Azomethine phthalimides fluorescent E -> Z photoswitches

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Herein, we report the synthesis and E -> Z photoswitching behavior of two 4-substituted azomethine phthalimides containing anthracenyl and 4-(dimethylamino)phenyl moieties (EAMP1 and EAMP2). These compounds represent newly synthesized and unstudied photoswitches with dual fluorescence properties as E-isomers and at photostationary state (PSS) depending on the solvent polarity. Steady-state fluorescence measurements were performed in various solvents and the results show strong sensitivity on the environmental polarity. The kinetics of E -> Z photoswitching to PSS was studied in AcCN by visible light activation at 410 nm (EAMP1) and long wavelength UV-light activation at 350 nm (EAMP2). The quantitative and qualitative performance of the switching behavior was evaluated by the degree of photoisomerization (R) and the rate constant (k). It was found for EAMP1 R = 6.95 %, k = 8.87 x 10(-4) s(-1) and EAMP2 R = 88.72 %, k = 4.00 x 10(-4) s(-1), respectively. The reason for the lower photoconversion of EAMP1 compared to the EAMP2 was analyzed through optimization of the molecular geometry of E- and Z-isomers in the ground state (S-0) and first excited state (S-1) by DFT/TD-DFT calculations with B3LYP/6-31 + G(d,p) level of theory using IEFPCM in AcCN. It was found that Eisomers in the S-0 have nonplanar conformation, while the Z-isomer of EAMP1 prefers twisted conformation and the Z-isomer of EAMP2 T-shaped conformation is energetically advantageous compared to the twisted one. The reason is the weak H.....pi noncovalent interaction (NCI) between 4-(dimethylamino)phenyl moiety and phthalimide ring. Moreover, the Z-isomer of EAMP2 is unusual stable up to 600 min at room temperature in dark compared to the EAMP1, which undergoes full Z -> E relaxation for less than 60 min at the same conditions. The Z -> E relaxation of EAMP2 is achieved for 90 min at 60 degrees C. The fluorescence E -> Z switching behavior was studied by emission measurements in AcCN and 1,4-DOX as E-isomers and at PSS in room and liquid nitrogen (77 K) temperatures. In the polar and nonpolar solvents, red-shifted emissions with increased fluorescence quantum (Phi(fl)) yields have been observed at PSS compared to the E-isomers. The molecular rotor behavior was studied in the binary mixture of glycerol:ethanol and the results show a sensitivity of the emission bands depending on the environmental viscosity. Time-resolved fluorescence decay measurements were performed in AcCN and 1,4-DOX as E-isomers and at PSS to estimate the mechanism of fundamental fluorescence bands. We found that dyes at PSS have longer lifetime (tau) compared to the E-isomers, especially in less polar 1,4-DOX.

Phthalimides; Fluorescence photoswitches; E -> Z photoisomerization; Rate constant; Molecular rotors

GEORGIEV, A.; YORDANOV, D.; ZHIVKOV, I.; DIMOV, D.; NAZAROVA, D.; WEITER, M.; .

15. 4. 2020

ELSEVIER SCIENCE SA

LAUSANNE

1010-6030

Journal of Photochemistry and Photobiology A:Chemistry

393

112443

Švýcarská konfederace

1

14

14

https://www.sciencedirect.com/science/article/abs/pii/S1010603020302422