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Journal articles on the topic '1-Vinylimidazole'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Kurdziel, Krystyna, and Tadeusz Glowiak. "Palladium(II) Complexes of 1-vinylimidazole." Journal of Coordination Chemistry 55, no. 3 (2002): 327–34. http://dx.doi.org/10.1080/00958970211890.

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2

Gusarova, N. K., S. I. Verkhoturova, S. N. Arbuzova, T. I. Kazantseva, and B. A. Trofimov. "Nucleophilic addition of phosphine to 1-vinylimidazole." Russian Journal of General Chemistry 81, no. 12 (2011): 2522–24. http://dx.doi.org/10.1134/s107036321112019x.

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3

Danilovtseva, Elena N., Stanislav N. Zelinskiy, Viktor A. Pal’shin, Gayathri Kandasamy, Uma Maheswari Krishnan, and Vadim V. Annenkov. "Poly(1-vinylimidazole) Prospects in Gene Delivery." Chinese Journal of Polymer Science 37, no. 7 (2019): 637–45. http://dx.doi.org/10.1007/s10118-019-2240-1.

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4

Litvincev, Yuriy. "DIRECT PHOSPHORILATION OF 1-VINYLIMIDAZOLE WITH RED PHOSPHO-RUS." Scientific Papers Collection of the Angarsk State Technical University 2021, no. 1 (2021): 51–57. http://dx.doi.org/10.36629/2686-7788-2021-1-1-51-57.

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5

Levchenkova, Olga S., Vasiliy E. Novikov, and Konstantin N. Kulagin. "Combined preconditioning with tetra-(1-vinylimidazole) cobalt dichloride." Reviews on Clinical Pharmacology and Drug Therapy 15, no. 1 (2017): 26–32. http://dx.doi.org/10.17816/rcf15126-32.

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The aim of this study was to investigate the vinylimidazole derivative as pharmacological preconditioning in experimental acute hypoxia and cerebral ischemia. All experiments were conducted with mice and rats. Acute hypoxia with hypercapnia was modeled by placing the mice in a glass with a glass lid shtanglazy 250 ml. Acute hypobaric hypoxia was performed putting animals under a glass cope, where from the Kamovsky pump pumped up the air which is equal to the altitude of 5000 meters (moderate hypoxia) and 11 000 meters (severe hypoxia). Cerebral ischemia in rats was modeled by one-stage bilater

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6

Ivanova, A. A., A. I. Emel’yanov, S. A. Korzhova, and A. S. Pozdnyakov. "Study of metal-polymer copper nanocomposites using the method of UV spectroscopy." Proceedings of Universities. Applied Chemistry and Biotechnology 11, no. 1 (2021): 165–70. http://dx.doi.org/10.21285/2227-2925-2021-11-1-165-170.

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New polymer copper-containing nanocomposites based on poly-N-vinylimidazole were obtained. The formation of nanocomposites was carried out using the method of chemical reduction of copper ions from a solution of copper acetate with ascorbic acid in an aqueous medium in the presence of a polymer. Nanocomposites were prepared at the polymer:Cu (II) molar ratio of 10:1 and 5:1. The reduction reaction yielded powder nanocomposites of a red-brown colour and having a metallic shine. It was found that the content of copper in the obtained nanocomposites depends on the initial molar ratio of the stabi

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7

Samdal, Svein, and Harald Møllendal. "Microwave Spectrum and Conformational Composition of 1-Vinylimidazole." Journal of Physical Chemistry A 115, no. 26 (2011): 7559–65. http://dx.doi.org/10.1021/jp202319q.

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8

Hamilton, Jackie R., Asghar Abedini, Zhongtao Zhang, John W. Whitley, Jason E. Bara, and C. Heath Turner. "Enhancing the pre-polymerization coordination of 1-vinylimidazole." Chemical Engineering Science 138 (December 2015): 646–54. http://dx.doi.org/10.1016/j.ces.2015.08.045.

