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- W2014534246 abstract "We have measured spectrophotometrically the rates of cleavage by aqueous methanolic alkali of the aryl–tin bonds in a series of X·C6H4·SnMe3 compounds. In this reaction, the rate-determining step of which probably involves separation of the carbanion X·C6H4–, the effects of meta substituents are in accord with the Hammett σ constants (σ= 2·18), but the effects of para substituents show an abnormal pattern. For example, there is rate-acceleration not only by electron-withdrawing groups such as p-CF3 and p-Cl, but also by normally electron-releasing groups such as p-OMe and p-NMe2. For the para substituents, the effects are roughly in line with their σ1 constants." @default.
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- W2014534246 date "1967-01-01" @default.
- W2014534246 modified "2023-10-14" @default.
- W2014534246 title "Aromatic reactivity. Part XXXV. Alkali cleavage of aryltrimethylstannanes: an unusual electrophilic aromatic substitution" @default.
- W2014534246 doi "https://doi.org/10.1039/j29670001036" @default.
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