The Radical Cations and the Radical Anions of Some Weitz-Type S-Donors
✍ Scribed by Fabian Gerson; Georg Gescheidt; Jürgen Knöbel; Ichiro Murata; Kazuhiro Nakasuji
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- German
- Weight
- 409 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
The radical cations and the radical anions of 1,6-dithiapyrene (1) and 3,lO-dithiaperylene (2) as well as those of three further Weitz-type S-donors 3,4, and 5 have been studied by ESR spectroscopy. The experimental findings for 1: (widths and behaviour on saturation of hyperfine lines) suggest that the ground state of this radical anion is effectively degenerate. With the exception of 1 :, the ESR studies of all radical ions could be complemented by the use of the ENDOR and general TRIPLE resonance techniques. In addition to proton hyperfine data, 33S coupling constants have been determined for 1 (0.34 mT); they are in agreement with the predicted substantial n-spin populations at the S-atoms.
(0.53 mT), 2 (0.46 mT), and 4
📜 SIMILAR VOLUMES
## Abstract The radical anions of the following substituted [2.2]paracyclophanes have been characterized by ESR. and ENDOR. spectroscopy: 4, 16‐dicyano‐ (**__o__**‐**2**), 4, 12‐dicyano‐ (**__p__**‐**2**), 4,5,12,13‐tetracyano‐ (**3**) and 4,5,12,13‐tetrakis (alkoxycarbonyl)‐ [2.2]paracyclophanes (
## Abstract The radical anions of 5,6‐didehydrobenzocyclooctene (**3**), 5,6,9,10‐tetradehydrobenzocyclooctene (**4**) and 1,4,7,10‐tetramethyl‐5,6‐didehydrodibenzo[__a__, __e__]‐cyclooctene (**6**) were prepared __in situ__ from dibromo‐precursors and have been characterized by ESR and ENDOR spect
200 mL) was acidified with 3 drops of 32% HCI and stirred for 15 min at 50°C (exclusion of light). After extraction with CH,CI,, the organic phase was dried (Na,SO,) and purified on silica gel (20 8). After removal of the solvent there remained 0.53 g (72%) of a crystalline product. For further puri
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