Dynamic Nucleophilic Aromatic Substitution of Tetrazines

Cage Compounds Hot Paper Dynamic Nucleophilic Aromatic Substitution of Tetrazines TanausfflSantos,David S. Rivero,Yaiza P8rez-P8rez, Endika Mart&n-Encinas,Jorge Pas#n, Antonio Hern#ndez Daranas,and Romen Carrillo* Abstract: Adynamic nucleophilic aromatic substitution of tetrazines (SNTz) is presented herein. It combines all the advantages of dynamic covalent chemistry with the versatility of the tetrazine moiety.Indeed, libraries of compounds or sophisticated molecular structures can be easily obtained, which are susceptible to post-functionalization by inverse electron demand Diels–Alder (IEDDA) reaction, which also locksthe exchange.Additionally,the structures obtained can be disassembled upon the application of the right stimulus,either UV irradiation or asuitable chemical reagent. Moreover,S NTz is compatible with the imine chemistry of anilines.The high potential of this methodology has been proved by building two responsive supramolecular systems:Amacrocycle that displaysalight-induced release of acetylcholine;and atruncated [4++6] tetrahedral shape-persistent fluorescent cage,whichis disassembled by thiols unless it is post-stabilized by IEDDA. Introduction Dynamic covalent chemistry (DCC) has become apowerful tool in supramolecular chemistry and materials science. This is probably due to the ability of DCC to “error-checking” and “proof-reading”, as it is based on reversible covalent reactions under thermodynamic control. This allows to correct synthetic dead-ends as it happens in non-covalent chemistry,although with much more robust molecular systems.[1–4] Therelevance of DCC on current chemistry is clearly reflected by the number of reported application in the synthesis of sophisticated molecular architectures,[5–9] in polymer chemistry,[10,11] in finding novel porous materials,[12] or bioactive compounds,[13–17] and in systems chemistry.[18–20] Even when there are well-established reversible reactions such as imine chemistry,[21,22] disulfide exchange,[23,24] boronic linkages,[25,26] olefin metathesis,[27,28] and some other interesting examples,[29–35] there is still alimited set of reactions amenable to dynamic covalent chemistry.Therefore,scope and functionality of the molecular structures synthesized could be improved by new additions to the toolkit of DCC. Particularly interesting would be to envision anovel dynamic process which inherently displays relevant physico-chemical properties and which allows for further functionalization. In this regard, we thought that agood choice for arobust and versatile DCC reaction could be the nucleophilic aromatic substitutions (SNAr) of tetrazines.Infact, SNAr is known to be reversible in some cases,[36] yet its dynamic nature has been overlooked almost completely.[37,38] Obviously,S NAr requires an electron-poor aromatic ring to be involved. But this requirement offers the chance to explore tetrazines as apotentially optimal moiety for an extremely versatile dynamic process.Indeed, tetrazines are not only electron-poor aromatic rings amenable to SNAr,but they are also avery useful moiety.[39] Thus,they have been profusely used as away to attach different compounds and moieties by inverse electron demand Diels–Alder (IEDDA) reaction,[40] which has found many applications in biology,[41–46] and materials science.[47–51] Tetrazine is avaluable scaffold to build stimulating architectures such as corona[n]arenes.[52–57] They also show an interesting redox performance,[58–60] and some of them display fluorescence.