New Optoelectronic Materials Based on Bitriazines: Synthesis and Properties

Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction

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Organic Semiconducting Oligomers for Use in Thin Film Transistors

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Electron Transport Materials for Organic Light-Emitting Diodes

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New Conjugated Polymers with Donor−Acceptor Architectures: Synthesis and Photophysics of Carbazole−Quinoline and Phenothiazine−Quinoline Copolymers and Oligomers Exhibiting Large Intramolecular Charge Transfer

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Growth and Characterization of Sexithiophene Single Crystals

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Recent applications of 2,4,6-trichloro-1,3,5-triazine and its derivatives in organic synthesis

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On the Nature of Nonplanarity in the [N]Phenylenes

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Polycyanate esters: Science and applications

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Hierarchical Self-Organization of Perylene Bisimide–Melamine Assemblies to Fluorescent Mesoscopic Superstructures

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High-Efficiency Organic Electrophosphorescent Diodes Using 1,3,5-Triazine Electron Transport Materials

Inomata, H., Goushi, K., Masuko, T., Konno, T., Imai, T., Sasabe, H., Brown, J. J., & Adachi, C. (2004) · Chemistry of Materials · doi:10.1021/cm034689t · Cited by 232

High‐Performance Organic Light‐Emitting Diodes Based on Intramolecular Charge‐Transfer Emission from Donor–Acceptor Molecules: Significance of Electron‐ Donor Strength and Molecular Geometry

Kulkarni, A. P., Kong, X., & Jenekhe, S. A. (2006) · Advanced Functional Materials · doi:10.1002/adfm.200500722 · Cited by 172

Syntheses, structures, and electroluminescence of new blue luminescent star-shaped compounds based on 1,3,5-triazine and 1,3,5-trisubstituted benzene

Pang, J., Tao, Y., Freiberg, S., Yang, X., D'Iorio, M., & Wang, S. (2001) · Journal of Materials Chemistry · doi:10.1039/b105422h · Cited by 168

Cyanuric Chloride Derivatives. III. Alkoxy-s-triazines

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An Efficient Pyridine- and Oxadiazole-Containing Hole-Blocking Material for Organic Light-Emitting Diodes: Synthesis, Crystal Structure, and Device Performance

Wang, C., Jung, G. Y., Hua, Y., Pearson, C., Bryce, M. R., Petty, M. C., Batsanov, A. S., Goeta, A. E., & Howard, J. A. K. (2001) · Chemistry of Materials · doi:10.1021/cm0010250 · Cited by 151

Anisotropy of the mobility of pentacene from frustration

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New electron-transporting materials for light emitting diodes: 1,3,4-oxadiazole–pyridine and 1,3,4-oxadiazole–pyrimidine hybrids

Wang, C., Jung, G. Y., Batsanov, A. S., Bryce, M. R., & Petty, M. C. (2001) · Journal of Materials Chemistry · doi:10.1039/b106907c · Cited by 126

[1,3,5]-Triazine: A Versatile Heterocycle in Current Applications of Organic Chemistry

Giacomelli, G., Porcheddu, A., & Luca, L. D. (2004) · Current Organic Chemistry · doi:10.2174/1385272043369845 · Cited by 125

Synthesis and Characterization of Aromatic Poly(1,3,5-triazine−ether)s for Electroluminescent Devices

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Synthesis and Application of Dimeric 1,3,5-Triazine Ethers as Hole-Blocking Materials in Electroluminescent Devices

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Synthesis and Identification of [1,3,5]Triazine-pyridine Biheteroaryl as a Novel Series of Potent Cyclin-Dependent Kinase Inhibitors

Kuo, G., DeAngelis, A., Emanuel, S. L., Wang, A., Zhang, Y., Connolly, P. J., Chen, X., Gruninger, R. H., Rugg, C. A., Fuentes‐Pesquera, A. R., et al. (2005) · Journal of Medicinal Chemistry · doi:10.1021/jm040214h · Cited by 96

A Molecule‐Based Nanoporous Material Showing Tuneable Spin‐Crossover Behavior near Room Temperature

Quesada, M., O’Shea, V. A. D. L. P., Aromı́, G., Geremia, S., Massera, C., Roubeau, O., Gámez, P., & Reedijk, J. (2007) · Advanced Materials · doi:10.1002/adma.200602284 · Cited by 87

Silane- and triazine-containing hole and exciton blocking material for high-efficiency phosphorescent organic light emitting diodes