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9

Genç, Feyza, Cengiz Uzun, and Olgun Güven. "Quaternized poly(1-vinylimidazole) hydrogel for anion adsorption." Polymer Bulletin 73, no. 1 (2015): 179–90. http://dx.doi.org/10.1007/s00289-015-1479-0.

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10

Annenkov, V. V., E. N. Danilovtseva, E. A. Filina, and Y. V. Likhoshway. "Interaction of silicic acid with poly(1-vinylimidazole)." Journal of Polymer Science Part A: Polymer Chemistry 44, no. 2 (2005): 820–27. http://dx.doi.org/10.1002/pola.21190.

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11

Schiavone, R. J., and C. G. Overberger. "Reactions and polymerization of 1-trityl-4-vinylimidazole." Journal of Polymer Science Part A: Polymer Chemistry 26, no. 1 (1988): 107–15. http://dx.doi.org/10.1002/pola.1988.080260111.

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12

Nikolayenko, V. V., A. V. Nekrasov, V. V. Smolyaninov, and G. A. Bodun. "Copolymerization of 1-N-vinyl-1,2,4-triazole with 1-N-vinylimidazole." Polymer Science U.S.S.R. 31, no. 4 (1989): 861–67. http://dx.doi.org/10.1016/0032-3950(89)90125-1.

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13

Voronov, Vladimir K., Igor A. Ushakov, and Evgenia A. Funtikova. "NMR Spectra of 1-Vinylimidazole, Transformed by Paramagnetic Complexes." Applied Magnetic Resonance 50, no. 4 (2018): 569–77. http://dx.doi.org/10.1007/s00723-018-1076-0.

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14

Baikalova, L. V., V. I. Sokol, V. N. Khrustalev, E. A. Zel'bst, and B. A. Trofimov. "Crystal and Molecular Structure of Bis(1-Vinylimidazole)diacetatozinc." Russian Journal of General Chemistry 75, no. 9 (2005): 1469–74. http://dx.doi.org/10.1007/s11176-005-0448-y.

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15

Schmidt, Christian, and Gudrun Schmidt-Naake. "Grafting of 1-Vinylimidazole onto Pre-Irradiated ETFE Films." Macromolecular Materials and Engineering 292, no. 10-11 (2007): 1067–74. http://dx.doi.org/10.1002/mame.200700189.

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16

Goh, S. H., S. Y. Lee, and I. K. Tan. "Miscibility of poly(1-vinylimidazole)/ poly(p-vinylphenol) blends." Polymer Bulletin 37, no. 2 (1996): 253–57. http://dx.doi.org/10.1007/bf00294129.

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17

Chi, Hui, Pei Chen, Liqin Cao, Xiujuan Wu, and Jide Wang. "Characterization and adsorptive properties of cross-linked poly (1-vinylimidazole)-iron (III) complex synthesized in supercritical carbon dioxide." e-Polymers 16, no. 5 (2016): 403–10. http://dx.doi.org/10.1515/epoly-2016-0096.

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AbstractIn this study, poly (1-vinylimidazole)-iron(III) [PVIm-Fe(III)] complex was investigated along with adsorption behavior of bovine serum albumin (BSA). The cross-linked PVIm-Fe(III) was synthesized in supercritical carbon dioxide by using N,N′-methylenebisacrylamide (BIS) as a cross-linker. The obtained products were analyzed using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and X-ray photoelectron spectra (XPS) analysis. The results reveal that iron ion is complexed by coordination with basic (-N) functional groups of 1-vinylimidazole successfully. The effec

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18

Bren, Vladimir A., Ivan E. Tolpygin, Yurii V. Revinskii, Karina S. Tikhomirova, Alexander D. Dubonosov, and Vladimir I. Minkin. "Synthesis and properties of polymer chemosensors based on 1-vinylimidazole." Arkivoc 2018, no. 7 (2018): 28–38. http://dx.doi.org/10.24820/ark.5550190.p010.625.

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19

Zhao, Juan. "Bis(2-chlorobenzoato-κO)bis(1-vinylimidazole-κN3)copper(II)". Acta Crystallographica Section E Structure Reports Online 64, № 10 (2008): m1321. http://dx.doi.org/10.1107/s1600536808030237.

