Naphthalimide‐Fused Dipyrrins: Tunable Halochromic Switches and Photothermal NIR‐II Dyes

Abstract A family of tunable halochromic switches is developed using a naphthalimide‐fused dipyrrin as the core π‐conjugated motif. Electronic properties of these dipyrrins are tuned by substitution of their alpha and meso positions with aryl groups of variable donor–acceptor strength. The first protonation results in a conformational change that enhances electronic coupling between the dipyrrin chromophore and the meso substituent, leading to halochromic effects that occasionally exceed 200 nm and switch the absorption between the near‐infrared (NIR)‐I and NIR‐II ranges. A NIR‐II photothermal effect, switchable by acid–base chemistry is demonstrated for selected dipyrrins. Further protonation is possible for derivatives bearing additional amino groups, leading to up to four halochromic switching step. The most electron‐rich dipyrrins are also susceptible to chemical oxidation, yielding NIR‐absorbing radical cations and closed‐shell dications.


Introduction
-Conjugated organic chromophores with strong absorptions in the near-infrared (NIR) region have drawn considerable interest because of their diverse applications in biomedical research, materials science, and related fields. [1][2][3][4] NIR-active organic dyes are based on various structural motifs, for example, DOI: 10.1002/advs.202105886 rylenes, cyanines, squaraines, and porphyrinoids, [5][6][7][8][9] which often show additional intense absorption in the visible region. In a given class of organic dyes, bathochromic shifts of absorptions into the NIR region are typically achieved by extending the -system of the chromophore or by incorporation of donor and acceptor groups into the parent structure. [10,11] These two strategies have been explored in diverse families of dyes, such as cyanines, rylenes, BODIPYs, expanded porphyrins, and porphyrin tapes, all of which can be engineered to yield near-infrared activity. [4,[12][13][14][15][16][17][18][19][20][21][22][23][24][25] In spite of this progress, switchable NIR dyes that will change their absorption and emission signatures in response to external stimuli remain relatively rare in spite of their potential uses in bioimaging, sensing, and actuation. Base-induced halochromism was reported by the Würthner group in bay-substituted PDI dyes, [26,27] some of which were also found to produce distinct hydrochromism. [27] Solvatochromic switching between visible and NIR absorption and emission is also possible for systems that undergo significant solvent-dependent conformational changes. [28] Inspired by these examples, we reasoned that judicious use of conformational switching may also enhance halochromic responses of NIR dyes. Examples of profound protonation-induced conformational changes have been particularly well documented in porphyrinoid chemistry, [29] occasionally enabling multi-state switching of aromaticity. [30] However, the complexity of the conformational dynamics and prototropic equilibria in these systems makes it difficult to design and control protonationinduced switching equilibria. We accordingly considered exploring a smaller oligopyrrole motif, the dipyrrin, which has a single protonation site and well-defined acid-base chemistry. [31] Freebase dipyrrins adopt a Z-syn configuration stabilized by an intramolecular hydrogen bond, but become conformationally flexible upon protonation (Figure 1). [32][33][34] The resulting dipyrrinium cation may be seen as a special case of triarylmethinium (TAM) cation [35][36][37] bearing two strongly conjugated 2-pyrrolyl groups. TAM cations have propeller-like structures, and can be transformed into NIR-absorbing dyes by -extension of individual aryl groups. [38][39][40][41][42] Here we report on the halochromism and electronic structure properties of a family of dipyrrins bearing fused naphthal- imide (NMI) moieties ( Figure 1). NMI pyrroles [43] have been previously shown to be versatile building blocks for the synthesis of electron-deficient porphyrins, [43][44][45] azacoronenes, [46][47][48] bipyrroles, [49][50][51] and polymers. [52] The family comprises two series of dipyrrins 1a-1f and 2a-2e, bearing respectively phenyl, and p-(dimethylamino)phenyl groups at the pyrrolic (or 1,9) positions (G1), and aryl substituents with variable donor/acceptor strength at the meso bridge (G2). Aminophenyl substituents have been previously shown to affect electronic gaps of NIR dyes, and can also serve as additional protonation and oxidation sites. [4,[53][54][55][56][57] The placement of NMe 2 groups at the para positions of G2 (rather than ortho or meta) ensures the strongest possible coupling with the dipyrrin without introducing steric hindrance. Thus, geometrical factors affecting the conformations of free-base and protonated dipyrrins should be similar in the 1a-e and 2a-e series. In the present design, the NMI units do not only impart a distinct donor-acceptor character to the dipyrrin but also create steric hindrance around the meso-aryl group G1. As a result of this crowding, the G1 group is rotated perpendicular to the plane of the dipyrrin and is largely decoupled from the oligopyrrole system. Upon protonation, the conformation of the dipyrrinium cation changes enabling a more TAM-like conjugation that includes the meso substituent. Depending on the combination of G1 and G2 groups, the optical gaps of the neutral and cationic forms of the dipyrrins are differently affected, yielding highly variable halochromic responses extending into the NIR-II optical window. Substitution with dimethylaminophenyl groups enables additional protonation events of the corresponding dipyrrins and makes them highly susceptible to electrochemical and chemical oxidation.

