Electron spin resonance spectra and structure of some group IV and group V derivatives of dicyclopentadienyltitanium(III)

Author(s):  
J. G. Kenworthy ◽  
J. Myatt ◽  
M. C. R. Symons
1982 ◽  
Vol 229 (3) ◽  
pp. 215-222 ◽  
Author(s):  
Alwyn G. Davies ◽  
Zbigniew Florjańczyk ◽  
Ewa Lusztyk ◽  
Janusz Lusztyk

1981 ◽  
Vol 59 (1) ◽  
pp. 156-163 ◽  
Author(s):  
D. Plancherel ◽  
D. R. Eaton

Electron spin resonance spectra are reported from a number of radicals derived from 2,4-pentadione substituted at the 3 position with nitroxide-containing groups. If the substituent is t-butyl nitroxide no metal complexes are formed. This is attributed to steric factors which prevent the formation of the enol form of the β-diketone. If the substituent is trifluoromethyl nitroxide two types of metal complex have been observed. The esr spectra of the first type are very similar to that of the uncomplexed radical. Such complexes are formed with Co(III) and Al(III). The esr spectra of the second type show considerably increased 14N and 19F hyperfine coupling constants and in some cases large couplings to the metal nucleus. Complexes for the second type have been observed with Pd(II), Pt(II), and Rh(III). The possible structures of these radicals are discussed.


1968 ◽  
Vol 21 (5) ◽  
pp. 1155 ◽  
Author(s):  
R Colton ◽  
CJ Rix

Complexes of the general formula Mo(CO)2L2X2 (L = pyridine (py), 2,2'- dipyridyl (dipy), 1,l0-phenanthroline (phen); X = Cl, Br) have been isolated. The pyrldine derivatives are yellow monomeric compounds which are paramagnetic, but the complexes with dipy and phen contain diamagnetic seven-coordinate cations and are correctly formulated as [Mo(CO)2L2X]+X-. Conductance, infrared, magnetic, and electron spin resonance studies have been carried out.


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