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Journal articles on the topic 'Tetraalkylammonium'

Author: Grafiati

Published: 18 May 2024

Last updated: 26 July 2025

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1

Schwendt, P., J. Chrappová, and K. Lišcák. "Tetraalkylammonium fluorooxoperoxovanadates." Monatshefte für Chemie Chemical Monthly 128, no. 4 (1997): 317–22. http://dx.doi.org/10.1007/bf00810768.

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2

Kulapina, E. G., E. S. Pogorelova, N. M. Makarova, and L. A. Bazhanova. "Physicochemical properties of tetraalkylammonium tetraphenylborates and tetraalkylammonium dodecylsulfates." Russian Journal of Inorganic Chemistry 58, no. 1 (2013): 112–16. http://dx.doi.org/10.1134/s0036023613010129.

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3

Perez-Tejeda, P., A. Maestre, P. Delgado-Cobos, and J. Burgess. "Single-ion Setschenow coefficients for several hydrophobic non-electrolytes in aqueous electrolyte solutions." Canadian Journal of Chemistry 68, no. 2 (1990): 243–46. http://dx.doi.org/10.1139/v90-032.

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Setschenow coefficients have been derived from solubility measurements on cyclohexane, benzene, naphthalene, 1-naphthol, 1,5-dihydroxynaphthalene, and anthracene in alkali halide, tetraalkylammonium bromide, and tetraphenylarsonium chloride aqueous solutions at 298.2 K. Single ion Setschenow coefficients have thence been obtained by an assumption involving extrapolation of the tetraalkylammonium bromide results to zero cation volume. Setschenow coefficients for the tetraalkylammonium cations correlate well with a hydrophobicity parameter based on their transfer chemical potentials from water i

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4

Anastasio, Paola, Tiziana Del Giacco, Raimondo Germani, Nicoletta Spreti, and Matteo Tiecco. "Structure effects of amphiphilic and non-amphiphilic quaternary ammonium salts on photodegradation of Alizarin Red-S catalyzed by titanium dioxide." RSC Advances 7, no. 1 (2017): 361–68. http://dx.doi.org/10.1039/c6ra25421g.

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The role of surfactants such as single- and double-tailed tetraalkylammonium bromide and various non-amphiphilic tetraalkylammonium salts was investigated on the TiO<sub>2</sub>photocatalyzed degradation of Alizarin Red-S under UV light irradiation.

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5

Duan, Erhong, Peng Zhang, Kun Yang, et al. "Effect of alkyl and halide moieties on the absorption and stratification of SO2 in tetrabutylammonium halide aqueous solutions." RSC Advances 6, no. 60 (2016): 55401–5. http://dx.doi.org/10.1039/c6ra05677f.

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To explore the interactions between SO<sub>2</sub> and tetraalkylammonium halide, the effects of temperature, concentration, length of alkyl chain, and halide anion on the solubility of SO<sub>2</sub> in tetraalkylammonium halide aqueous solutions were investigated.

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6

Rowland, Clare E., Mercouri G. Kanatzidis, and L. Soderholm. "Tetraalkylammonium Uranyl Isothiocyanates." Inorganic Chemistry 51, no. 21 (2012): 11798–804. http://dx.doi.org/10.1021/ic301741u.

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7

Haldar, Purushottam, and Bijan Das. "Conductometric Study of Some Tetraalkylammonium Bromides in 2-Ethoxyethanol in the Temperature Range 35–50 °C." Zeitschrift für Physikalische Chemie 218, no. 9 (2004): 1129–38. http://dx.doi.org/10.1524/zpch.218.9.1129.41673.

