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Journal articles on the topic 'N-(4-nitrophenacyl)-4-(1-hexyl)pyridinium bromide'

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Published: 4 June 2021

Last updated: 12 February 2022

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1

Sundar, T. V., V. Parthasarathi, K. Sarkunam, M. Nallu, B. Walfort, and H. Lang. "1-[(4-Chlorobenzoyl)methyl]-4-(N,N-dimethylamino)pyridinium bromide sesquihydrate and 1-[(4-bromobenzoyl)methyl]-4-(N,N-dimethylamino)pyridinium bromide sesquihydrate." Acta Crystallographica Section C Crystal Structure Communications 60, no. 7 (2004): o464—o466. http://dx.doi.org/10.1107/s0108270104010923.

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2

Zaleski, J., Z. Daszkiewicz, and J. Kyzioł. "1-Methyl-4-(N-methylnitramino)pyridinium bromide." Acta Crystallographica Section C Crystal Structure Communications 55, no. 4 (1999): 691–93. http://dx.doi.org/10.1107/s0108270198014656.

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3

Sundar, T. V., V. Parthasarathi, K. Sarkunam, M. Nallu, B. Walfort, and H. Lang. "1-[(2,4-Dichlorobenzoyl)methyl]-4-(N,N-dimethylamino)pyridinium bromide." Acta Crystallographica Section E Structure Reports Online 60, no. 12 (2004): o2345—o2346. http://dx.doi.org/10.1107/s1600536804029083.

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4

Sharmila, N., T. V. Sundar, A. Yasodha, A. Puratchikody, and B. Sridhar. "Crystal structure of 4-amino-1-(4-methylbenzyl)pyridinium bromide." Acta Crystallographica Section E Structure Reports Online 70, no. 12 (2014): o1293—o1294. http://dx.doi.org/10.1107/s1600536814025343.

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The title molecular salt, C13H15N2+·Br−, crystallized with two independent ion pairs (AandB) in the asymmetric unit. In the cations, the planes of the pyridine and benzene rings are inclined to one another by 79.32 (8) and 82.30 (10)° in ion pairsAandB, respectively. In the crystal, the anions and cations are connected by N—H...Br hydrogen bonds, forming a centrosymmetric tetramer-like unit enclosing anR84(16) ring motif. These units are linkedviaC—H...Br hydrogen bonds, forming a three-dimensional network.

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5

Sundar, T. V., V. Parthasarathi, K. Sarkunam, M. Nallu, B. Walfort, and H. Lang. "1-[2-(Biphenyl-4-yl)-2-oxoethyl]-4-(N,N-dimethylamino)pyridinium bromide hemihydrate." Acta Crystallographica Section E Structure Reports Online 61, no. 4 (2005): o889—o891. http://dx.doi.org/10.1107/s1600536805006471.

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6

Lu, Norman, Rong-Jyun Wei, Kwan-Yu Lin, Mani Alagesan, Yuh-Sheng Wen, and Ling-Kang Liu. "Weak hydrogen bonding and fluorous interactions in the chloride and bromide salts of 4-[(2,2,3,3-tetrafluoropropoxy)methyl]pyridinium." Acta Crystallographica Section C Structural Chemistry 73, no. 4 (2017): 343–49. http://dx.doi.org/10.1107/s2053229617004016.

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Neutralization of 4-[(2,2,3,3-tetrafluoropropoxy)methyl]pyridine with hydrohalo acids HX(X= Cl and Br) yielded the pyridinium salts 4-[(2,2,3,3-tetrafluoropropoxy)methyl]pyridinium chloride, C9H10F4NO+·Cl−, (1), and 4-[(2,2,3,3-tetrafluoropropoxy)methyl]pyridinium bromide, C9H10F4NO+·Br−, (2), both carrying a fluorous side chain at theparaposition of the pyridinium ring. Single-crystal X-ray diffraction techniques revealed that (1) and (2) are isomorphous. The halide anions accept four hydrogen bonds from N—H,ortho-C—H and CF2—H groups. Two cations and two anions form a centrosymmetric dimeric

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7

Fujimoto, Kanji, Daiki Morisaki, Munehiro Yoshida, et al. "Antimalarial effect of bis-pyridinium salts, N,N′-hexamethylenebis(4-carbamoyl-1-alkylpyridinium bromide)." Bioorganic & Medicinal Chemistry Letters 16, no. 10 (2006): 2758–60. http://dx.doi.org/10.1016/j.bmcl.2006.02.030.

