L. J. Zhang, X. T. Zhai, Z. K. Li, B. J. Zhao, Z. H. Wang, X. Ma, Z. Q. Cai
{"title":"An Anderson-Type Nickel-Substituted Arsenomolybdate for Rapid Adsorption and Selective Separation of Methylene Blue","authors":"L. J. Zhang, X. T. Zhai, Z. K. Li, B. J. Zhao, Z. H. Wang, X. Ma, Z. Q. Cai","doi":"10.1134/S1070328425601001","DOIUrl":"10.1134/S1070328425601001","url":null,"abstract":"<p>The separation of mixtures derived from various dyes remains a significant challenge in the fields of chemical synthesis and pollutant treatment. In this paper, an arsenomolybdate (NH<sub>4</sub>)<sub>3</sub>[H(NiO<sub>6</sub>)Mo<sub>6</sub>O<sub>18</sub>(As<sub>3</sub>O<sub>3</sub>)<sub>2</sub>] (<b>I</b>) has been synthesized and characterized successfully. The structure of <b>I</b> was comprehensively analyzed using single crystal X-ray diffraction (SXRD), X-ray powder diffraction (XRPD), elemental analysis revealed that <b>I</b> is an ionic compound, comprising the anion [H(NiO<sub>6</sub>)Mo<sub>6</sub>O<sub>18</sub>(As<sub>3</sub>O<sub>3</sub>)<sub>2</sub>]<sup>3–</sup> and three counter cations <span>({text{NH}}_{4}^{ + })</span>. Notably, <b>I</b> exhibits efficient and selective adsorption of Methylene Blue (MB), allowing its separation from other dyes. Furthermore, <b>I</b> exhibited good stability and recyclability in the adsorption of Methylene Blue, which was confirmed by five cycle tests. This research presents a viable strategy for the effective separation of Methylene Blue from dye mixtures.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 12","pages":"1095 - 1102"},"PeriodicalIF":1.1,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147588542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
V. M. Korshunov, V. E. Gontcharenko, D. A. Metlina, M. M. Islamov, A. I. Ferulev, I. V. Taydakov
{"title":"Complexes Eu(III) and Gd(III) with 1-([1,1'-Biphenyl]-4-yl)-4,4,4-trifluorobutane-1,3-dione: π-Stacking and Luminescence Properties","authors":"V. M. Korshunov, V. E. Gontcharenko, D. A. Metlina, M. M. Islamov, A. I. Ferulev, I. V. Taydakov","doi":"10.1134/S1070328425601347","DOIUrl":"10.1134/S1070328425601347","url":null,"abstract":"<p>Two new coordination compounds of europium(III) and gadolinium(III) with biphenyl-substituted β-diketone and 1,10-phenanthroline (Phen) ligands, [Eu(BPhTFB)<sub>3</sub>(Phen)] and [Gd(BPhTFB)(Phen)] (HBPhTFB = 1-([1,1′-biphenyl]-4-yl)-4,4,4-trifluorobutane-1,3-dione), have been synthesized and comprehensively studied. The introduction of a biphenyl fragment into the β-diketone ligand extends the π-conjugation system and enhances light absorption in the near-visible region, while the use of Phen as an ancillary ligand eliminates inner-sphere water or alcohol molecules that typically cause luminescence quenching. Structural studies revealed that the biphenyl moiety adopts a twisted conformation, enabling π–π stacking interactions with the phenanthroline ligand. This stacking leads to the formation of intermolecular charge-transfer states, as evidenced by features observed in the excitation spectra. The europium complex [Eu(BPhTFB)(Phen)] exhibits intense red emission characteristic of the <sup>5</sup><i>D</i><sub>0</sub> → <sup>7</sup><i>F</i><sub><i>J</i></sub> transitions, with an internal quantum yield of 57% and an overall luminescence quantum yield of 32%. The gadolinium analogue serves as a non-luminescent reference, confirming the ligand-centered origin of the sensitization process. The combined structural and photophysical data demonstrate that introducing extended aromatic substituents and appropriate ancillary ligands effectively enhances the luminescence performance of europium β-diketonate complexes, making them promising candidates for use in photonic and sensing applications.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 12","pages":"1067 - 1073"},"PeriodicalIF":1.1,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147588545","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. O. Tolpygin, A. V. Cherkasov, G. K. Fukin, Y. V. Nelyubina, A. A. Trifonov
