Next Article in Journal
Recent Progress in Conjugated Polymers-Based Donor–Acceptor Semiconductor Materials for Photocatalytic Hydrogen Evolution from Water Splitting
Next Article in Special Issue
An Asymmetric Dinuclear Bis(ansa-Zirconocene) Complex: Synthesis and Performance in Olefin (co-)Polymerization
Previous Article in Journal
The Effect of Different g-C3N4 Precursor Nature on Its Structural Control and Photocatalytic Degradation Activity
Previous Article in Special Issue
Divergent Reactivity of D-A Cyclopropanes under PTC Conditions, Ring-Opening vs. Decyanation Reaction
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Catalysts
Volume 13
Issue 5
10.3390/catal13050849
catalysts-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Novel Copper(II) Complexes with BIAN Ligands: Synthesis, Structure and Catalytic Properties of the Oxidation of Isopropylbenzene

by
Iakov S. Fomenko
1,
Olga S. Koshcheeva
1,
Nina I. Kuznetsova
2,
Tatyana V. Larina
2,
Marko I. Gongola
3,
Medhanie Afewerki
3,
Pavel A. Abramov
1,
Alexander S. Novikov
4,5 and
Artem L. Gushchin
1,*
1
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of Russian Academy of Sciences, 3 Acad. Lavrentiev Ave., Novosibirsk 630090, Russia
2
Federal Research Center Boreskov Institute of Catalysis, 5 Acad. Lavrentiev Ave., Novosibirsk 630090, Russia
3
Novosibirsk State University, 1 Pirogova Str., Novosibirsk 630090, Russia
4
Saint Petersburg State University, Universitetskaya Nab. 7/9, Saint Petersburg 199034, Russia
5
Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya Street 6, Moscow 117198, Russia
*
Author to whom correspondence should be addressed.
Catalysts 2023, 13(5), 849; https://doi.org/10.3390/catal13050849
Submission received: 18 April 2023 / Revised: 4 May 2023 / Accepted: 4 May 2023 / Published: 8 May 2023
(This article belongs to the Special Issue Feature Papers in Catalysis in Organic and Polymer Chemistry)
Browse Figures
Review Reports Versions Notes

Abstract

:
Two new isomeric complexes [CuBr2(R-bian)] (R = 4-Me-Ph (1), 2-Me-Ph (2)) were obtained by reacting copper(II) bromide with 1,2-bis[(2-methylphenyl)imino]acenaphthene ligands and characterized. The crystal structure of 2 was determined by X-ray diffraction analysis. The copper atom has a distorted square-planar environment; the ω angle between the CuN2 and CuBr2 planes is 37.004°. The calculated ω parameters for optimized structures 1 and 2 were 76.002° and 43.949°, indicating significant deviations from the ideal tetrahedral and square-plane geometries, respectively. Molecules 2 form dimers due to non-covalent Cu···Br contacts, which were analyzed by DFT calculations. The complexes were also characterized by cyclic voltammetry and UV-Vis spectroscopy. A quasi-reversible Cu(II)/Cu(I) redox event with E1/2 potentials of 0.81 and 0.66 V (vs. SHE) was found for 1 and 2, respectively. The electronic absorption spectra showed the presence of Cu(I) species as a result of the partial reduction of the complexes in the acetonitrile solution. Both complexes were tested as homogenous catalysts for the oxidation of isopropylbenzene (IPB) in acetonitrile at low temperatures. Differences in the mechanism of the catalytic reaction and the composition of the reaction products depending on the oxidizing ability of the catalyst were revealed.

1. Introduction

Bis(imino)-acenaphthenes (BIANs) belong to the class of α-diimines, which combine 1,4-diazabutadiene and naphthalene fragments [1,2,3]. Due to this combination, BIANs have strong σ-donor and π-acceptor properties, providing stabilization of both high and low oxidation states of the metal upon coordination. BIANs form complexes with almost all main group elements [4,5,6,7,8] and transition metals [9,10,11,12,13,14,15,16,17,18,19,20]. The key feature of BIANs is their pronounced redox activity [21,22,23,24,25], and this property is widely exploited by scientists to implement various catalytic transformations [1]. Historically, the first BIAN-based catalysts were Brookhart’s catalysts for the polymerization of olefins [9,26]. The various stereoelectronic properties of BIAN ligands, including their oxidation states, allowed for the modulation of catalyst properties, polyethylene branching, and polymer microstructure [27,28,29].
Much less attention has been paid to the study of other catalytic processes involving metal/BIAN complexes. The most striking examples are reduction processes. These are hydrogenation [12,30,31,32,33,34,35,36,37,38,39,40,41], reduction of nitroarenes [42,43,44,45,46,47,48,49,50], and hydroamination [7,51,52,53,54,55]. Examples of oxidative transformations catalyzed by metal/BIAN complexes are even rarer, possibly due to the electron-withdrawing properties of ligands [56,57,58,59]. In particular, V(IV) complexes [VO(acac)(R-bian)]Cl efficiently catalyze the epoxidation of terminal and internal olefins with tert-butyl hydroperoxide or hydrogen peroxide [56], while the related complexes [VOCl2(R-bian)] provide easy CH-oxidation of alkanes with hydrogen peroxide [57,60].
It should be noted that the oxidation reactions catalyzed by BIAN complexes are limited to only one metal, vanadium. Similarly to vanadium(IV), copper(II) is capable of activating peroxides in hydrocarbon oxidation reactions. Indeed, copper(II) complexes with various nitrogen-donor ligands are effective catalysts in the processes of activation (oxygenation) of C-H bonds in saturated hydrocarbons and other organic compounds [61,62,63,64,65,66,67]. For example, one of the latest works reported on the high catalytic activity of Cu(II) complexes with N-donor dipinodiazafluorenes in the oxidation of alkanes and alcohols by peroxides [68]. At the same time, there are no data in the literature on the reactivity of copper(II) complexes with BIAN-type ligands in radical chain oxidations. It is only known that complexes of the [CuCl2(R-bian)] type (R = tmp, dpp) catalyze the radical polymerization of styrene in the presence of 2,2′-azobisisobutyronitrile as a free radical initiator [69].
In this work, we synthesized two new copper(II) complexes with redox-active BIAN ligands [CuBr2(R-bian)] (R = 4-Me-Ph (1), 2-Me-Ph (2)) and studied their structures, electrochemical properties, and reactivity in the oxidation of isopropylbenzene with oxygen. To the best of our knowledge, these are the first examples of the oxygenation of the C-H bond catalyzed by copper-BIAN complexes.

