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Relevant bibliographies by topics / N-(pyridin-4-yl)pyridin-4-amine

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Journal articles

Academic literature on the topic 'N-(pyridin-4-yl)pyridin-4-amine'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "N-(pyridin-4-yl)pyridin-4-amine"

1

Bussey, Katherine A., Annie R. Cavalier, Jennifer R. Connell, et al. "Structural studies of (prop-2-en-1-yl)bis[(pyridin-2-yl)methylidene]amine hetero-scorpionate copper complexes." Acta Crystallographica Section C Structural Chemistry 71, no. 7 (2015): 526–33. http://dx.doi.org/10.1107/s2053229615010335.

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The structures of five compounds consisting of (prop-2-en-1-yl)bis[(pyridin-2-yl)methylidene]amine complexed with copper in both the CuIand CuIIoxidation states are presented, namely chlorido{(prop-2-en-1-yl)bis[(pyridin-2-yl)methylidene]amine-κ3N,N′,N′′}copper(I) 0.18-hydrate, [CuCl(C15H17N3)]·0.18H2O, (1),catena-poly[[copper(I)-μ2-(prop-2-en-1-yl)bis[(pyridin-2-yl)methylidene]amine-κ5N,N′,N′′:C2,C3] perchlorate acetonitrile monosolvate], {[Cu(C15H17N3)]ClO4·CH3CN}n, (2), dichlorido{(prop-2-en-1-yl)bis[(pyridin-2-yl)methylidene]amine-κ3N,N′,N′′}copper(II) dichloromethane monosolvate, [CuCl2(C

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2

Reddy, B. Siva, and K. R. S. Prasad. "Design, Synthesis and Antibacterial Activity of N-(3-((4-(6-(2,2,2- Trifluoroethoxy)pyridin-3-yl)-1H-imidazol-2-yl)methyl)oxetan-3-yl)amide Derivatives." Asian Journal of Chemistry 33, no. 3 (2021): 577–82. http://dx.doi.org/10.14233/ajchem.2021.23039.

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A new series of N-(3-((4-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)-1H-imidazol-2-yl)methyl)oxetan-3- yl)amide derivatives (10a-h)were synthesized by the reaction of 3-((4-(6-(2,2,2-trifluoroethoxy)pyridin- 3-yl)-1H-imidazol-2-yl)methyl)oxetan-3-amine (8) with various carboxylic acids in the presence of T3P catalyst. The reaction is usually furnished within 60 min with good isolated yields. Coupling of 6-(2,2,2-trifluoroethoxy) nicotinic acid (1) with Weinreb amine hydrochloride gave N-methoxy-Nmethyl- 6-(2,2,2-trifluoroethoxy) nicotinamide (2). Compound 3 was synthesized by the Grignard reaction

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3

Böck, Denise, Andreas Beuchel, Richard Goddard, Adrian Richter, Peter Imming, and Rüdiger W. Seidel. "Protonation sites and hydrogen bonding in mono-hydrobromide salts of two N,4-diheteroaryl 2-aminothiazoles." Structural Chemistry 32, no. 3 (2021): 989–96. http://dx.doi.org/10.1007/s11224-021-01730-0.

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AbstractThe synthesis and structural characterization of N-(6-methoxypyridin-3-yl)-4-(pyridin-2-yl)thiazol-2-amine mono-hydrobromide monohydrate (3) and N-(6-methoxypyridin-3-yl)-4-(pyrazin-2-yl)thiazol-2-amine mono-hydrobromide 0.35 methanol solvate (4) are reported. The crystal structures of 3 (monoclinic, space group P21/n, Z = 4) and 4 (monoclinic, space group, C2/c, Z = 8) feature N,4-diheteroaryl 2-aminothiazoles showing similar molecular conformations but different sites of protonation and thus distinctly different intermolecular hydrogen bonding patterns. In 3, Namine–H⋯Br−, N+pyridine

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4

Unjaroen, Duenpen, Johann B. Kasper, and W. R. Browne. "Reversible photochromic switching in a Ru(ii) polypyridyl complex." Dalton Trans. 43, no. 45 (2014): 16974–76. http://dx.doi.org/10.1039/c4dt02430c.

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Fully reversible photoswitching of the coordination mode of the ligand MeN<sub>4</sub>Py (1,1-di(pyridin-2-yl)-N,N′-bis(pyridin-2-yl-methyl)-ethan-1-amine) in its ruthenium(ii) complex with visible light is reported.

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5

Guo, Huixia, Xiaohua Xi, Renxiang Yan та Xiaoquan Lu. "Theoretical study on the effect of different π-linker on the performance of sensitizer in carbazole-based dyes". Journal of Theoretical and Computational Chemistry 17, № 02 (2018): 1850019. http://dx.doi.org/10.1142/s0219633618500190.

