An investigation into the unusual linkage isomerization and nitrite reduction activity of a novel tris(2-pyridyl) copper complex

The copper-containing nitrite reductases (CuNIRs) are a class of enzymes that mediate the reduction of nitrite to nitric oxide in biological systems. Metal–ligand complexes that reproduce the salient features of the active site of CuNIRs are therefore of fundamental interest, both for elucidating the possible mode of action of the enzymes and for developing biomimetic catalysts for nitrite reduction. Herein, we describe the synthesis and characterization of a new tris(2-pyridyl) copper complex ([Cu1(NO2)2]) that binds two molecules of nitrite, and displays all three of the common binding modes for NO2−, with one nitrite bound in an asymmetric quasi-bidentate κ2-ONO manner and the other bound in a monodentate fashion with a linkage isomerism between the κ1-ONO and κ1-NO2 binding modes. We use density functional theory to help rationalize the presence of all three of these linkage isomers in one compound, before assessing the redox activity of [Cu1(NO2)2]. These latter studies show that the complex is not a competent nitrite reduction electrocatalyst in non-aqueous solvent, even in the presence of additional proton donors, a finding which may have implications for the design of biomimetic catalysts for nitrite reduction.


MDS, 0000-0001-8067-5240
The copper-containing nitrite reductases (CuNIRs) are a class of enzymes that mediate the reduction of nitrite to nitric oxide in biological systems. Metal-ligand complexes that reproduce the salient features of the active site of CuNIRs are therefore of fundamental interest, both for elucidating the possible mode of action of the enzymes and for developing biomimetic catalysts for nitrite reduction. Herein, we describe the synthesis and characterization of a new tris(2-pyridyl) copper complex ([Cu1(NO 2 ) 2 ]) that binds two molecules of nitrite, and displays all three of the common binding modes for NO 2 − , with one nitrite bound in an asymmetric quasi-bidentate κ 2 -ONO manner and the other bound in a monodentate fashion with a linkage isomerism between the κ 1 -ONO and κ 1 -NO 2 binding modes. We use density functional theory to help rationalize the presence of all three of these linkage isomers in one compound, before assessing the redox activity of [Cu1(NO 2 ) 2 ]. These latter studies show that the complex is not a competent nitrite reduction electrocatalyst in non-aqueous solvent, even in the presence of additional proton donors, a finding which may have implications for the design of biomimetic catalysts for nitrite reduction.  in a range of transformations between the various oxidation states of nitrogen [1]. The reduction of nitrite to nitric oxide (NO) is one such transformation, which is a critical step during the process of denitrification performed by a range of bacteria. The overall equation for this conversion is Various classes of enzymes are involved in this transformation, based on haems, molybdenum and copper [2]. In the case of Cu, the enzymes performing this reaction are known as the copper-containing nitrite reductases (CuNIRs), and the reaction performed can therefore be written as The crystal structure of CuNIR (isolated from Achromobacter cycloclastes) was first reported by Adman and co-workers in 1991 [3]. This and subsequent studies have revealed that the active site for nitrite reduction consists of a Cu(II) ion coordinated by three histidine ligands and a single water molecule in a distorted tetrahedral geometry [4]. During nitrite reduction, NO 2 − is believed to displace water from this complex and bind to the Cu(II) centre through both of its oxygen atoms (κ 2 -ONO binding mode; figure 1), leading to a distorted square-based pyramidal geometry at the Cu [2,5]. Subsequent electron transfer and protonation steps then lead to oxygen abstraction from the bound nitrite, NO liberation and the regeneration of the Cu(II) complex in its water-bound form, ready to enter the catalytic cycle again upon binding of additional nitrite [6,7]. The apparently rather simple active-site structure of CuNIR (a tripodal N-donor ligand which supports a copper centre undergoing a one-electron redox reaction) has led numerous groups of coordination chemists to attempt the synthesis of functional analogues of this enzyme [8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24]. Most of these complexes bind only one molecule of nitrite, but Woollard-Shore et al. [20] have reported two examples where two nitrite molecules are bound to a single Cu centre. In both of these examples, one nitrite is bound to the metal through both its oxygen atoms (κ 2 -ONO), while the other nitrite binds through a single oxygen (κ 1 -ONO). Lehnert and co-workers have also reported a series of copper complexes that bind nitrite in both a monodentate and a bidentate fashion (including a di-κ 1 -ONO complex and a κ 1 -ONO/κ 1 -NO 2 complex) [25].
