Gas‐Phase Electronic Structure of Phthalocyanine Ions: A Study of Symmetry and Solvation Effects

Abstract Research into and applications of phthalocyanines (Pc) are mostly connected to their intriguing electronic properties. Here, messenger‐type UV–vis spectroscopy of two metal‐free ions from the phthalocyanine family, cationic H2Pc+ and H2PcD+, along with their hydrates is performed. They show that the electronic properties of both ions can be traced to those in the conjugate base, Pc2–, however, they are affected by state splitting due to the reduced symmetry; in the H2Pc+ radical cation, a new band appears due to excitations into the singly‐occupied molecular orbital. Quantum chemical spectra modeling reproduces all important features of the measured spectra and provides insight into the nature of electronic transitions. Hydration of the ions has only a mild effect on the electronic spectra, showing the stability of the electronic structure with respect to solvation effects.


Introduction
Phthalocyanine (H 2 Pc) and its metallic derivatives (MPc) belong to the large family of aromatic organic compounds and received considerable attention within the last years due to their exceptional electronic, optical, and magnetic properties. [1]These molecules find widespread use in various technical applications, including optical data storage, gas sensors, and dyes in infrared laser systems.Of particular interest is their potential application as nonlinear optical materials, [2] sensitizers in photochemical reactions or photovoltaic cells, [3] photodynamic reagents in cancer therapy, [4] liquid crystals, [5] enzyme-like catalysts, [6] pigments and dyes. [7]Additionally, MPc can serve as model systems for studying biologically relevant, albeit more delicate, molecules such as heme and chlorophyll, owing to their structural similarities.
Spectroscopic investigations of H 2 Pc and its derivatives have been carried out in various environments, including surfaces, [8] solutions [9] or molecular matrices. [10]A range of techniques has DOI: 10.1002/advs.20230781610d,13] Gas-phase measurements, in comparison to studies conducted in solution or on surfaces, offer the advantage of revealing the intrinsic photophysical properties of the molecular systems without interference from the surrounding environment and allow for the controlled study of such interactions. [14]nother crucial step in improving the quality and reliability of spectroscopic data is cooling the molecules to reduce the distribution of populated quantum states.15d] Another well-established method to study molecules in the gas phase at extremely low temperatures involves embedding them in helium nanodroplets (HNDs). [16]These droplets, composed of weakly bound helium atoms, serve as a cold matrix that captures any molecule it collides with. [17]15b] Additionally, van der Waals clusters of H 2 Pc with Ar n (n = 1-4) [13b,19] and with H 2 O [10c,d] have been formed through sequential pickup within the helium nanodroplets and subjected to spectroscopic analysis.15d] The spectroscopic width of H 2 Pc has been observed to be temperature and energydependent when performing 2D spectroscopy on H 2 Pc in helium clusters (≈0.37 K) and in neon clusters (≈10 K).
In this contribution, our focus lies on the electronic spectroscopy of H 2 Pc cations, which are formed in multiply-charged HNDs. [20]We examine how the spectrum changes as we alter the environment, such as by forming deuterated H 2 Pc species or by attaching single (1 up to 15) water molecules.To eliminate an influence arising from solvation within HNDs, we employ a newly developed method. [21]This method utilizes HNDs to create and cool molecular ions to sub-Kelvin temperatures before gently extracting them from the helium matrix through collisions with additional helium gas at room temperature.This approach enables the efficient formation of weakly bound helium-tagged molecular ions, which are suitable for gasphase action spectroscopy by detecting the loss of the messenger helium following photoabsorption. [22]While the UV-vis spectrum of H 2 Pc + significantly differs from that of H 2 PcD + , the formation of hydrogen bonds with water molecules results in a slight blueshift of the broad absorption bands observed in both the visible and ultraviolet regions.Through quantum chemical analysis, we rationalize the dissociation patterns and track the character of spectral features to symmetry breaking, starting from the Pc 2-conjugate base of very high symmetry (D 4h ) through H 2 Pc and open-shell H 2 Pc + (D 2h ) to the deuterated H 2 PcD + ion (C s ).

