3-Hydroxyisonicotinaldehyde
3-Hydroxyisonicotinaldehyde, also known as 3-hydroxypyridine-4-carboxaldehyde, is a derivative of pyridine, with hydroxyl and aldehyde substituents. It has been studied as a simple analogue of vitamin B6. In 2020, it was reported as having the lowest molecular weight of all dyes which exhibit green fluorescence.
Preparation
3-Hydroxyisonicotinaldehyde was first prepared in 1958 by oxidation of 3-hydroxy-4-pyridinemethanol with manganese dioxide. Alternative syntheses have also been reported.Spectroscopic properties
The absorption spectrum of HINA has been the subject of studies dating back to the 1950s, owing to its relationship to vitamin B6 and pyridoxal, of which it is a simple analogue. However, its fluorescent properties were not described until 2020. It is noteworthy for having a green-emitting fluorophore with a wavelength of maximum emission at 525 nm in aqueous solution at alkaline pH, making it the compound of lowest molecular weight to display that property. In acidic solutions, the fluorescence is less intense and becomes blue; the compound has isosbestic points at 270 and 341 nm.The molecular basis of the observed properties is the presence of a push-pull fluorophore, a feature of many fluorescent and luminescent compounds. At pH above 7.1 in aqueous solutions, HINA is in its anionic form, with its absorbance peak at 385 nm and emission peak at 525 nm. The anion contains just 13 atoms, with a molecular mass of 122 Da. The quantum yield for the emission is 15%, with an emission lifetime of 1.0 ns. The observed Stokes shift of 6900 cm−1 is typical of push-pull dyes.