Artem S. Bogomyakov
Russian Academy of Sciences
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Inorganic Chemistry | 2010
Nikolay A. Semenov; Nikolay A. Pushkarevsky; Anton V. Lonchakov; Artem S. Bogomyakov; Elena A. Pritchina; Elizaveta A. Suturina; Nina P. Gritsan; Sergey N. Konchenko; R. Mews; Victor I. Ovcharenko; Andrey V. Zibarev
Decamethylchromocene, Cr(II)(eta(5)-C(5)(CH(3))(5))(2) (2), readily reduced [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazole (1) in a tetrahydrofuran solvent at ambient temperature with the formation of radical-anion salt [2](+)[1](-) (3) isolated in 97% yield. The heterospin salt 3 ([2](+), S = 3/2; [1](-), S = 1/2) was characterized by single-crystal X-ray diffraction as well as magnetic susceptibility measurements in the temperature range 2-300 K. The experimental data together with theoretical analysis of the salts magnetic structure within the CASSCF and spin-unrestricted broken-symmetry (BS) density functional theory (DFT) approaches revealed antiferromagnetic (AF) interactions in the crystalline 3: significant between anions [1](-), weak between cations [2](+), and very weak between [1](-) and [2](+). Experimental temperature dependences of the magnetic susceptibility and the effective magnetic moment of 3 were very well reproduced in the assumption of the AF-coupled [1](-)...[1](-) (J(1) = -40 +/- 9 cm(-1)) and [2](+)...[2](+) (J(2) = -0.58 +/- 0.03 cm(-1)) pairs. The experimental J(1) value is in reasonable agreement with the value calculated using BS UB3LYP/6-31+G(d) (-61 cm(-1)) and CASSCF(10,10)/6-31+G(d) (-15.3 cm(-1)) approaches. The experimental J(2) value is also in agreement with that calculated using the BS DFT approach (-0.33 cm(-1)).
Inorganic Chemistry | 2012
Victor I. Ovcharenko; S. V. Fokin; Elvina T. Kostina; G. V. Romanenko; Artem S. Bogomyakov; E. V. Tretyakov
The reaction of copper(II) hexafluoroacetylacetonate [Cu(hfac)2] with the stable nitronyl nitroxide 2-(1-ethyl-3-methyl-1H-pyrazol-4-yl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazole-3-oxide-1-oxyl (L(a)) resulted in a paired heterospin complex [[Cu(hfac)2]3(μ-O,N-L(a))2][Cu(hfac)2(O-L(a))2]. The crystals of the compound were found to be capable of a reversible single-crystal-to-single-crystal (SC-SC) transformation initiated by the variation of temperature. At room temperature, the molecular structure of [[Cu(hfac)2]3(μ-O,N-L(a))2][Cu(hfac)2(O-L(a))2] is formed by the alternating fragments of the pair complex. Cooling the crystals of the complex below 225 K caused considerable mutual displacements of adjacent molecules, which ended in a transformation of the molecular structure into a polymer chain structure. A reversible topotactic polymerization-depolymerization coordination reaction actually takes place in the solid during repeated cooling-heating cycles: [[Cu(hfac)2]3(μ-O,N-L(a))2][Cu(hfac)2(O-L(a))2] ⇌ Cu(hfac)2(μ-O,N-L(a))]∞. Polymerization during cooling is the result of the anomalously great shortening of intermolecular distances (from 4.403 Å at 295 K to 2.460 Å at 150 K; Δd = 1.943 Å) between the terminal Cu atoms of the trinuclear fragments {[[Cu(hfac)2]3(μ-O,N-L(a))2]} and the noncoordinated N atoms of the pyrazole rings of the mononuclear {[Cu(hfac)2(O-L(a))2]} fragments. When the low-temperature phase was heated above 270 K, the polymer chain structure was destroyed and the compound was again converted to the pair molecular complex. The specifics of the given SC-SC transformation lies in the fact that the process is accompanied by a magnetic anomaly, because the intracrystalline displacements of molecules lead to a considerable change in the mutual orientation of the paramagnetic centers, which, in turn, causes modulation of the exchange interaction between the odd electrons of the Cu(2+) ion and nitroxide. On the temperature curve of χT, this shows itself as a hysteresis loop. The nontrivial character of the recorded spin transition during the cooling of the sample below 225 K lies in the fact that the magnetic moment abruptly increased. In contrast, heating the sample above 270 K led to a drastic decrease in χT. This behavior of χT is caused by a stepwise change in the character of the exchange interaction in the {>N-(•)O-Cu(2+)-O(•)-N<} fragments. The lengthening of distances between the paramagnetic centers on cooling below 225 K led to a transition from antiferromagnetic to ferromagnetic exchange and, vice versa, the shortening of distances between the paramagnetic centers during the heating of the heterospin polymer above 270 K led to a transition from ferromagnetic exchange to antiferromagnetic exchange.
