Чмовж Тимофей Николаевич

Старший научный сотрудник научно-образовательного центра «Нанотехнологии»

Кандидат химических наук

E-mail:

chmovzhtn[at]susu[dot]ru

Индекс Хирша:

РИНЦ 0

Scopus 8

Web of Science 0

Научные профили:

Scopus ID: 56578500600

Статьи и монографии за последние три года:

Benzo[1,2-d:4,5-d′]bis([1,2,3]thiadiazole) and Its Bromo Derivatives: Molecular Structure and Reactivity / Chmovzh, T. //International Journal of Molecular Sciences.–2023.–Vol. 24 No. 10

Chmovzh, T. 5,6-Dihydro-[1,2,5]oxadiazolo[3,4-d]pyridazine-4,7-dione / T.. Chmovzh, K.. Gaisin, O.. Rakitin //MolBank.–2023.–Vol. 2023 No. 2

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) / Chmovzh, T. //Molecules.–2023.–Vol. 28 No. 9

Chmovzh, T. Benzobischalcogenadiazoles: synthesis and applications (microreview) / T.. Chmovzh, O.. Rakitin //Chemistry of Heterocyclic Compounds.–2022.–Vol. 58 No. 6-7.– P.307-309

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 / Chmovzh, T. //Molecules.–2022.–Vol. 27 No. 21

Small D-π-A-π-D organic dyes for near-infrared emitting OLEDs with excellent external quantum efficiency / V.. Korshunov //Dyes and Pigments.–2022.–Vol. 208

Candle light-style OLEDs with benzochalcogenadiazoles cores / V.. Korshunov //Dyes and Pigments.–2021.–Vol. 185

chmovzh, T. 7-bromo-[1,2,5]selenadiazolo[3,4-d]pyridazin-4(5h)-one / T.. chmovzh, O.. Rakitin //MolBank.–2021.–Vol. 2021 No. 2

chmovzh, T. Tert-butyl bis(4′-(hexyloxy)-[1,1′-biphenyl]-4-yl)carbamate / T.. chmovzh, O.. Rakitin //MolBank.–2021.–Vol. 2021 No. 3

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 / V.. Korshunov //Molecules.–2021.–Vol. 26 No. 10

A novel low-bandgap pyridazine thiadiazole-based conjugated polymer with deep molecular orbital levels / A.. Leventis //Polymer Chemistry.–2020.–Vol. 11 No. 2.– P.581-585

Reactions of 4,7-dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine with alcohols / Chmovzh, T. //Russian Chemical Bulletin.–2020.–Vol. 69 No. 11.– P.2167-2170

[1,2,5]Thiadiazolo[3,4-d]pyridazine as an internal acceptor in the D-A-π-A organic sensitizers for dye-sensitized solar cells / Chmovzh, T. //Molecules.–2019.–Vol. 24 No. 8

3,6-Dibromopyridazine-4,5-diamine / Chmovzh, T.N //MOLBANK.–2019.–Vol. 2019 No. 1

A novel candle light-style OLED with a record low colour temperature / V.. Korshunov //Chemical Communications.–2019.–Vol. 55 No. 89.– P.13354-13357

Safe synthesis of 4,7-dibromo[1,2,5]thiadiazolo [3,4-d]pyridazine and its SNAr reactions / Chmovzh, T.N //Molecules.–2018.–Vol. 23 No. 10

Synthesis of the 4,7-Dibromo Derivative of Highly Electron-Deficient [1,2,5]Thiadiazolo[3,4-d]pyridazine and Its Cross-Coupling Reactions / Chmovzh, T.N //European Journal of Organic Chemistry.–2018.–Vol. 2018 No. 41.– P.5668-5677