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Article

Trapping of Ag+ into a Perfect Six-Coordinated Environment: Structural Analysis, Quantum Chemical Calculations and Electrochemistry

by
Veronika I. Komlyagina
1,2,
Nikolay F. Romashev
1,
Vasily V. Kokovkin
1,
Artem L. Gushchin
1,*,
Enrico Benassi
2,*,
Maxim N. Sokolov
1 and
Pavel A. Abramov
1,3,*
1
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of Russian Academy of Sciences (SB RAS), 3 Akad. Lavrentiev Ave., 630090 Novosibirsk, Russia
2
Faculty of Natural Sciences, Novosibirsk State University, 2 Pirogova Str., 630090 Novosibirsk, Russia
3
Institute of Natural Sciences and Mathematics, Ural Federal University, 620002 Ekaterinburg, Russia
*
Authors to whom correspondence should be addressed.
Molecules 2022, 27(20), 6961; https://doi.org/10.3390/molecules27206961
Submission received: 28 September 2022 / Revised: 12 October 2022 / Accepted: 12 October 2022 / Published: 17 October 2022
(This article belongs to the Special Issue Synthesis, Characterization and Crystal Structure of Coordination Compounds II)
Browse Figures
Review Reports Versions Notes

Abstract

:
Self-assembly of (Bu4N)4[β-Mo8O26], AgNO3, and 2-bis[(2,6-diisopropylphenyl)-imino]acenaphthene (dpp-bian) in DMF solution resulted in the (Bu4N)2[β-{Ag(dpp-bian)}2Mo8O26] (1) complex. The complex was characterized by single crystal X-ray diffraction (SCXRD), X-ray powder diffraction (XRPD), diffuse reflectance (DR), infrared spectroscopy (IR), and elemental analysis. Comprehensive SCXRD studies of the crystal structure show the presence of Ag+ in an uncommon coordination environment without a clear preference for Ag-N over Ag-O bonding. Quantum chemical calculations were performed to qualify the nature of the Ag-N/Ag-O interactions and to assign the electronic transitions observed in the UV–Vis absorption spectra. The electrochemical behavior of the complex combines POM and redox ligand signatures. Complex 1 demonstrates catalytic activity in the electrochemical reduction of CO2.

1. Introduction

Ag+/L/polyoxometalate hybrid organic–inorganic systems are attractive candidates for engineering multifunctional coordination networks. In this field, numerous works have been contributed by Cronin [1,2,3,4,5], Wang [6,7], Sun [8,9,10], Mac [11], and Niu et al. [12,13]. The versatility of Ag-based supramolecular building blocks opens almost limitless opportunities to create coordination networks of different topologies and compositions [14,15,16,17,18,19,20,21,22]. Complexes with redox-active ligands have been mostly ignored in this field. We believe, however, that the usage of such ligands would offer an advantage to construct new semiconductors with controllable topologies.
Bis(arylimino)acenaphthenes (BIANs) are redox-active, sterically bulky ligands, widely used as N,N-bidentate ligands in coordination chemistry and catalysis [23,24]. The key feature of BIANs as strong π-acceptor molecules is their ability to accept up to four electrons, which can be reversibly exchanged with the coordinated metal-triggering redox-based chemical processes [25,26,27,28,29,30,31,32,33,34,35]. Many complexes of late transition metals with BIANs have been reported [36,37,38,39,40,41]. However, Ag complexes with BIANs remain scarcely explored: There are only seven structurally characterized examples of Ag-BIAN complexes [42,43,44,45]. The first mention is found in the report by Rosa and co-workers, who reported the preparation, spectroscopic, and computational studies of [Ag(dpp-bian)2]BF4 and [Ag(tmp-bian)2]BF4 [42].
In our recent studies, we paid particular attention to the Ag+ coordination environment in novel [β-{AgL}2Mo8O26]2− complexes, where the [β-Mo8O26]4− polymolybdate acts as a ditopic doubly tetradentate ligand towards Ag+ [46,47,48]. These works focus on the Ag+ coordination behavior and changing of the coordination number (CN) initiated by the auxiliary ligand L. In all cases, we used monodentate ligands for L, and found typical coordinations with CN 3 and 4. Moreover, Ag+ can form long-range contact with an additional DMF molecule, formally increasing its CN [46]. This situation may be more complicated without any auxiliary ligand when different monomeric and polymeric species have been detected [47]. Concerning bidentate ligands, either rigid (e.g., BIANs) or flexible (e.g., bpy and its derivatives) diimines with redox nature can be used, which opens numerous ways to construct new coordination networks, with relevance in the field of coordination polymers preparation. In this work we report a new complex, viz. (Bu4N)2[β-{Ag(dpp-bian)}2Mo8O26], indicating a unique Ag coordination environment. The electrochemical activity of the complex toward CO2 reduction was studied.

2. Results and Discussion

2.1. Synthesis and Structural Features

Mixing (Bu4N)4[β-Mo8O26] and AgSO3CF3 in DMF results in the coordination of Ag+ with [β-Mo8O26]4−, leading to [{Ag(DMF)x}2Mo8O26]2− (x = 1, 2) and other species [47]. The addition of dpp-bian to such a solution provided an orange precipitate. Brown block-shaped crystals of 1 suitable for X-ray diffraction analysis were obtained by diffusion of diethyl ether into a solution of 1 in DMF. The resulting crystalline complex 1 crystallized in monoclinic crystal system (C2/c space group) with the following unit cell parameters: a = 38.5675(16), b = 12.6898(6), c = 26.2540(11) Å, β = 116.858(1)° (Supplementary Materials Table S1). The main building blocks of the structure are hybrid [β-{Ag(dpp-bian)}2Mo8O26]2− anions (Figure 1).
It should be noted that using other bians (e.g., tmp-bian, or p-Cl-bian) with less bulky substituents always provided the corresponding [Ag(bian)2]SO3CF3 complexes. The most proposed cause of this is in bulkiness of the substituents.
The main structural feature in this complex is the unusual coordination environment of Ag+ (Figure 2, Table S2) consisting of four oxo ligands from polyoxomolybdate and two N-atoms from dpp-bian. The Ag-O bond distances ranged from 2.495 to 2.569 Å, while Ag-N distances were 2.386 and 2.461 Å. The asymmetric coordination of the dpp-bian ligand was likely caused by packing effects. The Ag+, therefore, resides inside a coordination environment that has six coordination bonds, as demonstrated by the quantum chemical calculations (vide postea). Unlike many other structures that involve multiple Ag···L contacts, the bond lengths vary in a relatively narrow range (0.18 Å) and cannot be divided into primary and secondary interactions. The coordination polyhedron of Ag+ is irregular, neither octahedral nor trigonal prismatic, but is similar to a monocapped octahedron, lacking a vertex in the capped face (Figure 3). The analysis with SHAPE (http://www.shapesoftware.com/ (accessed on 3 September 2022)) shows that this is a transition state between a pentagonal pyramid and a trigonal prism (Table S3).
The sum of the ionic radii of Ag+ (1.15 Å, Shannon for the CN 6) and O2− (1.35 Å, Shannon) is 2.50 Å. Purely van der Waals interactions were expected at 3.24 Å, which is the sum of the vdW radii of Ag (1.72 Å) and O (1.52 Å), while covalent radii are 1.45 (Ag) and 0.66 Å (O), which would provide Ag-O distances close to 2.1 Å for covalent bonding. Similar considerations apply, mutatis mutandis, for the Ag-N bond distances. We can describe this situation as Ag+ trapped inside a {N2O4} cage. It is interesting to compare the observed bonding arrangement around Ag+ with other reported data. We used the AgO4N2 coordination environment as the criterion for the structural search in CCDC. The relevant entries are summarized in Table 1. All hits were divided into five groups based on the ligand nature. The first one included complexes with sterically fixed pincer-type ligands based on pyridine as a central fragment and two O-donor arms. In such complexes, the Ag-N bonds were significantly shorter than Ag-O bonds.
However, in the case of HATSAZ, two tridentate ligands completed the coordination sphere of Ag+. Therefore, the discrimination between Ag-O and Ag-N bond distances cannot be done properly.
The second group combined complexes with crown-ethers and cryptands. In this environment, Ag+ was fixed inside the cages wherein Ag-O contacts were largely determined by ligand geometry. The Ag-N bond distances were shorter than Ag-O, except for TIBQIE, wherein the coordination sphere of Ag+ may include additional Ag-π donation (c.a. at 2.83 Å) and Ag-F contacts (2.71 Å). In this case, the bonding nature should be further studied through quantum chemical calculations, to shed light on the Ag+ complexes with very high coordination numbers. Remarkably, for such a group of complexes, coordination numbers were lower than the number of donor atoms.
The third group was constituted by POM-based complexes. In this group, an uncommon Ag+ coordination by the POM was observed in the case of ZULXOV, wherein there were two types of Ag (namely, Ag1 and Ag2), with a significant Ag-X bond distance distribution. Curiously, the values of d(Ag1-O) ranging from 1.960 to 2.097 Å were too short for Ag and might be attributed to the presence of a 3d metal.
Within the fourth group, no anomalies in the Ag+ coordination were revealed. The comparison of the bonding distribution around Ag followed the same trends as in the previous groups.
In the fifth group, more structures featured anomalous geometries. In most cases, the atom assigned as Ag looks more like a 3d metal, rather than Ag. In the case of ELEGIM structure, the “Ag” atom had CN 9 and might be a lanthanide.
From this structural analysis, it can be seen that the significant difference between Ag-N (shorter) and Ag-O (longer) bond distances is a rule. There are only two cases wherein this rule is infringed, viz. in SENJIE and TIBQIE. This might be due to a wrong refinement of N and O atoms or impurities in the initial ligands. High coordination numbers can be achieved only with the use of pincer ligands with fixed geometry, and there is no possibility to reach CN 6 (4 O and 2 N donor atoms) for Ag+ using mono or bidentate ligands. The example reported in this work, therefore, represents a unique case in the literature, which reveals a hitherto hidden aspect of Ag+ coordination behavior.

