کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1337384 | 1500252 | 2015 | 8 صفحه PDF | دانلود رایگان |
Two trinuclear centrosymmetric hetero-metallic copper(II)–mercury(II) complexes of general formula [(CuL)2HgX2] (where X = N3− for 1 and 1′ or OCN− for 2 and 2′) have been synthesized using [CuL] as ‘‘ligand complex” (where H2L = N,N′-bis(salicylidene)-1,4-butanediamine) and structurally characterized. Rapid crystallization of both the complexes yielded isomorphous crystals with two independent half molecules (Z′ = 1) in 1 and 2 but the crystals that were grown slowly from the same solutions are not isomorphous and contain single half molecule (1′ and 2′) in the asymmetric units (Z′ = 0.5). Crystal structure analyses reveal that the complexes have discrete trinuclear entity in which two square planar [CuL] units are bonded to a mercury ion through double phenoxido bridges. The Hg(II) is in a six-coordinate distorted octahedral environment being bonded additionally to two mutually trans nitrogen atoms of terminal azide (for 1 and 1′) and cyanate (for 2 and 2′). Higher Z′ compounds are stabilized probably due to weak interactions (C–H⋯N/O and C/H⋯π interactions) that help to hold two independent molecules together.
Two copper(II)–mercury(II) complexes have been synthesized using Cu(II)-salicylaldimine “ligand complex” and N3− or OCN− as coligand. Fast and slow crystallization results Z′ = 1 and Z′ = 0.5 crystals, respectively. The week interactions seem to stabilize the structures with higher Z′.Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 87, 17 February 2015, Pages 403–410