Results and Discussion
In this section, we delve into the spectroscopic properties of H 2 Pc + (H 2 O) n and H 2 PcD + (H 2 O) n , examining their absorption spectra and structural characteristics.

H 2 Pc + (H 2 O) n
We start our discussion with the spectroscopy of pure H 2 Pc + tagged with three He atoms.In Figure 1a, the Y Norm yield (normalized photofragment yield) of H 2 Pc + is plotted as a function of the laser photon energy.Two prominent and broad absorption bands, one in the visible wavelength range and one in the UV, are evident.A multi-Lorentzian fit reveals three maxima at ≈2.3, 2.5, and 4.0 eV, respectively.Figure 1b-d presents wavelength scans of mass-selected H 2 Pc + (H 2 O) n cluster ions, where n equals 1, 6 and 12.Additional absorption spectra of H 2 Pc +water clusters can be found in the SI, Figure S2 (Supporting Information).While these spectra share similarities, there is a noticeable trend: a slight narrowing and a blueshift of the absorption band in the visible range become apparent as more water molecules are attached to the clusters.Such effects have been reported for other gas-phase water-biomolecule clusters, for example for uracil-water clusters. [23]n Figure 1a, helium atoms serve as messengers for photoabsorption, whereas in Figure 1b-d, the loss of water molecules is used to extract the absorption spectra.For example, the mass spectrum associated with the wavelength scan in Figure 1d is shown in Figure 2a.Here, the quadrupole mass filter only allows ions with a mass-to-charge ratio of 730 (corresponding to H 2 Pc + (H 2 O) 12 ) to pass.The detected peak at a mass-per-charge ratio of 18 below the parent peak represents the loss of one water molecule due to collisions with residual gas after passing through the mass filter.Upon photoabsorption, two photofragment distributions emerge: one corresponding to the loss of 11 or 12 water molecules and the other to the loss of five to eight water molecules.The high abundance of H 2 Pc + (H 2 O) 5 indicates a particularly stable configuration.We disregard photofragments that In all subfigures, multi-Lorentzian fits were performed, in subfigures a) and b), three peaks were fitted (red, green, and grey), together with a cumulative fit (blue).In subfigures c) and d), data were each fitted with a multi-Lorentzian fit (blue) and with only two Lorentzian (grey and green).Due to visibility reasons, the region between 1.86 and 3.1 eV in subfigure a) and c) was multiplied by a factor of three.In the case of helium-tagged H 2 Pc + , we obtained a count rate of ≈250 cps for the parent peak H 2 Pc + He 3 and a count rate of ≈40 cps for the photofragment H 2 Pc + (at 316 nm).In the case of the hydrated H 2 Pc + , we obtained ≈1760 cps for the selected parent peak H 2 Pc + (H 2 O) 6 , and ≈160 cps for the photofragment H 2 Pc + (at 413 nm).
lose more than eight water molecules, as they stem from multiphoton absorption processes, as confirmed by laser power dependence measurements (see Figure S1, Supporting Information).
Photofragments that lose less than eight water molecules show unique wavelength-dependent absorption features, independent of the selected parent ion.The corresponding partial ion yields for different precursor ions, H 2 Pc + (H 2 O) n with n = 10, 12, 15 are displayed in Figure 2b-d.A clear trend of sequential water molecule loss with increasing absorbed energy is evident.Assuming the entire photon energy is converted into thermal energy upon excitation and equally distributed to the attached water molecules, we deduce a binding energy of 0.42(4) eV per H 2 O molecule from the experimental spectra (for more details see Figure S4, Supporting Information).
In Figure 3a,b, we show the calculated isomers of H 2 Pc and H 2 Pc + .In the most stable structure of both molecules, N0a/C0a, opposite inner nitrogen atoms are protonated, resulting in high D 2h symmetry.In the second most stable isomer of C 2v symmetry, N0b/C0b, the neighboring inner nitrogen atoms are protonated.Charging H 2 Pc almost does not influence the relative stability as the least bound electron occupies a delocalized  orbital (see below).As expected, structures with protonated outside nitrogen atoms are considerably less stable, see Figures S6 and S7 (Supporting Information).