[61–64] Even when it is known that some tetrazines,such as 3,6-dichloro-1,2,4,5tetrazine (Cl-Tz-Cl)can undergo SNAr,[65,66] the reversibility Figure 1. a) Tetrazine is avery versatile moiety with interesting properties. b) This work combines the intrinsic advantages of dynamic covalent reactions with the chemical versatility of the tetrazine ring. [*] T. Santos, D. S. Rivero, Y. P8rez-P8rez, Dr.E.Mart&n-Encinas, Dr.A.H.Daranas, Dr.R.Carrillo Functional Molecular Systems Group, Instituto de Productos NaturalesyAgrobiolog&a(IPNA-CSIC) Avda. Astrof&sico Fco. S#nchez 3, 38206 La Laguna(Spain) E-mail:r[email protected] Dr.J.Pas#n LaboratoriodeMateriales para An#lisis Qu&micos (MAT4LL), Departamento de F&sica, UniversidaddeLaLaguna (ULL) 38206 La Laguna, Tenerife (Spain) Supportinginformation and the ORCID identification number(s) for the author(s) of this article can be found under: https://doi.org/10.1002/anie.202106230. T2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution License, which permitsuse, distribution and reproduction in any medium, provided the original work is properly cited. A ngewandte Chemie Research Articles How to cite: Angew.Chem. Int. Ed. 2021,60,18783–18791 International Edition: doi.org/10.1002/anie.202106230 German Edition: doi.org/10.1002/ange.202106230 18783Angew.Chem. Int.Ed. 2021,60,18783–18791 T2021 TheAuthors.AngewandteChemieInternational Edition publishedbyWiley-VCH GmbH of the substitution is completely unexplored. In this regard, phenols or thiols may act both as good nucleophiles and as efficient leaving groups,and therefore it seems reasonable to focus on them as optimal candidates as substituents of tetrazine to achieve areversible SNAr. Having all that in mind, anovel tool for DCC is herein introduced:The nucleophilic aromatic substitution of tetrazines (SNTz) with phenols and alkyl thiols (Figure 1). This fast exchange reaction combines the intrinsic advantages of dynamic covalent chemistry with the chemical versatility of the tetrazine moiety.Infact, it allows not only to obtain dynamic libraries of compounds,orcomplex molecular structures in an easier way,but it also takes advantage of the tetrazine moiety itself,and its interesting physicochemical properties. Thedynamic nature of SNTz has been successfully confirmed by obtaining the same distribution of compounds in aseries of reactions conducted in both forward and reverse directions.Activation and deactivation of the exchange was observed by the presence or absence of abase,respectively. Additionally,other exciting features of this dynamic reaction were also proved:Post-functionalization by IEDDA, which also inhibits the exchange process;photolysis by UV irradiation;and finally this exchange reaction successfully proved its potential in some supramolecular systems.Indeed, light induced guest-release and responsive covalent cages were also achieved by SNTz. Results and Discussion 3,6-di-substituted tetrazines were prepared starting from the corresponding nucleophile and 3,6-dichloro-1,2,4,5-tetrazine (Cl-Tz-Cl)(Figure 2a), which can be synthesized in five steps in gram scale.[67] Amines and aliphatic alcohols were discarded from this work because previous studies,[39,66,68] and several experiments in our lab showed that di-substituted tetrazines are frequently hard to obtain with that kind of nucleophiles:Harsh conditions are required and usually only low yields are obtained. On the other hand both phenols and thiols give good yields of di-substituted tetrazines at room temperature and thus we focused on them for this work.[67] We took the reaction between cresol (1)and the disubstituted tetrazine with 4-methoxyphenol (2-Tz-2)as the reference process,which was compared with the reverse reaction, between 4-methoxyphenol (2)and the cresol disubstituted tetrazine (1-Tz-1), to test reversibility and exchange ability in SNTz (Figure 2b). One equivalent of the disubstituted tetrazine and two equivalents of the corresponding phenol were solved in different deuterated solvents, and finally 3equivalents of triethylamine were added. Fortunately,the experimentally indistinguishable NMR spectra obtained for reactions conducted in both forward and reverse directions demonstrate that equilibrium was achieved (Figure 2cand d). Interestingly,when reaction was set up directly from Cl-Tz-Cl and two equivalents of phenols 1and 2and Figure 2. a) Synthesis of the disubstituted tetrazines was carried out from Cl-Tz-Cl and the corresponding thiol or phenol. b) Reactions performed on both directions (forward and reverse) and also starting directly from Cl-Tz-Cl (neutral), led to identical product distribution. c) 1HNMR of the forward and reverse reactions in CD3CN. Unfortunately the peaks of 1-Tz-2 