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Journal articles on the topic '6-bis([1,2,4]-triazin-3-yl)-pyridine'

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Published: 4 June 2021

Last updated: 9 February 2022

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1

Höfener, Sebastian, Michael Trumm, Carsten Koke, et al. "Computing UV/vis spectra using a combined molecular dynamics and quantum chemistry approach: bis-triazin-pyridine (BTP) ligands studied in solution." Physical Chemistry Chemical Physics 18, no. 11 (2016): 7728–36. http://dx.doi.org/10.1039/c5cp07540h.

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2

Veliscek-Carolan, J., K. A. Jolliffe, and T. L. Hanley. "Correction: Effective Am(iii)/Eu(iii) separations using 2,6-bis(1,2,4-triazin-3-yl)pyridine (BTP) functionalised titania particles and hierarchically porous beads." Chemical Communications 51, no. 58 (2015): 11726. http://dx.doi.org/10.1039/c5cc90295a.

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Correction for ‘Effective Am(iii)/Eu(iii) separations using 2,6-bis(1,2,4-triazin-3-yl)pyridine (BTP) functionalised titania particles and hierarchically porous beads’ by J. Veliscek-Carolan et al., Chem. Commun., 2015, DOI: 10.1039/c5cc03957f.

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3

Yuan, Weijin, Yinyong Ao, Long Zhao, et al. "Influence of radiation effect on extractability of an isobutyl-BTP/ionic liquid system: quantitative analysis and identification of radiolytic products." RSC Adv. 4, no. 93 (2014): 51330–33. http://dx.doi.org/10.1039/c4ra08308c.

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Approaches were established for assessing the influence of radiation effect on the extractability of the 2,6-di(5,6-diisobutyl-1,2,4-triazin-3-yl)pyridine (isobutyl-BTP)/1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide ([C<sub>2</sub>mim][NTf<sub>2</sub>]) extraction system.

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4

Abushamleh, Ahmad S., Mustafa M. El-Abadelahb, and Wolfgang Voelter. "Transition Metal Complexes of Derivatized Chiral Dihydro-1,2,4-triazin-6-ones. Part III [1]. X-Ray Crystal Structure Analysis of N,N’-Bis[(1-phenyl-5-isopropyl-4,5-dihydro-6-oxo-1,2,4-triazin-3-yl)ethylidene]- propane-1,3-diamine Nickel(II)." Zeitschrift für Naturforschung B 55, no. 11 (2000): 1074–78. http://dx.doi.org/10.1515/znb-2000-1113.

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Template reaction of L-3-acetyl-1-phenyl-5-isopropyl-4,5-dihydro-1,2,4-triazin-6-one (lb) with 1,3-diaminopropane and nickel acetate gave the corresponding chiral complex 4 in high yield. X-ray structure determination showed that the nickel complex is square planar, and the ligand N,N’-bis[(l-phenyl-5-isopropyl-4,5-dihydro-6-oxo-1,2,4-triazin-3-yl)ethylid-ene]- propane-1,3-diamine is of tetra-aza type where the imine nitrogens and the ring HN(4) nitrogens are the coordinating sites. MS-FAB and NMR spectral data are in agreement with the X-ray structure.

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5

Drew, Michael G. B., Mark R. St J. Foreman, Andreas Geist, et al. "Synthesis, structure, and redox states of homoleptic d-block metal complexes with bis-1,2,4-triazin-3-yl-pyridine and 1,2,4-triazin-3-yl-bipyridine extractants." Polyhedron 25, no. 4 (2006): 888–900. http://dx.doi.org/10.1016/j.poly.2005.09.030.

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6

Roblou, Emmanuel, Hassan Aït-Haddou, Isabelle Sasaki, and Jean-Claude Daran. "2,6-Bis(5,6-dicyclohexyl-1,2,4-triazin-3-yl)pyridine–dichloromethane–water (1/1/0.625)." Acta Crystallographica Section E Structure Reports Online 59, no. 8 (2003): o1175—o1177. http://dx.doi.org/10.1107/s1600536803015745.

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7

Rawat, Neetika, A. Bhattacharyya, S. K. Ghosh, T. Gadly, and B. S. Tomar. "Thermodynamics of complexation of lanthanides with 2,6-bis(5,6-diethyl-1,2,4-triazin-3-yl) pyridine." Radiochimica Acta 99, no. 11 (2011): 705–12. http://dx.doi.org/10.1524/ract.2011.1867.

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8

Boucher, Carole, Michael G. B. Drew, Philip Giddings, et al. "12-coordinate complexes formed by the early lanthanide metals with 2,6-bis(-1,2,4-triazin-3-yl)-pyridine." Inorganic Chemistry Communications 5, no. 8 (2002): 596–99. http://dx.doi.org/10.1016/s1387-7003(02)00489-6.

