Tetra-2,3-Pyrazinoporphyrazines with Externally Appended Pyridine Rings 22 Synthesis, Physicochemical and Photoactivity Studies on In(III) Mono- and Heteropentanuclear Complexes

The basic macrocyclic octapyridinotetrapyrazinoporphyrazine InIII complex of formula [Py8TPyzPzIn(OAc)]·8H2O, prepared by reaction of the free ligand [Py8TPyzPzH2]·2H2O with In(OAc)3, is a stable-to-air species of which the structure has been studied by its X-ray powder diffraction and mass spectra and characterization operated by IR and UV-visible spectral behavior. The complex has been further examined and proven to be of potential interest for its response as an anticancer agent in the field of photodynamic therapy (PDT), the value of ΦΔ = 0.55 (in DMF) being in the range of 0.4–0.6 at the level of similar phthalocyanine and porphyrazine analogs and qualifying the species as a highly efficient anticancer agent. Planned parallel types of investigation, including their photoactive behaviour in PDT, have been extended to the mononuclear octacation [(2-Mepy)8TPyzPzIn(OAc)]8+ (salted by iodide ions) and the heteropentanuclear derivatives [(M’Cl2)4Py8TPyzPzIn(OAc)]·xH2O (M’ = PdII, x = 8; PtII, x = 1)) and [{(Pd(CBT)2)4}Py8TPyzPzIn(OAc)]·19H2O (CBT = m-carborane-1-thiolate anion).


Introduction
Among our extensive studies on macrocyclic porphyrazine metal derivatives often finalized to explore their tendency to behave as active agents in photodynamic therapy (PDT), a well-known anticancer curative modality [1][2][3][4], we previously reported on the mononuclear complexes of formula [TTDPzMX] (TTDPz = tetrakis(thiadiazole)porphyrazinato anion) carrying centrally MX groups (MX = Al III Cl, Ga III Cl, and In III OAc) (OAc = acetate anion) [5], and for the two Al III and Ga III macrocycles relevant data were obtained as to their potential photoactivity in PDT (Φ ∆ respectively 0.35 and 0.69) [6]. In recent times, a related type of investigation regarded the mono-and pentanuclear porphyrazine macrocycles of formula [Py 8 TPyzPzMCl]·xH 2 O and [(PdCl 2 ) 4 Py 8 TPyzPzMCl]·xH 2 O (Py 8 TPyzPz = tetrakis-2,3-[5,6-di(2-pyridyl)-pyrazino]porphyrazinato dianion; M = Al III , Ga III ) [7] (Figure 1), all data cited appearing well compatible with those known for similar phthalocyanine and porphyrin analogs. Based on these data, it was found interesting to add to these findings those regarding a series of In III related porphyrazine complexes, this allowing a comparison on the heavy metal effect along the triad of the Al III , Ga III , In III complexes and on the role played by the target macrocycle as a potential therapeutic agent in PDT.
[Py8TPyzPzH2]·2H2O (100.9 mg, 0.086 mmol) and In(OAc)3 (48.9 mg, 0.167 mmol) (molar ratio 1:2) were suspended in glacial CH3COOH (5 mL) and the mixture was heated under stirring at 135 °C for 2 h. After cooling to room temperature and the addition of H2O (5 mL), the suspension was kept in a refrigerator overnight. After centrifugation, the separated dark green solid was washed with H2O until neutrality of the washings and was brought to constant weight under vacuum (
[Py 8 TPyzPzIn(OAc)]·8H 2 O. [Py 8 TPyzPzH 2 ]·2H 2 O (100.9 mg, 0.086 mmol) and In(OAc) 3 (48.9 mg, 0.167 mmol) (molar ratio 1:2) were suspended in glacial CH 3 COOH (5 mL) and the mixture was heated under stirring at 135 • C for 2 h. After cooling to room temperature and the addition of H 2 O (5 mL), the suspension was kept in a refrigerator overnight. After centrifugation, the separated dark green solid was washed with H 2 O until neutrality of the washings and was brought to constant weight under vacuum ( Singlet Oxygen Quantum Yield Measurements. Measurements of singlet oxygen quantum yield (Φ ∆ ) were carried in DMF by an absolute method using 1,3-diphenylisobenzofuran (DPBF) as the scavenger of singlet oxygen ( 1 O 2 ), as previously reported [6]. Solutions of the complexes (ca. 10 −6 -10 −5 M) and DPBF (ca. 5 × 10 −5 M) in DMF were irradiated in a 10-mm path length quartz cell with monochromatic light (Premier LC Lasers/HG Lens, Global Laser). The irradiation wavelength (λ irr = 670 nm) was close to the maximum of the Q-band absorption peaks for each compound. The light intensity was set to 0.300 mW and the value accurately measured with a radiometer (ILT 1400A/SEL100/F/QNDS2, International Light Technologies). The decay of DPBF absorption at 414 nm (ε DPBF = 2.3 × 10 4 mol −1 L cm −1 ) was monitored at 20 • C by a Varian Cary 50 Scan UV-visible spectrophotometer. The Φ ∆ values were calculated from Stern-Volmer plots on the basis of Equation (1): where Φ DPBF is the quantum yield of the photoreaction, k d is the decay rate constant of 1 O 2 in the solvent, and k r is the rate constant for the reaction of DPBF with 1 O 2 . The 1/Φ ∆ values were obtained as the intercept of each linear plot (1/Φ DPBF versus 1/[DPBF]).