The discovery and investigation of more such binding mode isomers of tripodal N-donor copper complexes is important, both from the standpoint of understanding how the natural enzymes work and in terms of developing biomimetic copper catalysts for applications such as the removal of nitrite from water streams [26] and NO-release systems for biomedical applications [27]. However, to the best of our knowledge, no other examples of nitrite linkage isomerism in mononuclear copper complexes incorporating tripodal N-donor ligands have been reported to date, and no examples where nitrite is present in all three of its most common binding modes (κ 1 -NO 2 , κ 1 -ONO and κ 2 -ONO; figure 1) are known at all.
Herein, we report the synthesis and characterization of a new copper complex which contains a tripodal N-donor ligand (ligand 1) and two molecules of nitrite. This complex ([Cu1(NO 2 ) 2 ]) forms immediately upon addition of nitrite to a solution of the precursor copper complex [Cu(1) 2 ] 2+ , the synthesis and characterization of which we also report. [Cu(1) 2 ] 2+ shares a common geometry with a number of similar complexes reported in the 1990s by Jonas & Stack [28] although the effects of adding nitrite to these previously reported complexes have hitherto not been documented. [Cu1(NO 2 ) 2 ] (whose structure we determine by single crystal X-ray diffraction) displays all three common binding modes for NO 2 − , with one nitrite bound in an asymmetric quasi-bidentate κ 2 -ONO manner and the other bound in a monodentate fashion with linkage isomerism between κ 1 -ONO and κ 1 -NO 2

Experimental section 2.1. General experimental remarks
Unless otherwise stated, all syntheses were conducted under nitrogen in air-and moisture-free solvents obtained from a commercial solvent purification system. Sodium hydride (60% dispersion in mineral oil), methyl iodide (99%), [Cu(CH 3 CN) 4 ]PF 6 (97%), benzoic acid (99.5%) and tetrabutylammonium nitrite (97%, TBA-NO 2 ) were supplied by Sigma-Aldrich. Tetrabutylammonium hexafluorophosphate (TBA-PF 6 ) (98%) was obtained from Alfa Aesar. 6-methyl-tris(2-pyridyl)methanol was prepared according to the published procedure [29]. All 1 H and 13 C NMR spectra were recorded on a Bruker AV 400 instrument, at a constant temperature of 300 K. Chemical shifts are reported in parts per million from low to high field. Coupling constants (J) are reported in hertz (Hz). Standard abbreviations indicating multiplicity were used as follows: m, multiplet; d, doublet; s, singlet. UV-vis spectra were recorded on a JASCO V-670 spectrophotometer using 1 cm path length cuvettes. CHN analyses were collected by the services facility at the School of Chemistry, University of Glasgow, as were LM-MS mass spectra (ESI, positive mode, Bruker micrOTOF-Q machine). IR spectra were collected in the solid state on a Shimadzu IRAffinity-1S Fourier Transform Infrared Spectrophotometer. X-band electron paramagnetic resonance (EPR) spectra were recorded on a Bruker ELEXSYS E500 Spectrometer and simulations were performed using Bruker's Xsophe Program Package [30]. Melting points were gauged using an Electrothermal IA 9000 digital melting point machine. Experiments performed at 'room temperature' were carried out at 20°C. Electrochemical experiments were performed as below.

