Extractions with metal-dithiocarbamates as reagents

1975 ◽  
Vol 47 (11) ◽  
pp. 1813-1817 ◽  
Author(s):  
Armin. Wyttenbach ◽  
Sixto. Bajo
Crystals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 286
Author(s):  
Edward R.T. Tiekink

A search of the Cambridge Structural Database was conducted for pyridyl-substituted dithiocarbamate ligands. This entailed molecules containing both an NCS2− residue and pyridyl group(s), in order to study their complexation behavior in their transition metal and main group element crystals, i.e., d- and p-block elements. In all, 73 different structures were identified with 30 distinct dithiocarbamate ligands. As a general observation, the structures of the transition metal dithiocarbamates resembled those of their non-pyridyl derivatives, there being no role for the pyridyl-nitrogen atom in coordination. While the same is true for many main group element dithiocarbamates, a far greater role for coordination of the pyridyl-nitrogen atoms was evident, in particular, for the heavier elements. The participation of pyridyl-nitrogen in coordination often leads to the formation of dimeric aggregates but also one-dimensional chains and two-dimensional arrays. Capricious behaviour in closely related species that adopted very different architectures is noted. Sometimes different molecules comprising the asymmetric-unit of a crystal behave differently. The foregoing suggests this to be an area in early development and is a fertile avenue for systematic research for probing further crystallization outcomes and for the rational generation of supramolecular architectures.


2015 ◽  
Vol 3 (5) ◽  
pp. 704-712 ◽  
Author(s):  
Joseph C. Bear ◽  
Nathan Hollingsworth ◽  
Anna Roffey ◽  
Paul D. McNaughter ◽  
Andrew G. Mayes ◽  
...  

2012 ◽  
Vol 12 (12) ◽  
pp. 1216-1229 ◽  
Author(s):  
Eszter Márta Nagy ◽  
Luca Ronconi ◽  
Chiara Nardon ◽  
Dolores Fregona

1973 ◽  
Vol 26 (11) ◽  
pp. 2533 ◽  
Author(s):  
R Chant ◽  
AR Hendrickson ◽  
RL Martin ◽  
NM Rohde

The one-electron oxidation and reduction processes for some 80 dithiocarbamates of Cr, Mn, Fe, Co, Ni, and Cu reveal a marked dependence of redox potential on the metal 3dn electron configuration. For all the complexes examined, the relative ordering of the redox potentials with the dithiocarbamate substituents is remarkably consistent for both oxidation and reduction processes.


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