2. Results and Discussion

Synthesis. Complexes [CuBr2(4-Me-Ph-bian)] (1) and [CuBr2(2-Me-Ph-bian)] (2) were obtained in high yield by similar procedures by reacting copper(II) bromide with the appropriate BIAN ligand in acetonitrile under reflux conditions (Scheme 1). Earlier works reported the preparation of related complexes [CuCl2(R-bian)] (R = tmp, dpp) [69]. Copper complexes with Me-Ph-bians have not been previously described. Complexes 1 and 2 are structural isomers with respect to each other and differ in the position of the methyl group in the aryl ring of the bian. They have different solubilities. Complex 2 is highly soluble in both dichloromethane and acetonitrile, while complex 1 is less soluble in these solvents.
The IR spectra of both complexes are very similar. IR spectra of 1 and 2 show typical vibration bands of the CH group in the region of 3046–2863 cm−1 (for 1) and 3056–2857 cm−1 (for 2), as well as ν(C-C) and ν(C-N) bands in the 1624–1044 cm−1 (for 1) and 1634–1049 cm−1 (for 2) range.
Crystal structure. Single crystals of [CuBr2(2-Me-Ph-bian)] (2) suitable for X-ray diffraction were obtained by layering hexane on a solution of 2 in dichloromethane (Table S1 in the Supplementary Materials). Unfortunately, our attempts to crystallize complex 1 were unsuccessful. The molecular structure of 2 is shown in Figure 1. The coordination environment around copper(II) center is a distorted square-planar, which is defined by two N and two Br atoms. The ω angle between the CuN2 and CuBr2 planes is 37.004°, where ω = 0° for a perfect square-planar coordination, whereas for a tetrahedral one, ω = 90° [69]. Thus, the geometry of the coordination node for 2 should be considered distorted square-planar. A high degree of distortion is confirmed by DFT calculations (see below). On the contrary, less distorted structures were found for related complexes: [CuCl2(tmp-bian)] (ω = 23.67°) and [CuCl2(dpp-bian)] (ω = 1.54°) [69]. The aryl substituents are not co-directed relative to each other, forming a dihedral angle between the planes of the phenyl rings equal to 30.040(5)°. The bond lengths of the C = N and C-C are 1.2803(2) and 1.5015(2) Å indicating the neutral state of the 2-Me-C6H4-bian. The 2-Me-C6H4-bian ligand is coordinated symmetrically, the Cu-N bond lengths are 2.026(2) and 2.039(3) Å. In the [CuCl2(tmp-bian)] and [CuCl2(dpp-bian)] complexes, these distances are 2.048 and 2.051 Å, respectively [69]. The Cu-Br bond lengths in 2 are slightly different (2.3517(6) and 2.3385(6)Å). Cu-Br distances are in the range of 2.354–2.391 Å in Cu(II) complexes with dipinodiazafluorenes [68].
An interesting feature of crystal packing 2 is the formation of weakly bounded dimers (Figure 2) with intermolecular contacts Cu···Br at 3.666 Å. These interactions were analyzed by DFT calculations (see below).These dimers are connected into infinite supramolecular chains via π–π interactions (Figure S1 in the Supplementary Materials). The chains are directed in the [100] crystal direction (Figure S2 in the Supplementary Materials).
DFT calculations. The lack of experimental X-ray structural data for complex 1 prompted us to perform DFT calculations and a full geometry optimization procedure for model structures 1 and 2 in order to compare the geometry of the coordination environment around copper(II) at least in idealized model systems and calculate the corresponding ω parameters. Results of our DFT calculations reveal that ω angles between the CuN2 and CuBr2 planes in optimized equilibrium model structures 1 and 2 are 76.002° and 43.949°, respectively. Thus, the optimized equilibrium model structure of 1 could be considered distorted tetrahedral, whereas the optimized equilibrium model structure of 2 is distorted square-planar and close to the experimental X-ray structure (ω = 37.004°). In both cases, the geometry of the coordination CuBr2N2 node is far from ideal (tetrahedral or square-planar), and a strong distortion typical of Cu(II) takes place.
Inspection of the crystallographic data revealed the presence of interesting intermolecular noncovalent interactions Cu···Br (3.666 Å) in the X-ray structure 2. In order to confirm or disprove the hypothesis on the existence of these intermolecular noncovalent interactions in the solid state and approximately quantify their strength from a theoretical viewpoint, the DFT calculations followed by the topological analysis of the electron density distribution were carried out at the ωB97XD/DZP-DKH level of theory for model supramolecular associates (see Computational details and Tables S2 and S3 in the Supplementary Materials). Results of topological analysis of the electron density distribution are summarized in Table 1 (the Poincare–Hopf relationship was satisfied), the contour line diagram of the Laplacian of electron density distribution ∇2ρ(r), bond paths, and selected zero-flux surfaces, visualization of electron localization function (ELF), and reduced density gradient (RDG) analyses for intermolecular noncovalent interactions Cu···Br in 2 are shown in Figure 3.
The topological analysis of the electron density distribution in the model supramolecular associate demonstrates the presence of bond critical point (3, −1) for Cu···Br interactions (Table 1). The low magnitude of the electron density (0.006 a.u.), positive value of the Laplacian of electron density (0.018 a.u.), and zero energy density in this bond critical point (3, −1) are typical for such weak contacts in similar chemical systems [71,72,73,74,75,76,77,78]. The balance between the Lagrangian kinetic energy G(r) and potential energy density V(r) at the bond critical point (3, −1) (viz. –G(r)/V(r) ≥ 1) indicates the absence of covalent contribution in these weak contacts [79]. The Laplacian of electron density is typically decomposed into the sum of contributions along the three principal axes of maximal variation, giving the three eigenvalues of the Hessian matrix (λ1, λ2 and λ3), and the sign of λ2 can be utilized to distinguish bonding (attractive, λ2 < 0) weak interactions from non-bonding ones (repulsive, λ2 > 0) [80,81]. Thus, intermolecular noncovalent Cu···Br interactions are attractive.
UV-Vis spectra. The diffuse reflectance spectra (converted to absorption spectra) of solid samples are characterized by broad bands in the high and low energy regions. (Figure S3). In the high energy region of the spectrum of 1, there is a band at 315 nm as well as a broad band in the range of 370–550 nm (the edge of this band extends to 680 nm). A poorly resolved wide band in the range of 720–850 nm was found in the low energy region. The spectrum of 2 demonstrates a slightly different pattern. Similar to complex 1, there is a band at 315 nm and a shoulder at 418 nm. An almost linear increase in absorption with a maximum at 700 nm was detected in the region of 450–700 nm. The high-energy bands in both spectra can be attributed to the π–π* and n–π* transitions of the BIAN ligand. The low energy bands correspond to d-d transitions of the Cu(II) ion (3d9). The hypsochromic shift of the d-d band found for 2 reflects the different coordination environment of the Cu(II) center in the structures (see above).
The UV-Vis spectra of 1 and 2 in acetonitrile solution (Figure S4) show similar absorption bands in the low and high energy regions as for solid samples. Differences appear in the visible region and are associated with the appearance of absorption in the range of 500–700 nm for both complexes. This absorption is especially pronounced for complex 1 with a maximum at 630 nm. We assume that the appearance of a new band is associated with the formation of the Cu(I) species due to the partial reduction of Cu(II). Absorption in this region is most likely associated with MLCT transitions, which are characteristic of Cu(I) complexes [19,82,83,84,85]. Apparently, complex 1 is involved in this redox transformation to a greater extent than 2. This is consistent with electrochemical data, according to which complex 1 is a stronger oxidizing agent than complex 2 (see below).
Cyclic voltammetry (CV). In order to determine the redox potential of the Cu(II)/Cu(I) couple, cyclic voltammograms of 1 and 2 in acetonitrile were recorded (Figure S5). A quasi-reversible Cu(II)/Cu(I) redox process centered at E1/2 = 0.62 (ΔE = 96 mV) and 0.47 V (ΔE = 137 mV) (vs. Ag/AgCl) or 0.81 and 0.66 V (vs. SHE) was found for 1 and 2, respectively. An irreversible reduction at 0.49 V and 0.44 V (vs. SHE) was previously reported for the related complexes [CuCl2(tmp-bian)] and [CuCl2(dpp-bian)], respectively [69]. The authors attribute the irreversibility of this process to the instability of the reduction product in terms of Cl− elimination. In our case, the reduction is quasi-reversible, which indicates a higher stability of the reduced Cu(I) species. Note that the Cu(II)/Cu(I) potential for 1 is noticeably shifted to a more positive region compared to 2, which indicates a higher oxidizing ability of Cu(II) in 1.
Catalytic studies. Both complexes 1 and 2 were tested as homogeneous catalysts for the oxidation of IPB with oxygen at low temperatures (30–50 °C). Oxygen uptake for 1 and 2 began without an induction period (Figure 4), although its presence is typical of many aerobic hydrocarbon oxidations. In solution 1, a stationary oxygen uptake was established immediately, while in solution 2, the initial intense uptake gradually slowed down to a stationary value. The steady-state rate of the reaction increased with an increase in the temperature of the experiment (inset in Figure 4). For comparison, oxygen consumption by solutions of 4-Me-Ph-bian (L1) or 2-Me-Ph-bian (L2) developed slowly and differed little from that of the control experiment in the absence of any catalyst (Figure 4, curves L1 and L2). In contrast to complexes 1 and 2, the CuBr2-catalyzed oxidation of IPB at 30 °C began after an induction period (Figure S6A) associated with the slow reduction of Cu(II) to Cu(I) [86]. The harder-to-reduce CuCl2 exhibited a long induction period at 30 °C and higher temperatures (Figure S6B).
The catalysis of the aerobic oxidation of hydrocarbons by transition metal compounds is based on the initiation of radical chains. In our case, the oxidation of IPB in acetonitrile solutions of 1 and 2 is initiated by the decomposition of isopropylbenzene hydroperoxide (IPBHP) due to the Cu(II)/Cu(I) redox couple with the formation of radicals RO• and ROO• (Equations (1) and (2)). The Cu(II)/Cu(I) redox process seems to be facilitated by the presence of the redox-active BIAN ligand, which ensures the reversibility of this process and a rather high oxidizing ability of Cu(II) in 1 and 2 (see CV part). This favors Equations (1) and (2). The initial rate of oxygen consumption by solution of 2 was slightly higher than by 1. (Figure 4). It decreases with time to a stationary value. IPBHP is contained in a small amount in the initial reaction solution (0.03 mol.%) and accumulates during cycling (Equations (3)–(5)). Termination of the radical chains is usually regarded as bimolecular interactions or self-termination [87]. During the stationary reaction, the rates are close in magnitude for 1 and 2, with some advantage for 1, which is especially noticeable at higher temperatures.
Cu(I) + ROOH = Cu(II) + RO• + OH-
Cu(II) + ROOH = Cu(I) + ROO• + H+
RO• + RH = R• + ROH
ROO• + RH = R• + ROOH
R˙• + O2 = ROO•
The UV-Vis spectra show the redox transformations of the complexes during catalysis. The spectrum of the initial solution of 2 in acetonitrile (Figure 5B, black line) does not change after the addition of IPB at room temperature, while significant changes occur during the oxidation of IPB under catalytic conditions (Figure 5B, red line). The absorption in the region of the MLCT transitions of Cu(I) (approx. 530 nm) decreases. On the contrary, the absorption in the region of the d–d transitions of Cu(II) (approx. 680 nm) increases. In contrast to 2, the spectrum of the initial solution of 1 (Figure 5A, black line) changes after the addition of IPB at room temperature (Figure 5A, green line). The decrease in Cu(II) absorption at approx. 800 nm is accompanied by the appearance of an intense Cu(I) absorption band at 605 nm. Under catalytic conditions, absorption in the region of MLCT transitions of Cu(I) (Figure 5A, red line) is retained.
A similar trend was observed in the spectra of solutions 1 and 2 after the addition of IPBHP (Figure S7). The content of Cu(II) increases in solution 2 (Figure S7B) and decreases in solution 1 (Figure S7A). This is in line with the higher oxidizing ability of complex 1. Thus, complexes 1 and 2 demonstrate a facile change in the oxidation state at the copper center during reactions both with IPB and IPBHP, wherein both procedures gave spectrally identical results.
According to the radical chain mechanism (Equations (1)–(5)), the oxidation of IPB should give mostly IPBHP and less 1-phenyl-1-propanol (PP). However, GC analysis together with iodometric titration of solutions 1 and 2 after catalysis revealed the formation of IPBHP, PP, as well as acetophenone (AP) and alpha-methylstyrene (AMS) (Scheme 2 and Table 2).
(*) The conditions are given in the caption to Figure 4. (**) Admixture of AMS appeared from dehydration of PP in the GC column.
The selectivity for IPBHP turned out to be quite low even at 30 °C, and it further decreased as the oxidation temperature increased to 40 and 50 °C (Table 2). While the Cu(II)/Cu(I) redox couples initiate the formation of IPBHP (Equations (1)–(5)), the Cu(II) complexes catalyze the subsequent conversion of IPBHP. It has been confirmed that IPBHP reacts with 1 and 2 in CH3CN solutions to form PP and AP at 30 °C (Table S4). The same products were previously obtained by decomposition of Cu(II)-IPB peroxo complexes or by decomposition of IPBHP catalyzed by Cu(II) complexes [88,89,90]. It seems reasonable to suggest the catalyzed by 1 and 2 decomposition of IPBHP follows the same mechanism (Equations (6)–(9)).
Cu(II) + ROOH = CuII-OH• + RO•
RO• + RH =ROH + R•
RO• = AP + CH3•
CuII-OH• + RH = Cu(II) + H2O +R•
The homolytic O-O bond cleavage of the peroxide moiety (Equation (6)) produces IPB-oxyl radical to form PP (Equation (7)) and AP (Equation (8)) via CH3-scission, in contrast to a less common for Cu(II) complexes heterolytic mechanism, which gives only PP [91]. Calculations of energetics confirm the homolytic cleavage to be favorable for the decomposition of any Cu(II)-alkylperoxo complexes [92], and comparable to the reductive cleavage of the CuII-O to form Cu(I) (similar to Equation (1)). According to the data of Table 2, the ratio of PP and AP varied within 1.5–2.8, that could be interpreted as indicator of the homolytic mechanism. Homolytic decomposition of IPBHP through the breaking of the O-O bond (Equation (6)) results in formation of CuII-OH• adduct that can participate in the activation of the C-H bond of hydrocarbons [93]. Apart from Equations (1) and (2), the initiation of the cyclic oxidation is intensified by Equations (6)–(9) during the oxidation of IPB. Comparing the catalytic activity of solutions 1 and 2, we can conclude that a more intense decomposition of IPBHP by complex 1 (Table S4) causes a lower selectivity for IPBHP, but a more intense oxidation of IPB.

