Three-State Switching of an Anthracene Extended Bis-thiaxanthylidene with a Highly Stable Diradical State

Abstract

A multistable molecular switching system based on an anthracene-extended bis-thiaxanthylidene with three individually addressable states that can be interconverted by electrochemical, thermal, and photochemical reactions is reported. Besides reversible switching between an open-shell diradical- and a closed-shell electronic configuration, our findings include a third dicationic state and control by multiple actuators. This dicationic state with an orthogonal conformation can be switched electrochemically with the neutral open-shell triplet state with orthogonal conformation, which was characterized by EPR. The remarkably stable diradical shows kinetic stability as a result of a significant activation barrier for isomerization to a more stable neutral closed-shell folded geometry. We ascribe this activation barrier of ΔG^⧧(293 K) = 25.7 kcal mol^–1 to steric hindrance in the fjord region of the overcrowded alkene structure. The folded closed-shell state can be converted back to the diradical state by irradiation with 385 nm. The folded state can also be oxidized to the dicationic state. These types of molecules with multiple switchable states and in particular stable diradicals show great potential in the design of new functional materials such as memory devices, logic gates, and OFETs.

Introduction

Artificial molecular switches and motors play a prominent role in the transition from molecules with static function to dynamic molecular systems in contemporary chemistry.¹⁻³ Taking inspiration from biology, e.g., the process of vision, it is evident that molecular switching offers numerous opportunities for the reversible control of material properties,⁴ molecular information content,⁵ or biological function.⁶ Switching between redox and geometric states can be induced by external stimuli including electricity, light, and heat.^7,8 A molecular switch can typically form either of two stable isomers, so-called bistability, to control, for example, magnetic, electronic, and optical properties, supramolecular assembly, and molecular recognition or complex functions such as catalysis.⁹⁻¹⁵

Moving beyond bistability, the design of multiple switchable molecular systems that can reach various stable states triggered by distinct and orthogonal external inputs e.g., photochemical, thermal, and electrochemical, remains particularly challenging. Herein, we report reversible switching between three states in a single molecule, including a highly stable diradical state, controlled through multiple actuators (electricity, light, and heat). Stable organic diradicals feature unique electronic properties and therefore show great potential for applications in molecular electronics such as organic field-effect transistors (OFETs).¹⁶ Reversible switching between open-shell diradical (or diradicaloid) and closed-shell electronic configurations of organic molecules is fascinating both experimentally and theoretically.¹⁷⁻²⁰ The system we describe here adds a third state that is interconvertible with the open-shell diradical state via redox chemistry. We anticipate that such a system with three independently addressable states will open doors toward smart, tunable electronics such as memory devices and logic gates.²¹

The systems presented here are based on bistricyclic aromatic enes (BAEs),²² a class of molecules that includes the overcrowded alkene light-driven molecular motors, which are robust examples of multistage switchable molecular systems.²³ In BAEs, the steric crowding in the fjord region plays a key role in the relative stability of various isomers.²² Two such geometries are described as folded (F) and twisted (T) (Figure 1). Facing the challenge to design orthogonal switching systems to allow ultimately more complex dynamic and responsive behavior, bisthiaxanthylidenes, a specific class of BAEs, offer the opportunity to combine multiple effectuators and states.¹² Bisthiaxanthylidenes undergo geometrical changes induced by either redox or photochemical reactions. A photochemical-redox luminescent switch based on bisthiaxanthylidenes was developed earlier by our group, in which oxidation leads to a stable dicationic state with a nearly orthogonal (O) orientation of the two tricyclic aromatic moieties (Figure 1a).¹²

Figure 1.

(a) Reversible switching of bis-thiaxanthylidenes from our earlier studies,¹² (b) Tschitschibabins’s hydrocarbon,²⁴ (c) DMA-based switch from Kubo et al.,¹⁸ and (d) our current work on aromatically extended bis-thiaxanthylidene switches.