Kang, J.-W., Lee, D.-S., Park, H.-D., Park, Y.-S., Kim, J. W., Jeong, W.-I., Yoo, K.-M., Go, K., Kim, S.-H., & Kim, J.-J. (2007) · Journal of Materials Chemistry · doi:10.1039/b705741e · Cited by 82

Electroluminescence from a new distyrylbenzene based triazine dendrimer

Lupton, J. M., Hemingway, L. R., Samuel, I. D. W., & Burn, P. L. (2000) · Journal of Materials Chemistry · doi:10.1039/a908816d · Cited by 71

Spin‐Crossover Studies on a Series of 1D Chain and Dinuclear Iron(II) Triazine‐Dipyridylamine Compounds

Neville, S. M., Leita, B. A., Offermann, D. A., Duriska, M. B., Moubaraki, B., Chapman, K. W., Halder, G. J., & Murray, K. S. (2007) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.200601034 · Cited by 63

Novel Diamino Derivatives of [1,2,4]Triazolo[1,5-a][1,3,5]triazine as Potent and Selective Adenosine A2aReceptor Antagonists

Vu, C. B., Pan, D., Peng, B., Kumaravel, G., Smits, G. J., Jin, X., Phadke, D., Engber, T. M., Huang, C., Reilly, J., et al. (2004) · Journal of Medicinal Chemistry · doi:10.1021/jm0498396 · Cited by 62

Liquid crystals in the series of 2,4,6-tristyryl-1,3,5-triazines

Holst, H. C., Pakuła, T., & Meier, H. (2004) · Tetrahedron · doi:10.1016/j.tet.2004.06.031 · Cited by 60

A New Class of Star-Shaped Discotic Liquid Crystal Containing a 2, 4, 6-Triphenyl-1, 3, 5-triazine Unit as a Core

Lee, C.-H., & Yamamoto, T. (2002) · Bulletin of the Chemical Society of Japan · doi:10.1246/bcsj.75.615 · Cited by 51

New Alternative Copolymer Constituted of Fluorene and Triphenylamine Units with a Tunable −CHO Group in the Side Chain. Quantitative Transformation of the −CHO Group to −CHCHAr Groups and Optical and Electrochemical Properties of the Polymers

Fang, Q., & Yamamoto, T. (2004) · Macromolecules · doi:10.1021/ma0359133 · Cited by 51

Light-Emitting Organic Materials with Variable Charge Injection and Transport Properties

Chen, A. C. ‐., Wallace, J. U., Wei, S. K. ‐., Zeng, L., Chen, S. H., & Blanton, T. N. (2005) · Chemistry of Materials · doi:10.1021/cm0519582 · Cited by 48

Chemical Reduction of 2,4,6-Tricyano-1,3,5-triazine and 1,3,5-Tricyanobenzene. Formation of Novel 4,4‘,6,6‘-Tetracyano-2,2‘-bitriazine and Its Radical Anion

Sesto, R. E. D., Arif, A. M., Novoa, J. J., Anusiewicz, I., Skurski, P., Simons, J., Dunn, B. C., Eyring, E. M., & Miller, J. S. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo025833h · Cited by 47

Symmetrical Bisquinolones via Metal-Catalyzed Cross-Coupling and Homocoupling Reactions

Hashim, J., Glasnov, T. N., Kremsner, J. M., & Kappe, C. O. (2006) · The Journal of Organic Chemistry · doi:10.1021/jo052283p · Cited by 44

Mesomorphic Block Molecules: Semiperfluorinated 1,3,5-Triazine Derivatives Exhibiting Lamellar, Columnar, and Cubic Mesophases

Kohlmeier, A., Janietz, D., & Diele, S. (2006) · Chemistry of Materials · doi:10.1021/cm0524502 · Cited by 36

New growth method of rubrene single crystal for organic field-effect transistor

Kim, K., Kim, M. K., Kang, H. S., Cho, M. Y., Joo, J., Kim, J. H., Kim, K. H., Hong, C. S., & Choi, D. H. (2007) · Synthetic Metals · doi:10.1016/j.synthmet.2007.05.013 · Cited by 34

Ab initio molecular orbital study of 1,3,5-triazine derivatives for phosphorescent organic light emitting devices

Chu, T., Ho, M., Chen, J.-F., & Chen, C. H. (2005) · Chemical Physics Letters · doi:10.1016/j.cplett.2005.08.149 · Cited by 32