Other physicochemical measurements. IR spectra were recorded on a Varian FT-IR 660 instrument in the range of 4000-250 cm −1 (KBr pellets or nujol mulls between CsI disks). UV-visible solution spectra of the synthesized compounds were recorded with a Varian Cary 5E spectrometer using quartz cuvettes (1 cm). Elemental analyses for C, H, N, and S were provided by the "Servizio di Microanalisi" at the Dipartimento di Chimica, Università "La Sapienza" (Rome), on an EA 1110 CHNS-O instrument. The ICP PLASMA In, Pd, and Pt analyses were performed on a Varian Vista MPX CCD simultaneous ICP-OES. X-ray powder diffraction spectra were run in the interval 500-5000 (2 ϑ/ • C) on a Philips PW1029 instrument interfaced with a computer (Software APD Philips), using a CuKα radiation. Mass spectra were recorded on a Shimadzu Biotech Axima Confidence spectrometer operating in MALDI-TOF modality (Collective Usage Center of Ivanovo State University of Chemical Technology supported by the Ministry of Science and Higher Education of Russia, grant No. 075-15-2021-671).  3 (Section 2), is generally obtained in good yield as a brilliant green solid. The X-ray powder spectrum of the complex (Figure 2A), indicative of a partial crystalline character, is closely approaching the X-ray powder of the spectra of the related macrocyclic analogs centrally carrying Al III Cl and Ga III Cl units ( Figure 2B,C) [7]. As established for the parallel series of tetrakis(thiadiazole)porphyrazines [TTDzPzMX] (M = Al III , Ga III ; X = Cl/M = In III , X = OAc), [5] schematically shown in Figure 3, and supported by the molecular arrangement of the corresponding Al III and Ga III species both elucidated by X-ray work [5] and by the findings for other similar tetrapyrrolic macrocycles given in ref. [7] (Table 1), providing for all of them (M = Al III , Ga III ) a distance M-C t of 0.3-0.4 Å, the In III center in the present basic macrocycle is given as axially positioned and residing out of the C t of the inner N 4 coordination site probably only very slightly exceeding the value of 0.4 Å. The water present in the complex, most likely involved in different forms of hydrogen bonds with the numerous N atoms of the macrocycle, could be eliminated by heating it under vacuum (100 • C, 10 −2 mmHg); nevertheless, rehydration took place at least partially by exposition of samples to the air. Only traces of water were present in the corresponding macrocyclic salt-like species, most likely explained by the fact that external N atoms once positively charged are no longer available for water attraction.       Useful information about the molecular formula of the basic In III complex is provided by its mass MALDI-TOF spectrum ( Figure 4). Peak positions at m/z = 1252.5 and 1287.5 were assigned, respectively, to the molecular fragments [Py 8 TPyzPzIn] and [Py 8 TPyzPzInCl], the latter formed clearly by the substitution of the OAc − group with Cl − caused by the utilized solvent (CHCl 3 ). In addition, a very low signal positioned at m/z 2391 was also observed as reasonably assigned to the formation of a mononuclear dimeric species [{Py 8 TPyzPz} 2 In] showing the metal center bridging two macrocyclic units. Noteworthy, a low intensity signal of the molecular peak at m/z = 1311.7 present in the bottom spectrum identified the species [Py 8 TPyzPzIn(OAc)]. It is noteworthy that, in the MALDI-TOF spectrum recorded using solution in CH 3 CN, the molecular ion peak corresponding to the species with axial chloride is absent, along with the stable cation [Py 8 TPyzPzIn] + peak of the bis(acetate) complex [Py 8 TPyzPzIn(OAc) 2 ] + , could be seen (see Figure S1 and related discussion in Supporting Information).