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AbstractThe electrical conductances of the solutions of four tetraalkylammonium bromide salts (R4NBr), namely tetraethylammonium bromide (Et4NBr), tetrapropylammonium bromide (Pr4NBr), tetrapentylammonium bromide (Pen4NBr) and tetraheptylammonium bromide (Hep4NBr) in 2-ethoxyethanol have been reported at 35, 40, 45 and 50 °C. The conductance data have been analyzed by the 1978 Fuoss conductance–concentration equation in terms of the limiting molar conductance (Λ0), the association constant (KA) and the association diameter (R). The ionic contributions to the limiting molar conductance have als

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8

Haldar, Purushottam, and Bijan Das. "Viscosities of some tetraalkylammonium bromides in 2-ethoxyethanol at 308.15, 313.15, 318.15, and 323.15 K." Canadian Journal of Chemistry 83, no. 5 (2005): 499–504. http://dx.doi.org/10.1139/v05-082.

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The viscosities of the solutions of tetraethylammonium bromide (Et4NBr), tetrapropylammonium bromide (Pr4NBr), tetrabutylammonium bromide (Bu4NBr), tetrapentylammonium bromide (Pen4NBr), and tetraheptylammonium bromide (Hep4NBr) in 2-ethoxyethanol have been reported at 308.15, 313.15, 318.15, and 323.15 K. The viscosity data have been analyzed by the JonesDole equation for the associated electrolytes to evaluate the viscosity B coefficients of the electrolytes. These data have also been analyzed by the transition-state treatment to obtain the contribution of the solutes to the free energy of

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9

Rybakova, I. A., R. I. Shekhtman, and E. N. Prilezhaeva. "Synthesis of tetraalkylammonium thiolates." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, no. 9 (1991): 1903–5. http://dx.doi.org/10.1007/bf00960427.

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10

Holba, Vladislav. "Activity Coefficients and Gibbs Energies of Transfer of Tetraalkylammonium Dianilinetetraisothiocyanatochromates(III)." Collection of Czechoslovak Chemical Communications 59, no. 8 (1994): 1738–44. http://dx.doi.org/10.1135/cccc19941738.

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The solubilities of tetraalkylammonium dianilinetetraisothiocyanatochromates(III) (alkyl = methyl, ethyl, 1-propyl, and 1-butyl) in water, water - methanol, water - tert-butyl alcohol and water - acetonitrile solutions were measured at 25 °C. The results were used to evaluate the activity coefficients and Gibbs energies of transfer of the saturating salts from water to the mixed systems. The Gibbs energies of transfer of the [Cr(C6H5NH2)2(NCS)4]- ion were obtained by means of known ionic transfer functions for the tetraalkylammonium ions based on the TATB assumption.

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11

Bakhtin, S.G., and A.V. Charyarov. "SPECTROPHOTOMETRIC DETERMINATION OF THE CONCENTRATION AND NUCLEOPHILICITY OF QUATERNARY AMMONIUM AND PHOSPHONIUM SALTS BASED ON THE REACTION OF NUCLEOPHILIC OPENING OF THE EPOXIDE RING." Bulletin of Donetsk National University. Series А. Natural Sciences, no. 4 (December 3, 2024): 26–32. https://doi.org/10.5281/zenodo.14276568.

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A new spectrophotometric method for determining the content of tetraalkylammonium or phosphonium salts is proposed, based on the chromogenic S<sub>N</sub>2 reaction of oxirane ring opening in the systems "epoxide – salt R<sub>4</sub>N<sup>+</sup><strong>X</strong><sup>–</sup> or R<sub>4</sub>P<sup>+</sup><strong>X</strong><sup>–</sup> – proton donor reagent". Formal kinetic patterns of the epoxide ring opening reaction in the proposed systems are investigated. <strong><em>Keywords:</em></strong><strong> </strong>tetraalkylammonium, tetraalkylphosphonium, oxirane, epoxid

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12

Anand, Hardeep, and Renu Verma. "Viscometric and Conductometric Studies of Solvation Behaviour of Tetraalkylammonium Salts in the Binary Mixtures of Dimethylsulfoxide and Methanol at 298.15 K." Zeitschrift für Physikalische Chemie 233, no. 5 (2019): 737–53. http://dx.doi.org/10.1515/zpch-2017-1015.