3. Experimental Section

General Procedures. All the experiments were carried out in air. Commercially available reagents (CuCl2.2H2O, CuBr2, PPh3, chlorobenzene) were used as purchased. 1,2-Bis[(2-methylphenyl)imino]acenaphthene (2-Me-Ph-bian) and 1,2-Bis[(4-methylphenyl)imino]acenaphthene (4-Me-Ph-bian) were prepared as reported [94]. Organic solvents (CH2Cl2, MeCN, glacial acetic acid, and hexane) were dried by standard methods before use. Cumene (99.9% purity, <0.0003 mmol/mL α-methylstyrene) was kindly donated by the Omskiy Caoutchouc factory.
Physical Measurements. Elemental C, H, N analyses were performed with a EuroEA3000 Eurovector analyzer. IR spectra were recorded in the 4000–300 cm–1 range with a Perkin–Elmer System 2000 FTIR spectrometer with samples in KBr pellets. A Shimadzu UV-2501 PC spectrometer equipped with an ISR-240A diffuse reflectance unit was used for UV-Vis spectroscopy of both solutions and solid samples. Diffuse reflectance (DR) spectra of the solid samples were recorded using BaSO4 as the reflectance standard in the wavelength range of 190–900 nm at room temperature. Samples (fraction < 0.25 mm) were placed in a quartz cuvette with a 2 mm optical path length. The obtained reflectance coefficients were transformed into absorption coefficients using the Kubelka–Munk function, F(R∞) = (1−R∞)2/2R∞. All DR spectroscopy data are presented in the following coordinates: Kubelka–Munk function, F(R∞) versus wavelength. The transmission spectra of the solutions were recorded relative to CH3CN in the wavelength range of 190–900 nm at room temperature. Samples of the solutions were placed in a quartz cuvette with a 1 cm optical path length. The obtained transmission coefficients were transformed into absorption coefficients using the Bouguer–Lambert–Beer law, A = −log(I/I0) = −logT = εlC. All absorption spectra are presented in the following coordinates: optical density, A or lgA versus wavelength.
Catalytic Experiments. The catalytic tests were carried out in a 25 mL glass reactor with a water heating jacket, connected to a thermostat (Huber ministat) by silicone tubes. The reactor had two valves for connection to a graduated gas burette and an oxygen cylinder. The reactor was loaded with 5 × 10−4 M acetonitrile solution of a catalyst (1.5 mL) and isopropylbenzene (IPB, 1 mL). The reactor, together with the burette, was purged with O2 at room temperature, sealed, and heated up to a desired temperature under intensive agitation by a magnetic stirrer. When the temperature and pressure stabilized, monitoring of O2 uptake started. After 130 min, the process was terminated, the reactor was quickly cooled to ~15 °C, and the contents were adjusted to 10 mL with acetonitrile and chlorobenzene (internal standard).
The amount of hydroperoxide in the reaction solutions was determined by standard iodometric titration. GC analysis of IPB oxidation products was undertaken on Agilent 7890B instrument equipped with FID and a SOLGEL-WAX 30 m × 0.25 mm × 1 μm column. Prior to GC, the solution was treated with PPh3 to reduce the isopropylbenzenehydroperoxide (IPBHP) to 2-phenyl-2-propanol (PP). Product concentrations were quantified by the internal standard method. The amount of PP formed during the catalytic oxidation was calculated as a difference between the data from GC and iodometric titration. Acetophenone (AP) and α-methylstyrene (AMS) were determined from appropriate GC signals.
X-ray Crystallography. Crystallographic data and refinement details for 2 are given in Table S1. The diffraction data were collected on a Bruker D8 Venture diffractometer with a CMOS PHOTON III detector and IµS 3.0 source (Mo Kα radiation, λ = 0.71073 Å) at 150 K. The φ- and ω-scan techniques were employed. Absorption correction was applied by SADABS (Bruker Apex3 software suite: Apex3, SADABS-2016/2 and SAINT, version 2018.7-2; Bruker AXS Inc.: Madison, WI, USA, 2017). Structures were solved by SHELXT [95] and refined by full-matrix least-squares treatment against |F|2 in anisotropic approximation with SHELX 2014/7 [96] in the ShelXle program [97]. H-atoms were refined in the geometrically calculated positions. The crystallographic data have been deposed in the Cambridge Crystallographic Data Centre under the deposition codes CCDC 2182022.
Computational details. The full geometry optimization procedure for all model structures and DFT calculations for model supramolecular associates based on the obtained experimental X-ray geometry of 2 have been carried out using the dispersion-corrected hybrid functional ωB97XD [98] with the help of Gaussian-09 [99] program package. The Douglas–Kroll–Hess 2nd order scalar relativistic calculations requested for the relativistic core Hamiltonian were carried out using the DZP-DKH basis sets [100,101,102,103] for all atoms. No symmetry restrictions were applied during the geometry optimization procedure. The Hessian matrices were calculated analytically for all optimized model structures to confirm the localization of true minima on the potential energy surface (no imaginary frequencies were found in all cases). The topological analysis of the electron density distribution has been performed using the Multiwfn program (version 3.7) [104]. The Cartesian atomic coordinates for all optimized equilibrium model structures and model supramolecular associates based on the obtained experimental X-ray geometry of 2 are presented in Tables S2 and S3 (Supplementary Materials).
Synthesis of [CuBr2(4-Me-Ph-bian)] (1). A mixture of CuBr2 (224 µmol, 50 mg) and 4-Me-Ph-bian (224 µmol, 80.7 mg) in 8 mL of acetonitrile was refluxed for 3 h. The resulting dark brown solution with the precipitate was evaporated to dryness and the residue was washed with hexane. Yield: 102 mg (78%). Anal. Calc. for C26H20Br2CuN2: C 53.4, H 3.5, N 4.8%; Found C 52.8, H 3.7, N 4.7%. IR (KBr) ν/cm−1: 3453 (br. vw), 3046 (w), 2976 (w), 2947 (w), 2919 (w), 2863 (w), 1661 (w), 1624 (w), 1587 (s), 1505 (s), 1486 (m), 1435 (m), 1422 (vs), 1381 (w), 1363 (w), 1314 (vs), 1288 (w), 1251 (m), 1227 (w), 1217 (w), 1186 (s), 1151 (w), 1135 (w), 1109 (vs), 1044 (m), 1022 (w), 981 (w), 933 (w), 829 (vs), 774 (vs), 742 (w), 711 (w), 701 (w), 652 (w), 636 (m), 616 (w), 589 (w), 553 (m), 527 (w), 488 (w), 450 (w), 419 (w).
Synthesis of [CuBr2(2-Me-Ph-bian)] (2). A mixture of CuBr2 (224 µmol, 50 mg) and 2-Me-Ph-bian (224 µmol, 80.7 mg) in 8 mL of acetonitrile was refluxed for 3 h. The resulting dark brown solution with the precipitate was evaporated to dryness and the residue was washed with hexane. Dark brown crystals were obtained by layering hexane on a solution of complex 2 in dichloromethane. Yield: 115 mg (88%). Anal. Calc. for C26H20Br2CuN2: C 53.4, H 3.5, N 4.8%; Found C 53.7, H 3.5, N 4.8%. IR (KBr) ν/cm−1: 3425 (br. vw), 3056 (m), 3018 (w), 2976 (vw), 2910 (w), 2857 (w), 1634 (vs), 1582 (vs), 1482 (s), 1460 (w), 1446 (w), 1434 (w), 1418 (m), 1378 (w), 1358 (w), 1293 (m), 1251 (w), 1226 (w), 1188 (w), 1153 (w), 1132 (w), 1121 (w), 1093 (w), 1049 (m), 954 (w), 940 (w), 859 (w), 835 (s), 777 (vs), 756 (vs), 717 (s), 627 (w), 615(w), 543 (m), 503(w), 445(w), 413 (w).

