Maerkl, Gottfried and Ehrl, Robert and Kreitmeier, Peter (2003) Oligomeric condensation products of (1E,3E,5E)-1,6-di(2-furyl)hexa-1,3,5-triene with acetaldehyde: Tetrahydro-tetramethyl-octaepoxy[60]annulene(6.1.6.1.6.1.6.1). HELVETICA CHIMICA ACTA, 86 (3). pp. 760-772. ISSN 0018-019X
Full text not available from this repository.Abstract
The Ca(NO3)(2)-induced condensation of(1E,3E,5E)-1,6-di(2-furyl)hexa-1,3,5-triene (6) with acetaldehyde yields the linear 'oligomers' 7-11 with 2-6 1,6-di(2-furyl)hexa-1,3,5-triene units and 1-4 acetaldehyde units, besides a cyclic condensation product 12 obtained from 4 equiv. of 6 with 4 equiv. of acetaldehyde. According to spectroscopic studies, 12 is the tetrahydro-tetramethyl-octaepoxy[60]annulene(6.1.6.1.6.1.6.1) as the most expanded annulene system known so far. While the dehydrogenation of 12 to give the tetramethyloctaepoxy[60]annulene(6.1.6.1.6.1.6.1) cannot be achieved, the oxidation of 12 with Br-2 yields a black, in all organic solvents nearly insoluble solid 14, which possibly is the tetramethyl-octaepoxy[58]annulene(6.1.6.1.6.1.6.1) dication. Because of the insolubility of 14, unfortunately most of its spectroscopic data are not available. However, the lambda(max) values in the UV/VIS/NIR spectrum of 14 (Soret and Q bands) are in line with the values of the tetraepoxy[26]annulene(4.2.4.2) dication, the tetraepoxy[30]annulene(4.4.4.4) dication, and the tetraepoxy[34]annulene(6.4.6.4) dication.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | DICATIONS; |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 25 Aug 2021 11:22 |
| Last Modified: | 25 Aug 2021 11:22 |
| URI: | https://pred.uni-regensburg.de/id/eprint/39458 |
Actions (login required)
 |
View Item |