species [{Py8TPyzPz}2In]
showing the metal center bridging two macrocyclic units. Noteworthy, a low intensity signal of the molecular peak at m/z = 1311.7 present in the bottom spectrum identified the species [Py8TPyzPzIn(OAc)]. It is noteworthy that, in the MALDI-TOF spectrum recorded using solution in CH3CN, the molecular ion peak corresponding to the species with axial chloride is absent, along with the stable cation [Py8TPyzPzIn] + peak of the bis(acetate) complex [Py8TPyzPzIn(OAc)2] + , could be seen (see Figure S1 and related discussion in Supporting Information).   8 ·H 2 O, which was obtained as a dark green solid by heating the basic In III neutral complex in the presence of CH 3 I in DMF (Section 2) and proved to be an amorphous material by its X-ray powder diffraction spectrum ( Figure S2). The restricted presence of water in the salted species is reasonably explained by the occurring engagement of the external N atoms in the methylation process and their associated quaternization. The newly reported related porphyrazine octacation [(2-Mepy)8TPyzPzIn(OAc)] 8+ schematically shown in Figure 5 is present in the corresponding iodide salt formulated as [(2-Mepy)8TPyzPzIn(OAc)](I)8·H2O, which was obtained as a dark green solid by heating the basic In III neutral complex in the presence of CH3I in DMF (Section 2) and proved to be an amorphous material by its X-ray powder diffraction spectrum ( Figure S2). The restricted presence of water in the salted species is reasonably explained by the occurring engagement of the external N atoms in the methylation process and their associated quaternization.  (Table 1)). In the spectrum of the octacationic-related  (Table 1)). In the spectrum of the octacationic-related macrocycle ( Figure 5, bottom), the essential skeletal absorptions of the macrocycle were kept in unchanged positions, with partly superimposed new peaks assigned to the presence of bending vibrations of the new CH 3 groups and changes determined by the introduced N + charged centers in the pyridine rings.  Table 1) taken in CH3CN and CHCl3 ( Figure S3) indicate the presence of the complex in its pure monomeric form with exclusive narrow intense absorptions in the Soret (370-380 nm) and Q-band region (660-670 nm), both assigned as π-π* transitions. Differently, the initial UV-visible spectrum of the complex shows in DMF (Figure 7), in addition to the presence of the Soret and Q-band peaks, an additional absorption of much lower intensity positioned immediately above 700 nm (peak at ca. 740 nm), which increases in intensity along with the time (4h), this effect paralleled by a concomitant increase of a broad absorption of an initial even lower intensity present in the region 500-600 nm. Both these absorptions, most likely indicative of the presence of some form of aggregation, moved in intensity in opposite direction with respect to that of the Soret and Q-band peaks, the spectra evidencing clean isosbestic points. These findings encouraged the hypothesis of an aggregation implying a monomer to dimer process. Moreover, a parallel evolution of the spectrum is observed in DMSO and pyridine ( Figure S4).  Table 1) taken in CH 3 CN and CHCl 3 ( Figure S3) indicate the presence of the complex in its pure monomeric form with exclusive narrow intense absorptions in the Soret (370-380 nm) and Q-band region (660-670 nm), both assigned as π-π* transitions. Differently, the initial UV-visible spectrum of the complex shows in DMF (Figure 7), in addition to the presence of the Soret and Q-band peaks, an additional absorption of much lower intensity positioned immediately above 700 nm (peak at ca. 740 nm), which increases in intensity along with the time (4h), this effect paralleled by a concomitant increase of a broad absorption of an initial even lower intensity present in the region 500-600 nm. Both these absorptions, most likely indicative of the presence of some form of aggregation, moved in intensity in opposite direction with respect to that of the Soret and Q-band peaks, the spectra evidencing clean isosbestic points. These findings encouraged the hypothesis of an aggregation implying a monomer to dimer process. Moreover, a parallel evolution of the spectrum is observed in DMSO and pyridine ( Figure S4). Interestingly, a systematic bathochromic shift of ca. 10-15 nm was observed by comparing the Q-band position (660-670 nm) for the present In III complex in its monomeric form in the different solvents (  [7]. In this respect, these overall findings also closely recall what was observed for the parallel known triad of [TTDPzMX] complexes (M = In III , X = OAc − ; Al III , Ga III ; X = Cl − , OH − ) [5].
