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Functionalized benzazines as luminescent materials and components for optoelectronics

Emiliya Vladimirovna Nosova 1, 2
Emiliya Vladimirovna Nosova
, 
Sylvain Achelle 3
Sylvain Achelle
, 
Galina Nikolaevna Lipunova 1, 2
Galina Nikolaevna Lipunova
, 
Valery Nikolaevich Charushin 1, 2
Valery Nikolaevich Charushin
, 
Oleg Nikolaevich Chupakhin 1, 2
Oleg Nikolaevich Chupakhin
1 I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences, Ekaterinburg
2 Ural Federal University named after the First President of Russia B. N. Yeltsin, Ekaterinburg
3 Institut des Sciences Chimiques de Rennes, UMR CNRS 6226, I.U.T. Lannion, Université de Rennes 1
10.1070/RCR4887
Published 30 November 2018
Review , RCR4887, Volume 88, Issue 11, 1128-1178
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Nosova E. V. et al. Functionalized benzazines as luminescent materials and components for optoelectronics // Russian Chemical Reviews. 2018. Vol. 88. No. 11. pp. 1128-1178.
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Nosova E. V., Achelle S., Lipunova G. N., Charushin V. N., Chupakhin O. N. Functionalized benzazines as luminescent materials and components for optoelectronics // Russian Chemical Reviews. 2018. Vol. 88. No. 11. pp. 1128-1178.
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TY - JOUR
DO - 10.1070/RCR4887
UR - https://rcr.colab.ws/publications/10.1070/RCR4887
TI - Functionalized benzazines as luminescent materials and components for optoelectronics
T2 - Russian Chemical Reviews
AU - Nosova, Emiliya Vladimirovna
AU - Achelle, Sylvain
AU - Lipunova, Galina Nikolaevna
AU - Charushin, Valery Nikolaevich
AU - Chupakhin, Oleg Nikolaevich
PY - 2018
DA - 2018/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 1128-1178
IS - 11
VL - 88
ER -
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@article{2018_Nosova,
author = {Emiliya Vladimirovna Nosova and Sylvain Achelle and Galina Nikolaevna Lipunova and Valery Nikolaevich Charushin and Oleg Nikolaevich Chupakhin},
title = {Functionalized benzazines as luminescent materials and components for optoelectronics},
journal = {Russian Chemical Reviews},
year = {2018},
volume = {88},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RCR4887},
number = {11},
pages = {1128--1178},
doi = {10.1070/RCR4887}
}
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Nosova, Emiliya Vladimirovna, et al. “Functionalized benzazines as luminescent materials and components for optoelectronics.” Russian Chemical Reviews, vol. 88, no. 11, Nov. 2018, pp. 1128-1178. https://rcr.colab.ws/publications/10.1070/RCR4887.
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Abstract

Extensive research on the synthesis and application of benzazine derivatives for electronic devices, luminescent elements, photoelectric conversion elements, and image sensors has been published recently. This review covers article data obtained within the period 2012---2018 on the synthesis and optical properties of functionalized quinolines, quinoxalines and quinazolines. Arylvinyl, arylethynyl and (het)aryl derivatives of these benzazines, their photoluminescence and photoisomerization are discussed. Examples of photosensitive annelated, oligo- and polymeric benzazines and also coordination compounds with benzazine ligands are reviewed.

The bibliography includes 267 references.

Funders

Russian Foundation for Basic Research
18-03-00112
Ministry of Education and Science of the Russian Federation
AAAA-A19-119012290117-6
Ural Branch of the Russian Academy of Sciences
18-3-3-16

References

1.
rcr_88_11_1128_bib1
Yersin
2008
2.
rcr_88_11_1128_bib2
Hannienen
2011
3.
rcr_88_11_1128_bib3
Ronda
2008
4.
rcr_88_11_1128_bib4
Mazzeo
2010
5.
rcr_88_11_1128_bib5
Bochkarev
2011
6.
Themed issue on “organic optoelectronic materials”
Hu W., Bao Z., Muellen K.
Journal of Materials Chemistry A , 2012
7.
Luminescent materials for modern light sources
Zak P.P., Lapina V.A., Pavich T.A., Trofimov A.V., Trofimova N.N., Tsaplev Y.B.
Russian Chemical Reviews , 2017
8.
Organic electroluminescent materials and devices emitting in UV and NIR regions
Pushkarev A.P., Bochkarev M.N.
Russian Chemical Reviews , 2016
9.
Coordination compounds of rare-earth metals with organic ligands for electroluminescent diodes
Katkova M.A., Vitukhnovsky A.G., Bochkarev M.N.
Russian Chemical Reviews , 2005
10.
rcr_88_11_1128_bib10
Liang
J. Mater. Chem. C , 2016
11.
Organic white-light emitting materials
Mukherjee S., Thilagar P.
Dyes and Pigments , 2014
12.