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8

Köppen, Robert, Franziska Emmerling, and Matthias Koch. "rac-1-(2-Aminocarbonyl-2-bromoethyl)pyridinium bromide." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1666. http://dx.doi.org/10.1107/s1600536812019721.

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In the crystal structure of the title compound, C8H10BrN2O+·Br−, intermolecular N—H...Br hydrogen bonds link the molecules into infinite chains along [001]. The inclined angle between the pyridine ring plane and the plane defined by the acid amide group is 63.97 (4)°.

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9

Skeberdis, Vytenis, Vida Gendvilienė, Danguolė Zablockaitė, Irma Martišienė, and Antanas Stankevičius. "inhibitor 2-[(4-methylphenyl)sulfonylcarbamido]-1-(4-nitrobenzyl)pyridinium bromide (2-AP27) is a muscarinic M2 receptor antagonist." Medicina 45, no. 7 (2009): 516. http://dx.doi.org/10.3390/medicina45070068.

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Aminopyridines are known to inhibit acetylcholine-activated K+ current (IKACh) in cardiac myocytes. The aim of this study was to examine the effect of 2-aminopyridine sulfonylcarbamide derivative 2-AP27 on isoprenaline-stimulated L-type Ca2+ current (ICaL) and to identify whether 2-AP27 acts via blocking of muscarinic M2-receptors in frog cardiomyocytes. The whole-cell configuration of the patch-clamp technique was used to record ICaL in enzymatically isolated cardiac myocytes. Isoprenaline (0.1 μM), an agonist of β1-β2-adrenoreceptors, stimulated the ICaL up to 475±61% (n=4) (P<0.05) vs. c

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10

Matsulevich, Zhanna V., Julia M. Lukiyanova, Vladimir I. Naumov, et al. "Bromination of bis(pyridin-2-yl) diselenide in methylene chloride: the reaction mechanism and crystal structures of 1H-pyridine-2-selenenyl dibromide and its cycloadduct with cyclopentene (3aSR,9aRS)-2,3,3a,9a-tetrahydro-1H-cyclopenta[4,5][1,3]selenazolo[3,2-a]pyridinium bromide." Acta Crystallographica Section E Crystallographic Communications 75, no. 5 (2019): 675–79. http://dx.doi.org/10.1107/s2056989019004997.

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1H-Pyridine-2-selenenyl dibromide, C5H5NSeBr2, 1, is a product of the bromination of bis(pyridin-2-yl) diselenide in methylene chloride recrystallization from methanol. Compound 1 is essentially zwitterionic: the negative charge resides on the SeBr2 moiety and the positive charge is delocalized over the pyridinium fragment. The C—Se distance of 1.927 (3) Å is typical of a single bond. The virtually linear Br—Se—Br moiety of 178.428 (15)° has symmetrical geometry, with Se—Br bonds of 2.5761 (4) and 2.5920 (4) Å, and is twisted by 63.79 (8)° relative to the pyridinium plane. The Se atom forms an

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11

Usta, Asu, and Hacer Taşkıran. "Synthesis and antimicrobial properties of N-substituted derivatives of (E)-2′,3″-thiazachalcones." Zeitschrift für Naturforschung C 70, no. 1-2 (2015): 45–50. http://dx.doi.org/10.1515/znc-2014-4182.