Of remarkable interest is the ensemble of the UV-visible spectral behavior observed for the octacationic macrocyclic complex (as its iodide salt) in the nonaqueous solvents CH3CN, DMF, DMSO, H2O and py (quantitative data in Table 1). Two main aspects need to be evidenced when observing the spectra run immediately after dissolution of the corresponding salt species in both CH3CN and DMF reported in the region 300-900 nm ( Figure 8). Both spectra show typical absorptions in the Soret and Q-band region located, respectively, at 355-360 nm and at 670-680 nm, as expected for a porphyrazine macrocyclic unit, with concomitant comparatively intense broad absorptions with the highest intensity present at ca. 550 and above 700 nm. These two latter combined absorptions are certainly indicative of the presence of a heavily more intense form of aggregation from that evidenced for the corresponding neutral species (Figure 6). The same form of aggregation becomes even more evident in DMSO and literally dominant in H2O (Figure 9). Similar behavior was observed in pyridine ( Figure S5). Interestingly, a systematic bathochromic shift of ca. 10-15 nm was observed by comparing the Q-band position (660-670 nm) for the present In III complex in its monomeric form in the different solvents (  [7]. In this respect, these overall findings also closely recall what was observed for the parallel known triad of [TTDPzMX] complexes (M = In III , X = OAc − ; Al III , Ga III ; X = Cl − , OH − ) [5].
Of remarkable interest is the ensemble of the UV-visible spectral behavior observed for the octacationic macrocyclic complex (as its iodide salt) in the nonaqueous solvents CH 3 CN, DMF, DMSO, H 2 O and py (quantitative data in Table 1). Two main aspects need to be evidenced when observing the spectra run immediately after dissolution of the corresponding salt species in both CH 3 CN and DMF reported in the region 300-900 nm ( Figure 8). Both spectra show typical absorptions in the Soret and Q-band region located, respectively, at 355-360 nm and at 670-680 nm, as expected for a porphyrazine macrocyclic unit, with concomitant comparatively intense broad absorptions with the highest intensity present at ca. 550 and above 700 nm. These two latter combined absorptions are certainly indicative of the presence of a heavily more intense form of aggregation from that evidenced for the corresponding neutral species (Figure 6). The same form of aggregation becomes even more evident in DMSO and literally dominant in H 2 O (Figure 9). Similar behavior was observed in pyridine ( Figure S5).

[(PdCl 2 ) 4 Py 8 TPyzPzIn(OAc)]·8H 2 O and [(PtCl 2 ) 4 Py 8 TPyzPzIn(OAc)]·H 2 O.