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9

Kovács, Attila, Christos Apostolidis, and Olaf Walter. "Comparative Study of Complexes of Rare Earths and Actinides with 2,6-Bis(1,2,4-triazin-3-yl)pyridine." Inorganics 7, no. 3 (2019): 26. http://dx.doi.org/10.3390/inorganics7030026.

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Complexes of group III metals (rare earth and actinides) with 2,6-bis(5,6-dipropyl-1,2,4-triazin-3-yl)pyridine (BTP) have been investigated by computational (DFT) and, in limited cases, by experimental (FT-IR, X-ray) techniques with the goal of determining the characteristics of metal–ligand interactions. The DFT calculations using the M062X exchange-correlation functional revealed that metal–ligand distances correlate with the ionic radii of the metals, in agreement with available X-ray diffraction results on the Sc, Y, La, U, and Pu complexes. A related blue-shift trend could be observed in

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10

Childs, Bradley J., Donald C. Craig, Marcia L. Scudder, and Harold A. Goodwin. "Coordination of the Strong Field Terimine System 6-Triazol-3-yl-2,2′-bipyridine and Substituted Derivatives. Electronic and Structural Properties of Bis(ligand)iron(II) Complexes." Australian Journal of Chemistry 51, no. 10 (1998): 895. http://dx.doi.org/10.1071/c97202.

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A terminal pyridine ring in terpyridine has been replaced by a triazole or substituted triazole moiety to give the tridentates 6-(1,2,4-triazol-3-yl)-2,2´-bipyridine, 6-(1-methyl-1,2,4-triazol-3-yl)-2,2´-bipyridine, 6-(5-methyl-1,2,4-triazol-3-yl)-2,2´-bipyridine and 6-(1,5-dimethyl-1,2,4-triazol-3-yl)-2,2´-bipyridine. The effects of coordination of these on the electronic and structural properties of the [FeN6]2+ species are considered. The primary effect is a reduction in the ligand field but salts of the [FeN6]2+ derivatives are essentially low spin (singlet ground state) at room temperatur

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11

Banik, Nidhu L., Melissa A. Denecke, Andreas Geist, Giuseppe Modolo, Petra J. Panak, and Jörg Rothe. "2,6-Bis(5,6-dipropyl-1,2,4-triazin-3-yl)-pyridine: Structures of An(III) and Ln(III) 1:3 complexes and selectivity." Inorganic Chemistry Communications 29 (March 2013): 172–74. http://dx.doi.org/10.1016/j.inoche.2012.11.032.

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12

Drew, Michael G. B., Denis Guillaneux, Michael J. Hudson, Peter B. Iveson, Mark L. Russell, and Charles Madic. "Lanthanide(III) complexes of a highly efficient actinide(III) extracting agent – 2,6-bis(5,6-dipropyl-1,2,4-triazin-3-yl)pyridine." Inorganic Chemistry Communications 4, no. 1 (2001): 12–15. http://dx.doi.org/10.1016/s1387-7003(00)00181-7.

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13

Kozhevnikov, Valery N., Dmitry N. Kozhevnikov, Olga V. Shabunina, Vladimir L. Rusinov, and Oleg N. Chupakhin. "An efficient route to 5,5″-diaryl-2,2′:6′,2″-terpyridines through 2,6-bis(1,2,4-triazin-3-yl)pyridines." Tetrahedron Letters 46, no. 9 (2005): 1521–23. http://dx.doi.org/10.1016/j.tetlet.2005.01.020.

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14

Veliscek-Carolan, J., K. A. Jolliffe, and T. L. Hanley. "Effective Am(iii)/Eu(iii) separations using 2,6-bis(1,2,4-triazin-3-yl)pyridine (BTP) functionalised titania particles and hierarchically porous beads." Chemical Communications 51, no. 57 (2015): 11433–36. http://dx.doi.org/10.1039/c5cc03957f.

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15

Ning, Shunyan, Qing Zou, Xinpeng Wang, Ruiqin Liu, and Yuezhou Wei. "Adsorption mechanism of silica/polymer-based 2,6-bis(5,6-diisohexyl-1,2,4-triazin-3-yl)pyridine adsorbent towards Ln(III) from nitric acid solution." Journal of Nuclear Science and Technology 53, no. 9 (2016): 1417–25. http://dx.doi.org/10.1080/00223131.2015.1123122.