A Novel Lighting OLED Panel Design
Zhang E., Xia W., Yan X.
Molecules , 2016
15.
Light Harvesting for Organic Photovoltaics
Hedley G.J., Ruseckas A., Samuel I.D.
Chemical Reviews , 2016
18.
rcr_88_11_1128_bib18
Achelle
Targets Heterocycl. Systems , 2013
19.
Photoluminescence Properties of Aryl-, Arylvinyl-, and Arylethynylpyrimidine Derivatives
Achelle S., Rodríguez-López J., Guen F.R.
ChemistrySelect , 2018
20.
Luminescent materials incorporating pyrazine or quinoxaline moieties
Achelle S., Baudequin C., Plé N.
Dyes and Pigments , 2013
22.
Azinylarylethenes: synthesis and photophysical and photochemical properties
Lipunova G.N., Nosova E.V., Trashakhova T.V., Charushin V.N.
Russian Chemical Reviews , 2011
23.
Functionalized Quinazolines and Pyrimidines for Optoelectronic Materials
Lipunova G.N., Nosova E.V., Charushin V.N., Chupakhin O.N.
Current Organic Synthesis , 2018
24.
Organic electroluminescent diodes
Tang C.W., VanSlyke S.A.
Applied Physics Letters , 1987
30.
Synthesis and optoelectronic properties of phenylenevinylenequinoline macromolecules
Flores-Noria R., Vázquez R., Arias E., Moggio I., Rodríguez M., Ziolo R.F., Rodríguez O., Evans D.R., Liebig C.
New Journal of Chemistry , 2014
31.
Domino synthesis of protochromic “ON–OFF–ON” luminescent 2-styryl quinolines
Cinar R., Nordmann J., Dirksen E., Müller T.J.
Organic and Biomolecular Chemistry , 2013
33.
Spectral and photochemical properties of isomeric styrylbenzoquinolines
Budyka M.F., Li V.M., Potashova N.I.
High Energy Chemistry , 2013
34.
Photochemical properties of 1-(9-Anthryl)-2-(2-Quinolyl)ethylene
Budyka M.F., Potashova N.I., Gavrishova T.N., Li V.M.
High Energy Chemistry , 2014
36.
Design, synthesis, and photochemistry of styrylquinoline -containing polymers
Kharchenko O., Smokal V., Krupka A., Kolendo A.
Molecular Crystals and Liquid Crystals , 2016
37.
Synthesis and photophysical properties of new styrylquinoline-containing polymers
Smokal V., Krupka A., Kharchenko O., Krupka O., Derkowska-Zielinska B., Kolendo A.
Molecular Crystals and Liquid Crystals , 2018
38.
Energy transfer, fluorescence and photoisomerization of styrylquinoline–naphthol dyads with dioxypolymethylene bridges
Budyka M.F., Sadykova K.F., Gavrishova T.N.
Journal of Photochemistry and Photobiology A: Chemistry , 2012
40.
Spectral and photochemical properties of bis(styrylquinoline) dyad with o-xylylene bridge
Budyka M.F., Gavrishova T.N., Potashova N.I., Chashchikhin O.V.
High Energy Chemistry , 2015
41.
Proton-driven “one-way” photoisomerization due to energy transfer switching in styrylquinoline–merocyanine dyad
Budyka M.F., Lee V.M., Gavrishova T.N.
Journal of Photochemistry and Photobiology A: Chemistry , 2014
42.
Budyka Mikhail Fedorovich, Li Vitalii Moeseevich
Mendeleev Communications , 2014
46.
A ratiometric probe based on coumarin-quinoline for highly selective and sensitive detection of Zn2+ ions in living cells
Wu G., Gao Q., Li M., Tang X., Lai K.W., Tong Q.
Journal of Photochemistry and Photobiology A: Chemistry , 2018
47.
Novel carbazole derivatives with quinoline ring: Synthesis, electronic transition, and two-photon absorption three-dimensional optical data storage
Li L., Wang P., Hu Y., Lin G., Wu Y., Huang W., Zhao Q.
Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy , 2015
48.
Molecular logic gates based on benzo-18-crown-6 ether of styrylquinoline: a theoretical study
Tzeli D., Petsalakis I.D., Theodorakopoulos G.
Physical Chemistry Chemical Physics , 2016
49.
Intense White Molecular Fluorescence from Naphthoxazole-Quinoline Derivatives
Zanocco R.P., Valdebenito S., Gidi Y., Zapata-Torres G., Lemp E., Nonell S., Zanocco A.L.
Photochemistry and Photobiology , 2018
50.
Long wavelength AIEgen of quinoline-malononitrile
Guo Z., Shao A., Zhu W.
Journal of Materials Chemistry C , 2016
51.
Synthesis, structure, and luminescent properties of 2-[2-(9-anthryl)vinyl]quinolines
Serdyuk O.V., Evseenko I.V., Dushenko G.A., Revinskii Y.V., Mikhailov I.E.
