The special role of B(C6F5)3 in the single electron reduction of quinones by radicals

In the presence of two molar equiv. of B(C6F5)3p-benzoquinone reacts with persistent radicals TEMPO, trityl or decamethylferrocene by single electron transfer to give the doubly O-borylated benzosemiquinone radical anion with TEMPO+, trityl cation or ferrocenium counter cations.


Introduction
Quinone/semiquinone/hydroquinone redox triads play important roles in biology. 1 They serve as redox mediators or active electron shuttles in a variety of processes involving intra-or intercellular electron transport, including e.g. the respiratory chain and photosynthesis. 2 Semiquinone radicals are important in superoxide and peroxide formation. 1e Some examples serve as chemical redox reagents in organic synthesis. 3 Anthraquinone/ anthrahydroquinone derivatives are involved as active agents in technical H 2 O 2 production. 4 In many of these redox examples sequential electron transfer plays a role, proceeding through intermediate semiquinone steps. Some such semiquinones are rather stable and have substantial half-lives. Biological systems containing hydro-quinone/semiquinone/quinone triads were structurally characterized at different redox stages. 5 Several Xray crystal structure analyses of semiquinones were published. 6 They usually show short C-O bonds, which are only slightly elongated as compared to their parent quinone systems (e.g. anthraquinone: 1.222Å). 7 Examples include p-benzosemiquinone [C]O distance: 1.295Å], tetrabromo-and tetrachlorobenzosemiquinone [d(C]O): 1.25(2)Å and 1.248(2)Å, depending slightly on the countercation]. The caesium salt of 2,3-dicyano-5,6-dichlorobenzosemiquinone shows a carbon oxygen bond length of 1.243 (1)Å (at 120 K). 8 In contrast quinhydrone shows two rather different C]O bond lengths of its pair of subunits, namely 1.234Å and 1.385/1.409Å, respectively. 9 Alkali metal semiquinones are not too easy to make; oen they are generated by exposure of the respective quinones to alkali metal mirrors. We regarded it desirable to search for a method that would easily and reliably allow for using kinetically favourable pathways for the preparation of suitable semiquinone derivatives, which would then show similar structural (and chemical) features to free metal containing semiquinones as they were described in the literature. We found that this could be achieved in a rather convenient way by the reaction of a number of quinones with persistent radicals or a suitable organometallic electron transfer reagent in the presence of two molar equivalents of the strong boron Lewis acid tris(penta-uorophenyl)borane B(C 6 F 5 ) 3 (1). Representative examples will be described in this account and some properties of the resulting borane containing semiquinones will be discussed.
There have been a few previous reports about the use of B(C 6 F 5 ) 3 in radical and electron transfer chemistry. Norton et al. 10,11 have shown that the [cB(C 6 F 5 ) 3 À ] radical anion (2) can be formed e.g. upon treatment of 1 with Cp * 2 Co serving as a single electron donor. The radical anion 2 was characterized by ESR spectroscopy. Stephan et al. recently proposed the involvement of the [cB(C 6 F 5 ) 3 À ] radical anion in FLP chemistry. 12 They have also shown that B(C 6 F 5 ) 3 reduces quinone derivatives in the presence of dihydrogen to give reactive paramagnetic semiquinone type boron containing radical products. 13 It was shown in the course of that study that pbenzoquinone (3a) underwent two electron reduction by two molar equivalents of decamethylferrocene (Cp * 2 Fe, 4) in the presence of B(C 6 F 5 ) 3 to yield the O-borylated hydroquinone dianion product 5a (with two Cp * 2 Fe þ cations). 14 Agapie et al. have shown a conceptionally related two electron reduction of dioxygen with Cp * 2 Fe and B(C 6 F 5 ) 3 to give borylated peroxide 6 (Scheme 1). 15 We have recently shown that O 2 could be reduced by suitable persistent radicals (TEMPO or the trityl radical) in the presence of B(C 6 F 5 ) 3 to yield paramagnetic superoxide products 7. 16 The sensitive superoxide radical anion systems 7 were characterized by X-ray diffraction, ESR spectroscopy and cyclic voltammetry. 14 The treatment of the systems 7 with suitable donors L (THF and DMSO) resulted in back electron transfer with the formation of respective L-B(C 6 F 5 ) 3 adducts and re-formation of triplet dioxygen. With additional trityl radicals or a second equivalent of Cp * 2 Fe the reduction of (superoxide)[B(C 6 F 5 ) 3 ] 2 À to (peroxide)[B(C 6 F 5 ) 3 ] 2 2À was achieved. 16

