Abstract:The copper(I) compounds [Cu + is a possible structural model compound for the metal site in Ace1 and Mac1 transcription factors. In compound 2, two neutral HL ligands bind a Cu I ion in an S,SЈ-isobidentate chelating fashion to
“…[1c-1e,4] In the reaction with Hg and Cu, it was also possible to separate solid compounds whose crystal structures showed the unusual presence of HL (SS) [1d, 5] As a natural development of this synthetic route, we selected the adduct HN(OPPh 2 )(SPPh 2 )·I 2 , HL (OS) ·I 2 , as the oxidising agent on the basis of the ligand containing mixed hard (O) and soft (S) donor atoms for better ion-complexing adaptability. The chemistry of this ligand has been studied far less than that of HL (SS) ; according to the complexes reported in the literature, chelation as an O,S-bidentate anionic ligand [L (OS) ; Scheme 1, structure I] is dominant, but not exclusive, with the S-monodentate coordination mode (Scheme 1, structure II) being adopted in a variety of complexes.…”
“…[1c-1e,4] In the reaction with Hg and Cu, it was also possible to separate solid compounds whose crystal structures showed the unusual presence of HL (SS) [1d, 5] As a natural development of this synthetic route, we selected the adduct HN(OPPh 2 )(SPPh 2 )·I 2 , HL (OS) ·I 2 , as the oxidising agent on the basis of the ligand containing mixed hard (O) and soft (S) donor atoms for better ion-complexing adaptability. The chemistry of this ligand has been studied far less than that of HL (SS) ; according to the complexes reported in the literature, chelation as an O,S-bidentate anionic ligand [L (OS) ; Scheme 1, structure I] is dominant, but not exclusive, with the S-monodentate coordination mode (Scheme 1, structure II) being adopted in a variety of complexes.…”
“…13 Polynuclear Cu I complexes were formed in all cases. X-Ray structure determination and 31 P{ 1 H} solid state CPMAS NMR spectra indicate the formation of the cyclic trimer [Cu 3 Q 1 3 ], and the same structure has been attributed to the complex [Cu 3 Q 2 3 ] on the basis of IR, NMR and ES-MS data. The trimers are formed by thiocarbonyl sulfur atoms in each compound.…”
Competitive transport experiments involving metal ions from an aqueous source phase through a chloroform membrane into an aqueous receiving phase have been carried out using a series of N-(thio)phosphorylated (thio)amide and thiourea ligands as ionophores in the organic phase. The source phase contained equimolar concentrations of Co(II), Ni(II), Cu(II), Zn(II), Ag(I), Cd(II) and Pb(II) with the source and receiving phases being buffered at different pH. Good transport properties were observed for Ag(I) in the case of (13). The best extraction properties have been shown by (3)L(1), (3)L(8), (2)L(7), (3)L(9) and (3)L(11) which contain an unsubstituted nitrogen atom at the C[double bond, length as m-dash]S groups ((3)L(1) and (3)L(9)), or a third nitrogen atom, capable of participating in additional coordination ((3)L(8), (2)L(7) and (3)L(11)). Reaction of Cu(NO(3))(2).6H(2)O with the potassium salt of the N-thiophosphorylated thiourea NH(2)C(S)NHP(S)(OiPr)(2) formed a new supramolecular Cu(I) complex, [{Cu(6)((2)L(1))(6)}{Cu(3)((2)L(1))(3)}.4Me(2)CO] that contains both trinuclear and hexanuclear forms in its solid state structure, and in solution.
The research of adamantane-type compounds has gained momentum in recent years, yielding remarkable new applications for this class of materials. In particular, organic adamantane derivatives (AdR4) or inorganic adamantane-type compounds...
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