Self-assembly and oligomerization of alkyne-terminated molecules on metal and oxide surfaces.

We report the self-assembly and subsequent oligomerization of organic molecules based on terthiophenes bearing a terminal alkyne moiety. Molecules with thioacetate and phosphonic acid functional groups were synthesized, enabling molecular self-assembly on metal (Au and Pd) and metal oxide [Al(2)O(3), HfO(2), and indium tin oxide (ITO)] surfaces, respectively. The molecules were assembled from solution and then oligomerized using either 2,5-norbornadiene-rhodium(I) chloride dimer or UV light.

Functionalizations of [6]- and [7]helicenes at their most sterically hindered positions.

Although the reactions of enol ethers of aryl methyl ketones with benzoquinone make it easy to prepare nonracemic helicenes that are substituted by hydroxyl groups at their 1,omega-positions, the hydroxyl groups fail to facilitate the introduction of electrophiles ortho to them. However, ethers of [6]- and [7]helicenols prepared in this way, seemingly because of the activation by the alkoxyl groups at the 6-positions, combine with electrophilic reagents to introduce bromines and acyl groups exactly into these positions. Moreover, these bromine and acyl groups can be transformed into other functional groups (including phosphine oxides and acetylenes), the ether functions adjacent to these functional groups can then be removed, and the phenols can be oxidized to quinone-acetals.