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20

Tekin, Nalan, A. Uğur Kaya, Kadir Esmer, and Ali Kara. "Adsorption and dielectric properties of poly(1-vinylimidazole) on sepiolite." Applied Clay Science 57 (March 2012): 32–38. http://dx.doi.org/10.1016/j.clay.2011.12.007.

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21

Chapiro, Adolphe. "Peculiar aspects of the free-radical polymerization of 1-vinylimidazole." International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry 40, no. 2 (1992): 89–93. http://dx.doi.org/10.1016/1359-0197(92)90063-l.

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22

Vasnin, S. V., J. Cetrullo, R. A. Geanangel, and I. Bernal. "Adducts of 1-vinylimidazole, 1-benzylimidazole, and 1,2,4-triazole with tin(II) chloride." Inorganic Chemistry 29, no. 4 (1990): 885–88. http://dx.doi.org/10.1021/ic00329a064.

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23

Kuznetsova, E. G., O. M. Kuryleva, L. A. Salomatina, et al. "On the possibility of therapeutic action after transdermal patch application." Russian Journal of Transplantology and Artificial Organs 24, no. 2 (2022): 119–24. http://dx.doi.org/10.15825/1995-1191-2022-2-119-124.

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Background. As scientific knowledge about the peculiarities of the structure and functional properties of the skin increased, it became clearer that during transdermal administration, drug may accumulate in the deep layers of the dermis and subsequently get diffused into the bloodstream even after the transdermal therapeutic system (TTS), also called transdermal patch, had been removed. Objective: to quantify active drug substances remaining in an animal skin after TTS application. Materials and methods. Two previously developed transdermal patches containing Russian-made drug substances were

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24

Sanchis-Perucho, Adrián, and José Martínez-Lillo. "Ferromagnetic exchange interaction in a new Ir(iv)–Cu(ii) chain based on the hexachloroiridate(iv) anion." Dalton Transactions 48, no. 37 (2019): 13925–30. http://dx.doi.org/10.1039/c9dt02884f.

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The new chloro-bridged heterobimetallic Ir<sup>IV</sup>Cu<sup>II</sup> chain of formula {IrCl<sub>5</sub>(μ-Cl)Cu(viim)<sub>4</sub>}<sub>n</sub> [viim = 1-vinylimidazole] is the first reported compound based on the Cu<sup>II</sup> and Ir<sup>IV</sup> metal ions.

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25

NAN, Alexandrina, and Rodica TURCU. "Poly(1-vinylimidazole) grafted on magnetic nanoparticles - attainment of novel nanostructures." Revue Roumaine de Chimie 65, no. 6 (2020): 611–16. http://dx.doi.org/10.33224/rrch.2020.65.6.12.

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26

Sargsyan, S. H., T. S. Sargsyan, K. M. Khizantsyan, I. G. Aghajanyan, A. S. Sargsyan, and K. S. Margaryan. "Electrosynthesis of 1-Vinylimidazole- and Acrylic-Acid-Based Metal-Containing Nanocomposites." Russian Journal of Electrochemistry 56, no. 1 (2020): 87–91. http://dx.doi.org/10.1134/s1023193520010073.

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27

Lingappan, Niranjanmurthi, Do Hoon Kim, Jong Myung Park, and Kwon Taek Lim. "Water Soluble Graphene Oxide/Poly(1-vinylimidazole) Composites: Synthesis and Characterization." Journal of Nanoscience and Nanotechnology 14, no. 8 (2014): 5713–17. http://dx.doi.org/10.1166/jnn.2014.8823.

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28

Voronov, V. K., I. A. Ushakov, and A. S. Dambinova. "Peculiarities of molecular structure of 1-vinylimidazole: High resolution NMR study." Journal of Molecular Structure 1048 (September 2013): 210–13. http://dx.doi.org/10.1016/j.molstruc.2013.04.075.

