1. Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts

    Semenov, N. A., Radiush, E. A., Chulanova, E. A., Slawin, A. M. Z., Woollins, J. D., Kadilenko, E. M., Bagryanskaya, I. Y., Irtegova, I. G., Bogomyakov, A. S., Shundrin, L. A., Gritsan, N. P. & Zibarev, A. V., 7 Nov 2019, In: New Journal of Chemistry. 43, 41, p. 16331-16337 7 p.

    Research output: Contribution to journalArticlepeer-review

  2. Comment on "computational Study on the Vinyl Azide Decomposition"

    Nguyen, M. T., Hang, T. D., Gritsan, N. P. & Kiselev, V. G., 24 Dec 2015, In: Journal of Physical Chemistry A. 119, 51, p. 12906-12907 2 p.

    Research output: Contribution to journalLetterpeer-review

  3. Chemistry of Herz radicals: A new way to near-IR dyes with multiple long-lived and differently-coloured redox states

    Makarov, A. Y., Volkova, Y. M., Shundrin, L. A., Dmitriev, A. A., Irtegova, I. G., Bagryanskaya, I. Y., Shundrina, I. K., Gritsan, N. P., Beckmann, J. & Zibarev, A. V., 16 Jan 2020, In: Chemical Communications. 56, 5, p. 727-730 4 p.

    Research output: Contribution to journalArticlepeer-review

  4. Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles

    Chulanova, E. A., Semenov, N. A., Pushkarevsky, N. A., Gritsand, N. P. & Zibarev, A. V., 1 Sept 2018, In: Mendeleev Communications. 28, 5, p. 453-460 8 p.

    Research output: Contribution to journalArticlepeer-review

  5. Chalcogen-bonded donor-acceptor complexes of 5,6-dicyano[1,2,5]selenadiazolo[3,4-b]pyrazine with halide ions

    Radiush, E. A., Pritchina, E. A., Chulanova, E. A., Dmitriev, A. A., Bagryanskaya, I. Y., Slawin, A. M. Z., Woollins, J. D., Gritsan, N. P., Zibarev, A. V. & Semenov, N. A., 4 Jul 2022, In: New Journal of Chemistry. 46, 30, p. 14490-14501 12 p.

    Research output: Contribution to journalArticlepeer-review

  6. Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine

    Mikhailovskaya, T. F., Makarov, A. G., Selikhova, N. Y., Makarov, A. Y., Pritchina, E. A., Bagryanskaya, I. Y., Vorontsova, E. V., Ivanov, I. D., Tikhova, V. D., Gritsan, N. P., Slizhov, Y. G. & Zibarev, A. V., 1 Mar 2016, In: Journal of Fluorine Chemistry. 183, p. 44-58 15 p.

    Research output: Contribution to journalArticlepeer-review

  7. Cadmium-inspired self-polymerization of {lniiicd2} units: Structure, magnetic and photoluminescent properties of novel trimethylacetate 1d-polymers (ln = sm, eu, tb, dy, ho, er, yb)

    Shmelev, M. A., Polunin, R. A., Gogoleva, N. V., Evstifeev, I. S., Vasilyev, P. N., Dmitriev, A. A., Varaksina, E. A., Efimov, N. N., Taydakov, I. V., Sidorov, A. A., Kiskin, M. A., Gritsan, N. P., Kolotilov, S. V. & Eremenko, I. L., 2 Jul 2021, In: Molecules. 26, 14, 4296.

    Research output: Contribution to journalArticlepeer-review

  8. Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: A pair of radical anions coupled by Te⋯N chalcogen bonding

    Puskarevsky, N. A., Smolentsev, A. I., Dmitriev, A. A., Vargas-Baca, I., Gritsan, N. P., Beckmann, J. & Zibarev, A. V., 1 Jan 2020, In: Chemical Communications. 56, 7, p. 1113-1116 4 p.

    Research output: Contribution to journalArticlepeer-review

  9. Beyond Classical Coordination Chemistry: The First Case of a Triply Bridging Phosphine Ligand

    Baranov, A. Y., Pritchina, E. A., Berezin, A. S., Samsonenko, D. G., Fedin, V. P., Belogorlova, N. A., Gritsan, N. P. & Artem'ev, A. V., 25 May 2021, In: Angewandte Chemie - International Edition. 60, 22, p. 12577-12584 8 p.

    Research output: Contribution to journalArticlepeer-review

  10. (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and (Azulene-1,3-diyl)-bis(iminonitroxide) and Their Copper Complexes

    Haraguchi, M., Tretyakov, E., Gritsan, N., Romanenko, G., Gorbunov, D., Bogomyakov, A., Maryunina, K., Suzuki, S., Kozaki, M., Shiomi, D., Sato, K., Takui, T., Nishihara, S., Inoue, K. & Okada, K., 16 Nov 2017, In: Chemistry - An Asian Journal. 12, 22, p. 2929-2941 13 p.

    Research output: Contribution to journalArticlepeer-review

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