Results and discussion
The TEMPO radical does not react with p-benzoquinone under our typical conditions (r.t., CD 2 Cl 2 ). However, this changed in the presence of the Lewis acid B(C 6 F 5 ) 3 . The mixing of p-benzoquinone with B(C 6 F 5 ) 3 leads to adduct formation. 14 The inspection of the NMR spectra at low temperature (193 K) indicated the formation of a mono-adduct when we started from 1 : 1 stoichiometry. In 1 : 2 stoichiometry there seemed to be a dynamic equilibration between the two possible adducts and free p-benzoquinone and B(C 6 F 5 ) 3 which was so rapid that we could not "freeze" it out on the NMR time scale even at low temperature (see the ESI † for details). The addition of one molar equiv. of TEMPO to the resulting red solution (r.t., 10 min) gave a dark brown mixture. The NMR spectra indicated that a reaction with the apparent formation of a paramagnetic product had taken place. We monitored the broad 1 H NMR signals due to the (diamagnetic) oxoammonium cation [i.e. TEMPO + ] of the product 8a (Scheme 2). The diffusion of pentane vapour into the dichloromethane solution at À35 C (48 h) yielded crystalline compound 8a (59% isolated). It was characterized by X-ray diffraction ( Fig. 1 and Table 1).
The X-ray crystal structure analysis conrmed the formation of the doubly B(C 6 F 5 ) 3 bonded p-benzosemiquinone radical anion with one TMP oxoammonium countercation. It features a semiquinone core that has a B(C 6 F 5 ) 3 moiety attached to each of its oxygen atoms in a bent arrangement. The B1-O1 bonds are relatively long and the O1-C41 linkage of the central organic unit is only slightly elongated. The core has retained a long/ short/long p-benzoquinone like carbon-carbon bond lengths sequence of the central p-phenylene moiety. The TEMPO + oxoammonium counter cation shows a short N1-O3 bond length (1.191(3)Å) and a planar-trigonal coordination geometry at the nitrogen atom N1 ( P N1 OCC ¼ 360 ). p-Benzoquinone reacts with the Gomberg dimer by two-fold addition of the trityl radical to the pair of carbonyl oxygen atoms to form the respective bis-trityl hydroquinone ether 10. 17 This typical reaction pathway becomes completely suppressed in the presence of B(C 6 F 5 ) 3 . We reacted the red solution that was obtained by mixing p-benzoquinone with two molar equiv. of B(C 6 F 5 ) 3 in dichloromethane with half an equivalent of the Gomberg dimer 9 (Scheme 2). The workup of the dark red reaction mixture involving layering with pentane and crystallization at À35 C gave the diborylated benzosemiquinone trityl salt 8b, which we isolated in 65% yield as a dark red crystalline material. In CD 2 Cl 2 solution we have monitored the 1 H/ 13 C NMR features of the trityl cation, but the semiquinone radical anion part of 8b appears NMR silent. The doubly borylated semiquinone system 8b was positively identied and structurally characterized by X-ray crystal structure analysis. This revealed bonding of a pair of (C 6 F 5 ) 3 B-moieties to the oxygen atoms of the semiquinone nucleus. The structural parameters of the central core of 8b are very similar to those of its oxoammonium congener 8a (Table 1), but it shows a planar tricoordinate trityl cation, of course. The structure of compound 8b is depicted in the ESI. † The treatment of the p-benzoquinone/2 B(C 6 F 5 ) 3 mixture with one molar equiv. of Cp * 2 Fe also took place by one electron transfer and we isolated the decamethylferrocenium/semiquinone radical anion salt 8c (Scheme 2), which also had a pair of stabilizing (C 6 F 5 ) 3 B-moieties attached to the core oxygen atoms. Dark red crystals of compound 8c were isolated in 63% yield. The compound was characterized by X-ray diffraction (the structure is depicted in the ESI, † see Table 1 for selected structural parameters). It features a broad paramagnetically shied 1 H NMR feature of the Cp * 2 Fe þ ferrocenium cation at d ¼ À36.7. The semiquinone radical anion part of compound 8c appears NMR silent.
