Unusual Fluorenylidene-philic Interactions for Effective Conformational Induction
✍ Scribed by Young-A. Lee; Ok-Sang Jung
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 132 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
✦ Synopsis
Control of the conformation of the fluorenylidene moiety is achieved through an intramolecular interaction between the fluorenylidene moiety and the axial ligand during the oxidative addition and successive substitution of [Pt (fm)] to give [Pt (X)(X')(fm)] (fm=9-fluorenylidenemalonate; see scheme). The conformation of the fm moiety can be effectively induced by the fluorenylidene-philicity of the axial X/X' ligands, OOCCH >OCH >OH.
📜 SIMILAR VOLUMES
The conformational preferences of oxymethylpyridines have been investigated by ab initio calculations and compared to similar calculations for oxymethylbenzene. The C-0 bond in the pyridine compounds was found to prefer eclipsing with a C-C bond in the ring, in agreement with previous observations b
## Abstract The interaction of the La(III) and Tb(III) ions with adenosine‐5′‐monophosphate (5′‐AMP), guanosine‐5′‐monophosphate (5′‐GMP), and 2′‐deoxyguanosine‐5′‐monophosphate (5′‐dGMP) anions with metal/nucleotide ratios of 1 and 2 has been studied in aqueous solution in acidic and neutral pHs.