Polypyridyl-functionalizated alkynyl gold(I) metallaligands supported by tri- and tetradentate phosphanes

摘要

A series of alkynyl gold(I) tri and tetratopic metallaligands of the type [Au-3(C C-R)(3)(mu(3)-triphosphane)] (R = 2,2'-bipyridin-5-yl or C10H7N2, 2,2': 6',2 ''-terpyridin-4-yl or C15H10N3; triphosphane = 1,1,1-tris(diphenylphosphanyl) ethane or triphos, 1,3,5-tris(diphenylphosphanyl) benzene or triphosph) and [Au-4(C C-R)(4) (mu(4)-tetraphosphane)] (R = C10H7N2, C15H10N3; tetraphosphane = tetrakis(diphenylphosphanylmethyl) methane or tetraphos, 1,2,3,5-tetrakis(diphenylphosphanyl) benzene or tpbz, tetrakis(diphenylphosphaneylmethyl)-1,2-ethylenediamine or dppeda) were obtained in moderate to good yields. All complexes could be prepared by a reaction between the alkynyl gold(I) polymeric species [Au(C C-R)](n) and the appropriate polyphosphane. An alternative strategy that required the previous synthesis of the appropriate acetylacetonate precursors [Au-n(acac)(n)(mu(n)-polyphosphane)] ("acac method") was assayed, nevertheless only the polyacac derivatives [Au-3(acac)(3)(mu(3)-triphosphane)] (triphosphane = triphos and triphosph) and [Au-4(acac)(4)(mu(4)-tetraphos)] could be isolated and characterized. All compounds were characterized by IR, multinuclear NMR spectroscopy and ESI (+) mass spectrometry. The X-ray crystal structure of complexes [Au-4(C C-C10H7N2)(4)(mu(4)-tetraphos)] and [Au-4(C C-C10H7N2)(4)(mu(4)-tpbz)] showed the involvement of all the gold atoms in close intramolecular Au. Au contact as well as intermolecular p stacking interactions between the aromatic rings of the polypyridyl ligands. The photophysical properties of the synthesized compounds were carefully studied and used as a probe of their possible use as multidentate ligands for Cu(I) and Zn(II). The UV-Vis speciation studies of the complexation reactions were conducted via metal titration and, in most cases the dangling units of the ligand were found to behave in a fairy independent manner. While in the case of Cu(I) multiple equilibria exist in solution a single complex is detected for Zn(II) under the conditions studied.