and those of the homodimersoverlap, so no quantification of all the compounds of the reaction mixture can be performed by 1HNMR. d) The 13CNMR shows slight differences between homo and hetero dimers of tetrazine, and therefore aquantitative experimentcan be carried out to obtain the ratios of all the compounds in equilibrium. A ngewandte Chemie Research Articles 18784 www.angewandte.org T2021 TheAuthors.AngewandteChemieInternational Edition publishedbyWiley-VCH GmbH Angew.Chem. Int.Ed. 2021,60,18783–18791 15213773, 2021, 34, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/anie.202106230 by Biblioteca Universitaria Upv/Ehu, Wiley Online Library on [24/01/2024]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License triethylamine in acetonitrile (neutral in Figure 2b), exactly the same distribution of products than the forward and reverse reaction was found.[67] As expected, polar aprotic solvents accelerate the reaction (Table 1). Indeed, in CDCl3reaction was very slow at room temperature,although progression was evident at 5088C, and after 15 hours at that temperature,equilibrium was reached. On the other hand, in deuterated DMSO at room temperature,reaction equilibrated so fast that it was impossible to be followed by NMR, while in acetonitrile it was complete in less than two hours at room temperature or in 30 minutes heating at 5088C. Thechoice of the base also affects the kinetics of the exchange.Triethylamine (TEA) and di-isopropylethylamine (DIPEA) yield the fastest exchange,while less basic compounds such as N-methylmorpholine(NMM) take longer times to completion, and pyridine was not even able to induce the exchange.Inorganic bases such as Cs2CO3in DMSO were detrimental to the reaction.[69] It was also shown that abase is required for asuccessful exchange of phenols.Infact, when trifluoroacetic acid was added after 10 minutes to the reaction in acetonitrile,the progress of the reaction was stopped. After additional 10 minutes,anew addition of triethylamine allows to reinitiate the exchange to finally reach equilibrium. Therefore,S NTz can be stopped and activated by the proper addition of an acid or abase,respectively,and reminds in this sense to the imine exchange,but with the opposite Scheme of activation/deactivation.[67] Obviously,animportant part of this work was to quantify all the species coexisting in the equilibrium. However,inthe 1HNMR spectra, the peaks corresponding to the heterodimer 1-Tz-2 overlap with those of the homodimers 1-Tz-1 and 2-Tz2,and therefore it is not possible to distinguish each compound in the mixture and as aconsequence,the ratio of all the species of the reaction cannot be calculated by 1HNMR (Figure 2b). Conversely,some of the peaks in the 13CNMR spectrum can be unambiguously assigned to the heterodimer,and therefore aquantitative 13CNMR could be used to quantify each and every chemical species in the reaction mixture.(Figure 2d and Table 2, entry 1). It is clear from Table 2(entry 1) that the equilibrium is shifted towards the release of cresol 1while phenol 2tends to bind the tetrazine.This result is reasonable considering the respective Hammett sigma of both substituents on the phenol, being 1the best leaving group ([email protected] for methoxy, sp= @0.170 for methyl group). Reversibility of this process was further proved by shifting the equilibrium backwards,i.e. towards the unfavorable direction by increasing the concentration of one of the chemical species in solution.[70] Specifically,once the equilibrium was reached in the reaction between 2and 1-Tz-1,which implies that most of 2is attached to the tetrazine ring, we added 10 more equivalents of cresol 1,inorder to force the release of phenol 2.Itisclearly seen by NMR that 2is almost completely detached from the tetrazine ring.[67] Table 1: Equilibration time observed for the reverse reference reaction. Solvent Base t[min] CDCl3TEA 1000[a] CD3CN TEA 90 (30)[a] [D6]DMSO TEA <5[b] [D6]DMSO DIPEA <5 [D6]DMSO NMM 600 [D6]DMSO Pyridine n.r.