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Published:
Oct 7, 2015Keywords:
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A Coloured Spin Trap which works as a pH Sensor
Abstract
Nitration of 4-hydroxybenzaldehyde afforded 2,6-dinitro-4-hydroxybenzaldehyde 2, which in the presence of thionyl chloride is converted to 4-chloro-2,6-dinitrobenzaldehyde 3. This compound is very reactive towards nucleophiles, and reacts easily with methoxyamine, affording the intermediate 4-aminomethoxy-2,6-dinitrobenzaldehyde 4. Reaction of 4 with N-t-butylhydroxylamine led to a new spin trap of the nitrone type, namely 4-aminomethoxy-3,5-dinitrophenyl-1-t-butylnitrone 6. The spin-trapping capabilities of the new compound have been tested in a classical system, in which short-lived radicals were generated by irradiation. The new compound 6 contains an acidic proton with a pKa value of 7.8, and removal of this by a base induces a colour change, from yellow to green-blue. In a similar way, a new stable nitronyl-nitroxide radical 8 has been obtained from the intermediate 4.
Keywords: Synthesis; free radical; spin-trapping; pH sensor; nitrone