Synthesis and Characterization
Initial design of the dipyrrin targets was guided by density functional theory (DFT) calculations, which provided semiquantitative information on electronic gaps, halochromism, and charge-transfer (CT) character of these chromophores. Dipyrrins 1a-1f and 2a-2e, selected for further investigations on the basis of their predicted properties, were prepared from the common monopyrrole building block 3, following a three-step procedure outlined in Scheme 1 (for details, see the Supporting Information). Bromopyrrole 3 was subjected to Suzuki coupling followed by decarboxylation and saponification, to produce -arylpyrroles 6 and 7, bearing respectively phenyl and p-(dimethylamino)phenyl substituents. Trifluoroacetic acid (TFA)-catalyzed condensation [58] of 6 and 7 with appropriate arylaldehydes, followed by oxidation with DDQ, furnished the desired dipyrrins, 1a-1f and 2a-2e in satisfactory yields. The dipyrrins yielded 1 H NMR and 13 C NMR, and mass spectrometric analyses that were consistent with the proposed structures. In particular, the NH resonances of all dipyrrins appeared at ≈14-15 ppm, indicating the presence of an intramolecular hydrogen bond. The upfield relocation of one of the naphthalene resonances (≈4.5-5.0 ppm) is consistent with the shielding ef-  fect of the meso-aryl substituent, which is held in perpendicular alignment in between the edges of the two NMI units.
Single crystals of free-base dipyrrins 1a, 1b, 1e, and 2e, suitable for X-ray diffraction analysis, were obtained using slow vapor diffusion of n-hexane or methanol into concentrated solutions of the dipyrrins in chloroform or other solvents. In the solid state, all dipyrrins showed near planar conformations characterized by small 2 and 3 angles (Figure 2 and Table 1, see Supporting Information for additional data). In all cases, the large torsional angles 1 (73-84°), and relatively long C meso -C ipso distances (1.49-1.51 Å) are indicative of disrupted conjugation between the dipyrrin and the meso substituent. Free bases 1b, 1e, and 2e form centrosymmetric -stacked dimers in the solid state, character-ized by an antiparallel alignment of the dipyrrins, and relatively small interplanar distances of ≈3.6 Å (Figure 2A,C). In the crystals of 1a, centrosymmetric -stacked tetramers were observed consisting of two types of symmetry-independent molecules (Figure 2D). The close stacking distances in all these assembles are achieved in spite of relatively bulky substitution of the dipyrrin cores and are likely promoted by the dipolar character of the NMIpyrrole subunits.
Diffraction-quality crystals of dipyrrinium salts [1a-H]Br and [1b-H]Cl were obtained from chloroform solutions of respective free bases acidified respectively with HBr and HCl. In the salts, the dipyrrinium cations [1a-H] + and [1b-H] + were found to adopt the Z-anti conformation, with one of the pyrrole units turned Table 1. Selected torsion angles (°), bond lengths (Å), and mean-plane deviations (Å) for dipyrrins in the neutral and protonated forms obtained from the X-ray crystal structures.   Figure S8, Supporting Information, for definition) d) mesoaryl angle from DFT calculations.
away from its original orientation in the free base ( Figure 2E-F). This change results in a significant reduction of the 1 torsion (to 46°and 29°respectively), permitting a more efficient communication with the meso substituent. The resulting propeller conformations of the dipyrrinium cations resemble those adopted by TAM cations. The latter analogy is especially valid for [1b-H] + , which shows a more flattened structure and near equalization of C-C bond lengths around the meso carbon (1.419, 1.427, and 1.431 Å). In the solid state, the salts form cyclic hydrogen-bonded assemblies consisting of two dipyrrinium cations bridged by two halide anions ( Figure 2G-H).
