A two-dimensional network formed by self-associating silver(I) perchlorate with 3-[4-(2-thienyl)-2H-cyclopenta[d]pyridazin-1-yl]benzonitrile

作者:Li Xiao Yan; Liu Qi Kui; Ma Jian Ping; Huang Ru Qi; Dong Yu Bin*
来源:Acta Crystallographica Section C-Crystal Structure Communications, 2009, 65(2): M45-M47.
DOI:10.1107/S0108270108043643

摘要

In the organometallic silver(I) supramolecular complex poly[[silver(I)-mu(3)-3-[4-(2-thienyl)-2H-cyclopenta[d] pyridazin-1- yl] benzonitrile] perchlorate methanol solvate], {[Ag(C(18)H(11)N(3)S)](ClO(4))center dot CH(3)OH}(n), there is only one type of Ag(I) center, which lies in an {AgN(2)S pi} coordination environment. Two unsymmetric multidentate 3-[4-(2-thienyl)-2H-cyclopenta[d]pyridazin-1-yl] benzonitrile (L) ligands link two Ag(I) atoms through pi-Ag(I) interactions into an organometallic boxlike unit, from which two 3- cyanobenzoyl arms stretch out in opposite directions and bind two Ag(I) atoms from neighboring box-like building blocks. This results in a novel two-dimensional network extending in the crystallographic bc plane. These two-dimensional sheets stack together along the crystallographic a axis to generate parallelogram-like channels. The methanol solvent molecules and the perchlorate counter-ions are located in the channels, where they are fixed by intermolecular hydrogen-bonding interactions. This architecture may provide opportunities for host-guest chemistry, such as guest molecule loss and absorption or ion exchange. The new fulvene-type multidentate ligand L is a good candidate for the preparation of Cp-Ag(I)-containing (Cp is cyclopentadienyl) organometallic coordination polymers or supramolecular complexes.