Tatiana G. Chulkova

Tatiana G. Chulkova

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Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 May 2016 in Zeitschrift für Kristallographie - Crystalline Materials
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Journal Article
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AAAnastasiia M. Afanasenko
Anastasiia M. Afanasenko
MAMargarita S. Avdontceva
Margarita S. Avdontceva
Alexander S. NovikovAlexander S. Novikov
Alexander S. Novikov
TCTatiana G. Chulkova
Tatiana G. Chulkova
The weak intermolecular noncovalent interactions in the solvatecis-[PtCl2(C2H5CN)2]·CHCl3were studied by XRD and DFT methods. Special attention was paid to a chloroform molecule as a potential donor of both hydrogen and halogen bonds. On the one hand, the H atom of chloroform links two Cl atoms ofcis-[PtCl2(C2H5CN)2] (Hchloroform–Clcomplex(2.660 Å, 2.811 Å)), and on the other side, the weak Clchloroform–Clcomplex(3.247 and 3.497 Å) interactions were found. According to DFT calculation, only the Hchloroform–Clcomplex(2.660 and 2.811 Å) and Clchloroform–Clcomplex(3.247 Å) interactions can be classified as weak noncovalent bonds, whereas the contacts Clchloroform–Cnitrile(3.391 Å) and Clchloroform–Clcomplex(3.497 Å) are due to the crystal packing effect.

1 January 2020 in Journal of Molecular Structure
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Journal Article
Closed access
AAAnastasiia M. Afanasenko
Anastasiia M. Afanasenko
Alexander S. NovikovAlexander S. Novikov
Alexander S. Novikov
TCTatiana G. Chulkova
Tatiana G. Chulkova
YGYakov M. Grigoriev
Yakov M. Grigoriev
IKIlya E. Kolesnikov
Ilya E. Kolesnikov
Mikhail ElinsonMikhail Elinson
Mikhail Elinson

26 December 2018 in Organometallics
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Journal Article
Closed access
DBDina V. Boyarskaya
Dina V. Boyarskaya
Evgeny BulatovEvgeny Bulatov
Evgeny Bulatov
IBIrina A. Boyarskaya
Irina A. Boyarskaya
TCTatiana G. Chulkova
Tatiana G. Chulkova
VRValentin A. Rassadin
Valentin A. Rassadin
Matti HaukkaMatti Haukka
Matti Haukka

1 October 2017 in Journal of Molecular Structure
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Journal Article
Closed access
AAAnastasiia M. Afanasenko
Anastasiia M. Afanasenko
DBDina V. Boyarskaya
Dina V. Boyarskaya
IBIrina A. Boyarskaya
Irina A. Boyarskaya
TCTatiana G. Chulkova
Tatiana G. Chulkova
YGYakov M. Grigoriev
Yakov M. Grigoriev
Mikhail ElinsonMikhail Elinson
Mikhail Elinson

1 May 2010 in Inorganic Chemistry Communications
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Journal Article
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TCTatiana G. Chulkova
Tatiana G. Chulkova
PGPavel V. Gushchin
Pavel V. Gushchin
MHMatti Haukka
Matti Haukka
VKVadim Yu. Kukushkin
Vadim Yu. Kukushkin

12 August 2023 in Materials
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Journal Article
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Anton YakimanskiyAnton Yakimanskiy
Anton Yakimanskiy
KKKsenia Kaskevich
Ksenia Kaskevich
EZElena V. Zhukova
Elena V. Zhukova
IBIvan A. Berezin
Ivan A. Berezin
LLLarisa Livinova
Larisa Livinova
AYAlexander Yakimansky
Alexander Yakimansky
Using palladium-catalyzed Suzuki polycondensation, we synthesized new light-emitting fluorene copolymers containing the dicyano derivatives of stilbene and phenanthrene and characterized them by gel permeation chromatography, UV-vis absorption spectroscopy, spectrofluorimetry, and cyclic voltammetry. The photoluminescence spectra of the synthesized polymers show significant energy transfer from the fluorene segments to the dicyanostilbene and 9,10-dicyanophenanthrene units, which is in agreement with the data of theoretical calculations. OLEDs based on these polymers were fabricated with an ITO/PEDOT-PSS (35 nm)/p-TPD (30 nm)/PVK (5 nm)/light emitting layer (70–75 nm)/PF-PO (20 nm)/LiF (1 nm)/Al (80 nm) configuration. Examination of their electroluminescence revealed that copolymers of fluorene with dicyanostilbene show yellow-green luminescence, while polymers with 9,10-dicyanophenanthrene have a greenish-blue emission. The 9,10-dicyanophenanthrene units have a more rigid structure compared to dicyanostilbene and, in OLEDs based on them, an increase in maximum brightness is observed with an increase in the content of the additive to the polymer chain. In particular, the device using fluorene copolymer with 9,10-dicyanophenanthrene (2.5 mol%) exhibited a maximum brightness of 9230 cd/m2 and a maximum current efficiency of 3.33 cd/A.