The conformational behavior of protonated 1b was investigated in solution using 1 H NMR spectroscopy ( Figure S23, Supporting Information). When treated with 1 equiv of camphorsulfonic acid, 1b produced a spectrum consistent with the formation of a monocation, [1b-H] + , which apparently adopts the Z-anti conformation analogous to that found in the solid state. In particular, two NH resonances of equal intensities were found at 12.60 and 12.39 ppm, respectively. These signals were shifted to higher field relative to the NH signal of the free-base 1b (13.98 ppm), consistent with the absence of an intramolecular hydrogen bond in the monocation. Some of the signals in the 6-9 ppm range were dynamically broadened, but the overall number of observed resonances was consistent with rapid flipping of pyrrole units in the Z-anti conformer. A different spectrum was obtained upon addition of dilute sulfuric acid, indicating the formation of a higher protonated form, [1b-H 2 ] 2+ . Two NH resonances were also observed for the latter species, while the number of aromatic resonances appeared to correspond to slow conformational selfexchange.
-Extended dipyrrins 1a-1e form emerald-green solutions in dichloromethane (Figure 3 and Figure S20, Supporting Information and Table 2). Their absorption spectra feature one weakly structured band, with a maximum in the 723-734 nm range and an extinction coefficient in the order of 10 4 dm 3 mol −1 cm −1 . Such weak dependence of the electronic gap on meso-substitution agrees well with the weak coupling expected for the free base dipyrrins. In the 2a-2e series, the presence of electron donating substituents results in a significant red shift of the principal band further into the NIR-I region ( max = 840 to 883 nm) and somewhat greater sensitivity to meso-substitution in comparison with 1a-1e (Figure 4). An analogous red shift is observed in the parent monopyrroles of both series ( max = 483 and 536 nm for 6 and 7, respectively, see the Supporting Information for additional data). In both series, the largest red shift is caused by electronwithdrawing meso-aryl groups, that is, pentafluorophenyl and 2,4-dinitrophenyl. Unlike the parent monopyrroles 6-7, which show noticeable positive solvatochromism in the visible range, the dipyrrins are only weaky solvatochromic (Figures S15-S19 and S34, Supporting Information). Dipyrrins 1a-1e are weakly fluorescent in the NIR range (QY < 0.1%, = 2 to 3 ns in toluene, Figures S34-S35 and Table S8, Supporting Information). Emission maxima for 1a-1c are at ≈760 nm in toluene, while those of 1d and 1e are bathochromically shifted to ≈780 nm. All species are moderately solvatofluorochromic ( max em ≈ 780 nm for 1a-1c and 810 nm for 1d and 1e). Nonradiative rate constants determined for the entire series are by 1 to 2 orders of magnitude larger than the corresponding radiative constants ( Figure S35 and Table S9, Supporting Information), implying efficient nonradiative decay channels, possibly involving vibrational relaxation or the CT character of the excited states.
To acquire insights into excited-state dynamics of 1a and 1b, we performed the femtosecond transient absorption (fs-TA) measurements. The excitation pump at 670 nm was employed to probe the TA spectra in the visible region. The fs-TA spectra of 1a and 1b in toluene displayed ground-state bleaching (GSB) sig-    nals corresponding to their steady-state absorption spectra in the region of 630-760 nm overlaid with very weak stimulated emission (SE) bands in the NIR region, as well as the excited-state absorption, features below 630 nm ( Figure S35, Supporting Information). Both species exhibited similar TA decay profiles with time constants of ≈4 to 6 ps and ≈2.0 to 2.3 ns, respectively. Regarding the monotonous spectral evolution in the observed time window, we assigned the faster decay to the structural relaxation from two dipyrrin moieties and the latter to the excited singlet state lifetime. The latter decay component matches well with the fluorescence lifetime obtained by the TCSPC measurement, and is followed by the residual triplet state population. The TA spectra of 1a in benzonitrile showed comparable spectral evolution and dynamics to those in toluene. Some disparities were, however, observed for 1b: the TA spectral evolution in the polar medium revealed an initial rise and broadening of the GSB band in the region of 550-725 nm with a decreased GSB signal below 740 nm with a time constant of 14 ps. After that, the ensuing TA spectra monotonically decreased with a time constant of 30 ps. The accelerated excited-state dynamics and spectral evolution indicate the formation of a CT state from the local singlet excited-state, and then charge recombination to the ground state. [59] These results show that, in the more polar benzonitrile, the formation of the CT state of 1b may be attributed to the effect of the electron-donating meso substituent.
