Second-sphere hydrogen-bonding in heteroditopic mercaptopyridinium copper(I) frameworks

作者:Bianketti Slawomir; Blake Alexander J; Wilson Claire; Hubberstey Peter*; Champness Neil R; Schroder Martin
来源:CrystEngComm, 2009, 11(5): 763-769.
DOI:10.1039/b813672f

摘要

A series of Cu(I) complexes of 4-mercaptopyridine (LH) are reported that form three-dimensional hydrogen-bonded frameworks in the solid-state. The 4-mercaptopyridine ligands co-ordinate to the Cu(I) cations via thiolate donors, leaving a pyridinium hydrogen-bond donor available for interaction with the relevant counter-anions. Four new Cu(I) complexes, [Cu(2)(LH)(6)]center dot 2Cl 1, [Cu(2)(LH)(6)]center dot SiF(6)center dot 2MeOH 2, [Cu(4)(LH)(10)]center dot-4NO(3)center dot MeOH center dot H(2)O 3 and {[Cu(6)(LH)(13)]center dot 2BF(4)center dot 2SiF(6)center dot 7.5MeOH}(infinity) 4 are reported and have been structurally characterised by single crystal X-ray diffraction. In each case hydrogen-bonded arrays are formed via N-H center dot center dot center dot anion hydrogen-bonds or by including hydrogen-bonding to guest solvent molecules. Whereas compound 1 adopts a rutile-like structure with [Cu(2)(LH)(6)](2 ) and Cl(-) nodes adopting six- and three-connected arrangements, respectively, compounds 2 and 3 adopt six-connected nets of alpha-Po (4(12)6(3)) topology. Compound 4 forms a thiolate bridged co-ordination polymer constructed from repeating units of six Cu(I) centres connected by ten bridging and three terminal thiolate-bound LH donors, with complex hydrogen-bonding observed between the polymer cation and counter-anions.

  • 出版日期2009