Russian Journal of Inorganic Chemistry | 2009
Zh. V. Dobrokhotova; G. G. Aleksandrov; Yu. A. Velikodnyi; V. N. Ikorskii; Artem S. Bogomyakov; L. N. Puntus; V. M. Novotortsev; I. L. Eremenko
Methods of synthesis of binuclear pivalate complexes L2Ln2(μ-O,η2-OOCCMe3)2(μ2-O,O′-OOCCMe3)2(η2-OOCCMe3)2, where Ln = Sm, Eu, Gd, or Er and L = 2,2′-dipyridyl (Bipy) or 1,10-phenanthroline (Phen), from the corresponding binuclear complexes Ln2(μ2-OOCCMe3)4(OOCCMe3)2(HOOCCMe3)6 · HOOCCMe3(I–IV), as well as of coordination polymers {Ln(OOCCMe3)3}n, were suggested. The compounds were characterized by X-ray crystallography and X-ray powder diffraction and their magnetic properties, solid-phase thermolysis, and the phase composition of solid decomposition products were studied. The structures of the metal carboxylate core and surrounding ligands were shown to have an effect on the thermal stability of the complexes. The luminescence properties of the Eu(III) complexes were analyzed.
Russian Journal of Coordination Chemistry | 2009
A. S. Burlov; S. A. Nikolaevskii; Artem S. Bogomyakov; I. S. Vasil’chenko; Yu. V. Koshchienko; V. G. Vlasenko; A. I. Uraev; D. A. Garnovskii; E. V. Sennikova; G. S. Borodkin; A. D. Garnovskii; Vladimir I. Minkin
The bidentate chelate Cu(II) complexes of phenylazosalicylaldehyde azomethines are synthesized for the first time and their magnetic properties are studied. The complexes with the intermetallic bridge of the nitrogen atoms are characterized by the antiferromagnetic interaction, whereas the ferromagnetic exchange is typical of analogous coordination compounds with the sulfur bridge.
Inorganic Chemistry | 2013
Nikolay A. Semenov; Nikolay A. Pushkarevsky; Elizaveta A. Suturina; Elena A. Chulanova; Natalia V. Kuratieva; Artem S. Bogomyakov; Irina G. Irtegova; Nadezhda V. Vasilieva; Lidia S. Konstantinova; Nina P. Gritsan; Oleg A. Rakitin; Victor I. Ovcharenko; Sergey N. Konchenko; Andrey V. Zibarev
Bis(toluene)chromium(0), Cr(0)(η(6)-C7H8)2 (3), readily reduced [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazole (1) and [1,2,5]thiadiazolo[3,4-b]pyrazine (2) in a tetrahydrofuran solvent with the formation of heterospin, S1 = S2 = ½, radical-ion salts [3](+)[1](-) (4) and [3](+)[2](-) (5) isolated in high yields. The salts 4 and 5 were characterized by single-crystal X-ray diffraction (XRD), solution and solid-state electron paramagnetic resonance, and magnetic susceptibility measurements in the temperature range 2-300 K. Despite the formal similarity of the salts, their crystal structures were very different and, in contrast to 4, in 5 anions were disordered. For the XRD structures of the salts, parameters of the Heisenberg spin Hamiltonian were calculated using the CASSCF/NEVPT2 and broken-symmetry density functional theory approaches, and the complex magnetic motifs featuring the dominance of antiferromagnetic (AF) interactions were revealed. The experimental χT temperature dependences of the salts were simulated using the Van Vleck formula and a diagonalization of the matrix of the Heisenberg spin Hamiltonian for the clusters of 12 paramagnetic species with periodic boundary conditions. According to the calculations and χT temperature dependence simulation, a simplified magnetic model can be suggested for the salt 4 with AF interactions between the anions ([1](-)···[1](-), J1 = -5.77 cm(-1)) and anions and cations ([1](-)···[3](+), J2 = -0.84 cm(-1)). The magnetic structure of the salt 5 is much more complex and can be characterized by AF interactions between the anions, [2](-)···[2](-), and by both AF and ferromagnetic (FM) interactions between the anions and cations, [2](-)···[3](+). The contribution from FM interactions to the magnetic properties of the salt 5 is in qualitative agreement with the positive value of the Weiss constant Θ (0.4 K), whereas for salt 4, the constant is negative (-7.1 K).
