Effects of ionization on stability of 1-methylcytosine — DFT and PCM studies

Consequences of ionization were studied by quantum-chemical methods (DFT and PCM) for 1-methylcytosine (MC)—a model of the nucleobase cytosine (C) connected with sugar in DNA. For calculations, three prototropic tautomers (one amino and two imino forms) and two imino zwitterions were considered, including conformational or configurational isomerism of exo heterogroups. Ionization and interactions between neighboring groups affect intramolecular proton-transfers, geometric and thermodynamic parameters, and electron delocalization for individual isomers. We discovered that an imino isomer is present in the isomeric mixture in the highest amount for positively ionized MC. Its contribution in neutral and negatively ionized MC is considerably smaller. Acid-base parameters for selected radical ions were estimated in the gas phase and compared to those of neutral MC. Gas-phase acidity of radical cations is close to that of the conjugate acid of MC, and gas-phase basicity of radical anions is close to that of the conjugate base of MC. Various routes of amino-imino conversion between neutral and ionized isomers were considered. Energetic-barrier for intramolecular proton-transfer in MC is close to that in the parent system—formamidine. Electronic supplementary material The online version of this article (doi:10.1007/s00894-016-3020-2) contains supplementary material, which is available to authorized users.


Introduction
Ionization reactions, in which a neutral molecule (M) changes its oxidation state and transforms into charged radicals, radical cation (Me → M +• ) or radical anion (M + e → M -• ), are well recognized in chemistry [1,2]. A large number of documents can be found in the literature for simple inorganic and organic species, as well as for more complex biomolecules. Energetic parameters, called the Bionization potential^(IP) or Bionization energy^(IE) for positive ionization and the Belectron affinity^(EA) for negative ionization, have been experimentally determined in the gas phase for about a thousand compounds and compiled in the NIST Chemistry Web Book, available online since 1996 [3].
Ionized forms, radical cations and radical anions, can be generated in the presence of ionizing agents, e.g., electrons, atoms, ions, etc. They can be identified in various types of mass spectrometers during positive or negative ionization [3][4][5][6]. They can also be detected by other spectroscopic techniques such as zero kinetic energy photoelectron spectroscopy [7], infrared depletion spectroscopy [8,9], or time-resolved resonance Raman spectroscopy combined with pulse radiolysis [10][11][12][13][14]. Ionization reactions and mechanisms of one-electron loss or one-electron gain can be analyzed by quantum-chemical methods, applied to isolated (in vacuo), as well as to solvated Electronic supplementary material The online version of this article (doi:10.1007/s00894-016-3020-2) contains supplementary material, which is available to authorized users. molecules [15][16][17][18][19][20][21]. For simple molecules, the IP (or IE) and EA values are associated with an atom or group which loses or gains one-electron [15]. For more complex biomolecules, for which prototropic tautomerism coupled with resonance very often takes place, isomers favored for neutral forms not always predominate for charged radicals [22][23][24], and it is difficult to indicate the ionization site from simple experiments. To understand the ionization processes and to explain the mechanisms of ionization reactions for tautomeric systems, quantum-chemical calculations should be performed for complete tautomeric mixtures of neutral and ionized forms, and physicochemical properties analyzed in detail.
For free nucleobases, uracil (U), thymine (T), cytosine (C), adenine (A), guanine (G), and for their model compounds, imidazole, purine, hydroxy-and amino-azines, the complete tautomeric mixtures in the gas phase have already been investigated [23][24][25][26][27][28]. One-electron loss and one-electron gain change acid-base properties of tautomeric groups, and consequently, change compositions of tautomeric mixtures and properties of nucleobases. These effects shed light on chemical changes in DNA, affecting aging processes, as well as various diseases, tumors, and cancers.
The phenomenon of prototropic tautomerism in heterocycles was already well known in the 1950s [29], when the molecular structure of nucleic acids was proposed by Watson and Crick [30]. The authors suggested that point mutations can occur in nucleic acids when canonical tautomeric forms of nucleobases change into their rare forms [31]. In normal nucleic acids, nucleobases have their canonical forms: amide and amino forms. Nevertheless, their rare tautomers, iminol, and imino forms are also possible ( Fig. 1). In normal DNA, cytosine (C) is paired with guanine (G), and thymine (T) is paired with adenine (A) [30]. However, the pairing can be impossible when the tautomeric preferences change. For example, the rare isomer of cytosine can be paired with adenine, and during DNA replication it can be replaced by thymine leading to the GC → AT transition [31]. Mispairs can also take place when one of the bases is ionized [32]. This type of mispair seems to occur most frequently than the mispairs being a consequence of neutral rare forms.
