Spectral and emission properties of the water-soluble cationic Pd(II) complex with Nile red
Feoktistova V. A.
1, Baichurin R. I.
1, Novikova T. A.
1, Plekhanov A. Yu.
2, Puzyk M. V.
11Herzen State Pedagogical University of Russia, St. Petersburg, Russia
2 Smorodintsev Research Institute of Influenza (a Russian Ministry of Health federal institution), St. Petersburg, Russia
Email: vik.feok.108@mail.ru, ruslanio85@mail.ru, tamaranovikova52@mail.ru, puzyk@mail.ru
Procedure for the synthesis of a cationic water-soluble Pd(II) complex with 9-diethylamino-5H-benzo[a]phenoxazin-5-one (Nile red) [PdEnNR]OAc (where En - is ethylenediamine, NR - is deprotonated Nile red, OAc - is outer-sphere acetate-ion) is developed. The positive solvatochromism of the luminescent properties of the Pd(II) complex has been established. The influence of DNA on the spectral-luminescent properties of [PdEnNR]OAc was studied. Intercalation of the complex into DNA in water was found. Keywords: cyclometallated Pd(II) complex, Nile red, luminescence, intercalation of the Pd(II) complex in DNA. DOI: 10.61011/EOS.2023.02.55796.4480-22
- J.F. Thorpe. J. Chem. Soc., 91, 324 (1907). DOI: 10.1039/CT9079100324
- P. Greenspan, E.P. Mayer, S.D. Fowler. J. Cell Biology, 100 (3), 965 (1985). DOI: 10.1083/jcb.100.3.965
- M. La Deda, M. Ghedini, I. Aiello, T. Pugliese, F. Barigelletti, G. Accorsi. J. Organomet. Chem., 690 (4), 857 (2005). DOI: 10.1016/j.jorganchem.2004.10.028
- T. Pugliese, N. Godbert, I. Aiello, M. La Deda, M. Ghedini, M. Amati, S. Belviso, F. Lelj. Dalton Trans., 6563 (2008). DOI: 10.1039/b810561h
- K. Liu, X. Kong, Y. Ma, W. Lin. Angew. Chem. Int. Ed., 56 (43), 13489 (2017). DOI: 10.1002/anie.201707518
- D. Madea, M. Marti nek, L. Muchova, J. Vavna, L. Vi tek, P. Klan. J. Org. Chem., 85 (5), 3473 (2020). DOI: 10.1021/acs.joc.9b03217
- A. Ionescu, N. Godbert, A. Crispini, R. Termine, A. Golemme, M. Ghedini. J. Mater. Chem., 22 (44), 23617 (2012). DOI: 10.1039/C2JM34946A
- B. Rosenberg, L. VanCamp, J.E. Trosko, V.H. Mansour. Nature, 222, 385 (1969). DOI: 10.1038/222385a0
- C.R. Brodie, J.G. Collins, J.R. Aldrich-Wright. Dalton Trans., 1145 (2004). DOI 10.1039/b316511f
- S.J. Lippard. Accounts of Chem. Res., 11 (5), 211 (1978). DOI: 10.1021/ar50125a006
- S.A. Lee, H. Grimm, W. Pohle, W. Scheiding, L. van Dam, Z. Song, M.H. Levitt, N. Korolev, A. Szabo, A. Rupprecht. Phys. Rev. E, 62 (5), 7044 (2000). DOI: 10.1103/physreve.62.7044
- A. Szabo, S.A. Lee. J. Biomolec. Struct. Dynamics, 26 (1), 93 (2008). DOI: 10.1080/07391102.2008.10507227
- A.J. Gordon, R.A. Ford. The Chemist's Companion: A Handbook of Practical Data, Techniques, and References (1st Edition. 1976)
- E.A. Katlenok, M.V. Puzyk, K.P. Balashev. Rus. J. Gen. Chem., 81 (8), 1711 (2011). DOI: 10.1134/S1070363211080214
- P.I. Baichurin, I.T. Dulanova, A.M. Puzyk, M.V. Puzyk. Opt. i spektr., 130 (14), 2108 (2022). DOI: 10.21883/EOS.2022.14.53995.2253-21
- M.V. Puzyk, M.A. Ivanov, K.P. Balashev. Opt. Spectrosc., 95 (4), 581 (2003). DOI: 10.1134/1.1621442
- Yu.E. Moskalenko, A.Yu. Men'shikova, N.N. Shevchenko, V.V. Faraonova, A.V. Gribanov. High Energy Chem., 45 (3), 183 (2011). DOI: 10.1134/S0018143911030118
- M. Ghedini, I. Aiello, A.Crispini, A. Golemme, M. La Deda, D. Pucci. Coord. Chem. Rev., 250 (11-12), 1373 (2006). DOI: 10.1016/j.ccr.2005.12.011
- J.F. Deye, T.A. Berger, A.G. Anderson. Anal. Chem., 62 (6), 615 (1990). DOI: 10.1021/ac00205a015
- N. Sarkar, K. Das, D.N. Nath, K. Bhattacharyya. Langmuir, 10 (1), 326 (1994). DOI: 10.1021/la00013a04
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