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Abstract N-alkyl substituted 2′,3″-thiazachalcones {3-[(1E)-3-(4-methylthiophene-2-yl)-3-oxoprop-1-en-1-yl]-1-alkyl (C5–12,14) pyridinium bromides} were synthesized by a two-step reaction. The newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR, elemental analysis and mass spectral studies. The synthesized compounds were tested for antibacterial activities and found to be more active against Gram-positive as compared to Gram-negative bacteria.

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12

Mikeš, František, Jiří Labský, Drahomír Výprachtický, and Jiří Chalabala. "Microenvironment of polymer chains in solution: pKa of indicators bound to the polymer chain." Collection of Czechoslovak Chemical Communications 55, no. 9 (1990): 2226–32. http://dx.doi.org/10.1135/cccc19902226.

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Polymers bearing at the end of side chains acidobasic indicator moieties exhibiting a solvatochromic absorption band were prepared by a polymeranalogous reaction of copolymers N-(2-hydroxy propyl) methacrylamide-N-methacryloylated 4-nitrophenyl ester ω-aminoacids with 1-(2-aminoethyl)-4-(4-hydroxystyryl)pyridinium bromide. It was found that pKa of reporters bound at a medium long side chain (six methylene groups) is close to pKa of a low-molecular model compound, while pKa of a reporter bound close to the polymer backbone is approximately by one pKa unit higher. Changes in the pKa value of the

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13

Iqbal, Nadeem, Zhong-Yong Wei, Glen B. Baker, and Edward E. Knaus. "Synthesis of 4,4-bis(2-methylphenyl)-3-butenyl (and butyl) analogs of 4-phenyl-1,4- and 6-phenyl-1,6-dihydropyridine-3-carboxylic acids and their evaluation as neuronal GABA-uptake inhibitors." Canadian Journal of Chemistry 75, no. 6 (1997): 601–10. http://dx.doi.org/10.1139/v97-071.

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Treatment of 3-[2-(4,4-dimethyl-4,5-dihydrooxazolin-2-yl)]-4-phenyl-1,4-dihydropyridine (13) with NaH–DMSO, and then reaction with 1,1-bis(2-methylphenyl)-4-bromobutane (12c) afforded 1-[4,4-bis(2-methylphenyl)butyl]-3-[2-(4,4-dimethyl-4,5-dihydrooxazolin-2-yl)]-4-phenyl-1,4-dihydropyridine (14). Reaction of methyl nicotinate with 2.1 equivalents 12c or 1,1-bis(2-methylphenyl)-4-bromo-1-butene (11b) afforded 4,4-bis(2-methylphenyl)butyl 1-[4,4-bis(2-methylphenyl)butyl]pyridinium-3-carboxylate bromide (17) or 4,4-bis(2-methylphenyl)-3-butenyl 1-[4,4-bis(2-methylphenyl)-3-butenyl]pyridinium-3-ca

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14

Chen, Ming, Xiao-Yan Tang, Ming-Zhen Chen, Jin-Xiang Chen, and Wen-Hua Chen. "Lanthanide-Based Polymers with Charged Ligand Backbones: Triple-Stranded Chain Structures and their DNA Cleavage Studies." Australian Journal of Chemistry 68, no. 3 (2015): 493. http://dx.doi.org/10.1071/ch14025.

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Four rare-earth metal complexes, [Ln(Ccbp)3(H2O)3]n (Ln = La (1), Ce (2), Pr (3) and Nd (4)) are synthesised from the ligand H2CcbpBr (H2CcbpBr = 4-carboxy-1-(4-carboxybenzyl)pyridinium bromide) and the respective lanthanide metal ions. Complexes 1–4 are isostructural in that every three Ccbp– ligands juxtapose two Ln3+ ions in a monodentate coordination mode to form triple-stranded one-dimensional chain structures. Each central Ln3+ atom further associates with three H2O molecules, furnishing a monocapped square-antiprism geometry. Agarose gel electrophoresis studies indicate that 1–4 are cap

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15

Pergushov, Dmitry V., Ulrich Oertel, Bettina Pilch, Simona Schwarz, and Jürgen Nagel. "Adsorption of poly(N-ethyl-4-vinyl pyridinium bromide) onto langmuir-blodgett films built up from amphiphilic polymers." Macromolecular Symposia 164, no. 1 (2001): 145–57. http://dx.doi.org/10.1002/1521-3900(200102)164:1<145::aid-masy145>3.0.co;2-1.