Procedures for the synthesis of these two pentanuclear macrocycles as hydrated species, developed by reaction of the mononuclear complex [Py 8 TPyzPzIn(OAc)]·8H 2 O with [(C 6 H 5 CN) 2 PdCl 2 ] or [(C 6 H 5 CN) 2 PtCl 2 ] (Section 2), led to the formation of amorphous green brilliant solids, as proven by X-ray powder spectra ( Figure S6).     The IR spectra of both macrocycles in the region 1800-300 cm −1 (Figure 10) recall aspects mainly observed for the respective mononuclear species, a well distinct spectral feature being instead for them the presence of the absorption at ca. 340 cm −1 assigned, as due to ν (M-Cl) (M = Pd II , Pt II ) . Worth notice is also, for both species, the lowered intensity reproducibly observed in the region 1000-950 cm −1 of the absorption positioned at 995 cm −1 as compared to that present at ca. 950 cm −1 , both appearing for the mononuclear species of more comparable relative intensity ( Figure 5), a difference which can be taken as indicative of the change mono-to pentanuclear species, these findings recalling those occurring for the homo/heteropentanuclear macrocyclic analogs carrying centrally bivalent [10,11] and tervalent metal centers [7]. aspects mainly observed for the respective mononuclear species, a well distinct spectral feature being instead for them the presence of the absorption at ca. 340 cm −1 assigned, as due to ν(M-Cl) (M = Pd II , Pt II ). Worth notice is also, for both species, the lowered intensity reproducibly observed in the region 1000-950 cm −1 of the absorption positioned at 995 cm −1 as compared to that present at ca. 950 cm −1 , both appearing for the mononuclear species of more comparable relative intensity ( Figure 5A), a difference which can be taken as indicative of the change mono-to pentanuclear species, these findings recalling those occurring for the homo/heteropentanuclear macrocyclic analogs carrying centrally bivalent [10,11] and tervalent metal centers [7]. The present two hydrated pentanuclear macrocycles [(MCl2)4Py8TPyzPzIn(OAc)]ˑxH2O (M = Pd II , Pt II ) assigned a structure similar to that reported in Figure 1 for the related Al III and Ga III corresponding species and having peripherally coordination sites of the type represented schematically in Figure 1 involving either PdCl2 or PtCl2 units are less soluble in DMSO and DMF than the corresponding neutral mononuclear In III complex. Their initial UV-visible spectra in the two solvents, similarly to what observed for the respective mononuclear macrocycle, indicate the occurrence of some form of aggregation more heavily increasing with the time (ca. 24h), as evident for the spectra taken for both species in DMSO ( Figure 11) and in DMF ( Figure  S7).
The reproducible bathochromic shift observed for the process mono-to pentanuclear species (2-6 nm in DMSO and DMF, 10 nm in CH3CN, nul in pyridine; data in Table 1) indicates that peripheral binding of the PdCl2 and PtCl2 units only scarcely increments the electron-deficient character of the central macrocycle, parallel effects previously observed  Figure 1 for the related Al III and Ga III corresponding species and having peripherally coordination sites of the type represented schematically in Figure 1 involving either PdCl 2 or PtCl 2 units ar e less soluble in DMSO and DMF than the corresponding neutral mononuclear In III complex. Their initial UV-visible spectra in the two solvents, similarly to what observed for the respective mononuclear macrocycle, indicate the occurrence of some form of aggregation more heavily increasing with the time (ca. 24 h), as evident for the spectra taken for both species in DMSO ( Figure 11) and in DMF ( Figure S7).
The reproducible bathochromic shift observed for the process mono-to pentanuclear species (2-6 nm in DMSO and DMF, 10 nm in CH 3 CN, nul in pyridine; data in Table 1) indicates that peripheral binding of the PdCl 2 and PtCl 2 units only scarcely increments the electron-deficient character of the central macrocycle, parallel effects previously observed also for their Pd II and Pt II homo/heteropentanuclear analogs [10][11][12][13]. Moreover, prolonged contact with pyridine determines the external release of the MX 2 units and complete formation of the related mononuclear In III species, in line with previous findings for the previously studied pentanuclear macrocycles [(PdCl 2 ) 4 Py 8 TPyzPzM] (M = bivalent metal center) [10,11]. [

[{Pd(CBT)2}4Py8TPyzPzIn(OAc)]•19H2O (CBT = m-carborane-1-thiolate anion).
