Next Article in Journal
Drosophila melanogaster as a Translational Model System to Explore the Impact of Phytochemicals on Human Health
Next Article in Special Issue
New Functional Alkoxysilanes and Silatranes: Synthesis, Structure, Properties, and Possible Applications
Previous Article in Journal
Uncovering the Role of Natural and Synthetic Small Molecules in Counteracting the Burden of α-Synuclein Aggregates and Related Toxicity in Different Models of Parkinson’s Disease
Previous Article in Special Issue
Determination of Kinetic Parameters and Identification of the Rate-Determining Steps in the Oxygen Exchange Process for LaNi0.6Fe0.4O3−δ
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 24
Issue 17
10.3390/ijms241713371
ijms-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 thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

New Ruthenium Nitrosyl Complexes Combining Potentially Photoactive Nitrosyl Group with the Magnetic Nitroxide Radicals as Ligands

by
Gennadiy A. Kostin
1,*,
Ruslan Kozlov
2,
Artem Bogomyakov
3,
Svyatoslav Tolstikov
3,
Dmitriy Sheven
1 and
Sergey Korenev
1
1
Nikolaev Institute of Inorganic Chemistry Siberian Branch of Russian Academy of Science, Lavrentieva, 3, 630090 Novosibirsk, Russia
2
Department of Natural Sciences, Novosibirsk State University, Pirogova, 2, 630090 Novosibirsk, Russia
3
International Tomography Center Siberian Branch of Russian Academy of Science, Institutskaya, 3a, 630090 Novosibirsk, Russia
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2023, 24(17), 13371; https://doi.org/10.3390/ijms241713371
Submission received: 27 July 2023 / Revised: 24 August 2023 / Accepted: 25 August 2023 / Published: 29 August 2023
(This article belongs to the Special Issue State-of-the-Art Materials Science in Russia—2nd Edition)
Browse Figures
Versions Notes

Abstract

:
Two ruthenium nitrosyl complexes of Na[RuNOCl4L] with nitronyl nitroxide radicals coordinated to ruthenium with N-donor pyridine rings were prepared and described. The crystal structure of both complexes is 1D or 2D polymeric, due to the additional coordination of sodium cation by bridging the chloride ligands or oxygen atoms of nitroxides. Partially, the oligomeric forms remain in the solutions of the complexes in acetonitrile. The magnetic measurements in the solid state demonstrate the presence of antiferromagnetic interactions through the exchange channels, with the distance between paramagnetic centers equal to 3.1–3.9 Å. The electrochemical behavior of the prepared complexes was investigated in acetonitrile solutions.

1. Introduction

Magnetic materials based on nitroxide radicals of different types have been of great interest for the last several decades. The magnetic exchange between nitroxide moieties and other paramagnetic centers can result in ferromagnetics [1], spin-crossover compounds [2], “breathing crystals” with the “single-crystal-to-single-crystal” transition [3], solvent sensible magnetics [2,4], etc. Usually, the combination of organic radicals with paramagnetic metal ions is explored to achieve special magnetic properties. Still, diamagnetic cations can be used to modulate the interactions between radical centers in the solid state [5,6].
The idea of optically switched magnetic materials was realized for the first time for the example of mixed cobalt iron cyanide (Prussian blue type) [7]. Since that time, a large number of photo-switchable magnetics have been prepared on the basis of cyanide complexes [8,9], complexes with switching spin crossover [10], and organic photo-switchable ligands [11,12,13]. Photo-switching can be realized directly in the magnetic center by changing the Jahn–Teller effect or the spin state of the paramagnetic ion [10,14,15]. Another approach is based mainly on the switching of structure by changing the distance between paramagnetic centers [12,13].
Ruthenium nitrosyl complexes are one of the most interesting examples of a photo-switching group, since the Ru-NO moiety can exist in three different isomeric forms [16,17,18]. The most stable is the ground state (GS), in which the Ru-NO (N-coordinated NO) group can be transferred by light irradiation with a specific wavelength to metastable MS1 (Ru-ON, O coordinated) or MS2 (Ru < NO, η2 coordinated). All three isomers possess different physical and chemical characteristics, in particular the well-defined photochromism. Thus, it can be considered as a three-position switch in contrast to most of the switching fragments.
In our previous work, we have shown the principal possibility of combining nitronyl nitroxide radicals (L) with ruthenium nitrosyl, and reported the first structure of Na[RuNOCl4L] [19]. The present paper is devoted to the development of our approach and the investigation of some of the properties of prepared complexes. For the first time, we describe the magnetic properties of such complexes and investigate their electrochemical behavior.