Russian Journal of Organic Chemistry , 2012
52.
Synthesis and spectral-luminescence properties of 2-[2-(pyridin-4-yl)vinyl]quinolines
Mikhailov I.E., Svetlichnyi D.A., Burov O.N., Revinskii Y.V., Dushenko G.A., Minkin V.I.
Russian Journal of General Chemistry , 2015
53.
Synthesis and spectral-luminescent properties of methyl and benzyl ethers of 2-[(E)-2-(pyridin-3-yl)vinyl]quinolin-8-ol
Mikhailov I.E., Svetlichnyi D.A., Burov O.N., Dushenko G.A., Revinskii Y.V., Kurbatov S.V.
Russian Journal of General Chemistry , 2016
54.
Synthesis and Photophysical Studies of a Series of Quinazoline Chromophores
Achelle S., Rodrı́guez-López J., Robin-le Guen F.
Journal of Organic Chemistry , 2014
55.
Trialkylalanes in palladium-catalyzed chemo- and regioselective alkylations
Mangalagiu I., Benneche T., Undheim K.
Tetrahedron Letters , 1996
56.
rcr_88_11_1128_bib56
Huang
2008
57.
Emission Tuning of Fluorescent Kinase Inhibitors: Conjugation Length and Substituent Effects
Dhuguru J., Liu W., Gonzalez W.G., Babinchak W.M., Miksovska J., Landgraf R., Wilson J.N.
Journal of Organic Chemistry , 2014
58.
Synthesis and antituberculosis activity of novel 5-styryl-4-(hetero)aryl-pyrimidines via combination of the Pd-catalyzed Suzuki cross-coupling and SNH reactions
Kravchenko M.A., Verbitskiy E.V., Medvinskiy I.D., Rusinov G.L., Charushin V.N.
Bioorganic and Medicinal Chemistry Letters , 2014
59.
Synthesis and Photophysical Investigation of a Series of Push–Pull Arylvinyldiazine Chromophores
Achelle S., Barsella A., Baudequin C., Caro B., Robin-le Guen F.
Journal of Organic Chemistry , 2012
61.
Dipicolylamine styryldiazine derivatives: Synthesis and photophysical studies
Achelle S., Rodríguez-López J., Bureš F., Robin-le Guen F.
Dyes and Pigments , 2015
62.
The synthesis and photophysical studies of quinoxaline and pyridopyrazine derivatives
THIRUMURUGAN P., MURALIDHARAN D., PERUMAL P.
Dyes and Pigments , 2009
64.
Palladium-catalyzed C–H alkenylation of quinoxaline N-oxide enabled by a mono-N-protected amino acid
Freire Franco M.S., de Paula M.H., Glowacka P.C., Fumagalli F., Clososki G.C., da Silva Emery F.
Tetrahedron Letters , 2018
65.
Direct arylalkenylation of furazano[3,4- b ]pyrazines via a new C–H functionalization protocol
Kazin N.A., Kvashnin Y.A., Irgashev R.A., Dehaen W., Rusinov G.L., Charushin V.N.
Tetrahedron Letters , 2015
66.
Synthesis, antimycobacterial and antifungal evaluation of some new 1-ethyl-5-(hetero)aryl-6-styryl-1,6-dihydropyrazine-2,3-dicarbonitriles
Verbitskiy E.V., Slepukhin P.A., Kravchenko M.A., Skornyakov S.N., Evstigneeva N.P., Kungurov N.V., Zil’berberg N.V., Rusinov G.L., Chupakhin O.N., Charushin V.N.
Bioorganic and Medicinal Chemistry Letters , 2015
67.
High thermally stable D–π–A chromophores with quinoxaline moieties in the conjugated bridge: Synthesis, DFT calculations and physical properties
Kalinin A.A., Sharipova S.M., Burganov T.I., Levitskaya A.I., Dudkina Y.B., Khamatgalimov A.R., Katsyuba S.A., Budnikova Y.H., Balakina M.Y.
Dyes and Pigments , 2018
69.
rcr_88_11_1128_bib69
Achelle
RSC Adv. , 2015
70.
Luminescence Behavior of Protonated Methoxy-Substituted Diazine Derivatives: Toward White Light Emission
Achelle S., Rodríguez-López J., Katan C., Robin-le Guen F.
Journal of Physical Chemistry C , 2016
72.
rcr_88_11_1128_bib72
Zhu
Chem. Commun. , 2018
73.
rcr_88_11_1128_bib73
Chauhan
2015
74.
Ferrocene–quinoxaline Y-shaped chromophores as fascinating second-order NLO building blocks for long lasting highly active SHG polymeric films
Senthilkumar K., Thirumoorthy K., Dragonetti C., Marinotto D., Righetto S., Colombo A., Haukka M., Palanisami N.
Dalton Transactions , 2016
75.
