Abstract

The reaction of [Cu(CH3CN)4](BF4) with 1-methyl-1,3-imidazolidine-2-thione {SC3H4(NMe)NH}, under aerobic conditions at room temperature, yielded an unusual one-dimensional coordination polymer, namely, catena-poly[[[(1-meth-yl-1,3-imidazolidine-2-thione-κS)copper(I)]-μ-(1-methyl-1,3-imidazolidine-2-thione)-κ2 S:S-copper(I)-μ-[3,3'-(sulfanedi-yl)bis-(1-methyl-1,3-imidazolidine-2-thione)]-κ5 S,S',S'':S,S''] bis-(tetra-fluorido-borate)], {[Cu2(C4H8N2S)2(C8H14N4S3)](BF4)2} n or [Cu4(κ5:L 1-N-S-N-L 1)2(κ1:L 1-NH)2(κ2:L 1-NH)2] n (BF4)4n 1 [L 1 = SC3 H4(NMe)NH] with sulfur-bridged {CuI 4S10} n central cores. The in situ generated bis-(1-methyl-1,3-imidazolidinyl-2-thione) sulfide [{SC3H4(NMe)NSN(NMe)C3H4S; abbrev. L 1-N-S-N-L 1] ligand, in combin-ation with 1-methyl-1,3-imidazolidine-2-thione (L 1-NH) ligands, construct this coordination polymer. Each CuI ion is bonded to four sulfur donor atoms in a distorted tetra-hedral geometry and the formation of this polymer solely by sulfur donor atoms with {CuI 4S10} n central cores, is the first such example in copper-heterocyclic-2-thione chemistry.

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