Inorganic Chemistry | 2011
Victor I. Ovcharenko; Sergei V. Fokin; Elena Fursova; Olga Kuznetsova; E. V. Tretyakov; G. V. Romanenko; Artem S. Bogomyakov
The crystals of heterospin complexes [M(hfac)(2)L(2)] (where M = Cu, Ni, Co, or Mn; hfac = hexafluoroacetylacetonate; and L = nitronyl nitroxide, 4,4,5,5-tetramethyl-2-(1-methyl-1H-imidazol-5-yl)-4,5-dihydro-1H-imidazole-3-oxide-1-oxyl) were found to make unusual jumping motions. Under ambient conditions, the jumping and various displacements of crystals lasted for several weeks. The mechanical motion was accompanied by the cracking and disintegration of crystals, and a solid [M(hfac)(2)(L(1))(2)] complex with the corresponding imino nitroxide 4,4,5,5-tetramethyl-2-(1-methyl-1H-imidazol-5-yl)-4,5-dihydro-1H-imidazole-1-oxyl (L(1)) was detected. The jumping was accompanied by the spontaneous elimination of oxygen, the source of which was the nitronyl nitroxyl fragment of coordinated L. An X-ray study of [M(hfac)(2)L(2)] (where M = Cu, Ni, Co, or Mn) showed that the molecular structure of all [M(hfac)(2)L(2)] and their packing in the solid state were identical. The packing of [M(hfac)(2)L(2)] was concluded to be critical to the mechanical effect. In complexes with different stoichiometries or different sets of diamagnetic ligands ([Cu(hfac)(2)L](2), [Cu(hfac)(acac)L]·EtOH, [CuPiv(2)L(2)]·2CH(2)Cl(2), and [Cu(hfac)(2)L(2)Cu(2)Piv(4)]·3C(7)H(8) (where acac is acetylacetonate and Piv is trimethylacetate), or free L), the effect vanished when the packing changed.
Inorganic Chemistry | 2012
Evgeny V. Tretyakov; Svyatoslav E. Tolstikov; Anastasiya O. Suvorova; Aleksey V. Polushkin; G. V. Romanenko; Artem S. Bogomyakov; Sergey L. Veber; Matvey V. Fedin; D. V. Stass; Edward J. Reijerse; Wolfgang Lubitz; Ekaterina M. Zueva; Victor I. Ovcharenko
Breathing crystals based on polymer-chain complexes of Cu(hfac)(2) with nitroxides exhibit thermally and light-induced magnetostructural anomalies in many aspects similar to a spin crossover. In the present work, we report the synthesis and investigation of a new family of Cu(hfac)(2) complexes with tert-butylpyrazolylnitroxides and their nonradical structural analogues. The complexes with paramagnetic ligands clearly exhibit structural rearrangements in the copper(II) coordination units and accompanying magnetic phenomena characteristic for breathing crystals. Contrary to that, their structural analogues with diamagnetic ligands do not undergo rearrangements in the copper(II) coordination environments. This confirms experimentally the crucial role of paramagnetic ligands and exchange interactions between them and copper(II) ions for the origin of magnetostructural anomalies in this family of molecular magnets.
Inorganic Chemistry | 2014
Oleg A. Varzatskii; Larysa V. Penkova; Svitlana V. Kats; Alexander V. Dolganov; Anna V. Vologzhanina; Alexander A. Pavlov; Valentin V. Novikov; Artem S. Bogomyakov; Victor N. Nemykin; Yan Z. Voloshin
Chloride ion-aided one-pot template self-assembly of a mixed pyrazoloxime ligand with phenylboronic acid on a corresponding metal(II) ion as a matrix afforded the first boron-capped zinc, cobalt, iron, and manganese pseudoclathrochelate tris-pyrazoloximates. The presence of a pseudocross-linking hydrogen-bonded chloride ion is critical for their formation, as the same chloride-capped complexes were isolated even in the presence of large excesses of bromide and iodide ions. As revealed by X-ray diffraction, all complexes are capped with a chloride ion via three N-H···Cl hydrogen bonds that stabilize their pseudomacrobicyclic frameworks. The MN6 coordination polyhedra possess a distorted trigonal prismatic geometry, with the distortion angles φ between their nonequivalent N3 bases of approximately 0°. Temperature dependences of the effective magnetic moment for the paramagnetic complexes showed the encapsulated metal(II) ions to be in a high-spin state in the temperature range of 2-300 K. In the case of the iron(II) pseudoclathrochelate, density functional theory (DFT) and time-dependent DFT calculations were used to assess its spin state as well as the (57)Fe Mössbauer and UV-vis-NIR parameters. Cyclic voltammetry studies performed for these pseudomacrobicyclic complexes showed them to undergo irreversible or quasi-reversible metal-localized oxidations and reductions. As no changes are observed in the presence of a substantial excess of bromide ion, no anion-exchange reaction occurs, and thus the pseudoclathrochelates have a high affinity toward chloride anions in solution.