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Abstract Molar conductance and viscosity of some tetraalkylammonium perchlorates (R4NClO4 where R = Methyl, Ethyl, Propyl, Butyl) have been measured in the concentration range (30–500) × 10−4 mol kg−1 at 298.15 K in the binary mixtures of dimethylsulfoxide (DMSO) + methanol (MeOH) containing 0, 20, 40, 50, 60, 80 and 100 mol% methanol. Conductance data has been analyzed using the Shedlovsky equation and the viscosity data by Jones-Dole equation. The limiting ionic conductances ($\lambda_{\pm}^{o}$) were used to calculate the solvated radii (ri) of the ions. The A and B coefficients of the Jone

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13

Clough, Matthew T., Karolin Geyer, Patricia A. Hunt, et al. "Azoniaspiro salts: towards bridging the gap between room-temperature ionic liquids and molten salts." Physical Chemistry Chemical Physics 18, no. 4 (2016): 3339–51. http://dx.doi.org/10.1039/c5cp07209c.

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14

Marin-Montesinos, I., J. C. Paniagua, M. Vilaseca, et al. "Self-assembled trityl radical capsules – implications for dynamic nuclear polarization." Physical Chemistry Chemical Physics 17, no. 8 (2015): 5785–94. http://dx.doi.org/10.1039/c4cp05225k.

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15

Lieffrig, Julien, Arnode G. Niassy, Olivier Jeannin, and Marc Fourmigué. "Halogen-bonded halide networks from chiral neutral spacers." CrystEngComm 17, no. 1 (2015): 50–57. http://dx.doi.org/10.1039/c4ce01935k.

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16

Emami, Marzieh, Katarzyna Anna Ślepokura, Monika Trzebiatowska, Nader Noshiranzadeh, and Vasyl Kinzhybalo. "Oxyanion clusters with antielectrostatic hydrogen bonding (AEHB) in tetraalkylammonium hypodiphosphates." CrystEngComm 20, no. 35 (2018): 5209–19. http://dx.doi.org/10.1039/c8ce00880a.

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17

Rahman, Shofiur, Ahmed Zein, Louise N. Dawe, Grigory Shamov, Pall Thordarson, and Paris E. Georghiou. "Supramolecular host–guest complexation of Lash's calix[4]azulene with tetraalkylammonium halides and tetrafluoroborate salts: binding and DFT computational studies." RSC Advances 5, no. 68 (2015): 54848–52. http://dx.doi.org/10.1039/c5ra07802d.

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18

Boudesocque, S., A. Mohamadou, L. Dupont, A. Martinez, and I. Déchamps. "Use of dicyanamide ionic liquids for extraction of metal ions." RSC Advances 6, no. 109 (2016): 107894–904. http://dx.doi.org/10.1039/c6ra18991a.

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19

Verma, Meenakshi, Kultar Singh, and Mandeep Singh Bakshi. "Surface active magnetic iron oxide nanoparticles for extracting metal nanoparticles across an aqueous–organic interface." Journal of Materials Chemistry C 7, no. 34 (2019): 10623–34. http://dx.doi.org/10.1039/c9tc03109j.

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20

Epand, Richard M., Robert J. B. Chen, and Kelli S. Robinson. "Tetraalkylammonium salts and phospholipid polymorphism." Journal of the American Chemical Society 111, no. 17 (1989): 6833–35. http://dx.doi.org/10.1021/ja00199a052.

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21

Jansson, Mikael, Angela Jönsson, Puyong Li, and Peter Stilbs. "Aggregation in tetraalkylammonium dodecanoate systems." Colloids and Surfaces 59 (November 1991): 387–97. http://dx.doi.org/10.1016/0166-6622(91)80261-l.

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22

Yushina, Irina, Boris Rudakov, Igor Krivtsov, and Ekaterina Bartashevich. "Thermal decomposition of tetraalkylammonium iodides." Journal of Thermal Analysis and Calorimetry 118, no. 1 (2014): 425–29. http://dx.doi.org/10.1007/s10973-014-3944-7.