First hyperpolarizabilities of triazine derivatives. Ab initio studies and Hammett correlation

Park, G., & Cho, B. R. (2004) · Journal of Physical Organic Chemistry · doi:10.1002/poc.709 · Cited by 24

Synthesis and characterization of triallylphenoxytriazine and the properties of its copolymer with bismaleimide

Fang, Q., & Jiang, L. (2001) · Journal of Applied Polymer Science · doi:10.1002/app.1547 · Cited by 18

Electro-optic properties of thiol-ene polymer stabilized ferroelectric liquid crystals

Beckel, E. R., Cramer, N. B., Harant, A. W., & Bowman, C. N. (2003) · Liquid Crystals · doi:10.1080/02678290310001605910 · Cited by 18

Diffusion properties of reactive dyes into net modified cotton cellulose with triazine derivative

Xie, K., Sun, Y. P., & Hou, A. (2006) · Journal of Applied Polymer Science · doi:10.1002/app.25097 · Cited by 14

Polymer Plating of 6-Substituted-1, 3, 5-Triazine-2, 4-Dithiols on Magnesium Alloys and Applications of the Plated Alloys

Mori, K., Hirahara, H., Oishi, Y., & Sasaki, H. (2001) · MATERIALS TRANSACTIONS · doi:10.2320/matertrans.42.1219 · Cited by 12

Diazine and triazine herbicides

Ishii, A., & Katsumata, Y. (2005) · Springer eBooks · doi:10.1007/3-540-27579-7_65 · Cited by 9

Recent progress in porphyrin-based materials for organic solar cells

Mahmood, A., Hu, J.-Y., Xiao, B., Tang, A., Wang, X., & Zhou, E. (2018) · Journal of Materials Chemistry A · doi:10.1039/c8ta06392c · Cited by 311

Star-Shaped Donor-π-Acceptor Conjugated Oligomers with 1,3,5-Triazine Cores: Convergent Synthesis and Multifunctional Properties

Ren, S., Zeng, D., Zhong, H., Wang, Y., Qian, S., & Fang, Q. (2010) · The Journal of Physical Chemistry B · doi:10.1021/jp104710y · Cited by 97

A General and Selective Copper‐Catalyzed Cross‐Coupling of Tertiary Grignard Reagents with Azacyclic Electrophiles

Hintermann, L., Xiao, L., & Labonne, A. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200803312 · Cited by 88

Conjugated Asymmetric Donor‐Substituted 1,3,5‐Triazines: New Host Materials for Blue Phosphorescent Organic Light‐Emitting Diodes

An, Z., Chen, R., Yin, J. L., Xie, G., Shi, H., Tsuboi, T., & Huang, W. (2011) · Chemistry - A European Journal · doi:10.1002/chem.201101118 · Cited by 83

One‐Step Synthesis of 2‐Amino‐5H‐pyrimido[5,4‐b]indoles, Substituted 2‐(1,3,5‐triazin‐2‐yl)‐1H‐indoles, and 1,3,5‐Triazines from Aldehydes

Biswas, S., & Batra, S. (2012) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201200276 · Cited by 69

Transition metal-catalyzed cross-coupling methodologies for the engineering of small molecules with applications in organic electronics and photovoltaics

Zani, L., Dessì, A., Franchi, D., Calamante, M., Reginato, G., & Mordini, A. (2019) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2019.04.007 · Cited by 69

New Conjugated Triazine Based Molecular Materials for Application in Optoelectronic Devices: Design, Synthesis, and Properties

Zhong, H., Lai, H., & Fang, Q. (2011) · The Journal of Physical Chemistry C · doi:10.1021/jp109806m · Cited by 63

Star‐Shaped D‐π‐A Molecules Containing a 2,4,6‐Tri(thiophen‐2‐yl)‐1,3,5‐triazine Unit: Synthesis and Two‐Photon Absorption Properties

Zou, L., Liu, Z., Yan, X., Liu, Y., Fu, Y., Liu, J., Huang, Z., Chen, X., & Qin, J. (2009) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200900641 · Cited by 61

Shining a Light on s-Triazine-Based Polymers

Butchosa, C., McDonald, T. O., Cooper, A. I., Adams, D. J., & Zwijnenburg, M. A. (2014) · The Journal of Physical Chemistry C · doi:10.1021/jp411854f · Cited by 58

