Dr James Walton's Outputs (2)

A new ratiometric switch “two-way” detects hydrazine and hypochlorite via a “dye-release” mechanism with a PBMC bioimaging study (2022)
Journal Article
Das, S., Patra, L., Pratim Das, P., Ghoshal, K., Gharami, S., Walton, J. W., Bhattacharyya, M., & Mondal, T. K. (2022). A new ratiometric switch “two-way” detects hydrazine and hypochlorite via a “dye-release” mechanism with a PBMC bioimaging study. Physical Chemistry Chemical Physics, 24(35), 20941-20952. https://doi.org/10.1039/d2cp02482a

A new ratiometric fluorescent probe (E)-2-(benzo[d]thiazol-2-yl)-3-(8-methoxyquinolin-2-yl)acrylonitrile (HQCN) was synthesised by the perfect blending of quinoline and a 2-benzothiazoleacetonitrile unit. In a mixed aqueous solution, HQCN reacts with... Read More about A new ratiometric switch “two-way” detects hydrazine and hypochlorite via a “dye-release” mechanism with a PBMC bioimaging study.

Enolate SNAr of unactivated arenes via [(η6-arene)RuCp]+ intermediates (2022)
Journal Article
Williams, L. J., Bhonoah, Y., & Walton, J. W. (2022). Enolate SNAr of unactivated arenes via [(η6-arene)RuCp]+ intermediates. Chemical Communications, 58(80), 11240-11243. https://doi.org/10.1039/d2cc02508f

A series of complexes of the general formula [(η6-arene)RuCp][PF6] (where arene = aryl halides or nitroarenes) were synthesised and the arene ring was found to be reactive towards an intermolecular nucleophilic aromatic substitution (SNAr) reaction w... Read More about Enolate SNAr of unactivated arenes via [(η6-arene)RuCp]+ intermediates.