Synthesis of ligand 1
6-methyl-tris(2-pyridyl)methanol (0.380 g, 1.37 mmol, 1 eq.) was dissolved in THF (7 ml) under nitrogen. Meanwhile, a suspension of NaH (60% dispersion in mineral oil, 0.274 g, 6.85 mmol, 5 eq.) was prepared in 25 ml THF under nitrogen. To this suspension, the solution of 6-methyl-tris(2-pyridyl)methanol was then added via cannula, followed by 0.43 ml (0.972 g, 6.85 mmol, 5 eq.) of methyl iodide to give an offwhite suspension. The reaction mixture was then heated up to 60°C under nitrogen overnight, during which time it was observed to turn orange. After cooling to room temperature, the reaction mixture was diluted with 100 ml CHCl 3 and then washed with water and then brine. The organic phase was dried over MgSO 4 to give a clear orange solution, which was concentrated in vacuo to yield a reddish-orange oil. To this oil was added 25 ml acetonitrile and the resulting suspension was extracted with 25 ml of pentane, whereupon two clear phases became evident: an upper colourless (pentane) layer and a lower bright yellow (acetonitrile) layer. Collection of the acetonitrile layer after further washing with pentane (2 × 25 ml) and concentration under reduced pressure then yielded compound 1 as an off-white solid (0.373 g, 93%), m.p. = 101-103°C. Anal. calcd. for C 18  Assignments of signals to groups of protons are based on two-dimensional (COSY) spectra and the expected coupling patterns of the peaks, although the symmetry of the molecule prevents unambiguous assignments. Letter codes correspond to those shown in scheme 1. The 1 H NMR spectrum of this compound is shown in electronic supplementary material, figures S1 and S2. 13   30 min at room temperature, producing a bright yellow solution. After complete addition, the reaction mixture was stirred for a further 90 min at room temperature, resulting in a yellow solution and a white precipitate. The solution was then filtered under air, and the volume of the filtrate reduced by half. Diethyl ether was then added to the filtrate. This yellow solution was subsequently sealed to prevent evaporation of the solvents and allowed to stand at room temperature under air for two weeks. After this time, the reaction mixture was observed to consist of a lilac solution and a blue-green precipitate. The precipitate was removed by filtration and the purple filtrate concentrated in vacuo to yield [Cu (1)

Electrochemical methods
Electrochemical studies were performed in a single-chamber cell with a three-electrode configuration using a CH Instruments CHI700 series potentiostat. The supporting electrolyte was 0.1 M TBA-PF 6 in acetonitrile. A large surface area strip of carbon felt (Alfa Aesar) was used as the counter electrode, along with an Ag/AgNO 3 pseudo-reference electrode. Potentials are reported relative to the ferrocenium/ferrocene couple, the position of which was judged by adding ferrocene to the samples analysed. Working electrodes were washed with acetone and deionized water prior to use. Cyclic voltammograms were collected at room temperature under an atmosphere of Ar at a scan rate of 100 mV s −1 . A glassy carbon disc electrode (area = 0.071 cm 2 , CH Instruments) was used as the working electrode for cyclic voltammetry. Measurements were conducted without stirring and with iR compensation enabled.

Computational methods
All calculations were performed with the program Gaussian 09 [31] at the DFT level. The M06-L exchange-correlation functional was used, [32] which is a pure functional of the meta-GGA type, which has been shown to perform well for transition-metal complexes [33,34]. The def2-TZVP basis set was used, [35] with the 'W06' auxiliary basis for density fitting [36]. The effect of exact exchange was gauged by comparing to the M06 functional, [37] which is a hybrid meta-GGA with 27% exactexchange admixture. No significant differences in structures, energies or spin density distributions were found. Interestingly, however, vibrational frequencies calculated with M06 were blue-shifted by as much as 80 cm -1 compared with M06-L. Modes involving N-O stretching were particularly strongly affected. The agreement with experiment was significantly better for the M06-L frequencies.
All computational results reported in the paper were therefore obtained with M06-L/def2-TZVP; data obtained with M06 are available via the University of Glasgow's open access online data repository [38]. All structures were fully optimized; stationary points were identified as minima by the absence of imaginary frequencies. Gibbs free energies were calculated based on the usual harmonic-oscillator/rigidrotor/ideal-gas approximation at 298. 15

Crystallography
Crystallographic data were collected at the University of Glasgow on a Bruker APEX-II CCD diffractometer. A green, column-shaped crystal of dimensions 0.46 × 0.1 × 0.06 mm was used for single crystal X-ray diffraction data collection. C 18  Mo Kα radiation, λ = 0.71073 Å. The structure was solved using SHELXS and refined using SHELXL (both within OLEX2) [43,44]. OLEX2 was also used for molecular graphics and to prepare material for publication. CCDC 1547352 contains the supplementary crystallographic data for this paper. More details on the crystallographic data and its collection can be found in the electronic supplementary material. Hence, deprotonation of 6-methyl-tris(2-pyridyl)methanol [29] with NaH followed by methylation with methyl iodide yielded the free ligand (1) in excellent yield after purification. Compound 1 was methylated in this way in order to prevent any coordination of the alcohol group to the metal centre, which it was feared might interfere in the subsequent binding of the metal centre to any small molecule ligands that were subsequently added.

