Twisted-Planar-Twisted expanded porphyrinoid dimer as a rudimentary reaction-based methanol indicator

Directly linked porphyrin dimers have attracted considerable attention because of their intriguing electronic features. Most emphasis has been placed on either dimers with large dihedral angles between the constituent planar monomeric subunits or those with overall planarity, referred to as “Planar-Twisted-Planar” and “Planar-Planar-Planar”, respectively. Herein, we report a “Twisted-Planar-Twisted” framework, the hexaphyrin dimer D that exists in a trans configuration. Treatment of D with MeOH affords two isomeric dimers, MD1 and MD2, both of which incorporate a methoxy moiety and exist in cis orientations with respect to the tethering linkage. The methanol-promoted conversion is accompanied by a readily discernible color change from green to brown and is not induced to an appreciable level by other alcohols. Dimer D thus acts as a rudimentary, albeit highly selective, reaction-based methanol indicator. This work provides a promising approach for constructing reaction-based chemosensors using porphyrinoid dimers of nonplanar subunits with biased reactivity.

N aturally occurring tetrapyrrolic pigments, including porphyrin (Fig. 1a), play essential roles in both aquatic and terrestrial life, while various synthetic analogs have seen extensive application in a wide range of application areas, including in materials and medicinal chemistry 1,2 . This importance has provided an incentive to create porphyrin analogs, i.e., porphyrinoids, including expanded porphyrins, contracted porphyrins, core-modified porphyrins and isomeric porphyrins 3,4 .
The first member of this ever-increasing family, the pentapyrrolic macrocycle sapphyrin 5 , was disclosed by Woodward in 1966 as being an unexpected reaction by-product. Since then, numerous expanded porphyrins have been prepared and studied in light of their flexible conformations, rich coordination chemistry, unique redox activity, and unusual chemical reactivity [6][7][8] . Often these features have no parallel in the chemistry of simple porphyrins. Early on, for instance, it was found that under certain conditions sapphyrin would undergo nucleophilic attack by methanol to produce a formally non-aromatic derivative 9 . Similar chemistry has been occasionally observed in the case of other porphyrinoid systems [10][11][12][13][14] . However, systematic efforts to exploit this reaction in the context of chemical sensing ("chemosensing") are to our knowledge unknown. Here we report a "Twisted-Planar-Twisted" dimeric expanded porphyrin system (D; Fig. 1) that reacts with methanol selectively and functions as a rudimentary, albeit selective, methanol chemosensor (formally a reaction-based indicator). In recent years, considerable effort has been devoted to extending the chemistry of porphyrin analogs beyond the limits of simple macrocyclic systems to encompass, inter alia, two-/ three-dimensional structures 15,16 , linear porphyrin tapes 17,18 , and annular nano-rings 19,20 . Directly linked porphyrin dimers have received particular attention within the context of this general paradigm because of their interesting optical and electrochemical features 21,22 . Confused porphyrins 22,23 (containing a pyrrole unit linked at the α,β′ positions) have also been used for constructing such dimers. In this case, the unoccupied α position may also be exploited to link the subunits in addition to the βand mesopositions that normally serve as inter-porphyrinoid linkage sites ( Fig. 1b) 10,24 , reflecting the inherent biased (and relatively high) reactivity of the α-pyrrolic positions. However, the directly linked bipyrroles that result from dimerization are usually severely twisted (reflected in large dihedral angles), presumably as the result of steric hindrance between the planar monomeric subunits. This results in "Planar-Twisted-Planar" dimers ( Fig. 1b) and little electronic communication between the individual macrocyclic components. To address this limitation, post-linkage reactions have been used to fuse the two porphyrin units to give "Planar-Planar-Planar" porphyrin dimers 25,26 (Fig. 1c). Less well explored, and all but unknown, are porphyrinoid dimers with an overall "Twisted-Planar-Twisted" structure ( Fig. 1d). Although a number of expanded porphyrins with twisted conformations (e.g., "figure-of-eight" structures) are known, they usually do not exhibit biased reactivity and are not readily dimerized in high yield 27,28 . However, we felt that if the confusion-and expansionbased approaches to porphyrin analog generation were combined, it might prove possible to obtain such dimers. Recently, we reported a neo-fused hexaphyrin FHP, a 5,5,5,7-tetracyclic ring system with a figure-of-eight structure, and an apparently accessible α position 29 . Here we show that, when FHP is treated with p-chloranil in chloroform, an α-α double-bond linked neohexaphyrin dimer D is obtained in high yield (65%) (Fig. 2). The directly linked central bipyrrolic subunit in D is exactly coplanar, and the whole molecule is centrosymmetrical. Also noteworthy is that, relative to FHP, dimer D displays a narrowed highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) gap, which leads to greater reactivity. Notably, D can react with MeOH under mild conditions while FHP is inert toward MeOH under the identical conditions. Upon treating D with a mixture of tetrahydrofuran (THF)/methanol under either basic or acidic conditions, a pair of isomeric dimers MD1 and MD2 are obtained into which a methoxy moiety is regioselectively attached (Fig. 2). Both MD1 and MD2 are characterized by relatively small HOMO-LUMO energy gaps, red-shifted absorption spectral features, and higher reactivity, compared to the FHP monomer. As a result, all the three dimers can be readily decomposed to give monomeric daughter products under mild conditions. Importantly, the initial insertion reaction that serves to convert D to MD1 and MD2 is relatively rapid and apparently selective for MeOH over other common alcohols, including ethanol. It also gives rise to a dramatic color change, from green to brown, that allows methanol to be differentiated from other alcohols visually without need for elaborate instrumentation.