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16

Sun, Jing, Wang Jiang, and Chao-Guo Yan. "Convenient construction of dibenzo[b,d]furanes and 2,6-diaryl-4-(2-hydroxyphenyl)pyridines via domino reaction of pyridinium ylides with 2-aryl-3-nitrochromenes." Organic Chemistry Frontiers 6, no. 9 (2019): 1428–32. http://dx.doi.org/10.1039/c9qo00079h.

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The DBU promoted domino annulation reaction of 2-aryl-3-nitrochromenes with two molecular 4-(N,N-dimethylamino)-1-phenacylpyridinium bromides in DMF resulted in unprecedented 1-benzoyl-2,4-diaryldibenzo[b,d]furane derivatives in good yields.

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17

Kantlehner, Willi, Markus Vettel, and Bernhard Eppinger. "Orthoamide und Iminiumsalze, LXXVI [1]. Ein weiterer Beitrag zur Chemie der Trialkoxyacetonitrile/ Orthoamides and Iminium Salts LXXVI [1]. A Further Contribution to the Chemistry of Trialkoxyacetonitriles." Zeitschrift für Naturforschung B 67, no. 4 (2012): 373–88. http://dx.doi.org/10.1515/znb-2012-0412.

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An improved procedure for the preparation of trimethoxyacetonitrile (3a) starting from trichloroacetonitrile and sodium methanolate is described. Carbanions, obtained by the action of sodium hydride on nitriles, ethyl acetate and methylketones, react with trialkoxyacetonitriles 3 to give α- imino-orthocarboxylic acid trialkylesters 12, 14 and 20, which form an equilibrium with the tautomeric enamines 13, 15 and 21. The enamines 21 react with N,N-dimethylformamide dimethylacetal (24) to give amidines 25 which are cyclized to pyridinium salts 28 and 29 on treatment with benzyl bromide and acetyl

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18

Peng, Qingrong, Fengmao Liu, and Chunrong Zhang. "Efficacy of Difenoconazole Emulsifiable Concentrate with Ionic Liquids against Cucumbers Powdery Mildew." International Journal of Chemical Engineering 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/8286358.

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Among eight ionic liquids (ILs) examined, 1-n-butyl-4-methyl-pyridinium bromide (BMPyBr, 5) was used in this study as an appropriate alternative to benzene homologs and derivatives to be used in 10 wt% water-insoluble difenoconazole emulsifiable concentrate (EC). Moreover, 10 wt% difenoconazole EC with BMPyBr (5) exhibited the same efficacy as 10 wt% difenoconazole wettable powder (WP) against powdery mildew on cucumbers under field conditions. The results revealed that difenoconazole EC with BMPyBr (5) had excellent stability at 268 K and 327 K after 14 days through high-performance liquid ch

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19

Lozano, Virginia, Oliver Moers, Peter G. Jones, and Armand Blaschette. "Polysulfonylamine, CLXIX. Intermolekulare Wechselwirkungen in kristallinen Di(organosulfonyl)aminen. Teil 1. Di(4-brombenzolsulfonyl)amin: Zwei Konformationspolymorphe und Strukturverwandtschaft eines Polymorphs mit dem entsprechenden 2,4-Dimethylpyridinium-Salz / Polysulfonylamines, CLXIX. Intermolecular Interactions in Crystalline Di(organosulfonyl)- amines. Part 1. Di(4-bromobenzenesulfonyl)amine: Two Conformational Polymorphs and the Structural Relationship of one Polymorph to the Corresponding 2,4-Dimethylpyridinium Salt." Zeitschrift für Naturforschung B 59, no. 6 (2004): 661–72. http://dx.doi.org/10.1515/znb-2004-0606.