Novel bipolar host materials based on 1,3,5-triazine derivatives for highly efficient phosphorescent OLEDs with extremely low efficiency roll-off

Liu, X., Zheng, C., Xiao, J., Ye, J., Liu, C.-L., Wang, S., Zhao, W., & Zhang, X. (2012) · Physical Chemistry Chemical Physics · doi:10.1039/c2cp41542a · Cited by 56

Nickel-Catalyzed One-Pot Deoxygenation and Reductive Homocoupling of Phenols via C–O Activation Using TCT Reagent

Iranpoor, N., & Panahi, F. (2014) · Organic Letters · doi:10.1021/ol503560e · Cited by 56

Synthesis and properties of bipolar derivatives of 1,3,5-triazine and carbazole

Matulaitis, T., Kostiv, N., Gražulevičius, J. V., Pečiulytė, L., Simokaitienė, J., Jankauskas, V., Łuszczyńska, B., & Ulański, J. (2015) · Dyes and Pigments · doi:10.1016/j.dyepig.2015.11.001 · Cited by 53

Efficient co-sensitization of dye-sensitized solar cells by novel porphyrin/triazine dye and tertiary aryl-amine organic dye

Sharma, G. D., Angaridis, P. A., Pipou, S., Zervaki, G. E., Nikolaou, V., Misra, R., & Coutsolelos, A. G. (2015) · Organic Electronics · doi:10.1016/j.orgel.2015.06.048 · Cited by 53

Excited State Luminescence of Multi-(5-phenyl-1,3,4-oxadiazo-2-yl)benzenes in an Electron-Donating Matrix: Exciplex or Electroplex?

Yang, C.-C., Hsu, C., Chou, P., Cheng, H. C., Su, Y. O., & Leung, M. (2009) · The Journal of Physical Chemistry B · doi:10.1021/jp9093063 · Cited by 50

Recent progress in organic hole transport materials for energy applications

Nhari, L. M., El‐Shishtawy, R. M., & Asiri, A. M. (2021) · Dyes and Pigments · doi:10.1016/j.dyepig.2021.109465 · Cited by 49

A Propeller‐Shaped, Triazine‐Linked Porphyrin Triad as Efficient Sensitizer for Dye‐Sensitized Solar Cells

Zervaki, G. E., Papastamatakis, E., Angaridis, P. A., Nikolaou, V., Singh, M., Kurchania, R., Kitsopoulos, T. N., Sharma, G. D., & Coutsolelos, A. G. (2014) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.201301278 · Cited by 47

Synthesis and photovoltaic performances of donor–π–acceptor dyes utilizing 1,3,5-triazine as π spacers

Liu, J., Wang, K., Xu, F. Y., Tang, Z., Zheng, W., Zhang, J., Li, C., Yu, T., & You, X. (2011) · Tetrahedron Letters · doi:10.1016/j.tetlet.2011.09.116 · Cited by 47

“Scorpion”-shaped mono(carboxy)porphyrin-(BODIPY) 2 , a novel triazine bridged triad: synthesis, characterization and dye sensitized solar cell (DSSC) applications

Zervaki, G. E., Agapi, N., Nikolaou, V., Sharma, G. D., & Coutsolelos, A. G. (2015) · Journal of Materials Chemistry C · doi:10.1039/c4tc02902j · Cited by 46

Triazine‐containing benzoxazine and its high‐performance polymer

Wang, D., Li, B., Zhang, Y., & Lu, Z. (2012) · Journal of Applied Polymer Science · doi:10.1002/app.37816 · Cited by 43

Star-shaped D-π-A compounds with a 1,3,5-triazine core and N-aryl chromophore substituted fluorene arms: Synthesis, aggregation induced emission and two-photon absorption

Liu, R., Shu, M., Hu, J., Zhu, S., Shi, H., & Zhu, H. (2016) · Dyes and Pigments · doi:10.1016/j.dyepig.2016.10.015 · Cited by 43

Effect of trace hydrofluoric acid in a LiPF 6 electrolyte on the performance of a Li–organic battery with an N-heterocycle based conjugated microporous polymer as the cathode

Chen, Z., Xu, N., Li, W., Zhao, R., Dong, Y., Liu, J., Su, C., Wang, J., & Zhang, C. (2019) · Journal of Materials Chemistry A · doi:10.1039/c9ta01810g · Cited by 43

1, 3, 5-Triazine-cored derivatives dyes containing triphenylamine based two-photon absorption: Synthesis, optical characterization and bioimaging

