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Acid-base isomerization of hybrid molecules based on fullerene C60 and spiropyrans

Airat Ramilevich Tuktarov 1
Airat Ramilevich Tuktarov
, 
Artur Albertovich Khuzin 1
Artur Albertovich Khuzin
, 
10.1016/j.mencom.2019.03.039
Published 2019-03-01
Communication , Volume 29, Issue 2, 229-231
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Tuktarov A. R., Khuzin A. A., Dzhemilev U. M. Acid-base isomerization of hybrid molecules based on fullerene C60 and spiropyrans // Mendeleev Communications. 2019. Vol. 29. No. 2. pp. 229-231.
GOST all authors (up to 50) Copy
Tuktarov A. R., Khuzin A. A., Dzhemilev U. M. Acid-base isomerization of hybrid molecules based on fullerene C60 and spiropyrans // Mendeleev Communications. 2019. Vol. 29. No. 2. pp. 229-231.
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TY - JOUR
DO - 10.1016/j.mencom.2019.03.039
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.03.039
TI - Acid-base isomerization of hybrid molecules based on fullerene C60 and spiropyrans
T2 - Mendeleev Communications
AU - Tuktarov, Airat Ramilevich
AU - Khuzin, Artur Albertovich
AU - Dzhemilev, Usein Memetovich
PY - 2019
DA - 2019/03/01
PB - Mendeleev Communications
SP - 229-231
IS - 2
VL - 29
ER -
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@article{2019_Tuktarov,
author = {Airat Ramilevich Tuktarov and Artur Albertovich Khuzin and Usein Memetovich Dzhemilev},
title = {Acid-base isomerization of hybrid molecules based on fullerene C60 and spiropyrans},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.03.039},
number = {2},
pages = {229--231},
doi = {10.1016/j.mencom.2019.03.039}
}
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Tuktarov, Airat Ramilevich, et al. “Acid-base isomerization of hybrid molecules based on fullerene C60 and spiropyrans.” Mendeleev Communications, vol. 29, no. 2, Mar. 2019, pp. 229-231. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.03.039.

Abstract

The reversible acid-base isomerization of fullerene C60 hybrid compounds with spiropyrans has been performed for the first time. It has been found that irradiation induces isomerization only for hybrid bearing NO2 group in the photochromic spiropyran part, while the treatment with trifluoroacetic acid induces isomerization for compounds containing NO2, Cl or F, i.e. irrespective of the nature of substituent in the spiropyran moiety.

References

2.
Barachevsky V.A.
Organic Photonics and Photovoltaics, 2015
3.
Spiropyran-based dynamic materials.
Klajn R.
Chemical Society Reviews, 2014
5.
Photoelectrochromic properties of a spirobenzopyran derivative
Jin Fang Zhi, Baba R., Hashimoto K., Fujishima A.
Journal of Photochemistry and Photobiology A: Chemistry, 1995
6.
Correlations between solvatochromism, Lewis acid-base equilibrium and photochromism of an indoline spiropyran
Song X., Zhou J., Li Y., Tang Y.
Journal of Photochemistry and Photobiology A: Chemistry, 1995
7.
SYNTHESIS OF A NEW SPIROPYRAN BASED ON [60]FULLERENE UNIT
Xu J., Li Y., Zhu D.
Synthetic Communications, 2002
9.
CO2 triggering and controlling orthogonally multiresponsive photochromic systems.
Darwish T.A., Evans R.A., James M., Malic N., Triani G., Hanley T.L.
Journal of the American Chemical Society, 2010
10.
Spiropyran-Amidine: A Molecular Canary for Visual Detection of Carbon Dioxide Gas
Darwish T.A., Evans R.A., James M., Hanley T.L.
Chemistry - A European Journal, 2011
11.
Force-induced activation of covalent bonds in mechanoresponsive polymeric materials
Davis D.A., Hamilton A., Yang J., Cremar L.D., Van Gough D., Potisek S.L., Ong M.T., Braun P.V., Martínez T.J., White S.R., Moore J.S., Sottos N.R.
Nature, 2009
13.
Elucidating the Mechanisms of Acidochromic Spiropyran-Merocyanine Interconversion
Wojtyk J.T., Wasey A., Xiao N., Kazmaier P.M., Hoz S., Yu C., Lemieux R.P., Buncel E.
Journal of Physical Chemistry A, 2007
14.
Multi-Responsive Photo- and Chemo-Electrical Single-Molecule Switches
Darwish N., Aragonès A.C., Darwish T., Ciampi S., Díez-Pérez I.
Nano Letters, 2014
15.
Directing and Sensing Changes in Molecular Conformation on Individual Carbon Nanotube Field Effect Transistors
Guo X., Huang L., O'Brien S., Kim P., Nuckolls C.
Journal of the American Chemical Society, 2005
16.
Functionalization of single-walled carbon nanotubes with optically switchable spiropyrans
Del Canto E., Flavin K., Natali M., Perova T., Giordani S.
Carbon, 2010
20.
Reversibly Light-Modulated Dirac Point of Graphene Functionalized with Spiropyran
Jang A., Jeon E.K., Kang D., Kim G., Kim B., Kang D.J., Shin H.S.
ACS Nano, 2012
22.
Photo- and pH-tunable multicolor fluorescent nanoparticle-based spiropyran- and BODIPY-conjugated polymer with graphene oxide.
Sharker S.M., Jeong C.J., Kim S.M., Lee J., Jeong J.H., In I., Lee H., Park S.Y.
Chemistry - An Asian Journal, 2014
23.
Synthesis, structure and photochromic properties of hybrid molecules based on fullerene C60 and spiropyrans
Tuktarov A.R., Khuzin A.A., Tulyabaev A.R., Venidictova O.V., Valova T.M., Barachevsky V.A., Khalilov L.M., Dzhemilev U.M.
RSC Advances, 2016
25.
Inheritance of Photochromic Properties of Nitro-Substituted and Halogenated Spiropyrans Containing the Pyrrolidino[60]fullerene
Pomogaev V.A., Barachevsky V.A., Tuktarov A.R., Avramov P.V., Artyukhov V.Y.
Journal of Physical Chemistry A, 2018
26.
Tuktarov A.R., Khuzin A.A., Khalilov L.M., Tulyabaev A.R., Akhmetov A.R., Dzhemilev U.M.
Mendeleev Communications, 2015
27.
Synthesis and photochromic properties of fullerene C 60 adducts with dithienylethenes
Tuktarov A.R., Khuzin A.A., Akhmetov A.R., Barachevsky V.A., Venidiktova O.V., Dzhemilev U.M.
Tetrahedron Letters, 2015
28.
Tuktarov A.R., Khuzin A.A., Akhmetov A.R., Khalilov L.M., Tulyabaev A.R., Barachevskii V.A., Venediktova O.V., Dzhemilev U.M.
Mendeleev Communications, 2016
29.
Synthesis and photochromic properties of hybrid molecules based on fullerene C60 and 3,3′-(cyclopent-1-ene-1,2-diyl)bis(5-chloro-2-methylthiophene)
Tuktarov A.R., Akhmetov A.R., Khuzin A.A., Venidiktova O.V., Barachevsky V.A., Dzhemilev U.M.
Russian Journal of Organic Chemistry, 2017