As the positive charge is markedly delocalized in H 2 Pc + , hydration patterns in H 2 Pc and H 2 Pc + are very similar.When a first water molecule is attached, two possible hydration sites can be distinguished, namely the outer nitrogen atoms and the central N/NH groups.Starting with a second water molecule, water clusters might be formed as well.10c] However, the alternative structure with a water molecule attached to the central protons, N1b/C1b, breaking the planarity of the phthalocyanine ring, lies close in energy.For two water molecules, two hydrogen bonds with outer nitrogen atoms are preferentially formed in H 2 Pc(H 2 O) 2 while a structure with a water dimer is more stable for H 2 Pc + (H 2 O) 2 .For larger clusters, water clustering seems to be preferred compared to attaching water molecules to several nitrogen sites (see Figures S8 and S9, Supporting Information for further structures).The calculated hydration energies are ≈0.5 eV per H 2 O, slightly higher than the hydration energy deduced from the experiment in case the whole excitation energy is used for water evaporation.Note that the experimental value is derived for larger clusters for which a decrease in average hydration energy is expected.Also, one might assume that the particular stability of H 2 Pc + (H 2 O) 5 could be connected to the formation of a hydrogen bonding bridge between the central nitrogen atoms and the outer ones that are evident already in N4a and C4a; however, more extensive exploration of possible structures would be needed to confirm this.
To understand the features observed in the electronic spectra of H 2 Pc + (H 2 O) n , we analyze the electronic structure in molecules with the phthalocyanine ring, starting with Pc 2-, the conjugate base of H 2 Pc, see Scheme 1.The Pc 2-anion has a high symmetry, D 4h , and degeneracies are possible due to the presence of the C 4 axis.When H 2 Pc or H 2 Pc + is formed, symmetry is reduced to D 2h, and degeneracies are split.The addition of a deuterium atom lowers the symmetry even further to C s .These effects are directly reflected in the electronic spectra.
Moreover, the open-shell character of H 2 Pc + allows a new class of electronic transitions into the singly-occupied molecular orbital (SOMO).
Figure 4 shows the electronic transitions in the calculated structures along with spectra modeled within the linearized reflection principle.We start our discussion with electronic spectra of Pc 2-and H 2 Pc.Although they were not probed experimentally here, they provide a basis for understanding the transitions in H 2 Pc + and H 2 PcD + .In Pc 2-, the three lowest bright transitions correspond to e g ← a 1u , e g ← a 2u, and e g ← a 1u , with two higher-lying transitions lying very close to each other, forming one band (see Figure 4 and Scheme 1).As expected, valence orbitals are delocalized over the  system (Figure S12, Supporting Information).Note that all transitions are doubly degenerate and thus split when the symmetry is lowered.This is indeed observed in H 2 Pc where the e g orbitals split into b 2g and b 3g orbitals, forming broader bands in the calculated spectrum.Within 4.3 eV, there are six bright electronic transitions present in H 2 Pc (see Figure 4; Figure S13 The spectra are only mildly sensitive to the position of the hydrogen atoms in isomers N0a/N0b.We note that the broad, structureless peaks are predicted due to the usage of the linearized reflection principle. Upon ionization of H 2 Pc, an electron is removed from the HOMO orbital of a u symmetry.The open-shell character of the H 2 Pc + ion significantly alters the spectrum, introducing several new electronic transitions within the energy range covered by the experiment (Figure 4).Our spectra modeling predicts three bands centered at ≈1.7, 2.6, and 4.3 eV.The first and third bands roughly correspond to the first and second bands found in Pc 2-/H 2 Pc (see Figure S14, Supporting Information).The second band newly appears as it corresponds to an excitation from a doubly occupied b 2g /b 3g orbital into the a u SOMO orbital as shown in Scheme 1. Again, the position of the hydrogen atoms has a rather mild effect on the spectral shape.