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29

Bay, R. F. C., S. P. Armes, C. J. Pickett, and K. S. Ryder. "Poly(1-vinylimidazole-co-4-aminostyrene): steric stabilizer for polyaniline colloids." Polymer 32, no. 13 (1991): 2456–60. http://dx.doi.org/10.1016/0032-3861(91)90089-2.

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30

Asayama, Shoichiro, Kozo Seno, and Hiroyoshi Kawakami. "Synthesis of Carboxymethyl Poly(1-vinylimidazole) as a Polyampholyte for Biocompatibility." Chemistry Letters 42, no. 4 (2013): 358–60. http://dx.doi.org/10.1246/cl.121263.

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31

Jiao, Hua, S. H. Goh, and S. Valiyaveettil. "Surfactant-Induced Mesomorphic Structures in Poly(1-vinylimidazole)−Alkanoic Acid Complexes." Langmuir 18, no. 4 (2002): 1368–73. http://dx.doi.org/10.1021/la011001n.

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32

Belyayeva, V. V., A. I. Skushnikova, A. L. Pavlova, Ye S. Domnina, and E. I. Brodskaya. "Spectroscopic study of complex formation between 1-vinylimidazole and acrylic acid." Polymer Science U.S.S.R. 31, no. 9 (1989): 2188–94. http://dx.doi.org/10.1016/0032-3950(89)90445-0.

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33

Danilovtseva, Elena N., Mikhail A. Chafeev, and Vadim V. Annenkov. "New polyelectrolytes based on 4-vinyl-1,2,3-triazole and 1-vinylimidazole." Journal of Polymer Science Part A: Polymer Chemistry 50, no. 8 (2012): 1539–46. http://dx.doi.org/10.1002/pola.25921.

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34

Tager, A. A., A. P. Safronov, V. A. Lopyrev, T. G. Yermakova, L. A. Tatarova, and T. N. Kashik. "Thermodynamics of aqueous solutions of poly-1-vinylimidazole and poly-1-vinyl-1,2,4-triazole." Polymer Science U.S.S.R. 29, no. 11 (1987): 2666–71. http://dx.doi.org/10.1016/0032-3950(87)90246-2.

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35

Schäffner, Friederike, Marco Drache, and Gudrun Schmidt-Naake. "Copolymerization of 2-Acrylamido-2-methyl-1-propanesulfonic Acid and 1-Vinylimidazole in Ethanol." Macromolecular Materials and Engineering 296, no. 6 (2011): 535–43. http://dx.doi.org/10.1002/mame.201000340.

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36

Li, Gui Zhen, Jun Bo Li, Chen Han, et al. "Complexs of Poly(1-vinylimidazole-co-methyl methacrylate) and Copper Ion as Catalysts for the Oxidation of Ethylbenzene." Advanced Materials Research 393-395 (November 2011): 1143–48. http://dx.doi.org/10.4028/www.scientific.net/amr.393-395.1143.

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This paper was reported a polymeric support metal catalyst and its application in oxidation of ethylbenzene with molecular oxygen. The Poly(1-vinylimidazole-co-methyl methacrylate) copolymer (PVM) was directly mixed with copper sulfate solution to prepare the catalyst of Cu(II)-PVM. The appropriate reaction temperature and amount of catalyst were 130°C and 0.2g. Recycling studies indicated that the catalyst could be recycled at least four times without significant decrease of catalytic activity.

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37

Gonsior, Nina, Fabian Mohr, and Helmut Ritter. "Synthesis of mesomeric betaine compounds with imidazolium-enolate structure." Beilstein Journal of Organic Chemistry 8 (March 13, 2012): 390–97. http://dx.doi.org/10.3762/bjoc.8.42.

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The synthesis of a heterocyclic mesomeric betaine by quaternization reaction of 1-butylimidazole and tetrabromo-1,4-benzoquinone is presented. The structure was verified by means of X-ray single-crystal analysis, NMR and IR spectroscopy. Inclusion complexes of the heterocyclic mesomeric betaine with randomly methylated (1.8) β-cyclodextrin were investigated by UV–vis spectroscopy. Furthermore, the reaction conditions were applied to poly(vinylimidazole) and 1,4-bis(1H-imidazol-1-yl)butane to obtain functionalized polymer networks and condensate polymers, respectively.

