Князева Екатерина Александровна

Князева Екатерина Александровна

Число
публикаций
Общее число
цитирований
Индекс
Хирша
28
250
9
9
159
6
к.х.н.
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: 3
Q4
4-(7-bromobenzo[d][1,2,3]thiadiazol-4-yl)morpholine
Gudim N.S., Knyazeva E.A., Obruchnikova N.V., Rakitin O.A., Popov V.V.
MolBank, 2021, цитирований: 0
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
9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-carbazole—A new donor building-block in the design of sensitizers for dye-sensitized solar cells
Mikhailov M.S., Gudim N.S., Knyazeva E.A., Tanaka E., Zhang L., Mikhalchenko L.V., Robertson N., Rakitin O.A.
Journal of Photochemistry and Photobiology A: Chemistry, 2020, цитирований: 8
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: 8
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: 13
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: 9
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
Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release
Konstantinova L.S., Knyazeva E.A., Gatilov Y.V., Zlotin S.G., Rakitin O.A.
Russian Chemical Bulletin, 2018, цитирований: 7
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: 5
Q4
Synthesis, crystal structure and electroluminescent properties of fac-bromotricarbonyl([1,2,5]oxadiazolo[3',4':5,6]pyrazino-[2,3-f][1,10]phenanthroline)rhenium (I)
Taydakov I.V., Vashchenko A.A., Lyssenko K.A., Konstantinova L.S., Knyazeva E.A., Obruchnikova N.V.
Arkivoc, 2017, цитирований: 3