Comparing the modeled spectrum of H 2 Pc + to the experimental data, the lowest-lying band falls outside the laser energy range and is not observed.However, the following two bands are well reproduced by our modeling with respect to their position, width, and relative intensity of ≈1:3.The structure of the lower-lying band with two Lorentzian functions used for fitting in Figure 1 can be explained by the e g orbital in Pc 2-splitting to b 2g /b 3g in H 2 Pc + .The calculated splitting of 0.21 eV for the a u ← b 2g /b 3g transitions is in good agreement with the 0.18 eV splitting obtained through the experimental fit.The higher-lying band is calculated to lie by ≈0.3 eV higher than the experimental data, most probably due to the limitations of the employed quantum chemical method.The spectra of the hydrated species (see Figure 4) give us an insight into the possible origin of the broadening and shifting of the spectra upon hydration (see Figure 1b-d).Electronic transitions in both H 2 Pc(H 2 O) n and H 2 Pc + (H 2 O) n are somewhat sensitive to the position of the water molecules, with a difference of the calculated maximum of the second band in C 1a and C 1b of 0.09 eV.With the increasing number of water molecules, the low-lying band undergoes minimal changes, while the higher-lying bands become broader and shift slightly to higher energies.As the transitions occur between highly delocalized orbitals, adsorbed water molecules have only a limited effect on the excitation energy.However, their presence still induces a subtle blue shift.This can be explained by the selective stabilization of the ground electronic state by the adsorbed water molecules while the electronically excited is either almost unaffected or even slightly destabilized by the presence of water.

H 2 PcD + (H 2 O) n
In the Next Step, we Investigate the spectroscopy of deuterated H 2 Pc + .We decided to deuterate instead of protonate our Scheme 1. Simplified comparison of the electronic structure and the main spectral features in Pc 2-, H 2 Pc, H 2 Pc + , and H 2 PcD + .See Figure 4 and Figures S12-S15 (Supporting Information) for spectra, transition energies, oscillator strengths, and transition character.
sample, due to the lower contribution of the H 2 Pc + isotopes to the H 2 PcD + rather than to the H 2 PcH + peak, which simplifies the evaluation.Deuterated H 2 Pc + ions are generated by predoping multiply charged HNDs with deuterium, leading to the formation of D 3 + ions distributed on the HND surface. [24]Further pick-up of D 2 molecules results in the formation of (D 2 ) n D + ions.Doping these predoped HNDs with H 2 Pc leads to the formation of H 2 PcD + (D 2 ) n via proton transfer processes.Once again, these ions are gently released from the HND through collisions with He gas in the evaporation chamber.For spectroscopic investiga- tions, the loss of weakly attached (D 2 ) n molecules is used as the messenger for photoabsorption.
Figure 5a displays the UV-vis wavelength scan of H 2 PcD + with three D 2 attached.The absorption spectrum exhibits two broad absorption bands, one spanning from ≈1.77 to 2.26 eV and anotherat ≈3.8 eV.A poor signal-to-noise ratio due to low laser power hinders the observation of distinct features in the spectrum, especially at laser photon energies lower than 1.9 eV.
Absorption spectra of H 2 PcD + (H 2 O) n , where n ranges from 1 to 12, are depicted in Figure 5b-k.These spectra are evaluated similarly to those in Figure 1b-d, with a notable difference in dissociation channels.While the corresponding spectra in Figure 1b-d mainly show the loss of H 2 O molecules, the mass spectra in Figure 5b-k reveal additional fragmentation channels due to the loss of DHO(H 2 O) n molecules (see Figure S3, Supporting Information).The relative loss of DHO itself increases exponentially with the number of detached water molecules (see Figure S3, Supporting Information, inset).Our analysis considers various fragmentation channels, protonated or deuterated, leading to no discernible spectroscopic differences between these species.As more water molecules are attached, the signal-tonoise ratio improves due to a higher ion yield, making the features more distinct.In addition to the reduced noise, we observe changes in the absorption properties.The peak at 1.96 eV narrows as more water molecules solvate the cluster.Moreover, an absorption feature appears at ≈1.79 eV in Figure 5g (indicated with a dashed line), which shifts to higher energies as additional water molecules are added (dashed line in Figure 5h-k).The experimentally derived hydration energy of 0.43 (5) eV per H 2 O molecule for H 2 PcD + (H 2 O) 12 clusters (see Figure S5, Supporting Information) is similar to the binding energy of water to the unprotonated H 2 Pc + .Earlier UV-vis spectra of cationic H 2 Pc In the case of deuterium tagged H 2 PcD + , we obtained a count rate of ≈1360 cps for the parent peak H 2 PcD + (D 2 ) 3 and a count rate of ≈50 cps for the photofragment H 2 PcD + (at 318 nm).In the case of the hydrated H 2 Pc + , we obtained ≈2000 cps for the selected parent peak H 2 PcD + (H 2 O) 6 , and ≈35 cps for the photofragment H 2 PcD + (at 582 nm).l) UV-vis spectrum of cationic H 2 Pc solvated in water performed by Bayrak. [25]lvated in water [25] (data is reproduced in Figure 5l) have shown unstructured broad absorption bands in the visible (max ≈625 nm) and UV (max ≈340 nm) wavelength range.It appears that solvation smoothens out the individual characteristics.