Tripodal molecules with triphenylamine core, diazine peripheral groups and extended π-conjugated linkers
Cvejn D., Achelle S., Pytela O., Malval J., Spangenberg A., Cabon N., Bureš F., Robin-le Guen F.
Dyes and Pigments , 2016
76.
Dipolar and V-shaped structures incorporating methylenepyran and diazine fragments
Achelle S., Kahlal S., Saillard J., Cabon N., Caro B., Robin-le Guen F.
Tetrahedron , 2014
77.
rcr_88_11_1128_bib77
Lin
2013
78.
Synthesis and Properties of Diarylamino-Substituted Linear and Dendritic Oligoquinolines for Organic Light-Emitting Diodes
Lee H., Xin H., Park S., Park S., Ahn T., Park D., Jenekhe S.A., Kwon T.
Bulletin of the Korean Chemical Society , 2012
79.
rcr_88_11_1128_bib79
Slodek
2014
80.
Facile Synthesis and Photophysical Characterization of New Quinoline Dyes
Santos G.C., de Andrade Bartolomeu A., Ximenes V.F., da Silva-Filho L.C.
Journal of Fluorescence , 2016
82.
Quinoline-Derived Two-Photon Sensitive Quadrupolar Probes
Tran C., Berqouch N., Dhimane H., Clermont G., Blanchard-Desce M., Ogden D., Dalko P.I.
Chemistry - A European Journal , 2017
83.
Theoretical-Experimental Photophysical Investigations of the Solvent Effect on the Properties of Green- and Blue-Light-Emitting Quinoline Derivatives
dos Santos G.C., Servilha R.O., de Oliveira E.F., Lavarda F.C., Ximenes V.F., da Silva-Filho L.C.
Journal of Fluorescence , 2017
84.
Synthesis of quinoline based heterocyclic compounds for blue lighting application
Kumar V., Gohain M., Van Tonder J.H., Ponra S., Bezuindenhoudt B.C., Ntwaeaborwa O.M., Swart H.C.
Optical Materials , 2015
87.
A quinoline-based fluorescence "on-off-on" probe for relay identification of Cu2+ and Cd2+ ions.
Han J., Tang X., Wang Y., Liu R., Wang L., Ni L.
Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy , 2018
89.
rcr_88_11_1128_bib89
Bonacorso
New J. Chem. , 2018
90.
New donor-acceptor-donor molecules based on quinoline acceptor unit with Schiff base bridge: synthesis and characterization
Kotowicz S., Siwy M., Filapek M., Malecki J.G., Smolarek K., Grzelak J., Mackowski S., Slodek A., Schab-Balcerzak E.
Journal of Luminescence , 2017
91.
Comprehensive exploration of the optical and biological properties of new quinoline based cellular probes
Czaplinska B., Maron A., Malecki J.G., Szafraniec-Gorol G., Matussek M., Malarz K., Mrozek-Wilczkiewicz A., Danikiewicz W., Musiol R., Slodek A.
Dyes and Pigments , 2017
92.
rcr_88_11_1128_bib92
Slodek
2016
93.
Highly efficient orange and deep-red organic light emitting diodes with long operational lifetimes using carbazole–quinoline based bipolar host materials
Chen C., Hsu L., Rajamalli P., Chang Y., Wu F., Liao C., Chiu M., Chou P., Huang M., Chu L., Cheng C.
Journal of Materials Chemistry C , 2014
95.
Octupolar chimeric compounds built from quinoline caged acetate moieties: a novel approach for 2-photon uncaging of biomolecules
Picard S., Genin E., Clermont G., Hugues V., Mongin O., Blanchard-Desce M.
New Journal of Chemistry , 2013
96.
Investigations into the flexibility of the 3D structure and rigid backbone of quinoline by fluorine addition to enhance its blue emission
Alapour S., Zamisa S.J., Silva J.R., Alves C.N., Omondi B., Ramjugernath D., Koorbanally N.A.
CrystEngComm , 2018
98.
Fluorescent periodic mesoporous organosilica nanoparticles dual-functionalized via click chemistry for two-photon photodynamic therapy in cells
Croissant J.G., Picard S., Aggad D., Klausen M., Mauriello Jimenez C., Maynadier M., Mongin O., Clermont G., Genin E., Cattoën X., Wong Chi Man M., Raehm L., Garcia M., Gary-Bobo M., Blanchard-Desce M., et. al.
Journal of Materials Chemistry B , 2016
99.
A two-photon fluorescent probe for viscosity imaging in vivo
Ning P., Dong P., Geng Q., Bai L., Ding Y., Tian X., Shao R., Li L., Meng X.
Journal of Materials Chemistry B , 2017
100.
A ratiometric two-photon fluorescent probe for selective detection of endogenous formaldehyde via Aza-Cope reaction
Yang H., Fang G., Guo M., Ning P., Feng Y., Yu H., Meng X.
Sensors and Actuators, B: Chemical , 2018
103.
rcr_88_11_1128_bib103
Liu
Chem. Commun. , 2013
105.