[c] [D6]DMSO Cs2CO3–[d] [a] Heating at 5088C. [b] Equilibrium reached already in the first NMR spectrum acquired. [c] No progress of the reaction was observed after 5days. [d] Decomposition of the reagents. Table 2: Quantification of different equilibria and their corresponding constants. [a] Nucleophiles employed.[b] Schematic equilibria and their corresponding constants. [c] All reactions were carried out in 0.5 mL of the specified solvent (chosen owing to solubility and kinetic reasons),and 0.02 mmol of the corresponding phenol or thiol, which were adjusted to the correct stoichiometry,prior to the addition of 5 mLoftriethylamine. Reactionswere followed by 1HNMR until no further changes were observed.Equilibrationtimes range from less than 5minutes to 24 hours. [d] Only the peaks corresponding to the compounds displayed at one of the ends of the equilibria can be seen by 1HNMR, and we assumed that less than 1% of the rest of the compounds is present in the mixture, so we could estimate aconstant.n.d.: not determined. A ngewandte Chemie Research Articles 18785Angew.Chem. Int.Ed. 2021,60,18783–18791 T2021 TheAuthors.AngewandteChemieInternational Editionpublished by Wiley-VCHGmbH www.angewandte.org 15213773, 2021, 34, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/anie.202106230 by Biblioteca Universitaria Upv/Ehu, Wiley Online Library on [24/01/2024]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License To examine the scope of this dynamic process and the effect of the nature of the nucleophile in the outcome of the equilibrium, aseries of different reactions were set up in deuterated solvents at room temperature (Table 2). Both the forward and the reverse reactions were followed until no further changes were observed. Then, quantification of all the compound in the reaction mixture was performed by quantitative 13CNMR,[67] except for the reaction with 4-bromophenol 3(entry 2), that could be quantified by 1HNMR. Moreover, as in most of the cases acomplete quantification of the species in equilibrium could be achieved, then calculation of the corresponding equilibrium constants was trivial (Table 2). Curiously,there are scarce papers about dynamic covalent reactions where the equilibrium constants of the exchanges are calculated,[71,72] even when it is akey physico-chemical property for areversible process and it provides agreat deal of information. From Table 2, it is clear that electron rich phenols tend to remain attached to the tetrazine ring (smaller constants) while electron poor ones are more prone to be released (larger constants) (entries 1–4). Actually,4-bromophenol 3 (entry 2) is mostly found free in the equilibrium, and when the extremely electron poor pentafluorophenol 4is compared to cresol 1(entry 3), the equilibrium is completely shifted towards the release of 4. It is worth mentioning that phenols with substituents in ortho position also reached the equilibrium, although much more slowly.Indeed, 5and 6only equilibrated after 24 hours in acetonitrile (entry 5). Thiols on the other hand might be problematic in this reaction. Many of them, such as N-acetylL-cysteine,2-mercaptoethanol or all the thiophenols tested led to acompetitive redox process:Reduction of the tetrazine ring to 1,4-dihydro-s-tetrazine,with the concomitant oxidation of the thiol to the corresponding disulfide.[67,73] Only some aliphatic thiols such as dodecanethiol and benzylmercaptan display an efficient exchange reaching equilibrium so fast that it cannot be followed by NMR (entry 7). Interestingly,alkyl thiols tend to displace phenols from the tetrazine very efficiently.Indeed dodecanethiol 7completely displaces cresol from the tetrazine in 5hours (entry 6),[67] while in the other direction of the reaction, cresol 1is not able to substitute the thiol attached to the tetrazine core. Dynamic covalent chemistry in aqueous environments is challenging for some reactions such as imines and boronic esters exchanges due to their labile nature.