Synthesis and Structure of Heterometallic Compounds with Dimethyl Pyridine-2,6-dicarboxylate
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BULHAK, Ion, URECHE, Dumitru, KRAVTSOV, Victor, BOUROSH, Pavlina. Synthesis and Structure of Heterometallic Compounds with Dimethyl Pyridine-2,6-dicarboxylate. In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 2023, vol. 49, pp. 77-85. ISSN -. DOI: https://doi.org/10.1134/S1070328422700245
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Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
Volumul 49 / 2023 / ISSN - /ISSNe 1070-3284

Synthesis and Structure of Heterometallic Compounds with Dimethyl Pyridine-2,6-dicarboxylate

DOI:https://doi.org/10.1134/S1070328422700245

Pag. 77-85

Bulhak Ion1, Ureche Dumitru1, Kravtsov Victor2, Bourosh Pavlina2
 
1 Institute of Chemistry, MSU,
2 Institute of Applied Physics, MSU
 
 
Disponibil în IBN: 8 iunie 2023


Rezumat

Dimethyl pyridine-2,6-carboxylate (L) was prepared by refluxing pyridine-2,6-dicarbonyl dichloride in methanol. The reactions of L with Ca(II), Sr(II), and Ba(II) salts and with cobalt(II) thiocyanate resulted in the formation of three heterometallic complexes: [CaL3][Co(NCS)4] (I), [SrL3][Co(NCS)4] (II), and [BaCoL3(μ-NCS)2(NCS-κN)2] (III). The composition and structure of compounds L and I–III were determined by elemental analysis, infrared spectroscopy, and X-ray diffraction (CCDC nos. 2166019–2166022, respectively). It was found that isostructural Ca(II) and Sr(II) compounds are ionic and are formed by the [CaL3]2+ and [SrL3]2+ complex cations and [Co(SCN)4]2– complex anion, while the Ba(II) derivative is a molecular complex in which [BaL3]2+ and [Co(NCS)4]2– moieties are linked by two (NCS) bridging units of the complex anions. In any of the three compounds, three tridentate L ligands are coordinated to the alkaline earth metal ion. 

Cuvinte-cheie
and Ba(II)/Cо(II) complexes, dimethyl pyridine-2, 6-dicarboxylate, heterometallic Ca(II), IR spectra, Sr(II), X-ray diffraction

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<titles>
<title xml:lang='en'>Synthesis and Structure of Heterometallic Compounds with Dimethyl Pyridine-2,6-dicarboxylate</title>
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<subject>and Ba(II)/Cо(II) complexes</subject>
<subject>dimethyl pyridine-2</subject>
<subject>6-dicarboxylate</subject>
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<subject>IR spectra</subject>
<subject>Sr(II)</subject>
<subject>X-ray diffraction</subject>
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<description xml:lang='en' descriptionType='Abstract'><p>Dimethyl pyridine-2,6-carboxylate (L) was prepared by refluxing pyridine-2,6-dicarbonyl dichloride in methanol. The reactions of L with Ca(II), Sr(II), and Ba(II) salts and with cobalt(II) thiocyanate resulted in the formation of three heterometallic complexes: [CaL<sub>3</sub>][Co(NCS)<sub>4</sub>] (I), [SrL<sub>3</sub>][Co(NCS)<sub>4</sub>] (II), and [BaCoL<sub>3</sub>(&mu;-NCS)<sub>2</sub>(NCS-&kappa;N)<sub>2</sub>] (III). The composition and structure of compounds L and I&ndash;III were determined by elemental analysis, infrared spectroscopy, and X-ray diffraction (CCDC nos. 2166019&ndash;2166022, respectively). It was found that isostructural Ca(II) and Sr(II) compounds are ionic and are formed by the [CaL<sub>3</sub>]<sup>2+</sup>&nbsp;and [SrL<sub>3</sub>]<sup>2+</sup>&nbsp;complex cations and [Co(SCN)<sub>4</sub>]<sup>2&ndash;</sup>&nbsp;complex anion, while the Ba(II) derivative is a molecular complex in which [BaL<sub>3</sub>]<sup>2+</sup>&nbsp;and [Co(NCS)<sub>4</sub>]<sup>2&ndash;</sup>&nbsp;moieties are linked by two (NCS)<sup>&ndash;</sup>&nbsp;bridging units of the complex anions. In any of the three compounds, three tridentate L ligands are coordinated to the alkaline earth metal ion.&nbsp;</p></description>
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