Abstract
Lithium complexes of 2-(diphenylphosphinoamino)pyridine and N,2-bis(diphenylphosphanyl)benzeneamine have been synthesized from the corresponding neutral compounds. In the former complex, the metal ion is coordinated to both nitrogen atoms, forming a constrained four-membered ring, whereas the latter complex forms a five-membered ring as the metal ion coordinates preferentially to the phosphorus atom. Coordination of the metal ion in both complexes is dictated primarily by soft-hard interactions and, subsequently, by the constrained geometry of the ring formed. Both lithium complexes and the corresponding neutral compounds have been characterized by single-crystal X-ray diffraction. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004).
| Original language | English |
|---|---|
| Pages (from-to) | 4795-4802 |
| Number of pages | 8 |
| Journal | European Journal of Inorganic Chemistry |
| DOIs | |
| Publication status | Published - 17 Dec 2004 |
Keywords
- lithium complexes (Diphenylphosphanylamino)pyridine
- N,2-bis(diphenylphosphanyl)benzeneamine
- hard-soft interactions
- N,N-chelation
- N,P-chelation
- X-ray diffraction
- COORDINATION CHEMISTRY
- CRYSTAL-STRUCTURES
- STRUCTURAL CHARACTERIZATION
- BENZAMIDINATE COMPLEXES
- METAL COORDINATION
- GROUP-13 METALS
- LIGAND
- POLYMERIZATION
- REACTIVITY
- ZIRCONIUM
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