Paper
The 2,4,6-Tris(trifluoromethyl)phenyl Substituent: An Ideal Combination of Steric and Electronic Stabilization
Published 1992 · F. Edelmann
Comments on Inorganic Chemistry
Q1 SJR score
35
Citations
0
Influential Citations
Abstract
Abstract The chemistry of the 2,4,6-tris(trifluoromethyl)phenyl substituent (RF) is reviewed. This ligand combines steric bulk with the possibility of electronic stabilization. Despite the electron-withdrawing nature of the CF3 groups, the electrondonating ability via the lone pairs at the fluorine atoms is the most important factor in the stabilization of low-coordinated main-group derivatives. This is demonstrated by a number of X-ray structure determinations which show significant intramolecular metal-fluorine interactions.
Study Snapshot
The 2,4,6-tris(trifluoromethyl)phenyl substituent offers steric bulk and electronic stabilization, enabling the stabilization of low-coordinated main-group derivatives through fluorine lone pairs.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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