ECE mechanisms as a tool for the investigation of unstable metal complexes. 3. Polarographic studies of ligand dissociation of dibromocobalt(II) and dibromocobalt(III) complexes

1981 ◽  
Vol 20 (7) ◽  
pp. 2090-2093 ◽  
Author(s):  
Akifumi. Yamada ◽  
Tadatsugu. Yoshikuni ◽  
Nobuyuki. Tanaka
1987 ◽  
Vol 52 (4) ◽  
pp. 838-847 ◽  
Author(s):  
Josef Hanzlík ◽  
Jan Hovorka ◽  
Anna Maria Camus

Transfer of trisbipyridine transition metal complexes [M(bpy)3]2+ (bpy = bipyridine) across the water-1,2-dichloroethane interface can be classified as a simple transfer of a divalent cation in case that the central atom M = Fe, Ni, Ru or Os, while for M = Co, Cu or Zn the charge transfer is accompanied by considerable chemical changes, such as the ligand dissociation and the solvolysis. Thermodynamic and transport parameters characterizing the transfer of [M(bpy)3]2+ ions from water to 1,2-dichloroethane have been determined from voltammetric measurements.


2020 ◽  
Vol 7 (3) ◽  
pp. 786-794 ◽  
Author(s):  
Jingqi Han ◽  
Kin-Man Tang ◽  
Shun-Cheung Cheng ◽  
Chi-On Ng ◽  
Yuen-Kiu Chun ◽  
...  

A new class of luminescent cyclometalated Ir(iii) complexes with readily tunable mechanochromic properties derived from the mechanically induced trans-to-cis isomerization have been developed.


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