{"title":"Coordination variety of phenyltetrazolato and dimethylamido ligands in dimeric Ti, Zr, and Ta complexes.","authors":"Galina A Bikzhanova, Ilia A Guzei","doi":"10.1107/S2053229624007411","DOIUrl":null,"url":null,"abstract":"<p><p>Three structurally diverse 5-phenyltetrazolato (Tz) Ti, Zr, and Ta complexes, namely, (C<sub>2</sub>H<sub>8</sub>N)[Ti<sub>2</sub>(C<sub>7</sub>H<sub>5</sub>N<sub>4</sub>)<sub>5</sub>(C<sub>2</sub>H<sub>6</sub>N)<sub>4</sub>]·1.45C<sub>6</sub>H<sub>6</sub> or (Me<sub>2</sub>NH<sub>2</sub>)[Ti<sub>2</sub>(NMe<sub>2</sub>)<sub>4</sub>(2,3-μ-Tz)<sub>3</sub>(2-η<sup>1</sup>-Tz)<sub>2</sub>]·1.45C<sub>6</sub>H<sub>6</sub>, (1·1.45C<sub>6</sub>H<sub>6</sub>), [Zr<sub>2</sub>(C<sub>7</sub>H<sub>5</sub>N<sub>4</sub>)<sub>6</sub>(C<sub>2</sub>H<sub>6</sub>N)<sub>2</sub>(C<sub>2</sub>H<sub>7</sub>N)<sub>2</sub>]·1.12C<sub>6</sub>H<sub>6</sub>·0.382CH<sub>2</sub>Cl<sub>2</sub> or [Zr<sub>2</sub>(Me<sub>2</sub>NH)<sub>2</sub>(NMe<sub>2</sub>)<sub>2</sub>(2,3-μ-Tz)<sub>3</sub>(2-η<sup>1</sup>-Tz)<sub>2</sub>(1,2-η<sup>2</sup>-Tz)]·1.12C<sub>6</sub>H<sub>6</sub>·0.38CH<sub>2</sub>Cl<sub>2</sub> (2·1.12C<sub>6</sub>H<sub>6</sub>·0.38CH<sub>2</sub>Cl<sub>2</sub>), and (C<sub>2</sub>H<sub>8</sub>N)<sub>2</sub>[Ta<sub>2</sub>(C<sub>7</sub>H<sub>5</sub>N<sub>4</sub>)<sub>8</sub>(C<sub>2</sub>H<sub>6</sub>N)<sub>2</sub>O]·0.25C<sub>7</sub>H<sub>8</sub> or (Me<sub>2</sub>NH<sub>2</sub>)<sub>2</sub>[Ta<sub>2</sub>(NMe<sub>2</sub>)<sub>2</sub>(2,3-μ-Tz)<sub>2</sub>(2-η<sup>1</sup>-Tz)<sub>6</sub>O]·0.25C<sub>7</sub>H<sub>8</sub> (3·0.25C<sub>7</sub>H<sub>8</sub>), where TzH is 5-phenyl-1H-tetrazole, have been synthesized and structurally characterized. All three complexes are dinuclear; the Ti center in 1 is six-coordinate, whereas the Zr and Ta atoms in 2 and 3 are seven-coordinate. The coordination environments of the Ti centers in 1 are similar, and so are the ligations of the Ta centers in 3. In contrast, the two Zr centers in 2 bear a different number of ligands, one of which is a bidentate η<sup>2</sup>-5-phenyltetrazolato ligand that has not been observed previously for d-block elements. The dimethylamido ligand, present in the starting materials, remained unchanged, or was converted to dimethylamine and dimethylammonium during the synthesis. Dimethylamine coordinates as a neutral ligand, whereas dimethylammonium is retained as a hydrogen-bonded entity bridging Tz ligands.</p>","PeriodicalId":7115,"journal":{"name":"Acta Crystallographica Section C Structural Chemistry","volume":" ","pages":"576-583"},"PeriodicalIF":0.7000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11371001/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Crystallographica Section C Structural Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1107/S2053229624007411","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/23 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Three structurally diverse 5-phenyltetrazolato (Tz) Ti, Zr, and Ta complexes, namely, (C2H8N)[Ti2(C7H5N4)5(C2H6N)4]·1.45C6H6 or (Me2NH2)[Ti2(NMe2)4(2,3-μ-Tz)3(2-η1-Tz)2]·1.45C6H6, (1·1.45C6H6), [Zr2(C7H5N4)6(C2H6N)2(C2H7N)2]·1.12C6H6·0.382CH2Cl2 or [Zr2(Me2NH)2(NMe2)2(2,3-μ-Tz)3(2-η1-Tz)2(1,2-η2-Tz)]·1.12C6H6·0.38CH2Cl2 (2·1.12C6H6·0.38CH2Cl2), and (C2H8N)2[Ta2(C7H5N4)8(C2H6N)2O]·0.25C7H8 or (Me2NH2)2[Ta2(NMe2)2(2,3-μ-Tz)2(2-η1-Tz)6O]·0.25C7H8 (3·0.25C7H8), where TzH is 5-phenyl-1H-tetrazole, have been synthesized and structurally characterized. All three complexes are dinuclear; the Ti center in 1 is six-coordinate, whereas the Zr and Ta atoms in 2 and 3 are seven-coordinate. The coordination environments of the Ti centers in 1 are similar, and so are the ligations of the Ta centers in 3. In contrast, the two Zr centers in 2 bear a different number of ligands, one of which is a bidentate η2-5-phenyltetrazolato ligand that has not been observed previously for d-block elements. The dimethylamido ligand, present in the starting materials, remained unchanged, or was converted to dimethylamine and dimethylammonium during the synthesis. Dimethylamine coordinates as a neutral ligand, whereas dimethylammonium is retained as a hydrogen-bonded entity bridging Tz ligands.
期刊介绍:
Acta Crystallographica Section C: Structural Chemistry is continuing its transition to a journal that publishes exciting science with structural content, in particular, important results relating to the chemical sciences. Section C is the journal of choice for the rapid publication of articles that highlight interesting research facilitated by the determination, calculation or analysis of structures of any type, other than macromolecular structures. Articles that emphasize the science and the outcomes that were enabled by the study are particularly welcomed. Authors are encouraged to include mainstream science in their papers, thereby producing manuscripts that are substantial scientific well-rounded contributions that appeal to a broad community of readers and increase the profile of the authors.