Compounds 8a, 8b and 8c in dichloromethane solution show a broad ESR signal at g ¼ 2.0049. The best-resolved spectra are observed at low temperatures (180 K) whereas resolution is gradually lost when the measurement temperature is increased. We attribute the general lack in resolution observed here to the low solubility of the radical in organic solvents of low polarity probably leading to ion pair aggregation. Solvents offering increased polarity such as THF and DMSO either lead to the decomposition of the semiquinone derivative, due to their Lewis basicity, or do not allow ESR measurements at sufficiently low temperatures (for more information see the ESI †).
The line shapes measured at 180 K in CH 2 Cl 2 can be simulated in terms of magnetic hyperne couplings to two equivalent boron nuclei and two pairs of equivalent protons (Fig. 2). The simulated spectra displayed are based on parameters which minimize deviations from the experimental data for both the rst and the second derivative spectra. The inequivalence of the ring protons suggests that at 180 K conformational reorientations are slow on the ESR timescale. The 11 B hyperne coupling constant (6.4 MHz) was conrmed independently by measuring a fully deuterated sample of an identical radical in compound 8c (Fig. 2). The further loss in resolution with increasing temperature suggests that the line-shape is additionally inuenced by exchange phenomena due to conformational dynamics occurring on the ESR timescale.
The compounds 8 are sensitive toward Lewis base donor ligands that typically add to the B(C 6 F 5 ) 3 Lewis acid forming the respective Lewis adducts. 18 This leads to back electron transfer. In the case of the oxoammonium/benzosemiquinone[B(C 6 F 5 ) 3 ] 2 salt 8a the reaction with THF occurs readily and leads to the formation of the TEMPO radical (as shown by ESR spectroscopy), the (C 6 F 5 ) 3 B-THF adduct and p-benzoquinone (both were identied by their NMR spectra from the reaction mixture). The treatment of 8a with DMSO furnished a similar result (Scheme 3 and the ESI † for details).
The reaction of the trityl cation salt 8b with DMSO takes a slightly different course. Here the exposure to the Lewis basic reagent leads to back electron transfer with the formation of the DMSO$B(C 6 F 5 ) 3 adduct. In this case the re-formation of the trityl radical apparently results in the redox reaction with reformed p-benzoquinone to the known diamagnetic product 10. We observed an approximately equal amount of 10 and p-benzoquinone 3a in the product mixture (Scheme 3).
Back electron transfer also ensues apparently upon treatment of the decamethylferrocenium/benzosemiquinone-[B(C 6 F 5 ) 3 ] 2 salt 8c with DMSO. We observed the formation of the DMSO$B(C 6 F 5 ) 3 adduct, p-benzoquinone and the doubly borylated hydroquinone dianion. This indicates the single electron transfer of the in situ generated Cp * 2 Fe to remaining 8c, forming the bis-B(C 6 F 5 ) 3 adduct 5a with the hydroquinone dianion (Scheme 3 and the ESI † for details). 9,10-Anthraquinone (3b), acenaphthenequinone (3c) or 9,10phenanthrenequinone (3d) were neither reduced with TEMPO nor with the Gomberg dimer or Cp * 2 Fe under our typical   conditions in the absence of the B(C 6 F 5 ) 3 Lewis acid. Even the anthraquinone/2 B(C 6 F 5 ) 3 mixture did not react with TEMPO. However, the trityl radical from its equilibrium with the Gomberg dimer reduced the quinone 3b in a single electron transfer process to generate the trityl cation/anthrasemiquinone-[B(C 6 F 5 ) 3 ] 2 radical anion salt 11b (Scheme 4). We tried to isolate compound 11b from the dark green reaction mixture by crystallization, but this product proved to be too sensitive. We only obtained a mixture of dark green compounds admixed with a colourless (apparently diamagnetic) material. The NMR spectra showed the presence of 3b. However, we found some green single crystals that were suited for the characterization of compound 11b by X-ray diffraction. The X-ray crystal structure analysis of compound 11b (Fig. 3) shows an anthrasemiquinone core with B(C 6 F 5 ) 3 groups attached to the pair of oxygen atoms. Consequently, the carbon-oxygen bonds were found slightly elongated as are the carboncarbon bonds proximal to the carbonyl carbon atom. The annulated pair of phenylene rings shows the slightly alternating p-system that is typical of quinoid aromatic structures. 19 The system is bent at oxygen and the pair of boron-oxygen vectors is found oriented markedly outside of the central anthrasemiquinone plane. The overall structure is close to (but not crystallographically exactly) C 2 -symmetric.