In comparison to fluorescence excitation, spectroscopic investigations utilizing HNDs as an ultracold matrix, which show narrow absorption bands (<0.1 cm -1 ) [13a] including the electronic band origin S 1 ← S 0 of neat H 2 Pc at 15 089 cm −1 (1.87 eV), [15b,26] no distinct peaks were observed in our measurements.Several factors may contribute here.The main difference between these former fluorescence excitation spectroscopic measurements and our results, besides the fact that we are studying H 2 Pc analogs in their cationic and not neutral form, is, that our measurements include excitation into higher vibrational states, which cannot be resolved well, likely due to a high density of vibrational states with similar Franck-Condon overlap.Additionally, lifetime broadening may be a contributing factor. [27]Furthermore, our measurements were conducted at higher temperatures, with dopant ions fully or nearly fully liberated from the He matrix, and we employed an OPO laser system with linewidths on the order of 4-5 cm -1 .The presence of multiple isomers may also broaden the absorption bands.
Calculated structures of H 2 PcD + (H 2 O) n , with n ranging from 0 to 4, are presented in Figure 3c.Among the various protonation possibilities, the most favorable involves adding a proton to an outer nitrogen atom of the H 2 Pc molecule, yielding the isomers D0a and D0b.Protonating an inner nitrogen atom is less favored, as seen in D0c (see Figure S10, Supporting Information for further isomers).The most favorable position for hydration is then the protonated side, represented by isomer D1a.As further water molecules attach, water clusters are predicted to be preferred, with a hydration energy close to 0.6 eV per H 2 O molecule, slightly higher than the experimental value due to the analysis of the cluster with n = 12 in the experiment.
Modeled electronic spectra of H 2 PcD + (H 2 O) n ions are shown in Figure 4.As these ions have closed-shell character and the additional proton does not influence the  system considerably, their electronic structure closely resembles that of the H 2 Pc(H 2 O) n clusters previously discussed.As a result, the spectrum of H 2 PcD + predicts two broad bands: one centered at ≈1.9 eV, the other at ≈3.8 eV.
The lower-energy band consists of two transitions that correspond to the e g ← a 1u transition in Pc 2-, with a separation of 0.25 eV between them.The transitions in the higher-energy peak primarily correlate with e g ← a 2u in Pc 2-, as illustrated in Scheme 1.The calculated bands closely match the experimental results in terms of their position, width, and intensity with a ratio of ≈1:1.As these transitions occur between highly delocalized orbitals (see Figure S15, Supporting Information), the spectra exhibit remarkable similarity among different isomers, regardless of the deuteration site.
When H 2 PcD + forms complexes with water, minimal shifts in the spectral position and intensity are observed, as exemplified for D1a-c isomers in Figure 4.This observation is consistent with the experimental spectra, where any significant changes in the absorption spectra would imply a shift in the deuteration site.With increasing hydration, a slight blueshift is noted in the calculated spectra, up to 0.05 and 0.1 eV for the first and second bands, respectively, in agreement with the experimental findings.