DNA mutations were theoretically modeled by Löwdin in the 1960s [33,34]. Taking the Watson and Crick hypothesis into account, the author proposed a model in which a double intermolecular proton-transfer in base pair GC or AT is possible. This proton-transfer can change the canonical forms of nucleobases into their rare forms. Consequently, after multiple DNA replications the GC pair can be substituted by the AT pair and vice versa. This pioneering model of double intermolecular protontransfer for neutral and ionized pairs has been extensively studied by various quantum-chemical methods in the last 20 years. Some representative reports are cited here [32,. Kumar and Sevilla [32], reviewing changes occurring in DNA exposed to high-energy radiation, paid attention to very fast (<20 ns) proton-coupled electrontransfer and discussed numerous experimental and theoretical works on intermolecular proton-transfer for radical ions. The authors found that in frozen aqueous solution upon one-electron loss a nucleobase becomes more acidic and can be deprotonated by a base, and upon one-electron gain it becomes more basic and can be protonated by an acid [56].
However, in the gas phase and in less polar environments, such as lipids and proteins present in living organisms, acidbase properties and proton-transfer reactions can be different from those in aqueous solution. For example, in aqueous solution amino acids and peptides exist in their zwitterionic forms, whereas in the gas phase intramolecular proton-transfers from acidic to basic groups for amphiprotic compounds are prohibited (ΔG > 100 kcal mol -1 ) [57]. Another example is guanidine which is a very strong base in aqueous solution (pK a > 13), whereas in the gas phase its basicity is lower than that of triethylamine [3,58]. Hence, it is possible that acid-base properties of radical ions, their stabilities and reactivities can be different in the gas phase than in aqueous solution. Some information on stability of gaseous radicals of nucleobases can be found in reports of Tureček [5,6], who used MS technologies. Nevertheless, there are little data on their acid-base properties. More information can be found for hydrated radicals of nucleobases [12-14, 32, 56]. For example, Sevilla and co-workers [56] proposed singly (pH 7-9) and doubly (pH > 11) deprotonated species for the guanine canonical radical cation in frozen aqueous solution, whereas Choi et al. [12] showed that the deprotonated guanine radical cation can be rapidly converted by protonation to a new radical cation, its tautomer. The authors employed different spectroscopic techniques. Sevilla and co-workers used ESR and UVvisible spectroscopy, whereas Choi et al. applied timeresolved resonance Raman spectroscopy combined with pulse radiolysis. The phenomena observed by Sevilla, Choi, and their co-workers clearly showed that proton-transfer reactions for ionized nucleobases, not yet paired in the DNA structure, may be crucial for better understanding various aging and disease processes. These fascinating experiments and interesting discussions between the authors [13,14], encouraged us to continue our studies on free nucleobases and their models, undertaken about ten years ago.
In this work, we chose 1-methylcytosine (MC in Chart 1) for modeling some tendencies of cytosine, combined with sugar in the DNA structure, to intramolecular proton-transfers. MC is frequently chosen to understand various properties of cytosine included in nucleic acids [59][60][61][62][63][64], because its substitution at N1 eliminates one labile proton and reduces a large number of prototropic tautomers occurring for isolated cytosine [28] to that possible for cytosine connected with sugar. This change can induce significant differences in geometric parameters and in relative stabilities of canonical and rare forms of cytosine. For our investigations, the neutral (MC), positively ionized (MCe → MC +• ), and negatively ionized forms (MC + e → MC -• ) were taken into account.