Recently, photochemical and thermal interconversion of stable closed-shell and open-shell diradical states of an organic compound (with a concomitant geometry change) has emerged as a new modality of molecular switching.¹⁸ Organic compounds with an open-shell diradical resonance contributor in the ground state date back to Tschitschibabin’s hydrocarbon, reported in 1907 (Figure 1b).^24,25 Noting the importance of stable open-shell systems, other organic compounds with diradicaloid ground states have since been described.²⁶⁻²⁹ Bistability between open- and closed-shell states can be achieved when the activation barriers are sufficiently high,¹⁸ while low barriers (with respect to k_BT) lead to thermal equilibration over the states.^30,31 The open-shell diradical configurations are stabilized by a combination of factors including steric hindrance, delocalization of spin density, and aromaticity.^32,33 In 2020, Kubo reported an organic compound capable of controlled switching between open-shell diradical and closed shell state: this BAE, based on the 9,10-dihydro-10,10-dimethyl-9-anthryl (DMA) motif, undergoes conversion from a triplet open-shell diradical state to a neutral closed-shell thermally, which can then be converted back to the open-shell state photochemically (Figure 1c).¹⁸

The anthracene-extended bis-thiaxanthylidene 1 described here allows for three-state reversible switching (Figure 1d). In our design the peripheral thioxanthene motif enables redox switching by stabilizing a dicationic state (1²⁺) by virtue of the sulfur heteroatom, which enables full conjugation to an “anthracene-like” delocalized structure facilitated by mesomeric electron donation (an effect that is entirely lacking in the DMA motif).^12,34 The thioxanthenes also stabilize an open-shell diradical configuration (1-O) in the neutral form by spin density delocalization.^35,36 Steric crowding in the fjord region caused by the central anthracene linker induces additional kinetic stabilization to the diradical. The stable open-shell orthogonal diradical converts thermally to a lower energy closed-shell folded geometry (1-F), and irradiation restores the compound to its orthogonal diradical state. In contrast, the analogous benzene-bridged bis-thiaxanthylidene 2 (Figure 1d) displays a thermal equilibrium between an open-shell diradical state (2-O) and a lower energy closed-shell folded state (2-F), which demonstrates the effect of steric crowding in the fjord region.

Results and Discussion

Synthetic Procedures

The arene-extended bisthioxanthylium salts 1²⁺ and 2²⁺ were prepared with anthracene and benzene spacers, respectively (Scheme 1). Thioxanthen-9-one 3 was iodinated to obtain 4, which was then functionalized with ethoxy groups through an Ullmann coupling to increase the solubility of these compounds in organic solvents. Dilithiation of 9,10-dibromoanthracene and 1,6-dibromobenzene and subsequent reaction with 5 produced diols 7 and 9, respectively, which after dehydration with aqueous HBF₄ yielded the dicationic BF₄^– salts 1²⁺ and 2²⁺. Characterization of compound 1²⁺ by ¹H NMR spectroscopy was precluded by the presence of traces of paramagnetic species, which is probably a monoradical impurity that facilitates fast electron exchange on the NMR time scale and consequent line broadening. The presence of a monoradical impurity is supported by an EPR signal that is typical for a doublet species (Figure S8). The salts 1²⁺ and 2²⁺ were reduced chemically with cobaltocene to obtain the neutral compounds 1-O and 2-F. The ¹H NMR spectrum of compound 1-O (Figure S2) shows paramagnetic shifts and broadening, consistent with open-shell diradical character. This is not the case for compound 2-F, which we therefore expect to be in the lowest energy folded closed-shell state (DFT calculations vide infra), and we denote it as 2-F. Reoxidation of 1-O and 2-F to their respective dicationic salts 1²⁺ and 2²⁺ was achieved with NOBF₄ (Figures S2 and S3).

Scheme 1. Synthesis of Compounds 1²⁺, 2²⁺, 1-O, and 2-F.

X-ray Crystallography

Single-crystal X-ray analysis of 1²⁺ and 2-F revealed the structures shown in Figure 2. DFT-optimized structures of 1-O and 2²⁺ are shown in Figure 3. Both the anthracene-bridged dication 1²⁺ (Figure 2a) and the benzene-bridged dication 2²⁺ (DFT-optimized structure, Figure 3b) adopt an almost orthogonal conformation of the aromatic spacers relative to the thioxanthylium units with dihedral angles of 80° and 75°, respectively. In both structures the two thioxanthylium motifs are coplanar. For 1²⁺, the C1–C2 and C2–C3 distances are 1.494(3) and 1.407(3) Å, respectively, which shows that it does not have a quinoidal structure. DFT calculations predict a similar quasi orthogonal conformation for 1-O similar to the dications with a dihedral angle of 82° between the anthracene spacer relative to the thioxanthenes (Figure 3a). In contrast, 2-F has a double-folded boat-like structure (Figure 2b). Within one thiaxanthylidene the fold angle between the two C₆H₃OEt rings is 133°. The bond length of ∼1.38 Å between C5–C8 and C1–C2 and ∼1.35 Å between C6–C7 and C3–C4 are consistent with double-bond character. On the other hand, single-bond character was noted between C2–C7, C2–C3, C4–C5, and C5–C6 (∼1.45 Å). This reveals that 2-F has a quinoidal closed-shell structure in the solid state.