We could also achieve the single electron reduction of 9,10anthraquinone (3b) with Cp * 2 Fe in the presence of B(C 6 F 5 ) 3 . The treatment of 3b with one molar equiv. of the electron-rich ferrocene derivative in the presence of two molar equiv. of B(C 6 F 5 ) 3 gave a dark green reaction mixture. In this case we were able to isolate the respective product 11c sufficiently pure. Aer crystallization it was isolated in 88% yield and characterized by C, H elemental analysis, by NMR spectroscopy [Cp * 2 Fe þ : d ¼ À36.5 ( 1 H)], by ESR spectroscopy (broad unstructured signal in CD 2 Cl 2 at g ¼ 2.0043) and by X-ray diffraction. Compound 11c shows the structural parameters of the anthrasemiquinone$ [B(C 6 F 5 ) 3 ] 2 radical anion core that are very similar to those of 11b (see the ESI † about the details of the characterization of compound 11c). Compound 11c could be further reduced by treatment of Cp * 2 Fe to give the bis-borane adduct (5c) of the respective 9,10-anthracenediolate dianion. The compound was characterized by X-ray diffraction. Table 2 shows a comparison of the structural parameters of the radical anion system 11c with the dianion system 5c. The structure of compound 5c is depicted in the ESI. † The reactions of acenaphthenequinone (3c) with the single electron donors used in this study are slightly more complicated. We made sure that 3c did not react with TEMPO, the Gomberg dimer or Cp * 2 Fe under our typical conditions in the absence of the activating B(C 6 F 5 ) 3 Lewis acid. However, acenaphthenequinone was not reduced by the TEMPO radical even in the presence of two molar equiv. of B(C 6 F 5 ) 3 . The trityl radical is a stronger electron donor than TEMPO. 16,20 We found that the exposure of 3c to the Gomberg dimer at r.t. (0.5 equiv. 1 h in CD 2 Cl 2 ) in the presence of two molar equiv. of B(C 6 F 5 ) 3 led to the generation of the respective acenaphthene-semiquinone bis [B(C 6 F 5 ) 3 ] product 12b. The dark green solution was investigated by NMR spectroscopy, which indicated the formation of a paramagnetic product. We could not isolate the very sensitive product 12b in bulk as a clean solid but obtained a few dark green single crystals by low temperature (À35 C, 7 d) crystallization from dichloromethane/pentane by the diffusion method. This allowed for the characterization of compound 12b by X-ray diffraction (the structure is depicted in the ESI †). The compound features two strong boron-oxygen linkages [B1-O1: 1.522(5)Å, B2-O2: 1.514(5)Å, and adjacent O-C bonds: 1.282(4) A (O1-C41), 1.279(4)Å (O2-C52)]; the connecting C-C bond is rather long [1.453(5)Å (C41-C52)] (atom numbering as for 12c, see Fig. 4 below).
The reaction of a red acenaphthenequinone (3c)/2 B(C 6 F 5 ) 3 solution with one molar equiv. of Cp * 2 Fe in CD 2 Cl 2 gave a dark green solution, from which the crystalline compound 12c precipitated upon cooling to À35 C (24 h). The ½Cp * 2 Fe þ acenaphthene-semiquinone$2 B(C 6 F 5 ) 3 product 12c (Scheme 5) was characterized by C, H elemental analysis and ESR spectroscopy (broad signal at g ¼ 2.0046) in solution (CH 2 Cl 2 ). In solution the acenaphthene-semiquinone core of compound 12c is NMR silent. We only observed a single broadened 19 F NMR signal of the -B(C 6 F 5 ) 3 moieties and a typically paramagnetically shied ½Cp * 2 Fe þ 1 H NMR resonance at d ¼ À36.7. The X-ray crystal structure analysis shows the presence of the ½Cp * 2 Fe þ cation.