2.2. Quantum Chemical Calculations

The natural bond orbital (NBO) analysis was conducted on the electron density of the optimized cluster to clarify the nature of the Ag-involving electron density delocalization interactions (ESI, Tables S4 and S5). Ag may play the role both of electron density donor and acceptor. As a donor, the NBO of Ag involved are core orbitals (CR 100% p in nature; with occupancy > 1.998) or lone pairs (LP 100% d in nature; with occupancy > 1.990). From Ag, the electron density shifted to empty virtual Rydberg orbitals (RY*) of C atoms or bond orbital BD*(C-C). When Ag plays the role of acceptor, the virtual NBO of Ag involved are 4 LP* and 6 RY*. Their nature and occupancy is variegated; however, 2 LP* are almost 100% p orbitals; 1 LP* is s33%p67%; 1 LP* is s65%p35%; RY* orbitals involve d orbitals (in particular, one RY* is 100% d). In these cases, the donors are CR belonging to O, N, C, or Mo atoms, BD(C-C), BD(C-N), or BD(C-H).
The non-covalent interaction (NCI) analysis confirmed that Ag has CN = 6, showing four strongly attractive interactions (Figure 4, blue regions) with as many O atoms (red arrows) + 2 with as many N atoms (blue arrows), involving each Ag atom. In those regions, bond critical points (BCPs) were identified by means of the topological analysis based on the atoms-in-molecules (AIM) theory (ESI, Table S6).
The UV–Vis absorption spectrum (Figure 5a) indicates two main bands, which do not represent two single transitions, but cover multiple transitions. The four transitions with higher intensities are found at 478 and 303 nm, each of which shows double degeneration. They are characterized by a complex composition in terms of molecular orbitals, and we hence decided to analyze their nature by means of natural transition orbitals (NTO) analysis (Figure 5b). Both absorption bands corresponded to CT transitions, and in both cases, Ag d orbitals donated electron density. The band at 478 nm was mostly Ag → L (the [Mo8O26]4− ligand was almost excluded from this electronic transition), and is dipolar in nature. Contrary to this, the other band at 303 nm involved the octamolybdate and was quadrupolar in nature.

2.3. Electrochemistry

The structure of 1 combines a redox-active polymolybdate, Ag+, and non-innocent dpp-bian ligand. Since the [{Ag(L)x}2Mo8O26]2− complexes are unstable in solution [46], their electrochemical behavior can be correctly studied only in solid state.
The redox behavior of 1 in the paste electrode in acetonitrile was studied with cyclic voltammetry (Figure 6, black curve). For the sake of comparison, a cyclic voltammogram for the (Bu4N)4[Mo8O26] under the same conditions was recorded (Figure 6, red curve). The comparison of paste electrodes behavior and blank solution is presented in Supplementary Materials (Figure S2). The corresponding data are provided in Table 2 and Table 3. In both cases, a large number of quasi-reversible and irreversible electrochemical transitions were observed, viz. from six (for the precursor) to eight (for the complex). The redox properties of the precursor were due to its ability to undergo multistage reduction processes, which is a characteristic feature of POMs. The presence of an additional redox-active dpp-bian fragment in the complex, known for its ability to multielectron reduction, increased the number of electrochemical transitions.
The electrochemistry of octamolybdates was reported in a number of works. Xie et al. reported synthesis and electrochemical behavior of [MoO3(TPMA)]·4H2O, {[Cu(TPMA)(H2O)]2(β-Mo8O26)·3H2O}4, [Co(TPMA)(β-Mo8O26)0.5], [Co(TPMA)(γ-Mo8O26)0.5], and [Cu3(TPMA)2(1,3-ttb)2(β-Mo8O26)]·H2O (TPMA = tris[(2-pyridyl)methyl]amine; 1,3-ttb = 1-(tetrazo-5-yl)-3-(triazo-1-yl)benzene) [49]. The electrochemical properties were measured for paste electrodes (CPE) in 0.5 M Na2SO4 + 0.1 M H2SO4 aqueous solution at different scan rates. The authors postulate that “when the scan rate is 100 mV·s−1, the mean peak potentials E1/2 = (Epa + Epc)/2 are +185 mV (I–I′) for [MoO3(TPMA)]·4H2O-CPE, 367 mV (I–I′) and 204 mV (II–II′) for [Co(TPMA)(β-Mo8O26)0.5]-CPE, 228 mV (I–I′) and 120 mV (II–II′) for [Co(TPMA)(γ-Mo8O26)0.5]-CPE, and 204 mV (I–I′) and 83 mV (II–II′) for [Cu3(TPMA)2(1,3-ttb)2(β-Mo8O26)]·H2O-CPE′′. They assigned these processes to Mo6+ reduction. However, in our opinion, ligand-centered redox reactions or redox reactions involving a heterometal that might occur in this region cannot be excluded. Indeed, for the initial (Bu4N)4[Mo8O26], we did not observe any reduction peaks in the positive region. Only oxidation peaks (peaks 4, 5, and 6 in the red curve in Figure 6) were found in the anodic curve and they can be attributed to the oxidation of electrochemically generated reduced species during cycling. On the other hand, the absence of cathodic peaks in the positive region for (Bu4N)4[Mo8O26] in comparison with related complexes can be explained by the influence of the medium and the shift of the Mo6+ reduction peaks to a more anodic region caused by the participation of protons in redox processes.
The same redox behavior was reported by Hoi et al. for H2{[Cu3(PCAP)4(H2O)2](β-Mo8O26)}·10H2O, H{[Cu(PCAP)(H2O)](β-Mo8O26)0.5} and H2[Co(H2O)6][Co2(PCAP)4(γ-Mo8O26)(H2O)2]·10H2O [50]. In both papers, the authors reported the electrochemical activity of the Cu-Mo8O26 complexes toward H2O2 reduction.
On the other hand, solid-state electrochemistry of bulk molybdates has been attracting increasing interest for possible technological applications, such as MgMoO4, which has been used for supercapacitor and battery applications [51], or CoMoO4, which has shown a specific capacitance of 79 F·g−1, an energy density of 21 W h·kg−1, and excellent cycling stability (retaining over 75% of its initial capacitance after 2000 cycles), which makes it a very promising candidate for large-scale energy-storage applications.
Recently, Schöfberger et al. reported the catalytic activity of [AgI(bian)2]BF4 in electrochemical CO2 reduction [52]. A drop-casted ink of [AgI(4-OMe-Ph-bian)2]BF4 immobilized onto carbon paper gas diffusion electrodes in a flow cell with 1.0 M KHCO3 aqueous electrolyte, resulting in Faradic efficiency of 51% for CO at a current density of 50 mA cm−2. This observation prompted us to use (Bu4N)2[β-{Ag(dpp-bian)}2Mo8O26] as the electroactive matter of the carbon-based paste electrode for CO2 reduction. The electrochemical activity was tested in a CO2-saturated 1.0 M KHCO3 aqueous solution. Figure 7 shows a CV series recorded in the range of −1.4/1.4 V relative to a saturated Ag/AgCl reference electrode at a 10 mV/s scan rate for a paste electrode containing 1. The red arrow in Figure 7 shows the cathodic potential sweep direction; the beginning of the first cycle corresponds to the 0.50 V point. In the region from approx. −0.9 to −1.2 V, there is a cathodic plateau that is most likely related to CO2 reduction. The black arrow on this plateau displays the sequential increase in current from the first to subsequent scans. At potentials below −1.2 and above 1.0 V, there was a sharp increase in current due to HER and OER, respectively. The voltammograms also revealed regions at potentials of ~0.10 (cathodic current peaks) and ~0.50 V (anodic current peaks), which are responsible for the presence of complex 1 in the paste. The dependence of the current in the peak on the square root of the potential scan (Figures S3 and S4 in Supplementary Materials) indicates the diffusion nature of the current for the redox reaction of complex 1 and its stability.
Comparison of CVs (Figure 8) recorded in the absence (red curve, blank) and in the presence of complex 1 (grey curve) in a 1.0 M KHCO3 solution saturated with CO2 or in a solution unsaturated with CO2 (blue curve) showed that, in the region of cathodic currents, the area (on the gray curve) appears with potentials in the region of−1.16/−0.87 V (relative to Ag/AgCl), which, apparently, is responsible for the electrocatalysis of CO2 reduction to less deeply oxidized products. The conversion to the RHE scale provided the potential ranging from −1.35 to −1.06 V. According to the literature data, the direct reduction involved the following first step:
CO2 + e = CO2
•−E° = −1.48 V (vs. RHE)
When CO2 was saturated in the presence of 1, an increase in the cathodic current was observed (Figure 8). In this case, the difference in an area between the blue (1) and gray (1 + CO2) cathodic currents reached 5.0 mC or 29 mC/cm2 in the range of −1.16/−0.87 V. The total difference between the red (blank + CO2) and gray currents was 34 mC or 176 mC/cm2.
The cathodic peak at approximately −0.5 V observed on the red curve (Figure 8) refers to the Nafion matrix containing acidic SO3H groups capable of ion exchange [53]. This peak is slightly shifted towards positive potentials for the paste containing 1 (up to −0.25 V). On the other hand, in the potential region of 0.1–0.2 and 0.5–0.6 V (gray and blue curves), cathodic and anodic peaks were observed, marking the presence of 1 in the pastes.
Typically, currents observed under anhydrous conditions and in the solvent–water mixtures differ due to the presence of protons accessing alternative reduction mechanisms. It is well known that, without external proton sources, electrocatalytic CO2 reduction can proceed: (i) as reductive disproportionation forming carbonate and CO, or (ii) as dimerization of CO2•− anion-radical to oxalate, while proton addition opens pathways to numerous reduction products, such as CO, formic acid, methanol, methane, and higher carbon products, e.g., ethylene, ethanol, and acetic acid [54,55,56,57,58,59]. The possible reaction mechanism and catalytic activity of Ag+ coordinated by different BIANs are currently the object of a dedicated investigation in our group, both from an experimental and computational point of view. However, in the specific case investigated in the present work, taking into account the activity of the complex in the solid state, the through-space electron transfer from the reduced complex to CO2 is the only possible explanation. In fact, the direct coordination of CO2 cannot be hypothesized due to lack of coordination space near to Ag+ caused by the bulky side groups installed onto BIAN molecules.
To check this hypothesis, we calculated the first reduced state of [β-{Ag(dpp-bian)}2Mo8O26]. The obtained spin density profile is shown in Figure 9.
According to the calculated data, for the first reduced state (induced during electroreduction) the spin density was mostly located over two BIAN ligands. Moreover, its small portion affects both Ag atoms. Thus, we can conclude that electron transfer to CO2 can be indeed realized from the combination of Ag and BIAN electronic states.
The formation of formic acid as a possible product of CO2 reduction could be judged from a comparison of CV data for pure HCOOH in 0.1 M Na2SO4 and the CV data for a paste electrode containing 1 in the presence of CO2 under the same conditions (Figure 10).
On the CV of the blank paste (blue curves in Figure 10) in the range of −1.40/−1.00 V, a region of cathodic reduction of formic acid, was observed. This region intersected with an interval of −1.25/−0.80 V, which is responsible for the reduction of CO2 in the paste containing 1 (orange curves). Note that the other characteristic regions on the orange curves in Figure 10 (Na2SO4) are close to the data where the supporting electrolyte was KHCO3 (Figure 8): Nafion matrix peak at−0.5/−0.4 V; cathodic and anodic peaks of 1 at 0.1/0.2 and 0.3/0.5 V.

