Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1322024 | Journal of Organometallic Chemistry | 2012 | 4 Pages |
Treatment of 4,4′-diethynyl-2,2′-bipyridine with (3-tolyl)3PAuCl or tBu3PAuCl leads to the gold(I) phosphane decorated bis(alkynyl)-2,2′-bipyridine complexes 5 and 6 respectively. These complexes have been fully characterized and their single crystal structures reveal that the bulky nature of the phosphane substituents preclude intermolecular Au…Au close contacts. Both compounds are photoactive and emissive in solution, but when irradiated at 238 nm (for 5) or 234 nm (for 6), immediate decay of the emission spectrum is observed with growth of new bands; the observations are compared with related compounds in which the gold(I) phosphane units contain less sterically demanding substituents.
Graphical abstractReactions of 4,4′-diethynyl-2,2′-bipyridine with (3-tolyl)3PAuCl or tBu3PAuCl produce photoactive and emission gold(I) phosphane decorated bis(alkynyl)-2,2′-bipyridine complexes. The effects of the bulky phosphane substituents on solid state structures and photodegradation are assessed.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Bis(alkynyl)-2,2′-bipyridines. ► Photoactive gold(I) phosphane derivatives and photodegradation. ► Crystallographic studies reveal no aurophilic interactions in the solid state.