Fluorine substitution, effect

A subsequent project focused on DFT study aimed at understanding structure/ reactivity relationships and fluorine substitution effects on carbocation stability in... 

The C—C distances in poly-fluorinated ethanes provide a particularly interesting sequence, for which unfortunately key values are still missing (Table 18). It appears that a-fluorination leads to a shorter C—C distance, while a, j3-fluorinations lengthen the C—C distance, with the exception of CF3—CHF2. Further studies of fluorinated ethanes are needed to provide data on the fluorine substitution effect. 

Yang H, Hay AS (1993) Fluorine substitutent effects on poly(2,6-diphenylphenylene ether). J Polym Sci A Polym Chem 31 2015-2029... 

Substitution of fluorine into an organic molecule results in enhanced chemical stabiUty. The resulting chemical reactivity of adjacent functional groups is drastically altered due to the large inductive effect of fluorine. These effects become more pronounced as the degree of fluorine substitution is increased, especially on the same carbon atom. This effect demonstrates a maximum in fluorocarbons and their derivatives. 

The 1,3-dipolar cycloadditions offluonnatedallenes provide a rich and varied chemistry Allenes, such as 1,1-difluoroallene and fluoroallene, that have fluorine substitution on only one of their two cumulated double bonds are very reactive toward 1,3-dipoles Such activation derives from the electron attracting inductive and hyperconjugative effects of the allylic fluorine substituent(s) that give nse to a considerable lowering of the energy of the LUMO of the C(2)-C(3) n bond [27]... 

The course of each of the free radical reactions shown in equations 19-21, where fluorine substitution alters the normal trans stereochemistry of addition, is ascnbed to endo fluonne stenc effects... 

Compare the effects of the successive fluorine substitutions en the various structural features of the molecule. 

Results for these CEBEs are presented in Table 1. As can be seen, for the carvone variants I-V the various substitutions have absolutely no effect at the carbonyl C=0 core, and are barely significant at the chiral center that lies between the carbonyl and substituent groups in these molecules. Only upon fluorine substitution at the tail (molecule VI) does the C=0 CEBE shift by one-half of an electronvolt the second F atom substitution adjacent to the C=0 in the difluoro derivative, VII contributes a further 0.6-eV shift. This effect can be rationalized due to the electron-withdrawing power of an F atom. Paradoxically, it is these fluorine-substituted derivatives, VI, VII, that arguably produce b curves most similar to the original carvone conformer, I, yet they are the only ones to produce a perturbation of the ground-state electron density at the C li core. This contributes further evidence to suggest that, at least for the C li... 

Comparing the potentials across each row, we can test the idea of additivity of ortAo-substituent effects for 2-fluoro, 6-chloro, and then 2-fluoro-6-chloro substitution. The definition of a = 0 changes across each row to permit easy visual addition of the potentials in the physically appropriate manner to assess the degree of additivity of ort/io-chlorine and ort/io-fluorine substituent effects. For o-fluorotoluene and 2-fluoro-6-chlorotoluene, a = 0 denotes the (minimum-energy) pseudo-trans conformation for o-chlorotoluene, a=0 denotes the pseudo-cis conformation. The notion of additivity has considerable merit in all three electronic states. 

Table 10 Effects of fluorine substitution on GABAa binding and efficacy...

Effects of Methyl and Fluorine Substitution on the Metabolic Activation and Tumorigenicity of Polycyclic Aromatic Hydrocarbons... 

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