We studied the effects of positive and negative ionization on MC isomers in two extreme environments, the gas phase and aqueous solution. Two levels of theory were chosen here: the density functional theory (DFT) method [65] with the three-parameter hybrid functional of Becke [66] and the non-local correlation functional of Lee, Yang, and Parr (B3LYP) [67], and the 6-311+G(d,p) basis set [68], and the polarizable continuum model (PCM) [69,70]. For selected isomers, we also tested the aug-cc-pVDZ basis set [71]. The PCM model does not include typical specific interactions with water molecules. Nevertheless, the PCM results can provide information on medium-polarity effects. The B3LYP functional was recommended and applied by Schaefer and coworkers for charged forms, particularly for radical anions [15,20,21,50,51], and used by Sevilla and co-workers for ionized nucleobases [52,53,56]. It has been successfully applied to proton-transfer reactions for mono-and polyfunctional bases [72,73] as well as to tautomeric conversions for simple [74][75][76][77][78][79][80][81][82] and more complex tautomeric systems including ionized nucleobases and their model compounds [24][25][26][27][28]. The PCM method was already used for investigations of radical ions of DNA bases and also for estimations of the IPs and/or EAs in aqueous solution [19,[83][84][85]. More details on selection of quantum-chemical methods are given in Electronic supplementary material (ESM).

Results and discussion
Possible isomers for MC Similar to the canonical form of cytosine included in DNA, MC possesses one proton at N8 that can be intramolecularly transferred between three tautomeric atoms, N8, O7, and N3. Each proton-transfer is accompanied by migration of double bond(s) [29]. The complete tautomeric mixture for MC consists of three prototropic tautomers (1-3) (Fig. 2). Gutowski and co-workers [23,93], characterizing the valence anionic states of MC, considered additionally two zwitterionic forms (4a and 5a) with the proton at C5 and C6. Rotational and/or geometric isomerism for exo groups (-OH and = NH, 9 respectively) are also possible. Hence, considering these four types of isomerism: prototropic tautomerism, formation of zwitterions, rotational and geometric isomerism, a mixture of 11 isomers of MC should be analyzed to obtain a complete picture of intramolecular proton-transfer. For neutral MC, zwitterionic forms probably do not exist. However, they can be stabilized by ions or free electrons [93]. They can occur for ionized (redox) forms. Analogous to cytosine, present in normal DNA, the amino isomer 1 of MC can be called the Bcanonical^tautomer [30], and the isomer 2a, responsible for DNA mutations, can be named the Brare^form [31]. The mixture of all 11 MC isomers can only be investigated by quantum-chemical methods. Experiments give a possibility to characterize the major forms [94]. Rare isomers, and sometimes even minor ones, are undetectable for tautomeric systems. Very often, their signals, being in the background, cannot be identified. Some isomers of neutral 1methylcytosine have already been studied in various environments [95][96][97][98][99][100][101]. There are also a few documents on radicals [102][103][104][105][106][107] and metal complexes [108][109][110]. However, literature data are not complete for MC and only a little information can be derived on ionization effects. Even for the neutral forms, conformational or configurational isomerism of the exo groups has not always been taken into account.
Geometries, charges, spin densities, and delocalization of n-and π-electrons DFT calculations showed that heavy atoms of neutral MC isomers are in the ring plane (Table S1 in ESM) indicating that n-and π-electrons are well delocalized. For the amino tautomer 1, its exo NH 2 group has a pyramidal conformation analogous to that in adenine and other amino derivatives of pyrimidine [24,26,81]. For the imino isomers 2a-3d, protontransfer from N8 to N3 or O7 does not destroy the ring planarity. The exo groups are in the ring plane. The CC and CX (X = N or O) bond lengths depend on position of labile proton and on isomerism of exo groups. Ionization affects the CC and CX bond lengths and the ring planarity. Similar to isolated cytosine [28], the exo NH 2 group is in the ring plane for 1 +• , while this group has a twisted pyramidal conformation for 1 -• . The exo =NH and −OH groups are more twisted for radical anions than for radical cations. However, the dihedral angle is not larger than 12°.
