## Abstract Analysis of the noise decoupled ^13^C spectra of doubly ^13^C labelled compounds where the two labelled carbons are identical, makes the determination of reltive signs of ^13^C^13^C coupling constants possible in a very simple way. The involved carbon form AA'X or AA'B spin systems.
13C13C coupling constants in derivatives of trans-stilbene and tetraphenylethylene. Determination of relative signs II
✍ Scribed by P. E. Hansen; O. K. Poulsen; A. Berg
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 493 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Magnitudes and signs of ^13^C^13^C coupling constants in compounds of the type Ph^13^CR^1^R^2^^13^CR^1^R^2^Ph have been determined and the results are discussed in a broader context. Two types of coupling constants, J(C‐i, C‐α) and J(C‐i, C‐β), between aromatic carbon atoms and the benzylic carbons, probably with different coupling mechanisms, are considered. Whereas ^2^J(C‐2, C‐α) are always found positive, ^2^J(C‐1, C‐β) in the present compounds are found to be negative or about zero. ^3^J(C‐3, C‐α) has the same sign as ^2^J(C‐2, C‐α). A ^4^J and a ^5^J were observed in trans‐stilbene.
📜 SIMILAR VOLUMES
## Abstract For mass spectrometric studies 1‐phenyl‐2‐phenyl‐1‐^13^C‐ethene‐1‐^13^C (trans‐stilbene) was synthesized from acetic‐1‐^13^C acid and acetic‐2‐^13^C acid via methylcyclohexene‐1‐^13^C and ‐α‐^13^C and toluene‐1‐^13^C and ‐α‐^13^C. No scrambling of the label was observed during the aroma
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