3. Materials and Methods

3.1. General Information

(NBu4)4[β-Mo8O26] and dpp-bian [60] were synthesized according to the standard procedures. All other reagents were of commercial purity (Sigma Aldrich, Buchs, Switzerland) and were used without any purification. Organic solvents (DMF and diethyl ether ((C2H5)2O)) were dried by standard methods before use. Elemental analysis was carried out on a Eurovector EA 3000 CHN analyzer. IR spectrum was recorded in the 4000–300 cm−1 range with a Perkin-Elmer System 2000 FTIR spectrometer (KBr pellets). DR was carried out on a UV–Vis–NIR spectrophotometer UV–3101 PC in an integrating sphere in a range of 240–800 nm (gap width 5 nm) at room temperature.

3.2. Synthesis of (Bu4N)2[{Ag(dpp-bian)}2Mo8O26] (1)

A mixture of (Bu4N)4Mo8O26 (100 mg, 46 mmol) and AgCF3SO3 (23.7 mg 92 mmol) was dissolved in DMF (2 mL). The solution was stirred for 30 min at 60 °C. After the reagents were dissolved, dpp-bian (46.2 mg, 92 mmol) was added. The mixture was stirred for 30 min at room temperature. The resulting orange solid was filtered, washed with diethyl ether, and dried in a vacuum. Yield 102 mg (76%). Crystals of 1, suitable for X-ray diffraction analysis, were obtained by diffusion of diethyl ether onto the reaction solution of 1 in DMF. Anal. Calc. for C110H152N6O26Mo8Ag2: C 43.29; 5.31; N 2.91%. Found: C 43.1, H 5.1, N 2.8% IR (Figure S5, KBr, cm−1): 3452 (m), 3064 (w), 2960 (vs), 2929 (s), 2872 (m), 1869 (w), 1662 (m), 1626 (m), 1587 (m), 1518 (w), 1483 (m), 1464 (m), 1431 (m), 1383 (w), 1362 (w), 1327 (w), 1279 (w), 1254 (w), 1223 (w), 1192 (w), 1150 (w), 1107 (w), 1061 (w), 1045 (w), 943 (vs), 926 (vs), 905 (vs), 839 (s), 808 (w), 795 (w), 781 (m), 756 (m), 727 (m), 704 (s), 656 (m), 573 (w), 556 (w), 523 (m), 480 (w), 465 (w), 448 (w), 413 (m). TGA (Figure S6).

3.3. SCXRD

Single-crystal XRD data for 1 were collected with a Bruker D8 Venture diffractometer (Bruker, Billerica, MA, USA) with a CMOS PHOTON III detector and IµS 3.0 source (Mo Kα radiation, λ = 0.71073 Å, Montel mirror optics, nitrogen flow thermostat). φ- and ω-scan techniques were employed to collect data for crystal structure refinement; full φ-scans were used for investigation of temperature dependence of unit cell parameters in 80–280 K range (increasing of temperature by 5–10 K steps was used). The unit cell parameters were refined using APEX3 Determine Unit Cell routines with the refinement of beam position instrumental parameters and may have similar systematic errors (~0.01 Å, ~0.1°) [61]. Integration and absorption corrections were applied with the use of APEX3 program suite (Bruker APEX3 software suite (APEX3 v.2019.1-0, SADABS v.2016/2, SAINT v.8.40a), Bruker Nonius (2003–2004), Bruker AXS (2005–2018), Bruker Nano (2019): Madison, WI, USA). Structures were solved by SHELXT [62] and refined by full-matrix least-squares treatment against |F|2 in anisotropic approximation with SHELX 2014/7 [63] in the ShelXle program [64]. The main geometrical parameters are present in Table S2. H-atoms were refined in calculated positions. One of TBA+ was disordered over two closed positions with 0.4/0.6 occupancies. C-atoms of such parts were refined isotropically.
The crystallographic data were deposited In the Cambridge Crystallographic Data Centre under the deposition codes, CCDC 2189249.

3.4. Quantum Chemical Calculations

The molecular geometry of the monomer and model dimer was fully optimized using density functional theory (DFT), as well as using the long-range corrected hybrid functional CAM-B3LYP [65] coupled with the Pople 6-311+G** triple-ζ basis set for H, C, N, and O [66,67,68,69,70,71,72,73,74], the LANL2DZ double-ζ basis set on the Mo and Ag valence shell, and the LANL2DZ effective core potential on the core [75,76,77,78]. The vibrational frequencies and thermochemical values were subsequently computed at the same levels of theory, within the harmonic approximation, at T = 298.15 K and p = 1 atm; no imaginary frequencies were found.
The natural bond orbital (NBO) [79,80,81,82,83,84,85], the atoms-in-molecules (AIM) Bader’s theory [86,87,88], and the non-covalent interaction [89,90,91,92] analyses were carried out on the ground state electron densities to investigate the nature of the interactions.
The UV–Vis absorption spectra for the equilibrium geometries were calculated at a time-dependent density functional theory (TD-DFT) level, accounting for S0 → Sn (n = 1 to 120) transitions. The nature of the vertical excited electronic state was analyzed via natural transition orbital (NTO) analysis [93].
The integration grid was set to 250 radial shells and 974 angular points. The convergence criteria for the self-consistent field were set to 10−12 for the RMS change in the density matrix and 10−10 for the maximum change in the density matrix. The convergence criteria for optimizations were set to 2 × 10−6 a.u. for the maximum force, 1 × 10−6 a.u. for the RMS force, 6 × 10−6 a.u. for the maximum displacement, and 4 × 10−6 a.u. for the RMS displacement.
The location of the CPs and subsequent calculation of SF values were performed using a modified version of the PROAIMV program [94]. The NCI analyses were conducted and plotted using homemade code. All the other calculations were performed using the GAUSSIAN G16.A03 package [95].

3.5. Electrochemistry

The CV measurements were carried out in a three-electrode cell with a paste electrode, an auxiliary electrode, and a reference electrode using a potentiostat-galvanostat P-45X (Elins, Chernogolovka, Russia) at 25 °C. The description of the cell and the measurement procedure have been previously reported [96,97,98]. The composition of the paste included carbon powder:EAS:Nafion = 100:10:4 mg (Nafion, 10% aqueous dispersion calculated on dry matter) for the complex 1 and the precursor. Based on the weights of the dry mixture, the concentration of 1 in the paste was ~0.030 and the precursor ~0.070 mol/kg. Initially, the measurements were carried out in the acetonitrile solutions containing 0.10 M Bu4NPF6 (supporting electrolyte). In total, in these experiments, three types of pastes were tested, viz. the pastes contained the complex 1, the precursor, and the blank (without EAS). The blank paste contained only the carbon powder and the Nafion dispersion in the ratio 100:4 mg.
CO2 reduction experiments were performed in an aqueous 1.0 M KHCO3 solution. Based on the weight of the dry mixture, the concentration of 1 in the paste was 0.030 mol/kg. The blank paste contained only the carbon powder and the Nafion dispersion (as in experiments with acetonitrile solutions). First, the electrochemical experiments were carried out in solutions saturated with CO2. Then, the measurements were continued in the same solution, but without its saturation with CO2. Finally, to compare the obtained results, measurements were also carried out on the blank pastes.
Some additional experiments were done with paste electrodes in an aqueous solution of 0.10 M Na2SO4. The composition of the paste was the same as in the previous series. In this case, we tried to find the difference in the CV behavior between the blank paste in solution with the addition of formic acid (0.038 M) and the paste after saturation with CO2.