An analysis of charge and total atomic spin densities (Table S2 in ESM) shows important differences in ionization mechanisms. One electron can be taken from different heteroatoms and/or π-bonds in MC isomers. Various sites in MC isomers can also attach one electron. Generally, the labile proton position (N8, N3, O7, C5, or C6) generates the charge distribution and unpaired spin density on other atoms. For MC +• isomers, the spin density is delocalized on the following atoms: N1 (for 1-3d), N3 (for 1 and 3a-5b), N9 (for 2a-5b), O7 (for 1, 4a and 4b), and C5 (for 1-3d, 5a, and 5b). For MC -• isomers, the spin density is mainly carried by carbon atoms: C2 (for 3a-3d), C4 (for 1-3d), C5 (for 3a-3d, 5a, and 5b), and C6 (for 1-2b, 4a, and 4b), but its high concentration also exists on N3 (for 1) and N9 (for 2a and 2b). Detailed analysis showed clearly that the unpaired electron stabilizes the structures 4a, 4b, 5a, and 5b, which were not found for neutral MC as zwitterions. Delocalization of n-and π-electrons in neutral and ionized MC isomers can be quantitatively measured using the geometry-based HOMED indices. Estimations were made for geometries optimized at the DFT level for the ring (six bonds -HOMED6) and for the whole tautomeric system, including exo groups (eight bonds -HOMED8). The calculated HOMED6 and HOMED8 values are given in Table S3 (ESM). For the neutral canonical MC-isomer 1, n-π conjugation in the six-membered ring (HOMED6 = 0.768) is analogous to that for the corresponding isomer of cytosine (HOMED6 = 0.785 [28]). The HOMED8 index is slightly larger for both MC (0.779) and C (0.791). For the neutral imino MC-isomers 2a, 2b, and 3a-3d, electron delocalization slightly decreases, and the HOMED6 and HOMED8 indices (0.64-0.73) are lower than those for 1. Additionally, favorable and unfavorable interactions between exo and endo groups affect electron delocalization. The HOMED indices are larger for isomers with favorable interactions. These effects are more important for 1-methylcytosine than for cytosine, indicating an important geometric difference between MC and C.
Positive or negative ionization decreases electron delocalization for 1, in higher degree for its radical cation ( H O M E D 8 = 0 . 5 9 9 ) t h a n f o r i t s r a d i c a l a n i o n (HOMED8 = 0.700). Ionization of imino isomers induces different effects on electron delocalization. For example, the HOMED8 indices (> 0.9) for 3a +• -3d +• strongly increases, while for 2a +• and 2b +• they slightly decrease (< 0.7). For radical anions, there is no important difference in the HOMED indices between 3a -• -3d -• and 2a -• -2b -• (HOMED8 0.56-0.76). Nevertheless, different conformations of exo -OH group cause stronger effect on the HOMED index (ΔHOMED8 0.18) than various configurations of exo =NH group (ΔHOMED8 ≤ 0.04). Moreover, the charged radicals 4a and 4b (HOMED8 < 0.5) are less delocalized than 5a and 5b (HOMED8 > 0.5). Differences between the HOMED8 indices of 5a and 4a and also between the HOMED8 indices of 5b and 4b are larger for radical cations (ΔHOMED8 > 0.4) than for radical anions (ΔHOMED8 < 0.2). Due to these differences and various ionization mechanisms for individual isomers, no linear relationship exists between the geometrybased indices of positively and negatively ionized isomers of 1-methylcytosine ( Fig. S1 in ESM).
It should be noted here that the HOMED indices estimated for 1-3d of MC, MC +• , and MC -• are not parallel to those found previously for the corresponding isomers of cytosine [28]. Lack of linear relationships between the geometry-based indices (Fig. 3) indicates that the total effect of Me, substituted at N1, is completely different for individual isomers. For example, when going from cytosine to 1-methylcytosine the HOMED8 index decreases in different degree for the neutral (by 0.012), positively (0.267), and negatively ionized (0.003) amino form 1. For the imino isomers 2a and 2b, the HOMED8 indices decrease for radical cations and increase for neutral and negatively charged forms. For the imino isomers 3a-3d, variations of the HOMED8 indices depend on conformation of exo −OH group. They increase for neutral 3a and 3c, and they decrease for neutral 3b and 3d. Reverse effects occur for 3a -• -3d -• . For 3a +• -3d +• , which are very well delocalized for MC +• and C +• (HOMED8 > 0.9), variations of the HOMED8 indices are very small (< 0.02).

Relative thermodynamic parameters
The isomers 4a, 4b, 5a, and 5b (Fig. 2) exist only for positively and negatively ionized 1-methylcytosine. For neutral MC, zwitterions are unstable and during optimization the initially built isomers 4a and 4b transform into open-ring structures with the N1−C2 bond broken, whereas 5a and 5b go to bicyclic structures with the additional N3−C5 bond formed. The instability of the neutral isomers 4a and 5a has already been signaled [93]. For all stable isomers of MC, neutral 1-3d and ionized 1-5b, real frequencies were found for minima.
