T. Chmovzh

发表

Safe Synthesis of 4,7-Dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine and Its SNAr Reactions

K. Lyssenko, O. Rakitin, T. Chmovzh, 2018, Molecules.

Synthesis of the 4,7-Dibromo Derivative of Highly Electron-Deficient [1,2,5]Thiadiazolo[3,4-d ]pyridazine and Its Cross-Coupling Reactions

O. Rakitin, I. Golovanov, T. Chmovzh, 2018, European Journal of Organic Chemistry.

A novel candle light-style OLED with a record low colour temperature.

O. Rakitin, I. Taydakov, I. Avetissov, 2019, Chemical communications.

Reactions of 4,7-dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine with alcohols

N. V. Krukovskaya, O. Rakitin, T. Chmovzh, 2020, Russian Chemical Bulletin.

Novel D-A-D Fluorescent Dyes Based on 9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-carbazole as a Donor Unit for Solution-Processed Organic Light-Emitting-Diodes

O. Rakitin, I. Taydakov, A. A. Vashchenko, 2021, Molecules.

3,4-Diaminopyridine-2,5-dicarbonitrile

T. Chmovzh, Oleg A. Rakitin, 2022, Molbank.

A novel low-bandgap pyridazine thiadiazole-based conjugated polymer with deep molecular orbital levels

M. Heeney, O. Rakitin, Y. Han, 2020 .

Small D-π-A-π-D organic dyes for near-infrared emitting OLEDs with excellent external quantum efficiency

O. Rakitin, I. Taydakov, M. Minyaev, 2022, Dyes and Pigments.

Efficient Synthesis of 4,8-Dibromo Derivative of Strong Electron-Deficient Benzo[1,2-d:4,5-d’]bis([1,2,3]thiadiazole) and Its SNAr and Cross-Coupling Reactions

O. Rakitin, T. Chmovzh, D. A. Alekhina, 2022, Molecules.

4,7-Di(9H-carbazol-9-yl)-[1,2,5]oxadiazolo[3,4-d]pyridazine

O. Rakitin, T. Chmovzh, Timofey A. Kudryashev, 2022, Molbank.

6-Dibromopyridazine-4 , 5-diamine

O. Rakitin, T. Chmovzh, E. A. Knyazeva, 2019 .

Synthesis of conformationally restricted Analogs of γ-aminobutyric acid

T. Kuznetsova, E. Averina, N. V. Yashin, 2014, Review Journal of Chemistry.

New D–A–D luminophores of the [1,2,5]thiadiazolo[3,4-d]pyridazine series

O. Rakitin, G. Chkhetiani, I. Taydakov, 2022, Mendeleev Communications.

3,6-Dibromopyridazine-4,5-diamine

O. Rakitin, T. Chmovzh, E. A. Knyazeva, 2019, Molbank.

Dye-sensitized solar cells: Investigation of D-A-π-A organic sensitizers based on [1,2,5]selenadiazolo[3,4-c]pyridine

N. Robertson, Wenjun Wu, O. Rakitin, 2017 .

4,7-Bis(5-(9-hexyl-9H-carbazol-3-yl)thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-d]pyridazine

O. Rakitin, I. Taydakov, V. Korshunov, 2022, Molbank.

7-Bromo-[1,2,5]selenadiazolo[3,4-d]pyridazin-4(5H)-one

O. Rakitin, T. Chmovzh, 2021, Molbank.

Edinburgh as an Internal Acceptor in the D-A--A Organic Sensitizers for Dye-Sensitized Solar Cells

N. Robertson, O. Rakitin, T. Chmovzh, 2019 .

4,7-Bis(2,3,3a,8b-tetrahydrocyclopenta[b]indol-4(1H)-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine

O. Rakitin, T. Chmovzh, 2022, Molbank.

Candle light-style OLEDs with benzochalcogenadiazoles cores

O. Rakitin, J. Woollins, I. Taydakov, 2021 .

Benzo[1,2-d:4,5-d′]bis([1,2,3]thiadiazole) and Its Bromo Derivatives: Molecular Structure and Reactivity

O. Rakitin, A. Korlyukov, R. Aysin, 2023, International journal of molecular sciences.

Benzobischalcogenadiazoles: synthesis and applications (microreview)

O. Rakitin, T. Chmovzh, 2022, Chemistry of Heterocyclic Compounds.

Benzo[1,2-d:4,5-d′]bis([1,2,3]thiadiazole)-4-carbonitrile

O. Rakitin, T. Chmovzh, Timofey A. Kudryashev, 2023, Molbank.

Palladium-Catalyzed Direct (Het)arylation Reactions of Benzo[1,2-d:4,5-d′]bis([1,2,3]thiadiazole and 4,8-Dibromobenzo[1,2-d:4,5-d′]bis([1,2,3]thiadiazole)

O. Rakitin, T. Chmovzh, D. A. Alekhina, 2023, Molecules.