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23

Kariv-Miller, Essie, and Vesna Svetličić. "Stoichiometry of a tetraalkylammonium “amalgam”." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 205, no. 1-2 (1986): 319–22. http://dx.doi.org/10.1016/0022-0728(86)90243-3.

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24

Kariv-Miller, Essie, and Phillip B. Lawin. "Tetraalkylammonium-lead: electrogeneration and stoichiometry." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 247, no. 1-2 (1988): 345–49. http://dx.doi.org/10.1016/0022-0728(88)80156-6.

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25

Stellwagen, Earle, and Nancy Stellwagen. "Interaction of Tetraalkylammonium+ and DNA." Biophysical Journal 110, no. 3 (2016): 562a—563a. http://dx.doi.org/10.1016/j.bpj.2015.11.3009.

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26

Dunwell, M., Junhua Wang, Y. Yan, and B. Xu. "Surface enhanced spectroscopic investigations of adsorption of cations on electrochemical interfaces." Physical Chemistry Chemical Physics 19, no. 2 (2017): 971–75. http://dx.doi.org/10.1039/c6cp07207k.

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27

Li, Jiaye, Haijin Zhu, Xiaoen Wang, Douglas R. MacFarlane, Michel Armand, and Maria Forsyth. "Increased ion conduction in dual cation [sodium][tetraalkylammonium] poly[4-styrenesulfonyl(trifluoromethylsulfonyl)imide-co-ethylacrylate] ionomers." Journal of Materials Chemistry A 3, no. 39 (2015): 19989–95. http://dx.doi.org/10.1039/c5ta04407c.

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28

Thielemann, Gabi, and Stefan Spange. "Polarity of tetraalkylammonium-based ionic liquids and related low temperature molten salts." New Journal of Chemistry 41, no. 16 (2017): 8561–67. http://dx.doi.org/10.1039/c7nj00443e.

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29

Pérez-Pérez, Jovana, Uvaldo Hernández-Balderas, Diego Martínez-Otero, and Vojtech Jancik. "Bifunctional silanol-based HBD catalysts for CO2 fixation into cyclic carbonates." New Journal of Chemistry 43, no. 47 (2019): 18525–33. http://dx.doi.org/10.1039/c9nj04840e.

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Unprecedented silanol-based bifunctional HBD catalysts with tetraalkylammonium units directly incorporated into their structures were prepared from tailor-made silanols and used in the preparation of cyclic carbonates.

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30

Cougnon, Charles, and Jacques Simonet. "Are tetraalkylammonium cations inserted into palladium cathodes? Formation of new palladium phases involving tetraalkylammonium halides." Journal of Electroanalytical Chemistry 507, no. 1-2 (2001): 226–33. http://dx.doi.org/10.1016/s0022-0728(01)00431-4.

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31

Molina-Muriel, Ricardo, J. Ramón Romero, Yifan Li, Gemma Aragay, and Pablo Ballester. "The effect of solvent on the binding of anions and ion-pairs with a neutral [2]rotaxane." Organic & Biomolecular Chemistry 19, no. 45 (2021): 9986–95. http://dx.doi.org/10.1039/d1ob01845k.

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32

Matsumoto, Kazuhiko, Ukyo Harinaga, Ryo Tanaka, Akira Koyama, Rika Hagiwara, and Katsuhiko Tsunashima. "The structural classification of the highly disordered crystal phases of [Nn][BF4], [Nn][PF6], [Pn][BF4], and [Pn][PF6] salts (Nn+ = tetraalkylammonium and Pn+ = tetraalkylphosphonium)." Phys. Chem. Chem. Phys. 16, no. 43 (2014): 23616–26. http://dx.doi.org/10.1039/c4cp03391d.

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33

Fernandez-Maestre, R., C. Wu, and H. H. Hill. "Separation of asparagine, valine and tetraethylammonium ions overlapping in an ion mobility spectrum by clustering with methanol introduced as a modifier into the buffer gas." Analytical Methods 7, no. 3 (2015): 863–69. http://dx.doi.org/10.1039/c4ay01814a.

