Russian Journal of Coordination Chemistry最新文献

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Bis(o-Aminophenolato)germanium(II) and Tin(II) Complexes in Hydroboration Reactions of Aromatic Aldehydes 双(邻氨基酚)锗(II)和锡(II)配合物在芳香醛的硼化加氢反应中的应用
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-07-10 DOI: 10.1134/S1070328425600238
K. V. Arsen’eva, A. V. Klimashevskaya, A. V. Cherkasov, A. V. Piskunov
{"title":"Bis(o-Aminophenolato)germanium(II) and Tin(II) Complexes in Hydroboration Reactions of Aromatic Aldehydes","authors":"K. V. Arsen’eva,&nbsp;A. V. Klimashevskaya,&nbsp;A. V. Cherkasov,&nbsp;A. V. Piskunov","doi":"10.1134/S1070328425600238","DOIUrl":"10.1134/S1070328425600238","url":null,"abstract":"<p>Stable tin(II) (<sup>dipp</sup>AmP)<sub>2</sub>Sn (<b>I</b>) and germanium(II) (<sup>dipp</sup>AmP)<sub>2</sub>Ge (<b>II</b>) complexes based on 4,6-di-<i>tert</i>-butyl-<i>N</i>-(2,6-diisopropylphenyl)-<i>o</i>-aminophenol were synthesized and characterized. The compounds are monomeric and contain, in addition to covalent element(II)–oxygen bonds, additional coordination bonds involving the secondary amino groups of the chelating ligand. The synthesized compounds were tested as homogeneous catalysts for the hydroboration of various substituted aldehydes to the corresponding boronate esters. Optimization of the catalytic reaction conditions made it possible to reduce the catalyst loading to 0.02 mol % while maintaining quantitative conversion under mild conditions. The molecular structure of complex <b>II</b> was established by X-ray diffraction analysis (CCDC no. 2423247, <b>II</b>).</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 4","pages":"246 - 254"},"PeriodicalIF":1.1,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145164255","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}
引用次数: 0
The [(Dpp-BIAN)LnI(Solv)x] Complexes (Ln = Nd, Dy, Tm) and Their Reduction Reactions [(Dpp-BIAN)LnI(Solv)x]配合物(Ln = Nd, Dy, Tm)及其还原反应
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-07-10 DOI: 10.1134/S1070328424601596
V. A. Dodonov, V. M. Makarov, D. A. Razborov, E. V. Baranov, I. L. Fedushkin
{"title":"The [(Dpp-BIAN)LnI(Solv)x] Complexes (Ln = Nd, Dy, Tm) and Their Reduction Reactions","authors":"V. A. Dodonov,&nbsp;V. M. Makarov,&nbsp;D. A. Razborov,&nbsp;E. V. Baranov,&nbsp;I. L. Fedushkin","doi":"10.1134/S1070328424601596","DOIUrl":"10.1134/S1070328424601596","url":null,"abstract":"<p>The reduction of Dpp-BIAN with neodymium metal in the presence of equimolar amounts of iodine gave the neodymium complex with acenaphthene-1,2-diimine ligand in the dianion form, [(Dpp-BIAN)NdI(DME)<sub>2</sub>] (<b>I</b>) (Dpp-BIAN is (1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene, DME is dimethoxyethane). The treatment of the complexes [(Dpp-BIAN)LnI(Solv)<sub><i>n</i></sub>] (Solv is ether solvent), (Ln = Nd, Dy, Tm) with solutions of thex [Dpp-BIANK<sub>2</sub>] molecular iodine resulted in the formation of bis-ligand ate-complexes [(Dpp-BIAN)<sub>2</sub>Nd][K(Et<sub>2</sub>O)<sub>2.62</sub>(THF)<sub>0.38</sub>]Et<sub>2</sub>O (<b>II</b>), [(Dpp-BIAN)<sub>2</sub>Dy][K(DME)<sub>4</sub>](DME)<sub>0.28</sub> (<b>III</b>), and [(Dpp-BIAN)<sub>2</sub>Tm][K(Et<sub>2</sub>O)<sub>3</sub>]Et<sub>2</sub>O (<b>IV</b>). The reaction of [(Dpp-BIAN)NdI(DME)<sub>2</sub>] with lithium trimethylsilylamide gave the product [(Dpp-BIAN)<sub>2</sub>Nd][Li(DME)(Et<sub>2</sub>O)<sub>2</sub>] (<b>V</b>). The molecular structure of complexes <b>I</b>–<b>V</b> was established by X-ray diffraction analysis (CCDC no. 2409375 (<b>I</b>), 2409376 (<b>II</b>), 2409377 (<b>III</b>), 2409378 (<b>IV</b>), 2409379 (<b>V</b>)).</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 4","pages":"227 - 235"},"PeriodicalIF":1.1,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145164271","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}