Results and discussion
After methylation, copper was then inserted into ligand 1 by stirring the free ligand with [Cu(CH 3 CN) 4 ]PF 6 at room temperature. Subsequent exposure to air then yielded the purple complex [Cu(1) 2 ](PF 6 ) 2 . The electronic absorption spectrum of this complex (figure 2a, black line) showed strong similarities to that reported for the analogous complex (containing an -OMe substituent on the pyridyl ring in place of the methyl substituent) reported previously by Jonas & Stack ([Cu(1) 2 ] 2+ displays λ max at 560 nm, with an extinction coefficient of 56 M −1 cm −1 , while the -OMe derivative has λ max = 580 nm with ε = 57 M −1 cm −1 ) [28]. The position of the absorption maximum for this transition at a value well below 600 nm was previously rationalized on the basis of the Jahn-Teller distortion which is expected for a d 9 Cu(II) ion ligated by six almost equivalent ligands. This distortion, it was argued, should lead to ligand field transitions at higher energies as the distortion away from octahedral geometry becomes greater (and as the Cu−N bonds in the equatorial plane therefore become shorter). A λ max value of 560 nm therefore corresponds to a complex in which the geometry is significantly distorted away from octahedral symmetry. To obtain further insight into the nature of the geometry around the copper centre in [Cu (1)   g || > g ⊥ > g e (free electron g-value) and A || A ⊥ . The simulation gave spin-Hamiltonian parameters: g = (2.057, 2.058, 2.227); A{ 63,65 Cu} = (10, 10, 193) × 10 -4 cm -1 ; A{ 14 N} = (13, 13, 12) × 10 -4 cm -1 . Although the superhyperfine coupling from the 14 N nuclei was less than the experimental linewidth, it was nonetheless included and approximated by matching the average value to the one obtained from the isotropic spectrum. There is a slight drift away from strict axial symmetry, with the best fit obtained with inequivalent g x and g y values. This stems from the methylation of one pyridyl arm in 1. The spectral profile is near-identical to that reported by Jonas & Stack [28] for their analogous complex with methoxylated pyridyl groups, and is typical of complexes of Cu(II) in five-coordinate and distorted octahedral geometries with pyridyl ligands [45][46][47].

Synthesis and structure of complex [Cu1(NO 2 ) 2 ]
Upon addition of nitrite to [Cu(1) 2 ](PF 6 ) 2 , the complex undergoes rapid reaction as signalled by an immediate colour change from lilac to bottle-green. Hence, when 10 equivalents of tetrabutylammonium nitrite (TBA-NO 2 ) were added to a 1.2 mM solution of [Cu(1) 2 ](PF 6 ) 2 in acetonitrile, the colour change was instantaneous and gave rise to the absorption spectrum shown as the red line in figure 2a (λ max = 643 nm, ε = 120 M −1 cm −1 ). This reaction was repeated on a preparative scale, allowing green crystals of [Cu1(NO 2 ) 2 ] to be obtained by vapour diffusion of diethyl ether into an acetonitrile solution of [Cu1(NO 2 ) 2 ]. These crystals then proved suitable for X-ray diffraction ( figure 3).
The crystal structure of [Cu1(NO 2 ) 2 ] shows the copper centre to be coordinated octahedrally, with three Cu−N bonds to the pyridine moieties in ligand 1 and a further three bonds between the Cu centre and two nitrite anions. The Cu-N bond lengths between the Cu and the nitrogen donors in ligand 1 are: Cu-N1 = 2.122(3), Cu-N2 = 2.009(3) and Cu-N3 = 2.169(4) Å, which are in reasonable agreement with the distances reported previously by Tanaka and co-workers for Cu(II)-tris(2-pyridyl) complexes with only one bound nitrite [48,49] and Kodera et al. [50] for Cu(II)-tris(2-pyridyl) complexes featuring two bound bromides.
More interestingly, the structure also displays isomerism in the two bound nitrite ligands. The first nitrite (defined by nitrogen N1A/N1B and oxygens O1A/O1B and O2A/O2B) is bound to the Cu(II) centre in an asymmetric quasi-bidentate manner with some disorder in the bond lengths, reminiscent of that observed by Lehnert and co-workers [25]. This disorder comes about as a result of the two Cu−O bond lengths being slightly different in the two isomers, which have N1A/B occupancies in a ratio of approximately 0.55 : 0.45. For example, the Cu−O1B bond length is 2.010(18) Å, while the Cu−O2B distance is considerably longer at 2.66(2) Å. Similar quasi-bidentate interactions of nitrite with a Cu(II) centre in a tris(2-pyridyl) complex have previously been reported by Woollard-Shore et al. [20] who found a long Cu−O interaction of 2.5620 Å.      [51][52][53][54]).