Methanol is a key industrial chemical and a recognized human toxin. It is used as a denaturant in laboratory and industrial-grade ethanol but can also be present in distilled beverages whose quality is not carefully controlled 30,31 . Not surprisingly, therefore, considerable effort has been devoted to the problem of sensing methanol in the presence of ethanol and other potentially competing analytes 32,33 . Currently, physical techniques, such as gas chromatography 34 , Fourier transform infrared spectroscopy 35 , and Raman spectroscopy 36 , define the gold standard for methanol sensing. However, these methods rely on relatively expensive instrumentation. Electrochemical and bioanalytical approaches based on nanomaterials are also known 37,38 . In addition, several chemical indicators have been developed in recent years 39,40 . However, the number of bona fide colorimetric sensors and reaction-based indicators for methanol that allow its presence to be detected through simple color changes remain limited and  selectivity remains an issue [41][42][43] . It is thus possible that the "Twisted-Planar-Twisted" dimer D may have a role to play in addressing this need.
Reaction-based chemosensors are usually based on analytespecific reactions involving appropriately chosen functional groups 44,45 . The post-synthetic functionalization at a specific position of a macrocycles, such as a porphyrinoid, could provide an alternative approach. However, such transformations are usually challenging to implement due to the low selectivity or/and poor yields 46 . As a matter of fact, synthetic macrocycles used as analyte-specific sensors are usually based on supramolecular interactions like weak coordination bonds, hydrogen bonding, and electrostatics 44 , rather than reactivity. In contrast, the rational design and construction of macrocycles incorporating highly reactive N-confused pyrrole units with biased reactivity that can serve as reaction-based chemosensors represents an all but unexplored area of research. As detailed below, the "Twisted-Planar-Twisted" system D may serve as a model for this type of putative reaction-based indicator.

Synthesis of dimers.
When FHP was treated with 5 equivalents of tetrachloro-p-benzoquinone (p-chloranil) under reflux in chloroform for 24 h (Fig. 2), dimer D was obtained as a lightgreen powder in 65% yield. The high-resolution mass spectrum (HRMS) of D revealed a molecular ion peak at 2561.1683 (Supplementary Fig. 13, see Supporting Information), assignable to a homodimer of FHP produced formally through the elimination of four hydrogen atoms. The 1 H spectrum of D in CDCl 3 is characterized by features consistent with a symmetrical structure ( Supplementary Fig. 1). Moreover, a singlet at 6.95 ppm corresponding to the β protons on the two bridging pyrrole subunits is seen, as would be expected for a dimer linked via the neighboring α-pyrrolic positions. No signal corresponding to the latter protons is seen in D, in contrast to what is observed for FHP. Four NH proton resonances are seen at δ = 11.29 and 9.09 ppm, respectively, as expected given the proposed structure.