Acid titrations of the NMI dipyrrins revealed a highly variable behavior dependent on the identity of both meso and substituents (Figures 3 and 4 and Figures S20 and S21, Supporting Information, Table 2). When treated with trifluoroacetic acid (TFA) in CH 2 Cl 2 , the all-phenyl derivative 1a produced the corresponding dipyrrinium cation [1a-H] + . The latter species showed a relatively small relocation of the low-energy absorption band to 744 nm, corresponding to a small change of the energy gap of ΔE g = −0.05 eV, which was accompanied by a notable increase of maximum absorbance. Analogs containing electronwithdrawing meso groups, 1d and 1e, showed more significant positive halochromism, with the principal band shifted up to ≈800 nm into the NIR range. The [1f-H] + cation, for which a CT band had been predicted by TD-DFT, showed an absorption spectrum very similar to that of [1a-H] + , with no observable CT features. Two-step protonation was observed for 1b, bearing the p-dimethylaminophenyl meso-substituent. The first protonation induced a negative halochromic effect (from 728 to 694 nm), whereas a marked shift to longer wavelengths (from 694 to 774 nm) was induced by the second protonation (achieved using sulfuric acid). Apparently, the second protonation takes place at the NMe 2 group, which thus becomes electron-deficient, yielding a significant red shift. A two-stage protonation was also observed for 1c, which however showed a different behavior. The first protonation produced a spectrum containing a slightly red shifted maximum at 731 nm, which was accompanied by a broader, redshifted band with a maximum at ≈820-830 nm. The latter band was found to correspond to a CT transition, as discussed below. The second protonation resulted in a spectrum closely resembling that of [1a-H] + , and was consequently assumed to occur at the terminal meso NMe 2 group. For all members of the 1a-1e series, the spectral changes in the NIR region caused by protonation are accompanied by variation of the visible absorption profiles, which lead to noticeable color changes of the dipyrrin solutions.
Acid titrations of the -NMe 2 -substituted dipyrrins 2a-2e produced complex absorption responses in the vis-NIR range, with a marked bathochromic shift relative to their 1a-1e congeners ( Figure 4). The simplest derivative, meso-phenyl-substituted 2a, revealed a three-stage protonation, exhibiting clean isosbestic points, which was ascribed to the availability of two -NMe 2 groups. The first protonation step apparently produced the dipyrrinium cation [2a-H] + characterized by an absorption at 983 nm, corresponding to a halochromic change of −0.21 eV. The increase of absorbance induced by first protonation is smaller for 2a than for 1a. This trend is preserved for other members of the series and could be semi-quantitatively reproduced by TD-DFT calculations. Subsequent protonations resulted in a negative halochromic effect, which reflected the progressive shortening of the conjugation length in the system. The ultimate absorption spectrum of [2a-H 3 ] 3+ ( max = 713 nm) resembles that of [1a-H] + indicating a similar electronic structure. Interestingly, in contrast to electron-withdrawing groups placed at the meso position, which yield a bathochromic shift of the absorption maximum, alpha substitution with acceptor groups (herein, -NHMe 2 + ) results in a hypsochromic shift (relative to [1a-H] + ). 2d and 2e showed a qualitatively similar three-step response to acids, but the positions of absorptions displayed by the protonated forms were redshifted relative to those observed for 2a. The bathochromic shifts for the dipyrrinium cations [2d-H] + and [2e-H] + were particularly large ( max = 1081 and 1090 nm, respectively). The latter value corresponds to the largest positive halochromic effect observed in all dipyrrins (+213 nm or −0.28 eV).