To clarify the energetic and electronic aspects of the two types of isomerism and to analyse the structures of the different forms, we undertook a series of DFT calculations. There are four isomeric forms to consider: both of the κ 1 -bound linkage isomers (κ 1 -ONO and κ 1 -NO 2 ) can exist in two forms, depending on which of the Cu-O bonds of the quasi-chelating κ 2 -ONO ligand is short or long. Because these two forms are de facto enantiomeric (but for the methyl groups, which are remote from the metal centre), they are energetically degenerate for all intents and purposes, which is consistent with the approximately 1 : 1 occupancy in the X-ray structure. It is, therefore, sufficient to consider in the following only one form of each of these linkage isomers.
As can be seen from figure 5, the corresponding copper-donor distances for the two linkage isomers are very similar. The quasi-chelating κ 2 -ONO ligand is bound asymmetrically, with one short and one long Cu-O interaction, as seen in the X-ray structure. This asymmetry in the coordination is mirrored in the Cu-N pyr distances trans to the bidentate nitrite: the two short Cu-N/O bonds are (approx.) trans to each other, as are the two long ones. This feature is not apparent from the X-ray structure, where these Cu-N pyr bonds have similar lengths (2.12 and 2.17 Å) and the nitrogens have unique positions. Such asymmetry in the coordination is expected for an octahedral d 9 system: the two long Cu-N/O bonds define the Jahn-Teller axis, along which the octahedron is tetragonally distorted (elongated).
Looking at the spin density distributions and Mulliken spin populations for the two linkage isomers (figure 6), there is again very little difference between them. In essence, around half of the spin of one electron is localized on the metal and approximately 0.2 of the spin of one electron is localized on each of the nitrite ligands. The nitrites therefore carry a significant fraction of the unpaired spin density. The shape of the spin density on copper is clearly recognizable as that corresponding to the d x 2 −y 2 orbital, which is the SOMO in these complexes (noting that the Jahn-Teller axis is taken to be the z-axis by definition).
The two linkage isomers are nearly energetically degenerate. The κ 2 -ONO, κ 1 -NO 2 isomer is calculated to be less stable than the κ 2 -ONO, κ 1 -ONO isomer by 4 kJ mol -1 in terms of potential energy and just 1 kJ mol -1 in terms of Gibbs free energy. The small energy difference is consistent with the concurrent presence of both isomers in the crystal in approximately equal proportion. Similarly, small energy differences between O-and N-coordinated nitrite isomers have been reported before by Lehnert and co-workers for their series of Cu complexes [25].
The infrared spectrum of [Cu1(NO 2 ) 2 ] reveals a number of peaks that fall in the frequency range characteristic of bound nitrite. However, the assignment of these is complicated by the fact that several of these bands (bands 1, 2 and 6 in figure 7  Based on the literature, two alternatives then exist for the assignment of these bands. In the first scenario, the bands at 1373 and 1131 cm −1 emanate from terminal and internal N-O stretches of Obound nitrite, respectively [48]. Meanwhile, the band at 1327 cm −1 is assigned to the κ 1 -NO 2 symmetric stretching mode [20]. In the second scenario, the two bands at 1373 and 1327 cm −1 are assigned to terminal N-O stretches from O-bound nitrites, and now the band at 1131 cm −1 is assigned to the κ 1 -NO 2 symmetric stretching mode [25]. Our calculated vibrational data suggest that perhaps the first scenario is the more likely. Taking into account that the M06-L functional somewhat overestimates vibrational frequencies (especially modes involving N-O stretching), we predict that the κ 1 -NO 2 symmetric stretch should appear between 1340 and 1300 cm −1 . Furthermore, we predict that a terminal N-O stretch from  ligands in the first coordination sphere were obscured. The spectrum was simulated with g iso = 2.132 and A iso = 63 × 10 -4 cm -1 . The smaller Cu hyperfine coupling reveals less spin density localized on the Cu centre, consistent with a six-coordinate complex. A frozen solution spectrum of this complex recorded in an acetonitrile/dichloromethane glass at 130 K is shown in the electronic supplementary material, figure S5.