Relative thermodynamic parameters {Δ(E + ZPE), ΔH, TΔS, ΔG), equilibrium constants (as pK), and percentage contents (%) estimated at the DFT level for the MC, MC +• , and MC -• isomers in vacuo are summarized in Table S4 (ESM). First perusal of these values clearly indicates that the canonical form 1 is the favored isomer at each oxidation state. As could be expected [28,93,[95][96][97][98][99], the isomers 3a-3d can be neglected in the isomeric mixture of neutral 1methylcytosine. The MC mixture consists mainly of three neutral isomers: 1 (97.3 %), 2a (2.6 %), and 2b (0.1 %). A small amount of 2a and 2b has been detected in a frozen argon matrix [95]. Positive or negative ionization dramatically changes the composition of the isomeric mixture of MC in the gas phase.
Positive ionization of 1-methylcytosine affects the percentage contents of the three isomers: • . The isomers 4a-5b (< 1⋅10 -20 %) have no importance for the structure and properties of MC +• . Since analogous calculations were performed for isolated cytosine [28], DFT results for MC +• and C +• can be analyzed. This analysis clearly shows that stability of 2a strongly increases when cytosine is substituted at N1. This isomer becomes a minor one for MC +• in the gas phase, whereas it is a rare form for C +• (< 3 %). For negatively ionized forms, the contribution of 2a in the isomeric mixture of MC -• (0.6 %) is analogous to that for C -• (0.1 %). Interestingly, the amounts of 4a-5b strongly increase for MC -• , and one of them (4a, 1.8 %) cannot be neglected in the isomeric mixture. This mixture mainly contains the canonical tautomer 1 (97.6 %). The other imino isomers (< 0.005 %) can be neglected. A use of larger basis set (aug-cc-pVDZ) in DFT calculations for the negatively ionized isomers 1, 2a, and 4a confirms the tautomeric preference (1, 98.2 %) for MC -• . Relative thermodynamic parameters for the MC, MC +• , and MC -• isomers can be plotted against those previously calculated at the same level of theory for the corresponding isomers of cytosine [28]. The plots of the calculated ΔG values for MC, MC +• , and MC -• isomers against those for cytosine (Fig. 4) show significant differences for 3b and 3d, for which the exo −OH group unfavorably interacts with Me at N1 in MC, and favorably interacts with N1 in C. These opposite intramolecular interactions lead to strong deviations of points referring to these two isomers. For other MC isomers, the ΔG values correlate quite well with those of the corresponding C isomers. For example, the slope of linear relationship for neutral isomers (1.05) and the correlation coefficient (r = 0.999 9 ) are close to unity. The same is true for ionized isomers, radical cations and radical anions. Generally, relative parameters for neutral and ionized isomers of 1-methylcytosine (except 3b and 3d) are parallel to those of cytosine.
An application of the PCM(water) model to the DFToptimized geometries of MC isomers displays an interesting effect of medium polarity (Table S5 in ESM, ZPEs estimated at the DFT level were applied to the total electronic energies calculated at the PCM(water) level). For neutral MC isomers, the canonical form 1 is favored in aqueous solution (100 %, assuming that thermal corrections and entropy terms in aqueous solution are the same as those in the gas phase). Relative energies of 2a and 2b are larger than 6 kcal mol -1 , and thus their contributions in the isomeric mixture of neutral MC may be lower than 0.01 %. Relative energies of 3a-3d do not change very much when going from nonpolar (gas phase) to polar environment (aqueous solution). Their amounts can be neglected in the isomeric mixture of MC. Generally, the relative energies calculated at the PCM(water) level are almost parallel to those estimated at the DFT level, and a good linear relationship is found (r = 0.991) for neutral isomers of MC (Fig. 5). The slope of this line (0.87) is slightly lower than unity indicating some attenuation of isomerization effects in aqueous solution.
