New monomers for (bi)pyridine-containing polymers
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Li ZR, editor. Organic Light-Emitting Materials and Devices. Boca Raton: CRC Press, 2015. 813 p.
Wang C, Kilitziraki M, MacBride JAH, Bryce MR., Horsburgh LE, Sheridan AK, Monkman AP, Samuel IDW. Tuning the optoelectronic properties of pyridine-containing polymers for light-emitting devices. Adv Mater. 2000;12:217–22. doi:10.1002/(SICI)1521-4095(200002)12:3<217::AID-ADMA217>3.0.CO;2-Y
Sato Y, Kagotani M, Yamamoto T, Souma Y. Novel Effective Poly(2,2′-Bipyridine-5,5′-Diyl)-CuCl2 Catalyst for Synthesis of Dimethyl Carbonate (DMC) by Oxidative Carbonylation of Methanol. Appl Catal A-Gen. 1999;185:219–26. doi:10.1016/S0926-860X(99)00175-1
Xiao L, Zhang H, Jana T, Scanlon E, Chen R, Choe E-W, Ramanathan LS, Yu S, Denicewicz BC. Synthesis and characterization of pyridine-based polybenzimidazoles for high temperature polymer electrolyte membrane fuel cell applicationsx. Fuel cells. 2005;5:287–95. doi:10.1002/fuce.200400067
Yang L, Mihali V-A, Brandell D, Strømme M, Sjödin M. Conjugated Pyridine-Based Poly-mers Characterized as Conductivity Carrying Components in Anode Materials. J Phys Chem C. 2014;118:25956–63. doi:10.1021/jp509606c
Kozhevnikov VN, Kozhevnikov DN, Shabunina OV, Rusinov VL, Chupakhin ON. An effi-cient route to 5-(hetero)aryl-2,4′- and 2,2′-bipyridines through readily available 3-pyridyl-1,2,4-triazines. Tetrahedron Lett. 2005;46:1791–3. doi:10.1016/j.tetlet.2005.01.135
Pabst GR, Sauer J. A new and simple 'LEGO' system for the synthesis of 2,6-oligopyridines. Tetrahedron Lett. 1998;39:6687–90. doi:10.1016/S0040-4039(98)01437-3
Rykowski A, Branowska D, Kielak J. A novel one-pot synthesis of annulated 2,2′-bipyridine ligands by inverse electron demand Diels–Alder reaction of 5,5′-bi-1,2,4-triazines. Tetrahedron Lett. 2000;41:3657–9. doi:10.1016/S0040-4039(00)00436-6
Kozhevnikov VN, Shabunina OV, Kopchuk DS, Ustinova MM, König B, Kozhevnikov DN. Facile synthesis of 6-aryl-3-pyridyl-1,2,4-triazines as a key step toward highly fluorescent 5-substituted bipyridines and their Zn(II) and Ru(II) complexes. Tetrahedron. 2008;64:8963–73. doi:10.1016/j.tet.2008.06.040
Starnovskaya ES, Kopchuk DS, Khasanov AF, Tanya OS, Santra S, Giri K, Rahman M, Ko-valev IS, Zyryanov GV, Majeed A, Charushin VN. Synthesis and photophysics of new unsym-metrically substituted 5,5′-diaryl-2,2′-bypiridine-based “push-pull” fluorophores. Dyes Pigm. 2019;162:324–30. doi:10.1016/j.dyepig.2018.10.040
Kopchuk DS, Chepchugov NV, Starnovskaya ES, Khasanov AF, Krinochkin AP, Santra S, Zyryanov GV, Das P, Majee A, Rusinov VL, Charushin VN. Synthesis and optical properties of new 2-(5-arylpyridine-2-yl)-6-(het)arylquinoline-based “push-pull” fluorophores. Dyes Pigm. 2019;167:151–6. doi 10.1016/j.dyepig.2019.04.029
Kozhevnikov VN, Ustinova MM, Slepukhin PA, Santoro A, Bruce DW, Kozhevnikov DN. From 1,2,4-triazines towards substituted pyridines and their cyclometallated Pt complexes. Tet-rahedron Lett. 2008;49:4096–8. doi:10.1016/j.tetlet.2008.04.138
Saraswathi TV, Srinivasan VR. A novel synthesis of 1,2,4-triazines. Tetrahedron Lett. 1971;12:2315–6. doi:10.1016/S0040-4039(01)96849-2
Saraswathi TV, Srinivasan VR. Syntheses and spectral characteristics of 6-mono-, 3,6-di and 3,5,6-trisubstituted-1,2,4-triazines. Tetrahedron. 1977;33:1043–51. doi:10.1016/0040-4020(77)80223-8
Shtaitz YaK, Savchuk MI, Kopchuk DS, Taniya OS, Santra S, Zyryanov GV, Suvorova AI, Rusinov VL, Chupakhin ON. Efficient Synthesis of Methyl 6-(6-Aryl-1,2,4-triazin-3-yl)pyridine-2-carboxylates. Russ J Org Chem. 2020;56:548–51. doi:10.1134/S1070428020030306
Khan MS, Al-Mandhary MRA, Al-Suti MK. Feeder N, Nahar S, Koehler A, Friend RH, Wil-son PJ, Raithby PR. Synthesis, characterisation and electronic properties of a series of plati-num(II) poly-ynes containing novel thienyl-pyridine linker groups. Dalton Trans. 2002;12:2441–8. doi:10.1039/B201073A
Hu B, Fu S-J, Xu F, Tao T, Zhu H-Y, Cao K-S, Huang W, You X-Z. Linear heterocyclic ar-omatic fluorescence compounds having various donor-acceptor spacers prepared by the combi-nation of carbon-carbon bond and carbon-nitrogen bond cross-coupling reactions. J Org Chem. 2011;76:4444–56. doi:10.1021/jo200065d
DOI: https://doi.org/10.15826/chimtech.2020.7.4.13
Copyright (c) 2020 Krinochkin A.P., Savchuk M.I., Starnovskaya E.S., Shtaitz Y.K., Kopchuk D.S., Nikonov I.L., Kovalev I.S., Zyryanov G.V., Rusinov V.L., Chupakhin O.N.
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