2. Results and Discussion

2.1. Structure and Synthesis

Earlier, we investigated the reaction of Na2[RuNOCl5] with N-donor heterocycles to prepare the first example of [RuNOCl4L]− complexes with a nitronyl-nitroxide radical [19]. In the present paper, we examine the approach to the synthesis of complexes with similar ligands. Since the nitroxides themselves are relatively weak ligands, that could be crucial for inert ruthenium complexes, we exploited nitroxides with an additional N-donor center. For both the investigated ligands, the only complex with a cis-position of NO and L is formed, according to single-crystal X-ray diffraction. The vibration spectra of both complexes contain the only absorption band corresponding to ν(NO) vibrations (1872 and 1868 cm−1) that could be assigned to the trans-NO-Ru-Cl coordinate. The vibrations of the N-O fragment in a nitronyl nitroxide ligand are usually located at 1370–1400 cm−1 [20]; thus, the strong band in the spectra of both compounds at 1372–1373 cm−1 could be assigned to the nitroxide NO stretching vibrations.
Generally, the substitution of one chloride ligand to N-heterocycle (L) in [RuNOCl5]2− can result in the formation of a trans(L,NO)- or cis(L,NO) isomer. Arion et al. reported that the reaction of [RuNOCl5]2− with different amino acids (AA) results in only one isomer, namely mer(Cl)-trans(O, NO) [RuNOCl3(AA-H)] [21]. The reaction of [RuNOCl5]2− with N-heterocycles in different alcohols with the molar ratio heterocycle Ru < 2 results in both cis- and trans-isomers of [RuNOCl4L]−; the longer reaction time seems to be favorable for cis-isomer formation [22]. The reaction of [RuNOCl5]2− with the 5–10 molar excess of N-heterocycles in boiling DMF only results in fac-[RuNOCl3L2] [23]. The strong π-acceptor properties of the NO ligand result in the strong labialization of the trans-to-NO ligand due to the kinetic trans-effect [24]; thus, the trans-isomers seem to be the products of the kinetic control, while the formation of cis-isomers results from the thermodynamic control of the reaction.
Both new crystal structures (2)–(3), as well as the previously reported structure (1), are built from the anionic [RuNOCl4L]− fragments, which are combined into 1D or 2D structures due to the additional interactions of the chloride ligands or oxygen atoms of nitroxide radicals with sodium cations. The structural parameters of the [RuNOCl4L]− moiety in all three structures (Table 1) are close to typical for nitrosyl complexes [23,25,26]. The Ru-Cl distances vary in the range of 2.34–2.40 Å. The Ru-NO bond and the bond between nitrogen and oxygen atoms in the nitrosyl group are quite short, due to the dual nature of the NO ligand, which is both the σ-donor and π-acceptor. The RuNO fragment is close to linear in all the investigated compounds. That kind of geometry is typical of ruthenium nitrosyl complexes, whose electronic structure can be represented as Ru2+-NO+. In all structures, an interplane angle between the pyridine ring and nitroxide fragment sufficiently deviates from the coplanar, prohibiting the distribution of spin density on the pyridine ring.
Structure (2) crystallizes in the triclinic (P-1) group. The asymmetric unit consists of two ruthenium anions, two sodium cations, and one acetonitrile molecule. In the crystal structure (2), 2D layers are formed by the additional interactions between sodium cations and the oxygen atoms of nitroxide radicals or bridging chloride ligands. There are three independent positions of sodium atoms in the crystal structure (Figure 1). In the first position, Na1 is coordinated by three bridging chloride ligands with Na-Cl distances of 2.798(3)–2.800(3) Å, two oxygen atoms from two nitroxide radicals with Na-O distances being equal to 2.323(3)–2.415(3) Å, and an additional acetonitrile molecule with an Na-N distance equal to 2.450(2) Å. The coordination environment of Na1 can be represented as a distorted square pyramid with two chlorine atoms, an oxygen atom and a nitrogen atom at the base. The sodium cation in the second position is disordered in two positions with equal occupation (50%). The coordination environment of Na2 can be represented as a distorted square with a trans-arrangement of two coordinated oxygen atoms from the nitroxide radicals (2.233(2) and 2.356(2) Å) and two nitrogen atoms from the acetonitrile molecules (2.512(3) and 2.507(3) Å). The sodium cation Na3 is in the private position (0.5, 0.5, 0). The coordination environment of Na3 is a distorted octahedron from six chlorine atoms with distances of 2.681(3)–2.849(3) Å.
In two-dimensional grids oriented perpendicular to the a axis, rows formed by Na1 fragments alternate with rows formed by Na3 and Na2 fragments (Figure 2). Additionally, the network is stabilized by -pi-stacking interactions between the pyridine rings of the ligands with distances between the ring planes of 3.786 Å. According to the CCDC database, bridging sodium cations are not rare for the crystal structures of chloride complex salts. Similar short Na…Cl contacts in the solid state were revealed for different complexes of transition metals, such as ruthenium [27,28], iridium [29], and rhenium [30]. The Na…O distances in the studied structures are also short enough to be considered as coordination bonds. Similar distances were observed earlier for the sodium complexes of crown ethers [31,32].
Complex (3) crystallizes in the orthorhombic (P212121) space group. The asymmetric unit contains one ruthenium anion, one sodium cation, and a water molecule. The structure (3) is formed on the basis of the RuCl4-Na-RuCl4 chain motif, in which each sodium cation is bonded to the two neighboring ruthenium anions by the two bridging chloride ligands. The sodium coordination environment is a distorted octahedron of four chlorine atoms and two oxygen atoms from the nitroxide radical and water molecule. The Na-Cl bond lengths are in the range of 2.786(1)–3.004(1) Å and the Na-O distances are 2.281(3) and 2.299(3) Å. In the crystal lattice, these chains are oriented along the a axis and are linked by hydrogen bonds between the oxygen atom of the water molecule coordinated to sodium and one of the oxygen atoms of the nitroxide radical with an O…O distance of 2.72 Å (Figure 3). The presence of water in the crystal structure (3) is also confirmed by the IR spectra, where corresponding vibration bonds are located at 3580 cm−1 (ν(OH)) and 1616 cm−1 (δ(OH)).

2.2. Hirshfeld Surfaces Analysis

A Hirshfeld surfaces analysis was performed for the anionic fragments [RuNOCl4L]− in structures (2) and (3) to study the weak interactions in the complexes, such as hydrogen bond, π-π, molecular packing in crystal, and van der Waals interactions. The dnorm (Figure 4) and cool contact detachment provide a comprehensive relationship between the distances of any superficial point and the surrounding internal (di) and exterior (de) atoms along the van der Waals distance.
The mostly red zones in Figure 4 correspond to the earlier mentioned interactions between sodium cations and chlorine or oxygen atoms responsible for the polymeric nature of structures. Still, the analysis of 2D fingerprints allows additional weak interactions to be revealed, which include the ruthenium nitrosyl group or nitroxide groups. The contribution of certain atoms to the anion Hirshfeld surfaces in structures (2) and (3) is similar. The most significant contribution is made by hydrogen atoms (48% for both structures), chlorine atoms (29.8 for (3) and 29.9% for (2)), and oxygen atoms (9.7% for (3) and 13.3% for (2)) (Supplementary Materials Figure S3a,b).
The relatively short contacts of ruthenium nitrosyl groups and nitroxide groups are shown in Figure 5. In structure (2), the distance between nitroxide oxygen atoms is equal to 3.632(2) Å and the additional interactions between nitroxide oxygen and the methyl groups of adjacent nitroxide are also revealed, with the distance O…C equal to 3.459(3) Å. In structure (3) the contacts between nitroxide fragments are longer with the distance O…O equal to 3.908(3) Å. The shortest contacts of nitroxide oxygens in structure (3) (2.720(3) Å) correspond to the weak hydrogen bonding with the water molecule coordinated to the sodium cation. The oxygen atoms of the nitrosyl group in both structures are surrounded by the nitroxide ligands of the neighboring [RuNOCl4L]− fragments; in structure (2), the nitrosyl groups are also surrounded by the chlorine ligands of the neighboring fragments.