In the area of anticancer BNCT (boron neutron capture therapy), only two "low molecular weight" curative agents have so far been used in clinical trials, i.e., sodium borocaptate (BSH, Na2B12H11SH) and the dihydroxyboryl derivative of phenylalanine (BPA), others being of only recently proposed intent or under evaluation [14] (including carboranyl porphyrins and porphyrazines) [15]. Since, in this area, we recently reported on the This heteropentanuclear species is obtained as a light green substantially amorphous ( Figure S8), highly hydrated solid material by reaction of the parent pentanuclear complex [(PdCl 2 ) 4 Py 8 TPyzPzIn(OAc)]·8H 2 O with m-carborane-1-thiol (Section 2), this implying full peripheral substitutions of Cl − by CBT − anions on the external Pd II centers. Its IR spectrum ( Figure 13) shows in the range 3600-3200 cm −1 a broad absorption due to the O-H stretching of water and, in the adjacent region, the low intensity peak at 3042 cm −1 and the much more intense peak at 2588 cm −1 assigned, respectively, to the stretching of the C-H and B-H bonds internal to the m-carborane-1-thiolate anion. As expected, complete absence was observed in the region 400-300 cm −1 of the peak due to ν (Pd-Cl) presence in the spectrum of the related starting species. hypothesis of potentialities in BNCT of two low molecular weight species, i.e., cis-[(bipy)Pd(CBT)2] and trans-[(py)2Pd(CBT)2] (CBT = m-carborane-1-thiolate anion) [16], and also on the macrocyclic porphyrazine complexes of formula [{Pd(CBT)2}4Py8PyzPzM]·xH2O (M = Mg II (H2O), Zn II , Pd II ) [17] specifically thought as a bimodal PDT/BNCT active species, added here is the synthesis and physicochemical characterization of the complex [{Pd(CBT)2}4Py8TPyzPzIn(Oac)]·19H2O of the proposed structure shown in Figure 12. This heteropentanuclear species is obtained as a light green substantially amorphous ( Figure S8), highly hydrated solid material by reaction of the parent pentanuclear complex [(PdCl2)4Py8TPyzPzIn(OAc)]·8H2O with m-carborane-1-thiol (Section 2), this implying full peripheral substitutions of Cl − by CBT − anions on the external Pd II centers. Its IR spectrum ( Figure 13) shows in the range 3600-3200 cm −1 a broad absorption due to the O-H stretching of water and, in the adjacent region, the low intensity peak at 3042 cm −1 and the much more intense peak at 2588 cm −1 assigned, respectively, to the stretching of the C-H and B-H bonds internal to the m-carborane-1-thiolate anion. As expected, complete absence was observed in the region 400-300 cm −1 of the peak due to ν(Pd-Cl) presence in the spectrum of the related starting species. The present pentanuclear CBT derivative, insoluble in H2O and in the nonaqueous solvents acetone, THF and CHCl3, dissolves better (c ~ 10 −5 M) in DMSO, DMF and pyridine. Its UV-visible spectra in these solvents ( Figure 14) exhibit features, in terms of peaks due to ligand-centered π-π* transitions, recalling those shown by the above reported In III -related mono/pentanuclear macrocycles. The observed intense broad peak present in the region 400-500 nm, not observed in the spectrum of the complex [(PdCl2)4Py8TPyzPzIn(OAc)] from which the CBT derivative is generated, nor in that of the related In III mononuclear species is interesting. The same characteristic absorption is instead systematically present in the UV-visible spectra of the previously reported homo/heteropentanuclear analogs [{Pd(CBT2)}4Py8TPyzPzM] [17] also carrying externally Pd(CBT)2 units with the CBT groups being necessarily in a vicinal position, i.e., cisarranged. From these data, it clearly appeared that the observed 400-500 nm absorption was in intimate relationship with the presence in the macrocycle of the Pd(CBT)2 units. Of remarkable additional importance is that in recent work conducted on the two low molecular weight CBT derivatives i.e., cis-[(bipy)Pd(CBT)2] and trans-[py2Pd(CBT)2], both of the elucidated structures [16], only the cis structure exhibit the same type of absorption in the region 400-500 nm, which has also been observed in the UV-visible spectra of all pertinent macrocycles cited above, [17] whereat it is definitely absent in the spectrum of the trans-species. This clearly means that the origin of the absorption is intimately connected with the presence of two cis-arranged CBT groups in M(CBT)2 units, either in macrocyclic species or in low molecular weight compounds, all the exposed findings supported