Upon treating FHP with p-chloranil in a mixture of chloroform and methanol (4/1, v/v) under reflux and an N 2 atmosphere, a heterodimer MD1 and its isomer MD2 were separated as brown solids in 18 and 2% yield, respectively. The HRMS of MD1 exhibits a molecular ion peak at m/z = 2592.1881 ( Supplementary   Fig. 14). This value is ca. 31 amu higher than the corresponding peak in the HRMS of D, leading us to infer that a methoxy moiety is incorporated into the dimer during the oxidative coupling process. The addition of a single methoxy group was expected to disrupt the symmetry of the overall dimeric molecule. Indeed, 1 H and 13 C nuclear magnetic resonance (NMR) spectroscopic analyses of MD1 in CDCl 3 revealed features consistent with this presumed lack of symmetry. For instance, separate signals for the two distinct monomeric units could be observed (Supplementary Figs. [3][4][5]. In addition, the peaks at 3.41 and 51.5 ppm, readily assigned to the methoxy substituents, were seen in the 1 H and 13 C NMR spectra, respectively (Supplementary Figs. 3,5). Similar HRMS and NMR spectral features were seen for MD2 (Supplementary Figs. 6 and 15). All three dimers proved soluble in a variety of organic solvents, including CH 2 Cl 2 , MeCN, THF, toluene, acetone, and dimethylformamide (DMF). This high solubility, which is not recapitulated in most Planar-Planar-Planar dimers, may reflect the twisted nature of the FHP unit and an inability to stack effectively in a layer-bylayer fashion.
Dimers MD1 and MD2 can also be obtained directly from dimer D. When a common inorganic base, such as K 2 CO 3 , Cs 2 CO 3 , or KOH, was added into a solution of D in THF and methanol, a rapid color change from green to brown was observed. After stirring for 5 min, MD1 and MD2 could be isolated in yields of ca. 56 and 41%, respectively. On the other hand, when common acids, such as HCl, H 2 SO 4 , TFA, and p-TsOH, were used instead of the base, MD1 and MD2 were obtained in yields of ca. 63 and 15%, respectively. While not studied in detail, the relatively higher yields of MD1 and the increased MD1/MD2 ratios under acidic conditions can be rationalized in terms of slightly different mechanisms that are considered operative under these disparate conditions (Supplementary Figs. 20 and 21).
In contrast to dimer D, the corresponding monomer FHP was not observed to react with MeOH under similar conditions, even if the reaction time was prolonged from 5 min to a few days. The higher reactivity of D is considered to reflect the dramatically narrowed HOMO-LUMO gap and the strong electron-deficient character of the central bipyrrolic unit (vide infra), both of which are expected to facilitate nucleophilic attack by methanol. Decomposition of the dimers to monomers. Although FHP is quite stable in MeOH and other common organic solvents in the presence of air, dimers D, MD1, and MD2 are much more reactive and tend to decompose to afford monomers. However, the symmetrical dimer D and the unsymmetrical dimers MD1/ MD2 exhibit quite different decomposition reactivities. In particular, Ag(I) salts (CF 3 COOAg, AgPF 6 , AgNO 3 , etc.), anhydrous FeCl 3 , DDQ, and even air (O 2 ) can induce the decomposition of D to give monomer FHPO 2 (Fig. 2), along with other unidentified side products. The reaction is not clean and the best yield of FHPO 2 , obtained when CF 3 COOAg was used as the oxidant, was no higher than 8%. The 1 H NMR spectrum of FHPO 2 revealed the absence of a methoxy moiety within the expected 3.0-4.0 ppm chemical shift range ( Supplementary  Fig. 7 Fig. 11). We thus conclude that the silver(I)promoted decomposition reactions of the unsymmetrical dimers MD1 and MD2 are much simpler and cleaner than those of the homodimer D, a difference attributed to the effect of the methoxy group. Furthermore, FHPMO was found to undergo a highly regioselective monochlorination reaction to afford FHPMOCl in 78% yield when treated with anhydrous FeCl 3 in chloroform/ methanol. Evidence for the formation of In both unsymmetrical dimers, a methoxy group is attached to one of the hexaphyrin units. In MD1, this group is attached at C29, which is best described as being an sp 3 -hybridized carbon center. The surrounding C-N, C-O and C-C bond lengths are in the range of 1.40-1.54 Å, typical for single bonds. It is noteworthy that pyrrole D is tilted from the A-A' plane with a relatively large dihedral angle of 80.6°. On the other hand, the methoxy-free subunit of MD1 is more planar, with pyrroles C' and D' tilted from A-A' at smaller dihedral angles of 37.9°and 36.8°, respectively. In MD2, the corresponding values are 31.9°and 34.8°, respectively, slightly smaller than those observed for MD1. These dihedral angles are all larger than the corresponding values in D, indicative of greater distortion.