4. Conclusions

Three components, and five building blocks’ self-assembly, produced a [{Ag(dpp-bian)}2Mo8O26]2− complex which had a non-typical coordination environment for Ag+ cation, wherein Ag had six comparable distances to both O and N donor atoms. There was no remarkable difference between all Ag-N and Ag-O bond lengths; however, the Ag-N bond was revealed to be covalent in nature, whereas Ag-O had a predominant ionic character. Quantum–chemical calculations confirmed the CN of Ag+ cation and indicated the charge-transfer character of the two bands in the UV–Vis absorption spectrum. Solid (Bu4N)2[β-{Ag(dpp-bian)}2Mo8O26] showed rich electrochemistry which involved both organic components and octamolybdate ligands with an electrochemical window of ca. 2.5 V between two quasi-reversible processes in both extremes of the cycling route. The complex also demonstrated a catalytic activity toward electrochemical CO2 reduction. CO2 activation most likely occurs at the Ag-bian redox site.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/molecules27206961/s1, Figure S1. X-ray powder diffraction patterns comparison, Figures S2–S5. CV data for 1, Figure S6. TGA data for 1, Table S1. SCXRD experimental details, Table S2. Selected geometric parameters, Table S3. Shape results, Tables S4–S6. Quantum chemical calculations data for 1.

Author Contributions

V.I.K. and N.F.R.: investigation (synthesis); V.V.K. and A.L.G.: investigation (electrochemistry); P.A.A.: project administration, investigation (SCXRD), writing—original draft; E.B.: investigation (quantum chemical calculations), writing—review and editing; M.N.S.: writing—review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the grant of the President of the Russian Federation for young scientists—Doctors of Sciences MD-396.2021.1.3.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The crystallographic data have been deposited in the Cambridge Crystallographic Data Centre under the deposition codes CCDC 2189249.

Acknowledgments

The authors are grateful to the Siberian Supercomputer Centre of Institute of Computational Mathematics and Mathematical Geophysics (Russian Academy of Sciences, Novosibirsk, Russian Federation) for kindly providing the computational resources. The technical staff of the Institute is also thanked for the assistance. The NIIC team thanks the Ministry of Science and Higher Education of the Russian Federation for an access to XRD facilities. The authors thank Anna Kuznetsova for graphical abstract preparation.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Samples of the compounds are available from the authors.

