer a rationale for the factors behind the small quantum yield of the reaction.
Results and discussion
The first step of our study is to select the level of theory for the electronic-structure calculations, especially for the nonadiabatic surface-hopping dynamics simulations. We commence by computing the lowest-energy band of the density of triplet states, which involves the T 1 and T 2 electronic states, of a thymine–thymine stacked pair embedded in a solvated single strand (dT)12. Triplet excitation energies were calculated with an electrostatic QM/MM  scheme where the two nucleobases in the middle of the strand were described by multistate complete active space second-order perturbation  (MS-CASPT2) theory and the rest of the system by a force field [25, 26]. The QM region was also described by state-average complete active space self-consistent field (SA-CASSCF)  to investigate whether dynamical correlation is necessary to describe the lowest-energy triplet band. In addition, the MS-CASPT2/MM calculations have been performed employing two different active spaces, namely (4,4) and (8,8). The first one only includes the four π orbitals and the four electrons involved in the dimerization reaction (orbitals π 3, π 4, π 5*, and π 6* in Fig. 9). The second active space has two additional electrons and two additional π orbitals for each nucleobase. The calculations were performed on an ensemble of 250 geometries taken from a previous ground-state QM/MM molecular dynamics simulation . The density-of-states bands computed at the different levels of theory are plotted in Fig. 2a. The MS-CASPT2(8,8)/MM band is blue shifted by only 0.08 eV with respect to the MS-CASPT2(4,4)/MM one. This means that the smaller active space is enough to describe most of the static correlation. The small energy difference of 0.12 eV between MS-CASPT2(4,4)/MM and SA-CASSCF(4,4)/MM shows that a correct qualitative picture can be obtained without including dynamical correlation in the calculation. The electrostatic effect of the solvated DNA environment in the triplet excited states is small. This can be seen by comparing the SA-CASSCF(4,4)/MM and SA-CASSCF(4,4)/gas phase bands, whose energy maxima differ only by 0.04 eV. Overall, the energy difference between the highest level of theory [MS-CASPT2(8,8)/MM] and the lowest level of theory [SA-CASSCF(4,4) in the gas phase] employed here is 0.24 eV. Therefore, based on these results at the Franck–Condon region, SA-CASSCF calculations in the gas phase seem to be suitable to describe the lowest-energy triplet states of the thymine dimer embedded in a DNA strand.
The first step of the reaction is the population of T1 after TTET. The character of the T1 state can either be 3L or 3BR depending on its electronic configuration (see Fig. 1). For most of the geometries within the Franck–Condon region, it is expected that the T 1 electronic state corresponds to the locally excited configuration 3L as the relatively large rise distance (3.5 Å) between stacked nucleobases in DNA strands mostly precludes the direct formation of 3BR state, where the C6–C6′ bond is already preformed. The excited electronic density in 3L is completely located at one of the thymine nucleobases (Fig. 1c), while 3BR has the spin density equally distributed over the ethylenic C5 and C5′ atoms of both thymine bases (Fig. 1d, e). Since the C6–C6′ bond is already preformed in the 3BR species, it is likely that the T〈〉T dimerization is triggered by the formation of the biradical intermediate, as suggested in the literature [5, 14].
Even if the C6–C6′ bond is not preformed within the Franck–Condon region, we found it interesting to investigate whether any initial geometrical configuration presents 3BR character. To this aim, we analyzed the electronic transition density [21, 28, 29] of the triplet states that compose the density of states, from which the delocalization length (DL), defined as the number of nucleobases involved in the excitation process , was computed. For 3L, the excitation is localized in only one of the thymine bases (DL = 1), while in 3BR both thymine monomers are involved in the excitation (DL = 2). Figure 2b shows the calculated density of triplet states in the gas phase decomposed by delocalization length. We find that the lowest-energy triplet band is mainly composed by local excitations 3L, while the contribution of excitations delocalized over the two monomers is very small. Since the photosensitizer employed in the experiments  was initially excited at ∼ 4 eV, the calculated states composing this band (between 2.7 and 4.4 eV) are the only ones energetically accessible by triplet–triplet energy transfer. Unequivocally, most of the states populated at the Franck–Condon region are locally excited states, i.e. correspond to the 3L triplet state.
After having established that the 3L state is initially populated, in agreement with spectroscopic measurements, the next step is the formation of the 3BR state. Figure 3a shows the MS-CASPT2 energies of the S 0, T 1, and T 2 state in a static scan from the 3L state to the 3BR minimum and from the 3BR minimum to the dimer. In qualitative agreement with the barrier obtained in Ref. , a barrier of 0.27 eV separates the 3L and the 3BR minima in T 1. This energy barrier agrees very well with the barrier of 0.30 eV that is obtained by using the Arrhenius equation at a temperature of 300 K and using the experimental deactivation time of 22 ns , despite the approximations taken. The relatively large energy barrier is likely the first reason that explains the low yield of the reaction as in many cases the system has enough time to return to the ground state by intersystem crossing before overcoming the barrier.