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16

Ruff, Christian M., Udo Müllich, Andreas Geist, and Petra J. Panak. "Complexation of Cm(iii) and Eu(iii) with a hydrophilic 2,6-bis(1,2,4-triazin-3-yl)-pyridine studied by time-resolved laser fluorescence spectroscopy." Dalton Transactions 41, no. 48 (2012): 14594. http://dx.doi.org/10.1039/c2dt31748f.

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17

Trumm, Sascha, Petra J. Panak, Andreas Geist, and Thomas Fanghänel. "A TRLFS Study on the Complexation of CmIII and EuIII with 2,6-Bis(5,6-dipropyl-1,2,4-triazin-3-yl)pyridine in Water/Methanol Mixture." European Journal of Inorganic Chemistry 2010, no. 19 (2010): 3022–28. http://dx.doi.org/10.1002/ejic.201000230.

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18

Beele, Björn B., Andrej Skerencak-Frech, Arnulf Stein, et al. "2,6-Bis(5,6-diisopropyl-1,2,4-triazin-3-yl)pyridine: a highly selective N-donor ligand studied by TRLFS, liquid–liquid extraction and molecular dynamics." New Journal of Chemistry 40, no. 12 (2016): 10389–97. http://dx.doi.org/10.1039/c6nj02657e.

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19

Dotray, Peter A., and Cynthia B. McKenney. "Established and Seeded Buffalograss Tolerance to Herbicides Applied Preemergence." HortScience 31, no. 3 (1996): 393–95. http://dx.doi.org/10.21273/hortsci.31.3.393.

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Experiments were conducted to evaluate established and seeded buffalograss [Buchloe dactyloides (Nutt.) Engelm.] tolerance to herbicides applied preemergence at labeled use rates. Established buffalograss tolerated benefin, benefin plus oryzalin, benefin plus trifluralin, DCPA, dithiopyr, isoxaben, oryzalin, pendimethalin, and prodiamine. For established buffalograss treated with atrazine, diuron, or metolachlor, the injury rating was 27% to 71% at 6 weeks after treatment (WAT) and 22% to 84% at 15 WAT. Buffalograss tolerated cyanazine, metsulfuron, propazine, and pyrithiobac applied in the se

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20

Geist, Andreas, Udo Müllich, Daniel Magnusson, et al. "Actinide(III)/Lanthanide(III) Separation Via Selective Aqueous Complexation of Actinides(III) using a Hydrophilic 2,6-Bis(1,2,4-Triazin-3-Yl)-Pyridine in Nitric Acid." Solvent Extraction and Ion Exchange 30, no. 5 (2012): 433–44. http://dx.doi.org/10.1080/07366299.2012.671111.

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21

Chupakhin, Oleg N., Anton M. Prokhorov, Dmitry N. Kozhevnikov, et al. "1,2,4-Triazinylcarboranes: a new approach to the synthesis and the crystal structures of 1-(3,6-ditolyl-1,2,4-triazin-5-yl)-2-phenyl-1,2-dicarba-closo-dodecaborane and 1,7-bis[6-phenyl-3-(4-chlorophenyl)-1,2,4-triazin-5-yl]-1,7-dicarba-closo-dodecaborane." Mendeleev Communications 13, no. 4 (2003): 165–67. http://dx.doi.org/10.1070/mc2003v013n04abeh001773.

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22

Xiao, Haihua, Pingliang Li, Dongcai Guo, Jinhui Hu, Yuchao Chai, and Wei He. "Synthesis and antibacterial activity evaluation of 2,6-bis(6-substituted-1,2,4-triazolo[3,4-b][1,3,4]thiadiazol-3-yl)pyridine derivatives." Medicinal Chemistry Research 23, no. 4 (2013): 1941–49. http://dx.doi.org/10.1007/s00044-013-0790-2.

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23

Tan, Cunmin, Xin Zhang, Shiwei Cao, et al. "Solvent extraction of americium(III) and europium(III) with 2,6-bis(5,6-diethyl-1,2,4-triazin-3-yl) pyridine in ionic liquids: Experimental study and molecular dynamics simulation." Separation and Purification Technology 192 (February 2018): 302–8. http://dx.doi.org/10.1016/j.seppur.2017.09.033.

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24

Scudder, Marcia L., Donald C. Craig, and Harold A. Goodwin. "Hydrogen bonding influences on the properties of heavily hydrated chloride salts of iron(ii) and ruthenium(ii) complexes of 2,6-bis(pyrazol-3-yl)pyridine, 2,6-bis(1,2,4-triazol-3-yl)pyridine and 2,2′∶6′,2″-terpyridine." CrystEngComm 7, no. 107 (2005): 642. http://dx.doi.org/10.1039/b511825e.