The acenaphthene-semiquinone radical anion has a pair of -B(C 6 F 5 ) 3 units attached to its oxygen atoms. The B-O bonds are oriented close to anti-periplanar at the framework. The bonding parameters of 12c and 12b (see above) are similar (see Fig. 4 and the ESI † for details). The semiquinone salt 12c reacted only slowly with tetrahydrofuran; aer 72 h there was still some 12c le. The reaction of 12c with DMSO was much faster. Within 1 h at r.t. back electron transfer was complete to give acenaphthenequinone (3c), Cp * 2 Fe and the (DMSO)B(C 6 F 5 ) 3 adduct (for details see the ESI †). 9,10-Phenanthrenequinone (3d) did not react with the electron transfer reagents in the absence of B(C 6 F 5 ) 3 . However, the reaction of B(C 6 F 5 ) 3 with 3d (2 : 1 molar ratio) in dichloromethane followed by the treatment of the resulting dark brown solution with Cp * 2 Fe (one molar equiv.) 21 gave the respective [(C 6 F 5 ) 3 B] 2 -9,10-phenanthrene-semiquinone radical anion, which was isolated as the ½Cp * 2 Fe þ salt 13c as a brown crystalline material in 81% yield aer workup involving crystallization at À35 C (Scheme 6). Compound 13c was characterized by C, H elemental analysis. In dichloromethane solution compound 13c showed an ESR signal at 2.0047 g with a septet-like hyperne coupling pattern. Our DFT-supported simulations suggest that this pattern is mainly caused by hyperne interactions with the adjacent 1 H nuclei (see the ESI † for details), whereas the nuclear hyperne interactions with 11 B and 10 B are signicantly weaker (A( 11 B) ¼ 1.3 MHz). Similar results were previously obtained for a radical of a similar structure exhibiting only one B(C 6 F 5 ) 2 moiety. 13a We have also reacted the quinone 3d with two molar equiv. of Cp * 2 Fe in the presence of two molar equiv. of B(C 6 F 5 ) 3 . This resulted in a reduction to the bis-alkoxide, isolated as the twofold B(C 6 F 5 ) 3 O-borylated dianion with two ½Cp * 2 Fe þ countercations. The green crystalline product 14c was isolated in 95%   This journal is © The Royal Society of Chemistry 2018 yield. It was characterized by C, H elemental analysis. The low temperature NMR spectra (233 K) show that the two parts of the dianion are symmetry-equivalent. We observed four separate equal intensity 1 H NMR CH signals of the aromatic nucleus. The 19 F NMR spectrum shows six o-F signals of the three boron bound -C 6 F 5 groups of the symmetry equivalent pair of -B(C 6 F 5 ) 3 groups, three p-F and six m-F resonances. This indicates a frozen conformation of these groups at 233 K on the NMR time scale. The 11 B NMR feature is at d ¼ À2.7 and there is a broad ½Cp * 2 Fe þ methyl 1 H NMR resonance at d ¼ À50.3 (see the ESI † for details).
Both the semiquinone radical anion salt 13c and the dianion salt 14c were characterized by X-ray diffraction (see Table 3 for a structural comparison of the same core data). The semiquinone radical anion in 13c shows rather long B-O bonds (Table 3) which probably indicates a marked structural quinone resemblance. In contrast, the B-O bonds of the diolate dianion in 14c are much shorter. Consistently, the O-C bonds in 13c are short, featuring a remaining partial carbon-oxygen double bond character. The C-O bonds in 14c are markedly longer. The connecting C-C bond in 14c shows a typical double bond character, while the connecting C-C bond in 13c is much longer, almost with a typical value of a C(sp 2 )-C(sp 2 ) single bond. The structure of the 9,10-phenanthrene-semiquinone salt is depicted in Fig. 5; see the ESI † for a projection of the structure of the dianion bis½Cp * 2 Fe þ salt 14c. The reduction of the semiquinone-[B(C 6 F 5 ) 3 ] 2 Lewis acid adducts 8 to the borylated hydroquinone dianion systems was also investigated by cyclic voltammetry. For the parent p-benzosemiquinone-[B(C 6 F 5 ) 3 ] 2 system cyclic voltammetry experiments revealed a redox potential of À0.03 V vs. the ferrocene/ ferrocenium redox couple for the reduction of the semiquinone 8c to the O-borylated hydroquinone dianion 5a in dichloromethane (0.1 M Bu 4 NPF 6 ). The reduction of p-benzoquinone 3a to the semiquinone and dianion in dichloromethane (0.1 M Bu 4 NPF 6 ) in the absence of B(C 6 F 5 ) 3 occurs at redox potentials of À0.99 V and approx. À1.8 V vs. Fc/Fc + , respectively (see the ESI † for the voltammograms and additional information). Hence, the adduct formation of 3a with B(C 6 F 5 ) 3 leads to a signicant shi (approx. 1.8 V) of the redox potentials which is just in accordance with the experimental observations. 