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We introduced methanol into the buffer gas of an ion mobility spectrometer-mass spectrometer and mobilities changed depending on ion structures; baseline separation of valine, asparagine, and tetraalkylammonium ions was achieved.

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34

Dib, Eddy, Antoine Gimenez, Tzonka Mineva, and Bruno Alonso. "Preferential orientations of structure directing agents in zeolites." Dalton Transactions 44, no. 38 (2015): 16680–83. http://dx.doi.org/10.1039/c5dt02558c.

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The local structure of MFI-type zeolites is modified using asymmetric tetraalkylammonium structure directing agents R(Pr)<sub>3</sub>N<sup>+</sup> cations that adopt preferential orientations at the crossing between channels.

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35

Yamada, Shinji, Azusa Iwaoka, Yuka Fujita, and Seiji Tsuzuki. "Tetraalkylammonium-Templated Stereoselective Norrish–Yang Cyclization." Organic Letters 15, no. 23 (2013): 5994–97. http://dx.doi.org/10.1021/ol4028732.

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36

Abramov, Alexander A., Magomed S. A. Dzhigirkhanov, Yurii I. Matyunin, and Boris Z. Iofa. "Extraction of oxoanions by tetraalkylammonium salts." Mendeleev Communications 11, no. 3 (2001): 121–22. http://dx.doi.org/10.1070/mc2001v011n03abeh001443.

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37

Manin, N. G., A. V. Kustov, and O. A. Antonova. "Heat capacities of crystalline tetraalkylammonium salts." Russian Journal of Physical Chemistry A 86, no. 5 (2012): 878–80. http://dx.doi.org/10.1134/s0036024412050226.

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38

Gittleman, C. S., S. S. Lee, A. T. Bell, and C. J. Radke. "Zeolite synthesis from tetraalkylammonium silicate gels." Microporous Materials 3, no. 4-5 (1995): 511–30. http://dx.doi.org/10.1016/0927-6513(94)00062-z.

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39

Su, Yuan, Debra J. Searles, and Liguang Wang. "Semiclathrate hydrates of methane + tetraalkylammonium hydroxides." Fuel 203 (September 2017): 618–26. http://dx.doi.org/10.1016/j.fuel.2017.05.005.

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40

German, K. E., S. V. Krjuchkov, L. I. Belyaeva, and V. I. Spitsyn. "Ion association in tetraalkylammonium pertechnetate solutions." Journal of Radioanalytical and Nuclear Chemistry Articles 121, no. 2 (1988): 515–21. http://dx.doi.org/10.1007/bf02041440.

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41

Shirakawa, Seiji, Shiyao Liu, Shiho Kaneko, et al. "Tetraalkylammonium Salts as Hydrogen-Bonding Catalysts." Angewandte Chemie International Edition 54, no. 52 (2015): 15767–70. http://dx.doi.org/10.1002/anie.201508659.

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42

Shirakawa, Seiji, Shiyao Liu, Shiho Kaneko, et al. "Tetraalkylammonium Salts as Hydrogen-Bonding Catalysts." Angewandte Chemie 127, no. 52 (2015): 15993–96. http://dx.doi.org/10.1002/ange.201508659.

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43

Guncheva, Maya, Momtchil Dimitrov, Paula Ossowicz, and Ewa Janus. "Tetraalkylammonium acetates and tetraalkylammonium tetrafluoroborates as new templates for room-temperature synthesis of mesoporous silica spheres." Journal of Porous Materials 25, no. 3 (2017): 935–43. http://dx.doi.org/10.1007/s10934-017-0505-z.

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44

Tayama, Eiji, Noriko Naganuma, Hajime Iwamoto, and Eietsu Hasegawa. "Double axial chirality promoted asymmetric [2,3] Stevens rearrangement of N-cinnamyl l-alanine amide-derived ammonium ylides." Chem. Commun. 50, no. 52 (2014): 6860–62. http://dx.doi.org/10.1039/c4cc02536a.