Redox activity of [Cu1(NO 2 ) 2 ] and nitrite electroreduction studies
On account of the known nitrite electroreduction activity of allied Cu-tris(2-pyridyl) complexes [22,23,48], we hypothesized that [Cu1(NO 2 ) 2 ] might also be active for this transformation. Initially, cyclic voltammetry was performed on a nitrite-free solution of [Cu(1) 2 ](PF 6 ) 2 in acetonitrile containing 0.1 M tetrabutylammonium hexafluorophosphate (TBA-PF 6 ) as the supporting electrolyte. This evinced a reduction process centred at around −0.5 V (versus the ferrocenium/ferrocene couple), which we attribute to reduction of the Cu(II) centre to the Cu(I) oxidation state by analogy to previous studies of such complexes in non-aqueous solvents (black trace in figure 9a) [28]. However, this redox event is only quasi-reversible, with the re-oxidation event occurring over a rather broad range and with considerable separation between the cathodic and anodic peaks. Such behaviour has been noted previously for complexes consisting of two tripodal ligands coordinated to one Cu(II) centre [28] and would be consistent with extensive ligand rearrangements taking place as a result of reduction and re-oxidation of the copper centre. Hence, reduction of the Cu(II) centre in [Cu(1) 2 ] 2+ would produce a Cu(I) centre, which would be likely to exist preferentially in a tetrahedral coordination environment. Hence, loss of one of the bound tripodal ligands may occur or both of the tripodal ligands may remain bound but undergo significant rearrangements as a result of reduction. Re-oxidation would then require a change in geometry back to a higher coordination number. Such a scenario would also be consistent with the reproducible nature of the CVs of [Cu(1) 2 ] 2+ under these conditions: repeated cycling over the range shown by the black trace in figure 9a does not lead to any decrease in the signal or alteration in the shape of the voltammogram, consistent with slow ligand rearrangements that accommodate the preferred coordination geometry of these two oxidation states of copper [28].
Upon addition of two equivalents of a soluble nitrite source to [Cu(1) 2 ] 2+ , the colour of the solution turns from lilac to green (indicating the formation of [Cu1(NO 2 ) 2 ]) and the redox wave attributed to the Cu(II)/Cu(I) couple appears to shift to slightly more anodic potentials, as shown by the red trace in figure 9a. Upon addition of excess nitrite, the Cu(II)/Cu(I) couple becomes less well defined (black trace in figure 9b). Meanwhile, the oxidation events that were evident upon the addition of two equivalents of nitrite (at 0 V and above) become more pronounced. However, these oxidation events seem to be due mainly to the background oxidation of nitrite as indicated by the red trace in figure 9b, which shows that these waves are present when the nitrite salt is dissolved in the electrolyte in the absence of any copper complex.
Further additions of nitrite to solutions of [Cu1(NO 2 ) 2 ] show an increase in the wave corresponding to background nitrite oxidation, but do not show any catalytic waves that could be attributed to the  reduction of nitrite (figure 10a, black trace). Hence, we concluded that no electrocatalytic reduction of nitrite as a result of the presence of our copper complex was occurring under these conditions. This is perhaps not unexpected, as equations (1.1) and (1.2) clearly show that the most probable nitrite reduction reactions all require protons. We therefore attempted to switch on electrocatalysis in our system by the addition of a soluble proton source (in this case, benzoic acid). Tripodal copper complexes have previously been used to demonstrate nitrite electroreduction to NO in aqueous solution, and these studies have shown that nitrite reduction does not occur at pH values above 9, on account of the dearth of protons [22,23,48]. There was, therefore, good reason to suppose that addition of an external proton source would be efficacious in our case. However, the red trace in figure 10a shows that adding 20 equivalents of benzoic acid to a solution containing 20 equivalents of nitrite and one equivalent of copper complex fails to produce any reductive features that could be interpreted as a catalytic wave. Indeed, figure 10b shows an overlay of the red trace from figure 10a with the CV displayed by the [Cu(1) 2 ] 2+ ion on its own, without any nitrite or benzoic acid present. This clearly shows that there is no reductive activity in the presence of nitrite and benzoic acid that exceeds in magnitude the current for the reduction of the complex alone. On this basis, we are forced to conclude that [Cu1(NO 2 ) 2 ] is not an active electrocatalyst for nitrite reduction under these conditions, even in the presence of an external proton source.