22 Unfortunately, the rst reduction of the quinones to the semiquinone stage in the presence of tris(pentauorophenyl) borane remained inconclusive in our cyclic voltammetry experiments under various conditions. Hence, for a qualitative assessment we looked at the redox potentials of the uncomplexed quinones instead. 9,10-Anthraquinone 3b is reduced at À1.49 V and À2.0 V vs. Fc/Fc + , respectively, under our typical cyclic voltammetry conditions (in dichloromethane, 0.1 M Bu 4 NPF 6 ). The reduction to the dianion stage could not be observed for acenaphthenequinone 3c under the described experimental conditions and is, therefore, expected to occur at <À2.1 V vs. Fc/Fc + . The rst reduction step takes place at À1.43 V vs. Fc/Fc + . The reduction of 9,10-phenanthrenequinone 3d to the semiquinone and subsequently the dianion occurs at À1.13 V and À1.8 V vs. Fc/Fc + in dichloromethane (0.1 M Bu 4 NPF 6 ). The redox potentials of the reducing agents (decamethylferrocene: À0.59 V vs. Fc/Fc + ; trityl radical: À0.18 V vs. Fc/ Fc + ; TEMPO: 0.24 V vs. Fc/Fc + ) were determined under the same experimental conditions. This sequence in redox potentials might qualitatively explain why TEMPO, the weakest of the here utilized reductants, was only able to reduce p-benzoquinone to the borane stabilized semiquinone under our conditions in the presence of B(C 6 F 5 ) 3 but failed to do so for the benzannulated quinones. We could positively show that anthraquinone 3b and acenaphthenquinone 3c were reduced readily to the respective borylated semiquinones by trityl radical, and decamethylferrocene reduced all of the quinones investigated here in the presence of the B(C 6 F 5 ) 3 Lewis acid.

Conclusions
We have found that the here studied quinones did not react with a stoichiometric amount of the members of the trio of  electron donor reagents used in this study, namely TEMPO, trityl radical and decamethylferrocene, under our typical conditions in the absence of B(C 6 F 5 ) 3 . The addition of two molar equiv. of the borane Lewis acid then resulted in a rapid and complete single electron transfer in the 1 : 1 stoichiometry experiments in these cases. In some examples the energetically least potent reductant, the TEMPO radical, was inert towards oxidation by some quinones, but mostly, single electron transfer was possible and rapidly realized. In some cases further reduction to the diamagnetic dianion could be realized.
The X-ray crystal structure analyses of the resulting semiquinone-[B(C 6 F 5 ) 3 ] 2 products revealed some interesting structural effects: the C]O bonds in the various O-B(C 6 F 5 ) 3 borylated semiquinone systems investigated in our study are almost identical in lengths to the reported structurally characterized free semiquinone examples. 6-9 In addition, the B-O lengths are rather long as compared to the respective borylated hydroquinone systems (which consequently show much longer C-O bonds). So, we conclude that the attachment of the boranes to the pairs of semiquinone oxygen atoms has only a marginal structural effect. Consequently, the essential role of the added B(C 6 F 5 ) 3 Lewis acid component seems to be kinetic quinone activation and thermodynamic semiquinone radical anion stabilization, but structurally, the attachment of the pair of B(C 6 F 5 ) 3 Lewis acid moieties seems to only marginally alter the structural features of the semiquinone radical anions.
The obtained systems showed another interesting feature of potentially general signicance. The systems were prone to rapid back electron transfer. This became visible upon addition of suitable donor reagents, tetrahydrofuran or even better dimethyl sulfoxide, which trapped B(C 6 F 5 ) 3 from the borylated semiquinone radical anions to form the respective THF-B(C 6 F 5 ) 3 or DMSO-B(C 6 F 5 ) 3 Lewis adducts, and thereby opened the way to efficient back electron transfer. This re-formed the respective radicals, e.g. TEMPO from TEMPO + , and regenerated the quinone systems (or products derived from them). So, in addition to promoting the formation of the semiquinone radical anion stage, the B(C 6 F 5 ) 3 Lewis acid serves in a role that apparently makes electron-shuttling between semiquinone radical anions and quinone oxidation states easier. We will see if that may lead to a closer similarity of such well-characterized molecular electron-transfer models in their function close to the related systems in biology.

Conflicts of interest
There are no conicts to declare.