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The iron complex of dimethyl chlorin e6–thioctic acid conjugate and its monolayers on the water and gold surfaces

Alexander Vladimirovich Nyuchev
Evgeny Nikolaevich Kochetkov 2
Evgeny Nikolaevich Kochetkov
Kirill Vasil'evich Schegravin 1
Kirill Vasil'evich Schegravin
Maxim Aleksandrovich Baten’kin 3
Maxim Aleksandrovich Baten’kin
Maxim Andreevich Samsonov 3
Maxim Andreevich Samsonov
Oscar Iosifovich Koifman 4
Oscar Iosifovich Koifman
Yulia Vital'evna Romanenko 4
Yulia Vital'evna Romanenko
Nina Borisovna Melnikova 2
Nina Borisovna Melnikova
Published 2017-10-30
CommunicationVolume 27, Issue 6, 610-612
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Nyuchev A. V. et al. The iron complex of dimethyl chlorin e6–thioctic acid conjugate and its monolayers on the water and gold surfaces // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 610-612.
GOST all authors (up to 50) Copy
Nyuchev A. V., Kochetkov E. N., Schegravin K. V., Zamyshlyayeva O. G., Baten’kin M. A., Samsonov M. A., Koifman O. I., Romanenko Y. V., Melnikova N. B., Fedorov A. Y. The iron complex of dimethyl chlorin e6–thioctic acid conjugate and its monolayers on the water and gold surfaces // Mendeleev Communications. 2017. Vol. 27. No. 6. pp. 610-612.
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TY - JOUR
DO - 10.1016/j.mencom.2017.11.024
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.024
TI - The iron complex of dimethyl chlorin e6–thioctic acid conjugate and its monolayers on the water and gold surfaces
T2 - Mendeleev Communications
AU - Nyuchev, Alexander Vladimirovich
AU - Kochetkov, Evgeny Nikolaevich
AU - Schegravin, Kirill Vasil'evich
AU - Zamyshlyayeva, Olga Georgievna
AU - Baten’kin, Maxim Aleksandrovich
AU - Samsonov, Maxim Andreevich
AU - Koifman, Oscar Iosifovich
AU - Romanenko, Yulia Vital'evna
AU - Melnikova, Nina Borisovna
AU - Fedorov, Alexey Yur'evich
PY - 2017
DA - 2017/10/30
PB - Mendeleev Communications
SP - 610-612
IS - 6
VL - 27
ER -
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@article{2017_Nyuchev,
author = {Alexander Vladimirovich Nyuchev and Evgeny Nikolaevich Kochetkov and Kirill Vasil'evich Schegravin and Olga Georgievna Zamyshlyayeva and Maxim Aleksandrovich Baten’kin and Maxim Andreevich Samsonov and Oscar Iosifovich Koifman and Yulia Vital'evna Romanenko and Nina Borisovna Melnikova and Alexey Yur'evich Fedorov},
title = {The iron complex of dimethyl chlorin e6–thioctic acid conjugate and its monolayers on the water and gold surfaces},
journal = {Mendeleev Communications},
year = {2017},
volume = {27},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.024},
number = {6},
pages = {610--612},
doi = {10.1016/j.mencom.2017.11.024}
}
MLA
Cite this
MLA Copy
Nyuchev, Alexander Vladimirovich, et al. “The iron complex of dimethyl chlorin e6–thioctic acid conjugate and its monolayers on the water and gold surfaces.” Mendeleev Communications, vol. 27, no. 6, Oct. 2017, pp. 610-612. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2017.11.024.

Abstract

A μ-oxo-Fe3+ complex of chlorin e6–thioctic acid conjugate was synthesized and explored as a new sensing material for nitric oxide. This conjugate can be used as a model for NO-binding potential biosensors.