References

  1. McGlone, T.; Streb, C.; Busquets-Fité, M.; Yan, J.; Gabb, D.; Long, D.-L.L.; Cronin, L. Silver Linked Polyoxometalate Open Frameworks (Ag-POMOFs) for the Directed Fabrication of Silver Nanomaterials. Cryst. Growth Des. 2011, 11, 2471–2478. [Google Scholar] [CrossRef]
  2. McGlone, T.; Streb, C.; Long, D.L.; Cronin, L. Assembly of Pure Silver-Tungsten-Oxide Frameworks from Nanostructured Solution Processable Clusters and Their Evolution into Materials with a Metallic Component. Adv. Mater. 2010, 22, 4275–4279. [Google Scholar] [CrossRef] [PubMed]
  3. Streb, C.; Tsunashima, R.; MacLaren, D.A.; McGlone, T.; Akutagawa, T.; Nakamura, T.; Scandurra, A.; Pignataro, B.; Gadegaard, N.; Cronin, L. Supramolecular Silver Polyoxometalate Architectures Direct the Growth of Composite Semiconducting Nanostructures. Angew. Chem.—Int. Ed. 2009, 48, 6490–6493. [Google Scholar] [CrossRef] [PubMed]
  4. Wilson, E.F.; Abbas, H.; Duncombe, B.J.; Streb, C.; Long, D.-L.; Cronin, L. Probing the Self-Assembly of Inorganic Cluster Architectures in Solution with Cryospray Mass Spectrometry: Growth of Polyoxomolybdate Clusters and Polymers Mediated by Silver(I) Ions. J. Am. Chem. Soc. 2008, 130, 13876–13884. [Google Scholar] [CrossRef]
  5. Abbas, H.; Pickering, A.L.; Long, D.-L.; Kögerler, P.; Cronin, L. Controllable Growth of Chains and Grids from Polyoxomolybdate Building Blocks Linked by Silver(I) Dimers. Chem.—A Eur. J. 2005, 11, 1071–1078. [Google Scholar] [CrossRef]
  6. Wang, X.; Zhao, D.; Tian, A.; Ying, J. Three 3D Silver-Bis(Triazole) Metal–Organic Frameworks Stabilized by High-Connected Wells–Dawson Polyoxometallates. Dalt. Trans. 2014, 43, 5211. [Google Scholar] [CrossRef]
  7. Yang, H.X.; Zhu, W.J.; Jin, L.Y.; Bai, Y.; Dang, D.B. Synthesis, Crystal Structure, and Electrochemical Properties of One Polyoxometalate-Based Silver(I) Compound with Keggin-Type [PW12O40]3− Anions. Russ. J. Coord. Chem. 2018, 44, 466–472. [Google Scholar] [CrossRef]
  8. Hu, T.-P.; Zhao, Y.-Q.; Mei, K.; Lin, S.-J.; Wang, X.-P.; Sun, D. A Novel Silver(I)-Keggin-Polyoxometalate Inorganic–Organic Hybrid: A Lewis Acid Catalyst for Cyanosilylation Reaction. CrystEngComm 2015, 17, 5947–5952. [Google Scholar] [CrossRef]
  9. Xie, A.; Wang, Z.; Cheng, L.-P.; Luo, G.-G.; Liu, Q.-Y.; Sun, D. An Extended Ag I Cluster-Based Framework Solid: Silver-Thiolate Cluster Linked Polyoxometalate Including Ag I ···H-C Anagostic Interactions. Eur. J. Inorg. Chem. 2019, 2019, 496–501. [Google Scholar] [CrossRef]
  10. Wang, Z.; Gupta, R.K.; Luo, G.; Sun, D. Recent Progress in Inorganic Anions Templated Silver Nanoclusters: Synthesis, Structures and Properties. Chem. Rec. 2020, 20, 389–402. [Google Scholar] [CrossRef]
  11. Zhao, X.-L.; Mak, T.C.W. New Polyoxometalate Species Stabilized in Coordination Networks Constructed with the Multinuclear Silver(I) Ethynediide Aggregate C2@Agn (n = 6 and 7). Inorg. Chem. 2010, 49, 3676–3678. [Google Scholar] [CrossRef]
  12. Dang, D.; Zheng, Y.; Bai, Y.; Guo, X.; Ma, P.; Niu, J. Assembly of Polyoxometalate-Based Metal–Organic Frameworks with Silver(I)-Schiff Base Coordination Polymeric Chains as Building Blocks. Cryst. Growth Des. 2012, 12, 3856–3867. [Google Scholar] [CrossRef]
  13. Bai, Y.; Zhang, G.-Q.; Dang, D.-B.; Ma, P.-T.; Gao, H.; Niu, J.-Y. Assembly of Polyoxometalate-Based Inorganic–Organic Compounds from Silver–Schiff Base Building Blocks: Synthesis, Crystal Structures and Luminescent Properties. CrystEngComm 2011, 13, 4181. [Google Scholar] [CrossRef]
  14. Artem’ev, A.V.; Bagryanskaya, I.Y.; Doronina, E.P.; Tolstoy, P.M.; Gushchin, A.L.; Rakhmanova, M.I.; Ivanov, A.Y.; Suturina, A.O. A New Family of Clusters Containing a Silver-Centered Tetracapped [Ag@Ag4(μ3-P)4] Tetrahedron, Inscribed within a N 12 Icosahedron. Dalt. Trans. 2017, 46, 12425–12429. [Google Scholar] [CrossRef] [Green Version]
  15. Artem’ev, A.V.; Ryzhikov, M.R.; Berezin, A.S.; Kolesnikov, I.E.; Samsonenko, D.G.; Bagryanskaya, I.Y. Photoluminescence of Ag(I) Complexes with a Square-Planar Coordination Geometry: The First Observation. Inorg. Chem. Front. 2019, 6, 2855–2864. [Google Scholar] [CrossRef]
  16. Artem’ev, A.V.; Shafikov, M.Z.; Schinabeck, A.; Antonova, O.V.; Berezin, A.S.; Bagryanskaya, I.Y.; Plusnin, P.E.; Yersin, H. Sky-Blue Thermally Activated Delayed Fluorescence (TADF) Based on Ag(I) Complexes: Strong Solvation-Induced Emission Enhancement. Inorg. Chem. Front. 2019, 6, 3168–3176. [Google Scholar] [CrossRef]
  17. Artem’ev, A.V.; Davydova, M.P.; Berezin, A.S.; Samsonenko, D.G. Synthesis and Thermochromic Luminescence of Ag(I) Complexes Based on 4,6-Bis(Diphenylphosphino)-Pyrimidine. Inorganics 2020, 8, 46. [Google Scholar] [CrossRef]
  18. Rogovoy, M.I.; Berezin, A.S.; Samsonenko, D.G.; Artem’ev, A.V. Silver(I)–Organic Frameworks Showing Remarkable Thermo-, Solvato- And Vapochromic Phosphorescence As Well As Reversible Solvent-Driven 3D-to-0D Transformations. Inorg. Chem. 2021, 60, 6680–6687. [Google Scholar] [CrossRef]
  19. Rogovoy, M.I.; Frolova, T.S.; Samsonenko, D.G.; Berezin, A.S.; Bagryanskaya, I.Y.; Nedolya, N.A.; Tarasova, O.A.; Fedin, V.P.; Artem’ev, A.V. 0D to 3D Coordination Assemblies Engineered on Silver(I) Salts and 2-(Alkylsulfanyl)Azine Ligands: Crystal Structures, Dual Luminescence, and Cytotoxic Activity. Eur. J. Inorg. Chem. 2020, 2020, 1635–1644. [Google Scholar] [CrossRef]
  20. Awaleh, M.O.; Badia, A.; Brisse, F.; Bu, X.-H. Synthesis and Characterization of Silver(I) Coordination Networks Bearing Flexible Thioethers: Anion versus Ligand Dominated Structures. Inorg. Chem. 2006, 45, 1560–1574. [Google Scholar] [CrossRef]
  21. Ovsyannikov, A.S.; Ferlay, S.; Solovieva, S.E.; Antipin, I.S.; Konovalov, A.I.; Kyritsakas, N.; Hosseini, M.W. Molecular Tectonics: Silver Coordination Networks Based on Tetramercaptothiacalix[4]Arene in 1,3-Alternate Conformation Bearing Four Nitrile Groups. Russ. Chem. Bull. 2015, 64, 1955–1962. [Google Scholar] [CrossRef]
  22. Azizzadeh, S.; Nobakht, V.; Carlucci, L.; Proserpio, D.M. Self-Assembly of Three Cationic Silver(I) Coordination Networks with Flexible Bis(Pyrazolyl)-Based Linkers. Polyhedron 2017, 130, 58–66. [Google Scholar] [CrossRef]
  23. Wang, J.; Soo, H. Sen; Garcia, F. Synthesis, Properties, and Catalysis of p-Block Complexes Supported by Bis(Arylimino)Acenaphthene Ligands. Commun. Chem. 2020, 3, 113. [Google Scholar] [CrossRef]
  24. Singha Hazari, A.; Ray, R.; Hoque, M.A.; Lahiri, G.K. Electronic Structure and Multicatalytic Features of Redox-Active Bis(Arylimino)Acenaphthene (BIAN)-Derived Ruthenium Complexes. Inorg. Chem. 2016, 55, 8160–8173. [Google Scholar] [CrossRef]
  25. Stoll, T.; Castillo, C.E.; Kayanuma, M.; Sandroni, M.; Daniel, C.; Odobel, F.; Fortage, J.; Collomb, M.-N. Photo-Induced Redox Catalysis for Proton Reduction to Hydrogen with Homogeneous Molecular Systems Using Rhodium-Based Catalysts. Coord. Chem. Rev. 2015, 304–305, 20–37. [Google Scholar] [CrossRef]
  26. Luca, O.R.; Crabtree, R.H. Redox-Active Ligands in Catalysis. Chem. Soc. Rev. 2013, 42, 1440–1459. [Google Scholar] [CrossRef]
  27. Fedushkin, I.L.; Maslova, O.V.; Morozov, A.G.; Dechert, S.; Demeshko, S.; Meyer, F. Genuine Redox Isomerism in a Rare-Earth-Metal Complex. Angew. Chemie—Int. Ed. 2012, 51, 10584–10587. [Google Scholar] [CrossRef]
  28. Fedushkin, I.L.; Skatova, A.A.; Chudakova, V.A.; Fukin, G.K. Four-Step Reduction of Dpp-Bian with Sodium Metal: Crystal Structures of the Sodium Salts of the Mono-, Di-, Tri- and Tetraanions of Dpp-Bian. Angew. Chem.—Int. Ed. 2003, 42, 3294–3298. [Google Scholar] [CrossRef]
  29. Romashev, N.F.; Gushchin, A.L.; Fomenko, I.S.; Abramov, P.A.; Mirzaeva, I.V.; Kompan’kov, N.B.; Kal’nyi, D.B.; Sokolov, M.N. A New Organometallic Rhodium(I) Complex with Dpp-Bian Ligand: Synthesis, Structure and Redox Behaviour. Polyhedron 2019, 173, 114110. [Google Scholar] [CrossRef]
  30. Gushchin, A.L.; Romashev, N.F.; Shmakova, A.A.; Abramov, P.A.; Ryzhikov, M.R.; Fomenko, I.S.; Sokolov, M.N. Novel Redox Active Rhodium(Iii) Complex with Bis(Arylimino)Acenaphthene Ligand: Synthesis, Structure and Electrochemical Studies. Mendeleev Commun. 2020, 30, 81–83. [Google Scholar] [CrossRef]
  31. Fomenko, I.S.; Gushchin, A.L.; Shul’pina, L.S.; Ikonnikov, N.S.; Abramov, P.A.; Romashev, N.F.; Poryvaev, A.S.; Sheveleva, A.M.; Bogomyakov, A.S.; Shmelev, N.Y.; et al. New Oxidovanadium(iv) Complex with a BIAN Ligand: Synthesis, Structure, Redox Properties and Catalytic Activity. New J. Chem. 2018, 42, 16200–16210. [Google Scholar] [CrossRef]