2.3. Mass-Spectrometry

The electrospray ionization mass-spectra (ESI-MS, negative ions—NI) of the investigated compounds in acetonitrile solutions reveals the presence of an [RuNOCl4L]− anion for both complexes, and also the presence of oligomeric forms, corresponding to the parts of the molecular chains detected in the solid-state crystal structure. The forms were assigned based on the position of the most intensive line (Table 2) and verified by the characteristic patterns of isotopic distribution (Figure 6, Supplementary Materials, Figure S1a,b).
The presence of dimeric (C) and trimeric (D) forms was detected for both compounds. Moreover, for the complex with the ligand L1 (2), the signal of the dimeric form (C) was six times more intensive than for the monomeric anion (A). All the main signals (A), (C), (D) were accompanied by minor peaks with lower m/z, corresponding to the loss of one oxygen atom. The conversion of nitronyl nitroxide to an imino nitroxide radical is well-known and can be mediated by different factors (temperature, acidic media, the presence of reducing agents) [33,34,35]. Still, the EPR spectra of complex solutions in acetonitrile have only five specific lines corresponding to the nitronyl nitroxide ligand [19]; thus, the deoxygenated species (A)-O and (C)-O form in the process of ESI-MS.

2.4. Electrochemistry

The redox properties of complexes (2) and (3) were investigated in acetonitrile solutions with different scan rates (0.1–0.5 V/s). Both complexes demonstrated irreversible ox-red behavior, and the corresponding cathodic and anodic potentials were strongly dependent on the scan rate. Complex (2) showed two irreversible reduction processes (Figure 7a). The potential of the first peak was weakly dependent on the scan rate (0.88–0.85 V), while the second one shifted from −0.739 to −1.120 V with an increase in the scan rate (0.1–0.5 V/s). Also, three oxidation peaks could be revealed. The first one (−0.651–0.633 V) occurred only at the higher scan rates (0.2–0.5 V/s), the potential of the second peak decreased (1.24–0.98 V) with an increase in the scan rate, and the third one had a potential equal to 1.32–1.35 V. Similar processes can be revealed for complex (3) (Figure 7b, Table 3).
Since the nitronyl nitroxide ligands are compounds with a one-electron shell lying between the corresponding hydroxylamine (strong reducing agent) and oxoammonium salt (strong oxidizer), the pure ligands usually demonstrate two quasi-reversible waves. The potentials of the oxidation process (nitroxide–oxoammonium salt) are in the range of 0.4–0.8 V and the electron acceptors shift the potentials to higher values [36,37,38,39,40]. The potentials of the reduction process (nitroxide–hydroxylamine) varies from −1.4 to −0.8 V and the electron acceptors also shift the potentials to higher values [36]. Thus, we can suppose that the cathodic peaks are related to the nitroxide transformations, as well as the anodic peaks, with potentials of 0.6 and 1–1.2 V. The irreversible oxidation process at potentials of 1.2–1.4 V can be assigned to the oxidation of the (RuNO)3+ group according to the literature data for ruthenium nitrosyls [25,41].
If the redox process is chemically and electrochemically reversible, the difference between the anodic and cathodic peaks, called peak-to-peak separation, is close to 59 mV (2.303RT/F at 25 °C). The redox processes associated with nitroxide ligands (−0.7 and 0.9–1.2 V) obviously do not fit that requirement. Moreover, the peak-to-peak separation shifts with an increase in the scan rate, which indicates electrochemical quasi-reversibility [42,43]. Earlier, it was shown that pure ligands demonstrate reversible redox transformations [36,37,38,39,40]. The most probable reason for the irreversibility in the investigated complexes is the presence of the chemical reaction conjugated to the redox process, e.g., the interaction of a reduced ligand with the Ru-NO fragment. Nevertheless, a rigorous confirmation of this hypothesis requires additional studies.

2.5. Magnetic Measurements

The temperature dependencies of the effective magnetic moment (µeff) for complexes (1) and (3) are shown in Figure 8. The µeff values at 300 K are very close to a theoretical spin-only value of 1.73 µB for the monoradical of the molecular mass, corresponding to formulas (1) and (3). For complex (1) the µeff changes slightly as the temperature is lowered, and then decreases to 0.54 µB at 2 K. The decreasing in µeff is indicative of antiferromagnetic coupling due to short contacts (NO....ON 3.121 Å, NO...CH3 3.169 Å) (Supplementary Materials Figure S2a) between the paramagnetic fragments of nitroxides in the solid (1). An analysis of the experimental µeff(T) dependence with an alternating chain model (Spin Hamiltonian H = –2J1·Si–1Si – 2J2·SiSi+1) results in equal J1 and J2 values, so the uniform chain model was used (H = –2J·SiSi+1). The best-fit values of the g-factor and exchange coupling parameter J are 2.00 ± 0.01 and −7.7 ± 0.1 cm−1. In the case of complex (3), the µeff decreases below 25 K to 1.40 µB at 2 K. According to the X-ray diffraction data, radicals in the solid 2 form exchange-coupled chain have short contacts between nitroxide groups (NO....ON 3.904 Å, Supplementary Materials, Figure S2b). An analysis of the experimental µeff(T) dependence on the uniform chain model gives best-fit values of g = 1.99 ± 0.01 and −0.60 ± 0.01 cm−1.

3. Materials and Methods

3.1. General Procedures and Materials

All reagents and solvents were of standard pure grade (Merck) and used without additional purification. Na2[RuNOCl5]·6H2O [44] and the nitroxide radicals [45,46] (Scheme 1) were prepared according to the techniques described earlier. The elemental analysis was conducted on a EuroVector EA3000 analyzer (EuroVector, Pavia, Italy). IR spectra in KBr pellets in the range of 400–4000 cm−1 were recorded on the spectrometer FCM 2201 “Infraspec”.

3.2. Synthesis of Na[RuNOCl4L1]

Exact weights of Na2[RuNOCl5]·6H2O (46 mg, 0.1 mmol) and the ligand L1 (47 mg, 0.2 mmol) were mixed in 4 mL of acetonitrile, after that the mixture was stirred in a closely capped vial at 85 °C for 2 h. After cooling, the solution was filtered from NaCl and the blue filtrate was evaporated until dry at a reduced pressure. The final residue was dissolved in 1 mL of CH2Cl2, 4 mL of benzene was added, and the resulting suspension was stirred in a closely capped vial for 1 h at 75 °C. After cooling, the product precipitate was filtered, washed with benzene and diethyl ether, and air-dried. The final yield was 45 mg (80%). The IR spectra in cm−1 were: 2994(w), 2924(w), 2852(w), 1872(v.s.), 1452(m), 1402(m), 1372(s), 1324(m), 1215(m), 1177(m), 1135(m), 1068(m), 801(s), and 685(v).
NaRuCl4C12N4O3H16 found/calcd % were: N—10.3/10.6, C—27.1/27.2, and H—2.9/3.0.
Single crystals for X-ray analysis were prepared by the slow diffusion of diethyl ether in the acetonitrile solution. The different crystal phases for Na[RuNOCl4L1] were identified after diffusion in different conditions. Phase (1), prepared at 25 °C, is described earlier [19] and was stable in the absence of solvent. Phase (2), prepared at 5 °C, corresponds to the formula Na[RuNOCl4L1]·CH3CN and quickly loses solvent. For the magnetic measurements the stable phase (1) was used.