引用次数: 0
Halogen Bond in Supramolecular Associates of Antimony(V) Bromide Complexes with Tribromide Anion and Halogen-Containing Pyridinium Cations 锑(V)溴配合物与三溴阴离子和含卤吡啶阳离子的超分子结合物中的卤素键
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-07-10 DOI: 10.1134/S1070328425600160
I. A. Shentseva, A. N. Usol’tsev, N. A. Korobeinikov, I. V. Korol’kov, D. A. Ulybin, A. S. Novikov, S. A. Adonin
{"title":"Halogen Bond in Supramolecular Associates of Antimony(V) Bromide Complexes with Tribromide Anion and Halogen-Containing Pyridinium Cations","authors":"I. A. Shentseva,&nbsp;A. N. Usol’tsev,&nbsp;N. A. Korobeinikov,&nbsp;I. V. Korol’kov,&nbsp;D. A. Ulybin,&nbsp;A. S. Novikov,&nbsp;S. A. Adonin","doi":"10.1134/S1070328425600160","DOIUrl":"10.1134/S1070328425600160","url":null,"abstract":"<p>The reactions of a solution of Sb<sub>2</sub>O<sub>3</sub> in HBr, Br<sub>2</sub>, and 1,1'-(propane-1,3-diyl)bis(3-halogenpyridinium) bromides (halogen = Cl (<b>I</b>), Br (<b>II</b>)) afford bromoantimonates(V) Cat{[SbBr<sub>6</sub>](Br<sub>3</sub>)}, whose structures are determined by single-crystal X-Ray diffraction (SCXRD). Tribromide and hexabromoantimonate anions form supramolecular one-dimensional polymers due to the formation of a halogen bond between them, and the cations are also involved in halogen bond formation. The energies of the halogen bonds are estimated by quantum-chemical calculations.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 4","pages":"292 - 300"},"PeriodicalIF":1.1,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145164254","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}
引用次数: 0
Structure of Sodium and Calcium Metal-Organic Frameworks with 2,2'-Diiodobiphenyl-4,4'-dicarboxylic Acid Anions 含2,2'-二碘多联苯-4,4'-二羧酸阴离子的钠和钙金属有机框架的结构
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-07-10 DOI: 10.1134/S1070328425600147
M. A. Bondarenko, N. A. Korobeinikov, A. S. Zaguzin, R. V. Red’kin, E. A. Pilyukova, A. V. Zaitsev, S. A. Adonin
{"title":"Structure of Sodium and Calcium Metal-Organic Frameworks with 2,2'-Diiodobiphenyl-4,4'-dicarboxylic Acid Anions","authors":"M. A. Bondarenko,&nbsp;N. A. Korobeinikov,&nbsp;A. S. Zaguzin,&nbsp;R. V. Red’kin,&nbsp;E. A. Pilyukova,&nbsp;A. V. Zaitsev,&nbsp;S. A. Adonin","doi":"10.1134/S1070328425600147","DOIUrl":"10.1134/S1070328425600147","url":null,"abstract":"<p>The heteroleptic metal-organic frameworks {[Na(μ<sub>2</sub>-DMF)(HBpdc-I<sub>2</sub>)]}<sub><i>n</i></sub> (<b>I</b>) and {[Ca(DMF)<sub>2</sub>(Bpdc-I<sub>2</sub>)]} (<b>II</b>) were obtained by the reaction of sodium (NaOH) and calcium hydroxides (Ca(OH)<sub>2</sub>), respectively, with 2,2'-diiodobiphenyl-4,4'-dicarboxylic acid (H<sub>2</sub>(Bpdc-I<sub>2</sub>)) in <i>N</i>,<i>N</i>-dimethylformamide (DMF). The product structures were determined by X-ray diffraction. The compounds had two- and three-dimensional structures, respectively. A halogen bond was detected in <b>I</b> between the neighboring Bdc-I<sub>2</sub> ligands.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 4","pages":"255 - 262"},"PeriodicalIF":1.1,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145164272","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}