Ultraviolet/visible/near-infrared (UV/vis/NIR) absorption spectra. Compared with FHP, the absorption bands of the dimers tail further into the red (Fig. 4). They are also roughly twice as intense, as might be expected for dimers incorporating twice the number of chromophores on a per mole basis. In the case of D, a Soret-like band with a sharp peak centered at ca. 442 nm is seen, along with a broad and very intense Q-like band centered at 727 nm that tails out to ca. 1300 nm. In contrast, the spectrum of the unsymmetrical dimer MD1 is characterized by a split Soretlike band with local maxima centered at 423 and 479 nm, as well as a shoulder at ca. 693 nm. The absorption edge of MD1 extends to ca. 1070 nm, a reduction in the tailing compared to D that may reflect interruption in the local conjugation as a consequence of the incorporated methoxy group. The absorption spectrum of heterodimer MD2 resembles that of MD1. However, the absorption edge of MD2 approaches ca. 1250 nm, an observation consistent with the more extended conjugation expected for MD2 as the result of the double bond link that connects the two monomeric units (Supplementary Fig. 34). The absorption bands of FHPO 2 and FHPMO roughly mirror those of FHP, consistent with their monomeric structures. However, their absorption features tail a bit further to the red (to ca. 960 and 910 nm for FHPO 2 and FHPMO, respectively). In addition, the Soret-like feature is strongly split in the case of FHPO 2 .
Electrochemistry. The electrochemical properties of the dimers and monomers were studied using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) in CH 2 Cl 2 containing 0.1 M  Table 1). This observation is consistent with what was seen for the tailing absorption band edges. The inferred HOMO-LUMO gaps for the dimers are much smaller than that for FHP (1.73 eV). Again, this is consistent with effective π-conjugation occurring to a greater or lesser extent throughout the three dimers.
Theoretical calculations. Density functional theory (DFT) calculations using the Gaussian 16 program package 49 were performed on the dimers in an effort to understand further their distinct structures and properties. First, the energies of both the putative cis and trans isomers were calculated at different energy levels. The B3LYP/6-31G(d) 50 and extended basis sets (6-31G(d,p) and 6-311G(d,p)) 51,52 all gave similar values for the energy barriers between isomers D/D-a and MD1/MD1-a/MD2/MD2-a, respectively. The use of the BMK functional 53 gave similar results as the B3LYP functional. In addition, the Grimme D3 correction 54 was included for the B3LYP functional; this gave the same trend (Supplementary Tables 5 and 6). It was found that the relative energy of the trans dimer (D) is 17.3 kJ/mol lower than the corresponding cis isomer D-a (Fig. 6a). Such a computational finding is consistent with the observation that D is obtained as the sole product and in relatively high yield when FHP is subject to oxidative coupling. In contrast, the isomeric cis dimers (MD1 and MD2) were both calculated to lie at much lower energies than their corresponding trans dimers MD1-a and MD2-a; again, this finding agrees well with experiment, specifically the finding that neither MD1-a nor MD2-a could be detected under the conditions of the methanol insertion reaction (Fig. 6b). On the other hand, the energy of MD2 is slightly higher than its isomer MD1 (by +2.1 kJ/ mol), roughly consistent with the observation that the synthetic yields for MD1 are higher than MD2 under the various synthetic conditions tested in the context of this study (vide supra). Notably, the frontier molecular orbitals of D, MD1, and MD2 are all remarkably different (Fig. 7a-c). For D, the LUMO orbital is mainly distributed over the central multiply fused unit showing a relatively low energy of −3.78 eV. This results in a narrow HOMO-LUMO gap of 1.26 eV, which is ca. 0.74 eV smaller than that of FHP. This is taken as evidence of the pronounced electron-deficient character of the two bridging imino-type pyrrolic units (A-A'), an inference that, in turn, explains the susceptibility to nucleophilic attack by MeOH (or its alkoxide anion) to form MD1/2. Such an inference is consistent with the positive shifts in the first two reduction waves seen in D (vide supra). The HOMO and HOMO-1 of D are almost degenerate (orbital energies: −5.04 and −5.06 eV, respectively) with the orbitals extended over the two hexaphyrin macrocycles except for the central multiply fused units. The high symmetry and relatively strong interaction between the two hexaphyrin units may be responsible for the near-degeneracy [54][55][56][57] . For MD1, the HOMO and LUMO are both delocalized over the methoxycontaining hexaphyrin unit. Specifically, the LUMO is delocalized over the whole hexaphyrin macrocycle, while the HOMO is distributed over the macrocycle except for the fused tetracyclic unit (ABCD rings; see Fig. 3b). No evidence of degenerate orbitals is seen for the HOMO of MD1, which may reflect the reduced symmetry of this unsymmetrical dimer relative to D. In the case of MD2, the LUMO orbital is mainly located on the methoxycontaining hexaphyrin moiety, as well as the pyrrolic unit (A') of the other hexaphyrin moiety. The HOMO, however, is mainly distributed over the methoxy-free hexaphyrin unit. The obviously different orbital distributions of MD1 and MD2 can be rationalized by the fact that the conjugation pathway in MD1 is disturbed, which results in relatively weak interaction between the two hexaphyrin units, while a fuller conjugated pathway exists in MD2 (Supplementary Fig. 34).