{"title":"Y3+ and Nd3+ Complexes Coordinated by ansa-Bis(amidinate) Ligands. Synthesis, Structural Features, and Catalytic Performance in Ring-Opening Polymerization of rac-Lactide and ε-Caprolactone","authors":"A. O. Tolpygin, A. V. Cherkasov, G. K. Fukin, Y. V. Nelyubina, A. A. Trifonov","doi":"10.1134/S1070328425601335","DOIUrl":"10.1134/S1070328425601335","url":null,"abstract":"<p>The reaction of equimolar amounts of disodium derivative of <i>ansa</i>-bis(amidine) (L<sup>1</sup>Na<sub>2</sub>) (L<sup>1</sup> = [C<sub>6</sub>H<sub>4</sub>-1,2-{NC(Bu<sup><i>t</i></sup>)N(2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)}<sub>2</sub>]<sup>2–</sup>) with [YCl<sub>2</sub>(N(SiMe<sub>3</sub>)<sub>2</sub>)] affords the tris(amidinate) complex Y{κ<sup>4</sup>-L<sup>1</sup>}{κ<sup>2</sup>-L<sup>amd</sup>} (2) (L<sup>amd</sup> = ((2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>N)<sub>2</sub>CBu<sup><i>t</i></sup>)<sup>–</sup>). For the bulkier analogue the reactions of L<sup>2</sup>Na<sub>2</sub> (L<sup>2</sup> = [C<sub>6</sub>H<sub>4</sub>-1,2-{NC(Bu<sup><i>t</i></sup>)N(2,6-Pr<sup><i>i</i></sup><sub>2</sub>C<sub>6</sub>H<sub>3</sub>)}<sub>2</sub>]<sup>2–</sup>) with [LnCl<sub>2</sub>(N(SiMe<sub>3</sub>)<sub>2</sub>)] (Ln = Y, Nd) led to the formation of ionic compounds [Na(DME)<sub>3</sub>][Nd{κ<sup>3</sup>-L<sup>2</sup>}{κ<sup>2</sup>-L<sup>2</sup>}] (<b>3</b>) and [Na(DME)<sub>3</sub>][Y{κ<sup>3</sup>-L<sup>2</sup>}<sub>2</sub>] (<b>4</b>) featuring different types of coordination of <i>ansa</i>-bis(amidinate) ligands. Complexes <b>2</b>–<b>4</b> proved to be efficient catalysts for <i>rac</i>-lactide polymerization. Complexes <b>3</b> and <b>4</b> in the presence of Pr<sup><i>i</i></sup>OH allow to perform controlled polymerization and obtaining PLAs with molecular weights close to the theoretical ones. Complexes <b>2</b>–<b>4</b> are also active in ε-caprolactone polymerization achieving full conversion of up to 500 equivalents of ε-CL in 1–10 min giving polycaprolactone samples characterized by high M<sub>n</sub> (34.9–542.0 × 10<sup>3</sup>) and somewhat broaden molecular weight distribution <i>M</i><sub>w</sub>/<i>M</i><sub>n</sub> = 1.31–2.61.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 12","pages":"1187 - 1199"},"PeriodicalIF":1.1,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147588541","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
P. A. Egorov, T. A. Tripol’skaya, E. A. Mel’nik, A. A. Mikhaylov, P. V. Prikhodchenko
{"title":"Synthesis and Crystal Structure of Triphenylgermanium Cumylperoxide","authors":"P. A. Egorov, T. A. Tripol’skaya, E. A. Mel’nik, A. A. Mikhaylov, P. V. Prikhodchenko","doi":"10.1134/S1070328425601591","DOIUrl":"10.1134/S1070328425601591","url":null,"abstract":"<p>The triphenylgermanium cumylperoxide, Ph<sub>3</sub>GeOOCm was synthesized and characterized using single-crystal X-ray diffraction (scXRD), powder X-ray diffraction (PXRD), FTIR and Raman spectroscopy, thermal analysis, and elemental analysis. According to the single-crystal X-ray diffraction analysis triphenylgermanium cumylperoxide crystallizes in the triclinic <span>(Pbar {1})</span> space group with <i>Z</i> = 2. The stability of Ph<sub>3</sub>GeOOCm complex to hydrolysis was characterized by <sup>1</sup>H NMR spectroscopy in toluene, DMSO, and DMF.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 12","pages":"1074 - 1081"},"PeriodicalIF":1.1,"publicationDate":"2026-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147588543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. S. Vikulova, K. P. Cheremnykh, A. S. Sukhikh, I. Yu. Ilyin, A. A. Vinogradova, D. P. Pishchur, N. B. Morozova