Emission properties of diazines chromophores: Structure-properties relationship
Achelle S., Robin-le Guen F.
Journal of Photochemistry and Photobiology A: Chemistry , 2017
106.
rcr_88_11_1128_bib106
Nosova
2016
107.
Nosova Emiliya Vladimirovna, Moshkina Tatyana Nikolaevna, Lipunova Galina Nikolaevna, Baklanova Inna Viktorovna, Kopchuk Dmitrii Sergeevich, Slepukhin Pavel Alexandrovich, Charushin Valery Nikolaevich
Mendeleev Communications , 2017
108.
Nosova Emiliya Vladimirovna, Moshkina Tatyana Nikolaevna, Lipunova Galina Nikolaevna, Kelbysheva Elena Sergeevna, Loim Nikolay Mikhailovich, Slepukhin Pavel Alexandrovich, Charushin Valery Nikolaevich, Baklanova Inna Viktorovna
Mendeleev Communications , 2017
109.
rcr_88_11_1128_bib109
Wang
J. Org. Chem. , 2018
114.
New 2,3-Bis(5-arylthiophen-2-yl)quinoxaline Derivatives: Synthesis and Photophysical Properties
Moshkina T.N., Nosova E.V., Lipunova G.N., Valova M.S., Charushin V.N.
Asian Journal of Organic Chemistry , 2018
115.
Synthesis and Two-Photon Absorption Property Characterizations of Small Dendritic Chromophores Containing Functionalized Quinoxaliniod Heterocycles
Lin T., Lee Y., Liu C., Huang B., Tsai M., Huang Y., Lin J., Shen Y., Wu C.
Chemistry - A European Journal , 2012
116.
rcr_88_11_1128_bib117
Harsha
Chem. Select , 2018
122.
Copper-catalyzed aerobic oxidative coupling of o-phenylenediamines with 2-aryl/heteroarylethylamines: direct access to construct quinoxalines
Gopalaiah K., Saini A., Chandrudu S.N., Rao D.C., Yadav H., Kumar B.
Organic and Biomolecular Chemistry , 2017
123.
Azinyl derivatives of ferrocene and cymantrene. Synthesis and properties
Utepova I.A., Musikhina A.A., Chupakhin O.N.
Russian Chemical Bulletin , 2016
125.
rcr_88_11_1128_bib126
Xu
ACS Appl. Mater. Interfaces , 2017
126.
Functionalization of Quinoxalines by Using TMP Bases: Preparation of Tetracyclic Heterocycles with High Photoluminescene Quantum Yields
Nafe J., Herbert S., Auras F., Karaghiosoff K., Bein T., Knochel P.
Chemistry - A European Journal , 2014
127.
Controlling the Charge Transfer in D–A–D Chromophores Based on Pyrazine Derivatives
Lu X., Fan S., Wu J., Jia X., Wang Z., Zhou G.
Journal of Organic Chemistry , 2014
128.
The optoelectronic properties of organic materials based on triphenylamine that are relevant to organic solar photovoltaic cells
Bourass M., Touimi Benjelloun A., Benzakour M., Mcharfi M., Jhilal F., Hamidi M., Bouachrine M.
New Journal of Chemistry , 2017
130.
Benzimidazolylquinoxalines: novel fluorophores with tuneable sensitivity to solvent effects
Burganov T.I., Zhukova N.A., Mamedov V.A., Bannwarth C., Grimme S., Katsyuba S.A.
Physical Chemistry Chemical Physics , 2017
131.
Four- and Five-Component Syntheses and Photophysical Properties of Emission Solvatochromic 3-Aminovinylquinoxalines
Gers-Panther C.F., Fischer H., Nordmann J., Seiler T., Behnke T., Würth C., Frank W., Resch-Genger U., Müller T.J.
Journal of Organic Chemistry , 2016
133.
Three-Component Activation/Alkynylation/Cyclocondensation (AACC) Synthesis of Enhanced Emission Solvatochromic 3-Ethynylquinoxalines
Merkt F.K., Höwedes S.P., Gers-Panther C.F., Gruber I., Janiak C., Müller T.J.
Chemistry - A European Journal , 2018
135.
An efficient exciton harvest route for high-performance OLEDs based on aggregation-induced delayed fluorescence
Yu L., Wu Z., Xie G., Zhong C., Zhu Z., Ma D., Yang C.
Chemical Communications , 2018
136.
rcr_88_11_1128_bib137
Yu
Chem. Commun. , 2016
138.
Organic light emitting diodes with horizontally oriented thermally activated delayed fluorescence emitters
Kim D.H., Inada K., Zhao L., Komino T., Matsumoto N., Ribierre J.C., Adachi C.
Journal of Materials Chemistry C , 2017
139.
Synthesis and Characterization of Quinoxaline Derivative as Organic Semiconductors for Organic Thin-Film Transistors
Kim H., Reddy M.R., Hong S., Kim C., Seo S.