Zhou, H., Zheng, Z., Xu, G.-Y., Yu, Z., Yang, X., Cheng, L., Tian, X., Kong, L., Wu, J., & Tian, Y. (2012) · Dyes and Pigments · doi:10.1016/j.dyepig.2012.03.017 · Cited by 42

s-Triazine-based functional monomers with thermocrosslinkable propargyl units: Synthesis and conversion to the heat-resistant polymers

Zhou, J., Wang, J., Jin, K., Sun, J., & Fang, Q. (2016) · Polymer · doi:10.1016/j.polymer.2016.09.027 · Cited by 41

Synthesis, crystal structures, molecular docking and in vitro cytotoxicity studies of two new copper( ii ) complexes: special emphasis on their binding to HSA

Shen, F., Liu, Y., Li, S., Jiang, C.-K., Wang, B., Xiong, Y., Mao, Z., & Le, X. (2017) · New Journal of Chemistry · doi:10.1039/c7nj02351k · Cited by 40

Negishi coupling in the synthesis of advanced electronic, optical, electrochemical, and magnetic materials

Huo, S., Mroz, R., & Carroll, J. (2015) · Organic Chemistry Frontiers · doi:10.1039/c4qo00322e · Cited by 40

Functionalized 1,3,5-triazine derivatives as components for photo- and electroluminescent materials

Nosova, E. V., Lipunova, G. N., Zyryanov, G. V., Чарушин, В. Н., & Чупахин, О. Н. (2022) · Organic Chemistry Frontiers · doi:10.1039/d2qo00961g · Cited by 39

A mono(carboxy)porphyrin-triazine-(bodipy) 2 triad as a donor for bulk heterojunction organic solar cells

Sharma, G. D., Siddiqui, S. A., Nikiforou, A., Zervaki, G. E., Georgakaki, I., Ladomenou, K., & Coutsolelos, A. G. (2015) · Journal of Materials Chemistry C · doi:10.1039/c5tc01076d · Cited by 36

Triazine dyes as photosensitizers for dye-sensitized solar cells

Liu, J., Wang, K., Zhang, X., Li, C., & You, X. (2012) · Tetrahedron · doi:10.1016/j.tet.2012.10.046 · Cited by 34

Polymers with alkyl main chain pendent biphenyl carbazole or triphenylamine unit as host for polymer light emitting diodes

Chuang, C., Chuang, H.-J., Wang, Y.-X., Chen, S., Huang, J., Leung, M., & Hsieh, K.-H. (2012) · Polymer · doi:10.1016/j.polymer.2012.08.042 · Cited by 34

Synthesis, two-photon absorption properties and bioimaging applications of mono-, di- and hexa-branched pyrimidine derivatives

Wang, H., Zhang, Q., Zhang, J., Li, L., Zhang, Q., Li, S., Zhang, S., Wu, J., & Tian, Y. (2013) · Dyes and Pigments · doi:10.1016/j.dyepig.2013.11.013 · Cited by 31

Photosensitizing porphyrin–triazine compound for bulk heterojunction solar cells

Luechai, A., Gasiorowski, J., Petsom, A., Neugebauer, H., Sariciftci, N. S., & Thamyongkit, P. (2012) · Journal of Materials Chemistry · doi:10.1039/c2jm33840h · Cited by 30

Synthesis and photophysical properties of hyperbranched polyfluorenes containing 2,4,6-tris(thiophen-2-yl)-1,3,5-triazine as the core

Zou, L., Liu, Y., Ma, N., Maçôas, E., Martinho, J. M. G., Pettersson, M., Chen, X., & Qin, J. (2011) · Physical Chemistry Chemical Physics · doi:10.1039/c0cp03014g · Cited by 28

Preparation of 2-Magnesiated 1,3,5-Triazines via an Iodine−Magnesium Exchange

Peng, Z., Haag, B. A., & Knochel, P. (2010) · Organic Letters · doi:10.1021/ol102173z · Cited by 26

Dye-sensitized solar cells based on triazine-linked porphyrin dyads containing one or two carboxylic acid anchoring groups

Zervaki, G. E., Angaridis, P. A., Koukaras, E. Ν., Sharma, G. D., & Coutsolelos, A. G. (2014) · Inorganic Chemistry Frontiers · doi:10.1039/c3qi00095h · Cited by 25

