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ol051572x_si_004.pdb (7.52 kB)

1,3,6,9,12,14,17,20-Octaethynyltetrabenz[a,b,f,j,k,o]-4,5,10,11,15,16,21,22- octadehydro[18]annulene:  A Carbon-Rich Hydrocarbon

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posted on 2005-09-01, 00:00 authored by Ognjen Š. Miljanić, Daniel Holmes, K. Peter C. Vollhardt
Dodecaynes 1ad have been prepared via a convergent strategy that employs Sonogashira couplings as the carbon−carbon bond-forming tool. Due to the steric bulk of the DMTS groups, 1c adopts a nonplanar conformation, the dynamics of which have been probed by VT-NMR. The cobalt-catalyzed isomerization of 1a,b produced the new conjugated phenylenes 2a,b and 3a,b, respectively.

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