3.3. Synthesis of Na[RuNOCl4L2]·H2O

The complex was prepared using the same synthetic pathway as for the ligand L1. The final yield of blue-green precipitate was 40 mg (70%). IR spectra in sm−1 were: 3580(b.m.), 2994(w), 2924(w), 2852(w), 1868(v.s.), 1616(s), 1451(m), 1404(m), 1373(s), 1323(m), 1224(m), 1171(m), 1136(m), 1063(m), 1028(m), 832(s), and 689(v).
NaRuCl4C12N4O4H18 found/calcd % were: N—10.6/10.2, C—26.9/26.3, and H—3.6/3.3.
Single crystals for X-ray analysis were prepared by the slow diffusion of diethyl ether in the acetonitrile solution. Only one crystal phase Na[RuNOCl4L2]·H2O (3) was formed at temperatures of 25 and 5 °C and was used for the magnetic measurements.

3.4. Physical methods

The magnetic susceptibility of the polycrystalline samples was measured with a Quantum Design MPMSXL SQUID magnetometer in the temperature range 2–300 K with a magnetic field of up to 5 kOe. Diamagnetic corrections were made using the Pascal constants. The effective magnetic moment was calculated as μeff(T) = [(3k/NAμB2)χT]1/2 ≈ (8χT)1/2. The analysis of the experimental magnetic data was performed using the PHI program [47].
Mass spectrometric data were obtained on an Agilent liquid chromatograph-mass spectrometer system (LC-MS) 6130 Quadrupole MS, 1260 infinity LC. The analyses were performed in an m/z range from 200 to 2500 mass units, in SCAN mode for positive and negative ions. Electrospray ionization (ESI) was used as an ion source. The following parameters were used: nitrogen as a drying gas, a temperature of 350 °C, a flow rate of 7 L min−1, a spraying gas (nitrogen) pressure of 60 psig, and a voltage on the capillary of 4000 V. The voltage on the fragmentator was established to be 100 V in all experiments. A 5 µL acetonitrile (HPLC grade) solution of the studied compound with a concentration of 10−4–10−3 M was injected into the mobile phase, consisting of acetonitrile (special purity grade), at a rate of 0.4 mL min−1, sprayed, and ionized. The mass spectra (MS) were interpreted by matching signals to the proposed ions, including a comparison of the calculated and experimental isotopic peak distributions.
Cyclic voltammetry was carried out on an Elins P-20X8 voltammetry analyzer using a three-electrode scheme with a glassy carbon (GC) working electrode, a Pt auxiliary electrode, and an Ag/AgCl/3.5 M KCl reference electrode. Investigations were carried out for 2·10−3 M solutions of (2) and (3) with 0.1 M Bu4NBF4 in acetonitrile. Tetracyanoquinodimethane (TCNQ) was used as the internal standard.
The Hirshfeld surfaces were calculated using Crystal Explorer [48]. This program allows the normalized contact distance dnorm to be mapped onto the generated Hirshfeld surface. It is customary to map dnorm using a red–white–blue scheme, where red denotes close intermolecular contacts (negative dnorm), blue denotes longer contacts (positive dnorm), and white denotes intermolecular contacts equal to the van der Waals radii of atoms in contact (dnorm = 0). It is possible to obtain two-dimensional plots (fingerprint plots) from the surfaces mapped with dnorm values. Derived from the Hirshfeld surface, these 2D-fingerprint plots provide a visual summary of the frequency of each combination of de (radius of external atom) and di (radius of internal atom) across the surface of a molecule, so they not only indicate which intermolecular interactions are present, but also the relative area of the surface corresponding to each kind of interaction. Points on the plot with no contribution to the surface are left uncolored, and points with a contribution to the surface are colored blue for a small contribution through green to red for points with the largest contribution.
Single crystal X-ray diffraction data were collected by a Bruker Apex Duo diffractometer with CCDs using graphite-monochromated MoKα radiation (λ = 0.71073 Å) via 0.5° ω- and φ-scan techniques. An experimental data reduction was performed using the APEX2 suite. The structures were solved by SHELXT and refined by the full-matrix least-squares technique SHELXL [49]. Atomic displacement parameters of the non-H atoms were refined using anisotropic approximation. The hydrogen atoms of organic ligands were located geometrically and refined using the riding model. CCDC 2279338–2279339 contains the supplementary crystallographic data. The crystal data and structure refinement for the (2) and (3) are given in Table 4. These data can be obtained free of charge via http://www.ccdc.cam.ac.uk/conts/retrieving.html (accessed on 5 July 2023), or by e-mail.

4. Conclusions

The relatively simple synthetic approach allows us to combine the photochemically active ruthenium nitrosyl group with the magnetic nitronyl nitroxides in one coordination anion [RuNOCl4L]−. The prepared compounds are the first examples of the combination of inorganic (RuNO) and organic (nitroxides) NO groups in one coordination sphere. The crystal structure of sodium salts depends on the structure of nitroxide radicals, but the main features can be generalized. All the investigated crystal structures have 1D or 2D topology, due to the additional interactions between cations (Na+) and chloride ligands or the oxygen atoms of coordinated nitroxide ligands. Surprisingly the oligomeric fragments (n= 2, 3) with bridging sodium cations were also detected in acetonitrile solutions of the investigated complexes. The electrochemical behavior of the synthesized complexes demonstrates two quasi-reversible processes of the oxidation or reduction of nitroxide ligands and the irreversible oxidation of the (RuNO)3+ fragment. The irreversibility of (RuNO)3+ oxidation was well-established earlier, while the quasi-reversible redox processes of nitroxide ligands significantly differ from those of pure ligands. The magnetic properties of solid phases indicate that antiferromagnetic coupling at low temperatures goes through the exchange channels with short contacts between the paramagnetic centers of nitroxide ligands. Since the coordination fragment [RuNOCl4L]− has an anionic nature, it could be combined further with different paramagnetic cations to prepare magnetic materials with different paramagnetic centers. Taking into account the potential photochemical activity of the RuNO group, these materials can demonstrate the photoswitching of magnetic properties.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms241713371/s1.

