237764-57-7Relevant academic research and scientific papers
Mechanism of Alkaline Hydrolysis of Some HO-π-COOAr Acyl Derivatives
Cevasco, Giorgio,Thea, Sergio
, p. 5422 - 5426 (2007/10/03)
To gain knowledge on the role played by the nature of the bridge interposed between hydroxyl and carbonyl groups in esters of the title type, in principle able to hydrolyze through dissociative pathways via the conjugate base of the substrate (E1cB mechanism), we have studied the alkaline hydrolyses of 2,4-dinitrophenyl esters in which the π-system is a biphenyl, azobenzene, benzylide-neaniline, or stilbene skeleton. Kinetic data, such as reactivity comparisons and Arrhenius parameters, show that these substrates react through the usual, associative, BAc2 mechanism. This outcome is discussed and interpreted from both structural and energetic standpoints. The data suggest that a value of 0.0 is the most appropriate assignment of the σp value for the benzylidenamino substituent (C6H5CH=N-).