4. Conclusions

Two novel Cu(II) complexes with redox-active BIAN ligands [CuBr2(R-bian)] (R = 4-Me-Ph (1), 2-Me-Ph (2)) were obtained in good yield by a ligand exchange reaction from copper(II) bromide. The complexes are structural isomers and differ only in the position of the methyl group in BIAN. For complex 2, the crystal structure was determined by X-ray diffraction analysis. The coordination environment of the Cu(II) center is distorted square-planar. On the contrary, the CuBr2N2 geometry in structure 1 is closer to a distorted tetrahedron, according to the DFT calculations. To the best of our knowledge, complexes 1 and 2 are the first examples of copper complexes with Me-Ph-bian ligands. The redox properties of complexes 1 and 2 in CH3CN were studied using cyclic voltammetry. The coordination of the redox-active Me-Ph-bian ligand to the Cu(II) center leads to both the reversibility of the Cu(II)/Cu(I) process and a rather high oxidizing ability of Cu(II), providing the E1/2 potentials of 0.81 and 0.66 V (vs. SHE) for 1 and 2, respectively. Accordingly, a partial reduction of Cu(II) to Cu(I) in solution was detected using UV-Vis spectroscopy. The differences in redox potentials can be related to the different structure of the CuBr2N2 coordination site. Both complexes 1 and 2 were tested as homogeneous catalysts for IPB oxidation. During the catalytic reaction, the ratio of Cu(II) and Cu(I) species differed from the initial one in the CH3CN solution. That was consistent with the radical chain oxidation initiated with the Cu(II)/Cu(I) couple. Simultaneously, complexes 1 and 2 were able to decompose IPBHP with the formation of RO• radicals without changing the oxidation state of Cu(II). The decomposition of IPBHP catalyzed by 1 or 2 resulted in the formation of products of homolytic cleavage of the O-O bond, which indicated the possibility of a Cu(II)-IPBperoxide adduct forming as an intermediate.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/catal13050849/s1, Table S1: Crystal data and structure refinement for 2; Table S2: Cartesian atomic coordinates for all optimized equilibrium model structures; Table S3: Cartesian atomic coordinates for model supramolecular associate based on the obtained experimental X-ray geometry of 2; Table S4: Conversion of IPBHP and products obtained in CH3CN solutions of 1 and 2. Conditions: 0.001 mmol of 1 or 2, 4 mmol of IPBHP in 2.5 mL CH3CN, 30 °C, 130 min, Ar; Figure S1: Formation of π-π interactions between the dimers in the crystal structure of 2; Figure S2: Crystal packing of 2; Figure S3: UV-Vis diffuse reflectance spectra of complexes 1 and 2 in solid state; Figure S4: UV-Vis absorption spectra of CH3CN solutions of complexes 1 and 2 (5 × 10−4 M); Figure S5: Cyclic voltammograms of 1 (A) and 2 (B) in CH3CN in the −2.3–2.0 V region (black line) and the 0–1.0 V region (blue line) at a potential scan rate of 100 mV/s; Figure S6: Kinetic curves of oxygen uptake by CuBr2 (A) and CuCl2 (B) solutions. Conditions: 1 mL of IPB, 1.5 mL of CH3CN, 5·10−4 M of catalyst; Figure S7: UV-Vis spectra of 1 (A) and 2 (B) (3 × 10−4 M) in CH3CN solution (1), 10 min after addition of IPBHP (2), 40 min after addition of IPBHP (3).

Author Contributions

I.S.F.: Investigation. Synthesis and description of copper complex compounds; O.S.K.: Investigation, Writing—original draft preparation. Investigation on catalysis of copper complexes. Description of catalytic data; N.I.K.: Investigation, Writing—original draft. Carrying out catalytic reactions catalyzed by copper complexes. Generalization and description of catalytic data; T.V.L.: Investigation. Conducting a spectroscopic study of copper complexes; M.I.G.: Investigation. Synthesis and purification of ligands; M.A.: Investigation. Crystallization and purification of copper complexes; P.A.A.: Investigation. Interpretation of X-ray diffraction data; A.S.N.: Investigation. DFT calculations; A.L.G.: Conceptualization, Writing—review & editing. Writing and editing the first draft of the article. Communication with the editor of the journal. All authors have read and agreed to the published version of the manuscript.