Author Contributions

G.A.K.—methodology, writing—original draft preparation, review and editing; R.K.—investigation; A.B.—investigation, resources; S.T.—investigation, data curation; D.S.—investigation, resources, data curation; S.K.—supervision, conceptualization. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Russian Science Foundation (no. 22-23-00407) and supported by the Ministry of Science and Higher Education of the Russian Federation (no. 121031700313-8).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

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

Acknowledgments

The authors thank the XRD Facility of NIIC SB RAS and personally thank Sukhih A. for the data collection.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Luneau, D.; Rey, P. Magnetism of Metal-Nitroxide Compounds Involving Bis-Chelating Imidazole and Benzimidazole Substituted Nitronyl Nitroxide Free Radicals. Coord. Chem. Rev. 2005, 249, 2591–2611. [Google Scholar] [CrossRef]
  2. Gass, I.A.; Tewary, S.; Rajaraman, G.; Asadi, M.; Lupton, D.W.; Moubaraki, B.; Chastanet, G.; Létard, J.-F.; Murray, K.S. Solvate-Dependent Spin Crossover and Exchange in Cobalt(II) Oxazolidine Nitroxide Chelates. Inorg. Chem. 2014, 53, 5055–5066. [Google Scholar] [CrossRef] [PubMed]
  3. Ovcharenko, V.; Bagryanskaya, E. Breathing Crystals from Copper Nitroxyl Complexes. In Spin-Crossover Materials; John Wiley & Sons, Ltd.: Hoboken, NJ, USA, 2013; pp. 239–280. [Google Scholar] [CrossRef]
  4. Romanenko, G.V.; Maryunina, K.Y.; Bogomyakov, A.S.; Sagdeev, R.Z.; Ovcharenko, V.I. Relationship between the Thermally Induced Reorientations of Aromatic Solvate Molecules in Cu(Hfac)2–Nitroxide Breathing Crystals and the Character of the Magnetic Anomaly. Inorg. Chem. 2011, 50, 6597–6609. [Google Scholar] [CrossRef]
  5. Ershova, I.V.; Piskunov, A.V.; Cherkasov, V.K. Complexes of Diamagnetic Cations with Radical Anion Ligands. Russ. Chem. Rev. 2020, 89, 1157. [Google Scholar] [CrossRef]
  6. Oshio, H.; Watanabe, T.; Ohto, A.; Ito, T.; Ikoma, T.; Tero-Kubota, S. Ferromagnetic Interactions between Imino Nitroxides through Diamagnetic Metal Ions:  Crystal Structures, Magnetism, and Electronic Properties of [M(I)(Imino Nitroxide)2](PF6) (M = Cu(I) and Ag(I)). Inorg. Chem. 1997, 36, 3014–3021. [Google Scholar] [CrossRef]
  7. Sato, O.; Iyoda, T.; Fujishima, A.; Hashimoto, K. Photoinduced Magnetization of a Cobalt-Iron Cyanide. Science 1996, 272, 704–705. [Google Scholar] [CrossRef]
  8. Stefańczyk, O.; Ohkoshi, S. Photoswitchable High-Dimensional CoII–[WV(CN)8] Networks: Past, Present, and Future. J. Appl. Phys. 2021, 129, 110901. [Google Scholar] [CrossRef]
  9. Arczyński, M.; Stanek, J.; Sieklucka, B.; Dunbar, K.R.; Pinkowicz, D. Site-Selective Photoswitching of Two Distinct Magnetic Chromophores in a Propeller-Like Molecule To Achieve Four Different Magnetic States. J. Am. Chem. Soc. 2019, 141, 19067–19077. [Google Scholar] [CrossRef]
  10. Gütlich, P.; Hauser, A.; Spiering, H. Thermal and Optical Switching of Iron(II) Complexes. Angew. Chem. Int. Ed. Engl. 1994, 33, 2024–2054. [Google Scholar] [CrossRef]
  11. Matsuda, K.; Irie, M. Photoswitching of Magnetic Properties by Using Diarylethene Photochromic Spin Coupler. Mol. Cryst. Liq. Cryst. Sci. Technol. Sect. A Mol. Cryst. Liq. Cryst. 2000, 345, 155–160. [Google Scholar] [CrossRef]
  12. Rogacz, K.; Brzozowska, M.; Baś, S.; Kurpiewska, K.; Pinkowicz, D. Low-Coordinate Erbium(III) Single-Molecule Magnets with Photochromic Behavior. Inorg. Chem. 2022, 61, 16295–16306. [Google Scholar] [CrossRef]
  13. Dommaschk, M.; Schütt, C.; Venkataramani, S.; Jana, U.; Näther, C.; Sönnichsen, F.D.; Herges, R. Rational Design of a Room Temperature Molecular Spin Switch. The Light-Driven Coordination Induced Spin State Switch (LD-CISSS) Approach. Dalt. Trans. 2014, 43, 17395–17405. [Google Scholar] [CrossRef] [PubMed]
  14. Kaszub, W.; Marino, A.; Lorenc, M.; Collet, E.; Bagryanskaya, E.G.; Tretyakov, E.V.; Ovcharenko, V.I.; Fedin, M.V. Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet. Angew. Chem. 2014, 53, 10636–10640. [Google Scholar] [CrossRef] [PubMed]
  15. Canton, S.E.; Biednov, M.; Pápai, M.; Lima, F.A.; Choi, T.-K.; Otte, F.; Jiang, Y.; Frankenberger, P.; Knoll, M.; Zalden, P.; et al. Ultrafast Jahn-Teller Photoswitching in Cobalt Single-Ion Magnets. Adv. Sci. 2023, 10, 2206880. [Google Scholar] [CrossRef]
  16. Schaniel, D.; Imlau, M.; Weisemoeller, T.; Woike, T.; Krämer, K.W.; Güdel, H.-U. Photoinduced Nitrosyl Linkage Isomers Uncover a Variety of Unconventional Photorefractive Media. Adv. Mater. 2007, 19, 723–726. [Google Scholar] [CrossRef]
  17. Mikhailov, A.A.; Stolyarova, E.D.; Kostin, G.A. PHOTOCHEMISTRY OF RUTHENIUM NITROSYL COMPLEXES IN SOLIDS AND SOLUTIONS AND ITS POTENTIAL APPLICATIONS. J. Struct. Chem. 2021, 62, 497–516. [Google Scholar] [CrossRef]