For MC +• isomers, polar solvent seems to influence tautomeric equilibria and isomeric preferences. In aqueous solution, the rare isomer 2a seems to be the favored one (45.0 %). Its rotamer 2b also contributes in the isomeric mixture (32.0 %). The canonical form 1 is rather a minor form (22.9 %). The other iminol isomers can be neglected. A change of the relative energies for MC +• isomers when going from one extreme environment to the other one slightly destroys the linear relation observed for neutral isomers (Fig. 5). Larger deviations of points are found for MC -• isomers. The canonical form 1 predominates for MC -• (97.9 %) in aqueous solution. The contribution of the rare isomers 2a and 2b is very small (< 0.01 %). The very rare isomers 3a-3d (<< 0.01 %) can be neglected. The isomer 4a (1.7 %) significantly contributes in the isomeric mixture of MC -• . The amounts of 4b (0.3 %), 5a (0.08 %), and 5b (0.03 %) seem to be larger than those in the gas phase but they do not exceed 0.5 %. Generally, polarity of water affects the relative energies of imino isomers. It also reduces differences between the relative

Properties of the favored neutral and ionized isomeric mixtures
Considering only major, minor, and rare isomers (> 0.001 %) for neutral and ionized 1-methylocytosine, the following ionization processes can be drawn (Scheme 1). In vacuo, the neutral and positively ionized isomeric mixtures of MC contain three isomers (1, 2a, and 2b), whereas at least five isomers (1, 2a, 2b, 4a, and 5a) can be considered for the negatively ionized molecule. For each oxidation state, the canonical isomer 1 is the favored form for 1-methylcytosine. The rare isomer 2a seems to be present in the highest amount (ca. 20 %) only for MC +• . For MC and MC -• , its contribution in the isomeric mixture is considerably lower (< 3 % and < 1 %, respectively). In aqueous solution, composition of the isomeric mixture dramatically changes only for MC +• . In this case, the rare isomer 2a becomes the favored one (45 %), and the canonical isomer 1 is rather a minor form (23 %). 2b also has an important contribution (32 %). For neutral and negatively ionized 1-methylcytosine, the isomer 2a is indeed the rare form (< 1 %). The isomers 4a-5b, strongly stabilized by an unpaired electron, can also be considered as rare forms for MC -• (≤ 2 %). The positive and negative ionization processes can be characterized by the ionization potential (IP) and by the electron affinity (EA), respectively. Unfortunately, there are no experimental data for 1-methylcytosine. However, there are experimental data for canonical cytosine (IP = 8.45 eV [111] and EA = 0.23 eV [112]) and for unsubstituted pyrimidine (IP = 9.33 eV [3] and EA < −0.25 eV [113]). It should be noted that the level of theory applied here {(B3LYP/6-311+G(d,p)} reproduce well the IP (9.18 eV) and EA (−0.14 eV) for pyrimidine. Moreover, the DFT-calculated EA for pyrimidine is close to that (−0.17 eV) found at the G3MP2B3 level [3]. This confirms that the level of theory applied here is sufficient and appropriate for neutral and ionized species, radical cations, and radical anions.
If we assume that removing or adding one electron does not very much affect the structure of MC isomers, we can calculate in vacuo and in aqueous solution the microscopic IP and EA for the individual tautomers-rotamers 1-3d, taking the energies of neutral and ionized forms into account (Table S6 in ESM). The macroscopic parameters referring to the isomeric mixture of MC (Scheme 1) can also be estimated. They are as follows: IP = 8.2 and 6.3 eVand EA = −0.4 and 1.8 eV in the gas phase and aqueous solution, respectively. Polarity of water changes the ionization parameters (IP and EA) by ca. 2 eV. An analogous hydration effect has been found for nucleic acid bases and their models [16-19, 24, 26]. The negative adiabatic EA value for MC, close to that for pyrimidine [113], confirms our spin-density analysis (Table S2 in ESM). Upon negative ionization the pyrimidine ring preferentially takes one electron. Additionally, the negative EAs for MC isomers indicate that negatively ionized forms, possessing energies very close to that of neutral ones, do not exist for a suitable time period. EA measurements cannot be performed with good precision. There are also other molecules which possess negative EAs in the gas phase [3,15,113]. Nevertheless, they can be investigated in solution or clusters, for which the EAs are positive.