Funding

Financial support from the Russian Science Foundation (grant No. 22-23-20123) and the government of the Novosibirsk region (contract r-39) is acknowledged.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The DFT calculations and topological analysis of the electron density distribution were supported by the RUDN University Strategic Academic Leadership Program. The authors thank the Ministry of Science and Higher Education of the Russian Federation, the Centre of Collective Usage of NIIC SB RAS for the XRD data collection as well as the shared research center “National center of investigation of catalysts” of BIC SB RAS for the UV-Vis studies.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bernauer, J.; Pölker, J.; Jacobi von Wangelin, A. Redox-active BIAN-based Diimine Ligands in Metal-Catalyzed Small Molecule Syntheses. ChemCatChem 2022, 14, e202101182. [Google Scholar] [CrossRef] [PubMed]
  2. Kaim, W. Chelate Rings of Different Sizes with Non-Innocent Ligands. Dalton Trans. 2019, 48, 8521–8529. [Google Scholar] [CrossRef] [PubMed]
  3. Abakumov, G.A.; Piskunov, A.V.; Cherkasov, V.K.; Fedushkin, I.L.; Ananikov, V.P.; Eremin, D.B.; Gordeev, E.G.; Beletskaya, I.P.; Averin, A.D.; Bochkarev, M.N.; et al. Organoelement Chemistry: Promising Growth Areas and Challenges. Russ. Chem. Rev. 2018, 87, 393–507. [Google Scholar] [CrossRef]
  4. Hill, N.J.; Vargas-Baca, I.; Cowley, A.H. Recent Developments in the Coordination Chemistry of Bis(Imino)Acenaphthene (BIAN) Ligands with s- and p-Block Elements. Dalton Trans. 2009, 2, 240–253. [Google Scholar] [CrossRef] [PubMed]
  5. Fedushkin, I.L.; Moskalev, M.V.; Lukoyanov, A.N.; Tishkina, A.N.; Baranov, E.V.; Abakumov, G.A. Dialane with a Redox-Active Bis-Amido Ligand: Unique Reactivity towards Alkynes. Chem. Eur. J. 2012, 18, 11264–11276. [Google Scholar] [CrossRef]
  6. Fedushkin, I.L.; Skatova, A.A.; Bazyakina, N.L.; Chudakova, V.A.; Khvoinova, N.M.; Nikipelov, A.S.; Eremenko, O.V.; Piskunov, A.V.; Fukin, G.K.; Lyssenko, K.A. Syntheses and Structures of Magnesium, Calcium, Europium, Gallium, and Zinc Complexes with Bis(Imino)Acenaphthene Ligands. Russ. Chem. Bull. 2013, 62, 1815–1828. [Google Scholar] [CrossRef]
  7. Arrowsmith, M.; Hill, M.S.; Kociok-Köhn, G. Dearomatized BIAN Alkaline-Earth Alkyl Catalysts for the Intramolecular Hydroamination of Hindered Aminoalkenes. Organometallics 2014, 33, 206–216. [Google Scholar] [CrossRef]
  8. Wang, J.; Ganguly, R.; Yongxin, L.; Díaz, J.; Soo, H.S.; García, F. Synthesis and the Optical and Electrochemical Properties of Indium(III) Bis(Arylimino)Acenaphthene Complexes. Inorg. Chem. 2017, 56, 7811–7820. [Google Scholar] [CrossRef]
  9. Johnson, L.K.; Killian, C.M.; Brookhart, M. New Pd(II)- and Ni(II)-Based Catalysts for Polymerization of Ethylene and .Alpha.-Olefins. J. Am. Chem. Soc. 1995, 117, 6414–6415. [Google Scholar] [CrossRef]
  10. 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]
  11. Fedushkin, I.L.; Makarov, V.M.; Sokolov, V.G.; Fukin, G.K.; Maslov, M.O.; Ketkov, S.Y. Compounds of Chromium, Titanium, and Zirconium with Different Reduced Forms of Acenaphthene-1,2-Diimine. Russ. Chem. Bull. 2014, 63, 870–882. [Google Scholar] [CrossRef]
  12. Villa, M.; Miesel, D.; Hildebrandt, A.; Ragaini, F.; Schaarschmidt, D.; Jacobi von Wangelin, A. Synthesis and Catalysis of Redox-Active Bis(Imino)Acenaphthene (BIAN) Iron Complexes. ChemCatChem 2017, 9, 3203–3209. [Google Scholar] [CrossRef]
  13. Quintal, S.; Pires da Silva, M.J.; Martins, S.R.M.; Sales, R.; Félix, V.; Drew, M.G.B.; Meireles, M.; Mourato, A.C.; Nunes, C.D.; Saraiva, M.S.; et al. Molybdenum(II) Complexes with p -Substituted BIAN Ligands: Synthesis, Characterization, Biological Activity and Computational Study. Dalton Trans. 2019, 48, 8449–8463. [Google Scholar] [CrossRef] [PubMed]
  14. Tanahashi, H.; Ikeda, H.; Tsurugi, H.; Mashima, K. Synthesis and Characterization of Paramagnetic Tungsten Imido Complexes Bearing α-Diimine Ligands. Inorg. Chem. 2016, 55, 1446–1452. [Google Scholar] [CrossRef]
  15. 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]
  16. 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]
  17. 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]
  18. Romashev, N.F.; Mirzaeva, I.V.; Bakaev, I.V.; Komlyagina, V.I.; Komarov, V.Y.; Fomenko, I.S.; Gushchin, A.L. Structure of a Binuclear Rhodium(I) Complex with the Acenaphthene-1,2-diimine Ligand. J. Struct. Chem. 2022, 63, 242–251. [Google Scholar] [CrossRef]
  19. Ng, Y.Y.; Tan, L.J.; Ng, S.M.; Chai, Y.T.; Ganguly, R.; Du, Y.; Yeow, E.K.L.; Soo, H. Sen Spectroscopic Characterization and Mechanistic Studies on Visible Light Photoredox Carbon–Carbon Bond Formation by Bis(Arylimino)Acenaphthene Copper Photosensitizers. ACS Catal. 2018, 8, 11277–11286. [Google Scholar] [CrossRef]
  20. Yambulatov, D.S.; Nikolaevskii, S.A.; Kiskin, M.A.; Kholin, K.V.; Khrizanforov, M.N.; Budnikova, Y.G.; Babeshkin, K.A.; Efimov, N.N.; Goloveshkin, A.S.; Imshennik, V.K.; et al. Generation of a Hetero Spin Complex from Iron(II) Iodide with Redox Active Acenaphthene-1,2-Diimine. Molecules 2021, 26, 2998. [Google Scholar] [CrossRef]
  21. Koptseva, T.S.; Moskalev, M.V.; Skatova, A.A.; Rumyantcev, R.V.; Fedushkin, I.L. Reduction of CO 2 with Aluminum Hydrides Supported with Ar-BIAN Radical-Anions (Ar-BIAN = 1,2-Bis(Arylimino)Acenaphthene). Inorg. Chem. 2022, 61, 206–213. [Google Scholar] [CrossRef] [PubMed]
  22. Moskalev, M.V.; Razborov, D.A.; Skatova, A.A.; Bazanov, A.A.; Fedushkin, I.L. Alkali Metal Reduction of 1,2-Bis[(2,6-dibenzhydryl-4-methylphenyl)Imino]Acenaphthene (Ar BIG-bian) to Radical-Anion. Eur. J. Inorg. Chem. 2021, 2021, 458–463. [Google Scholar] [CrossRef]
  23. Romashev, N.F.; Bakaev, I.V.; Komlyagina, V.I.; Fomenko, I.S.; Laricheva, Y.A.; Petrov, P.A.; Gushchin, A.L. Synthesis and Structure of a Binuclear Pd(Ii) Chloranilate Complex. J. Struct. Chem. 2021, 62, 1573–1579. [Google Scholar] [CrossRef]
  24. Fomenko, I.S.; Nadolinnyi, V.A.; Efimov, N.N.; Kokovkin, V.V.; Gushchin, A.L. Binuclear Oxidovanadium(IV) Complex with the Bridging Chloranilate Ligand: Synthesis and Magnetic Properties. Russ. J. Coord. Chem. 2019, 45, 776–781. [Google Scholar] [CrossRef]
  25. 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]
  26. Ittel, S.D.; Johnson, L.K.; Brookhart, M. Late-Metal Catalysts for Ethylene Homo- and Copolymerization. Chem. Rev. 2000, 100, 1169–1204. [Google Scholar] [CrossRef]
  27. Zhao, M.; Chen, C. Accessing Multiple Catalytically Active States in Redox-Controlled Olefin Polymerization. ACS Catal. 2017, 7, 7490–7494. [Google Scholar] [CrossRef]
  28. Anderson, W.C.; Rhinehart, J.L.; Tennyson, A.G.; Long, B.K. Redox-Active Ligands: An Advanced Tool To Modulate Polyethylene Microstructure. J. Am. Chem. Soc. 2016, 138, 774–777. [Google Scholar] [CrossRef]
  29. Kaiser, J.M.; Anderson, W.C.; Long, B.K. Photochemical Regulation of a Redox-Active Olefin Polymerization Catalyst: Controlling Polyethylene Microstructure with Visible Light. Polym. Chem. 2018, 9, 1567–1570. [Google Scholar] [CrossRef]
  30. van Asselt, R.; Elsevier, C.J. Homogeneous Catalytic Hydrogenation of Alkenes by Zero-Valent Palladium Complexes of Cis-Fixed Dinitrogen Ligands. J. Mol. Catal. 1991, 65, L13–L19. [Google Scholar] [CrossRef]
  31. Handbook of Homogeneous Hydrogenation. Available online: https://dare.uva.nl/search?metis.record.id=275294 (accessed on 29 June 2022).
  32. van Laren, M.W.; Elsevier, C.J. Selektive Palladium(0)-Katalysierte Homogene Hydrierung von Alkinen Zu (Z)-Alkenen. Angew. Chem. 1999, 111, 3926–3929. [Google Scholar] [CrossRef]
  33. Dedieu, A.; Humbel, S.; Elsevier, C.; Grauffel, C. Theoretical Study of the Semihydrogenation of Alkynes Catalyzed by Pd(0) Complexes: Is a Zwitterionic Pathway Possible? Theor. Chem. Acc. 2004, 112, 305–312. [Google Scholar] [CrossRef]
  34. Kluwer, A.M.; Koblenz, T.S.; Jonischkeit, T.; Woelk, K.; Elsevier, C.J. Kinetic and Spectroscopic Studies of the [Palladium(Ar-Bian)]-Catalyzed Semi-Hydrogenation of 4-Octyne. J. Am. Chem. Soc. 2005, 127, 15470–15480. [Google Scholar] [CrossRef] [PubMed]
  35. Guo, H.; Zheng, Z.; Yu, F.; Ma, S.; Holuigue, A.; Tromp, D.S.; Elsevier, C.J.; Yu, Y. [Pd(Ar-BIAN)(Alkene)]-Catalyzed Highly Chemo-, Regio-, and Stereoselective Semihydrogenation of 1,2-Allenyl Phosphonates and Related Compounds. Angew. Chem. 2006, 118, 5119–5122. [Google Scholar] [CrossRef]
  36. Wekesa, F.S.; Arias-Ugarte, R.; Kong, L.; Sumner, Z.; McGovern, G.P.; Findlater, M. Iron-Catalyzed Hydrosilylation of Aldehydes and Ketones under Solvent-Free Conditions. Organometallics 2015, 34, 5051–5056. [Google Scholar] [CrossRef]
  37. Sandl, S.; Maier, T.M.; van Leest, N.P.; Kröncke, S.; Chakraborty, U.; Demeshko, S.; Koszinowski, K.; de Bruin, B.; Meyer, F.; Bodensteiner, M.; et al. Cobalt-Catalyzed Hydrogenations via Olefin Cobaltate and Hydride Intermediates. ACS Catal. 2019, 9, 7596–7606. [Google Scholar] [CrossRef]
  38. Maier, T.M.; Sandl, S.; Shenderovich, I.G.; Jacobi von Wangelin, A.; Weigand, J.J.; Wolf, R. Amine-Borane Dehydrogenation and Transfer Hydrogenation Catalyzed by A-Diimine Cobaltates. Chem. Eur. J. 2019, 25, 238–245. [Google Scholar] [CrossRef]
  39. Saini, A.; Smith, C.R.; Wekesa, F.S.; Helms, A.K.; Findlater, M. Conversion of Aldimines to Secondary Amines Using Iron-Catalysed Hydrosilylation. Org. Biomol. Chem. 2018, 16, 9368–9372. [Google Scholar] [CrossRef]
  40. Tamang, S.R.; Cozzolino, A.F.; Findlater, M. Iron Catalysed Selective Reduction of Esters to Alcohols. Org. Biomol. Chem. 2019, 17, 1834–1838. [Google Scholar] [CrossRef]
  41. Maier, T.M.; Gawron, M.; Coburger, P.; Bodensteiner, M.; Wolf, R.; van Leest, N.P.; de Bruin, B.; Demeshko, S.; Meyer, F. Low-Valence Anionic α-Diimine Iron Complexes: Synthesis, Characterization, and Catalytic Hydroboration Studies. Inorg. Chem. 2020, 59, 16035–16052. [Google Scholar] [CrossRef]
  42. Ferretti, F.; Formenti, D.; Ragaini, F. The Reduction of Organic Nitro Compounds by Carbon Monoxide as an Effective Strategy for the Synthesis of N-Heterocyclic Compounds: A Personal Account. Rend. Lincei. 2017, 28, 97–115. [Google Scholar] [CrossRef]
  43. Ferretti, F.; Ramadan, D.R.; Ragaini, F. Transition Metal Catalyzed Reductive Cyclization Reactions of Nitroarenes and Nitroalkenes. ChemCatChem 2019, 11, 4450–4488. [Google Scholar] [CrossRef]