  18. Mikhailov, A.A.; Wenger, E.; Kostin, G.A.; Schaniel, D. Room-Temperature Photogeneration of Nitrosyl Linkage Isomers in Ruthenium Nitrosyl Complexes. Chem.-A Eur. J. 2019, 25, 7569–7574. [Google Scholar] [CrossRef]
  19. Kostin, G.A.; Tolstikov, S.E.; Kuratieva, N.V.; Nadolinny, V.A.; Ovcharenko, V.I. FIRST EXAMPLE OF RUTHENIUM NITROSO COMPLEXES WITH A NITROXYL RADICAL AS A LIGAND. J. Struct. Chem. 2023, 64, 169–178. [Google Scholar] [CrossRef]
  20. Rintoul, L.; Micallef, A.S.; Bottle, S.E. The Vibrational Group Frequency of the N–O Stretching Band of Nitroxide Stable Free Radicals. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 2008, 70, 713–717. [Google Scholar] [CrossRef]
  21. Rathgeb, A.; Böhm, A.; Novak, M.S.; Gavriluta, A.; Dömötör, O.; Tommasino, J.B.; Enyedy, É.A.; Shova, S.; Meier, S.; Jakupec, M.A.; et al. Ruthenium-Nitrosyl Complexes with Glycine, l-Alanine, l-Valine, l-Proline, d-Proline, l-Serine, l-Threonine, and l-Tyrosine: Synthesis, X-Ray Diffraction Structures, Spectroscopic and Electrochemical Properties, and Antiproliferative Activity. Inorg. Chem. 2014, 53, 2718–2729. [Google Scholar] [CrossRef]
  22. Büchel, G.E.; Gavriluta, A.; Novak, M.; Meier, S.M.; Jakupec, M.A.; Cuzan, O.; Turta, C.; Tommasino, J.-B.; Jeanneau, E.; Novitchi, G.; et al. Striking Difference in Antiproliferative Activity of Ruthenium- and Osmium-Nitrosyl Complexes with Azole Heterocycles. Inorg. Chem. 2013, 52, 6273–6285. [Google Scholar] [CrossRef]
  23. Rechitskaya, E.D.; Kuratieva, N.V.; Lider, E.V.; Eremina, J.A.; Klyushova, L.S.; Eltsov, I.V.; Kostin, G.A. Tuning of Cytotoxic Activity by Bio-Mimetic Ligands in Ruthenium Nitrosyl Complexes. J. Mol. Struct. 2020, 1219, 128565. [Google Scholar] [CrossRef]
  24. Coe, B.J.; Glenwright, S.J. Trans-Effects in Octahedral Transition Metal Complexes. Coord. Chem. Rev. 2000, 203, 5–80. [Google Scholar] [CrossRef]
  25. Stolyarova, E.D.; Mikhailov, A.A.; Ulantikov, A.A.; Eremina, J.A.; Klyushova, L.S.; Kuratieva, N.V.; Nadolinny, V.A.; Kostin, G.A. Blue-to-Red Light Triggered Nitric Oxide Release in Cytotoxic/Cytostatic Ruthenium Nitrosyl Complexes Bearing Biomimetic Ligands. J. Photochem. Photobiol. A Chem. 2021, 421, 113520. [Google Scholar] [CrossRef]
  26. Rechitskaya, E.D.; Vorobiev, V.A.; Kuratieva, N.V.; Kostin, G.A. MIXED-LIGAND NITROSYL AND 3-CYANOPYRIDINE COMPLEX OF RUTHENIUM(II): SYNTHESIS, CRYSTAL STRUCTURE, AND BOND ISOMERISM. J. Struct. Chem. 2021, 62, 256–264. [Google Scholar] [CrossRef]
  27. Piggot, P.M.T.; Hall, L.A.; White, A.J.P.; Williams, D.J. Synthesis of Ruthenium(II) Monosubstituted Squarates: 1. Procedural Considerations. Inorganica Chim. Acta 2004, 357, 250–258. [Google Scholar] [CrossRef]
  28. Chyba, J.; Novák, M.; Munzarová, P.; Novotný, J.; Marek, R. Through-Space Paramagnetic NMR Effects in Host–Guest Complexes: Potential Ruthenium(III) Metallodrugs with Macrocyclic Carriers. Inorg. Chem. 2018, 57, 8735–8747. [Google Scholar] [CrossRef]
  29. Hołyńska, M. Iridium(III) Products Isolated in a Reaction of IrCl3 with Phenyl 2-Pyridyl Ketoxime. Z. Krist.-Cryst. Mater. 2013, 228, 72–76. [Google Scholar] [CrossRef]
  30. Müller, U.; Noll, A. (Na-15-Krone-5)2ReCl6·4 CH2Cl2, Eine Struktur Mit CH2Cl2-Molekülen in Pseudohexagonalen Kanälen. Z. Krist.-Cryst. Mater. 2003, 218, 699–702. [Google Scholar] [CrossRef]
  31. Liddle, S.T.; Clegg, W. A Homologous Series of Crown-Ether-Complexed Alkali Metal Amides as Discrete Ion-Pair Species: Synthesis and Structures of [M(12-Crown-4)2][PyNPh·PyN(H)Ph] (M=Li, Na and K). Polyhedron 2003, 22, 3507–3513. [Google Scholar] [CrossRef]
  32. Liebing, P.; Schmeide, M.; Kühling, M.; Witzorke, J. The Alkali Metal Salts of Methyl Xanthic Acid. Eur. J. Inorg. Chem. 2020, 2020, 2428–2434. [Google Scholar] [CrossRef]
  33. Vostrikova, K.E.; Peresypkina, E.V.; Drebushchak, V.A. Cucurbituril-Assisted Transformation of Nitronyl Nitroxide into Imino Nitroxide in the Solid State. CrystEngComm 2011, 13, 3241–3245. [Google Scholar] [CrossRef]
  34. Luneau, D. Coordination Chemistry of Nitronyl Nitroxide Radicals Has Memory. Eur. J. Inorg. Chem. 2020, 2020, 597–604. [Google Scholar] [CrossRef]
  35. Goldstein, S.; Russo, A.; Samuni, A. Reactions of PTIO and Carboxy-PTIO with ·NO, ·NO2, and O2¯*. J. Biol. Chem. 2003, 278, 50949–50955. [Google Scholar] [CrossRef] [PubMed]
  36. Budnikova, Y.G.; Gryaznova, T.V.; Kadirov, M.K.; Tret’yakov, E.V.; Kholin, K.V.; Ovcharenko, V.I.; Sagdeev, R.Z.; Sinyashin, O.G. Electrochemistry of Nitronyl and Imino Nitroxides. Russ. J. Phys. Chem. A 2009, 83, 1976–1980. [Google Scholar] [CrossRef]
  37. Lee, J.; Lee, E.; Kim, S.; Bang, G.S.; Shultz, D.A.; Schmidt, R.D.; Forbes, M.D.E.; Lee, H. Nitronyl Nitroxide Radicals as Organic Memory Elements with Both N- and p-Type Properties. Angew. Chem. 2011, 123, 4506–4510. [Google Scholar] [CrossRef]
