An indenide-tethered N-heterocyclic stannylene

The structure of (μ-1κ :2(η ),κ , '-(2-{[2,6-bis(propan-2-yl)phen-yl]aza-nid-yl}eth-yl)[2-(1 -inden-1-yl)eth-yl]aza-nido)(1,4,7,10,13,16-hexa-oxa-cyclo-octa-dec-ane-1κ )lithiumtin, [LiSn(C H O )(C H N )], at 100 K has monoclinic ( 2 / ) symmetry. Analysis of the coordination of the Sn to the in...

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Veröffentlicht in:Acta crystallographica. Section E, Crystallographic communications Crystallographic communications, 2020-02, Vol.76 (Pt 2), p.254-256
Hauptverfasser: Bischof, Tobias, Evans, Kieren J, Haddow, Mairi F, Mansell, Stephen M
Format: Artikel
Sprache:eng
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Zusammenfassung:The structure of (μ-1κ :2(η ),κ , '-(2-{[2,6-bis(propan-2-yl)phen-yl]aza-nid-yl}eth-yl)[2-(1 -inden-1-yl)eth-yl]aza-nido)(1,4,7,10,13,16-hexa-oxa-cyclo-octa-dec-ane-1κ )lithiumtin, [LiSn(C H O )(C H N )], at 100 K has monoclinic ( 2 / ) symmetry. Analysis of the coordination of the Sn to the indenyl ring shows that the Sn inter-acts in an η fashion. A database survey showed that whilst this coordination mode is unusual for Ge and Pb compounds, Sn displays a wider range of coordination modes to cyclo-penta-dienyl ligands and their derivatives.
ISSN:2056-9890
2056-9890
DOI:10.1107/S205698902000047X