Two spectral features of H 2 PcD + (H 2 O) n observed experimentally in the 1.8-2.4eV region can be attributed to two distinct transitions corresponding to the e g ← a 1u transition in Pc 2-.The calculated splitting of 0.21-0.25 eV for H 2 PcD + (H 2 O) n , where n = 0-4, agrees with the separation of ≈0.1-0.2 eV observed experimentally for various degrees of hydration.The experimental spectrum is more structured as the vibrational progression cannot be reproduced within linearized reflection principle approximation.However, our analysis does not suggest the presence of several isomers with different protonation sites.

Conclusion
We employed an innovative experimental setup to investigate the spectra of mass-selected phthalocyanine cations, which were either pure, deuterated, or complexed with water molecules.Our observations reveal broad absorption bands in the ultraviolet and visible regions.To comprehend these spectral characteristics, we established connections between the electronic structures of H 2 Pc + and H 2 PcD + and the high-symmetry Pc 2-anion.While two absorption features in the closed-shell H 2 PcD + cation correlate directly with e g ← a 1u and e g ← a 2u transitions in Pc 2-, an additional band corresponding to the excitation into a SOMO is observed in the spectrum of the H 2 Pc + radical cation.Upon attaching single water molecules (ranging from 1 to 15), we note a slight blueshift and a narrowing of the absorption bands in our experimental data.Our calculations indicate that the initial water molecule preferentially adsorbs to the outer nitrogen atoms in both ions and as more water molecules are introduced, water clusters form.Theoretical analysis further confirms that the electronic transitions between highly delocalized orbitals are only minimally affected by the presence of the adsorbed water molecules.

Experimental Section
In the experiment, helium nanodroplets with a size of several million helium atoms were produced by supersonic expansion of helium at a pressure of 22 bar and a temperature of 8.5 Kelvin through a 5 μm nozzle.The HNDs were ionized by electron impact, mass-per-charge selected by an electrostatic sector, and doped in a differentially pumped chamber which was equipped with a resistively heated oven and a gas inlet system.In this study, the oven was utilized to vaporize H 2 Pc, and the gas inlet system to introduce water vapor.The picked-up H 2 Pc molecules were attracted to the charged regions on the HND surface and were ionized through charge transfer processes.Further pick-up of H 2 Pc and/or water molecules results in the formation of cluster ions, denoted as (H 2 Pc) n + (H 2 O) m , where n and m were tuned by varying the oven temperature as well as by the valvecontrolled gas inlet system, respectively.Subsequently, the doped HNDs collided with additional helium gas at room temperature in a separate, differentially pumped evaporation chamber.These collisions serve to reduce the size of the droplets and gently release the helium-tagged dopant ions from the helium nanodroplet.Depending on the helium pressure in the evaporation chamber, additional collisions of these ejected cluster ions with He atoms reduce the number of He atoms attached to a desired value.
After mass-to-charge selection using a quadrupole mass filter, the ions were merged with a laser beam generated by a pulsed OPO laser system (EKSPLA NT242).The resulting products were then directed into a timeof-flight mass spectrometer.The mass spectrometer was operated at a frequency of 10 kHz, while the laser operated at 1 kHz, allowing for the recording of mass spectra with and without laser irradiation on an alternating basis.For a more detailed description of the experimental setup, additional information can be found elsewhere. [22]rom the measured mass spectra, the normalized photofragment yield Y Norm related to absorption using the following formula was calculated: where N Frag , N BG , N Parent, and N Photon were the integrated counts of the fragments resulting from photoabsorption, the background counts at this mass per charge value without photoabsorption, the parent ion peak without photoabsorption, and the number of photons, respectively.Caution was exercised to select only the desired photofragments and to avoid photoproducts resulting from multiphoton processes.Further details can be found in Figure S1 (Supporting Information).