The energy levels of the LUMO orbitals for MD1 and MD2 are dramatically negatively shifted to −3.09 and −3.27 eV, respectively, relative to FHP (−2.90 eV). The corresponding HOMO levels are located at −4.84 and −4.75 eV, respectively. This represents a slight positive shift compared to FHP (−4.90 eV). As a result of the dramatically lowered LUMO orbitals, the HOMO-LUMO gaps of D, MD1, and MD2 are 1.26, 1.75, and 1.48 eV, respectively (Fig. 6c). They are thus much smaller than those of FHP (2.00 eV). These reductions in the HOMO-LUMO gaps are fully consistent with the trends inferred from the spectroscopic and electrochemical analyses discussed above. As mentioned above, the experimental absorption spectra of the three dimers appear to be very simple in the low energy region beyond 600 nm. These features are quite different from those of traditional porphyrin dimers [55][56][57] . To provide further insight into these observations and understand the dramatically different absorption features for the three dimers, time-dependent (TD) DFT calculations were carried out. At first, the energy of the S 1 state (nm) for the dimers were calculated by different functionals (B3LYP, PBE0, ω-B97XD, M062X, CAM-B3LYP, BMK, etc.) using the 6-31G(d) basis set and the polarizable continuum model (PCM) model (dichloromethane (DCM) as a solvent) (Supplementary Table 7). Relative to the observed absorption spectra, both the B3LYP 58 and PBE0 59 functionals underestimate the energy of the first S 0 → S 1 transition for D and MD2. On the other hand, the long-range corrected CAM-B3LYP 60 functional slightly overestimates the energy of the S 0 → S 1 electronic transition for MD1, while it overestimates the energy of the S 0 → S 1 electronic transition for dimer D. For the ω-B97XD 61 and M062X 62 functionals, the difference between the S 0 → S 1 electronic transition of MD1 and MD2 is not fully revealed. In contrast, the BMK functional, which usually gives improved accuracy for transition state barriers 53 , gave relatively reasonable results for all the three dimers compared to the other functionals employed. For D, the exceptionally strong and broad absorption band in the 600-900 nm region can be rationalized in terms of a HOMO-2 → LUMO transition with quite a large oscillator strength (f = 1.81). Both the HOMO-2 and LUMO orbitals are localized on the bridging bipyrrolylidene fragment (Fig. 7a), indicating that this band mainly originates from a localized π-π* transition, instead of an intramolecular charge transfer (ICT) from the hexaphyrin core to the central multiply fused linking unit [63][64][65] . The Q-like band of compound D corresponds to the quasidegenerated S 0 → S 1 and S 0 → S 2 transitions, and the oscillator strengths (f = 0.26/0.005) are much smaller than those of the HOMO-2 → LUMO transition (f = 1.81) (Supplementary Fig. 35 and Supplementary Table 9). Hence, the lower energy band is observed to be submerged within the strong broad band in the 600-900 nm region. As a result, no clearly resolved Q-like bands could be observed in contrast to other reported dimers characterized by different linking modes 55 .