by detailed theoretical DFT and TDDFT calculations [17]. The present pentanuclear CBT derivative, insoluble in H 2 O and in the nonaqueous solvents acetone, THF and CHCl 3 , dissolves better (c~10 −5 M) in DMSO, DMF and pyridine. Its UV-visible spectra in these solvents ( Figure 14) exhibit features, in terms of peaks due to ligand-centered π-π* transitions, recalling those shown by the above reported In III -related mono/pentanuclear macrocycles. The observed intense broad peak present in the region 400-500 nm, not observed in the spectrum of the complex [(PdCl 2 ) 4 Py 8 TPyzPzIn(OAc)] from which the CBT derivative is generated, nor in that of the related In III mononuclear species is interesting. The same characteristic absorption is instead systematically present in the UV-visible spectra of the previously reported homo/heteropentanuclear analogs [{Pd(CBT 2 )} 4 Py 8 TPyzPzM] [17] also carrying externally Pd(CBT) 2 units with the CBT groups being necessarily in a vicinal position, i.e., cis-arranged. From these data, it clearly appeared that the observed 400-500 nm absorption was in intimate relationship with the presence in the macrocycle of the Pd(CBT) 2 units. Of remarkable additional importance is that in recent work conducted on the two low molecular weight CBT derivatives i.e., cis-[(bipy)Pd(CBT) 2 ] and trans-[py 2 Pd(CBT) 2 ], both of the elucidated structures [16], only the cis structure exhibit the same type of absorption in the region 400-500 nm, which has also been observed in the UV-visible spectra of all pertinent macrocycles cited above, [17] whereat it is definitely absent in the spectrum of the trans-species. This clearly means that the origin of the absorption is intimately connected with the presence of two cis-arranged CBT groups in M(CBT) 2 units, either in macrocyclic species or in low molecular weight compounds, all the exposed findings supported by detailed theoretical DFT and TDDFT calculations [17]. The present highly hydrated CBT derivative has been observed via its UV-visible spectral behavior in DMSO and DMF (Figure 14, up and center) to remain practically unchanged during 24 h, some persistent aggregation being present as indicated by the absorption observed in the region above 750 nm. In pyridine solution (Figure 14, bottom), The present highly hydrated CBT derivative has been observed via its UV-visible spectral behavior in DMSO and DMF (Figure 14, up and center) to remain practically unchanged during 24 h, some persistent aggregation being present as indicated by the absorption observed in the region above 750 nm. In pyridine solution (Figure 14, bottom), during the same time, progressive decreasing of the 400-500 nm absorption was observed, known to be associated, as previously observed for the CBT analogs, [17] to progressive releasing of the external Pd(CBT) 2 units with concomitant formation of the related mononuclear In III macrocycle.
Singlet Oxygen Quantum Yield Studies. Photodynamic therapy (PDT) is an anticancer treatment based on the use of the components light and dioxygen ( 3 O 2 ); a third component is a photosensitizer, possibly a macrocyclic tetrapyrrolic metal derivative, able to absorb energy in the range 600-850 nm undergoing excitation from the ground state S 0 to the triplet state T 1 with a high quantum yield, and also on having an adequate T 1 energy and lifetime for a proper energy transfer to dioxygen for the process 3 O 2 to 1 O 2 to occur, 1 O 2 operating as the main cytotoxic agent responsible for the therapeutic effect [1][2][3][4]18,19]. The type of metal center in the macrocycle can strongly influence this process and, in this regard, it is known that incorporation of closed-shell metal ions such as Zn II , Mg II , Al III , Ga III , and Si IV give the complexes desirable photophysical properties in terms of high triplet quantum yields and long triplet lifetimes, which are essential for an efficient photosensitization process, as do, in some cases, open shell diamagnetic d 8 metal centers, such as Pd II and Pt II . Among tetrapyrrolic macrocycles carrying centrally tervalent metal ions, the most popular is the Al-photosensitizer PcAlS mix (Photosens ® ), a mixture of Al III hydroxide phthalocyanines with sulphonated side-groups, which is nowadays approved in Russia for various anticancer treatments [20,21]; Ga III and In III phthalocyanine complexes have also received increasing attention as photosensitizers in PDT [22][23][24][25].