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Two crystal structures (polymorphs) of di(4-bromobenzenesulfonyl)amine (1), as determined by low-temperature single-crystal X-ray diffraction, are reported: Form A, monoclinic, P21/c, Z' = 1; form B: monoclinic, P21/c, Z' = 2. In A, the molecule adopts an extended conformation approximating to C2 symmetry, whereas the two independent molecules of form B display a folded hair-pin conformation with pseudo-mirror symmetry [torsion τ (C-S···S’-C’) and intercentroid distance dIC of the aromatic rings in A: 173.2° and 750.8 pm, in B: −5.4/−8.90° and 364.1/366.5 pm]. The packings of both polymorphs c

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20

Kawabata, N., K. Yamazaki, T. Otake, I. Oishi, and Y. Minekawa. "Removal of pathogenic human viruses by insoluble pyridinium-type resin." Epidemiology and Infection 105, no. 3 (1990): 633–42. http://dx.doi.org/10.1017/s0950268800048275.

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SUMMARYCross-linked poly(N-benzyl-4-vinylpyridinium bromide) (BVP resin) was found to be very efficient in removing pathogenic human viruses from aqueous solution. In batch removal experiments using 50 g/1 of BVP resin at 35 °C. the level of infectivity in suspensions of enterovirus. herpes simplex virus, poliovirus, and human immunodeficiency virus was reduced 1000–100000 fold during a 2 h period. Those of coxsackievirus and echovirus were reduced 60–600 fold during 1 h contact. The haemagglutination titres of solutions of human rotavirus, influenza virus, human adenovirus. and Japanese encep

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21

Herodes, Koit, Ivo Leito, Juta Koppel, Christian Reichardt, and Ilmar A. Koppel. "UV-Vis spectroscopic study of the hydrophilic and solvatochromic 4-[2,6-diphenyl-4-(pyridin-4-yl)pyridinium-1-yl]-2,6-bis(pyridin-3-yl)phenolate betaine dye in aqueous tetra-n-butylammonium bromide." Journal of Physical Organic Chemistry 18, no. 10 (2005): 1013–17. http://dx.doi.org/10.1002/poc.958.

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22

Gu, Yingchun, Dayong Lin, Ran Li, Yalin Tang, Xuening Fei, and Jianguo Zhou. "Spectra, stability and labeling of 1-(5-carboxypentyl)-4-(2-(N-ethyl-carbazole-3-yl) vinyl) pyridinium bromide with a large Stokes shift." Luminescence 31, no. 2 (2015): 380–87. http://dx.doi.org/10.1002/bio.2970.

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23

Stoean, Bianca, Dumitrita Rugina, Monica Focsan, et al. "Novel (Phenothiazinyl)Vinyl-Pyridinium Dyes and Their Potential Applications as Cellular Staining Agents." International Journal of Molecular Sciences 22, no. 6 (2021): 2985. http://dx.doi.org/10.3390/ijms22062985.

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We report here the synthesis and structural characterization of novel cationic (phenothiazinyl)vinyl-pyridinium (PVP) dyes, together with optical (absorption/emission) properties and their potential applicability as fluorescent labels. Convective heating, ultrasound irradiation and mechanochemical synthesis were considered as alternative synthetic methodologies proficient for overcoming drawbacks such as long reaction time, nonsatisfactory yields or solvent requirements in the synthesis of novel dye (E)-1-(3-chloropropyl)-4-(2-(10-methyl-10H-phenothiazin-3-yl)vinyl)pyridin-1-ium bromide 3d and

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24

Štrop, Petr, František Mikeš, Marie Havranová, and Václav Žižkovský. "Human serum albumin. A study of the nature of its hydrophobic binding sites." Collection of Czechoslovak Chemical Communications 52, no. 5 (1987): 1362–74. http://dx.doi.org/10.1135/cccc19871362.