The most complicated behavior was observed upon protonation of 2b and 2c, each of which contains four potential protonation sites: the dipyrrin, two -NMe 2 groups, and one meso-NMe 2 group ( Figure 4B,C). 2c was first protonated at the dipyrrin core, yielding the expected dipyrrinium monocation [2c-H] + , which however did not display a CT similar to the one observed for [2a-H] + . Subsequent addition of acid caused a composite process consisting of initial slight relocation of the maximum to higher wavelengths followed by the appearance of a more blueshifted maximum at 888 nm. Comparison with 1c and 2a suggests that this stage consists of initial meso-NMe 2 protonation, which is closely followed by protonation of one of the -NMe 2 groups, to yield the trication [2c-H 3 ] 3+ . The latter species is ultimately protonated to form the tetracation [2c-H 4 ] 4+ , which produces the expected blue-shifted, narrow band ( max = 722 nm). Interestingly, 2b, which differs from 2c by the length of the meso linker between the dipyrrin and the NMe 2 group, showed a significantly different sequence of acid-induced spectral changes. The difference is reflected in the particularly rich palette of colors observed during titration (Figure 4). The spectrum of the initial dipyrrinium cation [2b-H] + is already unusual, with two lowenergy absorptions at 742 and 883 nm. Subsequent acidification led to an apparent two-step process that ended in the formation of an unprecedented green species characterized by a markedly blue-shifted spectrum with two maxima at 644 and 698 nm. The latter species, which may be assigned to a trication [2b-H 3 ] 3+ , undergoes one final protonation, which leads to a spectrum that resembles those observed for doubly -protonated forms discussed above. The final species could thus be tentatively identified as the fully protonated [2b-H 4 ] 4+ . Since its spectrum is red-shifted relative to the spectrum of [2b-H 3 ] 3+ , it may be presumed that the final protonation leading to [2b-H 4 ] 4+ may actually occur at the meso-NMe 2 . Such a sequence would indicate that the latter group is less basic than the -NMe 2 groups in 2b. Lack of isosbestic points in the final protonation stage further suggests that the overall process may involve additional species, differentiated not only by their protonation level, but also by conformations and interactions with anions.
Importantly, the first protonation of 2d and 2e switches the principal absorption between the therapeutically relevant NIR-I and NIR-II ranges, providing an opportunity to use these compounds as pH-sensitive photothermal agents (PTAs). [60,61] In a preliminary photothermal experiment (Figure 5), a 16 μM solution of 2e in toluene was irradiated with the same laser source (3 W, 24 W cm −2 ) for 15 min. Since the free base 2e has a negligible absorbance at this wavelength, we observed only a residual photothermal effect of ≈1°C. However, when the solution was treated with TFA to produce the dipyrrinium cation [2e-H] + , the sample temperature increased significantly when the laser source was turned on, reaching 64°C after ≈10 min of continuous irradiation ( Figure 5A). The effect was reproducible in consecutive irradiation cycles ( Figure 5B), with a minor decrease of the maximum temperature attributable to gradual evaporation of TFA caused by heating. Indeed, after addition of triethylamine to the solution, the free base 2e was recovered, as evidenced by the change of the absorption spectrum, and the sample no longer showed any thermal response upon irradiation. The dipyrrinium cation [2d-H] + showed a similar switching behavior, producing comparable temperature changes upon irradiation ( Figure S37, Supporting Information). Photothermal conversion efficiencies (PCE, ) estimated for [2e-H] + and [2d-H] + were relatively low (4-6%), but can likely be improved in an optimized experimental setup. These results demonstrate that the photothermal effect can be reversibly turned on and off in the NIR-II range by changing the protonation status of the dipyrrin. encouraging their further exploration as NIR-II organic PTAs. [62][63][64][65][66] DFT calculations, performed for the neutral and protonated dipyrrins at the B3LYP-GD3BJ/6-31G(d,p) level of theory, cor- relate well with the experimental results, providing additional insight into the electronic structures of these dyes and their halochromism. For the dipyrrinium cations, the propeller-like Zanti conformation was found to be the most stable one, in line with experimental findings (Table S12, Supporting Information). S 1 -S 0 transition energies obtained from TD-DFT calculations show a generally very good linear correlation with the electronic energy gaps estimated for dipyrrins and the dipyrrinium monocations ( Table 2). The correlation is less accurate for halochromic ΔE g values, although the experimental trend is reproduced by TD data.