[74–76] However the bonds involved in SNTz are more robust. Thus we tested one exchange between 1-Tz-1 and sodium 2-mercaptoethanesulfonate 9in amixture of deuterated water and acetonitrile (8:2). We found that 0.1 Msodium carbonate is enough to promote asuccessful exchange (Figure 3). Theinitial suspension of 1-Tz-1 slowly reacts,and while the mixture homogenizes,the solution progressively gets colored. Thefinal result is amixture of water-soluble compounds:cresol 1,9-Tz-9 and 1-Tz-9,which are stable for days in those conditions. Considering the basic conditions required for SNTz, we thought that it might be possible to combine it with imine chemistry that it is usually performed under acidic conditions. Combination of two or more dynamic covalent reactions in an orthogonal way is increasingly interesting because it eases the synthesis of multifunctional molecular architectures.[77–82] Consequently,dialdehyde 10-Tz-10 was synthesized and exposed to toluidine in acetonitrile (Figure 4). Thecorresponding imine precipitated from the reaction mixture,itwas filtrated and solved in deuterated DMSO.The 1HNMR clearly shows the formation of 11-Tz-11 and therefore confirms that SNTz is compatible with the imine chemistry of anilines. Obviously,one of the strengths of this novel dynamic reaction is the ability of post-functionalization by inverse electron demand Diels—Alder (IEDDA). Additionally,itis interesting to check if,once the Diels–Alder reaction transforms the tetrazine into an electron-richer 1,2-diazine,the exchange is interrupted. Thus,the IEDDAreaction between 2-Tz-2 and aslight excess of bicyclic compound 12 was examined (Figure 5a). We thought that 12 was an optimal dienophile to follow the reaction by NMR, because it displays only three singlet peaks,and once the initial cycloaddition finishes and one molecule of N2is released, then aretro Diels–Alder is expected to occur, giving the diazine 2-Dz-2 and the furan 13 which displays just two singlets in the 1HNMR. Fortunately,IEDDAreaction was carried out in high yield as it can be told by the stacked NMR spectra displayed in Figure 5b. After 48 hours heating at 5088CinCDCl3the 1HNMR only showed peaks corresponding to the expected final products and the remaining 12.The isolated yield of such post-functionalization was 94%. Interestingly the exchange reaction was inhibited after the functionalization (Figure 5c). Indeed, heating 2-Dz-2,and triethylamine in the presence of cresol 1or dodecanethiol 7led to no reaction at all, even after 5days,neither in DMSO at room temperature,nor heating at 5088CinCDCl3.Therefore,post-functionalization by IEDDA is not only an efficient way to attach different molecules to the dynamic libraries of compounds obtained, but it is also acomplementary way to cancel the exchange.Interestingly, when an intramolecular IEDDAreaction is possible,such as in compound 6-Tz-6,then heating the mixture gives the Figure 3. SNTz in aqueous environments. Figure 4. Combination of SNTz and imine chemistry. A ngewandte Chemie Research Articles 18786 www.angewandte.org T2021 TheAuthors.AngewandteChemieInternational Edition publishedbyWiley-VCH GmbH Angew.Chem. Int.Ed. 2021,60,18783–18791 15213773, 2021, 34, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/anie.202106230 by Biblioteca Universitaria Upv/Ehu, Wiley Online Library on [24/01/2024]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License corresponding diazine (6-Dz)in96% yield, which concomitantly implies that an irreversible self-inhibition of the exchange can be triggered by high temperatures.This property might be used for the kinetic control of the dynamic libraries of compounds obtained.[83–88] There are alternative ways to manipulate some of the tetrazine compounds obtained by SNTz. Inspired by the work by A. B. Smith III and R. M. Hochstrasser,[89,90] it is possible to break down the S,S-tetrazine derivatives by photolysis which gives two molecules of the corresponding thiocyanate and one molecule of nitrogen. Indeed, by UV irradiation with amedium pressure Hg lamp (450W), complete transformation of 7-Tz-7 into n-dodecyl thiocyanate 14 was achieved in two hours (Figure 6a). It is worth mentioning,that an O,Otetrazine such as 1-Tz-1 or an O,S-tetrazines such as 1-Tz-7 are not degraded by UV light. Therefore,all the S,S-tetrazine derivatives obtained by SNTz are potentially photo-cleavable. Controlling the behavior of molecular structures is essential to develop functional