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25

Malmbeck, Rikard, Daniel Magnusson, Stéphane Bourg, et al. "Homogenous recycling of transuranium elements from irradiated fast reactor fuel by the EURO-GANEX solvent extraction process." Radiochimica Acta 107, no. 9-11 (2019): 917–29. http://dx.doi.org/10.1515/ract-2018-3089.

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Abstract The EURO-GANEX process was developed for co-separating transuranium elements from irradiated nuclear fuels. A hot flow-sheet trial was performed in a counter-current centrifugal contactor setup, using a genuine high active feed solution. Irradiated mixed (carbide, nitride) U80Pu20 fast reactor fuel containing 20 % Pu was thermally treated to oxidise it to the oxide form which was then dissolved in HNO3. From this solution uranium was separated to >99.9 % in a primary solvent extraction cycle using 1.0 mol/L DEHiBA (N,N-di(2-ethylhexyl)isobutyramide in TPH (hydrogenated tetrapropene

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26

Bhattacharyya, Arunasis, Eunja Kim, Philippe F. Weck, Paul M. Forster, and Kenneth R. Czerwinski. "Trivalent Actinide and Lanthanide Complexation of 5,6-Dialkyl-2,6-bis(1,2,4-triazin-3-yl)pyridine (RBTP; R = H, Me, Et) Derivatives: A Combined Experimental and First-Principles Study." Inorganic Chemistry 52, no. 2 (2012): 761–76. http://dx.doi.org/10.1021/ic301881w.

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27

Bhattacharyya, A., P. K. Mohapatra, T. Gadly, D. R. Raut, S. K. Ghosh, and V. K. Manchanda. "Liquid–liquid extraction and flat sheet supported liquid membrane studies on Am(III) and Eu(III) separation using 2,6-bis(5,6-dipropyl-1,2,4-triazin-3-yl)pyridine as the extractant." Journal of Hazardous Materials 195 (November 2011): 238–44. http://dx.doi.org/10.1016/j.jhazmat.2011.08.033.

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28

Fedosseev, A. M., M. S. Grigoriev, I. A. Charushnikova, N. A. Budantseva, Z. A. Starikova, and Ph Moisy. "Synthesis, crystal structure and some properties of new perrhenate and pertechnetate complexes of Nd3+ and Am3+ with 2,6-bis(tetramethylfurano)-1,2,4-triazin-3-yl)-pyridine, tris(2-pyridylmethyl)amine and N,N′-tetraethylmalonamide." Polyhedron 27, no. 8 (2008): 2007–14. http://dx.doi.org/10.1016/j.poly.2007.12.029.

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29

Claramunt, Rosa Ma, María de la Concepción Foces-Foces, Félix Hernández Cano, et al. "Molecular structure in the solid state (X-ray crystallography) and in solution (1H and13C nuclear magnetic resonance spectroscopy) of 1,3-diazetidines and pentasubstituted biguanides. X-Ray molecular structure of 2,4-bis-(6-methyl-3-methylthio-5-oxo-4,5-dihydro-1,2,4-triazin-4-yl)-5,5-pentamethylene-1,3-diphenylbig anide and 1,3-bis-(p-chlorophenyl)-5-dimethylamino-2,4-bis-(6-methyl-3-methylthio-5-oxo-4,5-dihydro-1,2,4-triazin-4-yl)biguanide." J. Chem. Soc., Perkin Trans. 2, no. 11 (1990): 1859–69. http://dx.doi.org/10.1039/p29900001859.

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30

Lasley, Robert D., Gentian Kristo, Byron J. Keith, and Robert M. Mentzer. "The A2a/A2b receptor antagonist ZM-241385 blocks the cardioprotective effect of adenosine agonist pretreatment in in vivo rat myocardium." American Journal of Physiology-Heart and Circulatory Physiology 292, no. 1 (2007): H426—H431. http://dx.doi.org/10.1152/ajpheart.00675.2006.

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There is increasing evidence for interactions among adenosine receptor subtypes in the brain and heart. The purpose of this study was to determine whether the adenosine A2a receptor modulates the infarct size-reducing effect of preischemic administration of adenosine receptor agonists in intact rat myocardium. Adult male rats were submitted to in vivo regional myocardial ischemia (25 min) and 2 h reperfusion. Vehicle-treated rats were compared with rats pretreated with the A1 agonist 2-chloro- N6-cyclopentyladenosine (CCPA, 10 μg/kg), the nonselective agonist 5′- N-ethylcarboxamidoadenosine (N

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31

Li, Chun, Xin Wang, Zi Jiao, et al. "Functionalized Porous Silica-Based Nano/Micro Particles for Environmental Remediation of Hazard Ions." Nanomaterials 9, no. 2 (2019): 247. http://dx.doi.org/10.3390/nano9020247.