  38. Fedyushin, P.A.; Zayakin, I.A.; Tolstikov, S.E.; Lalov, A.V.; Akyeva, A.Y.; Syroeshkin, M.A.; Romanenko, G.V.; Tretyakov, E.V.; Egorov, M.P.; Ovcharenko, V.I. Synthesis and Redox Properties of Imidazol-2-Yl-Substituted Nitronyl Nitroxides. Russ. Chem. Bull. 2022, 71, 722–734. [Google Scholar] [CrossRef]
  39. Zayakin, I.A.; Akyeva, A.Y.; Syroeshkin, M.A.; Bagryanskaya, I.Y.; Tretyakov, E.V.; Egorov, M.P. Synthesis, Structure, and Electrochemistry of Nitronyl Nitroxide-Substituted 1,4-Naphthoquinone. Russ. Chem. Bull. 2023, 72, 213–222. [Google Scholar] [CrossRef]
  40. Souza, D.A.; Moreno, Y.; Ponzio, E.A.; Resende, J.A.L.C.; Jordão, A.K.; Cunha, A.C.; Ferreira, V.F.; Novak, M.A.; Vaz, M.G.F. Synthesis, Crystal Structure, Magnetism and Electrochemical Properties of Two Copper(II) Furoyltrifluoroacetonate Complexes with Nitroxide Radical. Inorganica Chim. Acta 2011, 370, 469–473. [Google Scholar] [CrossRef]
  41. Swain, P.; Mallika, C.; Jagadeeswara Rao, C.; Kamachi Mudali, U.; Natarajan, R. Electrochemical Studies on the Reduction Behaviour of Ruthenium Nitrosyl Ions in Nitric Acid Medium. J. Appl. Electrochem. 2015, 45, 209–216. [Google Scholar] [CrossRef]
  42. 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] [PubMed]
  43. Barmi, M.J.; Minakshi, M. Tuning the Redox Properties of the Nanostructured CoMoO4 Electrode: Effects of Surfactant Content and Synthesis Temperature. ChemPlusChem 2016, 81, 964–977. [Google Scholar] [CrossRef]
  44. Emel’yanov, V.A.; Gromilov, S.A.; Baidina, I.A.; Virovets, A.V.; Belyaev, A.V.; Logvinenko, V.A. Synthesis and Crystal Structure of Na2[RuNOCl5]·6H2O. J. Struct. Chem. 1999, 40, 883–891. [Google Scholar] [CrossRef]
  45. Tolstikov, S.E.; Artiukhova, N.A.; Romanenko, G.V.; Bogomyakov, A.S.; Zueva, E.M.; Barskaya, I.Y.; Fedin, M.V.; Maryunina, K.Y.; Tretyakov, E.V.; Sagdeev, R.Z.; et al. Heterospin Complex Showing Spin Transition at Room Temperature. Polyhedron 2015, 100, 132–138. [Google Scholar] [CrossRef]
  46. Zhang, J.; Zhao, M.; Cui, G.; Peng, S. A Class of Novel Nitronyl Nitroxide Labeling Basic and Acidic Amino Acids: Synthesis, Application for Preparing ESR Optionally Labeling Peptides, and Bioactivity Investigations. Bioorganic Med. Chem. 2008, 16, 4019–4028. [Google Scholar] [CrossRef]
  47. Chilton, N.F.; Anderson, R.P.; Turner, L.D.; Soncini, A.; Murray, K.S. PHI: A Powerful New Program for the Analysis of Anisotropic Monomeric and Exchange-Coupled Polynuclear d- and f-Block Complexes. J. Comput. Chem. 2013, 34, 1164–1175. [Google Scholar] [CrossRef]
  48. Spackman, M.A.; Jayatilaka, D. Hirshfeld Surface Analysis. CrystEngComm 2009, 11, 19–32. [Google Scholar] [CrossRef]
  49. Sheldrick, G.M. SHELXT-Integrated Space-Group and Crystal-Structure Determination. Acta Crystallogr. Sect. A Found. Adv. 2015, 71, 3–8. [Google Scholar] [CrossRef]
Ijms 24 13371 g001
Figure 1. The different crystallographic positions of sodium cations in the crystal structure of (2). Hydrogen atoms are omitted for clarity.
Figure 1. The different crystallographic positions of sodium cations in the crystal structure of (2). Hydrogen atoms are omitted for clarity.
Ijms 24 13371 g001
Ijms 24 13371 g002
Figure 2. (a) 2D layer in the structure (2). Stacking interactions are marked with red dashes. (b) The view of structure (2) along the b axis. Hydrogen atoms are omitted for clarity.
Figure 2. (a) 2D layer in the structure (2). Stacking interactions are marked with red dashes. (b) The view of structure (2) along the b axis. Hydrogen atoms are omitted for clarity.
Ijms 24 13371 g002
Ijms 24 13371 g003
Figure 3. (a) Chain building block in structure (3). (b) View of the crystal structure (3) along the a axis. Hydrogen bonds are marked with red dashes. Hydrogen atoms are omitted for clarity.
Figure 3. (a) Chain building block in structure (3). (b) View of the crystal structure (3) along the a axis. Hydrogen bonds are marked with red dashes. Hydrogen atoms are omitted for clarity.
Ijms 24 13371 g003
Ijms 24 13371 g004
Figure 4. Hirshfeld surfaces for the anions in structure (2) (a,b)—two crystallographically independent units—and (3) (c).
Figure 4. Hirshfeld surfaces for the anions in structure (2) (a,b)—two crystallographically independent units—and (3) (c).
Ijms 24 13371 g004
Ijms 24 13371 g005
Figure 5. The shortest contacts of RuNO and nitroxide fragments in structure (2) (a–c) and (3) (d,e).
Figure 5. The shortest contacts of RuNO and nitroxide fragments in structure (2) (a–c) and (3) (d,e).
Ijms 24 13371 g005
Ijms 24 13371 g006
Figure 6. Mass spectra of the acetonitrile solutions of (2) and (3). The assignment of the main forms corresponds to Table 2. Experimental and calculated isotopic distribution patterns (red lines) corresponding to the [RuNOCl4L]− form are shown on the insets.