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38

Racovita, Stefania, Nicolae Baranov, Ana Maria Macsim, et al. "New Grafted Copolymers Carrying Betaine Units Based on Gellan and N-Vinylimidazole as Precursors for Design of Drug Delivery Systems." Molecules 25, no. 22 (2020): 5451. http://dx.doi.org/10.3390/molecules25225451.

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New grafted copolymers possessing structural units of 1-vinyl-3-(1-carboxymethyl) imidazolium betaine were obtained by graft copolymerization of N-vinylimidazole onto gellan gum followed by the polymer-analogous reactions on grafted polymer with the highest grafting percentage using sodium chloroacetate as the betainization agent. The grafted copolymers were prepared using ammonium persulfate/N,N,N′,N′ tetramethylethylenediamine in a nitrogen atmosphere. The grafting reaction conditions were optimized by changing one of the following reaction parameters: initiator concentration, monomer concen

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39

Fouzia Chang, Fouzia Chang, Najma Memon Najma Memon, Shahabuddin Memon Shahabuddin Memon, Ayaz Ali Memon Ayaz Ali Memon, Saddam Hussain Bughio Saddam Hussain Bughio, and Muhammad Nawaz Tahir and Abdul Sattar Chang Muhammad Nawaz Tahir and Abdul Sattar Chang. "Self-Assembled Synthesis and Characterization of Novel [Co(1-vinylimidazole)6].NO3 Polymer: Highly Efficient Antimicrobial Agent." Journal of the chemical society of pakistan 43, no. 6 (2021): 706. http://dx.doi.org/10.52568/000973/jcsp/43.06.2021.

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Cobalt coordination polymer i.e. [Co(1-VI)6]and#183;NO3 was successfully synthesized with cobalt metal and (VI = vinylimidazole) and characterized by elemental analysis, FTIR, UV/Vis spectroscopy and X-ray crystallography. The structure of the compound was determined by single X-ray crystallography at temperature 296 K with a Bruker APEX II CCD diffractometer using Mo-Kα radiations (λ = 0.71073 and#197;), R = 0.0642 and 0.0989. Orthorhombic unit cell parameters are a = 16.1341 (6) and#197;, b = 16.5179(16) and#197;, c = 18.2664(16) and#197;, V= 4868.0 (8) and#197;, Dx = 4, Mr = 937.91. The X-r

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40

Stumphauser, Tímea, György Kasza, Attila Domján, et al. "Nanoconfined Crosslinked Poly(ionic liquid)s with Unprecedented Selective Swelling Properties Obtained by Alkylation in Nanophase-Separated Poly(1-vinylimidazole)-l-poly(tetrahydrofuran) Conetworks." Polymers 12, no. 10 (2020): 2292. http://dx.doi.org/10.3390/polym12102292.

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Despite the great interest in nanoconfined materials nowadays, nanocompartmentalized poly(ionic liquid)s (PILs) have been rarely investigated so far. Herein, we report on the successful alkylation of poly(1-vinylimidazole) with methyl iodide in bicontinuous nanophasic poly(1-vinylimidazole)-l-poly(tetrahydrofuran) (PVIm-l-PTHF) amphiphilic conetworks (APCNs) to obtain nanoconfined methylated PVImMe-l-PTHF poly(ionic liquid) conetworks (PIL-CNs). A high extent of alkylation (~95%) was achieved via a simple alkylation process with MeI at room temperature. This does not destroy the bicontinuous n

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41

Şen, Fatih, Ramazan Şahin, Ömer Andaç та Murat Taş. "trans-Bis(nitrato-κO)tetrakis(1-vinyl-1H-imidazole-κN3)copper(II)". Acta Crystallographica Section E Structure Reports Online 68, № 8 (2012): m1045. http://dx.doi.org/10.1107/s1600536812030607.

