Dehydrogenative homocoupling of terminal alkenes on copper surfaces: a route to dienes

Angew Chem Int Ed Engl. 2015 Apr 7;54(15):4549-52. doi: 10.1002/anie.201412307. Epub 2015 Feb 20.

Abstract

Homocouplings of hydrocarbon groups including alkynyl (sp(1) ), alkyl (sp(3) ), and aryl (sp(2) ) have recently been investigated on surfaces with the interest of fabricating novel carbon nanostructures/nanomaterials and getting fundamental understanding. Investigated herein is the on-surface homocoupling of an alkenyl group which is the last elementary unit of hydrocarbons. Through real-space direct visualization (scanning tunneling microscopy imaging) and density functional theory calculations, the two terminal alkenyl groups were found to couple into a diene moiety on copper surfaces, and is contrary to the common dimerization products of alkenes in solution. Furthermore, detailed DFT-based transition-state searches were performed to unravel this new reaction pathway.

Keywords: copper surfaces; density functional calculations; dimerization; homocoupling; surface chemistry.