## Abstract A model of the paramagnetism in cobalt(II) porphyrin complexes has been developed which successfully calculates paramagnetic shifts for protons not affected by the contact term. The model utilizes a single large dipole positioned on the cobalt(II) atom, and calculates the pseudoβcontact
Evaluation of dipolar shifts and paramagnetic anisotropy in penta coordinated cobalt(II) complexes
β Scribed by M.M. Dhingra; M.D. Zingde; R.N. Mukherjee
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 364 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
The isotropic proton shifts for the pyridine N-oxide and ypicoline N-oxide protons have been observed in the pcnta coordinated adducts of these bases with bis[diCn-tolyl)dithioplrosphinato] cobalt[II). The con~bution to the observed shifts due to dipolar interaction has been calculated. Prom the dipolar shifts, it ~3s ascertained that the pyridine N-oside complexes have a bent structure in solution with a Co.-O-N angle of 12.5". An estimate of the pvamagnetic anisotropy of the cobalt complex yields Kii--ir, = 4244 X lo-' cm3/mole.
π SIMILAR VOLUMES
## Abstract Fiveβcoordinate complexes have been prepared, of the general formulae [CoX(L'L~3~)]^+^ and [RhX(L'L~3~)], where X = halogen and L'L~3~ = a quadridentate tripodβlike ligand containing various Group V donor atom sets. The electronic spectra and magnetism of the cobalt(II) series can be in
31 P NMR measurements on CoADP bound to creatine kinase designed to estimate the relative contribution of scalar and dipolar interactions to 31 P spin relaxation rates show that these rates are primarily due to distance-dependent dipolar interactions and that the contribution of the scalar interacti
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