A quantitative analysis of frontier molecular orbitals (MOs) was used to explore the influence of protonation, as well asand meso-substitution, on the electronic structure of the dipyrrins (Figure 6 and Figures S38-S58, Supporting Information). In  particular, contributions of key molecular fragments, namely 1) the NMI-dipyrrin unit, 2) -substituents, and 3) meso substituents, were evaluated for frontier MOs. For 1a, the highest occupied molecular orbital (HOMO, −5.49 eV) is localized mainly on the NMI-dipyrrin unit and on the -phenyls (81% and 18% respectively), whereas the lowest unoccupied molecular orbital (LUMO, −3.47 eV) is almost exclusively confined to the NMI-dipyrrin fragment. For both molecular orbitals (MOs), the contribution of the meso-Ph group is negligible (≤1%), in line with the conformation-induced decoupling of the latter substituent. In the dipyrrinium cation [1a-H] + , the composition of the HOMO remains similar to that observed for the free base whereas an increased contribution of the meso substituent (10%) is observed for the LUMO. The latter effect is observed for all dipyrrins: the resultant lowering of LUMO energy caused by electron-withdrawing meso-substituents, explains the red shift they induce in dipyrrinium cations. While the HOMO levels are insignificantly affected by the C 6 F 5 and 2,4-dinitrophenyl meso-substituents, dramatic changes are produced by the NMe 2bearing groups. In 1b, the meso contribution to the HOMO is 29%, whereas in 1c the HOMO is localized almost exclusively on the meso substituent (99%). The HOMO-LUMO transition for the free base 1c is however dipole-forbidden according to TD calculations, and consequently, the associated CT band is not observed experimentally. For [1c-H] + , the HOMO-LUMO transition is predicted to have a high oscillator strength, thus validating the assignment of the 840 nm CT band. In the 2a-2e series, contributions of -substituents to highest occupied MOs are much larger (>50%) than in the 1a-1e series, resulting in significant elevation of HOMO energies and consequent reduction of the electronic gaps. Thus, -and meso-substitution in the NMI dipyrrins have complementary effects on the electronic structure of the chromophore.
Electrochemical measurements revealed rich redox chemistry of the NMI dipyrrins, which showed up to five one-electron oxidations and up to five one-electron reductions in the −2.5 to 1.5 V range of potentials (versus Fc/Fc + , Figure 7 and Figures S30 and S31 and Table S10, Supporting Information). Remarkably, the majority of these redox events are electrochemically reversible, with each system possessing at least five stable oxidation states. Scheme 2. Protonation-coupled redox reactivity of dipyrrin 2d. Reagents and conditions: a) 0 to 2.5 eq. BAHA, CH 2 Cl 2 ; b) AgPF 6 , CH 2 Cl 2 ; c) excess BAHA, CH 2 Cl 2 ; b) excess AgPF 6 , CH 2 Cl 2 ; e) hydrazine hydrate or KO 2 , CH 2 Cl 2 .
These features result from the combined effect of NMI fusion, which is known to stabilize multiply reduced states, [43,46,47] and the presence of electron-rich -dimethylaminophenyl groups, which confer significant stability to the first two oxidized forms in the 2a-2e series.