Figure 6. Mass spectra of the acetonitrile solutions of (2) and (3). The assignment of the main forms corresponds to Table 2. Experimental and calculated isotopic distribution patterns (red lines) corresponding to the [RuNOCl4L]− form are shown on the insets.
Ijms 24 13371 g006
Ijms 24 13371 g007
Figure 7. Cyclic voltammogram of a solution of 2.0 mM of (2) (a) and (3) (b) in acetonitrile containing 0.1 m TBAPF6 using a glassy carbon electrode with different scan rates. The arrows show the redox peaks mentioned in Table 3.
Figure 7. Cyclic voltammogram of a solution of 2.0 mM of (2) (a) and (3) (b) in acetonitrile containing 0.1 m TBAPF6 using a glassy carbon electrode with different scan rates. The arrows show the redox peaks mentioned in Table 3.
Ijms 24 13371 g007
Ijms 24 13371 g008
Figure 8. The µeff(T) dependencies for complexes (1) (a) and (3) (b). Solid lines are theoretical curves.
Figure 8. The µeff(T) dependencies for complexes (1) (a) and (3) (b). Solid lines are theoretical curves.
Ijms 24 13371 g008
Ijms 24 13371 sch001
Scheme 1. The ligands used in the investigation.
Scheme 1. The ligands used in the investigation.
Ijms 24 13371 sch001
Table 1. Selected parameters in the structure of (1)–(3).
Table 1. Selected parameters in the structure of (1)–(3).
ParameterNaRuNOCl4L 1 (1) [19]NaRuNOCl4L 1 (2)NaRuNOCl4L 2 (3)
d (Ru-Cl), Å2.349(1)–2.398(1)2.345(1)–2.382(1)2.347(1)–2.400(1)
d (Ru-NL), Å2.102(3)2.111(2)–2.118(2)2.110(4)
d (Ru-NO), Å1.726(3)1.736(3)–1.752(3)1.799(4)
d (RuN-O), Å1.133(4)1.110(3)–1.124(3)1.011(5)
∠Ru-N-O, °178.1(3)173.6(3)–179.0(3)177.8(4)
d (N-O(L)), Å1.275(3)–1.303(3)1.273(3)–1.296(3)1.260(5)–1.272(5)
∠NN-Py *, °49.5(4)41.0(4), 48.2(4)33.5(2)
* An interplane angle between the pyridine ring and C1N2O2 plane of the nitroxide fragment.
Table 2. Main assigned forms in the mass-spectra (negative ions) of (2) and (3).
Table 2. Main assigned forms in the mass-spectra (negative ions) of (2) and (3).
Complex Forms(2)(3)
m/z
RuNOCl4274274
RuNOCl4L− (A)508508
(A)-O492492
NaRuNOCl4(RuNOCl4L) (B)805805
Na(RuNOCl4L)2 (C)10391039
(C)-O10231023
(C) + CH3CN-1080
Na2(RuNOCl4L)3 (D)15681568
Na3(RuNOCl4L)4 (E)2068-
Table 3. Electrochemical characteristics of (2) and (3) and the corresponding assigned processes.
Table 3. Electrochemical characteristics of (2) and (3) and the corresponding assigned processes.
Scan Rate, V/sEpc, VEpa, V
N-O·→ N-O−N+ = O → N-O·N-O− → N-O·N-O → N+ = O·(Ru2+-NO+) →(Ru3+-NO+)
Complex (2)
0.1−0.750.88ND1.261.36
0.25−1.140.86−0.650.971.28
0.5−1.130.86−0.640.981.31
Complex (3)
0.1−0.730.93ND1.241.39
0.25−1.090.92−0.681.011.23
0.5−1.100.90−0.671.001.26
Table 4. Crystal data and structure refinement.
Table 4. Crystal data and structure refinement.
(2)(3)
Empirical formulaC28H38Cl8N10Na2O6Ru2C12H18Cl4N4NaO4Ru
Formula weight1142.40548.16
Crystal systemtriclinicorthorhombic
Space groupP-1P212121
a/Å10.4158(2)6.9913(2)
b/Å10.8548(2)15.1057(3)
c/Å20.9285(4)18.7215(5)
α/°99.831(1)90
β/°94.477(1)90
γ/°109.036(1)90
Volume/Å32181.12(7)1977.15(9)
Z24
ρcalcg/cm31.7391.842
μ/mm−11.2541.381
F(000)1140.01092.0
2Θ range for data collection/°4.714 to 66.5023.464 to 66.392
Index ranges−16 ≤ h ≤ 16, −16 ≤ k ≤ 16, −32 ≤ l ≤ 29−10 ≤ h ≤ 10, −23 ≤ k ≤ 22, −28 ≤ l ≤ 28
Reflections collected43,67426,074
Independent reflections16,301 [Rint = 0.0452, Rsigma = 0.0718]7563 [Rint = 0.0388, Rsigma = 0.0426]
Data/restraints/parameters16,301/0/5157563/4/245
Goodness-of-fit on F20.8611.058
Final R indexes [I ≥ 2σ (I)]R1 = 0.0460, wR2 = 0.1217R1 = 0.0400, wR2 = 0.0838
Final R indexes [all data]R1 = 0.0835, wR2 = 0.1466R1 = 0.0486, wR2 = 0.0875
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

Kostin, G.A.; Kozlov, R.; Bogomyakov, A.; Tolstikov, S.; Sheven, D.; Korenev, S. New Ruthenium Nitrosyl Complexes Combining Potentially Photoactive Nitrosyl Group with the Magnetic Nitroxide Radicals as Ligands. Int. J. Mol. Sci. 2023, 24, 13371. https://doi.org/10.3390/ijms241713371

AMA Style

Kostin GA, Kozlov R, Bogomyakov A, Tolstikov S, Sheven D, Korenev S. New Ruthenium Nitrosyl Complexes Combining Potentially Photoactive Nitrosyl Group with the Magnetic Nitroxide Radicals as Ligands. International Journal of Molecular Sciences. 2023; 24(17):13371. https://doi.org/10.3390/ijms241713371

Chicago/Turabian Style

Kostin, Gennadiy A., Ruslan Kozlov, Artem Bogomyakov, Svyatoslav Tolstikov, Dmitriy Sheven, and Sergey Korenev. 2023. "New Ruthenium Nitrosyl Complexes Combining Potentially Photoactive Nitrosyl Group with the Magnetic Nitroxide Radicals as Ligands" International Journal of Molecular Sciences 24, no. 17: 13371. https://doi.org/10.3390/ijms241713371

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