  44. Ragaini, F.; Cenini, S.; Gallo, E.; Caselli, A.; Fantauzzi, S. Fine Chemicals by Reductive Carbonylation of Nitroarenes, Catalyzed by Transition Metal Complexes. Curr. Org. Chem. 2006, 10, 1479–1510. [Google Scholar] [CrossRef]
  45. Ragaini, F.; Cenini, S.; Gasperini, M. Reduction of Nitrobenzene to Aniline by CO/H2O, Catalysed by Ru3(CO)12/Chelating Diimines. J. Mol. Catal. A Chem. 2001, 174, 51–57. [Google Scholar] [CrossRef]
  46. Ragaini, F.; Cenini, S.; Tollari, S. Reduction of Nitrobenzene to Aniline by CO/H2O, Catalysed by Ru3 (CO)12. Strong Activating Ability of Rigid α-Diimine Ligands. J. Mol. Catal. 1993, 85, L1–L5. [Google Scholar] [CrossRef]
  47. Viganò, M.; Ragaini, F.; Buonomenna, M.G.; Lariccia, R.; Caselli, A.; Gallo, E.; Cenini, S.; Jansen, J.C.; Drioli, E. Catalytic Polymer Membranes under Forcing Conditions: Reduction of Nitrobenzene by CO/H2O Catalyzed by Ruthenium Bis(Arylimino)Acenaphthene Complexes. ChemCatChem 2010, 2, 1150–1164. [Google Scholar] [CrossRef]
  48. Cenini, S.; Ragaini, F.; Tollari, S.; Paone, D. Allylic Amination of Cyclohexene Catalyzed by Ruthenium Complexes. A New Reaction Involving an Inter Molecular C−H Functionalization. J. Am. Chem. Soc. 1996, 118, 11964–11965. [Google Scholar] [CrossRef]
  49. Ragaini, F.; Cenini, S.; Tollari, S.; Tummolillo, G.; Beltrami, R. Allylic Amination of Unactivated Olefins by Nitroarenes, Catalyzed by Ruthenium Complexes. A Reaction Involving an Intermolecular C−H Functionalization. Organometallics 1999, 18, 928–942. [Google Scholar] [CrossRef]
  50. Ragaini, F.; Cenini, S.; Borsani, E.; Dompé, M.; Gallo, E.; Moret, M. Synthesis of N-Arylpyrroles, Hetero-Diels−Alder Adducts, and Allylic Amines by Reaction of Unfunctionalized Dienes with Nitroarenes and Carbon Monoxide, Catalyzed by Ru(CO)3 (Ar-BIAN). Organometallics 2001, 20, 3390–3398. [Google Scholar] [CrossRef]
  51. Arrowsmith, M.; Hill, M.S.; Kociok-Köhn, G. Suppression of Schlenk Equilibration and Heavier Alkaline Earth Alkyl Catalysis: A Dearomatization Strategy. Organometallics 2011, 30, 1291–1294. [Google Scholar] [CrossRef]
  52. Yakub, A.M.; Moskalev, M.V.; Bazyakina, N.L.; Fedushkin, I.L. Carbon—Carbon and Carbon—Nitrogen Bond Formation Reactions Catalyzed by the Magnesium and Calcium Acenaphthene-1,2-Diimine Complexes. Russ. Chem. Bull. 2018, 67, 473–478. [Google Scholar] [CrossRef]
  53. Cimino, A.; Moscatelli, F.; Ferretti, F.; Ragaini, F.; Germain, S.; Hannedouche, J.; Schulz, E.; Luconi, L.; Rossin, A.; Giambastiani, G. Novel Yttrium and Zirconium Catalysts Featuring Reduced Ar-BIANH 2 Ligands for Olefin Hydroamination (Ar-BIANH 2 = Bis-Arylaminoacenaphthylene). New J. Chem. 2016, 40, 10285–10293. [Google Scholar] [CrossRef]
  54. Li, L.; Lopes, P.S.; Figueira, C.A.; Gomes, C.S.B.; Duarte, M.T.; Rosa, V.; Fliedel, C.; Avilés, T.; Gomes, P.T. Cationic and Neutral (Ar-BIAN)Copper(I) Complexes Containing Phosphane and Arsane Ancillary Ligands: Synthesis, Molecular Structure and Catalytic Behaviour in Cycloaddition Reactions of Azides and Alkynes. Eur. J. Inorg. Chem. 2013, 2013, 1404–1417. [Google Scholar] [CrossRef]
  55. Li, L.; Lopes, P.S.; Rosa, V.; Figueira, C.A.; Lemos, M.A.N.D.A.; Duarte, M.T.; Avilés, T.; Gomes, P.T. Synthesis and Structural Characterisation of (Aryl-BIAN)Copper(i) Complexes and Their Application as Catalysts for the Cycloaddition of Azides and Alkynes. Dalton Trans. 2012, 41, 5144–5154. [Google Scholar] [CrossRef]
  56. Nunes, C.D.; Vaz, P.D.; Félix, V.; Veiros, L.F.; Moniz, T.; Rangel, M.; Realista, S.; Mourato, A.C.; Calhorda, M.J. Vanadyl Cationic Complexes as Catalysts in Olefin Oxidation. Dalton Trans. 2015, 44, 5125–5138. [Google Scholar] [CrossRef]
  57. 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]
  58. 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]
  59. Lukoyanov, A.N.; Fomenko, I.S.; Gongola, M.I.; Shul’pina, L.S.; Ikonnikov, N.S.; Shul’pin, G.B.; Ketkov, S.Y.; Fukin, G.K.; Rumyantcev, R.V.; Novikov, A.S.; et al. Novel Oxidovanadium Complexes with Redox-Active R-Mian and R-Bian Ligands: Synthesis, Structure, Redox and Catalytic Properties. Molecules 2021, 26, 5706. [Google Scholar] [CrossRef]
  60. Fomenko, I.S.; Gongola, M.I.; Shul’pina, L.S.; Ikonnikov, N.S.; Komarovskikh, A.Y.; Nadolinny, V.A.; Kozlov, Y.N.; Gushchin, A.L.; Shul’pin, G.B. Mononuclear Oxidovanadium(IV) Complexes with BIAN Ligands: Synthesis and Catalytic Activity in the Oxidation of Hydrocarbons and Alcohols with Peroxides. Catalysts 2022, 12, 1168. [Google Scholar] [CrossRef]
  61. Shul’pin, G.B.; Shul’pina, L.S. Oxidation of Organic Compounds with Peroxides Catalyzed by Polynuclear Metal Compounds. Catalysts 2021, 11, 186. [Google Scholar] [CrossRef]
  62. Petrenko, Y.P.; Piasta, K.; Khomenko, D.M.; Doroshchuk, R.O.; Shova, S.; Novitchi, G.; Toporivska, Y.; Gumienna-Kontecka, E.; Martins, L.M.D.R.S.; Lampeka, R.D. An Investigation of Two Copper(II) Complexes with a Triazole Derivative as a Ligand: Magnetic and Catalytic Properties. RSC Adv. 2021, 11, 23442–23449. [Google Scholar] [CrossRef] [PubMed]
  63. Gurbanov, A.V.; Andrade, M.A.; Martins, L.M.D.R.S.; Mahmudov, K.T.; Pombeiro, A.J.L. Water-Soluble Al(III), Fe(III) and Cu(II) Formazanates: Synthesis, Structure, and Applications in Alkane and Alcohol Oxidations. New J. Chem. 2022, 46, 5002–5011. [Google Scholar] [CrossRef]
  64. Shen, H.-M.; Wang, X.; Huang, H.; Liu, Q.-P.; Lv, D.; She, Y.-B. Staged Oxidation of Hydrocarbons with Simultaneously Enhanced Conversion and Selectivity Employing O2 as Oxygen Source Catalyzed by 2D Metalloporphyrin-Based MOFs Possessing Bimetallic Active Centers. J. Chem. Eng. 2022, 443, 136126. [Google Scholar] [CrossRef]
  65. Shul’pina, L.S.; Vinogradov, M.M.; Kozlov, Y.N.; Nelyubina, Y.V.; Ikonnikov, N.S.; Shul’pin, G.B. Copper Complexes with 1,10-Phenanthrolines as Efficient Catalysts for Oxidation of Alkanes by Hydrogen Peroxide. Inorg. Chim. Acta 2020, 512, 119889. [Google Scholar] [CrossRef]
  66. Fomenko, I.; Gushchin, A.; Abramov, P.; Sokolov, M.; Shul’pina, L.; Ikonnikov, N.; Kuznetsov, M.; Pombeiro, A.; Kozlov, Y.; Shul’pin, G. New Oxidovanadium(IV) Complexes with 2,2′-Bipyridine and 1,10-Phenathroline Ligands: Synthesis, Structure and High Catalytic Activity in Oxidations of Alkanes and Alcohols with Peroxides. Catalysts 2019, 9, 217. [Google Scholar] [CrossRef]
  67. Artem’Ev, A.V.; Kashevskii, A.V.; Bogomyakov, A.S.; Safronov, A.Y.; Sutyrina, A.O.; Telezhkin, A.A.; Sterkhova, I.V. Variable Coordination of Tris(2-Pyridyl)Phosphine and Its Oxide toward M(Hfac)2: A Metal-Specifiable Switching between the Formation of Mono- and Bis-Scorpionate Complexes. Dalton Trans. 2017, 46, 5965–5975. [Google Scholar] [CrossRef]
  68. Fomenko, I.S.; Afewerki, M.; Gongola, M.I.; Vasilyev, E.S.; Shul’pina, L.S.; Ikonnikov, N.S.; Shul’pin, G.B.; Samsonenko, D.G.; Yanshole, V.V.; Nadolinny, V.A.; et al. Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties. Molecules 2022, 27, 4072. [Google Scholar] [CrossRef]
  69. Fliedel, C.; Rosa, V.; Santos, C.I.M.; Gonzalez, P.J.; Almeida, R.M.; Gomes, C.S.B.; Gomes, P.T.; Lemos, M.A.N.D.A.; Aullón, G.; Welter, R.; et al. Copper(II) Complexes of Bis(Aryl-Imino)Acenaphthene Ligands: Synthesis, Structure, DFT Studies and Evaluation in Reverse ATRP of Styrene. Dalton Trans. 2014, 43, 13041. [Google Scholar] [CrossRef]
  70. Espinosa, E.; Molins, E.; Lecomte, C. Hydrogen Bond Strengths Revealed by Topological Analyses of Experimentally Observed Electron Densities. Chem. Phys. Lett. 1998, 285, 170–173. [Google Scholar] [CrossRef]
  71. Ivanov, D.M.; Kirina, Y.V.; Novikov, A.S.; Starova, G.L.; Kukushkin, V.Y. Efficient π-Stacking with Benzene Provides 2D Assembly of Trans-[PtCl2(p-CF3C6H4CN)2]. J. Mol. Struct. 2016, 1104, 19–23. [Google Scholar] [CrossRef]
  72. Rozhkov, A.V.; Novikov, A.S.; Ivanov, D.M.; Bolotin, D.S.; Bokach, N.A.; Kukushkin, V.Y. Structure-Directing Weak Interactions with 1,4-Diiodotetrafluorobenzene Convert One-Dimensional Arrays of [MII(Acac)2] Species into Three-Dimensional Networks. Cryst. Growth Des. 2018, 18, 3626–3636. [Google Scholar] [CrossRef]
  73. Katkova, S.A.; Mikherdov, A.S.; Kinzhalov, M.A.; Novikov, A.S.; Zolotarev, A.A.; Boyarskiy, V.P.; Kukushkin, V. (Isocyano Group π-Hole)⋅⋅⋅[D Z2 -M II] Interactions of (Isocyanide)[M II] Complexes, in Which Positively Charged Metal Centers (D 8-M = Pt, Pd) Act as Nucleophiles. Chem. Eur. J. 2019, 25, 8590–8598. [Google Scholar] [CrossRef]
  74. Baykov, S.V.; Filimonov, S.I.; Rozhkov, A.V.; Novikov, A.S.; Ananyev, I.V.; Ivanov, D.M.; Kukushkin, V.Y. Reverse Sandwich Structures from Interplay between Lone Pair−π-Hole Atom-Directed C···dz2[M] and Halogen Bond Interactions. Cryst. Growth Des. 2019, 20, 995–1008. [Google Scholar] [CrossRef]
  75. Usoltsev, A.N.; Adonin, S.A.; Novikov, A.S.; Samsonenko, D.G.; Sokolov, M.N.; Fedin, V.P. One-dimensional polymeric polybromotellurates(IV): Structural and theoretical insights into halogen⋯halogen contacts. CrystEngComm 2017, 19, 5934–5939. [Google Scholar] [CrossRef]
  76. Adonin, S.A.; Gorokh, I.D.; Novikov, A.S.; Abramov, P.A.; Sokolov, M.N.; Fedin, V.P. Halogen Contacts-Induced Unusual Coloring in Bi III Bromide Complex: Anion-to-Cation Charge Transfer via Br⋅⋅⋅Br Interactions. Chem. Eur. J. 2017, 23, 15612–15616. [Google Scholar] [CrossRef]
  77. Adonin, S.A.; Gorokh, I.D.; Novikov, A.S.; Samsonenko, D.G.; Plyusnin, P.E.; Sokolov, M.N.; Fedin, V.P. Bromine-Rich Complexes of Bismuth: Experimental and Theoretical Studies. Dalton Trans. 2018, 47, 2683–2689. [Google Scholar] [CrossRef]
  78. Rozhkov, A.V.; Krykova, M.A.; Ivanov, D.M.; Novikov, A.S.; Sinelshchikova, A.A.; Volostnykh, M.V.; Konovalov, M.A.; Grigoriev, M.S.; Gorbunova, Y.G.; Kukushkin, V.Y. Reverse Arene Sandwich Structures Based upon π-Hole⋅⋅⋅[MII] (D8 M=Pt, Pd) Interactions, Where Positively Charged Metal Centers Play the Role of a Nucleophile. Angew. Chem. Int. Ed. 2019, 58, 4164–4168. [Google Scholar] [CrossRef]
  79. Espinosa, E.; Alkorta, I.; Elguero, J.; Molins, E. From Weak to Strong Interactions: A Comprehensive Analysis of the Topological and Energetic Properties of the Electron Density Distribution Involving X–H⋯F–Y Systems. J. Chem. Phys. 2002, 117, 5529–5542. [Google Scholar] [CrossRef]
  80. Johnson, E.R.; Keinan, S.; 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]
