The synthesis and transition temperatures of 5-(4-alkyl- and 4-alkoxy-phenyl)-2-cyanobenzo [b] furans and a 5-(4′-alkylbiphenyl-4-yl)-2-cyanobenzo [b] furan:: a comparison with their biphenyl and terphenyl analogues

The synthesis and transition temperatures of a series of 5-(4-alkyl- and 4-alkoxy-phenyl)-cyanobenzo[b]furans and a 5-(4'-alkylbiphenyl-4-yl)-2-cyanobenzo [b]furan are presented. The 2-cyanobenzo[b]furans show similar mesophase types to the analogous biphenyl and terphenyl compounds, which are obtained by replacing the benzo[b]furan unit with a phenyl ring. The transition temperatures for the 2-cyanobenzo[b]furan compounds are always higher than for their biphenyl and terphenyl counterparts, but they are much lower than for the corresponding phenylnaphthalenes. Five mesogenic benzo[b]furans without a cyano group were prepared as intermediates and these compounds have lower clearing points than their biphenyl analogues.