Inorganic Chemistry | 2015
Alexander V. Piskunov; Irina V. Ershova; Artem S. Bogomyakov; A. G. Starikov; Georgy K. Fukin; V. K. Cherkasov
A number of pentacoordinated gallium complexes iSQ2GaR (1-7) (R = Et (1), Me (2), N3 (3), Cl (4), Br (5), I (6), NCS (7)) where iSQ is a radical anion of 4,6-di-tert-butyl-N-(2,6-diisopropylphenyl)-o-iminobenzoquinone were synthesized, and crystalline samples of 1-7 were characterized using magnetic susceptibility measurements. The character of magnetic exchange interaction between spins of o-iminosemiquinonate radicals was found to be strongly influenced by the nature of the apical substituent. The antiferromagnetic coupling is predominant when the apical position is occupied by halogens or other tested inorganic anions, and the value of exchange interaction parameter varies from -99 to -176 K for R = I and NCS, respectively. In the case of alkyl groups the ferromagnetic exchange prevails and, as the result, the triplet ground state for pentacoordianted biradical compounds was observed. Compounds 1-7 demonstrate a biradical X-band EPR spectrum in frozen toluene matrix. The molecular structures of 4, 6, and 7 have been established by single-crystal X-ray analysis. A computational DFT UB3LYP/6-31G(d,p) study was performed on complexes 1-7 in order to understand the reason for changes in the magnetic behavior of the related diradical gallium compounds. The calculations showed that the magnetic behavior of the complexes with inorganic anions is conditioned by the presence of antiferromagnetic exchange channel formed as a consequence of overlapping between donor atomic orbitals of iminoquinone with π-orbitals of halogen atoms (4-6) or nitrogen atom (3, 7).
Inorganic Chemistry | 2015
Nikolay A. Pushkarevsky; Nikolay A. Semenov; Alexey A. Dmitriev; Natalia V. Kuratieva; Artem S. Bogomyakov; Irina G. Irtegova; Nadezhda V. Vasilieva; Bela E. Bode; Nina P. Gritsan; Lidia S. Konstantinova; J. Derek Woollins; Oleg A. Rakitin; Sergey N. Konchenko; Victor I. Ovcharenko; Andrey V. Zibarev
Low-temperature interaction of [1,2,5]thiadiazolo[3,4-c][1,2,5]thiadiazole (1) with MoMes2 (Mes = mesitylene/1,3,5-trimethylbenzene) in tetrahydrofuran gave the heterospin (S1 = S2 = (1)/2) radical-ion salt [MoMes2](+)[1](-) (2) whose structure was confirmed by single-crystal X-ray diffraction (XRD). The structure revealed alternating layers of the cations and anions with the Mes ligands perpendicular, and the anions tilted by 45°, to the layer plane. At 300 K the effective magnetic moment of 2 is equal to 2.40 μB (theoretically expected 2.45 μB) and monotonically decreases with lowering of the temperature. In the temperature range 2-300 K, the molar magnetic susceptibility of 2 is well-described by the Curie-Weiss law with parameters C and θ equal to 0.78 cm(3) K mol(-1) and -31.2 K, respectively. Overall, the magnetic behavior of 2 is similar to that of [CrTol2](+)[1](-) and [CrCp*2](+)[1](-), i.e., changing the cation [MAr2](+) 3d atom M = Cr (Z = 24) with weak spin-orbit coupling (SOC) to a 4d atom M = Mo (Z = 42) with stronger SOC does not affect macroscopic magnetic properties of the salts. For the XRD structure of salt 2, parameters of the Heisenberg spin-Hamiltonian were calculated using the broken-symmetry DFT and CASSCF approaches, and the complex 3D magnetic structure with both the ferromagnetic (FM) and antiferromagnetic (AF) exchange interactions was revealed with the latter as dominating. Salt 2 is thermally unstable and slowly loses the Mes ligands upon storage at ambient temperature. Under the same reaction conditions, interaction of 1 with MoTol2 (Tol = toluene) proceeded with partial loss of the Tol ligands to afford diamagnetic product.