2005/11/01 by Matthew N. Gard, Matthew K. Kiesewetter, Richard C. Reiter +1 · 2 citations
Chemistry · Physics and Astronomy · #Cyclization and Aryne Chemistry #Synthesis and Properties of Aromatic Compounds #Advanced Chemical Physics Studies
paper · doi:10.1021/ja053886l
openalex publication_date 2005/11/01 · openalex created_date 2022/05/12 · openalex updated_date 2026/06/26
Only one isomer of o-benzyne ([6]annulyne or 1,2-didehydrobenzene) exists, but the dehydro analogue of the "ring-opened double benzene", [12]annulyne, was generated in several isomeric forms. 1,5-Hexadiyne undergoes self-condensation in the presence of potassium tert-butoxide to yield two isomers of [12]annulyne (3,11-di-trans-[12]annulyne and 5,9-di-trans-[12]annulyne), both of which exhibit a weak paratropic ring current in their 1H NMR spectra and are oxygen sensitive. They can be reduced to their respective dianions, which are diatropic. A third isomer (3,9-di-trans-[12]annulyne) was generated via the complete dehydrohalogenation of hexabromocyclododecene and found to be much less stable but can be tamed via one- or two-electron reduction. A tight association of the cation (K+) with the p(y)-orbitals within the alkyne moiety results in an unusually low-field resonance for an adjacent external proton.