  81. Contreras-García, J.; Johnson, E.R.; Keinan, S.; Chaudret, R.; Piquemal, J.-P.; Beratan, D.N.; Yang, W. NCIPLOT: A Program for Plotting Noncovalent Interaction Regions. J. Chem. Theory Comput. 2011, 7, 625–632. [Google Scholar] [CrossRef]
  82. Kern, T.; Monkowius, U.; Zabel, M.; Knör, G. Mononuclear Copper(I) Complexes Containing Redox-Active 1,2-Bis(Aryl-Imino)Acenaphthene Acceptor Ligands: Synthesis, Crystal Structures and Tuneable Electronic Properties. Eur. J. Inorg. Chem. 2010, 2010, 4148–4156. [Google Scholar] [CrossRef]
  83. Kern, T.; Monkowius, U.; Zabel, M.; Knör, G. Synthesis, Crystal Structure and Charge Transfer Spectra of Dinuclear Copper(I) Complexes Bearing 1,2-Bis(Arylimino)Acenaphthene Acceptor Ligands. Inorg. Chim. Acta 2011, 374, 632–636. [Google Scholar] [CrossRef]
  84. Papanikolaou, P.; Akrivos, P.D.; Czapik, A.; Wicher, B.; Gdaniec, M.; Tkachenko, N. Homoleptic Bis(Aryl)Acenaphthenequinonediimine–Cu I Complexes—Synthesis and Characterization of a Family of Compounds with Improved Light-Gathering Characteristics. Eur. J. Inorg. Chem. 2013, 2013, 2418–2431. [Google Scholar] [CrossRef]
  85. Green, O.; Gandhi, B.A.; Burstyn, J.N. Photophysical Characteristics and Reactivity of Bis(2.9-Di-Tert-Butyl-1,10-Phenanthroline) Copper(l). Inorg. Chem. 2009, 48, 5704–5714. [Google Scholar] [CrossRef]
  86. Kuznetsova, N.I.; Babushkin, D.E.; Zudin, V.N.; Koscheeva, O.S.; Kuznetsova, L.I. Low-Temperature Oxidation of Isopropylbenzene Mediated by the System of NHPI, Fe(Acac)3 and 1,10-Phenanthroline. Catal. Commun. 2021, 149, 106218. [Google Scholar] [CrossRef]
  87. Bhattacharya, A. Kinetic Modeling of Liquid Phase Autoxidation of Cumene. Chem. Eng. J. 2008, 137, 308–319. [Google Scholar] [CrossRef]
  88. Pella, B.J.; Niklas, J.; Poluektov, O.G.; Mukherjee, A. Effects of Denticity and Ligand Rigidity on Reactivity of Copper Complexes with Cumyl Hydroperoxide. Inorg. Chim. Acta 2018, 483, 71–78. [Google Scholar] [CrossRef]
  89. Tano, T.; Ertem, M.Z.; Yamaguchi, S.; Kunishita, A.; Sugimoto, H.; Fujieda, N.; Ogura, T.; Cramer, C.J.; Itoh, S. Reactivity of Copper(Ii)-Alkylperoxo Complexes. Dalton Trans. 2011, 40, 10326. [Google Scholar] [CrossRef]
  90. Shimizu, I.; Morimoto, Y.; Velmurugan, G.; Gupta, T.; Paria, S.; Ohta, T.; Sugimoto, H.; Ogura, T.; Comba, P.; Itoh, S. Characterization and Reactivity of a Tetrahedral Copper(II) Alkylperoxido Complex. Chem. Eur. J. 2019, 25, 11157–11165. [Google Scholar] [CrossRef]
  91. Tano, T.; Sugimoto, H.; Fujieda, N.; Itoh, S. Heterolytic Alkyl Hydroperoxide O–O Bond Cleavage by Copper(I) Complexes. Eur. J. Inorg. Chem. 2012, 2012, 4099–4103. [Google Scholar] [CrossRef]
  92. Chen, P.; Fujisawa, K.; Solomon, E.I. Spectroscopic and Theoretical Studies of Mononuclear Copper(II) Alkyl- and Hydroperoxo Complexes: Electronic Structure Contributions to Reactivity. J. Am. Chem. Soc. 2000, 122, 10177–10193. [Google Scholar] [CrossRef]
  93. Kim, B.; Jeong, D.; Cho, J. Nucleophilic Reactivity of Copper(II)–Alkylperoxo Complexes. Chem. Comm. 2017, 53, 9328–9331. [Google Scholar] [CrossRef]
  94. Ferretti, F.; Rota, L.; Ragaini, F. Unexpected Coordination Behavior of Ruthenium to a Polymeric α-Diimine Containing the Poly[Bis(Arylimino)Acenaphthene] Fragment. Inorg. Chim. Acta 2021, 518, 120257. [Google Scholar] [CrossRef]
  95. Sheldrick, G.M. SHELXT—Integrated Space-Group and Crystal-Structure Determination. Acta Crystallogr. A 2015, 71, 3–8. [Google Scholar] [CrossRef]
  96. Sheldrick, G.M. Crystal Structure Refinement with SHELXL. Acta Crystallogr. C Struct. Chem. 2015, 71, 3–8. [Google Scholar] [CrossRef]
  97. 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]
  98. Chai, J.-D.; Head-Gordon, M. Long-Range Corrected Hybrid Density Functionals with Damped Atom–Atom Dispersion Corrections. Phys. Chem. Chem. 2008, 10, 6615–6620. [Google Scholar] [CrossRef]
  99. Frisch, M.J.; Trucks, G.W.; Schlegel, H.B.; Scuseria, G.E.; Robb, M.A.; Cheeseman, J.R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G.A.; et al. Gaussian 09, Revision C.01; Gaussian Inc: Wallingford, CT, USA, 2010. [Google Scholar]
  100. Barros, C.L.; de Oliveira, P.J.P.; Jorge, F.E.; Canal Neto, A.; Campos, M. Gaussian Basis Set of Double Zeta Quality for Atoms Rb through Xe: Application in Non-Relativistic and Relativistic Calculations of Atomic and Molecular Properties. Mol. Phys. 2010, 108, 1965–1972. [Google Scholar] [CrossRef]
  101. Jorge, F.E.; Canal Neto, A.; Camiletti, G.G.; Machado, S.F. Contracted Gaussian Basis Sets for Douglas–Kroll–Hess Calculations: Estimating Scalar Relativistic Effects of Some Atomic and Molecular Properties. J. Chem. Phys 2009, 130, 064108. [Google Scholar] [CrossRef]
  102. de Berrêdo, R.C.; Jorge, F.E. All-Electron Double Zeta Basis Sets for Platinum: Estimating Scalar Relativistic Effects on Platinum(II) Anticancer Drugs. J. Mol. Struct. 2010, 961, 107–112. [Google Scholar] [CrossRef]
  103. Canal Neto, A.; Jorge, F.E. All-Electron Double Zeta Basis Sets for the Most Fifth-Row Atoms: Application in DFT Spectroscopic Constant Calculations. Chem. Phys. Lett. 2013, 582, 158–162. [Google Scholar] [CrossRef]
  104. Lu, T.; Chen, F. Multiwfn: A Multifunctional Wavefunction Analyzer. J. Comput. Chem. 2012, 33, 580–592. [Google Scholar] [CrossRef] [PubMed]
Catalysts 13 00849 sch001 550
Scheme 1. Synthetic routs towards complexes 1 and 2.
Scheme 1. Synthetic routs towards complexes 1 and 2.
Catalysts 13 00849 sch001
Catalysts 13 00849 g001 550
Figure 1. Molecular structure of complex 2. Main bond lengths (Å) and angles (°): C = N, 1.2805(2) and 1.2801(2); C-C, 1.5015(2); Cu-N, 2.026(2) and 2.039(3); Cu-Br, 2.3517(6) and 2.3385(6); N1-Cu-N2, 81.577(7); Br1-Cu-Br2, 99.419(7); N1-Cu-Br2, 95.083(7) and 95.083(7); N1-Cu-Br1, 149.778(8) and 155.648(8).
Figure 1. Molecular structure of complex 2. Main bond lengths (Å) and angles (°): C = N, 1.2805(2) and 1.2801(2); C-C, 1.5015(2); Cu-N, 2.026(2) and 2.039(3); Cu-Br, 2.3517(6) and 2.3385(6); N1-Cu-N2, 81.577(7); Br1-Cu-Br2, 99.419(7); N1-Cu-Br2, 95.083(7) and 95.083(7); N1-Cu-Br1, 149.778(8) and 155.648(8).
Catalysts 13 00849 g001
Catalysts 13 00849 g002 550
Figure 2. Electrostatic dimers in the crystal structure of 2. Cu···Br contacts are shown with dashed lines.
Figure 2. Electrostatic dimers in the crystal structure of 2. Cu···Br contacts are shown with dashed lines.
Catalysts 13 00849 g002
Catalysts 13 00849 g003 550
Figure 3. Contour line diagram of the Laplacian of electron density distribution ∇2ρ(r), bond paths, and selected zero-flux surfaces (left panel), visualization of electron localization function (ELF, center panel), and reduced density gradient (RDG, right panel) analyses for intermolecular noncovalent interactions Cu···Br in the X-ray structure 2. Bond critical points (3, −1) are shown in blue, nuclear critical points (3, −3)—in pale brown, ring critical points (3, +1)—in orange, bond paths are shown as pale brown lines, length units—Å, and the color scale for the ELF and RDG maps is presented in a.u.
Figure 3. Contour line diagram of the Laplacian of electron density distribution ∇2ρ(r), bond paths, and selected zero-flux surfaces (left panel), visualization of electron localization function (ELF, center panel), and reduced density gradient (RDG, right panel) analyses for intermolecular noncovalent interactions Cu···Br in the X-ray structure 2. Bond critical points (3, −1) are shown in blue, nuclear critical points (3, −3)—in pale brown, ring critical points (3, +1)—in orange, bond paths are shown as pale brown lines, length units—Å, and the color scale for the ELF and RDG maps is presented in a.u.
Catalysts 13 00849 g003
Catalysts 13 00849 g004 550
Figure 4. Kinetic curves of the oxygen uptake by solutions of 1 (bright symbols), 2 (light symbols), L1, L2 and in the absence of catalyst. Conditions: 1 mL of IPB, 1.5 mL of CH3CN, 3 × 10−4 M catalyst.
Figure 4. Kinetic curves of the oxygen uptake by solutions of 1 (bright symbols), 2 (light symbols), L1, L2 and in the absence of catalyst. Conditions: 1 mL of IPB, 1.5 mL of CH3CN, 3 × 10−4 M catalyst.
Catalysts 13 00849 g004
Catalysts 13 00849 g005 550
Figure 5. UV-Vis spectra of solutions 1 (A) and 2 (B) in CH3CN (3 × 10−4 M): initial (black spectra), reacted with IPB for 50 min at 40 °C (red spectra) or 10 min at 25 °C (green spectrum).
Figure 5. UV-Vis spectra of solutions 1 (A) and 2 (B) in CH3CN (3 × 10−4 M): initial (black spectra), reacted with IPB for 50 min at 40 °C (red spectra) or 10 min at 25 °C (green spectrum).
Catalysts 13 00849 g005
Catalysts 13 00849 sch002 550
Scheme 2. Scheme of IPB oxidation catalyzed by complexes 1–2.
Scheme 2. Scheme of IPB oxidation catalyzed by complexes 1–2.
Catalysts 13 00849 sch002
Table
Table 1. Values of the density of all electrons—ρ(r), Laplacian of electron density—∇2ρ(r) and appropriate λ2 eigenvalues, energy density—Hb, potential energy density—V(r), Lagrangian kinetic energy—G(r), and electron localization function—ELF (a.u.) at the bond critical point (3, −1), corresponding to intermolecular noncovalent interactions Cu···Br in the X-ray structure 2 and estimated strength for these weak contacts Eint [70] (kcal/mol).
Table 1. Values of the density of all electrons—ρ(r), Laplacian of electron density—∇2ρ(r) and appropriate λ2 eigenvalues, energy density—Hb, potential energy density—V(r), Lagrangian kinetic energy—G(r), and electron localization function—ELF (a.u.) at the bond critical point (3, −1), corresponding to intermolecular noncovalent interactions Cu···Br in the X-ray structure 2 and estimated strength for these weak contacts Eint [70] (kcal/mol).
Noncovalent
Interaction		ρ(r)∇2ρ(r)λ2HbV(r)G(r)ELFEint ≈ −V(r)/2
2
Cu···Br,
3.666 Å		0.0060.018−0.0060.000−0.0040.0040.0201.3
Table
Table 2. Results of IPB oxidation in CH3CN solutions of 1 and 2 (*).
Table 2. Results of IPB oxidation in CH3CN solutions of 1 and 2 (*).
ComplexT °CProducts, mmolTON, h−1Selectivity, %
IPBHPPP + AMS (**)AP
500.8250412.256.331.5
1400.530716.758.824.5
300.3119019.557.123.4
500.6439320.348.231.5
2400.4125222.653.124.3
300.3219723.257.119.7
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Fomenko, I.S.; Koshcheeva, O.S.; Kuznetsova, N.I.; Larina, T.V.; Gongola, M.I.; Afewerki, M.; Abramov, P.A.; Novikov, A.S.; Gushchin, A.L. Novel Copper(II) Complexes with BIAN Ligands: Synthesis, Structure and Catalytic Properties of the Oxidation of Isopropylbenzene. Catalysts 2023, 13, 849. https://doi.org/10.3390/catal13050849