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Derived from diarylamine sensitizer diphenyl-(7-pyridin-4-yl-9H-carbazol-2-yl)-amine (N13), a series of novel D[Formula: see text]A carbazole-based organic dye sensitizers with different [Formula: see text]-linkers were designed for searching more effective sensitizers in dye-sensitized solar cells (DSSCs) design. Optimized geometries, electronic structure, and other parameters, which can evaluate the performance of DSSCs effectively and intuitively, were theoretically calculated by density functional theory (DFT) and time-dependent DFT methods at the M06/6-31G(d,p) level. The results indicate

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6

Kansagara, N. N., V. R. Dangar, and V. R. Shah. "Synthesis, Characterization and Antimicrobial Evaluation of Schiff’s Base and Aryl Aminomethyl Derivatives." International Letters of Chemistry, Physics and Astronomy 64 (February 2016): 89–94. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.64.89.

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Schiff’s bases are obtained on heating an aldehydes with aromatic amine in presence of glacial acetic acid. These are the compounds containing characteristic –HC=N– group. Aryl amino methyl derivatives of heterocyclic compounds to synthesize by selective reduction of schiff’s bases (imine group) with sodiumborohydride in controlled experimental condition. Schiff’s base of N-Aryl-1-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]methanimines & Aryl amines of N-Aryl-1-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]methanamines were prepared. Their chemical structures were conf

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7

Padilha, Diego da S., Adailton J. Bortoluzzi, and Marciela Scarpellini. "An unusual partial occupancy of labile chloride and aqua ligands in cocrystallized isomers of a nickel(II) complex bearing a tripodal N 4-donor ligand." Acta Crystallographica Section C Structural Chemistry 76, no. 1 (2020): 17–22. http://dx.doi.org/10.1107/s2053229619015705.

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A novel Ni2+ complex with the N 4-donor tripodal ligand bis[(1-methyl-1H-imidazol-2-yl)methyl][2-(pyridin-2-yl)ethyl]amine (L), namely, aqua{bis[(1-methyl-1H-imidazol-2-yl-κN 3)methyl][2-(pyridin-2-yl-κN)ethyl]amine-κN}chloridonickel(II) perchlorate, [NiCl(C17H22N6)(H2O)]ClO4 or [NiCl(H2O)(L)Cl]ClO4 (1), was synthesized and characterized by spectroscopic and spectrometric methods. The crystal structure of 1 reveals an interesting and unusual cocrystallization of isomeric complexes, which are crystallographically disordered with partial occupancy of the labile cis aqua and chloride ligands. The

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8

Wolińska, Ewa. "Chiral oxazoline ligands with two different six-membered azaheteroaromatic rings – synthesis and application in the Cu-catalyzed nitroaldol reaction." Heterocyclic Communications 22, no. 2 (2016): 85–94. http://dx.doi.org/10.1515/hc-2016-0001.

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AbstractSynthesis and catalytic activity of chiral ligands 5,6-diphenyl-3-{3-[(4S/R)-4-R/Ar-4,5-dihydro-1,3-oxazol-2-yl]pyridin-2-yl}amino-1,2,4-triazines 2 and their analogs 3 possessing an N-oxide function in the pyridine ring are described. The pivotal step in the synthesis of ligands 2 is the Buchwald-Hartwig Pd-catalyzed cross-coupling reaction between 3-bromo-5,6-diphenyl-1,2,4-triazine (7a) and enantiopure 3-(4,5-dihydro-1,3-oxazol-2-yl)pyridin-2-amines 6a–d. Aromatic nucleophilic substitution of chlorine in 3-chloro-5,6-diphenyl-1,2,4-triazine (7b) with 3-(4,5-dihydro-1,3-oxazol-2-yl)p

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9

Jyotindra B, Mahyavanshi, Parmar Kokila A, and Mahato Anil K. "Synthesis, Structural Elucidation and Anti Microbial Screening of N-(4-aryl amine)-2-{[4-phenyl-5- (pyridin-4-yl)-4H-1,2,4-triazol-3-yl]sulfanyl}acetamide Derivatives." Indian Journal of Applied Research 4, no. 1 (2011): 91–94. http://dx.doi.org/10.15373/2249555x/jan2014/27.

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10

Jiang, Quan-Fu, and Chun-Xiong Lu. "N-{2-[4-(2-Methoxyphenyl)piperazin-1-yl]ethyl}pyridin-2-amine monohydrate." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1727. http://dx.doi.org/10.1107/s1600536810022816.

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