## Abstract All carbon resonances in the title compounds have been unequivocably assigned. Steric effects in the __peri__ substituted compounds have been compared with analogous effects in naphthalene and benzo[__b__]furan. The observed effects are not explained by current theory. Unusual deshieldi
13C NMR spectra of thiophenes. III—Bromothiophenes
✍ Scribed by Tyo Sone; Kunimi Fujieda; Kensuke Takahashi
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 266 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The ^13^C NMR spectra of all bromo substituted thiophenes have been obtained at 15·085 MHz. ^13^C signal assignments for monobromothiophenes have been confirmed by comparison with the spectra of their partially deuteriated derivatives; a revision is made for the assignment in 3‐bromothiophene. The substituent effect of bromine is generally additive for the ^13^C chemical shifts. The substituent effect on various types of ^13^C, ^1^H coupling constants is also obtained and discussed.
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