Figure 2.

ORTEP drawings of the (a) 1²⁺ and (b) 2-F structures. Hydrogen atoms, counterions, and solvent molecules are omitted for clarity.

Figure 3.

DFT-optimized structures of the (a) 1-O and (b) 2²⁺ structures. Hydrogen atoms are omitted for clarity.

Electronic Absorption and Emission Spectroscopy

The redox couple 1²⁺ and 1-O both display UV/vis absorption spectra (Figure 4a and c, Table 1) with absorptions at long wavelength in the visible region between 500 and 650 nm. These are common bands for twisted geometries.^{12,18,37−39} Thus, it seems likely that the conformation does not change significantly between 1²⁺ and 1-O. The absorption bands for 1²⁺ and 1-O between 325 and 400 nm with vibronic splitting are typical for anthracene.³³ In contrast, the spectra of 2²⁺ and 2-F (Figure 4b and d, Table 1) are consistent with a major change in geometry. 2-F shows a broad absorption band between 350 and 550 nm. The absorption bands at shorter wavelength are typical of an increase in S0–S1 gap expected for a folded structure. Its spectrum is similar to that observed for the folded anthracene-bridged bis-DMA, confirming its folded structure in solution,¹⁸ while 2²⁺ shows characteristic absorptions of a twisted conformation.¹² Compound 1²⁺ exhibits red emission (λ_max = 641 nm), whereas 1-O is not luminescent as expected due to its triplet diradical character (vide infra). Furthermore, emission spectroscopy shows that reduction of 2²⁺ to 2-F results in a change in luminescence with λ_max shifting from 682 nm (red) to 569 nm (yellow), respectively.

Figure 4.

UV/vis absorption and normalized emission spectra (dotted lines) of (a) 1²⁺ (6.25 × 10^–6 M), (b) 2²⁺ (6.25 × 10^–6 M), (c) 1-O (2.5 × 10^–5 M), and (d) 2-F (1.25 × 10^–5 M) in DCM. Excitation wavelengths: (a) 560 nm, (b) 520 nm, and (d) 450 nm.

Table 1. λ_max Values for 1²⁺, 2²⁺, 1-O, and 2-F.

	λmax (nm)
	UV/vis	emission (Φb)
(a) 12+	260, 299, 359, 377, 398, 448, 569	641 (0.02)
(b) 22+	253 (Sa), 303, 376, 443, 561	682 (4.0)
(c) 1-O	264, 284, 340 (S), 360, 376, 397, 444, 614
(d) 2-F	255, 391, 468	569

^aS = shoulder.

^bΦ = quantum yield in %.

EPR Spectroscopy

1-O shows a typical EPR spectrum for a triplet diradical in toluene at 77 K (Figure 5). Simulation (EasySpin, see the SI) yields a g-value of 2.0023 and zero field splitting parameters D = 183 MHz (65.3 G) and E = 3 MHz. D was used to estimate a spin–spin distance of 7.53 Å by the point-dipole approximation.²⁶ This distance is greater than the distance between the two carbons at the 9-position (5.87 Å), which indicates delocalization of the unpaired electrons.^26,40 The forbidden Δm_s = 2 signal is observed at 1722 G (effective g-value of 4.006), the intensity of which increases with decreasing temperature. The Δm_s = 2 double integrated intensity (I_EPR) vs 1/T (temperature range 70–8.6 K) plot was fitted with the Bleaney–Bowers equation (eq 1), where C is the Curie constant, J is the electron exchange interaction, 2J equals ΔE_S-T (=+22 × 10^–3 kcal mol^–1), and J = +3.9 cm^–1 (ferromagnetic coupling).

1

Figure 5.

Top: EPR signal of compound 1-O (4.4 × 10^–4 M) in toluene at 77 K with inset: forbidden Δm_s = 2 signal at 40 K. Bottom: Curie plot of 1-O with fit to the Bleaney–Bowers equation (adj. R-square = 0.9939).

