Publications

(Reverse chronological order, undergraduate co-authors underlined)

  1. Ehrhorn E., Lovell P., Svechkarev D., Romanova S., Mohs A. M. Optimizing the performance of silica nanoparticles functionalized with a near-infrared fluorescent dye for bioimaging applications. Nanotechnology (2024) accepted.

Prior to UNO:

  1. Laliwala A.,* Svechkarev D.,* Sadykov M. R., Endres J., Bayles K. W., Mohs A. M. Simpler procedure and improved performance for pathogenic bacteria analysis with a paper-based ratiometric fluorescent sensor array. Anal. Chem. 94 (2022) 2615-2624 (*equal contribution).
  2. Bhattacharya D. S., Bapat A., Svechkarev D., Mohs A. M. Water-soluble blue fluorescent non-conjugated polymer dots from hyaluronic acid and hydrophobic amino acids. ACS Omega 6 (2021) 17890-17901.
  3. Dereka B., Rosspeintner A., Svechkarev D., Vauthey E. Comment on “Theoretical Insights into the Excited State Decays of a Donor−Acceptor Dyad: Is the Twisted and Rehybridized Intramolecular Charge-Transfer State Involved?” J. Phys. Chem. B 124 (2020) 10578-10581.
  4. Bhattacharya D. S., Svechkarev D., Bapat A., Patil P., Hollingsworth M. A., Mohs A. M. Sulfation modulates the targeting properties of hyaluronic acid to P-selectin and CD44. ACS Biomater. Sci. Eng. 6 (2020) 3585-3598.
  5. Dereka B., Svechkarev D., Rosspeintner A., Aster A., Lunzer M., Liska R., Mohs A. M., Vauthey E. Solvent Tuning of Photochemistry upon Excited-State Symmetry Breaking. Nature Commun. 11 (2020) 1925.
  6. Svechkarev D., Sadykov M. R., Houser L. J., Bayles K. W., Mohs A. M. Fluorescent sensor arrays can predict and quantify the composition of multicomponent bacterial samples. Frontiers Chem. 7 (2020) 916.
  7. Mukadam I. Z., Machhi J., Herskovitz J., Hasan M., Oleynikov M. D., Blomberg W. R., Svechkarev D., Mohs A. M., Zhou Y., Dash P., McMillan J., Gorantla S., Garrison J., Kevadiya B. D., Gendelman H. Rilpivirine-associated aggregation-induced emission enables cell-based nanoparticle tracking. Biomaterials 231 (2020) 119669.
  8. Svechkarev D., Mohs A. M. Organic fluorescent dye-based nanomaterials: Advances in the rational design for imaging and sensing applications. Current Med. Chem. 26 (2019) 4042-4064 (invited review).
  9. Doroshenko A. O., Kyrychenko A. V., Valiashko O. M., Kotlyar V. N., Svechkarev D., 4’-methoxy-3-hydroxyflavone excited state intramolecular proton transfer reaction in alcoholic solutions: intermolecular versus intramolecular hydrogen bonding effect. J. Photochem. Photobiol. A: Chem. 383 (2019) 111964.
  10. Letrun R., Lang B., Yushchenko O., Wilcken R., Svechkarev D., Kolodieznyi D., Riedle E., Vauthey E. Excited-state dynamics of a molecular dyad with two orthogonally-oriented fluorophores. Phys. Chem. Chem. Phys. 20 (2018) 30219-30230 (2018 PCCP Hot Article).
  11. Svechkarev D., Kyrychenko A., Payne W. M., Mohs A. M. Probing the self-assembly dynamics and internal structure of amphiphilic hyaluronic acid conjugates by fluorescence spectroscopy and molecular dynamics simulations. Soft Matter 14 (2018) 4762-4771.
  12. Svechkarev D., Sadykov M. R., Bayles K. W., Mohs A. M. Ratiometric fluorescent sensor array as a versatile tool for bacterial pathogen identification and analysis. ACS Sensors 3 (2018) 700-708.
  13. Svechkarev D., Kyrychenko A., Payne W. M., Mohs A. M. Development of colloidally stable carbazole-based fluorescent nanoaggregates. J. Photochem. Photobiol. A: Chem. 352 (2018) 55-64.
