scholarly journals The Coordination Chemistry of Phosphoryl Compounds Containing the -N(CH3)2 Group, XII.

1973 ◽  
Vol 28 (3-4) ◽  
pp. 104-106 ◽  
Author(s):  
M.W.G. De Bolster ◽  
B. Nieuwenhuijse ◽  
J. Reedijk

Room temperature electron spin resonance powder spectra have been recorded for some compounds of the type Mn(ligand)p(anion)2 with hexamethylphosphoramide and nonamethylimidodiphosphoramide as ligands (p = 1 - 4) and BF-4, NO-3, Cl-, Br-, I- and NCS-as anions.The values for the zero-field parameters, D and λ, have been determined and are compared with literature data. It is shown that ESR spectroscopy can be very helpful in elucidating the structures of manganese(II) complexes.The high values for the hyperfine coupling constant of the solvates suggest that in these complexes the bonding between the ligands and the metal ion is essentially ionic.

1993 ◽  
Vol 58 (6) ◽  
pp. 1294-1298
Author(s):  
Ali H. Al-Mowali ◽  
Alhan D. Girgees

The linewidths of the hyperfine components of the ESR spectra of vanadyl tetraphenylporphyrin in liquid toluene have been measured as a function of temperature and analyzed in detail. This has allowed the separate contributions to the observed ESR line widths from spin rotational, g tensor anisotropy, hyperfine anisotropy and unresolved nitrogen hyperfine coupling to be evaluated. These results have been used to estimate the size of the nitrogen isotropic hyperfine coupling constant and thus the extent of delocalization of the unpaired electron onto the nitrogen atoms.


1972 ◽  
Vol 50 (12) ◽  
pp. 1981-1983 ◽  
Author(s):  
J. A. Howard

A tert-butylperoxy radical specifically labelled with 17O on the terminal oxygen has been prepared by photolysis of di-tert-butyl peroxide in perdeuterocyclopentane containing 17O enriched oxygen. The value of the 17O hyperfine coupling constant is 23.45 G.


1984 ◽  
Vol 62 (6) ◽  
pp. 1164-1168 ◽  
Author(s):  
Danial D. M. Wayner ◽  
Donald R. Arnold

Several 4-substituted benzyl radicals of the general form R(On)SC6H4CH2•(n = 0, 1, 2; R = Me, Ph, Tol, COCH3 OCH3) have been investigated by electron spin resonance (esr) spectroscopy. In general, the ability to delocalize spin density onto the substituent decreases as n increases. The effect of R on the spin density depends on the oxidation state of the sulphur. These trends are explained by considering the sulphur to be either a spin donor or a spin acceptor, depending on the oxidation state. The σ•α values are determined.


2003 ◽  
Vol 58 (5-6) ◽  
pp. 303-305 ◽  
Author(s):  
V. K. Jain

The electron spin resonance (ESR) of Cr3+ in K1−xTlxAl(SO4)2·12H2O has been studied at 300 K and 9.45 GHz. The ESR spectrum for x between 30 and 90% shows several chromium complexes. The variation of the zero-field splitting parameter D suggests that monovalent ions play an important role in the trigonal distortion of the water octahedron around the trivalent metal ion in alums. - PASC: 76.30 F.


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