  32. Fomenko, I.S.; Gushchin, A.L. Mono- and Binuclear Complexes of Group 5 Metals with Diimine Ligands: Synthesis, Reactivity and Prospects for Application. Russ. Chem. Rev. 2020, 89, 966–998. [Google Scholar] [CrossRef]
  33. Romashev, N.F.; Abramov, P.A.; Bakaev, I.V.; Fomenko, I.S.; Samsonenko, D.G.; Novikov, A.S.; Tong, K.K.H.; Ahn, D.; Dorovatovskii, P.V.; Zubavichus, Y.V.; et al. Heteroleptic Pd(II) and Pt(II) Complexes with Redox-Active Ligands: Synthesis, Structure, and Multimodal Anticancer Mechanism. Inorg. Chem. 2022, 61, 2105–2118. [Google Scholar] [CrossRef] [PubMed]
  34. Bendix, J.; Clark, K.M. Delocalization and Valence Tautomerism in Vanadium Tris(Iminosemiquinone) Complexes. Angew. Chemie Int. Ed. 2016, 55, 2748–2752. [Google Scholar] [CrossRef]
  35. Abramov, P.A.; Dmitriev, A.A.; Kholin, K.V.; Gritsan, N.P.; Kadirov, M.K.; Gushchin, A.L.; Sokolov, M.N. Mechanistic Study of the [(Dpp-Bian)Re(CO)3Br] Electrochemical Reduction Using in Situ EPR Spectroscopy and Computational Chemistry. Electrochim. Acta 2018, 270, 526–534. [Google Scholar] [CrossRef]
  36. De Frémont, P.; Clavier, H.; Rosa, V.; Avilés, T.; Braunstein, P. Synthesis, Characterization, and Reactivity of Cationic Gold(I) α-Diimine Complexes. Organometallics 2011, 30, 2241–2251. [Google Scholar] [CrossRef]
  37. Adams, C.J.; Fey, N.; Harrison, Z.A.; Sazanovich, I.V.; Towrie, M.; Weinstein, J.A. Photophysical Properties of Platinum(II)−Acetylide Complexes: The Effect of a Strongly Electron-Accepting Diimine Ligand on Excited-State Structure. Inorg. Chem. 2008, 47, 8242–8257. [Google Scholar] [CrossRef]
  38. Lohr, T.L.; Piers, W.E.; Parvez, M. Monomeric Platinum(II) Hydroxides Supported by Sterically Dominant α-Diimine Ligands. Inorg. Chem. 2012, 51, 4900–4902. [Google Scholar] [CrossRef]
  39. Adams, C.J.; Fey, N.; Weinstein, J.A. Near-Infrared Luminescence from Platinum(II) Diimine Compounds. Inorg. Chem. 2006, 45, 6105–6107. [Google Scholar] [CrossRef]
  40. Gray, K.; Page, M.J.; Wagler, J.; Messerle, B.A. Iridium(III) Cp* Complexes for the Efficient Hydroamination of Internal Alkynes. Organometallics 2012, 31, 6270–6277. [Google Scholar] [CrossRef]
  41. Parmene, J.; Krivokapic, A.; Tilset, M. Synthesis, Characterization, and Protonation Reactions of Ar-BIAN and Ar-BICAT Diimine Platinum Diphenyl Complexes. Eur. J. Inorg. Chem. 2010, 2010, 1381–1394. [Google Scholar] [CrossRef]
  42. Rosa, V.; Santos, C.I.M.; Welter, R.; Aullón, G.; Lodeiro, C.; Avilés, T. Comparison of the Structure and Stability of New α-Diimine Complexes of Copper(I) and Silver(I): Density Functional Theory versus Experimental. Inorg. Chem. 2010, 49, 8699–8708. [Google Scholar] [CrossRef]
  43. Fedushkin, I.L.; Skatova, A.A.; Dodonov, V.A.; Chudakova, V.A.; Bazyakina, N.L.; Piskunov, A.V.; Demeshko, S.V.; Fukin, G.K. Digallane with Redox-Active Diimine Ligand: Dualism of Electron-Transfer Reactions. Inorg. Chem. 2014, 53, 5159–5170. [Google Scholar] [CrossRef]
  44. Chen, S.; Huang, Y.; Fang, X.; Li, H.; Zhang, Z.; Hor, T.S.A.; Weng, Z. Aryl-BIAN-Ligated Silver(i) Trifluoromethoxide Complex. Dalt. Trans. 2015, 44, 19682–19686. [Google Scholar] [CrossRef]
  45. Papanikolaou, P.A.; Gdaniec, M.; Wicher, B.; Akrivos, P.D.; Tkachenko, N.V. Bis(Aryl)Acenaphthenequinonediimine Substituent Effect on the Properties and Coordination Environment of Ligands and Their Bis-Chelate Ag I Complexes. Eur. J. Inorg. Chem. 2013, 2013, 5196–5205. [Google Scholar] [CrossRef]
  46. Chupina, A.V.; Shayapov, V.; Novikov, A.S.; Volchek, V.V.; Benassi, E.; Abramov, P.A.; Sokolov, M.N. [{AgL}2Mo8O26]n– Complexes: A Combined Experimental and Theoretical Study. Dalt. Trans. 2020, 49, 1522–1530. [Google Scholar] [CrossRef]
  47. Chupina, A.V.; Mukhacheva, A.A.; Abramov, P.A.; Sokolov, M.N. Complexation and Isomerization of [β-Mo8O26]4− in the Presence of Ag+ and DMF. J. Struct. Chem. 2020, 61, 299–308. [Google Scholar] [CrossRef]
  48. Abramov, P.A.; Komarov, V.Y.; Pischur, D.A.; Sulyaeva, V.S.; Benassi, E.; Sokolov, M.N. Solvatomorphs of (Bu4N)2[{Ag(N2-Py)}2Mo8O26]: Structure, Colouration and Phase Transition. CrystEngComm 2021, 23, 8527–8537. [Google Scholar] [CrossRef]
  49. Guo, H.; Gong, C.; Zeng, X.; Xu, H.; Zeng, Q.; Zhang, J.; Zhong, Z.; Xie, J. Isopolymolybdate-Based Inorganic–Organic Hybrid Compounds Constructed by Multidentate N-Donor Ligands: Syntheses, Structures and Properties. Dalt. Trans. 2019, 48, 5541–5550. [Google Scholar] [CrossRef]
  50. Wang, X.; Liu, D.; Lin, H.; Liu, G.; Wang, X.; Le, M.; Rong, X. PH, Solvent and Metal Ion Induced Octamolybdate-Based Metal–Organic Complexes Decorated with a Pyridyl-Carboxylate Ligand Containing an Amide Group. CrystEngComm 2016, 18, 888–897. [Google Scholar] [CrossRef]
  51. Minakshi, M.; Mitchell, D.R.G.; Munnangi, A.R.; Barlow, A.J.; Fichtner, M. New Insights into the Electrochemistry of Magnesium Molybdate Hierarchical Architectures for High Performance Sodium Devices. Nanoscale 2018, 10, 13277–13288. [Google Scholar] [CrossRef] [Green Version]
  52. Krisch, D.; Sun, H.; Pellumbi, K.; Faust, K.; Apfel, U.-P.; Schöfberger, W. Tuning the Electronic Properties of Homoleptic Silver(I) Bis-BIAN Complexes towards Efficient Electrocatalytic CO2 Reduction. Catalysts 2022, 12, 545. [Google Scholar] [CrossRef]
  53. Zakharchuk, N.F.; Meyer, B.; Henning, H.; Scholz, F.; Jaworksi, A.; Stojek, Z. A Comparative Study of Prussian-Blue-Modified Graphite Paste Electrodes and Solid Graphite Electrodes with Mechanically Immobilized Prussian Blue. J. Electroanal. Chem. 1995, 398, 23–35. [Google Scholar] [CrossRef]
  54. Kinzel, N.W.; Werlé, C.; Leitner, W. Transition Metal Complexes as Catalysts for the Electroconversion of CO2: An Organometallic Perspective. Angew. Chemie Int. Ed. 2021, 60, 11628–11686. [Google Scholar] [CrossRef]
  55. Gonglach, S.; Paul, S.; Haas, M.; Pillwein, F.; Sreejith, S.S.; Barman, S.; De, R.; Müllegger, S.; Gerschel, P.; Apfel, U.-P.; et al. Molecular Cobalt Corrole Complex for the Heterogeneous Electrocatalytic Reduction of Carbon Dioxide. Nat. Commun. 2019, 10, 3864. [Google Scholar] [CrossRef] [Green Version]
  56. De, R.; Gonglach, S.; Paul, S.; Haas, M.; Sreejith, S.S.; Gerschel, P.; Apfel, U.; Vuong, T.H.; Rabeah, J.; Roy, S.; et al. Electrocatalytic Reduction of CO2 to Acetic Acid by a Molecular Manganese Corrole Complex. Angew. Chemie Int. Ed. 2020, 59, 10527–10534. [Google Scholar] [CrossRef]
  57. Kaiser, U.; Heitz, E. Zum Mechanismus Der Elektrochemischen Dimerisierung von CO2 Zu Oxalsäure. Ber. Der Bunsenges. Für Phys. Chem. 1973, 77, 818–823. [Google Scholar] [CrossRef]
  58. König, M.; Vaes, J.; Klemm, E.; Pant, D. Solvents and Supporting Electrolytes in the Electrocatalytic Reduction of CO2. iScience 2019, 19, 135–160. [Google Scholar] [CrossRef]
  59. Costentin, C.; Robert, M.; Savéant, J.-M. Catalysis of the Electrochemical Reduction of Carbon Dioxide. Chem. Soc. Rev. 2013, 42, 2423–2436. [Google Scholar] [CrossRef] [PubMed]
  60. Paulovicova, A.; El-Ayaan, U.; Shibayama, K.; Morita, T.; Fukuda, Y. Mixed-Ligand Copper(II) Complexes with the Rigid Bidentate Bis(N-Arylimino)Acenaphthene Ligand: Synthesis, Spectroscopic-, and X-Ray Structural Characterization. Eur. J. Inorg. Chem. 2001, 2001, 2641–2646. [Google Scholar] [CrossRef]
  61. Serebrennikova, P.C.; Komarov, V.Y.; Sukhikh, A.S.; Gromilov, S.A. On the accuracy of determining unit cell parameters of single crystals on modern laboratory diffractometers. J. Struct. Chem. 2021, 62, 682–691. [Google Scholar] [CrossRef]
  62. Sheldrick, G.M. SHELXT—Integrated Space-Group and Crystal-Structure Determination. Acta Crystallogr. Sect. A Found. Adv. 2015, 71, 3–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Sheldrick, G.M. Crystal Structure Refinement with SHELXL. Acta Crystallogr. Sect. C Struct. Chem. 2015, 71, 3–8. [Google Scholar] [CrossRef] [Green Version]
  64. Hübschle, C.B.; Sheldrick, G.M.; Dittrich, B. ShelXle: A Qt Graphical User Interface for SHELXL. J. Appl. Crystallogr. 2011, 44, 1281–1284. [Google Scholar] [CrossRef] [Green Version]
  65. Yanaia, T.; Tew, D.P.; Handy, N.C. A New Hybrid Exchange–Correlation Functional Using the Coulomb-Attenuating Method (CAM-B3LYP). Chem. Phys. Lett. 2004, 393, 51–57. [Google Scholar] [CrossRef] [Green Version]
