Abstract

Mononuclear barium and binuclear silver(I) complexes of bibracchial tetraimine Schiff-base macrocycles L1—L4 derived from the ‘2 + 2’ condensation of 2,6-diacetylpyridine and the functionalised triamines N,N-bis(2-aminoethyl)-2-(aminomethyl)pyridine, N,N-bis(3-aminopropyl)-2-(aminomethyl) pyridine, N,N-bis(3-aminopropyl)-2-methoxyethylamine, and N,N-(3-aminopropyl)-2-methoxybenzylamine, respectively, have been synthesised. The crystal structures of five complexes have been determined: [BaL1][ClO4]2 crystallises in the monoclinic space group C2/c(C62h, no. 15) and has unit-cell dimensions a= 20.310(38), b= 14.453(41), c= 15.137(29)A, β= 104.84(15)°, and Z= 4; [Ag2L1][ClO4]2 crystallises in the tetragonal space group I41cd(C124v, no. 110) with a= 28.11 (4), c= 21.618(16)A, and Z= 16; [Ag2L2][ClO4]2·0.5H2O crystallises in the triclinic space group P(C1i, no. 2) with a= 12.277(16), b= 13.899(14), c= 15.260(50)A, α= 77.30(20), β= 70.17(20), γ= 71.27(9)°, and Z= 2; [Ag2L3][ClO4]2· 0.5 H2O crystallises in the triclinic space group P(C1i), no. 2) with a= 14.171 (14), b= 18.323(16), c= 12.495(23)A, α= 99.20(12), β= 120.13(11), γ= 116.35(7)°, and Z= 2; [Ag2L4][ClO4]2 crystallises in the monoclinic space group P21/a(C52h, no. 14),a= 16.595(16), b= 13.363(11), c= 23.951 (25)A, β= 105.43(8)°, and Z= 4. The macrocycles fold to present molecular clefts into which the metals co-ordinate. Modification of the ring size and of the nature of the donor atom in the pendant arm leads to the Ag ⋯ Ag separation in the binuclear silver(I) complexes varying from 2.9 to 6.9 A.

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