For instance, dipyrrin 2a showed three reversible oxidations with (0.19, 0.30, and 1.03 V) suggesting that the radical cation and dication states might be accessible by chemical oxidation (Figure 7). 2a and 2d were accordingly treated with tris(4bromophenyl)ammoniumyl hexachloroantimonate (BAHA), and silver hexafluorophosphate (AgPF 6 ), [67] both of which were found to affect two-electron oxidation of the dipyrrins (Figure 8 and Figure S28, Supporting Information). In particular, stepwise addition of 2.5 equiv of BAHA to 2d resulted in the formation of a new absorption maximum at 1098 nm with a clear isosbestic point ( Figure 8A). In comparison, 2a showed the main maximum at 1000 nm accompanied by a much weaker broad band centered at ≈1850 nm. Upon further addition of BAHA (up to 5 equiv.) both 2d and 2a produced a new species, displaying two NIR bands ( max = 1077 and 1930 nm for 2d). When these final oxidation products were reduced with excess hydrazine hydrate, the resulting spectra were blue-shifted relative to the initial free base spectra (7-11 nm, Figure 8B and Figure S28, Supporting Information), suggesting a chemical modification of the starting dipyrrins. Indeed, for 2d, the ultimate oxidation product, denoted 3d, was subjected to a MALDI-TOF analysis and found to contain an additional chloro substituent ( Figure S152, Supporting Information). An XRD analysis of a disordered co-crystal of 3d and 2d showed that the chlorination occurred at the 3 position of the -(4-(dimethylamino)phenyl) substituents (total Cl occupancy of ≈0.4, Figure S13, Supporting Information). This type of reactivity, with the chlorine apparently originating from the SbCl 6 − anion, has been previously documented for other BAHA oxidations. [68] To avoid the chlorination, AgPF 6 was used as an alternative oxidant for 2d, yielding a somewhat different sequence of spectral changes ( Figure 8C). Interestingly, while the final spectrum www.advancedsciencenews.com www.advancedscience.com observed under these conditions was very similar to that obtained using BAHA, intact 2d was recovered after reduction of the AgPF 6 -oxidized mixture with either hydrazine hydrate or KO 2 . Oxidation of 2d with 2.5 equiv of BAHA under 1 H NMR control (CD 2 Cl 2 , 240 K, Figure S24, Supporting Information), showed that the primary species formed under these conditions is the diamagnetic dication [2d] 2+ , with a well-defined spectrum, which was partly analyzed using correlation spectroscopy. In particular, it was found that the rotation of the -aryl substituents is hindered in [2d] 2+ in comparison with the neutral 2d, suggesting a more quinoidal character of the dication. The coexistence of the radical cation [2d] •+ was inferred from the presence of an additional broadened set of signals corresponding to a dipp substituents (other resonances could not be observed because of paramagnetic broadening) ( Figure S25, Supporting Information). In comparison with 2a and 2d, the less electron-rich 1a appeared to undergo only partial oxidation to the radical cation [1a] •+ when treated with an excess of BAHA ( Figure S27, Supporting Information). This behavior appears to be consistent with the high first oxidation potential of 1a (0.82 V).
Combined experimental and TD-DFT data can be used to rationalize the different effects of excess BAHA and AgPF 6 oxidants on the equilibrium mixture of [2d] •+ and [2d] 2+ (Scheme 2, Figures S95-S102 and Tables S53-S60, Supporting Information). During BAHA oxidations, the dication reacts with chlorides released from the SbCl 6 − anions to produce an arenium intermediate that tautomerizes to the chloro-substituted dipyrrinium cation [3d-H] + , which immediately undergoes one-electron oxidation with excess BAHA, yielding the radical dication [3d-H] •2+ , which is stable under these conditions. The behavior observed with AgPF 6 may be related to the acidity of the salt, which, when used in excess, can apparently lead to protonation of the radical cation [2d] •+ . The resulting species, [2d-H] •2+ , is analogous to [3d-H] •2+ , and produces a very similar absorption spectrum, which can be accurately reproduced using TD-DFT calculations. The possibility to reduce [2d-H] •2+ back to the neutral dipyrrin 2d shows that no substitution takes place when the dipyrrin is oxidized with AgPF 6 ( Figures S26 and S29, Supporting Information).

Conclusion
In conclusion, we have developed a family of acid-and redoxresponsive -extended dipyrrins containing fused naphthalimide subunits. The electronic properties of these dyes can be finely tuned using the complementary effects of and meso substitution. Specifically, the energy gap is reduced by electrondonating groups, which increase the HOMO energy, and by electron-withdrawing meso groups, which stabilize the LUMO level. LUMO stabilization is also responsible for the reduction of energy gaps in dipyrrinium monocations, in which a significant positive halochromic effect is produced via enhanced coupling with the meso-substituent. The latter change is enhanced by a protonation-induced conformational change, which imparts a TAM-like character to the -system of the chromophore. As shown in our preliminary experiments, the unique combination of halochromism, photostability, and good photothermal efficiency of these dipyrrins makes them of interest as pH-selective NIR-II-active agents for photothermal therapy.

Experimental Section
All experimental details are included in the Supporting Information.
[CCDC 2108054, 2110050, 2110061, 2110067, 2110070, and 2110072 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif .]

Supporting Information
Supporting Information is available from the Wiley Online Library or from the author.