As can be seen from Fig. 7b, the occupied and unoccupied molecular orbitals of MD1 are mainly localized on either one of the hexaphyrin units. Therefore, the calculated lowest energy transitions of MD1 at 817 and 698 nm, mainly corresponding to HOMO-1 → LUMO and HOMO → LUMO+1 excitations, respectively, are both characteristic of weak oscillator strengths (f ≈ 0.1) because of the ICT nature associated with the electronic distribution ( Supplementary Fig. 36 and Supplementary Table 10). On the other hand, the high energy transitions in the range of 400-600 nm (Soret-like band) demonstrate relatively larger oscillator strengths (f = 0.3-0.7). Therefore, absorptions from the low energy transitions are submerged under the higher energy ones. As a result, MD1 exhibits only a shoulder peak at ca. 693 nm instead of well-resolved Q-like bands as observed for the traditional porphyrin dimers [55][56][57] . Similar to MD1, the lowest energy excitations of MD2 also correspond to HOMO-1 → LUMO and HOMO → LUMO+1 transitions (Supplementary Fig. 37 and Supplementary Table 11). Notably, the HOMO-1 orbitals are located over both of the hexaphyrin fragments, and the HOMO-1 → LUMO transition is symmetry allowed, leading to a larger oscillator strength (0.37) than that of MD1, a finding that serves to rationalize the slightly stronger Q-like band and longer wavelength band edge for MD2 in comparison with MD1.
Methanol response. As mentioned above, a dramatic solution color change from light green to brown was observed accompanying with the conversion from D to MD1/2. As a matter of fact, solutions of D in THF under basic conditions are very sensitive to methanol, while the response to ethanol and other alcohols is considerably slower. Presumably, this reflects the somewhat lowered nucleophilicity and greater steric hindrance of these higher alcohols. In principle, this reactivity difference could be used to differentiate methanol from other alcohols. As a test of this hypothesis, various alcohols (3.0 μL corresponding to ca. 25 mM after dilution) were added, respectively, into THF solutions of D (1.3 × 10 −2 mM in 3.0 mL) in the presence of excessive NaOH (s) (10 mg). Under these conditions, a discernible color change was found for the methanol sample within 5 min (Fig. 8). However, no obvious color change was observed in the case of any of the other alcohols during the same 5-min time period. Kinetic studies, involving the response of D toward methanol and ethanol as a function of time, were carried and provide support for the fact that these two alcohols give rise to remarkably different reaction rates ( Supplementary Figs. 22 and 23). Notably, when the amount of added methanol was decreased to 0.50 μL (corresponding to ca. 4.2 mM after dilution), a color change from green to light brown still occurs, although 24 h were required to effect essentially complete conversion (Supplementary Figs. 24 and 25). On this basis, we conclude that methanol may be readily differentiated from other alcohols by simply monitoring whether the distinctive color change is produced during a set time period. Furthermore, the detection limit 66 Fig. 26). On this basis, we proposed that D may emerge as a promising methanol indicator that can operate in the absence of relatively expensive analytical instrumentation.

Discussion
Oxidative coupling of an unusual twisted neo-fused hexaphyrin (FHP) with a protruding N-confused pyrrole gives rise to the "Twisted-Planar-Twisted" homodimer D with a trans configuration in high yield, leading us to suggest that introducing a reactive subunit into a twisted porphyrinoid is a promising approach for constructing functional dimers or even larger oligomers. Upon adding methanol to the reaction mixture under basic or acid conditions, regioselective addition of a methoxy moiety to D occurs to afford two isomeric heterodimers, MD1 and MD2, both of which contain cis-type central linkages. A strong interaction between the two hexaphyrin subunits of D is inferred from its spectral and physical properties and is ascribed to the presence of a coplanar central bipyrrolic linking unit and the roughly coplanar arrangement of the appended neo-fused hexaphyrin subunits. Compared with D, reduced intramolecular electronic interactions are seen in the case of MD1 and MD2. These latter isomeric species differ somewhat from one another, reflecting differences in their respective conjugation pathways and molecular conformations. The fact that D reacts readily and selectively with methanol under readily defined reaction conditions allows for the qualitative differentiation of methanol from ethanol and other alcohols by simple visual means. The associated sensing function could prove useful in detecting methanol in either an industrial or beverage-related setting. Further studies of this possibility are ongoing in our laboratory. The studies reported here not only illustrate a promising approach to synthesizing porphyrinoid dimers by oxidatively coupling the corresponding monomers through their accessible α-pyrrolic positions but also provide an approach for developing reaction-based chemosensors. The latter potential application takes advantage of the fact that the present dimers allow for biased high reactivity that reflects a synergetic effect of reduced HOMO-LUMO energy gaps and the presence of reactive Nconfused units. While further work will be needed to develop the present findings as a potentially generalizable strategy, the approach to sensing detailed here could provide a useful complement to current methods that typically involve the rational design of specific receptors or reactive constructs.