From both the paramagnetic ¹H NMR and EPR spectral data we conclude that 1-O has a triplet diradical ground state with a singlet diradical state slightly higher in energy. As expected, for compound 2-F a signal was not observed, consistent with its preferred closed-shell, folded (F) quinoidal structure (vide supra).

Computational Studies

DFT calculations on 1 and 2 were performed to further investigate the stabilities of the folded quinoidal geometries relative to the orthogonal diradical conformations. Computational investigation at the B3LYP/6-31** level of theory (for the selection of the computational method, see the SI) of the various possible geometries showed that the most stable geometry is a folded (F) structure for the neutral compounds 1 and 2 and an orthogonal (O) conformation for the dicationic compounds 1²⁺ and 2²⁺ (Tables S4, S5). More specifically, the most stable geometry of 1-F is in a doubly anti-folded state that minimizes steric hindrance with the anthracenyl bridge. For 2-F the steric hindrance is significantly lower, and it has a syn-folded orientation as its most stable form. However, the isomerization barriers of the neutral compounds differ greatly. Reduction of 1²⁺ leads to the diradical state 1-O without significant conformational change. 1-O is a local minimum (ΔE = 0.7 kcal mol^–1 relative to 1-F, Figure 6) kinetically trapped with a high barrier (ΔE^⧧ = 30.6 kcal mol^–1) for isomerization at room temperature toward the global minimum 1-F. Conversely, as deduced from electrochemistry (vide infra), the reduction of 2²⁺ does initially lead to 2-O, which subsequently isomerizes to 2-F. The calculated barrier for the latter process (ΔE^⧧ = 9.5 kcal mol^–1) supports the experimental observations. The low barrier and relative energy differences between 2-O and 2-F provide a rationale for the shape of the cyclic voltammogram (Figure 7e), where a relatively fast equilibrium means that both the orthogonal and folded structures are present in solution. This isomerization pathway was probed with a potential energy surface scan (Figures S22 and S23). The relative energies of the diradical singlets and the corresponding triplets for 1-O and 2-O are sufficiently close for population of both states (ΔE_S-T = −14 × 10^–3 kcal mol^–1 for 1-O and ΔE_S-T = −0.145 kcal mol^–1 for 2-O). The low ΔE_S-T for 1-O is in accordance with EPR data, although experimentally a triplet ground state was observed. However, the calculated energy difference is less than the expected error margin, and hence it can only be concluded that the energy levels are highly similar. For all diradical species we found that the spin density is mainly located on the thioxanthene motifs with negligible contribution from the bridging motifs.

Figure 6.

Schematic and graphic representation of the thermal isomerization pathway for the neutral geometries 1-O to 1-F and 2-O to 2-F based on DFT calculations (B3LYP/6-31G**). Hydrogens are omitted for clarity.

Figure 7.

Cyclic voltammograms of (a) 1²⁺, (b) 2²⁺, (c) 1-O, (d) 2-F (0.1 V s^–1), (e) 2-F at different scan rates, and (f) 2-F at −50 °C (0.1 V s^–1) recorded in DCM with 5 × 10^–4 M analyte and 0.1 M TBAPF₆.

Electrochemistry

Compounds 1²⁺ and 2²⁺ were characterized electrochemically by cyclic voltammetry in dichloromethane (DCM) at rt, and both show reversible electrochemical switching (Figure 7a and b, Table 2). For 1²⁺ splitting of the redox waves was seen in DCM, whereas in MeCN (Figure S9) a single reversible wave was observed. This difference is due to the better solvation of the radical cation in MeCN after the first reduction relative to DCM.⁴¹ In solvents with poor donor properties, such as DCM, the singly occupied molecular orbital (SOMO) can be delocalized over the entire molecule, stabilizing the radical cation.⁴² Therefore, in DCM, the second reduction of 1²⁺ is shifted to more negative potentials. The radical cation of 2²⁺ is less stabilized, and only a single reversible wave is observed independent of solvent. Cyclic voltammograms of 1-O and 2-F do not show hysteresis (Figure 7c and d, Table 2). This suggests that 1-O has a structure similar to 1²⁺. The open-shell diradical 1-O indeed has an almost orthogonal conformation. In contrast, it is proposed that the folded closed-shell 2-F is in equilibrium with the orthogonal open-shell diradical 2-O. This explains why 2-F exhibits a quasi-reversible cyclic voltammogram where the rapid prior equilibrium between 2-F and 2-O precedes the oxidation of 2-O to 2²⁺.^31,43,44 Hysteresis is not observed, as 2-O and 2²⁺ have similar conformations. At lower scan rate there is more time (within the time frame of the electrochemical experiment) for the equilibrium to shift toward 2-O, and the voltammogram shows increasing electrochemical reversibility (Figure 7e). Cyclic voltammetry at −50 °C shows the direct oxidation of 2-F to 2²⁺ (Figure 7f, Table 2). At this temperature the 2-O state is not populated, and the large geometrical change from the folded 2-F to the orthogonal 2²⁺ is responsible for the hysteresis.