Basicity and acidity of neutral and ionized MC in the gas phase
There are no solvent molecules in the gas phase and acid-base properties of organic compounds depend only on functional groups. Acidity or basicity can be described by thermodynamic parameters of the corresponding deprotonation or protonation reaction, ΔH and ΔG, which differ by the entropy term, ΔG = ΔH -TΔS [3,114]  In the case of neutral 1-methylcytosine, experimental gasphase acidity and gas-phase basicity parameters have been determined in 2008 by Lee and co-workers [97]. The authors used a Fourier transform ion cyclotron resonance mass spectrometer and the bracketing method, and derived the following macroscopic acid-base parameters: DPE = 349 ± 3 and GA = 342 ± 3 kcal mol -1 for deprotonation of neutral MC to its monoanion MC-H + (MC → MC-H + + H + ), and PA = 230 ± 3 and GB = 223 ± 3 kcal mol -1 for protonation of neutral MC to its monocation MCH + (MC + H + → MCH + ). Comparison of these experimental data with those found for other organic compounds in the gas phase [3] shows that 1-methylcytosine displays acidity close to that of pyrrole (DPE = 359.6 and GA = 351.8 kcal mol -1 ) and basicity close to that of imidazole (PA = 225.3 and GB = 217.3 kcal mol -1 ) and 2-aminopyridine (PA = 226.4 and GB = 218.8 kcal mol -1 ). Both pyrrole and 1methylcytosine belong to the family of NH acids, for which the NH group is deprotonated. On the other hand, imidazole, 2-aminopyridine, and 1-methylcytosine belong to the family of N bases which contain the amidine group >N−C=N− with the imino N site preferentially protonated.
To our knowledge, gas-phase acidity and gas-phase basicity for radical cations and radical anions of 1-methylcytosine have not yet been reported in the literature. Nevertheless, they can be estimated on the basis of our DFT calculations performed for selected neutral and charged radicals. According to Sevilla and co-workers experiments performed for nucleobases and their models [32,107], deprotonation of radical cation of 1-methylcytosine and protonation of its radical anion can lead to the corresponding neutral radical: MC + • − H + → MC-H • and MC -• + H + → MCH • . Acidity and basicity parameters for these deprotonation and protonation reactions in the gas phase can be predicted from the calculated thermodynamic parameters for the corresponding radicals by the same procedure applied for neutral 1-methylcytosine (see  (Fig. 6). Moreover, the radical cations 1 +• and 2a +• are stronger bases than neutral water (PA = 165.2 and GB = 157.7 kcal mol -1 [3]), indicating that water cannot deprotonate them in the gas phase (apolar environment). Water is too weak a base. Water is also too weak an acid (DPE = 390.3 and GA = 383.7 kcal mol -1 [3]), and cannot protonate the radical anions 1 -• and 2a -• . Other compounds, being stronger bases and stronger acids than 1-methylcytosine in the gas phase, can be considered in the future for deprotonation of its radical cations and for protonation of its radical anions in an apolar environment.
How the Bcanonical^form of MC can be converted into its Brare^form?
Various routes can be considered for transformation of the canonical tautomer 1 into the rare isomer 2a for neutral and ionized 1-methylcytosine, one-step, two-steps, or multi-steps amino-imino conversion. In the gas phase, the labile proton can be transferred intramolecularly from N8 to N3 through the corresponding transition state (Scheme 4). We found three transition states between the neutral isomers 1 and 2a (TS) and their positively (TS +• ) and negatively (TS -• ) ionized forms at the DFT(B3LYP)/6-311+G(d,p) level. Each of these transition states possesses one imaginary frequency. Inclusion of thermal corrections when proceeding from 0 to 298 K and entropy terms, leads to the following relative Gibbs energies (relative to the canonical tautomer) for TS, TS +• , and TS -• : ΔG = 40.4, 42.0, and 36.0 kcal mol -1 , respectively. The estimations indicate that positive ionization slightly increases the energetic-barrier for tautomeric conversion between the amino and imino isomers whereas negative ionization slightly decreases it. Our DFT calculations show additionally that the energetic-barrier for the neutral tautomers 1 and 2a is slightly lower than that found by Fogarasi [76]  . −NH 2 /H 2 N−CH=NH). When one water molecule participates in this conversion, the energetic-barrier diminishes by 25-30 kcal mol -1 . An analogous decrease of the energeticbarrier for amino-imino conversion may be expected for the MC isomers.
Tautomeric amino-imino conversion between the canonical and rare tautomers of 1-methylcytosine can also run through two-steps proton-transfer reaction. For neutral forms, the monoanion MC-H + or monocation MCH + can be an intermediate product between the isomers 1 and 2a as shown in Scheme 2. For radical ions, tautomeric conversion between 1 +• and 2a +• can run through the neutral radicals MC-H • and that between 1 -• and 2a -• can run through the other neutral radical MCH • as shown in Scheme 3.
