TY  - JOUR
AU  - Xie, Yun
AU  - Ilić, Stefan
AU  - Škaro Bogojević, Sanja
AU  - Maslak, Veselin
AU  - Glusac, Ksenija D.
PY  - 2017
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/998
AB  - The excited-state heterolysis of acridinol-based derivatives leads to the release of the OH- ion and the formation of the corresponding acridinium cations. To evaluate the parameters that control the reaction barriers, the kinetics of excited-state OH- release from a series of acridinol photobases were studied using transient absorption spectroscopy. The rate constants were obtained in three solvents (methanol, butanol, and isobutanol), and the data were modeled using Marcus theory. The intrinsic reorganization energies obtained from these fits were found to correlate well with the solvent reorganization energies calculated using dielectric continuum model, suggesting that the excited-state OH- release occurs along the solvent reaction coordinate. Furthermore, the ability of acridinol photobases to photoinitiate chemical reactions was demonstrated using the Michael reaction between dimethylmalonate and nitrostyrene.
PB  - Amer Chemical Soc, Washington
T2  - Journal of Physical Chemistry A
T1  - Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases
EP  - 457
IS  - 2
SP  - 448
VL  - 121
DO  - 10.1021/acs.jpca.6b10980
ER  - 

@article{
author = "Xie, Yun and Ilić, Stefan and Škaro Bogojević, Sanja and Maslak, Veselin and Glusac, Ksenija D.",
year = "2017",
abstract = "The excited-state heterolysis of acridinol-based derivatives leads to the release of the OH- ion and the formation of the corresponding acridinium cations. To evaluate the parameters that control the reaction barriers, the kinetics of excited-state OH- release from a series of acridinol photobases were studied using transient absorption spectroscopy. The rate constants were obtained in three solvents (methanol, butanol, and isobutanol), and the data were modeled using Marcus theory. The intrinsic reorganization energies obtained from these fits were found to correlate well with the solvent reorganization energies calculated using dielectric continuum model, suggesting that the excited-state OH- release occurs along the solvent reaction coordinate. Furthermore, the ability of acridinol photobases to photoinitiate chemical reactions was demonstrated using the Michael reaction between dimethylmalonate and nitrostyrene.",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Physical Chemistry A",
title = "Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases",
pages = "457-448",
number = "2",
volume = "121",
doi = "10.1021/acs.jpca.6b10980"
}

Xie, Y., Ilić, S., Škaro Bogojević, S., Maslak, V.,& Glusac, K. D.. (2017). Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases. in Journal of Physical Chemistry A
Amer Chemical Soc, Washington., 121(2), 448-457.
https://doi.org/10.1021/acs.jpca.6b10980

Xie Y, Ilić S, Škaro Bogojević S, Maslak V, Glusac KD. Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases. in Journal of Physical Chemistry A. 2017;121(2):448-457.
doi:10.1021/acs.jpca.6b10980 .

Xie, Yun, Ilić, Stefan, Škaro Bogojević, Sanja, Maslak, Veselin, Glusac, Ksenija D., "Excited-State Hydroxide Ion Release From a Series of Acridinol Photobases" in Journal of Physical Chemistry A, 121, no. 2 (2017):448-457,
https://doi.org/10.1021/acs.jpca.6b10980 . .