To analyze the structure, hydration energy, and electronic spectra of specific ions, quantum chemical calculations, optimizing Pc 2-, H 2 Pc, H 2 Pc + , and H 2 PcD + along with their hydrated forms employing density functional theory (DFT) at the B97XD/cc-pVDZ level of theory were performed. [28]or hydrated clusters, only representative structures with respect to the bonding patterns were picked to study the influence of the hydration on the electronic spectra (see the Supporting Information for details).The nomenclature of N, C, and D for neutral (H 2 Pc), cationic nondeuterated (H 2 Pc + ), and cationic deuterated clusters (H 2 PcD + ) was used, respectively.Additionally, we indicate the number of water molecules and use the letters a-i to represent the relative stability, e.g., D2b refers to the second most stable H 2 PcD + (H 2 O) 2 structure identified.The electronic transitions were calculated Within time-dependent DFT (TDDFT) theory at the TD-BMK/aug-cc-pVDZ level, [29] covering transitions up to 4.7 eV.The shape of the spectra was modeled using the linearized reflection principle approximation [30] that requires only calculations of molecular properties (vibrational frequencies in the ground state, excitation energies, and forces in every electronically excited state) in the ground-state minimum structure.However, the vibrational resolution was lost within this approach, and an unreasonable spectral width might be predicted for bound electronically excited states.Wave function stabilization was performed prior to each optimization and all calculations were done in the Gaussian package. [31]

Figure 1 .
Figure 1.Wavelength scan of different precursor ions.Subfigure a) shows a wavelength scan for H 2 Pc + He 3 , subfigure b-d) for the precursor H 2 Pc + (H 2 O) n with n = 1, 6, 12.In all subfigures, multi-Lorentzian fits were performed, in subfigures a) and b), three peaks were fitted (red, green, and grey), together with a cumulative fit (blue).In subfigures c) and d), data were each fitted with a multi-Lorentzian fit (blue) and with only two Lorentzian (grey and green).Due to visibility reasons, the region between 1.86 and 3.1 eV in subfigure a) and c) was multiplied by a factor of three.In the case of helium-tagged H 2 Pc + , we obtained a count rate of ≈250 cps for the parent peak H 2 Pc + He 3 and a count rate of ≈40 cps for the photofragment H 2 Pc + (at 316 nm).In the case of the hydrated H 2 Pc + , we obtained ≈1760 cps for the selected parent peak H 2 Pc + (H 2 O) 6 , and ≈160 cps for the photofragment H 2 Pc + (at 413 nm).

Figure 2 .
Figure 2. a) Mass spectrum of the precursor H 2 Pc + (H 2 O) 12 when photofragmentation occurs.The fragments are plotted in different colors and are multiplied by a factor of ten due to visibility reasons.Section b-d) shows the wavelength dependence of each photofragment for the precursor H 2 Pc + (H 2 O) n , n = 10,12,15.The black curve is the sum of all photofragments after 1-photon absorption.
, Supporting Information).Two transitions of the b 2g /b 3g ← a u character form a band at ≈2.1 eV, the second band at ≈4.2 eV corresponds mainly to b 2g /b 3g ← b 1u transitions.

Figure 3 .
Figure 3. Selected isomers of a) H 2 Pc(H 2 O) n , b) H 2 Pc + (H 2 O) n , c) H 2 PcD + (H 2 O) n , n = 0-4, along with the respective symmetry group and the relative stability for n = 0 and hydration energy for n = 1-4 corresponding to the M + n H 2 O → M(H 2 O) n reaction, M = H 2 Pc, H 2 Pc + , H 2 PcD + (in eV).Calculated at the B97XD/cc-pVDZ level of theory.See Figures S6-S9 (Supporting Information) for further structures.

Figure 5 .
Figure 5. a) Wavelength scan for H 2 PcD + (D 2 ) 3 ; b-k) Wavelength scan for the precursor ions H 2 PcD + (H 2 O) n for n = 1-6, 8, 10-12.In the case of deuterium tagged H 2 PcD + , we obtained a count rate of ≈1360 cps for the parent peak H 2 PcD + (D 2 ) 3 and a count rate of ≈50 cps for the photofragment H 2 PcD + (at 318 nm).In the case of the hydrated H 2 Pc + , we obtained ≈2000 cps for the selected parent peak H 2 PcD + (H 2 O) 6 , and ≈35 cps for the photofragment H 2 PcD + (at 582 nm).l) UV-vis spectrum of cationic H 2 Pc solvated in water performed by Bayrak.[25]