AMA Style

Fomenko IS, Koshcheeva OS, Kuznetsova NI, Larina TV, Gongola MI, Afewerki M, Abramov PA, Novikov AS, Gushchin AL. Novel Copper(II) Complexes with BIAN Ligands: Synthesis, Structure and Catalytic Properties of the Oxidation of Isopropylbenzene. Catalysts. 2023; 13(5):849. https://doi.org/10.3390/catal13050849

Chicago/Turabian Style

Fomenko, Iakov S., Olga S. Koshcheeva, Nina I. Kuznetsova, Tatyana V. Larina, Marko I. Gongola, Medhanie Afewerki, Pavel A. Abramov, Alexander S. Novikov, and Artem L. Gushchin. 2023. "Novel Copper(II) Complexes with BIAN Ligands: Synthesis, Structure and Catalytic Properties of the Oxidation of Isopropylbenzene" Catalysts 13, no. 5: 849. https://doi.org/10.3390/catal13050849

APA Style

Fomenko, I. S., Koshcheeva, O. S., Kuznetsova, N. I., Larina, T. V., Gongola, M. I., Afewerki, M., Abramov, P. A., Novikov, A. S., & Gushchin, A. L. (2023). Novel Copper(II) Complexes with BIAN Ligands: Synthesis, Structure and Catalytic Properties of the Oxidation of Isopropylbenzene. Catalysts, 13(5), 849. https://doi.org/10.3390/catal13050849

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop