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Joined 2026-09-21 Message
Jeffrey M. Robertson Created 2026-10-20 Updated 2026-11-05
Jeffrey M. Robertson used model reactions to investigate intermediates in liquid-crystal polymer synthesis. Trapping experiments with secondary amines supported formation of a quinoid ketene through E1cb elimination, connecting a proposed intermediate with an observable product.[ref]
Model experiments implicate a benzoquinoneketene intermediate in LCP synthesis by Jeffrey M. Robertson and colleagues. 2011, hydroxybenzoyl ester models, E1cB fragmentation and secondary-amine trapping
The three regions represent competing pathways whose leaving-group sensitivities differ.
- Region 1, : good leaving groups permit E1cB mechanism. OH first deprotonates the para phenol. The phenoxide lone pair then pushes through the ring, with loss of ArO from the acyl group, giving a quinoid ketene, schematically . Water/hydroxide traps the ketene and proton transfers restore the aromatic hydroxybenzoate. Rate-limiting fragmentation has extensive C–OAr cleavage, hence strong dependence on leaving-group basicity.
- Region 2, : as ArO becomes a worse leaving group, elimination slows steeply and ordinary hydroxide addition to neutral C becomes competitive/dominant. The tetrahedral acyl-substitution pathway is much less sensitive to leaving-group p.
- Region 3, : hydroxide attacks the deprotonated phenoxide ester C. Its low electrophilicity and anion-anion interaction make addition slow. The leaving group is little involved in that addition transition state. Combined with prior deprotonation, this is the third-order term.
The bend in the upper plot is a crossover of mechanisms, not a discontinuous change in the identity of the leaving group. The lower plot is the separate hydroxide-on-phenoxide pathway.
Parallel acyl-substitution and conjugate-base elimination pathways
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