Journal of Nanoscience and Nanotechnology , 2017
140.
rcr_88_11_1128_bib141
Yang
RSC Adv. , 2015
141.
rcr_88_11_1128_bib142
Gedefaw
2017
142.
Development of quinoxaline based polymers for photovoltaic applications
Yuan J., Ouyang J., Cimrová V., Leclerc M., Najari A., Zou Y.
Journal of Materials Chemistry C , 2017
143.
Quinoxaline-based conjugated polymers for polymer solar cells
Liu M., Gao Y., Zhang Y., Liu Z., Zhao L.
Polymer Chemistry , 2017
145.
The improved photovoltaic performance of phenothiazine-dithienopyrrole based dyes with auxiliary acceptors
Han M., Zhu Y., Liu S., Liu Q., Ye D., Wang B., Zheng J.
Journal of Power Sources , 2018
147.
rcr_88_11_1128_bib148
Wang
ACS Appl. Mater. Interfaces , 2016
150.
Dithienylpyrazine-based photosensitizers: Effect of swapping a connecting unit on optoelectronic properties and photovoltaic performances
Godfroy M., Aumaitre C., Caffy F., Kervella Y., Cabau L., Pellejà L., Maldivi P., Narbey S., Oswald F., Palomares E., Joly D., Demadrille R.
Dyes and Pigments , 2017
153.
rcr_88_11_1128_bib154
Lu
ACS Appl. Mater. Interfaces , 2014
154.
rcr_88_11_1128_bib155
Jia
J. Mater. Chem. A , 2014
155.
X-shaped organic dyes with a quinoxaline bridge for use in dye-sensitized solar cells
Lu X., Jia X., Wang Z., Zhou G.
Journal of Materials Chemistry A , 2013
156.
Incorporating quinoxaline unit as additional acceptor for constructing efficient donor-free solar cell sensitizers
Shen C., Wu Y., Zhang W., Jiang H., Zhang H., Li E., Chen B., Duan X., Zhu W.
Dyes and Pigments , 2018
157.
Molecular engineering of D–A–π–A sensitizers for highly efficient solid-state dye-sensitized solar cells
Li X., Xu B., Liu P., Hu Y., Kloo L., Hua J., Sun L., Tian H.
Journal of Materials Chemistry A , 2017
158.
High performance solid-state dye-sensitized solar cells based on organic blue-colored dyes
Shen Z., Xu B., Liu P., Hu Y., Yu Y., Ding H., Kloo L., Hua J., Sun L., Tian H.
Journal of Materials Chemistry A , 2017
161.
Two Novel Small Molecule Donors and the Applications in Bulk-Heterojunction Solar Cells
Qi X., Lo Y., Zhao Y., Xuan L., Ting H., Wong K., Rahaman M., Chen Z., Xiao L., Qu B.
Frontiers in Chemistry , 2018
162.
Non-planar perylenediimide acceptors with different geometrical linker units for efficient non-fullerene organic solar cells
Liu X., Liu T., Duan C., Wang J., Pang S., Xiong W., Sun Y., Huang F., Cao Y.
Journal of Materials Chemistry A , 2017
163.
Quinoxaline-Based Small Molecules: Synthesis and Investigation on Their Optoelectronic Properties
Deng J., Tao Q., Yan D., Huang X., Liao Y.
Materials Science-Poland , 2018
164.
rcr_88_11_1128_bib165
Xiao
ACS Appl. Mater. Interfaces , 2018
165.
Bipolar carbazole/quinoxaline-based host materials for efficient red PhOLEDs
Hu M., Xu Q., Jiang Y., Mu H., Gao L., Hu P., Huang J., Su J.
Dyes and Pigments , 2018
171.
rcr_88_11_1128_bib172
Fan
RSC Adv. , 2017
172.
rcr_88_11_1128_bib173
Jiang
J. Mater. Chem. C , 2017
173.
Key role of ancillary ligands in imparting blue shift in electroluminescence wavelength in ruthenium polypyridyl light-emitting diodes
Shahroosvand H., Rezaei S., Mohajerani E., Mahmoudi M., Kamyabi M.A., Nasiri S.
New Journal of Chemistry , 2014
174.
Supramolecular architecture and photophysical and biological properties of ruthenium(ii) polypyridyl complexes
Bhat S.S., Revankar V.K., Khan A., Butcher R.J., Thatipamula K.
New Journal of Chemistry , 2015
175.
rcr_88_11_1128_bib176
Yu
2016
177.
A fluorescent chemosensor for the sequential detection of copper(II) and histidine and its biological applications
Wang D., Zheng J., Zheng X., Fang D., Yuan D., Jin L.
Sensors and Actuators, B: Chemical , 2016
179.
rcr_88_11_1128_bib180
180.
rcr_88_11_1128_bib181
181.
rcr_88_11_1128_bib182
183.
rcr_88_11_1128_bib184
Verbitskii
2019
187.
