Colorimetric Method for Instant Detection of Lysine and Arginine Using Novel Meldrum's Acid‐Furfural Conjugate

Abstract In the past few years Meldrum's acid furfural conjugate (MAFC) have been extensively explored as starting material for the synthesis of photo switchable donor acceptor stenhouse adducts (DASA). Hereby, we have explored the interaction of MAFC with various amino acids. To our surprise, nitrogen rich amino acids like lysine and arginine interact spontaneously with MAFC to give colored adduct immediately, whereas other amino acids, including nitrogen rich histidine, didn't show any coloration. Naked eye detection of lysine in benign solvent make this reagent an attractive new entry to the collection of chemosensors for the colorimetric detection of lysine and arginine. Intense coloration corresponds to the absorption at 514 nm under UV‐Vis spectrometer. Lowest concentration of 100 μ m can be detected with UV‐Vis spectrometer. NMR titrations reveals that the appearance of color is due to ring opening of a furfural that leads to the formation of conjugated triene species. Compared to previously reported chemosensors for lysine and arginine, MAFC offers advantages including simple synthesis, easy handling, high speed, low cost, good sensitivity/selectivity.