Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
- B. Joseph, V.M. Tormyshev, O.Yu. Rogozhnikova, D. Akhmetzyanov, E.G. Bagryanskaya, T.F. Prisner
Selective High-Resolution Detection of Membrane Protein–Ligand Interaction in Native Membranes using Trityl-Nitroxide PELDOR
Angewandte Chemie International Edition, 2016, V, 55, N 38, Pp 11538-11542 doi:10.1002/anie.201606335, IF=11.709
- G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
- M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
Multi-Quantum Counting of Trityl Radicals
The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
- G. Audran, E.G. Bagryanskaya, P. Bremond, M.V. Edeleva, S.R.A. Marque, D.A. Parkhomenko, O.Yu. Rogozhnikova, V.M. Tormyshev, E.V. Tretyakov, D.V. Trukhin, S.I. Zhivetyeva
Trityl-based alkoxyamines as NMP controllers and spin-labels
Polym. Chem., 2016, 42(7), 6490-6499 doi:10.1039/C6PY01303A, IF=5.687
- L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
- B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857
- V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
- H. Chen, A.G. Maryasov, O. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M. Bowman
Electron spin dynamics and spin-lattice relaxation of trityl radicals in frozen solutions
Phys. Chem. Chem. Phys., 2016,18, 24954-24965 doi:10.1039/C6CP02649D, IF=4.448
- Y. Talmon, L. Shtirberg, W. Harneit, O.Yu. Rogozhnikova, V. Tormyshev, A. Blank
Molecular diffusion in porous media by PGSE ESR
Chem.Phys.Phys.Chem., 2010, 12(23), 5998–6007. doi:10.1039/b922060g, IF=4.116
- N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
- A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43
- O.Yu. Rogozhnikova, V.G. Vasiliev, T.I. Troitskaya, D.V. Trukhin, T.V. Mikhalina, H.J. Halpern, V.M. Tormyshev
Generation of Trityl Radicals by Nucleophilic Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations and Practical and Convenient Large-Scale Synthesis of Persistent Tris(4-carboxy-2,3,5,6-tetrathiaaryl)methyl Radical
European Journal of Organic Chemistry, 2013, V. 2013, N 16, P. 3347-3355. doi:10.1002/ejoc.201300176, IF=3.344
- G. Yu. Shevelev, O. A. Krumkacheva, A. A. Lomzov, A. A. Kuzhelev, D. V. Trukhin, O. Yu. Rogozhnikova, V. M. Tormyshev, D. V. Pyshnyi, M. V. Fedin, E.G. Bagryanskaya
Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
J. Phys. Chem. B, 2015, 119 (43), pp 13641-13648 doi:10.1021/acs.jpcb.5b03026, IF=3.302
- A.A. Kuzhelev, D.V. Trukhin, O.A. Krumkacheva, R.K. Strizhakov, O.Yu. Rogozhnikova, T.I. Troitskaya, M.V. Fedin, V.M. Tormyshev, E. G. Bagryanskaya
Room-Temperature Electron Spin Relaxation of Triarylmethyl Radicals at the X- and Q-Bands
J. Phys. Chem. B, 2015, 119 (43), pp 13630-13640 doi:10.1021/acs.jpcb.5b03027, IF=3.302
- V.M. Tormyshev, A.M. Genaev, G.E. Sal'nikov, O.Yu. Rogozhnikova, T.I. Troitskaya, D.V. Trukhin, V.I. Mamatyuk, D.S. Fadeev, H.J. Halpern
Triarylmethanols with Bulky Aryl Groups and the NOESY/EXSY Experimental Observation of a Two-Ring-Flip Mechanism for the Helicity Reversal of Molecular Propellers
Eur.J. Org. Chem., 2012, N 3, 623-629. doi:10.1002/ejoc.201101243, IF=3.206
- V. M. Tormyshev, O.Yu. Rogozhnikova, M. K. Bowman, D. V. Trukhin, T. I. Troitskaya, V. G. Vasiliev, L. A. Shundrin, H. J. Halpern
Preparation of Diversely Substituted Triarylmethyl Radicals by the Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations with C-, N-, P-, and S-Nucleophiles
European Journal of Organic Chemistry, 2014, V. 2014, N 2, pp 371-380. doi:10.1002/ejoc.201301161, IF=3.154
- Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
- V.M. Tormyshev, D.V. Trukhin, O.Yu. Rogozhnikova, T.V. Mikhalina, T.I. Troitskaya, A. Flinn
Aryl Alkyl Ketones in One-Pot Gewald Synthesis of 2-Aminothiophenes
SynLett., 2006, V. 3, N 16, 2559-2564. doi:10.1055/s-2006-951484, IF=2.69
- K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641