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The adsorption and separation of hazard metal ions, radioactive nuclides, or minor actinides from wastewater and high-level radioactive waste liquids using functional silica-based nano/micro-particles modified with various inorganic materials or organic groups, has attracted significant attention since the discovery of ordered mesoporous silica-based substrates. Focusing on inorganic and organic modified materials, the synthesis methods and sorption performances for specific ions in aqueous solutions are summarized in this review. Three modification methods for silica-based particles, the dire

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32

Drew, Michael G. B., Denis Guillaneux, Michael J. Hudson, Peter B. Iveson, and Charles Madic. "Unusual complexes formed by the early lanthanides with 2,6-bis(5,6-dialkyl-1,2,4-triazin-3-yl)-pyridines." Inorganic Chemistry Communications 4, no. 9 (2001): 462–66. http://dx.doi.org/10.1016/s1387-7003(01)00210-6.

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33

Zhen, Zhiqiang. "Crystal structure of 2,6-bis(3-(pyrazin-2-yl)-1H-1,2,4-triazol-5-yl)pyridine – 1-ethyl-3-methyl-1H-imidazol-3-ium bromide (1/1), C23H22N13Br." Zeitschrift für Kristallographie - New Crystal Structures 233, no. 1 (2018): 151–52. http://dx.doi.org/10.1515/ncrs-2017-0247.

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AbstractC23H22N13Br, triclinic, P1̅ (no. 2), a = 9.255(6) Å, b = 9.819(6) Å, c = 14.497(9) Å, α = 105.186(7)°, β = 90.030(7)°, γ = 102.228(7)°, V = 1240.3(13) Å3, Z = 2, Rgt(F) = 0.0434, wRref(F2) = 0.1116, T = 296(2) K.

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34

van Diemen, J. H., J. G. Haasnoot, R. Hage, E. Müller, and J. Reedijk. "Synthesis, x-ray structure, electrochemical and electronic properties of [3-(pyridin-2-yl)-4-methyl-1,2,4-triazole-bis(2-(2′-phenylato)pyridine)-iridium(III)] hexafluorophosphate." Inorganica Chimica Acta 181, no. 2 (1991): 245–51. http://dx.doi.org/10.1016/s0020-1693(00)86817-6.

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35

Kozhevnikov, Valery N., Dmitry N. Kozhevnikov, Olga V. Shabunina, Vladimir L. Rusinov, and Oleg N. Chupakhin. "An Efficient Route to 5,5′′-Diaryl-2,2′:6′,2′′-terpyridines Through 2,6-Bis(1,2,4-triazin-3-yl)pyridines." ChemInform 36, no. 25 (2005). http://dx.doi.org/10.1002/chin.200525138.

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36

Chupakhin, Oleg N., Anton M. Prokhorov, Dmitry N. Kozhevnikov, et al. "1,2,4-Triazinylcarboranes: A New Approach to the Synthesis and the Crystal Structures of 1-(3,6-Ditolyl-1,2,4-triazin-5-yl) -2-phenyl-1,2-dicarba-closo-dodecaborane and 1,7-Bis[6-phenyl-3-(4-chlorophenyl)-1,2,4-triazin-5-yl] -1,7-dicarba-closo-dodecaborane." ChemInform 35, no. 2 (2004). http://dx.doi.org/10.1002/chin.200402173.

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37

Kamal, Sabreen A. "In Vitro Antifunal Potential of Morganella morganii and Determination of its Chemical Composition by Gas Chromatography-Mass Spectrometry." International Journal of Current Pharmaceutical Review and Research 8, no. 02 (2017). http://dx.doi.org/10.25258/ijcprr.v8i02.9193.

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Bioactives were analyzed using gas chromatography-mass spectroscopy (GC-MS) techniques, then the in vitro antibacterial and antifungal activity of the methanolic extract was evaluated. GC-MS analysis of Morganella morganii revealed the existence of the Tricyclo[4.3.1.1(3.8)]undecan-1-amine, 3-Methoxybenzaldehyde semicarbazone, carboxaldehyde , 1-methyl-,oxime ,(Z)-(+), 1,5,5-Trimethyl-6-methylene-cyclohexene, 4-(2,5-Dihydro-3-methoxyphenyl)butylamine, Paromomycin , 9-Borabicyclo[3.31]nonane , 9-mercapto-, Benzenemethanol , 2-(2-aminopropoxy)-3-methyl, Acetamide , N-(6-acetylaminobenzothiazol-2

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