引用次数: 0
Lanthanum Bis(amidinate) Amido Complex {2-[Ph2Р(O)]C6H4NC(But)N(2,6-Me2C6H3)}2LaN(SiMe3)2: Synthesis, Structure, and Catalytic Activity in Ring-Opening Polymerization of rac-Lactide and ε-Caprolactone 双(氨基酸)氨基配合物{2-[Ph2Р(O)]C6H4NC(But)N(2,6- me2c6h3)}2LaN(SiMe3)2: racc -丙交酯和ε-己内酯开环聚合的合成、结构和催化活性
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-07-02 DOI: 10.1134/S107032842560041X
A. O. Tolpygin, A. V. Cherkasov, G. K. Fukin, A. A. Trifonov
{"title":"Lanthanum Bis(amidinate) Amido Complex {2-[Ph2Р(O)]C6H4NC(But)N(2,6-Me2C6H3)}2LaN(SiMe3)2: Synthesis, Structure, and Catalytic Activity in Ring-Opening Polymerization of rac-Lactide and ε-Caprolactone","authors":"A. O. Tolpygin,&nbsp;A. V. Cherkasov,&nbsp;G. K. Fukin,&nbsp;A. A. Trifonov","doi":"10.1134/S107032842560041X","DOIUrl":"10.1134/S107032842560041X","url":null,"abstract":"<p>The La(III) bis(amidinate) amido complex {2-[Ph<sub>2</sub>Р(O)]C<sub>6</sub>H<sub>4</sub>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>LaN(SiMe<sub>3</sub>)<sub>2</sub> (<b>I</b>) was synthesized by the reaction of 2-[Ph<sub>2</sub>Р(O)]C<sub>6</sub>H<sub>4</sub>NHC(Bu<sup><i>t</i></sup>)=N(2,6-Me<sub>2</sub>C<sub>6</sub>H<sub>3</sub>) (HL) and La[N(SiMe<sub>3</sub>)<sub>2</sub>]<sub>3</sub> in 2 : 1 molar ratio and isolated in 74% yield. X-ray analysis revealed that in <b>I</b> both monoanionic amidinate ligands are κ<sup>3</sup>-N,N,O-coordinated to La(III) ion. Complex <b>I</b> demonstrates high catalytic activity in ring-opening polymerization of cyclic esters and enables 100% conversion of 100–300 equiv of <i>rac</i>-lactide in 30 min or 100–500 equiv of ε-caprolactone in 1 min providing highly controlled polymerization. The obtained polymeric samples feature linear dependence of molecular weight vs. the monomer loading and rather narrow polydispersity (<i>M</i><sub>w</sub>/<i>M</i><sub><i>n</i></sub> = 1.36–1.88).</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 5","pages":"374 - 380"},"PeriodicalIF":1.1,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145161002","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}
引用次数: 0
Synthesis, Structures, and Thermal Behavior of Calcium, Strontium, Barium Bis(1-ferrocenyl-4,4,4-trifluorobutane-1,3-dionato) Complexes with Crown-Ethers 钙、锶、钡与冠醚配合物(1-二茂铁-4,4,4-三氟丁烷-1,3-dionato)的合成、结构和热行为
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-07-02 DOI: 10.1134/S1070328425600184
T. S. Pochekutova, B. I. Petrov, N. M. Lazarev, G. K. Fukin, E. V. Baranov, N. M. Khamaletdinova, A. A. Zolotukhin, A. A. Belikov, T. I. Lopatina, R. S. Kovylin
{"title":"Synthesis, Structures, and Thermal Behavior of Calcium, Strontium, Barium Bis(1-ferrocenyl-4,4,4-trifluorobutane-1,3-dionato) Complexes with Crown-Ethers","authors":"T. S. Pochekutova,&nbsp;B. I. Petrov,&nbsp;N. M. Lazarev,&nbsp;G. K. Fukin,&nbsp;E. V. Baranov,&nbsp;N. M. Khamaletdinova,&nbsp;A. A. Zolotukhin,&nbsp;A. A. Belikov,&nbsp;T. I. Lopatina,&nbsp;R. S. Kovylin","doi":"10.1134/S1070328425600184","DOIUrl":"10.1134/S1070328425600184","url":null,"abstract":"<p>The new ferrocenyl-containing β-diketonate complexes with crown-ethers [Ca(Fctfa)<sub>2</sub>(15-crown-5)] (<b>I</b>), [Sr(Fctfa)<sub>2</sub>(18-crown-6)] (<b>II</b>), [Sr(Fctfa)<sub>2</sub>(18-crown-6)](CH<sub>2</sub>Cl<sub>2</sub>) (<b>III</b>), [Ba(Fctfa)<sub>2</sub>(18-crown-6)] (<b>IV</b>) and [Ba(Fctfa)<sub>2</sub>(18-crown-6)](CH<sub>2</sub>Cl<sub>2</sub>) (<b>V</b>) (Fctfa = 1-ferrocenyl-4,4,4-trifluorobutane-1,3-dionato), 15-crown-5 = 1,4,7,10,13-pentanoxacyclopentadecane; 18-crown-6 = 1,4,7,10,13,16-hexaoxacyclooctadecane) have been synthesized. The compounds are characterized by infrared and <sup>1</sup>H NMR spectroscopy and X-ray diffraction analysis. The thermal behavior of complexes <b>I</b>, <b>II</b>, <b>IV</b> was investigated by thermal analysis. It was found that complexes are thermally stable up to 150°C for <b>I</b>, 215°C for <b>II</b> 180°C for <b>IV</b>. The decomposition behavior of <b>I</b>, <b>II</b>, <b>IV</b> studied by <sup>1</sup>H nuclear magnetic resonance investigation of substances, formed at decomposition of <b>I</b>, <b>II</b>, <b>IV</b> in dynamic vacuum. It was found, that the heating of <b>I</b>, <b>II</b>, <b>IV</b> in the ranges 150–800°C for <b>I</b>, 215–800°C for <b>II</b>, 180–800°C for <b>IV</b> affords the solid substances, containing alkaline-earth metals fluorides and iron oxides. Using topological analysis of the electron density distribution in <b>I</b>, <b>III</b>, <b>V</b>, intra- and intermolecular interactions were quantitatively estimated within the framework of Bader’s atoms in molecules theory. According to Espinosa–Mollins–Lecomte correlation, energies of the intermolecular interactions for <b>I</b>, <b>III</b>, <b>V</b> are close to the experimentally measured enthalpies of sublimation of related complexes published previously.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 5","pages":"348 - 362"},"PeriodicalIF":1.1,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145160913","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}
引用次数: 0
Estimating Strength of Cu–O Bonds in Cu(II) β-Diketonates from Electron Density Topology 从电子密度拓扑估计Cu(II) β-二酮酸酯中Cu - o键的强度
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-07-02 DOI: 10.1134/S1070328425600226
R. E. Afaunov, I. V. Mirzaeva, S. G. Kozlova
{"title":"Estimating Strength of Cu–O Bonds in Cu(II) β-Diketonates from Electron Density Topology","authors":"R. E. Afaunov,&nbsp;I. V. Mirzaeva,&nbsp;S. G. Kozlova","doi":"10.1134/S1070328425600226","DOIUrl":"10.1134/S1070328425600226","url":null,"abstract":"<p>Copper(II) β-diketonates are popular MOCVD precursors for production of copper and copper-containing coatings. For further development and targeted design of new precursors of this type it would be very useful to have a tool for fast indirect estimation of the energy of Cu–O bonds. In this work, we have searched for correlations between the energy of Cu–O bonds in Cu(II) β-diketonates and their topological characteristics. Several equations have been proposed.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 5","pages":"340 - 347"},"PeriodicalIF":1.1,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145161001","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}
引用次数: 0
Coordination Compounds of Cobalt(II) and Zinc(II) with N,N'-((Hydrazine-1,2-diylidene-bis(methanylylidene))bis(2,1-phenylene))bis(4-methylbenzenesulfonamide): Synthesis and Properties 钴(II)和锌(II)与N,N'-((肼-1,2-二乙基-双(甲基乙基))双(2,1-苯基))双(4-甲基苯磺酰胺)配位化合物的合成及性能
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-06-06 DOI: 10.1134/S1070328424601638
A. A. Kolodina, O. P. Demidov, N. I. Vikrishchuk, A. S. Galkina, N. N. Efimov, A. V. Chernyshev, L. D. Popov, A. V. Metelitsa, A. S. Burlov