  14. Payne W. M.,* Svechkarev D.,* Kyrychenko A., Mohs A. M. The role of hydrophobic modification on hyaluronic acid dynamics and self-assembly. Carbohydr. Polymers 182 (2018) 132-141 (*equal contribution).
  15. Dereka B., Svechkarev D., Rosspeintner A., Tromayer M., Liska R., Mohs A. M., Vauthey E. Direct Observation of a Photochemical Alkyne-Allene Reaction and of a Twisted and Rehybridized Intramolecular Charge-Transfer State in a Donor-Acceptor Dyad. J. Amer. Chem. Soc. 139 (2017) 16885-16893.
  16. Bhattacharya D., Svechkarev D., Souchek J. J., Hill T. K., Taylor M. A., Natarajan A., Mohs A. M. Impact of structurally modifying hyaluronic acid on CD44 interaction. J. Mater. Chem. B 5 (2017) 8183-8192.
  17. Payne W. M., Hill T. K., Svechkarev D., Holmes M., Sajja B., Mohs A. M. Multimodal imaging nanoparticles derived from hyaluronic acid for integrated preoperative and intraoperative cancer imaging. Contr. Media Molec. Imaging 2017 (2017) 9616791.
  18. Svechkarev D., Grygorovych O. V. Tournament of Young Chemists in Ukraine: Engaging Students in Chemistry through a Role-Playing Game-Style Competition. J. Chem. Educ. 93 (2016) 874-878.
  19. Dereka B., Letrun R., Svechkarev D., Rosspeintner A., Vauthey E. Excited-state dynamics of 3-hydroxyflavone anion in alcohols. J. Phys. Chem. B 119 (2015) 2434-2443.
  20. Svechkarev D., Kolodezny D., Mosquera-Vázquez S., Vauthey E. Complementary surface second harmonic generation and molecular dynamics investigation of the orientation of organic dyes at a liquid/liquid interface. Langmuir 30 (2014) 13869-13876.
  21. Dereka B., Svechkarev D., Doroshenko A. O. Facile ultrasensitive monitoring of mercury ions in water flow by fluorescent ratiometric detection. Centr. Eur. J. Chem. 11 (2013) 584-593.
  22. Kyrychenko A., Karpushina G. V., Svechkarev D., Kolodezny D., Bogatyrenko S. I., Kryshtal A. P., Doroshenko A. O. Fluorescence Probing of Thiol-Functionalized Gold Nanoparticles: Is Alkylthiol Coating of a Nanoparticle as Hydrophobic as Expected? J. Phys. Chem. C 116 (2012) 21059-21068.
  23. Svechkarev D. A., Doroshenko A. O., Kolodezny D. Yu. 1,4-bis-(3-hydroxy-4-oxo-4H-chromen-2-yl)-benzene (bis-flavonol): synthesis, spectral properties and principle possibility of the excited state double proton transfer reaction. Centr. Eur. J. Chem. 10 (2012) 205-215.
  24. Svechkarev D., Dereka B., Doroshenko A. Mercury ions complexation with a series of heterocyclic derivatives of 3-hydroxychromone: spectral effects and prospects for ultrasensitive Hg2+ probing. J. Phys. Chem. A 115 (2011) 4223-4230.
  25. Svechkarev D., Doroshenko A., Baumer V., Dereka B. Nature of dual fluorescence in 2-(quinolin-2-yl)-3-hydroxychromone: tuning between concurrent H-bond directions and ESIPT pathways. J. Lumin. 131 (2011) 253-261.
  26. Svechkarev D. A., Baumer V. N., Syzova Z. A., Doroshenko A. O. New benzimidazolic 3-hydroxychromone derivative with two alternative mechanisms of the excited state intramolecular proton transfer reaction. J. Mol. Struct. 882 (2008) 63-69.
  27. Svechkarev D. A., Karpushina G. V., Lukatskaya L. L., Doroshenko A. O. 2-(benzimidazol-2-yl)-3-hydroxy­chromone derivatives: spectroscopic properties and a possible alternative intramolecular proton phototransfer. Centr. Eur. J. Chem. 6 (2008) 443-449.
  28. Svechkarev D. A., Bukatich I. V., Doroshenko A. O. New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic polarity probes. J. Photochem. Photobiol. A: Chem. 200 (2008) 426-431.