Investigating gas-phase basicities of organic compounds by quantum-chemical methods, Makisć and co-workers [72] analyzed the following steps from neutral (B) to monoprotonated (BH + ) forms: positive ionization of base (B e → B +• ), formation of hydrogen atom (H + + e → H • ), and formation of conjugate acid (B +• + H • → BH + ). These steps are in agreement with experiment. Gas-phase basicities can be measured using various MS techniques with positive ionization, and ions B +• and BH + detected and analyzed [3,57,114]. Taking into account the MS experiments and the Btriadic analysis^, tautomeric conversion between 1 and 2a can also run through MCH + , 1 +• , and 2a +• . An analogous tautomeric conversion between 1 and 2a can be proposed for negative ionization in the gas phase, where 1 -• , 2a -• and MC-H + can be intermediates (Scheme 5).
Another conversion-route between the ionized canonical and rare isomer of 1-metylcytosine can be proposed on the basis of Choi et al. experiments for guanidine radical cations [12]. The authors observed the neutral radical as an intermediate between two ionized isomers. On the other hand, Sevilla, Tureček, and their co-workers [5,6,32,56,106,107] proposed a deprotonation reaction for radical cations and protonation reaction for radical anions, both leading to the corresponding neutral radicals. Taking these experimental observations into account, tautomeric conversion between the ionized canonical and rare isomers of 1-methylcytosine can also run through MC-H • or MCH • (Scheme 6).
The route of proton-transfer between the canonical and rare isomers of 1-methylcytosine may depend on the method of investigation. For example, in matrix isolation IR, MW, and REMPI experiments, the intramolecular proton-transfer proposed in Scheme 4a may take place for the neutral isomers. During experimental MS gas-phase acidity/basicity determinations, tautomeric conversion may run through the monocation MCH + or monoanion MC-H + (Scheme 5). The neutral radicals MC-H • or MCH • may be intermediates between the radical ions (Scheme 6) in zero kinetic energy photoelectron spectroscopic studies.

Conclusions
Our calculations carried out in the gas phase at the DFT level and in aqueous solution at the PCM(water) level for the isomeric mixture of neutral and ionized 1-methylcytosine show clearly that positive and negative ionization change both the geometry-and energy-based parameters. Electron delocalization in the pyrimidine ring and also in the whole tautomeric system dictates the isomeric preference only for neutral MC. The most delocalized amino isomer 1 (HOMED8 = 0.779) is favored for MC. When going from the neutral to charged radicals, electron delocalization changes dramatically. Due to completely different Me effects for individual MC isomers, the changes are not parallel to those observed earlier for cytosine (Fig. 3) [28]. Only relative thermodynamic parameters for MC isomers correlate well with those for the corresponding isomers of cytosine (Fig. 4). Some exceptions are the isomers a) positive ionization 3b and 3d with unfavorable interactions between OH and Me groups.
In the gas phase, which models apolar environments (lipids), positive or negative ionization does not change the tautomeric preference (Scheme 1). Ionization influences the isomeric mixture. The canonical isomer 1 is favored for MC, MC +• , and MC -• . The rare isomer 2a, responsible for DNA mutation [31], appears in detectable amounts in the isomeric mixture of MC, MC +• , and MC -• with the highest contribution for MC +• . Its percentage content increases in aqueous solution, which models a more polar environment (enzymes, receptors, proteins, nucleoproteins, etc.). The rare isomer 2a becomes the favored form for MC +• , while the canonical tautomer 1 is only a minor form. For MC -• , the percentage contents of the radical anions 4a-5b are larger than that of 2a. They are well stabilized by an unpaired electron. Polarity of water does not affect their contributions in the isomeric mixture. Positive ionization strongly increases the energies of 4a-5b such that they can be neglected in the isomeric mixture of MC +• . For neutral MC, they do not exist. Four rotamers of 3 can be neglected at each oxidation state in both extreme environments.
The most important effects observed for tautomeric 1methylcytosine seem to result from interactions of MC with positively ionized agents. They are completely different from those observed previously for isolated cytosine and better describe some tendencies of cytosine included in DNA to intramolecular proton-transfer than isolated cytosine. Interestingly, gas-phase acidities of radical cations of MC are close to that of its monocation, and gas-phase basicities of radical anions are close to that of its monoanion. Water in the gas phase is too weak a base to deprotonate MC +• and also it is too weak an acid to protonate MC -• . This observation suggests that radical ions may live a longer time in an apolar than polar environment and may be responsible for changes in nucleic acids. Figure 7 summarizes the DFT-calculated relative Gibbs energies of possible structures which 1-methylcytosine may adopt when proceeding from the canonical to rare isomer.