{"title":"Coordination Compounds of Cobalt(II) and Zinc(II) with N,N'-((Hydrazine-1,2-diylidene-bis(methanylylidene))bis(2,1-phenylene))bis(4-methylbenzenesulfonamide): Synthesis and Properties","authors":"A. A. Kolodina,&nbsp;O. P. Demidov,&nbsp;N. I. Vikrishchuk,&nbsp;A. S. Galkina,&nbsp;N. N. Efimov,&nbsp;A. V. Chernyshev,&nbsp;L. D. Popov,&nbsp;A. V. Metelitsa,&nbsp;A. S. Burlov","doi":"10.1134/S1070328424601638","DOIUrl":"10.1134/S1070328424601638","url":null,"abstract":"<p><i>N</i>,<i>N</i>'-((Hydrazine-1,2-diylidene-bis(methanylylidene))bis(2,1-phenylene))bis(4-methylbenzene-sulfonamide) (H<sub>2</sub>L) and its binuclear complexes Zn<sub>2</sub>L<sub>2</sub> and Co<sub>2</sub>L<sub>2</sub> are synthesized. The compositions and structures of H<sub>2</sub>L and its complexes are determined by elemental analysis and IR and <sup>1</sup>H NMR spectroscopy (for Zn<sub>2</sub>L<sub>2</sub>). The structures of H<sub>2</sub>L and Co<sub>2</sub>L<sub>2</sub> are determined by XRD (CIF files CCDC no. 2405868 for H<sub>2</sub>L and no. 2390599 for Co<sub>2</sub>L<sub>2</sub>·4DMSO). The magnetic properties of Co<sub>2</sub>L<sub>2</sub> and photoluminescence properties of H<sub>2</sub>L and Zn<sub>2</sub>L<sub>2</sub> are studied. The Zn(II) complex exhibits the photoluminescence properties in an acetonitrile solution and in the solid state (<span>(lambda _{{{text{max}}}}^{{{text{fl}}}})</span> = 584 and 532 nm) with quantum yields of 0.06 and 0.68, respectively. The Co(II) complex exhibits the properties of slow magnetic relaxation.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 3","pages":"175 - 183"},"PeriodicalIF":1.1,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145142575","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}
引用次数: 0
New Tetraiodomanganate(II) with Highly Efficient Short-Lived Phosphorescence 具有高效短寿命磷光的新型四锰酸盐(II)
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-06-06 DOI: 10.1134/S1070328425600123
M. P. Davydova, I. Yu. Bagryanskaya, A. S. Berezin, V. A. Kuimov, A. V. Artem’ev
{"title":"New Tetraiodomanganate(II) with Highly Efficient Short-Lived Phosphorescence","authors":"M. P. Davydova,&nbsp;I. Yu. Bagryanskaya,&nbsp;A. S. Berezin,&nbsp;V. A. Kuimov,&nbsp;A. V. Artem’ev","doi":"10.1134/S1070328425600123","DOIUrl":"10.1134/S1070328425600123","url":null,"abstract":"<p>Biphosphonium tetraiodomanganate(II) [DPEPhosMe<sub>2</sub>]MnI<sub>4</sub> has been synthesized by the reaction of MnI<sub>2</sub> with bis(phosphonium) salt [DPEPhosMe<sub>2</sub>]I<sub>2</sub>, which is prepared by the alkylation of DPEPhos with methyl iodide. At ambient temperature, polycrystalline samples of [DPEPhosMe<sub>2</sub>]MnI<sub>4</sub> exhibit bright green phosphorescence (λ<sub>max</sub> = 546 nm) with a quantum yield of 77%. The phosphorescence decay lifetime is 45 μs, which is rather short for Mn<sup>2+</sup>-centered phosphorescence.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 3","pages":"169 - 174"},"PeriodicalIF":1.1,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145142574","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}
引用次数: 0
Yttrium Polyphenylcyclopentadienyl Complexes with 1,3,5-Trimethyl-1,3,5-triazacyclohexane 与1,3,5-三甲基-1,3,5-三氮杂环己烷的钇聚苯基环戊二烯配合物
IF 1.1 3区 化学
Russian Journal of Coordination Chemistry Pub Date : 2025-06-06 DOI: 10.1134/S1070328424601444
D. A. Bardonov, K. A. Lysenko, I. E. Nifantiev, M. E. Minyaev, D. M. Roitershtein
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