systems.Asithas been proved, SNTz allows for aprecise chemical control of the compounds obtained, either by photodegradation under UV light or by the complete substitution of phenols by thiols. Those properties together with its dynamic nature make SNTz apotentially valuable tool for the synthesis of functional systems.With all this in mind, we decided to test some of its possible applications through two examples.Onone hand, we decided to prove that SNTz allows for the easy synthesis of photo cleavable receptors.Controlled release of guest by light is very attractive because it is aclean and switchable process which has been reported in several supramolecular systems.[91–95] Owing to the abovementioned intrinsical properties of S,S-tetrazines,they could be employed to create receptors with the ability to release their guest after disassembly triggered by light. Actually,tetrazine-bearing crown ether 15 was synthesized in two steps in 44%yield, and it displays an association constant of 1.1X102M@1with neurotransmitter acetylcholine hexafluorophosphate (ACh PF6)inacetonitrile (Figure 6b).[96–99] However,UVirradiation causes the macrocycle to break down into two molecules of dithiocyanate podand 16,which shows no binding with acetylcholine. Therefore,S NTz is not only an efficient way to click molecular fragments into afunctional structure,but it confers macrocycle 15 the ability to release acetylcholine triggered by UV irradiation, although it seems difficult to apply this results to biological systems for the time being, considering the potent irradiation required for hours for asuccessful release. On the other hand, SNTz allows clicking phenols together and declicking them with thiols.[100] Such ability could be used to synthesize responsive molecular architectures,that would be disassembled upon the presence of the right chemical environment. We decided to test it on ashape persistent cage, as it is one of the traditional uses of dynamic methodologies.[27,101–110] We reasoned that phloroglucinol and Cl-TzCl should lead to atruncated [4++6] tetrahedral cage,where each of the four faces is actually an i-corona[6]arene (Figure 7a).[111] As expected, cage 17 was successfully synthesized in one step in 43%yield. This covalent molecular capsule displays an orange fluorescence with amaximum emission wavelength in acetone of 532 nm (Figure 7b). Asuitable single crystal was obtained by slow diffusion of hexane into acetone/dichloromethane (1:1). Thecompound 17 crystallized in the noncentrosymmetric Pna21space group and asingle cage and two acetone solvent molecules form its asymmetric unit.[67] Each tetrahedral cage is formed by four phloroglucinol groups Figure 5. a) Inverse electron demand Diels–Alder(IEDDA) reaction on 2-Tz-2 with bicyclic dienophile 12.b)1HNMR of the reaction mixture before and after heating for 24 hand 48 h. c) Diazines do not undergo SNTz.d)Heating converts the exchangeable 6-Tz-6 into unreactive 6-Dz by an intramolecular IEDDA reaction. Figure 6. a) Photolysis of 7-Tz-7 by UV irradiation.b)Release of acetylcholine after macrocycle 15 is photo-cleaved. A ngewandte Chemie Research Articles 18787Angew.Chem. Int.Ed. 2021,60,18783–18791 T2021 TheAuthors.AngewandteChemieInternational Editionpublished by Wiley-VCHGmbH www.angewandte.org 15213773, 2021, 34, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/anie.202106230 by Biblioteca Universitaria Upv/Ehu, Wiley Online Library on [24/01/2024]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License located in the vertices and six tetrazine groups on the edges. They form an almost perfect tetrahedron able to accommodate asphere of 7 cof diameter inside.