{"title":"N-Benzyloxycarboxamides and Their Zirconium Complexes: Synthesis, Structures, and Thermal Properties","authors":"E. S. Vikulova, K. P. Cheremnykh, A. S. Sukhikh, I. Yu. Ilyin, A. A. Vinogradova, D. P. Pishchur, N. B. Morozova","doi":"10.1134/S1070328425601049","DOIUrl":"10.1134/S1070328425601049","url":null,"abstract":"<p><i>N</i>-Benzyloxycarboxamides (HL) and corresponding zirconium(IV) complexes [Zr(L)<sub>4</sub>] (L = R'C(O)NOR, R = CH<sub>2</sub>–C<sub>6</sub>H<sub>5</sub>; R' = CH<sub>3</sub> for L = baa or R' = C<sub>6</sub>H<sub>5</sub> for L = bba) are synthesized and characterized to reveal the influence of the aromatic substituent on the structures and thermal properties. The structures of Hbba, [Zr(baa)<sub>4</sub>], and [Zr(bba)<sub>4</sub>] (CIF files CCDC nos. 2 474 365, 2 474 366, and 2 474 367, respectively) are determined by single-crystal X-ray diffraction (SC-XRD) and compared with those of <i>N</i>‑methoxybenzamide analogues Hmba and [Zr(mba)<sub>4</sub>] (R = CH<sub>3</sub>, R' = C<sub>6</sub>H<sub>5</sub>). The compounds are also studied by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). The thermodynamic parameters for melting of Hbba and [Zr(baa)<sub>4</sub>] have been determined for the first time. In the [Zr(L)<sub>4</sub>] complexes, the introduction of the benzyl group into L results in the disappearance of the low-temperature structural transitions (L = mba) and a decrease in the melting points (L = baa, bba). The melting points of <i>N‑</i>alkoxybenzamides increase in the order L = mba < bba. Under the TGA conditions at comparable molecular weights, the [Zr(mba)<sub>4</sub>] complex partially evaporates, whereas [Zr(baa)<sub>4</sub>] decomposes.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 10","pages":"936 - 946"},"PeriodicalIF":1.1,"publicationDate":"2026-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145993644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. A. Ermakova, Yu. A. Golubeva, K. S. Smirnova, P. E. Savinykh, N. F. Romashev, L. S. Klyushova, E. Yu. Zyryanova, I. A. Utepova, E. V. Lider
{"title":"Zinc(II) Complex with 2-Ferrocenyl-1,10-phenanthroline: Synthesis, Structure, Study of Electrochemical and Cytotoxic Properties","authors":"E. A. Ermakova, Yu. A. Golubeva, K. S. Smirnova, P. E. Savinykh, N. F. Romashev, L. S. Klyushova, E. Yu. Zyryanova, I. A. Utepova, E. V. Lider","doi":"10.1134/S1070328425601293","DOIUrl":"10.1134/S1070328425601293","url":null,"abstract":"<p>The reaction of zinc(II) nitrate with 2-ferrocenyl-1,10-phenanthroline (L) produced the complex [ZnL(NO<sub>3</sub>)<sub>2</sub>] (<b>I</b>), which was analyzed by elemental analysis, powder X-ray diffraction, thermogravimetric analysis, cyclic voltammetry, and IR spectroscopy. According to the single-crystal X-ray diffraction analysis, the coordination environment of zinc(II) can be described as 5 + 1, and L acts as a chelating ligand that binds to the zinc(II) atom through the nitrogen atoms of the phenanthroline moiety. The cytotoxic properties of complex <b>I</b> were evaluated using the human two-dimensional cell lines Hep2 (laryngeal carcinoma cells), A549 (lung adenocarcinoma cells), and MRC5 (nontumor lung fibroblasts). Complex <b>I</b> exhibited cytotoxicity at concentrations between 50 and 100 μM. The activity of complex <b>I</b> in Hep2 spheroids (3D model) was found to be comparable to that in the two-dimensional model. The behavior of the complex in solution was studied using optical spectroscopy, conductometry, and cyclic voltammetry.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 10","pages":"867 - 877"},"PeriodicalIF":1.1,"publicationDate":"2026-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145993710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
