Fatima Setifi , Zouaoui Setifi , Hans Reuter , Mohammad Hadi Al-Douh , Abderezak Addala
{"title":"Bis(azido-κN)bis(quinolin-8-amine-κ2N,N′)iron(II) monohydrate","authors":"Fatima Setifi , Zouaoui Setifi , Hans Reuter , Mohammad Hadi Al-Douh , Abderezak Addala","doi":"10.1107/S2414314625002354","DOIUrl":null,"url":null,"abstract":"<div><div>In the title compound, [Fe(N<sub>3</sub>)<sub>2</sub>(C<sub>9</sub>H<sub>8</sub>N<sub>2</sub>)<sub>2</sub>]·H<sub>2</sub>O or [Fe(N<sub>3</sub>)<sub>2</sub>(AQ)<sub>2</sub>]·H<sub>2</sub>O, the Fe<sup>II</sup> ion is distorted octahedrally coordinated by two azide ions in a <em>cis</em> position with a <em>syn</em> orientation, while the two amino groups of the AQ ligands are in a <em>cis</em> and the two pyridiyl N atoms are in a <em>trans</em> position.</div></div><div><div>In the hydrated title complex, [Fe(N<sub>3</sub>)<sub>2</sub>(AQ)<sub>2</sub>]·H<sub>2</sub>O (AQ is 8-aminoquinoline, C<sub>9</sub>H<sub>9</sub>N<sub>2</sub>), the Fe<sup>II</sup> ion is coordinated in a distorted octahedral manner by two neutral, chelating AQ ligands and two anionic, monodentate azide (N<sub>3</sub><sup>−</sup>) ions in a <em>syn</em>,<em>cis</em>-configuration. From the two AQ ligands, the pyridyl N atoms are opposite to each other and the amino groups <em>trans</em> to the azide ligands. Distortion results from different Fe—N bond lengths [2.112 (2)–2.231 (2) Å] and 〈(N—Fe—N)<sub><em>cis</em></sub> [75.25 (6)–99.91 (7)°] and 〈(N—Fe—N)<sub><em>trans</em></sub> [159.98 (7)–170.62 (7)°] bond angles. The water molecule acts as the acceptor of hydrogen bonds with the NH<sub>2</sub> groups of both AQ-ligands in one and the same molecule, and as donor to the γ-N and α-N atoms of the azido ligands of two adjacent iron complexes. In addition, both terminal N atoms of the azido ligands are involved in hydrogen bonds with NH<sub>2</sub> groups in neighboring iron complexes, so that the hydrogen-bonding pattern leads to a rod-like arrangement of the molecules in the <em>b</em>-axis direction.<span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (345KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div>","PeriodicalId":94324,"journal":{"name":"IUCrData","volume":"10 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IUCrData","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2414314625000185","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In the title compound, [Fe(N3)2(C9H8N2)2]·H2O or [Fe(N3)2(AQ)2]·H2O, the FeII ion is distorted octahedrally coordinated by two azide ions in a cis position with a syn orientation, while the two amino groups of the AQ ligands are in a cis and the two pyridiyl N atoms are in a trans position.
In the hydrated title complex, [Fe(N3)2(AQ)2]·H2O (AQ is 8-aminoquinoline, C9H9N2), the FeII ion is coordinated in a distorted octahedral manner by two neutral, chelating AQ ligands and two anionic, monodentate azide (N3−) ions in a syn,cis-configuration. From the two AQ ligands, the pyridyl N atoms are opposite to each other and the amino groups trans to the azide ligands. Distortion results from different Fe—N bond lengths [2.112 (2)–2.231 (2) Å] and 〈(N—Fe—N)cis [75.25 (6)–99.91 (7)°] and 〈(N—Fe—N)trans [159.98 (7)–170.62 (7)°] bond angles. The water molecule acts as the acceptor of hydrogen bonds with the NH2 groups of both AQ-ligands in one and the same molecule, and as donor to the γ-N and α-N atoms of the azido ligands of two adjacent iron complexes. In addition, both terminal N atoms of the azido ligands are involved in hydrogen bonds with NH2 groups in neighboring iron complexes, so that the hydrogen-bonding pattern leads to a rod-like arrangement of the molecules in the b-axis direction.