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In the title compound, [Cu(NO3)2(C5H6N2)4], the CuIIion is located on an inversion centre. It features a Jahn–Teller-distorted octahedral coordination geometry, defined by four N atoms of four 1-vinylimidazole ligands in the equatorial plane and two nitrate O atoms in the axial positions. The nitrate anion is disordered over two sets of sites in a 0.801 (6):0.199 (6) ratio. In the crystal, the complex molecules are linked by weak intermolecular C—H...O and C—H...π interactions.

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42

Margaryan, K. S., S. H. Sargsyan, and A. S. Sargsyan. "Electrosynthesis of metal-containing polymeric coatings based on 1-vinylimidazole and acrylamide." Russian Journal of Applied Chemistry 89, no. 8 (2016): 1261–64. http://dx.doi.org/10.1134/s1070427216080073.

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43

Bojanic, Vaso. "Optimization of cellulose acrylate and grafted 4-vinylpyridine and 1-vinylimidazole synthesis." Chemical Industry 64, no. 6 (2010): 529–35. http://dx.doi.org/10.2298/hemind100401043b.

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Optimization of cellulose acrylate synthesis by reaction with sodium cellulosate and acryloyl chloride was carried out. Optimal conditions for conducting the synthesis reaction of cellulose acrylate were as follows: the molar ratio of cellulose/potassium-t-butoxide/acryloyl chloride was 1:3:10 and the optimal reaction time was 10 h. On the basis of elemental analysis with optimal conditions for conducting the reaction of cellulose acrylate, the percentage of substitution of glucose units in cellulose Y = 80.7%, and the degree of substitution of cellulose acrylate DS = 2.4 was determined. The g

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44

Li, Rong-Xun, Shao-Xiang Li, Qi-Ye Wu, Guang-Ye Liu та Fa-Qian Liu. "catena-Poly[[bis(1-vinylimidazole-κN3)zinc(II)]-μ-phthalato-κ2O1:O2]". Acta Crystallographica Section E Structure Reports Online 63, № 12 (2007): m2874. http://dx.doi.org/10.1107/s160053680705355x.

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45

Feng, Kai, Lei Liu, Beibei Tang, Nanwen Li, and Peiyi Wu. "Nafion-Initiated ATRP of 1-Vinylimidazole for Preparation of Proton Exchange Membranes." ACS Applied Materials & Interfaces 8, no. 18 (2016): 11516–25. http://dx.doi.org/10.1021/acsami.6b02248.

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46

Deng, Wenjin, Alexander Lobovsky, Scott T. Iacono, et al. "Poly (acrylonitrile – co -1-vinylimidazole): A new melt processable carbon fiber precursor." Polymer 52, no. 3 (2011): 622–28. http://dx.doi.org/10.1016/j.polymer.2010.11.054.

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47

Tian, Ai Hua, Ji-Young Kim, Jin Yi Shi, and Keon Kim. "Poly(1-vinylimidazole)/Pd-impregnated Nafion for direct methanol fuel cell applications." Journal of Power Sources 183, no. 1 (2008): 1–7. http://dx.doi.org/10.1016/j.jpowsour.2008.04.085.

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48

Annenkov, V. V., E. N. Danilovtseva, H. Tenhu, V. Aseyev, S. P. Hirvonen, and A. I. Mikhaleva. "Copolymers of 1-vinylimidazole and (meth)acrylic acid: Synthesis and polyelectrolyte properties." European Polymer Journal 40, no. 6 (2004): 1027–32. http://dx.doi.org/10.1016/j.eurpolymj.2003.12.014.

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49

Voronov, V. K., I. A. Ushakov, and L. V. Baikalova. "NMR spectra of paramagnetic complexes of 1-vinylimidazole with iron group metals." Russian Chemical Bulletin 54, no. 6 (2005): 1473–76. http://dx.doi.org/10.1007/s11172-005-0429-7.

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50

Lin, Jinrui, and Xiuyuan Ni. "Preparation of Graphene Oxide/Poly(1-vinylimidazole) Composites for Resistive Switching Memory." Journal of Nanoscience and Nanotechnology 18, no. 4 (2018): 2601–8. http://dx.doi.org/10.1166/jnn.2018.14320.

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