Formation of One-Dimensional Helical Columns and Excimerlike Excited States by Racemic Quinoxaline-Fused [7]Carbohelicenes in the Crystal
Sakai H., Shinto S., Araki Y., Wada T., Sakanoue T., Takenobu T., Hasobe T.
Chemistry - A European Journal , 2014
188.
rcr_88_11_1128_bib189
Sakai
J. Phys. Chem. , 2015
189.
Synthetic Control of the Excited-State Dynamics and Circularly Polarized Luminescence of Fluorescent “Push-Pull” Tetrathia[9]helicenes
Yamamoto Y., Sakai H., Yuasa J., Araki Y., Wada T., Sakanoue T., Takenobu T., Kawai T., Hasobe T.
Chemistry - A European Journal , 2016
192.
rcr_88_11_1128_bib193
193.
rcr_88_11_1128_bib194
Laramee-Milette
Chem. Select , 2017
197.
rcr_88_11_1128_bib198
Guo
RSC Adv. , 2015
198.
rcr_88_11_1128_bib199
Kang
2018
199.
A Medium Bandgap D–A Copolymer Based on 4-Alkyl-3,5-difluorophenyl Substituted Quinoxaline Unit for High Performance Solar Cells
Wang T., Lau T., Lu X., Yuan J., Feng L., Jiang L., Deng W., Peng H., Li Y., Zou Y.
Macromolecules , 2018
200.
rcr_88_11_1128_bib201
Yang
ACS Appl. Mater. Interfaces , 2018
203.
PANI Branches onto Donor-Acceptor Copolymers: Synthesis, Characterization and Electroluminescent Properties of New 2D-Materials
Jessop I., Díaz F., Terraza C., Tundidor-Camba A., Leiva Á., Cattin L., Bèrnede J.
Polymers , 2018
208.
High-Efficiency Tris(8-hydroxyquinoline)aluminum (Alq3) Complexes for Organic White-Light-Emitting Diodes and Solid-State Lighting
Pérez-Bolívar C., Takizawa S., Nishimura G., Montes V.A., Anzenbacher P.
Chemistry - A European Journal , 2011
215.
rcr_88_11_1128_bib216
216.
rcr_88_11_1128_bib217
Hsu
J. Am. Chem. Soc. , 2011
219.
Porous Cu(I) Triazolate Framework and Derived Hybrid Membrane with Exceptionally High Sensing Efficiency for Gaseous Oxygen
Liu S., Qi X., Lin R., Cheng X., Liao P., Zhang J., Chen X.
Advanced Functional Materials , 2014
220.
rcr_88_11_1128_bib221
Song
RSC Adv. , 2015
221.
Coordination polymer of silver(I) perrhenate with quinoxaline: Synthesis, crystal structure, and luminescence properties
Kokunov Y.V., Gorbunova Y.E., Kovalev V.V., Kozyukhin S.A.
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya , 2015
222.
A novel cobalt (I) coordination polymer with mixed thiocyanate and quinoline ligands: Crystal structure, magnetism and luminescent properties
Li L., Chen S., Zhou R., Bai Y., Dang D.
Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy , 2014
231.
Design and synthesis of heteroleptic ruthenium (II) complexes and their applications in nanocrystalline TiO2 solar cells
Ocakoglu K., Harputlu E., Guloglu P., Erten-Ela S.
Inorganic Chemistry Communication , 2012
232.
Ruthenium(II) complexes with quinoline carboxylate as a co-ligand
Małecki J.G., Maroń A., Gryca I., Mori A., Suzuki T.
Polyhedron , 2013
233.
Synthesis, Photophysical and Electrochemical Properties of Novel Ru(II) Complexes
Wang J., Shang Y.
Journal of the Korean Chemical Society , 2012
234.
rcr_88_11_1128_bib235
Stacey
Dalton Trans. , 2016
235.
Enhancement of luminescence performance from the alteration of stacking patterns of Pt(ii) dendrimers
Li H., Yuan W., Wang X., Zhan H., Xie Z., Cheng Y.
Journal of Materials Chemistry C , 2015
237.
Photophysical Properties of Cyclometalated Pt(II) Complexes: Counterintuitive Blue Shift in Emission with an Expanded Ligand π System
Bossi A., Rausch A.F., Leitl M.J., Czerwieniec R., Whited M.T., Djurovich P.I., Yersin H., Thompson M.E.
Inorganic Chemistry , 2013
238.
Highly Luminescent Dinuclear Platinum(II) Complexes Incorporating Bis-Cyclometallating Pyrazine-Based Ligands: A Versatile Approach to Efficient Red Phosphors
Culham S., Lanoë P., Whittle V.L., Durrant M.C., Williams J.A., Kozhevnikov V.N.
Inorganic Chemistry , 2013
240.
