## Abstract Values of one‐bond __J__(C^35^ Cl) and __T__~1~(^35^Cl) were determined for small chlorine‐containing molecules through ^13^C scalar relaxation in the rotating frame. A method is suggested for evaluating the contribution of scalar relaxation which eliminates experimental imperfections.
An investigation of 1H and 13C longitudinal relaxation and relaxation in the rotating frame in solid poly(N-vinylcarbazole)
✍ Scribed by Frank Heatley; Aglaia Karali; Photis Dais
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 118 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0959-8103
- DOI
- 10.1002/pi.727
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^1^H and ^13^C longitudinal relaxation times (T~1~) and relaxation times in the rotating frame (T~1ρ~) have been measured for poly(N‐vinylcarbazole) in the solid state in air and nitrogen atmospheres in an attempt to elucidate molecular motions. In air, the T~1~ relaxation of both ^1^H and ^13^C was dominated by interaction with absorbed paramagnetic oxygen. In nitrogen, the ^13^C T~1~ relaxation times were long (>300 s) and were averaged by ^13^C–^13^C spin diffusion. The ^13^C T~1ρ~ relaxation times showed an exponential dependence on the strength of the rotating ^13^C magnetic field and were thus controlled by spin–spin processes rather than spin–lattice processes.
© 2001 Society of Chemical Industry
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