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, A. V. Klimashevskaya, A. V. Cherkasov, 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}
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, V. M. Makarov, D. A. Razborov, E. V. Baranov, 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}
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, A. N. Usol’tsev, N. A. Korobeinikov, I. V. Korol’kov, D. A. Ulybin, A. S. Novikov, 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}
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, N. A. Korobeinikov, A. S. Zaguzin, R. V. Red’kin, E. A. Pilyukova, A. V. Zaitsev, 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}
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, A. V. Cherkasov, G. K. Fukin, 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}
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, 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","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}
{"title":"Estimating Strength of Cu–O Bonds in Cu(II) β-Diketonates from Electron Density Topology","authors":"R. E. Afaunov, I. V. Mirzaeva, 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}
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, O. P. Demidov, N. I. Vikrishchuk, A. S. Galkina, N. N. Efimov, A. V. Chernyshev, L. D. Popov, A. V. Metelitsa, 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}
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, I. Yu. Bagryanskaya, A. S. Berezin, V. A. Kuimov, 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}
D. A. Bardonov, K. A. Lysenko, I. E. Nifantiev, M. E. Minyaev, D. M. Roitershtein
{"title":"Yttrium Polyphenylcyclopentadienyl Complexes with 1,3,5-Trimethyl-1,3,5-triazacyclohexane","authors":"D. A. Bardonov, K. A. Lysenko, I. E. Nifantiev, M. E. Minyaev, D. M. Roitershtein","doi":"10.1134/S1070328424601444","DOIUrl":"10.1134/S1070328424601444","url":null,"abstract":"<p>The reaction of di-, tri-, and tetraphenylcyclopentadienylpotassium with yttrium chloride tetrahydrofuranate in the presence of 1,3,5-trimethyl-1,3,5-triazacyclohexane (Me<sub>3</sub>tach) gives complexes of the type [Cp'Y(Me<sub>3</sub>tach)Cl<sub>2</sub>] (Cp' = Ph<sub>2</sub>C<sub>5</sub>H<sub>3</sub> (Cp<sup>Ph2</sup>) (<b>I</b>), Ph<sub>3</sub>C<sub>5</sub>H<sub>2</sub> (Cp<sup>Ph3</sup>) (<b>II</b>), Ph<sub>4</sub>C<sub>5</sub>H (Cp<sup>Ph4</sup>) (<b>III</b>). The molecular structure of complexes <b>I</b>–<b>III</b> was established by X-ray diffraction (CCDC nos. 2406644 (<b>I</b>), 2406645 (<b>II</b>), 2406646 (<b>III</b>)). The main structural parameters of all of the obtained monocyclopentadienyl complexes were similar, irrespective of the number of phenyl substituents in the cyclopentadienyl ligand. According to NMR spectroscopy data, compounds <b>I</b> and <b>III</b> retained their structure in THF solution.</p>","PeriodicalId":759,"journal":{"name":"Russian Journal of Coordination Chemistry","volume":"51 3","pages":"211 - 217"},"PeriodicalIF":1.1,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145142592","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}