Abstract
The investigation demonstrates the analytical power of F-NMR spectroscopy for the identification of isomeric substituted fluorobiphenyls. The biphenyls are formed by u.v. irradiation of iodobenzenes in aromatic solvents. A special procedure for the identification is outlined and tendencies of the results—chemical shifts and relative rates for the production of isomers—are discussed in consideration of electronic and steric substituent effects.
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