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Relaxation studies of carbonyl rhenium clusters. Part 2—relaxation mechanisms and estimation of the 13C chemical shielding anisotropy in the [Re3(μ-H)4(CO)10]− anion at low temperature

✍ Scribed by Tiziana Beringhelli; Giuseppe D'Alfonso; Henriette Molinari


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
483 KB
Volume
24
Category
Article
ISSN
0749-1581

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✦ Synopsis


Application of the non-selective inversion recovery

technique to 13C spectra of moderately enriched [Re,(p-H),(CO),]-indicates that relaxation times, at low temperatures, are strongly field dependent and decrease with increasing field strength. Measurements performed at 183K and at 20.15, 50.31 and 67.88 MHz indicate that chemical shielding anisotropy is dominant at higher fields, which dBers from the behavionr previously observed at room temperature where the main relaxation pathway is scalar coupling with the quadrupolar rhenium isotopes. The =C chemical shielding anisotropy was estimated to be in the range 476 f 40 ppm. Interactions with quadrnpolar rhenium also affect the hydrogen spin-spin relaxation times.