  66. Binning, R.C.; Curtiss, L.A. Compact Contracted Basis Sets for Third-Row Atoms: Ga-Kr. J. Comput. Chem. 1990, 11, 1206–1216. [Google Scholar] [CrossRef]
  67. Blaudeau, J.-P.; McGrath, M.P.; Curtiss, L.A.; Radom, L. Extension of Gaussian-2 (G2) Theory to Molecules Containing Third-Row Atoms K and Ca. J. Chem. Phys. 1997, 107, 5016–5021. [Google Scholar] [CrossRef]
  68. McLean, A.D.; Chandler, G.S. Contracted Gaussian Basis Sets for Molecular Calculations. I. Second Row Atoms, Z = 11–18. J. Chem. Phys. 1980, 72, 5639–5648. [Google Scholar] [CrossRef]
  69. Krishnan, R.; Binkley, J.S.; Seeger, R.; Pople, J.A. Self-consistent Molecular Orbital Methods. XX. A Basis Set for Correlated Wave Functions. J. Chem. Phys. 1980, 72, 650–654. [Google Scholar] [CrossRef]
  70. Wachters, A.J.H. Gaussian Basis Set for Molecular Wavefunctions Containing Third-Row Atoms. J. Chem. Phys. 1970, 52, 1033–1036. [Google Scholar] [CrossRef]
  71. Hay, P.J. Gaussian Basis Sets for Molecular Calculations. The Representation of 3d Orbitals in Transition-metal Atoms. J. Chem. Phys. 1977, 66, 4377–4384. [Google Scholar] [CrossRef]
  72. Raghavachari, K.; Trucks, G.W. Highly Correlated Systems. Excitation Energies of First Row Transition Metals Sc–Cu. J. Chem. Phys. 1989, 91, 1062–1065. [Google Scholar] [CrossRef]
  73. McGrath, M.P.; Radom, L. Extension of Gaussian-1 (G1) Theory to Bromine-containing Molecules. J. Chem. Phys. 1991, 94, 511–516. [Google Scholar] [CrossRef]
  74. Curtiss, L.A.; McGrath, M.P.; Blaudeau, J.; Davis, N.E.; Binning, R.C.; Radom, L. Extension of Gaussian-2 Theory to Molecules Containing Third-row Atoms Ga–Kr. J. Chem. Phys. 1995, 103, 6104–6113. [Google Scholar] [CrossRef]
  75. Dunning Jr, T.H.; Hay, P.J. Methods of Electronic Structure Theory. In Modern Theoretical Chemistry; Schaefer, H.F., Ed.; Plenum Publishing Company: New York, NY, USA, 1977; pp. 1–28. [Google Scholar]
  76. Hay, P.J.; Wadt, W.R. Ab Initio Effective Core Potentials for Molecular Calculations. Potentials for the Transition Metal Atoms Sc to Hg. J. Chem. Phys. 1985, 82, 270–283. [Google Scholar] [CrossRef]
  77. Wadt, W.R.; Hay, P.J. Ab Initio Effective Core Potentials for Molecular Calculations. Potentials for Main Group Elements Na to Bi. J. Chem. Phys. 1985, 82, 284–298. [Google Scholar] [CrossRef]
  78. Hay, P.J.; Wadt, W.R. Ab Initio Effective Core Potentials for Molecular Calculations. Potentials for K to Au Including the Outermost Core Orbitals. J. Chem. Phys. 1985, 82, 299–310. [Google Scholar] [CrossRef]
  79. Foster, J.P.; Weinhold, F. Natural Hybrid Orbitals. J. Am. Chem. Soc. 1980, 102, 7211–7218. [Google Scholar] [CrossRef]
  80. Reed, A.E.; Weinhold, F. Natural Bond Orbital Analysis of Near-Hartree–Fock Water Dimer. J. Chem. Phys. 1983, 78, 4066–4073. [Google Scholar] [CrossRef]
  81. Reed, A.E.; Weinstock, R.B.; Weinhold, F. Natural Population Analysis. J. Chem. Phys. 1985, 83, 735–746. [Google Scholar] [CrossRef]
  82. Reed, A.E.; Weinhold, F. Natural Localized Molecular Orbitals. J. Chem. Phys. 1985, 83, 1736–1740. [Google Scholar] [CrossRef]
  83. Carpenter, J.E.; Weinhold, F. Analysis of the Geometry of the Hydroxymethyl Radical by the “Different Hybrids for Different Spins” Natural Bond Orbital Procedure. J. Mol. Struct. THEOCHEM 1988, 169, 41–62. [Google Scholar] [CrossRef]
  84. Reed, A.E.; Curtiss, L.A.; Weinhold, F. Intermolecular Interactions from a Natural Bond Orbital, Donor-Acceptor Viewpoint. Chem. Rev. 1988, 88, 899–926. [Google Scholar] [CrossRef]
  85. Weinhold, F.; Carpenter, J.E. The Natural Bond Orbital Lewis Structure Concept for Molecules, Radicals, and Radical Ions. In The Structure of Small Molecules and Ions; Springer US: Boston, MA, USA, 1988; pp. 227–236. [Google Scholar]
  86. Bader, R.F.W.; Essén, H. The Characterization of Atomic Interactions. J. Chem. Phys. 1984, 80, 1943–1960. [Google Scholar] [CrossRef]
  87. Bader, R.F.W. Atoms in Molecules: A Quantum Theory; Clarendon Press: Oxford, UK, 1990; ISBN 9780198558651. [Google Scholar]
  88. Bader, R.F.W. A Quantum Theory of Molecular Structure and Its Applications. Chem. Rev. 1991, 91, 893–928. [Google Scholar] [CrossRef]
  89. Bohórquez, H.J.; Matta, C.F.; Boyd, R.J. The Localized Electrons Detector as an Ab Initio Representation of Molecular Structures. Int. J. Quantum Chem. 2010, 110, 2418–2425. [Google Scholar] [CrossRef]
  90. Johnson, E.R.; Keinan, S.; Mori-Sánchez, P.; Contreras-García, J.; Cohen, A.J.; Yang, W.; Mori-Sánchez, P.; Contreras-García, J.; Cohen, A.J.; Yang, W. Revealing Noncovalent Interactions. J. Am. Chem. Soc. 2010, 132, 6498–6506. [Google Scholar] [CrossRef] [Green Version]
  91. Boto, R.A.; Contreras-García, J.; Tierny, J.; Piquemal, J.-P. Interpretation of the Reduced Density Gradient. Mol. Phys. 2016, 114, 1406–1414. [Google Scholar] [CrossRef] [Green Version]
  92. Andrés, J.; Berski, S.; Contreras-García, J.; González-Navarrete, P. Following the Molecular Mechanism for the NH3 + LiH → LiNH2 + H2 Chemical Reaction: A Study Based on the Joint Use of the Quantum Theory of Atoms in Molecules (QTAIM) and Noncovalent Interaction (NCI) Index. J. Phys. Chem. A 2014, 118, 1663–1672. [Google Scholar] [CrossRef]
  93. Martin, R.L. Natural Transition Orbitals. J. Chem. Phys. 2003, 118, 4775–4777. [Google Scholar] [CrossRef]
  94. Biegler-könig, F.W.; Bader, R.F.W.; Tang, T.-H. Calculation of the Average Properties of Atoms in Molecules. II. J. Comput. Chem. 1982, 3, 317–328. [Google Scholar] [CrossRef]
  95. Frisch, M.J.; Trucks, G.W.; Schlegel, H.B.; Scuseria, G.E.; Robb, M.A.; Cheeseman, J.R.; Scalmani, G.; Barone, V.; Petersson, G.A.; Nakatsuji, H.; et al. Gaussian 16, Revision C.01; Gaussian, Inc.: Wallingford, CT, USA, 2016. [Google Scholar]
  96. Kokovkin, V.V.; Kal’nyi, D.B.; Korotaev, E.V.; Shakirova, O.G.; Lavrenova, L.G. Electrochemical Studies of Iron(II) Complexeswith 4-amino-1,2,4-triazole Possessing Spin Crossover. Z. Für Anorg. Allg. Chem. 2021, 647, 1620–1624. [Google Scholar] [CrossRef]
  97. Vinnik, D.A.; Kokovkin, V.V.; Volchek, V.V.; Zhivulin, V.E.; Abramov, P.A.; Cherkasova, N.A.; Sun, Z.; Sayyed, M.I.; Tishkevich, D.I.; Trukhanov, A.V. Electrocatalytic Activity of Various Hexagonal Ferrites in OER Process. Mater. Chem. Phys. 2021, 270, 124818. [Google Scholar] [CrossRef]
  98. Mukhacheva, A.A.; Komarov, V.Y.; Kokovkin, V.V.; Novikov, A.S.; Abramov, P.A.; Sokolov, M.N. Unusual π–π Interactions Directed by the [{(C6H6)Ru}2W8O30(OH)2]6− Hybrid Anion. CrystEngComm 2021, 23, 4125–4135. [Google Scholar] [CrossRef]
Molecules 27 06961 g001 550
Figure 1. The structure of [β-{Ag(dpp-bian)}2Mo8O26]2−.
Figure 1. The structure of [β-{Ag(dpp-bian)}2Mo8O26]2−.
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Molecules 27 06961 g002 550
Figure 2. The coordination environment of Ag+ in the crystal structure of 1.
Figure 2. The coordination environment of Ag+ in the crystal structure of 1.
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Molecules 27 06961 g003 550
Figure 3. The coordination polyhedron of Ag+. O-atoms are red, N-atoms are blue.
Figure 3. The coordination polyhedron of Ag+. O-atoms are red, N-atoms are blue.
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Molecules 27 06961 g004 550
Figure 4. Plots of the isosurfaces of non-covalent interaction index mapped over the reduced density gradient (s = 1/2). Legend of colors: −0.012 a.u. (red; repulsion) to +0.012 a.u. (blue; attraction). Ag-O and Ag-N attractive NCIs are pointed out by red and blue arrows, respectively. The calculations were conducted on the optimized geometry.
Figure 4. Plots of the isosurfaces of non-covalent interaction index mapped over the reduced density gradient (s = 1/2). Legend of colors: −0.012 a.u. (red; repulsion) to +0.012 a.u. (blue; attraction). Ag-O and Ag-N attractive NCIs are pointed out by red and blue arrows, respectively. The calculations were conducted on the optimized geometry.
Molecules 27 06961 g004
Molecules 27 06961 g005 550
Figure 5. (a) Experimental (black line) and computed UV–Vis absorption spectra (red line) of complex 1 in the wavelengths’ region from 250 to 700 nm. No scale factor applied. (b) Natural transition orbital (NTO) analysis of the main transitions corresponding to the two electronic bands; two perspectives are depicted for each transition. Calculations were performed on the optimized geometry.