[67] In spite of the reported good anion binding abilities of icorona[6]arenes,[111] cage 17 shows no remarkable association constant with any anion tested. This fact is probably due to rigidity of the cage compared with i-corona[6]arenes:Inthe macrocycle the aromatic proton can be accommodated towards the cavity and plays akey role on the binding event, which is obviously not possible with the cage. Interestingly, 17 is able to respond to achemical stimulus such as the presence of athiol. Indeed dodecanethiol 7in the presence of triethylamine is able to rapidly disassemble the cage into phloroglucinol and 7-Tz-7 (Figure 7d). Such reaction can be followed by 1HNMR where the singlet peak of cage 17 disappears completely in less than 30 minutes,and an up field singlet corresponding to phloroglucinol shows up (Figure 7e). Notably,the fluorescence of the reaction mixture is lost as none of the final products is fluorescent. As expected, once cage 17 is conveniently functionalized by IEDDA, the resulting diazine cage 18 becomes unresponsive to the effect of thiols.Tothe best of our knowledge,there are only acouple of precedents of such post-stabilization by Diels–Alder reaction and in both cases,only for DCC products based on imines.[112,113] Conclusion We have shown that nucleophilic substitution of tetrazines (SNTz) with phenols and alkyl thiols is atruly dynamic covalent reaction. Theexamples reported herein may serve as glimpse of the numerous applications that SNTz can find. All those possibilities are related not only to the dynamic nature of the process itself,but also to the inherent chemical properties of the tetrazine.Indeed, it has been shown that post-functionalization by IEDDAofthe compounds obtained allows for the attachment of molecular fragments while at the same time it inhibits the exchange.Moreover the thiol derivatives can be photolized by UVirradiation as an efficient and clean way to break down irreversibly those compounds. Functional supramolecular systems such as atetrahedral responsive fluorescent cage and amacrocycle that releases acetylcholine upon irradiation were also studied. SNTz is arobust and versatile dynamic covalent reaction an therefore it unleashes ahuge potential of applications in the synthesis of porous organic cages,interlocked structures, covalent adaptable networks and COFs,all of which could be post-functionalized, and, in some cases they could also respond to the right stimulus,either UV irradiation or aspecific chemical reagent. Moreover,modulation of the compounds obtained through IEDDAormany other chemical reactions,[114–117] will ease the access to numerous functional systems.Other well-known properties of tetrazines such as fluorescence or an interesting redox behavior, foresee also abright future to SNTz in the fields of molecular sensors and electronics.There are undoubtedly plenty of possibilities for this novel dynamic covalent reaction awaiting to be explored. Acknowledgements This work was financially supported by Ministerio de Ciencia eInnovaciln(PGC2018-094503-B-C21 and MAT2017-90207R) and by Agencia Canaria de Investigaciln, Innovaciln ySociedad de la Informaciln(ACIISI) (ProID2020010089). J.P. thanks Cabildo de Tenerife for the Agust&ndeBetancourt research position at the University of La Laguna and also Nanotec,INTech, Cabildo de Tenerife and ULL for laboratory facilities.D.S.R. thanks Ministerio de Ciencia, InnovacilnyUniversidades for his FPU fellowship.E.M.-E. acknowledges his current contract financed by Cabildo de Tenerife,Program TF INNOVA 2016-21 (with MEDI & FDCANFunds). All the authors thank SEGAI-ULL, and SDS-IPNA, and they are particularly grateful with Nieves M. Rodr&guez and Manuel Cabrera for their technical support in this research. Figure 7. a) Synthesis of cage 17.b)Yellow–orange fluorescence of cage 17 under UV light. c) Single-crystalX-ray molecularstructure of 17.[118] One molecule of acetone lies inside the cavity while other is outside. d) Cage 17 is disassembledbythiol 7in the presence of triethylamine, however post-stabilization can be achieved by IEDDA. e) Stacked plot of the 1HNMR of pure 17,the crude of the disassembling reaction mixture after 30 minutes and phloroglucinol all in CD3CN. A ngewandte Chemie Research Articles 18788 www.angewandte.org T2021 TheAuthors.AngewandteChemieInternational Edition publishedbyWiley-VCH GmbH Angew.Chem. Int.Ed. 2021,60,18783–18791 15213773, 2021, 34, Downloaded from https://onlinelibrary.wiley.com/doi/10.1002/anie.202106230 by Biblioteca Universitaria Upv/Ehu, Wiley Online Library on [24/01/2024]. 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