Novel Nitroxide-Substituted Hydrazone Switch: Experimental and Theoretical Insights into Photoswitching Behavior

Novel Nitroxide-Substituted Hydrazone Switch: Experimental and Theoretical Insights into Photoswitching Behavior

Článek WoS

Hydrazones are a versatile class of molecular switches with dual responsiveness to both light and pH. To investigate their switching properties, we incorporated a nitroxide moiety, enabling analysis by not only conventional techniques such as H-1 NMR and UV-vis spectroscopy but also EPR spectroscopy, which provides valuable insights into structure and dynamics. A novel nitroxide-substituted hydrazone switch (2) was synthesized and fully characterized. However, initial experiments using H-1 NMR and UV-vis revealed restricted photoisomerization of 2. Theoretical studies employing DFT and TD-DFT methods revealed the presence of the D-1 excited state related to pi -> pi* electron transfer of the nitroxide moiety, and D-2 excited state related to pi -> pi* electron transfer within the hydrazone moiety. The latter excitation results in weakening of the C=N bond and enables the rotation around the hydrazone bond; however, the internal conversion D-2 -> D-1 process is most likely responsible for the quenching of photoisomerization in 2. Additionally, pH-induced switching was monitored using UV-vis and EPR spectroscopy, revealing that strong acids such as trifluoroacetic acid had no significant effect on the paramagnetic center.

Hydrazones are a versatile class of molecular switches with dual responsiveness to both light and pH. To investigate their switching properties, we incorporated a nitroxide moiety, enabling analysis by not only conventional techniques such as H-1 NMR and UV-vis spectroscopy but also EPR spectroscopy, which provides valuable insights into structure and dynamics. A novel nitroxide-substituted hydrazone switch (2) was synthesized and fully characterized. However, initial experiments using H-1 NMR and UV-vis revealed restricted photoisomerization of 2. Theoretical studies employing DFT and TD-DFT methods revealed the presence of the D-1 excited state related to pi -> pi* electron transfer of the nitroxide moiety, and D-2 excited state related to pi -> pi* electron transfer within the hydrazone moiety. The latter excitation results in weakening of the C=N bond and enables the rotation around the hydrazone bond; however, the internal conversion D-2 -> D-1 process is most likely responsible for the quenching of photoisomerization in 2. Additionally, pH-induced switching was monitored using UV-vis and EPR spectroscopy, revealing that strong acids such as trifluoroacetic acid had no significant effect on the paramagnetic center.

hydrazone switch; nitroxide radical; photoisomerization; pH-induced isomerization; computational studies

hydrazone switch; nitroxide radical; photoisomerization; pH-induced isomerization; computational studies

KOTÁSKOVÁ, L.; NEMEC, I.; HERCHEL, R.; SANTANA, V.; NEUGEBAUER, P.

2026

04.02.2026

American Chemical Society

ACS Organic & Inorganic Au

6

1

Spojené státy americké

64

75

12

https://pubs.acs.org/doi/pdf/10.1021/acsorginorgau.5c00068?utm_source=clarivate&getft_integrator=clarivate

http://hdl.handle.net/11012/256341