American Chemical Society, Journal of Physical Chemistry Letters, 1(5), p. 92-98, 2013
DOI: 10.1021/jz402280w
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A synthesized blue fluorescent protein (BFP) chromophore analogue 2-BFP ((4Z)-4-[(1H-imidazol-2-yl)methylene]-1-methyl-2-phenyl-1H-imidazol-5(4H)-one) displays dual fluorescent emission that arises from the same Z-isomer. The larger Stokes shift emission is a result of excited-state intramolecular proton transfer (ESIPT) mediated by an N–H···N type of hydrogen bond. Compared to other green fluorescent protein (GFP) analogues with ESIPT such as o-HBDI, 2-BFP possesses greatly enhanced quantum yields and much slower proton-transfer rates. In addition, fluorescence up-conversion experiments revealed two rising components of lifetime for the tautomer formation of 2-BFP. The results imply that the relaxation of the N* state in 2-BFP triggers the proton transfer of the molecule. The weaker photoacidity of N–H is proposed to be crucial for these photophysical and photochemical properties. Finally, the ESIPT process in 2-BFP is inhibited in protic solvents (MeOH) or by the formation of metal–chelate complexes, providing insights for further developments and applications of ESIPT molecules.