N. A. Shimin, L. B. Serezhkina, M. S. Grigoriev, A. V. Savchenkov, V. N. Serezhkin
{"title":"Features of Noncovalent Interactions in the Structures of New Uranyl Methacrylates R[UO2(C4H5O2)3], Where R = ({{({text{C}}{{{text{H}}}_{{text{3}}}})}_{2}}{text{NH}}_{2}^{ + }) or ({{({{{text{C}}}_{2}}{{{text{H}}}_{{text{5}}}})}_{2}}{text{NH}}_{2}^{ + })","authors":"N. A. Shimin, L. B. Serezhkina, M. S. Grigoriev, A. V. Savchenkov, V. N. Serezhkin","doi":"10.1134/S107032842560113X","DOIUrl":"10.1134/S107032842560113X","url":null,"abstract":"<p>The crystals of R[UO<sub>2</sub>(mac)<sub>3</sub>]<sub>2</sub> (where R is (CH<sub>3</sub>)<sub>2</sub><span>({text{NH}}_{2}^{ + })</span> (<b>I</b>) or (C<sub>2</sub>H<sub>5</sub>)<sub>2</sub><span>({text{NH}}_{2}^{ + })</span> (<b>II</b>), and mac is methacrylate ion <span>({{{text{C}}}_{{text{4}}}}{{{text{H}}}_{{text{5}}}}{text{O}}_{{text{2}}}^{ - })</span>) are synthesized and studied by IR spectroscopy and X-ray diffraction (XRD) (CIF files CCDC nos. 2476810 (<b>I</b>) and 2476811 (<b>II</b>)). The [UO<sub>2</sub>(mac)<sub>3</sub>]<sup>–</sup> complexes have the crystallochemical formula А(B<sup>01</sup>)<sub>3</sub>, where A is <span>({text{UO}}_{2}^{{2 + }})</span>, and B<sup>01</sup> is mac. A comparative analysis of noncovalent interactions in the crystal structures of compounds <b>I</b> and <b>II</b> is carried out using the Voronoi–Dirichlet molecular polyhedra (VDMP) and Hirshfeld surface methods. The results of these independent methods are well consistent for both qualitative and quantitative estimations of intermolecular contacts. Only the VDMP method allows one to characterize in detail any interatomic contacts that contribute to the real range of intermolecular interactions.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 10","pages":"904 - 911"},"PeriodicalIF":1.1,"publicationDate":"2026-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145993709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. E. Bolot’ko, M. A. Shmelev, A. A. Bovkunova, A. A. Sidorov, I. L. Eremenko
{"title":"Effect of the Nature of N-Donor Ligands on the Structure of Mixed-Anion Europium Benzoate Pentafluorobenzoate Compounds","authors":"A. E. Bolot’ko, M. A. Shmelev, A. A. Bovkunova, A. A. Sidorov, I. L. Eremenko","doi":"10.1134/S1070328425601207","DOIUrl":"10.1134/S1070328425601207","url":null,"abstract":"<p>The study addresses mixed-anion Eu(III) complexes with benzoic (Bz) and pentafluorobenzoic (Pfb) acid anions and 2,2'-bipyridine(Bpy), 4,4'-dimethyl-2,2'-bipyridine (Me<sub>2</sub>Bpy), 4,4'-di-<i>tert-</i>butyl-2,2'-bipyridine (<i>t</i>-Bu<sub>2</sub>Bpy), 4,4'-dinonyl-2,2'-bipyridine(Nn<sub>2</sub>Bpy), and 3,4,7,8-tetramethyl-1,10-phenanthroline: [Eu<sub>2</sub>(Bpy)<sub>2</sub>(Pfb)<sub>2.4</sub>(Bz)<sub>3.6</sub>] (<b>I</b>), [Eu<sub>2</sub>(Me<sub>2</sub>Bpy)<sub>2</sub>(Pfb)<sub>2.5</sub>(Bz)<sub>3.5</sub>] (<b>II</b>), [Eu<sub>2</sub>(Nn<sub>2</sub>Bpy)<sub>2</sub>-(Pfb)<sub>3.5</sub>(Bz)<sub>2.5</sub>]·2MeCN (<b>III</b>), [Eu<sub>2</sub>(<i>t</i>-Bu<sub>2</sub>Bpy)<sub>2</sub>(Pfb)<sub>5.5</sub>(Bz)<sub>0.5</sub>]<sub><i>n</i></sub>·2<i>n</i>MeCN (<b>IV</b>), and [Eu<sub>2</sub>(Me<sub>4</sub>Phen)<sub>2</sub>-(Pfb)<sub>4.8</sub>(Bz)<sub>1.2</sub>]<sub><i>n</i></sub> (<b>V</b>). According