𝔖 Bobbio Scriptorium
✦   LIBER   ✦

13C spin-relaxation times in some paramagnetic transition-metal acetylacetonate complexes. Importance of ligand-centred relaxation

✍ Scribed by David M. Doddrell; David T. Pegg; M.Robin Bendall; Hans P.W. Gottlieb; Anthony K. Gregson; Maurice Anker


Publisher
Elsevier Science
Year
1976
Tongue
English
Weight
352 KB
Volume
39
Category
Article
ISSN
0009-2614

No coin nor oath required. For personal study only.

✦ Synopsis


r3C spin-lattice relaxation times have been measured for some of the ligand positions of some metal acetylacetonate complexes. The results suggest that the relaxation process is dominated by dipolar interactions with unpaired eiectron spin residing on the ligand. A simple analysis of ligand-centred dipolar relaxation is used to quantify its importance and it is demonstrated that spin density greater than 10v3 of an unpaired electron may be significant.


📜 SIMILAR VOLUMES


Proton spin relaxation in some paramagne
✍ David M. Doddrell; David T. Pegg; M.Robin Bendall; Anthony K. Gregson 📂 Article 📅 1976 🏛 Elsevier Science 🌐 English ⚖ 437 KB

Proton spin-lattice (T1) and spin-spin (T2) relaxation times have been measured for CH3 protons in a series of paramagnetic transition-meta! acetylacetonatc complexes and the results interpreted in terms of current relaxation theory. r&the correlation time for molecular reorientation, was estimated

Structural studies of metalloporphyrins.
✍ J. Huet; A. Gaudemer 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 574 KB

## Abstract Rotation barriers around the metal—pyridine bond of various macrocyclic complexes of cobalt(III), rhodium(III), zinc(II) and magnesium(II) have been studied using the ^13^C longitudinal relaxation times, __T__~1~, of the carbon atoms of pyridine and the macrocycle. The data have been ra

High-resolution 13C NMR study of free an
✍ Hazime Saitô; Ryoko Tabeta; Motoko Yokoi 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 819 KB

High-resolution 13C NMR spectra of 15 samples of uncomplexed and metalcomplexed tetranactin and nonactin were recorded in the solid state, revealing characteristic displacements of peaks due to complex formation and the effect of crystalline packing on the 13C chemical shifts and spidattice relaxati