Symmetrical and unsymmetrical multibranched D–π–A molecules based on 1,3,5-triazine unit: synthesis and photophysical properties

Zhang, L., Zou, L., Xiao, J., Zhou, P., Zhong, C., Chen, X., Qin, J., Mariz, I. F. A., & Maçôas, E. (2012) · Journal of Materials Chemistry · doi:10.1039/c2jm32323k · Cited by 25

High yielding microwave-assisted synthesis of tri-substituted 1,3,5-triazines using Pd-catalyzed aryl and heteroarylamination

Dao, P., Garbay, C., & Chen, H. (2012) · Tetrahedron · doi:10.1016/j.tet.2012.03.041 · Cited by 23

A General and Selective Copper‐Catalyzed Cross‐Coupling of Tertiary Grignard Reagents with Azacyclic Electrophiles

Hintermann, L., Li, X., & Labonne, A. (2008) · Angewandte Chemie · doi:10.1002/ange.200803312 · Cited by 19

An X-shaped solution-processible oligomer having an anthracene unit as a core: A new organic light-emitting material with high thermostability and efficiency

Sun, J., Zhong, H., Xu, E., Zeng, D., Zhang, J., Xu, H., Zhu, W., & Fang, Q. (2009) · Organic Electronics · doi:10.1016/j.orgel.2009.09.030 · Cited by 19

A triazine di(carboxy)porphyrin dyad versus a triazine di(carboxy)porphyrin triad for sensitizers in DSSCs

Zervaki, G. E., Tsaka, V., Vatikioti, A., Georgakaki, I. P., Nikolaou, V., Sharma, G. D., & Coutsolelos, A. G. (2015) · Dalton Transactions · doi:10.1039/c5dt01141h · Cited by 17

Abnormal effect of hydroxyl on the longest wavelength maximum in ultraviolet absorption spectra for bis-aryl Schiff bases

Cao, C., Zhou, W., & Cao, C. (2016) · Journal of Physical Organic Chemistry · doi:10.1002/poc.3672 · Cited by 16

Structure property relationship of linear and angular pyrazine-based structural isomers with terminal D-A groups and evaluation of their photophysical properties

Meti, P., Park, D.-J., & Gong, Y. (2019) · Dyes and Pigments · doi:10.1016/j.dyepig.2019.04.057 · Cited by 15

Synthesis and Intramolecular Hydrogen Bonding Networks of 2,4,6-Tri(o-hydroxyaryl)-1,3,5-Triazines

Conn, G., & Eisler, S. (2011) · Organic Letters · doi:10.1021/ol201946f · Cited by 15

Microwave-Assisted Selective Synthesis of Mono- and Bistriazines with π-Conjugated Spacers and Study of the Optoelectronic Properties

Ruiz‐Carretero, A., Noguez, O., Herrera, T., Ramírez, J. R., Sánchez‐Migallón, A., & de la Hoz, A. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo500480r · Cited by 14

New solution processed bulk-heterojunction organic solar cells based on a triazine-bridged porphyrin dyad as electron donor

Sharma, G. D., Zervaki, G. E., Angaridis, P., & Coutsolelos, A. G. (2014) · RSC Adv. · doi:10.1039/c4ra07770a · Cited by 13

Potassium Tert‐Butoxide‐Promoted Synthesis of Fluorescent β‐Carboline Tethered 1,3,5‐Triazines and Assessment of Their Luminescent Properties

Singh, M., Jamra, R., Mehra, S., Rattan, S., & Singh, V. (2021) · Asian Journal of Organic Chemistry · doi:10.1002/ajoc.202100281 · Cited by 13

Synthesis and two-photon absorption properties of multi-branched styryl derivatives containing π-bond and σ-electron pair as bridge based on 1,3,5-triazine

Zheng, Z., Zhou, H., Xu, G.-Y., Yu, Z., Yang, X., Cheng, L., Kong, L., Feng, Y., Wu, J., & Tian, Y. (2012) · Tetrahedron · doi:10.1016/j.tet.2012.05.050 · Cited by 13

Influence of the side-group at C=N bridging bond of bis-aryl Schiff bases on the wavelength of absorption maximum of ultraviolet absorption spectra

Luo, Q., Cao, C., Cao, Z., & Cao, C. (2016) · Journal of Physical Organic Chemistry · doi:10.1002/poc.3550 · Cited by 13

Synthesis, structure and magnetism of homodinuclear complexes of Co, Ni and Cu supported by a novel bitriazine scaffold

