E. A. Khakina, I. A. Nikovskii, A. A. Danshina, E. P. Antoshkina, A. N. Rodionov, Yu. V. Nelyubina
{"title":"Synthesis of a New Cobalt Complex with Catechol Dianion and Study of the Kinetics of Its Redox-Activated Dissociation","authors":"E. A. Khakina, I. A. Nikovskii, A. A. Danshina, E. P. Antoshkina, A. N. Rodionov, Yu. V. Nelyubina","doi":"10.1134/S1070328424600669","DOIUrl":"10.1134/S1070328424600669","url":null,"abstract":"<p>A new redox-active cobalt(III) complex with a catechol dianion and two 4,4'-dimethoxy-2,2'-bipyridine ligands was synthesized. The reduction of the complex with ascorbic acid in an inert atmosphere was studied by NMR spectroscopy in situ. The reaction followed the first-order kinetics with respect to the starting complex, had a rate constant of 1.1 × 10<sup>–3</sup> s<sup>–1</sup>, and was accompanied by the release of catechol, which served as a model drug.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 10","pages":"791 - 801"},"PeriodicalIF":1.1,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142790358","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. S. Samulionis, J. K. Voronina, S. N. Melnikov, A. S. Gavronova, D. A. Utepova, N. V. Gogoleva, A. S. Goloveshkin, D. S. Yambulatov, S. A. Nikolaevskii, M. A. Kiskin, I. L. Eremenko
{"title":"Synthesis and X-ray Structures of Polymeric Calcium Carboxylates","authors":"A. S. Samulionis, J. K. Voronina, S. N. Melnikov, A. S. Gavronova, D. A. Utepova, N. V. Gogoleva, A. S. Goloveshkin, D. S. Yambulatov, S. A. Nikolaevskii, M. A. Kiskin, I. L. Eremenko","doi":"10.1134/S1070328424601043","DOIUrl":"10.1134/S1070328424601043","url":null,"abstract":"<p>The reactions of calcium hydroxide with pivalic, 1-naphthoic, and 2-furancarboxylic acids afford the corresponding polymeric calcium carboxylates. Depending on the crystallization conditions, calcium pivalate is isolated as two different coordination polymers: [Ca<sub>3</sub>(Piv)<sub>6</sub>(DMF)<sub>2</sub>]<sub><i>n</i></sub>·0.635<i>n</i>C<sub>6</sub>H<sub>6</sub>·0.365<i>n</i>DMF (<b>I</b>) and [Ca(Рiv)(H<sub>2</sub>O)<sub>2.333</sub>(DMF)<sub>0.666</sub>]<sub><i>n</i></sub>·<i>n</i>Рiv·0.333H<sub>2</sub>O (<b>II</b>). The synthesized calcium 1-naphthoate contains coordinated water molecules [Сa(Naph)<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>]<sub><i>n</i></sub> (<b>III</b>), and calcium furoate [Ca(Fur)<sub>2</sub>]<sub><i>n</i></sub> (<b>IV</b>) contains no ancillary ligands. The structures of compounds <b>I</b>–<b>IV</b> are determined by X-ray diffraction (XRD) (CIF files CCDC nos. 2342790–2342793, respectively). The structures of compounds <b>I</b>–<b>III</b> are characterized by the 1D polymeric structure, and compound <b>IV</b> is the 3D polymer.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 9","pages":"757 - 767"},"PeriodicalIF":1.1,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142790365","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}
{"title":"Octahedral Halide Clusters of Niobium and Tantalum Bearing the Cluster Core {M6X12}","authors":"M. V. Shamshurin, M. N. Sokolov","doi":"10.1134/S1070328424600384","DOIUrl":"10.1134/S1070328424600384","url":null,"abstract":"<p>Synthesis methods, molecular and electronic structures, and reactivity of the family of the octahedral clusters of niobium and tantalum halides bearing the {M<sub>6</sub>X<sub>12</sub>} cluster core are reviewed. Possible fields of the practical use of this class of compounds are considered.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 9","pages":"620 - 635"},"PeriodicalIF":1.1,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142790366","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}
I. A. Shentseva, A. N. Usol’tsev, N. A. Korobeinikov, S. A. Adonin
