REFERENCE DATA causes the electron density to be comparatively lower at C-3 and C-5 than at C-2 and C-4, so that the former signals resonate at lower fields. Distinction between the signals of the C-2/C-4 and C-3/C-5 pairs was achieved by comparing the C-H coupling patterns of 5 and 1. Compounds 1,
Carbon-13 spectra of some heterocyclic analogues of biphenylene
✍ Scribed by J. A. Hugh MacBride; Mei Ling Leow; (the late) Peter M. Wright; John P. Kilcoyne; Basil J. Wakefield
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 219 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 13C chemical shifts for 2,7-, 1,sand 1,6-diazabiphenylenes are reported, together with some coupling constants and the I3C chemical shifts of a benzothiophene analogue of biphenylene. The results can be explained by the existence of a paramagnetic ring current in the four-membered ring of the nitrogen-containing compounds which is absent in the case of the benzothiophene. A possible explanation is offered.
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