Reid, D. J., Cull, J. E. W., Chisholm, K. D. S., Langlois, A., Lin, P., Long, J., Lebel, O., Korobkov, I., Wang, R., Wuest, J. D., et al. (2011) · Dalton Transactions · doi:10.1039/c1dt00018g · Cited by 12

Efficient blue emitters based on 1,3,5-triazine for nondoped organic light emitting diode applications

Liu, J., Teng, M., Zhang, X.-P., Wang, K., Li, C., Zheng, Y., & You, X. (2012) · Organic Electronics · doi:10.1016/j.orgel.2012.06.013 · Cited by 11

Preparation and characterization of bis‐[1,3,5]triazinyl diazenes and their utilization as flame retardants in polypropylene films

Tirri, T., Aubert, M., Pawelec, W., Wilén, C., Pfaendner, R., Hoppe, H., Roth, M. R., & Sinkkonen, J. (2014) · Journal of Applied Polymer Science · doi:10.1002/app.40413 · Cited by 11

Synthesis and properties of solution-processible oligomers for the use of organic light-emitting diodes (OLEDs)

Sun, J., Lai, H., Zhong, H., & Fang, Q. (2011) · Thin Solid Films · doi:10.1016/j.tsf.2011.06.019 · Cited by 11

Efficient Hole-Blocker with Electron Transporting Property and Its Applications in Blue Organic Light-Emitting Devices

Tao, S., Lai, S., Yu, J., Jiang, Y., Zhou, Y., Lee, C., Zhang, X., & Lee, S. (2009) · The Journal of Physical Chemistry C · doi:10.1021/jp903330z · Cited by 10

Metal-catalyzed synthesis of triazine derivatives

Jain, S., Kumawat, J., Jain, P., Shruti, Malik, P., Dwivedi, J., & Kishore, D. (2022) · Monatshefte für Chemie - Chemical Monthly · doi:10.1007/s00706-022-02948-2 · Cited by 9

Triazine‐Triazole Conjugates as Potent Ligands for Cu–Catalyzed Sonogashira Reaction

Wang, Z., Wang, X., Sun, H., Zhu, Z., Zhang, G., Zhang, W., & Gao, Z. (2016) · ChemistrySelect · doi:10.1002/slct.201600113 · Cited by 9

Copper-catalyzed Facile Synthesis of Unsymmetrical Triazine–Triazole Conjugates

Wang, Z., Wang, X., Zhang, G., Zhang, W., & Gao, Z. (2015) · Chemistry Letters · doi:10.1246/cl.150569 · Cited by 8

Modulation of singlet and triplet excited states through σ spacers in ternary 1,3,5-triazines

An, Z., Wu, Q., Xiao, J., Chen, R., Yin, J. L., Shi, H., Tao, Y., Wang, Y., Wang, Z., Li, H., et al. (2013) · RSC Advances · doi:10.1039/c3ra41888j · Cited by 8

The synthesis and characterization of s-Triazine polymer complexes containing epoxy groups

Karakaya, N. O., & Uysal, Ş. (2019) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2019.127370 · Cited by 8

Linear and V‐Shaped Alkynyl‐1,3,5‐triazines

Gao, P., Wang, Z., Wang, X., Zhang, W., & Gao, Z. (2015) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201500948 · Cited by 7

Synthesis and Characterizations of s-Triazine Polymeric Complexes Including Epoxy Groups: Investigation of Their Magnetic and Thermal Properties

Tekin, O., & Uysal, Ş. (2019) · Journal of Inorganic and Organometallic Polymers and Materials · doi:10.1007/s10904-019-01132-0 · Cited by 6

Synthesis and Properties of the Derivatives of 2,4,6-Tris(Phenoxy)-1,3,5-Triazine

Dainyte, A., Gudeika, D., Buika, G., & Gražulevičius, J. V. (2014) · Molecular Crystals and Liquid Crystals · doi:10.1080/15421406.2013.873850 · Cited by 5

Chapter 6.3 (2008): Triazines, Tetrazines and Fused Ring Polyaza Systems

Kozhevnikov, D. N., & Kozhevnikov, V. N. (2009) · Progress in heterocyclic chemistry · doi:10.1016/s0959-6380(09)70042-x · Cited by 4

Synthesis and spectroscopic properties of propeller type 2,4,6-tri(anthracen-9-yl)-1,3,5-triazine