{"title":"1D Polymeric Iodoantimonates(III) with 1-Methylpyridinium and 3-Bromo-1-methylpyridinium Cations: Structures and Properties","authors":"I. A. Shentseva, A. N. Usol’tsev, N. A. Korobeinikov, S. A. Adonin","doi":"10.1134/S1070328424600700","DOIUrl":"10.1134/S1070328424600700","url":null,"abstract":"<p>The reactions of SbI<sub>3</sub> with iodides of cations of the pyridinium family in a mixture of acetonitrile and acetone afford two polymeric iodoantimonate complexes: (1-MePy){[SbI<sub>4</sub>]} (<b>I</b>) and (3-Br-1-MePy){[SbI<sub>4</sub>]} (<b>II</b>). Specific features of the crystal structures are determined by X-ray diffraction (XRD). The thermal stability of compounds <b>I</b> and <b>II</b> is evaluated by thermogravimetry. The optical forbidden bandgaps are estimated from the diffuse reflectance spectra.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 10","pages":"809 - 816"},"PeriodicalIF":1.1,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142790423","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. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, D. N. Dybtsev
{"title":"Cadmium(II)-Organic Frameworks with the Polynuclear Unit: Dimensionality Control and Luminescence Response to Pyridine","authors":"V. A. Dubskikh, A. A. Lysova, D. G. Samsonenko, D. N. Dybtsev","doi":"10.1134/S1070328424600864","DOIUrl":"10.1134/S1070328424600864","url":null,"abstract":"<p>New porous metal-organic frameworks (MOF) [Cd<sub>7</sub>(Btdc)<sub>7</sub>(Bpa)<sub>2</sub>(Dmf)<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>]·15Dmf·2H<sub>2</sub>O (<b>I</b>) and [Cd<sub>7</sub>(Btdc)<sub>7</sub>(Bpe)<sub>2</sub>(Dmf)<sub>2</sub>]·15Dmf·3H<sub>2</sub>O (<b>II</b>) (H<sub>2</sub>Btdc is 2,2′-bithiophene-5,5′-dicarboxylic acid, Bpa is 1,2-bis(4-pyridyl)ethane, Bpe is 1,2-bis(4-pyridyl)ethylene, and Dmf is <i>N</i>,<i>N</i>-dimethylformamide) are synthesized under solvatothermal conditions. The structures and compositions of the compounds are determined by single-crystal X-ray diffraction (XRD) (CIF files ССDС nos. 2364290 (<b>I</b>) and 2364289 (<b>II</b>)) and confirmed by powder XRD, elemental analysis, thermogravimetry, and IR spectroscopy. Compound <b>I</b> has a 2D structure based on the heptanuclear discrete building unit {Cd<sub>7</sub>} with the linear structure. Compound <b>II</b> is a 3D MOF in which the {Cd<sub>7</sub>} building units are linked into a continuous chain motif due to additional interactions. The formation of either discrete or continuous chains is directly related to the nature of the N-donor bridging ligand (Bpe or Bpa). Compounds <b>I</b> and <b>II</b> have open structures with the accessible volume about 50%. The solvate molecules are replaced by thiophene, benzene, and pyridine, and the luminescence properties of the prepared adducts are studied. Luminescence quenching in the presence of thiophene and an increase in the luminescence intensity in the presence of pyridine accompanied by a change in the quantum yield by 4–5 times are shown.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 9","pages":"653 - 661"},"PeriodicalIF":1.1,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142790425","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}
K. A. Vinogradova, M. I. Rakhmanova, M. D. Taigina, N. V. Pervukhina, D. Yu. Naumov, V. A. Sannikova, I. R. Filippov, D. S. Kolybalov, A. Yu. Vorob’ev
{"title":"Heteroleptic Ionic Copper(I) Complexes Based on Pyrazolo[1,5-a][1,10]phenanthrolines: Synthesis, Structure, and Photoluminescence","authors":"K. A. Vinogradova, M. I. Rakhmanova, M. D. Taigina, N. V. Pervukhina, D. Yu. Naumov, V. A. Sannikova, I. R. Filippov, D. S. Kolybalov, A. Yu. Vorob’ev","doi":"10.1134/S1070328424600657","DOIUrl":"10.1134/S1070328424600657","url":null,"abstract":"<p>Heteroleptic copper(I) tetrafluoroborate complexes with pyrazolo[1,5-<i>a</i>][1,10]phenanthrolines (L<sup><i>n</i></sup>, <i>n</i> = 1–3) and bis[(2-diphenylphosphino)phenyl] ether (POP) were synthesized and structurally characterized. The coordination compounds with the general formula [CuL<sup><i>n</i></sup>(POP)]BF<sub>4</sub>·Solv (<i>n</i> = 1, Solv = 0.5MeCN, complex <b>I</b>; <i>n</i> = 2, Solv = 0.5CH<sub>2</sub>Cl<sub>2</sub>, complex <b>II</b>; <i>n</i> = 3, Solv = 1.25Et<sub>2</sub>O, complex <b>III</b>·Et<sub>2</sub>O) were prepared by the reaction of CuBF<sub>4</sub> with L<sup><i>n</i></sup> and POP in organic solvents (MeCN/CH<sub>2</sub>Cl<sub>2</sub>/Et<sub>2</sub>O) at 1 : 1 : 1 molar ratio. Compound <b>III</b>·Et<sub>2</sub>O gradually loses solvate molecules to be converted to the complex [CuL<sup>3</sup>(POP)]BF<sub>4</sub> (<b>III</b>). According to single-crystal X-ray diffraction data, the complexes (<b>I</b>, <b>II</b>, <b>III</b>·Et<sub>2</sub>O) are ionic; in complex cation [CuLn(POP)]<sup>+</sup> the coordination environment of the copper atom is a distorted tetrahedron with CuN<sub>2</sub>P<sub>2</sub> chromophore. The photoluminescence properties of the obtained complexes (<b>I</b>–<b>III</b>) were studied in the solid state and in solution. In the absorption spectra of the complexes, a charge transfer band is observed at 380–385 nm; excitation in this range gives rise to two emission bands at 480 and 650 nm in solution. In the solid state, the complexes show photoluminescence only in the red range (λ<sub>max</sub> = 600–610 nm) with microsecond lifetimes. It was found that complexes <b>I</b> and <b>III</b> with a more perfect tetrahedral environment have quantum yields an order of magnitude higher than the quantum yield observed for complex <b>II</b>.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 8","pages":"567 - 578"},"PeriodicalIF":1.1,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142595487","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. E. Bardina, E. V. Makotchenko, K. P. Birin, E. S. Shremzer, P. A. Abramov, Yu. G. Gorbunova, A. L. Gushchin
{"title":"Synthesis and Structure of Gold(III) Compounds with i-Pr- and t-Bu-Substituted Tetraarylporphyrins","authors":"E. E. Bardina, E. V. Makotchenko, K. P. Birin, E. S. Shremzer, P. A. Abramov, Yu. G. Gorbunova, A. L. Gushchin","doi":"10.1134/S1070328424600591","DOIUrl":"10.1134/S1070328424600591","url":null,"abstract":"<p>Gold(III) compounds with tetrakis(4-<i>tert</i>-butylphenyl)porphyrin, [Au(TTBPP)][AuCl<sub>4</sub>] (<b>I</b>), and with tetrakis(4-isopropylphenyl)porphyrin, [Au(TIPPP)][AuCl<sub>4</sub>] (<b>II</b>), were synthesized for the first time. The obtained compounds were characterized by elemental analysis, <sup>1</sup>H NMR spectroscopy, cyclic voltammetry, and X-ray diffraction analysis of solvated complexes (CCDC no. 2333206 (<b>Ia</b>) and 2333207 (<b>IIa</b>)). Study of the structures of the obtained gold(III) complexes confirmed their specific character consisting in the formation of additional Au⋯Au and Au⋯Cl contacts between neighboring complexes giving weak intermolecular bonds.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 8","pages":"579 - 586"},"PeriodicalIF":1.1,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142595458","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. V. Avdeeva, A. S. Kubasov, I. V. Kozerozhets, S. E. Nikiforova, E. A. Malinina, N. T. Kuznetsov
{"title":"Synthesis and Structures of Mixed-Ligand Lead(II) Complexes with Decahydro-closo-decaborate Anion and Azheterocyclic Ligands","authors":"V. V. Avdeeva, A. S. Kubasov, I. V. Kozerozhets, S. E. Nikiforova, E. A. Malinina, N. T. Kuznetsov","doi":"10.1134/S1070328424600517","DOIUrl":"10.1134/S1070328424600517","url":null,"abstract":"<p>Lead(II) complexation reactions were studied in the presence of salts of the <i>closo</i>-decaborate anion [B<sub>10</sub>H<sub>10</sub>]<sup>2–</sup> and azaheterocyclic ligands 2,2'-bipyridyl (bipy) or 1,10-phenanthroline (phen) in water and organic solvents (acetonitrile, DMF). Binuclear complex Pb(bipy)<sub>2</sub>[B<sub>10</sub>H<sub>10</sub>] and polymer complex [Pb(phen)[B<sub>10</sub>H<sub>10</sub>]] were isolated. The effect of solvents and reagent ratios on the composition and structures of the final complexes was studied. The complex compounds were identified by elemental analysis, IR spectroscopy, and X-ray powder diffraction. The structure of complex [Pb(bipy)<sub>2</sub>[B<sub>10</sub>H<sub>10</sub>]]<sub>2</sub>·2CH<sub>3</sub>CN (CCDC no. 2325841) was determined by single-crystal X-ray diffraction.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 8","pages":"587 - 594"},"PeriodicalIF":1.1,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142595459","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. Bazhina, M. A. Shmelev, M. A. Kiskin, I. L. Eremenko