Nosova Emiliya Vladimirovna, Moshkina Tatyana Nikolaevna, Kopchuk Dmitrii Sergeevich, Lipunova Galina Nikolaevna, Slepukhin Pavel Alexandrovich, Charushin Valery Nikolaevich
Mendeleev Communications , 2016
242.
Red to near-infrared organometallic phosphorescent dyes for OLED applications
Ho C., Li H., Wong W.
Journal of Organometallic Chemistry , 2014
243.
Pure Red Phosphorescent Organic Light-Emitting Diodes Made of Iridium(III) Complex with Thiophene-Quinoline Ligand
Lim J.M., Kwon J., Xu F., Kim H.U., Hwang D.
Journal of Nanoscience and Nanotechnology , 2013
244.
Tetrazole iridium(iii) complexes as a class of phosphorescent emitters for high-efficiency OLEDs
Umamahesh B., Karthikeyan N.S., Sathiyanarayanan K.I., Malicka J.M., Cocchi M.
Journal of Materials Chemistry C , 2016
246.
Using Substituted Cyclometalated Quinoxaline Ligands To Finely Tune the Luminescence Properties of Iridium(III) Complexes
Langdon-Jones E.E., Hallett A.J., Routledge J.D., Crole D.A., Ward B.D., Platts J.A., Pope S.J.
Inorganic Chemistry , 2012
247.
rcr_88_11_1128_bib248
Han
Dalton Trans. , 2017
248.
Highly efficient orange-red electroluminescence of iridium complexes with good electron mobility
Han H., Cui R., Jing Y., Lu G., Zheng Y., Zhou L., Zuo J., Zhang H.
Journal of Materials Chemistry C , 2017
249.
rcr_88_11_1128_bib250
Lewis
Dalton Trans. , 2012
250.
rcr_88_11_1128_bib251
Singh
RSC Adv. , 2015
251.
Unusual O-Bridged Symmetric Quinoline-Based Ligand for the Formation of Luminescent Mono-Aqua Lanthanide Complexes
Hammoud H., de Bettencourt-Dias A., Schmitt M., Monteiro J.H., Rossini J.S., Lecointre A., Gallet S., Bourguignon J., Mameri S.
ChemistrySelect , 2016
252.
Structural and Spectroscopic Properties of New Chiral Quinoline-based Ln(III) Complexes
Mihorianu M., Leonzio M., Monari M., Ravotto L., Ceroni P., Bettinelli M., Piccinelli F.
ChemistrySelect , 2016
253.
Anion-Dependence of Ytterbium Complexes and Their NIR Luminescence
Wang J., Li H., Chen P., Zhang M., Sun W., Yan P.
Zeitschrift fur Anorganische und Allgemeine Chemie , 2016
254.
rcr_88_11_1128_bib255
Shen
RSC Adv. , 2016
255.
rcr_88_11_1128_bib256
Zhang
Dalton Trans. , 2015
256.
rcr_88_11_1128_bib257
Zhang
RSC Adv. , 2015
257.
Boron(III) Complexes with N,N’- and N,O-Heterocyclic Ligands: Synthesis and Spectroscopic Properties
Lipunova G.N., Nosova E.V., Charushin V.N., Chupakhin O.N.
Comments on Inorganic Chemistry , 2016
259.
rcr_88_11_1128_bib260
Balijapalli
2015
260.
Substituent Effect in 2-Benzoylmethylenequinoline Difluoroborates Exhibiting Through-Space Couplings. Multinuclear Magnetic Resonance, X-ray Diffraction, and Computational Study
Zakrzewska A., Kolehmainen E., Valkonen A., Haapaniemi E., Rissanen K., Chęcińska L., Ośmiałowski B.
Journal of Physical Chemistry A , 2012
261.
Substituent effects on the photophysical properties of fluorescent 2-benzoylmethylenequinoline difluoroboranes: A combined experimental and quantum chemical study
Zakrzewska A., Zaleśny R., Kolehmainen E., Ośmiałowski B., Jędrzejewska B., Ågren H., Pietrzak M.
Dyes and Pigments , 2013
262.
Photophysical Properties of Phenacylphenantridine Difluoroboranyls: Effect of Substituent and Double Benzannulation
Grabarz A.M., Jędrzejewska B., Zakrzewska A., Zaleśny R., Laurent A.D., Jacquemin D., Ośmiałowski B.
Journal of Organic Chemistry , 2017
264.
Synthesis, structure and photoluminescent properties of BF2 and BPh2 complexes with N,O-benzazine ligands
Nosova E.V., Moshkina T.N., Lipunova G.N., Baklanova I.V., Slepukhin P.A., Charushin V.N.
Journal of Fluorine Chemistry , 2015
265.
Synthesis and luminescent properties of BF2 complexes with N,O-benzazine ligands
Moshkina T.N., Nosova E.V., Lipunova G.N., Valova M.S., Taniya O.S., Slepukhin P.A., Charushin V.N.
Journal of Fluorine Chemistry , 2019