Journal
INORGANICS
Volume 9, Issue 9, Pages -Publisher
MDPI
DOI: 10.3390/inorganics9090070
Keywords
copper; dithiocarbamate; clusters; nanomaterials; disulfiram; anticancer agents
Categories
Funding
- King's College London
- Royal Society of Chemistry
- North-West University
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Copper dithiocarbamate complexes have diverse coordination chemistry and paramagnetic properties, with common forms being monomeric or dimeric in the solid state. They have been widely used as single-source precursors for nanoscale copper sulfides, showing a wide range of structural motifs and properties. Additionally, copper dithiocarbamates are known for their relevance in biology and medicine, especially as anticancer agents.
Copper dithiocarbamate complexes have been known for ca. 120 years and find relevance in biology and medicine, especially as anticancer agents and applications in materials science as a single-source precursor (SSPs) to nanoscale copper sulfides. Dithiocarbamates support Cu(I), Cu(II) and Cu(III) and show a rich and diverse coordination chemistry. Homoleptic [Cu(S2CNR2)(2)] are most common, being known for hundreds of substituents. All contain a Cu(II) centre, being either monomeric (distorted square planar) or dimeric (distorted trigonal bipyramidal) in the solid state, the latter being held together by intermolecular C center dot center dot center dot S interactions. Their d(9) electronic configuration renders them paramagnetic and thus readily detected by electron paramagnetic resonance (EPR) spectroscopy. Reaction with a range of oxidants affords d(8) Cu(III) complexes, [Cu(S2CNR2)(2)][X], in which copper remains in a square-planar geometry, but Cu-S bonds shorten by ca. 0.1 angstrom. These show a wide range of different structural motifs in the solid-state, varying with changes in anion and dithiocarbamate substituents. Cu(I) complexes, [Cu(S2CNR2)(2)](-), are (briefly) accessible in an electrochemical cell, and the only stable example is recently reported [Cu(S2CNH2)(2)][NH4]center dot H2O. Others readily lose a dithiocarbamate and the d(10) centres can either be trapped with other coordinating ligands, especially phosphines, or form clusters with tetrahedral [Cu(mu(3)-S2CNR2)](4) being most common. Over the past decade, a wide range of Cu(I) dithiocarbamate clusters have been prepared and structurally characterised with nuclearities of 3-28, especially exciting being those with interstitial hydride and/or acetylide co-ligands. A range of mixed-valence Cu(I)-Cu(II) and Cu(II)-Cu(III) complexes are known, many of which show novel physical properties, and one Cu(I)-Cu(II)-Cu(III) species has been reported. Copper dithiocarbamates have been widely used as SSPs to nanoscale copper sulfides, allowing control over the phase, particle size and morphology of nanomaterials, and thus giving access to materials with tuneable physical properties. The identification of copper in a range of neurological diseases and the use of disulfiram as a drug for over 50 years makes understanding of the biological formation and action of [Cu(S2CNEt2)(2)] especially important. Furthermore, the finding that it and related Cu(II) dithiocarbamates are active anticancer agents has pushed them to the fore in studies of metal-based biomedicines.
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