to X-ray diffraction data, in the structures of all compounds, Bz<sup>–</sup> and Pfb<sup>–</sup> anions are refined simultaneously in various ratios in some anion sites. It was shown that varying the substituents in the N-donor ligands affects the composition and geometry of the formed complexes. The complexes were characterized by X-ray diffraction, IR spectroscopy, and CHN analysis. The structures and crystal packing of the obtained complexes were analyzed in detail. The major contribution to stabilization of the crystal packing is made by π···π, C–H···F, and C–F···π interactions.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 10","pages":"886 - 898"},"PeriodicalIF":1.1,"publicationDate":"2026-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1134/S1070328425601207.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145993711","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. S. Degtyareva, M. E. Minyaev, I. E. Nifant’ev, D. M. Roitershtein
{"title":"Yttrium Chloride Complexes with 1,3,5-Trimethyl-1,3,5-triazacyclohexane: Unprecedented Structural Diversity","authors":"S. S. Degtyareva, M. E. Minyaev, I. E. Nifant’ev, D. M. Roitershtein","doi":"10.1134/S1070328425601177","DOIUrl":"10.1134/S1070328425601177","url":null,"abstract":"<p>Specific features of the structures of five various complexes [Y(Me<sub>3</sub>tach)Cl<sub>3</sub>(THF)<sub>2</sub>] (<b>I</b>), [Y(Me<sub>3</sub>tach)<sub>2</sub>Cl<sub>3</sub>] (<b>II</b>), [Y(Me<sub>3</sub>tach)Cl<sub>2</sub>(μ-Cl)<sub>2</sub>YCl<sub>2</sub>(THF)<sub>3</sub>] (<b>III</b>), [Y(Me<sub>3</sub>tach)Cl<sub>3</sub>(THF)]<sub>2</sub> (<b>IV</b>), and [Y(Me<sub>3</sub>tach)<sub>2</sub>Cl<sub>2</sub>]<sup>+</sup>[Y(Me<sub>3</sub>tach)Cl<sub>4</sub>]<sup>–</sup> (<b>V</b>) formed via the reaction of yttrium chloride tetrahydrofuranate with 1,3,5-trimethyl-1,3,5-triazacyclohexane (Me<sub>3</sub>tach) are compared. The molecular structures of newly synthesized complexes <b>IV</b> and <b>V</b> are determined by X-ray diffraction (XRD) (CIF files CCDC nos. 2484944 and 2484945, respectively). All complexes, except for complex <b>V</b>, demonstrate similar metal–ligand distances with a correction to the difference in coordination numbers regardless of the structure of the complex and metal to ligand ratio for both mono- and binuclear complexes.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 10","pages":"878 - 885"},"PeriodicalIF":1.1,"publicationDate":"2026-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145993712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
M. D. Gotsko, N. A. Korobeinikov, S. S. Opanasyuk, S. A. Adonin
{"title":"Heteroligand Co(II) and Cu(II) Complexes with 3,3-Bis(3,5-dimethylpyrazol-1-yl)-1-phenylpropan-1-one: Synthesis and Crystal Structure","authors":"M. D. Gotsko, N. A. Korobeinikov, S. S. Opanasyuk, S. A. Adonin","doi":"10.1134/S107032842560127X","DOIUrl":"10.1134/S107032842560127X","url":null,"abstract":"<p>The reaction of 3,3-bis(3,5-dimethylpyrazol-1-yl)-1-phenylpropan-1-one (L) with cobalt(II) chloride and copper(II) chloride yielded neutral, isostructural heteroligand complexes [LMCl<sub>2</sub>] with M = Co for <b>I</b> and M = Cu for <b>II</b>. Their structures were determined by direct X-ray diffraction methods (CCDC nos. 2478389 for <b>I</b>, 2478390 for <b>II</b>). In both complexes, the metal center has a tetrahedral coordination environment, and L coordinates to the metal ion in a bidentate manner.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 10","pages":"899 - 903"},"PeriodicalIF":1.1,"publicationDate":"2026-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145993728","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}