The electronic wavefunction of T 1 along the pathway between 3L and 3BR is analyzed in Fig. 3b, c. Specifically, the delocalization length (DL) and the charge-transfer fraction were computed from the electronic transition density [21, 28, 29]. The delocalization length clearly shows that the dimer is in a locally excited state (DL = 1) before the barrier and, after overcoming the barrier, it evolves towards the 3BR excited state (DL = 2). This 3BR excited state can be a Frenkel exciton state or a charge-resonance state (recall Fig. 1d, e). Due to the small separation between both thymine monomers at the 3BR minimum, the formation of charge-transfer states, favoured by orbital-overlap interactions , is possible. Therefore, the 3BR state could acquire charge-resonance character along the dimerization pathway. The solid line in Fig. 3b unambiguously shows that the charge-transfer contribution is very small along the path that connects 3L with 3BR. This demonstrates that 3BR is mainly a Frenkel exciton state. Only in the region near to the 3BR/S 0 crossing the charge-transfer contribution is around 0.15, indicating that the Frenkel state acquires a small degree of charge-transfer character. This conclusion is in contrast to the hypothesis put forward in Ref. , claiming that charge-transfer triplet states could be present in the T〈〉T dimerization. Our calculations clearly demonstrate that the precursor electronic state leading to dimerization is a Frenkel exciton state and not a charge-transfer state. Recent theoretical calculations predicted that T〈〉T dimerization in the singlet manifold is also mediated by an exciton intermediate . Figure 3d–f shows the same energy scan and wavefunction analysis computed at SA-CASSCF level. Since the energy and character of the states are very similar to the ones obtained by MS-CASPT2, as was also the case for the density of states computed at the Franck–Condon region, the subsequent gas-phase dynamics simulations are performed using SA-CASSCF for the electronic-structure calculations.
After the formation of the 3BR species, the system is trapped in the 3BR minimum (recall Fig. 3a). This minimum coincides with the crossing point with the ground state S 0. Dimerization takes place only when the appropriate region of the S 0 potential is populated after intersystem crossing from T 1. As the experimental  decay time constant is 62 ns for 3BR, the radiationless decay to the ground state is a very slow process. Once in the ground state, the system can dimerize or return to the reactant region without causing damage. The experimentally determined dimerization yield is only 4% . In order to determine the factors that govern this low yield, we have sampled the 3BR minimum of T 1 for at least 100 fs with non-adiabatic surface hopping molecular dynamics simulations in the gas phase using the SHARC code .
As expected, none of the trajectories that sampled the T 1 minimum showed intersystem crossing to the ground state during 100 fs. This is because the spin–orbit coupling around the 3BR/S 0 crossing, computed for one of the trajectories as the averaged spin–orbit coupling of 100 snapshots, is merely 1 cm−1. Since the intersystem crossing rate depends on the spin–orbit coupling , the system can survive in the T 1 minimum for a long time (see Fig. 4 for an example trajectory), in agreement with the large experimental deactivation time of 62 ns  and previous calculations . In order to simulate the last step of T〈〉T dimerization, 32 snapshots from the trajectories trapped in the T 1 state were chosen based on a combination of random selection and an 3BR/S 0 energy gap smaller than 0.15 eV. At these snapshots, the molecules were manually placed in the ground state, and the dynamics was continued. The selected geometries show an average 3BR/S 0 energy gap of 0.07 eV and were taken from the time region of 80–200 fs, based on the root mean squared displacement (RMSD) of the trajectories running in the T 1 state (see Fig. 5). The RMSD shows that at times shorter than 80 fs the geometry of the dimer is not equilibrated and at times longer than 200 fs the nucleobases go apart due to the lack of the sugar-phosphate backbone. Only 5 of these 32 trajectories lead to dimerization, while 27 trajectories returned to the reactant region. Figure 6 displays an example reactive trajectory, in which, first, the C6–C6′ bond formation is completed after 60 fs, and then, the C5–C5′ bond is formed after additional 40 fs. The low number of reactive trajectories qualitatively agrees with the low experimental yield of 4% obtained from spectroscopic measurements . However, due to the small number of trajectories employed here, we cannot make any comments on the statistics of the reaction.