In the present work, results are presented on the photosensitizing activity for the generation of singlet oxygen, of the above reported mono-and heteropentanuclear In III complexes. The singlet oxygen quantum yields values (Φ ∆ ) ( Table 2) were obtained in pure DMF with a macrocycle concentration of ca. 10 −6 -10 −5 M. The procedure described in the Section 2 was based on an absolute method, using a laser source at 670 nm close to the maximum of the Q-band absorption peaks of the examined species. Solutions of both monoand pentanuclear complexes were found stable under laser irradiation during the experiments. Data listed in Table 2 of the Φ ∆ values for the related derivatives [Py 8 TPyzPzMCl] (M = Al III and Ga III ) were obtained in preacidified DMF ([HCl ∼ = 1 × 10 −4 M) due to the instability of these species in DMF [7].  Figure 15 shows the UV-visible spectral data (A) and the relative Stern-Volmer analysis (B, Equation (1) in the Section 2) obtained in a typical experiment carried out with the mononuclear In III derivative [Py 8 TPyzPzIn(OAc)] and used to calculate the singlet oxygen quantum yield value (Φ ∆ ) of the complex. Figure 15A and the inset of Figure 15B illustrate the absorption decay recorded at 414 nm for the 1 O 2 scavenger, DPBF, during irradiation, as well as the stability of the complex. The ΦΔ value of [Py8TPyzPzIn(OAc)]·8H2O (0.55) falls in the range of the values 0.4-0.6 previously reported for a number of Zn II phthalocyanines and porphyrazines [26,27,28,29,30,31,32], including porphyrazine macrocycles studied by our group [10,11,12,13,17,33], and qualifies this compound as a highly efficient photosensitizer for the generation of singlet oxygen. Slightly lower values were obtained for the respective pentanuclear complexes [(MCl2)4[Py8TPyzPzIn(OAc)]ˑxH2O (M = Pd II , Pt II ). The values previously obtained in acidified DMF for the mononuclear complexes [Py8TPyzPzMCl] (M = Al III , Ga III ; 0.24 and 0.68) agree with the "heavy atom effect", which enhances the triplet excited state quantum yield for Ga III with respect to Al III . Indeed, the introduction of a heavier metal ion into a porphyrazine macrocycle increased the rate of intersystem crossing via enhancement of spin-orbit coupling, this favouring the formation of a triplet state T1 with adequate energy and lifetime to allow a proper energy transfer to dioxygen for the process 3 O2 to 1 O2. In this regard, although not higher than that for the Ga III analog, appreciable is the observed value for the mononuclear In III species. Irrelevant ΦΔ values  [26][27][28][29][30][31][32], including porphyrazine macrocycles studied by our group [10][11][12][13]17,33], and qualifies this compound as a highly efficient photosensitizer for the generation of singlet oxygen. Slightly lower values were obtained for the respective pentanuclear complexes [(MCl 2 ) 4 [Py 8 TPyzPzIn(OAc)]·xH 2 O (M = Pd II , Pt II ). The values previously obtained in acidified DMF for the mononuclear complexes [Py 8 TPyzPzMCl] (M = Al III , Ga III ; 0.24 and 0.68) agree with the "heavy atom effect", which enhances the triplet excited state quantum yield for Ga III with respect to Al III . Indeed, the introduction of a heavier metal ion into a porphyrazine macrocycle increased the rate of intersystem crossing via enhancement of spinorbit coupling, this favouring the formation of a triplet state T 1 with adequate energy and lifetime to allow a proper energy transfer to dioxygen for the process 3 O 2 to 1 O 2 . In this re-gard, although not higher than that for the Ga III analog, appreciable is the observed value for the mononuclear In III species. Irrelevant Φ ∆ values were obtained in pure or acidified DMF (0.0-0.1) for the water soluble salt-like macrocycle [(2-Mepy) 8 TPyzPzIn(OAc)](I) 8 ·H 2 O and as well for the heteropentanuclear CBT derivative [{Pd(CBT) 2 } 4 Py 8 TPyzPzIn(OAc)]·19H 2 O, both of these species highly involved, as shown by their UV-visible spectral behavior, in heavy forms of aggregation. Further studies are planned in an attempt to overcome this aspect and allow them to be examined as potential PDT or, tentatively, bimodal PDT/BNCT anticancer agents, eventually using intracellular transport by liposomes as operated by other porphyrazines [34].

Conclusions
Reaction of the macrocyclic porphyrazine free ligand [Py 8 TPyzPzH 2 ]·2H 2 O with In(OAc) 3 has allowed isolation of the new stable-to-air In III