Чмовж Тимофей Николаевич

Чмовж Тимофей Николаевич

Число
публикаций
Общее число
цитирований
Индекс
Хирша
15
83
6
15
93
7
к.х.н.
Q4
Tert-butyl bis(4-(hexyloxy)-[1,1-biphenyl]-4-yl)carbamate
Chmovzh T.N., Rakitin O.A.
MolBank, 2021, цитирований: 0
Q4
7-bromo-[1,2,5]selenadiazolo[3,4-d]pyridazin-4(5h)-one
Chmovzh T.N., Rakitin O.A.
MolBank, 2021, цитирований: 0
Q2
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
Korshunov V.M., Mikhailov M.S., Chmovzh T.N., Vashchenko A.A., Gudim N.S., Mikhalchenko L.V., Taydakov I.V., Rakitin O.A.
Molecules, 2021, цитирований: 0
Q1
Candle light-style OLEDs with benzochalcogenadiazoles cores
Korshunov V.M., Chmovzh T.N., Golovanov I.S., Knyazeva E.A., Mikhalchenko L.V., Saifutyarov R.S., Avetisov I.C., Woollins J.D., Taydakov I.V., Rakitin O.A.
Dyes and Pigments, 2021, цитирований: 5
Q3
Reactions of 4,7-dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine with alcohols
Chmovzh T.N., Knyazeva E.A., Krukovskaya N.V., Rakitin O.A.
Russian Chemical Bulletin, 2020, цитирований: 0
Q1
A novel low-bandgap pyridazine thiadiazole-based conjugated polymer with deep molecular orbital levels
Leventis A., Chmovzh T.N., Knyazeva E.A., Han Y., Heeney M., Rakitin O.A., Bronstein H.
Polymer Chemistry, 2020, цитирований: 9
Q2
[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, Knyazeva, Tanaka M.A., Popov, Mikhalchenko, Robertson, Rakitin
Molecules, 2019, цитирований: 10
Q4
3,6-dibromopyridazine-4,5-diamine
Chmovzh T., Knyazeva E., Ustimenko O., Rakitin O.
MolBank, 2019, цитирований: 2
Q1
A novel candle light-style OLED with a record low colour temperature
Korshunov V.M., Chmovzh T.N., Knyazeva E.A., Taydakov I.V., Mikhalchenko L.V., Varaksina E.A., Saifutyarov R.S., Avetissov I.C., Rakitin O.A.
Chemical Communications, 2019, цитирований: 8
Q2
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., Knyazeva E.A., Mikhalchenko L.V., Golovanov I.S., Amelichev S.A., Rakitin O.A.
European Journal of Organic Chemistry, 2018, цитирований: 14
Q2
Safe synthesis of 4,7-dibromo[1,2,5]thiadiazolo [3,4-d]pyridazine and its SNAr reactions
Chmovzh T., Knyazeva E., Lyssenko K., Popov V., Rakitin O.
Molecules, 2018, цитирований: 10
Q4
4,7-dichloro[1,2,5]oxadiazolo[3,4-d]pyridazine 1-oxide
Chmovzh T., Knyazeva E., Popov V., Rakitin O.
MolBank, 2018, цитирований: 2
Q3
Suzuki cross-coupling reactions of 4,7-dibromo[1, 2, 5]selenadiazolo[3,4-c]pyridine – a path to new solar cell components
Knyazeva E.A., Chmovzh T.N., Ustimenko O.O., Chkhetiani G.R., Paleva I.S., Konstantinova L.S., Mikhal’chenko L.V., Rakitin O.A.
Chemistry of Heterocyclic Compounds, 2017, цитирований: 6
Q1
Dye-sensitized solar cells: Investigation of D-A-Π-A organic sensitizers based on [1,2,5]selenadiazolo[3,4-c]pyridine
Knyazeva E.A., Wu W., Chmovzh T.N., Robertson N., Woollins J.D., Rakitin O.A.
Solar Energy, 2017, цитирований: 20
Q3
A short and safe method for the synthesis of [1,2,5]oxadiazolo[3,4-c] pyridine
Chmovzh T.N., Konstantinova L.S., Struchkova M.I., Rakitin O.A.
Chemistry of Heterocyclic Compounds, 2015, цитирований: 7