Table 2. Peak- and Half-Wave Potentials for 1²⁺, 2²⁺, 1-O, and 2-F.

	Ep,ox	Ep,red	E1/2
(a) 12+	–0.47/–0.36	–0.42/–0.54	–0.39/–0.50
(b) 22+	–0.29	–0.33	–0.31
(c) 1-O	–0.46/–0.34	–0.40/–0.52	–0.49/–0.37
(d) 2-F	–0.12	–0.35	–0.24
(e) 2-F (−50 °C)	0.14	–0.41

Thermal Equilibrium between 2-F and 2-O

Density functional theory (DFT) calculations indicated that the orthogonal diradical 2-O is thermally accessible. Variable-temperature NMR (VT-NMR) spectroscopy studies of 2-F (Figure 8a) show that the resolved signals at 25 °C become increasingly broadened with heating to 80 °C, consistent with the population of the excited triplet diradical state (2-O). Returning to 25 °C recovers the original spectrum as expected from the low activation barrier for the 2-O to 2-F conversion. These results are consistent with our electrochemical data and show that there is a thermal equilibrium between 2-F and 2-O.

Figure 8.

VT-NMR (500 MHz) spectroscopy studies of compounds (a) 2-F and (b) 1-O in toluene-d₈.

Switching between 1-O and 1-F

DFT calculations predict that 1-F is more stable than 1-O, but it was not observed after the chemical reduction of 1²⁺. We speculated that the as-synthesized 1-O was kinetically trapped. VT-NMR studies on the paramagnetic compound 1-O (Figure 8b) showed resolved signals, which are assigned to 1-F, that emerged as the temperature was increased to 100 °C. Cooling to 25 °C shows that the signals persist, consistent with a high activation barrier for interconversion between 1-F and 1-O. Full conversion to 1-F was achieved by holding the solution at 100 °C until its ¹H NMR spectrum at rt shows highly resolved signals. 1-O was converted in toluene at 90 °C to isolate and characterize 1-F. Single crystals of 1-F were grown and confirmed a double anti-folded geometry (Figure 9a). Within one thiaxanthylidene the fold angle between the two C₆H₃OEt rings is 129°. A quinoidal structure was confirmed by the double-bond character of the C5–C8 and C1–C2 bonds (∼1.35 Å) and the single-bond character of the C4–C5, C5–C6, C2–C7, and C2–C3 bonds (∼1.50 Å). Its UV/vis absorption spectrum supports the hypothesis that a geometrical change from orthogonal to folded occurred as the longest wavelength absorption is shifted to 450 nm (Figure 9b). The emission spectrum of 1-F has a maximum at 474 nm. Thus, by reversible switching between the 1²⁺, 1-O, and 1-F states (vide infra) the luminescence can be changed between red, nonluminescent, and blue, respectively. The activation barrier for the 1-O to 1-F transition was determined by UV/vis absorption spectroscopy in toluene. The decay in absorbance was monoexponential, and rates were used in an Eyring–Polanyi plot (Figure 9c). Eyring–Polanyi analysis yielded the free energy of activation ΔG^⧧(293 K) = 25.7 ± 0.2 kcal mol^–1. The activation barrier from 1-O to 1-F rationalizes why the reduction of 1²⁺ leads to trapping in the 1-O state, as can be seen from the cyclic voltammograms of the 1²⁺/1-O couple. The barriers are related to the increased steric hindrance in the fjord region, and this behavior is not seen for the 2O/2F couple. This restricted movement in the fjord region is also reflected in the onset of the oxidation potential of 1-F at 0.5 V (relative to the onset of the oxidation potential of 1-O at −0.6 V) (Figure 9d). The lack of chemical reversibility for the oxidation of 1-F is the result of the fast (within the time frame of the electrochemical experiment) chemical step 1-F²⁺ → 1²⁺. This chemical step leads to the observation of the following small reduction waves: 1-F²⁺ → 1-F^+· followed by 1-F^+· → 1-F at peak potentials 0.7 V (shoulder) and 0.6 V, respectively. Oxidation of 1-F (or 1-O) leads to 1²⁺, which can subsequently be reduced at −0.39 and −0.50 V to 1-O in the return sweep (from 1 to −1 V). This hysteresis in the cyclic voltammogram is caused by a geometrical change.^18,45 Irradiation at 385 nm leads to photochemical switching from 1-F to 1-O (Figure 9e). In toluene a band at 615 nm assigned to 1-O is observed. Heating at 90 °C results in this absorption band disappearing over 1 h. Repeated cycles of irradiation and heating confirm the excellent reversibility of this process not showing fatigue. Additional evidence for the photochemical back reaction of 1-F to 1-O was provided by EPR spectroscopy. Irradiation at 385 nm of the EPR-silent 1-F leads to the emergence of signals associated with 1-O (Figure 9f).

