C 30H38Cd2N10O2S4,m onoclinic, P121/c1(no. 14), a =7.4031(3) Å, b =26.526(1) Å, c =10.0970(4) Å, b =108.111(2)°, V =1884.6 Å 3 , Z =2,R gt (F) =0.024,
Source of materialAmethanol solution of Cd(OAc)2 · 2H 2 O(0.26 g, 1mmol) was added to amethanol solution (30 ml) of ammonium thiocyanate (0.15 g, 2mmol) and the Schiff base ligand (2-morpholin-4-ylethyl)-(1-pyridin-2-ylethylidene)amine (0.23 g, 1m mol) with stirring. The resulting solution was allowed to stand at room temperature for aweek, yielding colorless block-shaped single crystals.
Experimental detailsHatoms were constrained to ideal geometries, with d(C-H) = 0.93 -0.97 Å,and U iso(H) =1.2 Ueq(C) or 1.5 Ueq(C7).
DiscussionConsiderable attention has been focused on Schiff bases and their complexes because of the interesting structures and applications [1][2][3]. The cadmium(II) complexes are widely investigated for their fluorescent properties [4][5][6]. The title crystal structure is built up of acentrosymmetric dimeric cadmium(II) complex. The Cd···Cd distance is 5.936(2) Å.The Cd(II) atom is coordinated by three Na toms of the tridentate ligand 2-morpholin-4-ylethyl)-(1-pyridin-2-ylethylidene)amine, two Nand one Satoms from three thiocyante ligands, forming a distorted octahedron. The two halves of the dimer are related by a center of inversion. The distortion of the octahedral coordination can be observed on the bond angles: ∠N1-Cd1-N2 =68.43(7)°a nd ∠N2-Cd1-N3 =74.55°are much smaller than 90°,which is caused by the strain created by the five-membered chelate rings N1-Cd1-N2-C6-C1 and N2-Cd1-N3-C9-C8, respectively. The bond lengths d(Cd-N) are in the range of 2.99(2) -2.438(2) Å and d(Cd-S) =2.6712(6) Å,which is comparable to the similar cadmium(II) complexes with Schiff bases [7][8][9].