Electrochemical synthesis of pyridine-2-thionato complexes of zinc(II) and cadmium(II): the crystal structure of 1,10-phenanthroline-bis(pyridine-2-thionato)zinc(II)
References (38)
Coord. Chem. Rev.
(1985)- et al.
J. Chem. Soc. A.
(1969)et al.Z. Naturf.
(1975)et al.Inorg. Chim. Acta
(1983) Polyhedron
(1986)et al.Coord. Chem. Rev.
(1987)- G.M. Sheldrick, SHELXS-86, Program for the solution of crystal structures from diffraction data. University of...
The Enraf-Nonius CAD4 SDP, a realtime system for concurrent X-ray data collection and crystal structure determination
- et al.
J. Chem. Soc., Dalton Trans.
(1983) - et al.
J. Chem. Soc., Dalton Trans.
(1974) - et al.
Inorg. Chim. Acta
(1988) - et al.
J. Chem. Soc., Chem. Commun.
(1987) - et al.
Inorg. Chem.
(1987)
Inorg. Chem.
Can. J. Chem.
Acta Cryst.
J. Organomet. Chem.
J. Chem. Soc., Dalton Trans.
J. Chem. Soc., Dalton Trans.
Inorg. Chim. Acta
J. Chem. Soc., Dalton Trans.
Bull. Chem. Soc. Japan
Acta Cryst.
Bull. Chem. Soc. Japan
J. Am. Chem. Soc.
Cited by (42)
Heterocyclic-2-thione derivatives of group 10–12 metals: Coordination versatility, activation of C[dbnd]S (thione) bonds and biochemical potential
2021, Coordination Chemistry ReviewsCitation Excerpt :One Zn has ZnS3O and others have ZnN2SO cores. Polymeric ZnII complexes, {Zn(κ1S:1O-pySH-5-COO)2}n 540 [319], {Zn(κ1S:1O-pySH-3-COO)2}n 541 [320] and {Zn(imdtH2)2(S2O3)}n 542 [321], have been reported. In the polymers, 540 and 541, one S and one O are bridging atoms, while in 542, zinc(II) is bonded to two κ1S-imdtH2 thio-ligands and thiosulfate acts as S, O-bridge.
The use of sacrificial anodes for the electrochemical synthesis of metallic complexes
2015, Coordination Chemistry ReviewsCitation Excerpt :On the other side, the electrolysis of acetonitrile solutions of these thiones (HL1 and HL2) and bidentate co-ligands such as bipy or phen (L′) in the presence of a zinc anode gave the corresponding heteroleptic complexes [Zn(L1)2L′] and [Zn(L2)2L′]. The crystal structures of the octahedral Zn(II) complexes with 3-trifluoromethylpyridine-2-thionato [L2b]− and bipy or phen [24] are quite similar to that reported for [Zn(L2a)2(phen)] [279] and they exhibit the two monoanionic thionato ligands acting in a bidentate chelating (S,N) manner. In a difference, the structure of the tetrahedral Zn(II) complexes [Zn(L2c)2(bipy)] [24]; [Zn(L1b)2(phen)] [277]; and [Zn(L1c)2(bipy)] [277], which were obtained by electrolysis of acetonitrile solutions of the corresponding heterocyclic thione and the appropriate co-ligand in the presence of a zinc anode, contain the thionato ligand showing a monoanionic monodentate behavior.
Raman spectroscopic studies on surface coordination mechanism of benzotriazole and triphenylphosphine with metals
2009, Vibrational Spectroscopy