## Abstract A pulse sequence is presented which allows measurement of short __T__~1~ values (< 1 s) in solids, avoiding probe damage by the use of saturating sequences of 90° pulses. The use of the sequence is illustrated for a cross‐linked polymeric system which contains composite peaks having bot
Carbon-13 spin–lattice relaxation times as a probe for the study of electron donor–acceptor complexes
✍ Scribed by Barry J. Blackburn; Kenneth J. Friesen
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 300 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C spin–lattice relaxation times (T~1~'s) are reported for C‐3 of 2‐methylindole (methyl,3‐^13^C~2~) as a function of the concentration of added 1,3,5‐trinitrobenzene at 35°C in 1,2‐dichloroethane. The observed decreases in T~1~, with increasing concentrations of 1,3,5‐trinitrobenzene, are interpreted in terms of longer time‐averaged correlation times which result from (a) the formation of increasing amounts of electron donor–acceptor complex and (b) increases in viscosity. An equation is derived which makes it possible to obtain estimates of the equilibrium constant for complex formation, and the spin–lattice relaxation time of the complex, from the observed T~1~'s and viscosity measurements. From the data obtained, values of 6.4 × 10^−12^ and 14.1 × 10^−12^ s rad^−1^ were calculated for the effective correlation times (at 35°C and 0.686 centipoise) and 0.21 and 0.28 nm for the effective radii of free and complexed donor respectively.
📜 SIMILAR VOLUMES
## Abstract Relaxation times, __T__, due to the dipolar mechanism of relaxation of ^31^P nuclei were determined for eight pairs of 1,3‐dithianes with P‐containing substituents at the anomeric carbon atom. The separation of dipole–dipole from the total spin–lattice relaxation could be applied for th