The low dimerization yield is rationalized by analyzing the space of coordinates and velocities (phase space) at the moment of the 3BR/S 0 transition [34, 35]. Note that these 3BR/S 0 transitions are approximated by the selection process described above. The relevant internal coordinates that drive the reaction are the C5–C5′ and C6–C6′ distances, and the relevant velocities are those of the atoms involved in these distances. In Fig. 7a, b, the values of the C6–C6′ and C5–C5′ distances and average angle formed by the velocity vectors of the atoms C5 and C5′ with the C5–C5′ vector (θ 5 and θ 5′), and by the velocity vectors of the atoms C6 and C6′ with the C6–C6′ vector (θ 6 and θ 6′), are plotted at the moment of the 3BR/S 0 transition. Those trajectories that underwent dimerization are represented by green pentagons. Only when the C6–C6′ and C5–C5′ distances are lower than 2.1 and 3.0 Å, respectively, dimerization takes place. In addition, the C atoms of each monomer also need to move towards each other with a large degree of directionality, as indicated by the restricted values of the θ angles [larger than 100° for (θ 5 + θ 6)/2 and smaller than 80° for (θ 5′ + θ 6′)/2]. Therefore, although the phase space of the system is very wide, due to the large number of degrees of freedom of the system, only the population of a very small region of the phase space induces dimerization. This is the second reason that is responsible for the very small dimerization yield.
In summary, based on our theoretical results and previous experiments , we propose the following stepwise mechanism for the photosensitized T〈〉T dimerization, schematically represented in Fig. 8. First, the locally excited triplet state 3L of thymine is populated after triplet–triplet energy transfer from a photosensitizer [step (i) in Fig. 8]. Then, the system vibrationally relaxes to the 3L minimum where it stays for 22.5 ns (ii). After overcoming an energy barrier of ca. 0.3 eV (iii), a biradical intermediate 3BR with a lifetime of 62 ns is generated within a region that crosses with the electronic ground state. The populated triplet state of the intermediate species is a Frenkel exciton with a small degree of charge-transfer character. Finally, the system undergoes intersystem crossing from T 1 to the ground state (iv), from where it dimerizes with a very small yield, i.e. returning to the initial reactant geometries consisting of two separated thymines in most events (v) due to the tight phase-space restrictions that the system needs to satisfy at the moment of the T 1→S 0 transition.
QM/MM calculation of density of states
The density of states associated to the lowest-energy triplet band of the thymine dimer embedded in a solvated single strand (dT)12 and in the gas phase was computed. First, a isothermal-isobaric ensemble (NPT) classical molecular dynamics simulation for solvated (dT)12 was evolved at 300 K for 20 ns using the ff14SB  and TIP3P  force fields to describe DNA and water, respectively. The classical simulation was run with the graphical processing unit (GPU) module pmemd  implemented in the Amber14 package . Then, the last snapshot of the classical simulation was taken as the starting one for running quantum mechanics/molecular mechanics (QM/MM) molecular dynamics simulations in the NPT ensemble for 10 ps. The two nucleobases in the middle of the strand were described by the B3LYP functional  with D3 dispersion correction  and the 6-31G* basis set [40, 41] using the GPU-based code TeraChem1.9 [42, 43] through the interface to external QM programs implemented in Amber14 . More computational details about the molecular dynamics simulations can be found in Ref. .
An ensemble of 250 equidistant snapshots was selected from the last 5 ps of the QM/MM molecular dynamics simulation. For each snapshot, the electronic excitation energies of the lowest 3 triplet states were computed using an electrostatic embedding QM/MM scheme. The two nucleobases in the middle of the (dT)12 strand are described by state-averaged complete active space self-consistent field  (SA-CASSCF) using the cc-pVDZ basis set [44, 45], and also by multistate complete active space second-order perturbation (MS-CASPT2)  with the same basis set. To minimize the effect of intruder states the level-shift approach was applied with a real-valued shift of 0.3 a.u. The IPEA shift was set to zero, as it is recommended for organic chromophores . The rest of the DNA strand and the water molecules were described by a force field [25, 26]. In addition, the calculations were performed in the gas phase by removing the environment from the 250 snapshots. The two active spaces considered in the calculations consist of 8 electrons in 8 orbitals and of 4 electrons in 4 orbitals (see Fig. 9). These calculations were carried out with MOLCAS 8 [28, 47]. The resulting excitation energies were convoluted with Gaussian functions with a full width at half maximum of 0.20 eV. The intensity of the bands was scaled to unity. In addition, all electronic triplet states in the gas phase were classified as local states (3L) or biradical states (3BR) according to the electronic delocalization length, defined as the number of nucleobases involved in the excitation, computed from the electronic transition density [21, 29, 30]. For 3L, the excitation is localized in only one of the thymine bases (DL = 1), while in 3BR both thymine monomers are involved in the excitation (DL = 2). The MS-CASPT2/MM, SA-CASSCF/MM, and SA-CASSCF/gas phase density of states and the delocalization-length decomposition of the gas-phase band are plotted in Fig. 2.