Xu, L., Wang, P., Zhang, J., Wu, W., Shi, J., Yuan, J.-F., Han, H., & Wang, H. (2015) · RSC Advances · doi:10.1039/c5ra08833j · Cited by 4

Panchromatic Absorption of Unsymmetrical Donor‐Acceptor Dyes Based on a Meta‐Conjugated 1,3,5‐Heteroaryltriazine Core

Rothera, J. G., Taing, H., Cruz, M. V., Dmitrienko, A. S., Vukotic, V. N., Ryno, S. M., Risko, C. M., Raj, A. M., Skene, W. G., & Eichhorn, S. H. (2025) · Chemistry - A European Journal · doi:10.1002/chem.202403860 · Cited by 1

9-{4-[(E)-2-(4,6-Dimethyl-1,3,5-triazin-2-yl)ethenyl]phenyl}-9H-carbazole

Liu, C., Xue, G., Cui, Y., Li, T., & Ng, S. W. (2009) · Acta Crystallographica Section E Structure Reports Online · doi:10.1107/s1600536809030359 · Cited by 1

Triazine Dendrimers for DNA and siRNA Delivery: Progress, Challenges, and Opportunities

Mintzer, M. A., Merkel, O. M., Kissel, T., & Simanek, E. E. (2012) · Wiley eBooks · doi:10.1002/9781118275238.ch10 · Cited by 1

Synthesis of unsymmetrical trisubstituted 1,3,5-triazines compounds

Zhao, J., Chen, Y., Wang, X., Yang, W., Zhang, A., Qu, Z., Fu, H., & Ma, M. (2024) · Tetrahedron · doi:10.1016/j.tet.2024.134009 · Cited by 1

New Usage for Cyclotrimerization Reaction: A Facile Synthesis of 1,3,5-Triazine Derivatives

Ouyang, M., Yu, C. H., Zhang, N. Y., Song, Q. B., Sun, J. W., Hu, B., & Zhang, C. (2012) · Key engineering materials · doi:10.4028/www.scientific.net/kem.531-532.32

17.2.3.6 1,3,5-Triazines and Phosphorus Analogues (Update 2012)

Aggarwal, P., & Bebbington, M. W. P. (2012) · Haug Verlag in Georg Thieme Verlag KG eBooks · doi:10.1055/sos-sd-117-00295

Design, Synthesis and Study of Non-Linear Optical Properties of Phenyl Bridged Diphenylamine-s-triazine Based Donor-Acceptor Triads Containing Different π-Acceptor Groups

Suma, C. S., Dhanya, N. P., & Seena, S. (2021) · Asian Journal of Chemistry · doi:10.14233/ajchem.2021.23311

Triazatruxene-based materials for organic electronics and optoelectronics

Li, X., Wang, C., Lai, W., & Huang, W. (2016) · Journal of Materials Chemistry C · doi:10.1039/c6tc03832h · Cited by 99

One-Pot Synthesis of 4,8-Dibromobenzo[1,2-d;4,5-d′]bistriazole and Synthesis of its Derivatives as New Units for Conjugated Materials

Tam, T. L. D., Tan, H. H. R., Ye, W., Mhaisalkar, S. G., & Grimsdale, A. C. (2011) · Organic Letters · doi:10.1021/ol2031558 · Cited by 15

Synthesis of N+ -doped triphenylene derivatives by electrochemical intramolecular pyridination and their optoelectronic properties

大野, 雄., Ono, Y., 安藤, 匠., Ando, S., 古性, 大., Furusho, D., 一二三, 遼., Hifumi, R., 冨田, 育., Tomita, I., et al. (2024) · Institutional Repositories DataBase (IRDB)

Microwave-Assisted Selective Synthesis of Mono- and Bistriazines with π-Conjugated Spacers and Study of the Optoelectronic Properties

Ruiz‐Carretero, A., Noguez, O., Herrera, T., Ramírez, J. R., Sánchez‐Migallón, A., & de la Hoz, A. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo500480r · Cited by 14

Synthesis, characterization and optoelectronic investigations of bithiophene substituted 1,3,4-oxadiazole derivatives as green fluorescent materials

Deshapande, N., Belavagi, N. S., Sunagar, M. G., Gaonkar, S., Pujar, G. H., Wari, M. N., Inamdar, S. R., & Khazi, I. A. M. (2015) · RSC Advances · doi:10.1039/c5ra14550c · Cited by 40