Luminescence and photochemistry of transition metal complexes. I. Studies of temperature dependence of tervalent chromium complexes with oxygen-, nitrogen-, and carbon-coordinated ligands

1971 ◽  
Vol 24 (9) ◽  
pp. 1807 ◽  
Author(s):  
JL Laver ◽  
PW Smith

Experimental investigations of the luminescence exhibited by a range of tervalent chromium complexes are reported. The effects of the coordinated ligand on the temperature dependence of phosphorescence are examined and rationalized in terms of the 4T2-2E energy interval. In the case of hexaureachromium complexes which emit both phosphorescence and fluorescence the varying emission intensities observed for compounds with a variety of anions are interpreted in terms of competition between the non-radiative thermal repopulation process 2E ~~→ 4T2 and the radiative processes 2E → 4A2, 4T2 → 4A2.

1978 ◽  
Vol 31 (11) ◽  
pp. 2355 ◽  
Author(s):  
DM Doddrell ◽  
DT Pegg ◽  
MR Bendall ◽  
AK Gregson

Time modulation of the g-tensor by intramolecular reorientation between structurally equivalent molecular arrangements is postulated to dominate electron spin relaxation in solutions of some paramagnetic transition-metal complexes. The process is treated theoretically and it is shown that the resulting electron spin relaxation time depends on the correlation time for intramolecular reorientation. The temperature dependence of the nuclear T1 thus yields information concerning the potential energy profile for intramolecular reorientation. Experimental results on the field dependence of the temperature dependence of T1 of the methyl proton in Ru(acac)3 are in accord with the theory.


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