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Spectroscopic labels and hydrophobic chromatography on two different supports were used to compare the size and accessibility of the hydrophobic binding sites of human serum albumin with the accessibility of non-polar residues on the surface of other globular proteins. The binding of the labels 1-alkyl-4-(3-ethoxy-4-hydroxystyryl)pyridinium bromides (HPB) with alkyl chains of different length was investigated in the ultracentrifuge and by spectrophotometry. n-Butyl (C4-HPB) and decyl (C10-HPB) labels bind to albumin with association constants of 8 . 103 and 4 . 104, respectively, at pH 5·50, a

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25

Jeck, Reinhard, Michael Scholze, Anja Tischlich, Christoph Woenckhaus, and Jürgen Zimmermann. "New Reactive Coenzyme Analogues for Affinity Labeling of NAD+ and NADP+ Dependent Dehydrogenases." Zeitschrift für Naturforschung C 50, no. 7-8 (1995): 476–86. http://dx.doi.org/10.1515/znc-1995-7-803.

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Abstract Reactive coenzyme analogues ω-(3-diazoniumpyridinium)alkyl adenosine diphosphate were prepared by reaction of ω-(3-aminopyridinium)alkyl adenosine diphosphate with nitrous acid. In these compounds the nicotinamide ribose is substituted by hydrocarbon chains of varied lengths (n-ethyl to n-pentyl). The diazonium compounds are very unstable and decompose rapidly at room temperature. They show a better stability at 0 °C. L actate and alcohol dehydrogenase do not react with any of the analogues. Glyceraldehyde-3-phosphate dehydrogenase reacts rapidly with the diazonium pentyl compound. D

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26

Xu, Feng-Shun, Chen Yan, Jing Sun, and Chaoguo Yan. "Efficient Synthesis of Tetra- and Penta-substituted Benzenes via Domino Cycloaddition Reaction of pyridinium ylide and Chalcone o-Enolate." New Journal of Chemistry, 2021. http://dx.doi.org/10.1039/d1nj03772b.

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A very simple and high efficient synthetic protocol for tetra- and penta-substituted benzene derivatives has been provided by tetramethylguanidine (TMD) promoted reaction of 4-(N,N-dimethylamino)-1-phenacyl-pyridinium bromide with chalcone o-enolates in DMF...

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27

"An MD simulation study of Reichardt’s betaines in surfactant micelles: Unlike orientation and solvation of cationic, zwitterionic, and anionic dye species within the pseudophase." Kharkov University Bulletin Chemical Series, no. 30 (2018). http://dx.doi.org/10.26565/2220-637x-2018-30-03.

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Solvatochromic indicators of the pyridinium N-phenolate series, also known as Reichardt’s betaines, or Reichardt’s dyes, are often used for examining not only pure or mixed solvents, but also various colloidal aggregates, such as surfactant micelles, droplets of microemulsions etc. In order to disclose the locus of these molecular probes within the micellar pseudophase, we recently utilized the molecular dynamics (MD) simulations for the standard dye, i.e. 4-(2,4,6-triphenylpyridinium-1-yl)-2,6-diphenylphenolate, and three other dyes of this family of higher and lower hydrophobicity. Both zwit

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28

"Force field of tetrafluoroborate anion for molecular dynamics simulation: a new approach." Kharkov University Bulletin Chemical Series, no. 33 (2019). http://dx.doi.org/10.26565/2220-637x-2019-33-03.

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González A., Goikolea E., Barrena J. A., Mysyk R. Review on supercapacitors: Technologies and materials. Renew. Sustain. Energy Rev. 2016, 58 1189-1206. Zhong C., Deng Y., Hu W., Qiao J., Zhang L., Zhang J. A review of electrolyte materials and compositions for electrochemical supercapacitors. Chem. Soc. Rev. 2015, 44 (21), 7484-7539. Dahl K., Sando G., Fox D., Sutto T., Owrutsky J. Vibrational spectroscopy and dynamics of small anions in ionic liquid solutions. J. Chem. Phys. 2005, 123 084504. Zhang B., Yuan Z., li X., Ren X., Nian H., Shen Y., Yun Q. Ion-molecule interaction in solutions of

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