References

1.
10.1016/j.mencom.2017.11.024_bib0005
Osipov
Usp. Biol. Khim., 2007
2.
Protein-bound dinitrosyl–iron complexes appearing in blood of rabbit added with a low-molecular dinitrosyl–iron complex: EPR studies
Timoshin A.A., Vanin A.F., Orlova T.R., Sanina N.A., Ruuge E.K., Aldoshin S.M., Chazov E.I.
Nitric Oxide - Biology and Chemistry, 2007
3.
What is the real physiological NO concentration in vivo?
Hall C.N., Garthwaite J.
Nitric Oxide - Biology and Chemistry, 2009
4.
Dermal Application of Nitric Oxide In Vivo: Kinetics, Biological Responses, and Therapeutic Potential in Humans
Opländer C., Römer A., Paunel-Görgülü A., Fritsch T., van Faassen E.E., Mürtz M., Bozkurt A., Grieb G., Fuchs P., Pallua N., Suschek C.V.
Clinical Pharmacology and Therapeutics, 2012
6.
10.1016/j.mencom.2017.11.024_bib0030
Kalvinsh
Med. Hypothesis Res., 2006
7.
State of art in porphyrin Langmuir-Blodgett films as chemical sensors.
Giancane G., Valli L.
Advances in Colloid and Interface Science, 2012
8.
10.1016/j.mencom.2017.11.024_bib0040
Baschir
Dig. J. Nanomater. Biostruct., 2014
9.
Nitroxide malonate methanofullerene as biomimetic model of interaction of nitroxide species with antioxidants
Melnikova N.B., Korobko V.M., Gulenova M.V., Gubskaya V.P., Fazlleeva G.M., Zhiltsova O.E., Kochetkov E.N., Poddel’sky A.I., Nuretdinov I.A.
Colloids and Surfaces B: Biointerfaces, 2015
11.
Characterization of Self-Assembled Monolayers for Biosensor Applications
Nyquist R.M., Eberhardt A.S., Silks L.A., Li Z., Yang X., Swanson B.I.
Langmuir, 2000
14.
Novel NO Biosensor Based on the Surface Derivatization of GaAs by “Hinged” Iron porphyrins
Wu D.G., Ashkenasy G., Shvarts D., Ussyshkin R.V., Naaman R., Shanzer A., Cahen D.
Angewandte Chemie - International Edition, 2000
16.
Nitric Oxide Biosensors Based on the Immobilization of Hemoglobin on Mesoporous Titania Electrodes
17.
Naked Five-Coordinate FeIII(NO) Porphyrin Complexes: Vibrational and Reactivity Features
Lanucara F., Chiavarino B., Crestoni M.E., Scuderi D., Sinha R.K., Maı̂tre P., Fornarini S.
Inorganic Chemistry, 2011
18.
A highly sensitive nitric oxide biosensor based on hemoglobin–chitosan/graphene–hexadecyltrimethylammonium bromide nanomatrix
Wen W., Chen W., Ren Q., Hu X., Xiong H., Zhang X., Wang S., Zhao Y.
Sensors and Actuators, B: Chemical, 2012
19.
Ion recognition properties of self-assembled monolayers (SAMs)
Zhang S., Cardona C.M., Echegoyen L.
Chemical Communications, 2006
20.
Diode like electron transfer in mixed monolayer assembly
Berchmans S., Ramalechume C., Lakshmi V., Yegnaraman V.
Journal of Materials Chemistry A, 2002
22.
One-step covalent grafting of Fe4single-molecule magnet monolayers on gold
Rodriguez-Douton M.J., Mannini M., Armelao L., Barra A., Tancini E., Sessoli R., Cornia A.
Chemical Communications, 2011
23.
Research advances in the use of tetrapyrrolic photosensitizers for photodynamic therapy
Nyman E.S., Hynninen P.H.
Journal of Photochemistry and Photobiology B: Biology, 2004
25.
Imaging and Photodynamic Therapy: Mechanisms, Monitoring, and Optimization
Celli J.P., Spring B.Q., Rizvi I., Evans C.L., Samkoe K.S., Verma S., Pogue B.W., Hasan T.
Chemical Reviews, 2010
26.
Photodynamic therapy/oncology
Triesscheijn M., Baas P., Schellens J.H., Stewart F.A.
Oncologist, 2006
27.
Synthesis of Chlorin–(Arylamino)quinazoline Hybrids as Models for Multifunctional Drug Development
Fedorov A., Nyuchev A., Otvagin V., Gavryushin A., Romanenko Y., Koifman O., Belykh D., Schmalz H.
Synthesis, 2015
32.
10.1016/j.mencom.2017.11.024_bib0135
Frisch
Gaussian 03, Revision B.03, 2003
33.
Synthesis, Structure, and Electrochemistry of an Electron Deficient μ-Oxo Porphyrin Dimer, [(TPPBr4)Fe]2O
Kadish K.M., Autret M., Ou Z., Tagliatesta P., Boschi T., Fares V.
Inorganic Chemistry, 1997
34.
10.1016/j.mencom.2017.11.024_bib0145
Korenman
Novye titrimetricheskie metody (New Titrimetric Methods), 1983