Related Experiment Video
Updated: Jul 7, 2026

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyl(tropone)iron
Published on: August 12, 2019
The heteronuclear bonding between heavier Group 14 elements and transition metals: a novel trioxystannate-iron
Victor N Khrustalev1, Oleg V Chernov, Rinat R Aysin
1A. N. Nesmeyanov Institute of Organoelement Compounds of RAS, Vavilov Str., 28, Moscow, 119991, Russian Federation. vkh@xray.ineos.ac.ru
Abstract:
A new trioxystannate-transition metal complex, {[Li][(Me(2)NCH(2)CH(2)O)(3)Sn-Fe(CO)(4)]}(2) (3), exhibiting an unusual type of the heteronuclear bonding between heavier Group 14 elements and transition metals, has been synthesised and completely characterised by NMR, Raman and IR spectroscopy in solution as well as by Raman spectroscopy and X-ray diffraction analysis in the solid state.
More Related Videos
Related Concept Videos
Valence Bond Theory
Properties of Transition Metals
Ionic Bonding and Electron Transfer
Complexation Equilibria: Factors Influencing Stability of Complexes
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
Structural Isomerism
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...