Energy scan in the T 1 potential energy surface
The static calculations for the potential energy scan (Fig. 3), which goes from the Franck–Condon region to dimer formation, were carried out using MS-CASPT2 (Fig. 3a) and SA-CASSCF (Fig. 3d) with the previously described (4,4) active space and the cc-pVDZ basis set. The 3L geometry of the Franck–Condon region was taken from the ground state QM/MM molecular dynamics simulation explained above. Specifically, for every of the 30 snapshots whose vertical energy for T 1 is below 3.5 eV, which corresponds to the maxima of lowest-energy band of the density of states, the static scan was performed. Only the scan with the lowest energy barrier in the T 1 state, which tries to mimic a minimum-energy path calculation, is shown in Fig. 3. The geometry at the crossing point between S 0 and T 1 was taken from Ref. . The energies of the two lowest triplet states were computed along a linearly interpolated pathway between both geometries. From the crossing point a second linearly interpolated pathway was connected to the dimer structure, which was taken from our previous work . Moreover, the charge-transfer contribution and delocalization length were also computed along the interpolated pathway using both MS-CASPT2 (Fig. 3b, c) and SA-CASSCF (Fig. 3e, f) [21, 29].
Non-adiabatic molecular dynamics simulations
Non-adiabatic molecular dynamics simulations were run to sample the T 1/S 0 degeneracy region, in which the T 1 state presents biradical character. Therefore, an arbitrary initial geometry was built with interatomic C5–C5′ and C6–C6′ distances of 3.13 and 2.45 Å, respectively. From this geometry 1000 initial conditions (coordinates and velocities) were generated from a zero-Kelvin Wigner distribution  based on ground-state frequencies calculated at second-order Møller-Plesset (MP2) perturbation theory  using the cc-pVTZ basis set  implemented in MOLPRO . From these 1000 initial conditions, 25 were randomly selected to run dynamics on. All trajectories were initially excited to the T 1 state and ran for at least 100 fs or until they left the T 1/S 0 degeneracy region. As the dynamics starts at a close thymine–thymine distance, it was assumed that the reaction is already in progress at the start of the dynamics. Therefore, the initial velocities of all trajectories were modified so that the center of mass of each monomer moves towards each other at a velocity corresponding to the thermal energy (k B T) at a temperature of 298 K.
From the trajectories running in the degeneracy region, 32 geometries were chosen based on a combination of random selection as well as an 3BR/S 0 energy gap smaller than 0.15 eV and continued to run on the ground state potential energy surface. This approach was necessary as none of the trajectories that ran in T 1 hopped to the ground state during their simulation time. The geometries and velocities for the new trajectories running in S 0 were taken from the point where they manually hopped from the parent trajectory, and the electronic coefficients were adapted to put the population on the ground state.
The dynamics simulations were carried out using the ab initio molecular dynamics program SHARC (surface hopping including arbitrary couplings) [32, 51], which uses a modification of the Tully surface hopping method  allowing for treating both singlet and triplet states on the same footing. The time step used for the nuclear motion was 0.5 fs, and the time step for the integration of the time-dependent electronic Schrödinger equation was 0.02 fs. All electronic structure properties (energies, gradients, and couplings) were calculated at the SA-CASSCF level of theory using the above described (4,4) active space and the cc-pVDZ basis set. For both the singlet and the triplet state calculations, 3 states were averaged with equal weights each. The non-adiabatic couplings were calculated from the wavefunction overlaps by using a local-diabatization scheme . Additionally, this procedure monitors the wavefunction phase and makes sure that it is maintained throughout the dynamics . Moreover, the Persico decoherence correction , with a decoherence parameter of 0.1 a.u. was employed. To save computational time, the gradients of not-populated states were only calculated when their energy was within 0.5 eV of the currently populated state. This procedure is in accordance with previous studies showing that higher lying states only have a minimal effect on the potential of the populated states .
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Open access funding provided by University of Vienna. CR gratefully acknowledges the University of Vienna within the uni:docs programme for financial support. CR also thanks Chemical Monthly, Springer, the Austrian Academy of Sciences, and the Austrian Chemical Society (GÖCH) for a mobility fellowship. The authors thank Felix Plasser for fruitful discussions. The computational results have been achieved in part using the Vienna Scientific Cluster (VSC).
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Rauer, C., Nogueira, J.J., Marquetand, P. et al. Stepwise photosensitized thymine dimerization mediated by an exciton intermediate. Monatsh Chem 149, 1–9 (2018). https://doi.org/10.1007/s00706-017-2108-4
- Thymine dimerization
- Quantum chemical calculations
- Non-adiabatic dynamics
- Wavefunction analysis
- Charge transfer