Methods
General methods. Commercially available solvents and reagents were purchased from Adamas-Beta and used without further purification unless otherwise mentioned. Thin-layer chromatography was carried out on aluminum sheets coated with silica gel 60 F254 (MERCK). 1 H NMR (400 MHz) spectra were obtained using a Bruker AM 400 spectrometer. Chemical shifts are reported relative to tetramethylsilane (δ = 0) in ppm. 13 C NMR spectra were recorded at 101 MHz (Bruker AM 400) and the chemical shifts were reported relative to CDCl 3 (δ = 77.00), (CD 3 ) 2 CO (δ = 29.84), or DMSO-d 6 (δ = 39.52) in ppm; see Supplementary Figs. 1-12. HRMS analyses were performed using a Waters LCT Premier XE spectrometer or Bruker Solarix XR FTMS instrument for CH 2 Cl 2 solutions; see Supplementary Figs. 13-18. UV-vis-NIR absorption spectral studies were carried out using a Shimadzu UV2600 spectrophotometer with all spectra being recorded at room temperature.
Syntheses of compounds. Homodimer D was synthesized through a one-pot oxidation of the monomer FHP in methanol-free solvents, in yields of ca. 65%. The unsymmetrical dimers MD1 and MD2 can be obtained either from FHP or D, both in the presence of methanol. The monomers FHPO 2 and FHPMO were obtained by the direct oxidation of D and MD1 (MD2), respectively (see Supplementary Methods). The target compounds were fully characterized by single crystal X-ray diffraction analyses, as well as by NMR spectroscopy and HRMS analyses (Supplementary Methods).
Crystallography. Single crystals of D were obtained by the slow recrystallization from the DCM/heptane solution; crystals of D1 and FHPMOCl were obtained by the slow recrystallization from their DCM/octane solutions, and crystals of D2 and FHPMO 2 were obtained by the slow evaporation of their acetonitrile/water solutions. Single crystal X-ray analyses were performed on a SMART APEX equipped with CCD detector (Bruker) using MoKα (graphite, monochromated, λ = 0.71073 Å) radiation or CuKα (graphite, monochromated, λ = 1.54178 Å) radiation. The structures were solved by the direct method of SHELXS-97/2014/ 2018 and refined using the SHELXL-97/2014 or Olex2 1.2 program 49,67,68 . The positional parameters and thermal parameters of non-hydrogen atoms were refined anisotropically on F 2 by the full-matrix least-squares method. Hydrogen atoms were placed at calculated positions and refined riding on their corresponding carbon atoms. Detailed crystallographic data are provided in Supplementary Tables 2 and 3.
Electrochemical measurements. CV and DPV studies were carried out at 298 K using a CHI-730C Electrochemical Workstation. A three-electrode cell consisting of a glassy carbon (working electrode), platinum wire (counter electrode), and Ag/ AgCl (reference electrode) attached to a Chi-730D/620E electrochemistry station were used, with the potentials calibrated to the ferrocenium/ferrocene (Fc + /Fc) couple. Absolute DCM (CH 2 Cl 2 ) was purchased from Adamas-Beta and used as received and TBAClO 4 was purchased from Fluka Chemika, recrystallized from ethanol, and dried under vacuum at 40°C for at least 1 week prior to use.
Theoretical calculation details. All calculations were carried out using the Gaussian 16 suite of programs 49 . The geometries of all molecules under study were optimized using B3LYP 58 and the 6-31G(d) basis set 50 for all the atoms directly. No adjustment to the effective core potential was applied. All the optimized geometries were checked as the real minima on the potential energy surface by means of frequency calculations. At the optimized geometries, TD DFT calculations with the hybrid BMK functional 53 were carried out to simulate the absorption spectra. Solvent effects arising from CH 2 Cl 2 were accounted for using the PCM 69 .
Data availability CCDC 1886415-1886417, 1985682, and 1985685 contain 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. All other data supporting the findings of this study are available from the corresponding authors upon request.