Figure 9.

(a) ORTEP drawing of the 1-F structure (hydrogen atoms are omitted for clarity), (b) UV/vis absorption and normalized emission spectrum (λ_exc = 350 nm) of 1-F (2.5 × 10^–5 M) in DCM including λ_max values (quantum yield = 6.9%), (c) Eyring–Polanyi plot of the thermal conversion of 1-O to 1-F in toluene monitored at 615 nm obtained by fitting to the linearized form of the Eyring equation (adj. R-square = 0.9985). Dashed lines indicate 95% confidence intervals, (d) cyclic voltammogram of 1-F, E_p,ox1 = 0.66 V (shoulder) and E_p,ox2 = 0.75 V (5 × 10^–4 M in DCM/0.1 M TBAPF₆/0.1 V s^–1), (e) cycles of irradiating (1 × 10^–3 M) with 385 nm for 10 min (white areas) and heating at 90 °C for 1 h (gray areas) while monitoring the absorbance at 615 nm, and (f) EPR spectra of 1-F (5.3 × 10^–4 M) in toluene at 77 K: before irradiation (red) and after irradiation with 385 nm at rt for 10 min (black).

Conclusion

Here we report two arene-extended bis-thiaxanthylidines in which the introduction of an anthracene spacer allowed for redox switching between an orthogonal dicationic (1²⁺) and a diradical state (1-O), while thermal and photochemical switching allows modulation between 1-O and the folded state 1-F. The barrier between the neutral orthogonal open-shell triplet (1-O) and the folded closed-shell (1-F) form is high (ΔG^⧧(293 K) = 25.7 kcal mol^–1), showing that 1-O is a remarkably stable diradical. The reverse reaction from the closed-shell to the open-shell form has a higher activation barrier (ΔG^⧧ = 31.3 kcal mol^–1 (from DFT)). The resultant three stable states of this system show that the reduction of 1²⁺ leads to the kinetically trapped 1-O, which can be switched thermally to the more stable folded geometry 1-F. Irradiation of 1-F switches it back to the open-shell 1-O, while oxidation produces 1²⁺. For the benzene analogue, redox switching between an orthogonal dicationic (2²⁺) and a diradical state (2-O) was observed. A thermal equilibrium was found between the neutral more stable folded closed-shell (2-F) and orthogonal open-shell (2-O) forms with a low activation barrier from the transient 2-O to 2-F. At low temperature 2-F can be directly oxidized to 2²⁺. We ascribe the difference in activation barrier between 2-O to 2-Frelative to1-O to 1-F to the increased steric bulk in the fjord region. Overall, this means a robust three-state switch has been developed where the dication 1²⁺, diradical 1-O, and 1-F states can be individually addressed and interconverted by electricity, temperature control, or irradiation. This opens opportunities for the exploration of stable multistate photo- and electrochemical-responsive materials and devices.

Supporting Information Available

The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/jacs.1c05938.

• Crystallographic data (ZIP)

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Accession Codes

CCDC 2087865–2087867 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/data_request/cif, or by emailing data_request@ccdc.cam.ac.uk, or by contacting The Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033.

Author Contributions

The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript.

This work was supported financially by the European Research Council (ERC; advanced grant no. 694345 to B.L.F.) and the Dutch Ministry of Education, Culture and Science (Gravitation program no. 024.001.035).

The authors declare no competing financial interest.