2720-80-1Relevant articles and documents
Synthesis and coordination chemistry of fluorinated xanthate ligands
Fawcett, John,Hope, Eric G.,Stuart, Alison M.,Wood, Dan R.W.
, p. 1117 - 1124 (2005)
Alkali metal, copper, nickel and rhodium complexes of alkylated [S 2COC8H17] and fluoroalkylated xanthate ligands [S2COCmH2mCnF2n+1] (m = 2, n = 4, 6; m = 3, n = 1, 8) have been prepared in high yields and characterised by elemental analysis, mass spectrometry, IR and NMR spectroscopies. The structures of [Cu(S2COC8H 17)(PPh3)2], [Cu(S2COC 3H6CF3)(PPh3)2], [Ni(S2COC3H6CF3)2], [Cp*RhCl(S2COC8H17)] and [Cp*RhCl(S2COC3H6CF3)] have been determined by single crystal X-ray diffraction.
Syntheses, structures, and electrochemical studies of N,N′-bis(alkylthiocarbamate)butane-2,3-diimine Cu(II) complexes as pendent alkoxy derivatives of Cu(ATSM)
Vishnosky, Nicholas S.,Mashuta, Mark S.,Buchanan, Robert M.,Grapperhaus, Craig A.
, p. 45 - 51 (2017/03/01)
A series of N2S2-Cu(II) complexes based on N,N′-bis(alkylthiocarbamate)butane-2,3-diimine ligands have been synthesized and characterized by spectroscopic, electrochemical, and single crystal X-ray diffraction methods. This class of ligands contains a conjugated N2S2chelate framework with a non-coordinating, terminal alkoxy (–OR) group. Ligands and Cu(II) complexes were investigated for R = Me, Et,nPr,iPr, and octyl. Additionally, N,N′-bis(ethylthiocarbamate)hexane-3,4-diimine and its Cu(II) complex were analyzed. Single crystal X-ray diffraction studies on all six Cu(II) complexes confirm a square planar Cu(II) environment with no significant changes in the core structure as a function of R. Spectroscopic studies are consistent with a similar electronic environment in all complexes. However, electrochemical investigations reveal significant shifts in the CuII/Iand CuIII/IIreduction potentials throughout the series. The complexes are analogues of the well-known bis(thiosemicarbazone) Cu(II) which contain a similar donor core with terminal, non-coordinating amines. Substitution of the terminal amines of bis(thiosemicarbazones) with the alkoxy groups of N,N′-bis(alkylthiocarbamate)butane-2,3-diimines allows tuning of redox potentials with minimal changes in the physical and electronic structure.