| Autor: |
Gibson CM; Department of Chemistry, University of Sheffield , Sheffield, S3 7HF, U.K., Havenith RW, Fowler PW, Jenneskens LW |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of organic chemistry [J Org Chem] 2015 Feb 06; Vol. 80 (3), pp. 1395-401. Date of Electronic Publication: 2015 Jan 09. |
| DOI: |
10.1021/jo502179k |
| Abstrakt: |
In contrast to the equilibrium structure of the homoaromatic C(s) homotropenylium cation, C8H9(+) (1), which supports a pinched diatropic ring current, the C(2v) transition state (2) for inversion of the methylene bridge of 1 is antiaromatic and supports a two-lobe paratropic π current, as detected by plotting B3LYP/6-31G** ipsocentric current maps. Participation of the bridge CH bonds is crucial for the change in global character of the current in the transition state, as shown by the quenching of its paratropicity on substitution of H by F. Orbital-based arguments allow rationalization of this transition between homoaromaticity and hyper(conjugative) antiaromaticity. More generally, the hyperconjugative ring current in a family of C(2v) planar-constrained geometries of (CR2)C(N-1)H(N-1)(q) homoannulenes (R = H, F) can be switched from paratropic (antiaromatic) to diatropic (aromatic) by variation of ring size, charge, and bridge substituent. An orbital-based counting rule accounts for these systematic trends. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
|