Figure 5. (a) Experimental (black line) and computed UV–Vis absorption spectra (red line) of complex 1 in the wavelengths’ region from 250 to 700 nm. No scale factor applied. (b) Natural transition orbital (NTO) analysis of the main transitions corresponding to the two electronic bands; two perspectives are depicted for each transition. Calculations were performed on the optimized geometry.
Molecules 27 06961 g005
Molecules 27 06961 g006 550
Figure 6. Cyclic voltammogram (second cycle) of 1 (black curve) and a (Bu4N)4[Mo8O26] (red curve) in a paste electrode in acetonitrile with supporting electrolyte (0.10 M Bu4NPF6) at a sweep rate of 20 mV/s. Potentials vs. saturated Ag/AgCl reference electrode.
Figure 6. Cyclic voltammogram (second cycle) of 1 (black curve) and a (Bu4N)4[Mo8O26] (red curve) in a paste electrode in acetonitrile with supporting electrolyte (0.10 M Bu4NPF6) at a sweep rate of 20 mV/s. Potentials vs. saturated Ag/AgCl reference electrode.
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Molecules 27 06961 g007 550
Figure 7. CVs (four consecutive cycles) for the paste electrode including carbon powder, 1, and Nafion 10% aqueous dispersion in the ratio of 100:10:4 (the last component calculated as the dry mixture). The measurements were made at 10 mV/s scan rate in CO2-saturated 1.0 M KHCO3. Black arrows indicate the sequence of cycles, and red ones—the starting point and direction of CV starting potential. Potentials vs. saturated Ag/AgCl reference electrode.
Figure 7. CVs (four consecutive cycles) for the paste electrode including carbon powder, 1, and Nafion 10% aqueous dispersion in the ratio of 100:10:4 (the last component calculated as the dry mixture). The measurements were made at 10 mV/s scan rate in CO2-saturated 1.0 M KHCO3. Black arrows indicate the sequence of cycles, and red ones—the starting point and direction of CV starting potential. Potentials vs. saturated Ag/AgCl reference electrode.
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Molecules 27 06961 g008 550
Figure 8. CVs (second cycle) for the following pastes: red curve—blank in the CO2 saturated solution (without electroactive compound); blue—containing 1; and gray—containing 1 in the CO2 saturated solution; 1.0 M KHCO3 aqueous solutions at 10 mV/s scan rate. Potentials vs. saturated Ag/AgCl reference electrode.
Figure 8. CVs (second cycle) for the following pastes: red curve—blank in the CO2 saturated solution (without electroactive compound); blue—containing 1; and gray—containing 1 in the CO2 saturated solution; 1.0 M KHCO3 aqueous solutions at 10 mV/s scan rate. Potentials vs. saturated Ag/AgCl reference electrode.
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Molecules 27 06961 g009 550
Figure 9. The spin density distribution on [{Ag(dpp-bian)}2Mo8O26]3•− anion.
Figure 9. The spin density distribution on [{Ag(dpp-bian)}2Mo8O26]3•− anion.
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Molecules 27 06961 g010 550
Figure 10. The CV data (first five cycles) for 0.0373 M HCOOH in 0.1 M Na2SO4 aqueous solution (blue curves); CV data (first five cycles) for the paste electrode containing 1 after CO2 exposure into the 0.1 M Na2SO4 aqueous solution (orange curves). Potentials vs. saturated Ag/AgCl reference electrode. Scan rate 10 mV/s.
Figure 10. The CV data (first five cycles) for 0.0373 M HCOOH in 0.1 M Na2SO4 aqueous solution (blue curves); CV data (first five cycles) for the paste electrode containing 1 after CO2 exposure into the 0.1 M Na2SO4 aqueous solution (orange curves). Potentials vs. saturated Ag/AgCl reference electrode. Scan rate 10 mV/s.
Molecules 27 06961 g010
Table
Table 1. The analysis of CCDC data for Ag complexes with two N and four O-atoms in the coordination sphere.
Table 1. The analysis of CCDC data for Ag complexes with two N and four O-atoms in the coordination sphere.
REFCODEd(Ag-N)/Åd(Ag-O)/ÅCN
Group 1—Fixed Geometry Ligands
FOWWIA2.316, 2.3552.532–2.6416
GIFRIZ2.3622.502–2.6536
HATSAZ2.4702.420, 2.4786
IXEFAU2.3252.491–2.5736
IXEFEY2.3262.478. 2.6136
QOMQER2.3242.558, 2.6176
VAZDEF2.3152.522, 2.5886
Group 2—Crown-Ethers and Cryptands
FAFQUY2.4832.9234
GOXTAO2.275, 2.3042.681–2.7452
KISPUZ2.4372.558–2.7484
PIMCET2.219, 2.2352.736, 2.8502
QIFPEA2.323, 2.3422.564–2.741 3
QIFPIE2.3922.562–2.7373
ROQLOY2.3722.8342
SENJIE2.208, 2.7212.498–2.5575
TIBQIE2.585, 2.6942.478–2.6265
YUHDIO2.346, 2.3952.608–2.6844
Group 3—POM Complexes
PUCYES2.262, 2.3492.463, 2.606, 2.6783
ODEQOE2.3892.564–2.6326
XUJSAX2.270, 2.3602.385–2.8603
ZULXOV (Ag2)2.340, 2.3592.530–2.6436
Group 4—Other Complexes
PICVII2.303, 2.3202.529–2.8646
PURZUY2.232, 2.2832.547–2.7773
CAVWAY2.2492.6574
FEJFEF2.273, 2.3012.517–2.5745
HAXFOB2.3582.580–2.6196
KIJRIG2.4002.456–2.6336
LADFED2.338, 23402.291–2.7366
MEJBAE2.2702.548–2.5716
MIZAGN2.3722.600–2.6286
NAKLOB2.3822.605–2.6196
NELMAT2.4152.446–2.7904
RAWVER2.3322.609–2.6256
YIXDAM2.4022.508–2.5586
Group 5—Questionable Structures
ZULXOV (Ag1)1.960–2.0972.586, 2.3116
WOKRIY (3d)2.176, 2.1812.867, 2.9314
SIKJIH (3d)2.141, 2.1802.150, 2.1086
ELEGIM (Ln)2.440, 2.5442.470–2.5699
PYRCAG (3d)2.086, 2.2102.203–2.5426
SEHSAA (Ag2)2.1593.010–3.0742
SEHSAA (Ag1)2.1612.868–3.1782
Table
Table 2. Characteristics of half-wave potentials, as well as anodic and cathodic current peaks of the complex (Bu4N)2[β-{Ag(dpp-bian)}2Mo8O26]. Potentials vs. saturated Ag/AgCl reference electrode.
Table 2. Characteristics of half-wave potentials, as well as anodic and cathodic current peaks of the complex (Bu4N)2[β-{Ag(dpp-bian)}2Mo8O26]. Potentials vs. saturated Ag/AgCl reference electrode.
E1/2 (1,1′), V−1.585ΔE, V0.400quasi-reversible
Ea, V−1.390Ia, A−1.7 × 10−5
Ec, V−1.790Ic, A−2.1 × 10−3
E1/2 (2,2′), V−1.200ΔE, V0.400quasi-reversible
Ea, V−1.000Ia, A3.4 × 10−4
Ec, V−1.400Ic, A−1.8 × 10−3
E1/2 (3,3′), V ΔE, V irreversible
Ea, V−0.670Ia, A5.9 × 10−4
Ec, V Ic, A
E1/2 (4,4′), V−0.390ΔE, V0.520quasi-reversible
Ea, V−0.130Ia, A1.0 × 10−3
Ec, V−0.650Ic, A−1.8 × 10−3
E1/2 (5,5′), V ΔE, V irreversible
Ea, V0.090Ia, A1.0 × 10−3
Ec, V Ic, A
E1/2 (6,6′), V0.290ΔE, V0.780quasi-reversible
Ea, V0.680Ia, A1.6 × 10−3
Ec, V−0.100Ic, A−1.4 × 10−3
E1/2 (7,7′), V0.850ΔE, V0.640quasi-reversible
Ea, V1.170Ia, A1.7 × 10−3
Ec, V0.530Ic, A6.1 × 10−4
E1/2 (8,8′), V ΔE, V irreversible
Ea, V1.650Ia, A2.0 × 10−3
Ec, V Ic, A
a anodic; c cathodic
Table
Table 3. Characteristics of half-wave potentials, as well as anodic and cathodic current peaks of the (Bu4N)4[Mo8O26] precursor.
Table 3. Characteristics of half-wave potentials, as well as anodic and cathodic current peaks of the (Bu4N)4[Mo8O26] precursor.
E1/2 (1,1′), V ΔE, V irreversible
Ea, V Ia, A
Ec, V−2.050Ic, A−1.9 × 10−3
E1/2 (2,2′), V ΔE, V irreversible
Ea, V Ia, A
Ec, V−1.62Ic, A−1.8 × 10−3
E1/2 (3,3′), V−1.085ΔE, V0.670quasi-reversible
Ea, V−0.750Ia, A5.1 × 10−4
Ec, V−1.420Ic, A−1.8 × 10−3
E1/2 (4,4′), V−0.218ΔE, V0.785quasi-reversible
Ea, V0.175Ia, A1.1 × 10−3
Ec, V−0.610Ic, A−1.2 × 10−3
E1/2 (5,5′), V ΔE, V irreversible
Ea, V0.430Ia, A1.3 × 10−3
Ec, V Ic, A
E1/2 (6,6′), V ΔE, V irreversible
Ea, V1.140Ia, A1.45 × 10−3
Ec, V Ic, A
a anodic; c cathodic
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Komlyagina, V.I.; Romashev, N.F.; Kokovkin, V.V.; Gushchin, A.L.; Benassi, E.; Sokolov, M.N.; Abramov, P.A. Trapping of Ag+ into a Perfect Six-Coordinated Environment: Structural Analysis, Quantum Chemical Calculations and Electrochemistry. Molecules 2022, 27, 6961. https://doi.org/10.3390/molecules27206961

AMA Style

Komlyagina VI, Romashev NF, Kokovkin VV, Gushchin AL, Benassi E, Sokolov MN, Abramov PA. Trapping of Ag+ into a Perfect Six-Coordinated Environment: Structural Analysis, Quantum Chemical Calculations and Electrochemistry. Molecules. 2022; 27(20):6961. https://doi.org/10.3390/molecules27206961

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Komlyagina, Veronika I., Nikolay F. Romashev, Vasily V. Kokovkin, Artem L. Gushchin, Enrico Benassi, Maxim N. Sokolov, and Pavel A. Abramov. 2022. "Trapping of Ag+ into a Perfect Six-Coordinated Environment: Structural Analysis, Quantum Chemical Calculations and Electrochemistry" Molecules 27, no. 20: 6961. https://doi.org/10.3390/molecules27206961

APA Style

Komlyagina, V. I., Romashev, N. F., Kokovkin, V. V., Gushchin, A. L., Benassi, E., Sokolov, M. N., & Abramov, P. A. (2022). Trapping of Ag+ into a Perfect Six-Coordinated Environment: Structural Analysis, Quantum Chemical Calculations and Electrochemistry. Molecules, 27(20), 6961. https://doi.org/10.3390/molecules27206961

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