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1,3,7,9-Tetraazaperylene frameworks : Synthesis, photoluminescence properties, and thin film morphology. / Baranov, Denis S.; Uvarov, Mikhail N.; Glebov, Evgeni M. и др.

в: Dyes and Pigments, Том 150, 01.03.2018, стр. 252-260.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Baranov, DS, Uvarov, MN, Glebov, EM, Nevostruev, DA, Kazantsev, MS, Mostovich, EA, Fadeev, DS, Antonova, OV, Utkin, DE, Kuchinskaya, PA, Sukhikh, AS, Gromilov, SA & Kulik, LV 2018, '1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology', Dyes and Pigments, Том. 150, стр. 252-260. https://doi.org/10.1016/j.dyepig.2017.12.011

APA

Vancouver

Baranov DS, Uvarov MN, Glebov EM, Nevostruev DA, Kazantsev MS, Mostovich EA и др. 1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology. Dyes and Pigments. 2018 март 1;150:252-260. doi: 10.1016/j.dyepig.2017.12.011

Author

Baranov, Denis S. ; Uvarov, Mikhail N. ; Glebov, Evgeni M. и др. / 1,3,7,9-Tetraazaperylene frameworks : Synthesis, photoluminescence properties, and thin film morphology. в: Dyes and Pigments. 2018 ; Том 150. стр. 252-260.

BibTeX

@article{de79ac27a65f41f2b59f751c9c3bda14,
title = "1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology",
abstract = "Annulation of the two pyrimidine rings with anthraquinone through the simple condensation of the 1,5-diiodoanthraquinone with guanidine was employed to build 1,3,7,9-tetraazaperylene framework functionalized by NH2, C=O, aliphatic and alkoxy-groups. The properties of the synthesized 1,3,7,9-tetraazaperylenes were studied by cyclic voltammetry, optical and luminescence spectroscopy and DFT-calculations. Remarkably, the vacuum-deposited thin film of 1,3,7,9-tetraazaperylene functionalized by 2-ethylhexyloxy groups demonstrated photoluminescence quantum yield as high as 55%, which is even higher than that for toluene solution (33%).",
keywords = "Atomic force microscopy, Cyclic voltammetry, Optical absorption, Photoluminescence lifetime, Tetraazaperylenes, X-ray diffraction",
author = "Baranov, {Denis S.} and Uvarov, {Mikhail N.} and Glebov, {Evgeni M.} and Nevostruev, {Danil A.} and Kazantsev, {Maxim S.} and Mostovich, {Evgeny A.} and Fadeev, {Dmitry S.} and Antonova, {Olga V.} and Utkin, {Dmitriy E.} and Kuchinskaya, {Polina A.} and Sukhikh, {Aleksandr S.} and Gromilov, {Sergey A.} and Kulik, {Leonid V.}",
note = "Publisher Copyright: {\textcopyright} 2017 Elsevier Ltd Copyright: Copyright 2018 Elsevier B.V., All rights reserved.",
year = "2018",
month = mar,
day = "1",
doi = "10.1016/j.dyepig.2017.12.011",
language = "English",
volume = "150",
pages = "252--260",
journal = "Dyes and Pigments",
issn = "0143-7208",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - 1,3,7,9-Tetraazaperylene frameworks

T2 - Synthesis, photoluminescence properties, and thin film morphology

AU - Baranov, Denis S.

AU - Uvarov, Mikhail N.

AU - Glebov, Evgeni M.

AU - Nevostruev, Danil A.

AU - Kazantsev, Maxim S.

AU - Mostovich, Evgeny A.

AU - Fadeev, Dmitry S.

AU - Antonova, Olga V.

AU - Utkin, Dmitriy E.

AU - Kuchinskaya, Polina A.

AU - Sukhikh, Aleksandr S.

AU - Gromilov, Sergey A.

AU - Kulik, Leonid V.

N1 - Publisher Copyright: © 2017 Elsevier Ltd Copyright: Copyright 2018 Elsevier B.V., All rights reserved.

PY - 2018/3/1

Y1 - 2018/3/1

N2 - Annulation of the two pyrimidine rings with anthraquinone through the simple condensation of the 1,5-diiodoanthraquinone with guanidine was employed to build 1,3,7,9-tetraazaperylene framework functionalized by NH2, C=O, aliphatic and alkoxy-groups. The properties of the synthesized 1,3,7,9-tetraazaperylenes were studied by cyclic voltammetry, optical and luminescence spectroscopy and DFT-calculations. Remarkably, the vacuum-deposited thin film of 1,3,7,9-tetraazaperylene functionalized by 2-ethylhexyloxy groups demonstrated photoluminescence quantum yield as high as 55%, which is even higher than that for toluene solution (33%).

AB - Annulation of the two pyrimidine rings with anthraquinone through the simple condensation of the 1,5-diiodoanthraquinone with guanidine was employed to build 1,3,7,9-tetraazaperylene framework functionalized by NH2, C=O, aliphatic and alkoxy-groups. The properties of the synthesized 1,3,7,9-tetraazaperylenes were studied by cyclic voltammetry, optical and luminescence spectroscopy and DFT-calculations. Remarkably, the vacuum-deposited thin film of 1,3,7,9-tetraazaperylene functionalized by 2-ethylhexyloxy groups demonstrated photoluminescence quantum yield as high as 55%, which is even higher than that for toluene solution (33%).

KW - Atomic force microscopy

KW - Cyclic voltammetry

KW - Optical absorption

KW - Photoluminescence lifetime

KW - Tetraazaperylenes

KW - X-ray diffraction

UR - http://www.scopus.com/inward/record.url?scp=85038837852&partnerID=8YFLogxK

U2 - 10.1016/j.dyepig.2017.12.011

DO - 10.1016/j.dyepig.2017.12.011

M3 - Article

AN - SCOPUS:85038837852

VL - 150

SP - 252

EP - 260

JO - Dyes and Pigments

JF - Dyes and Pigments

SN - 0143-7208

ER -

ID: 9159796