{"title":"Coordination Polymers Ca(II)–Cr(III) and Ba(II)–Cr(III) with Cyclobutane-1,1-dicarboxylic Acid Anions","authors":"E. S. Bazhina, M. A. Shmelev, M. A. Kiskin, I. L. Eremenko","doi":"10.1134/S1070328424600566","DOIUrl":"10.1134/S1070328424600566","url":null,"abstract":"<p>The reactions of Cr(NO<sub>3</sub>)<sub>3</sub>·9H<sub>2</sub>O with barium and calcium salts of cyclobutane-1,1-dicarboxylic acid (H<sub>2</sub>Cbdc) in a ratio of 1 : 3 in an aqueous solution are studied. The reaction products isolated in the crystalline state are shown to be compounds formed by the binuclear tetraanionic units [Cr<sub>2</sub>(OH)<sub>2</sub>(Cbdc)<sub>4</sub>]<sup>4–</sup>, and the nature of the alkaline-earth metal ion introduced into the synthesis affects the dimensionality of the formed polymeric structure. The 2D polymeric compound {[Ba<sub>2</sub>Cr<sub>2</sub>(OH)<sub>2</sub>(Cbdc)<sub>4</sub>(H<sub>2</sub>O)<sub>5</sub>]·3H<sub>2</sub>O}<sub><i>n</i></sub> (<b>I</b>) is formed in the reaction with Ba(Cbdc), and the replacement of Ba<sup>2+</sup> by Ca<sup>2+</sup> results in the formation of the 1D coordination polymer {[Ca<sub>2</sub>Cr<sub>2</sub>(OH)(Cbdc)<sub>4</sub>(H<sub>2</sub>O)<sub>6</sub>]·8H<sub>2</sub>O}<sub><i>n</i></sub> (<b>II</b>). The crystal structures of compounds <b>I</b> and <b>II</b> are determined by single-crystal XRD (CIF files CCDC nos. 2344872 (<b>I</b>) and 2344873 (<b>II</b>), respectively).</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 8","pages":"603 - 611"},"PeriodicalIF":1.1,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142595488","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. A. Shmelev, T. D. Shatrov, O. V. Zvereva, A. A. Levina, Yu. K. Voronina, A. A. Sidorov, I. L. Eremenko
{"title":"Mixed-Carboxylate Cadmium–Europium Compounds with Monocarboxylic Acid Anions","authors":"M. A. Shmelev, T. D. Shatrov, O. V. Zvereva, A. A. Levina, Yu. K. Voronina, A. A. Sidorov, I. L. Eremenko","doi":"10.1134/S1070328424600554","DOIUrl":"10.1134/S1070328424600554","url":null,"abstract":"<p>A series of mixed-carboxylate EuCd compounds with 1,10-phenanthroline (phen) and anions of benzoic H(Bz), pentabenzoic H(Pfb), 3,5-dinitrobenzoic H(3,5-Nbz), and 3,5-di-<i>tert</i>-butylbenzoic H(Dtbbz) acids is synthesized: [Eu<sub>2</sub>Cd<sub>2</sub>(phen)<sub>2</sub>(Рfb)<sub>5,4</sub>(Bz)<sub>4,6</sub>]·2MeCN (<b>I</b>), [Eu<sub>2</sub>(H<sub>2</sub>O)<sub>2</sub>Cd<sub>2</sub>(phen)<sub>2</sub>(3,5-Nbz)<sub>4,1</sub>(Bz)<sub>5,9</sub>] (<b>II</b>), and [EuCd<sub>2</sub>(EtOH)<sub>4</sub>(Dtbbz)<sub>6</sub>(Pfb)] (<b>III</b>). The variation of combinations of aromatic anions makes it possible to reveal the influence of diverse factors on the compositions and structures of new compounds. In the case of benzoate‒pentafluorobenzoate compound <b>I</b> and 3,5-dinitrobenzoate‒benzoate compound <b>II</b>, the aromatic substituents of the anions have nonintegral populations and occupy close positions in the structure of the complex. The combination of the more bulky 3,5-di-<i>tert</i>-butylbenzoate and pentafluorobenzoate anions in compound <b>III</b> results in the formation of a compound with integral populations of the positions of the anions. The synthesized compounds are characterized by XRD, IR spectroscopy, and C,H,N elemental analysis.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"50 8","pages":"557 - 566"},"PeriodicalIF":1.1,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142595457","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}