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The base-induced asymmetric [2,3] Stevens rearrangement of N-cinnamyl tetraalkylammonium ylides derived from l-alanine amides proceeds via a double axially chiral intermediate to afford the corresponding α-substituted alanine derivatives with high enantio- and diastereoselectivities.

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45

Lima, Thamires A., Vitor H. Paschoal, Rafael S. Freitas, et al. "An inelastic neutron scattering, Raman, far-infrared, and molecular dynamics study of the intermolecular dynamics of two ionic liquids." Physical Chemistry Chemical Physics 22, no. 16 (2020): 9074–85. http://dx.doi.org/10.1039/d0cp00374c.

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The THz dynamics of ionic liquids based on tetraalkylammonium cations were investigated by a combined usage of inelastic neutron scattering (INS), Raman, and far-infrared (FIR) spectroscopies and the power spectrum calculated by molecular dynamics (MD) simulations.

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46

Mitsudo, Koichi, Kazuki Yoshioka, Takayuki Hirata, Hiroki Mandai, Koji Midorikawa, and Seiji Suga. "1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides." Synlett 30, no. 10 (2019): 1209–14. http://dx.doi.org/10.1055/s-0037-1611793.

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A 1,10-phenanthroline-promoted cyanation of aryl iodides has been developed. 1,10-Phenanthroline worked as an organocatalyst for the reaction of aryl iodides with tetraalkylammonium cyanide to afford aryl cyanides. A similar reaction occurred through an electroreductive process.

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47

S., K. SANYAL, and S. BANDYOPADHYAY (Miss). "Isothermal Diffusion Coefficient of Tetraalkylammonium Salts in Aqueous Solutions." Journal of Indian Chemical Society Vol. 64, Aug 1987 (1987): 511–13. https://doi.org/10.5281/zenodo.6216386.

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Department of Agricultural Chemistry and Soil Science, Bidhan Chandra Krishi Viswavidyalaya, Kalyani-741 235 <em>Manuscript received 27 January 1986, revised 12 January 1987, accepted 6 July 1987</em> Isothermal Diffusion Coefficient of Tetraalkylammonium Salts in Aqueous Solutions.

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48

P., K. BlSWAS, LAHIRI S.C., and P. DEY B. "lon-Solvent Interactions : Conductance Studies of Tetraalkylammonium Ions in Ethanol+ Water Mixtures." Journal of Indian Chemical Society Vol. 70, Feb 1993 (1993): 125–93. https://doi.org/10.5281/zenodo.5910595.

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United Bank of India, 507 R. B. C. Road, Garifa, North 24-Parganas Department of Chemistry, University of Kalyani, Kalyani-741 235 Department of Chemistry, Vivekananda Mission Mahavidyalaya, Viveknagar, P.O. Chaitanyapur (Haldia)-721 645 <em>Manuscript received 9 June 1992, revised 22 October 1992, accepted 2 December 1992</em> ln order to understand the nature of ion-solvent interactions and structural changes of the solvent mixtures associated with the addition of ions, conductance measurements of the tetraalkylammonium halides in ethanol + water mixtures  were made. The resul

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49

Nakano, Shu-ichi, Hirofumi Yamashita, Kazuya Tanabe, and Naoki Sugimoto. "Bulky cations greatly increase the turnover of a native hammerhead ribozyme." RSC Advances 9, no. 61 (2019): 35820–24. http://dx.doi.org/10.1039/c9ra06797c.

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Large tetraalkylammonium ions increase the turnover rate of the ribozyme derived from an intronic ribozyme in the human genome. The rate can be enhanced by more than a hundred-fold at the optimal concentrations of Mg<sup>2+</sup> and TPeA ions.

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50

Ali, Rana Faryad, Irene Andreu, and Byron D. Gates. "Green solvent assisted synthesis of cesium bismuth halide perovskite nanocrystals and the influences of slow and fast anion exchange rates." Nanoscale Advances 1, no. 11 (2019): 4442–49. http://dx.doi.org/10.1039/c9na00586b.

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Halide perovskite nanocrystals of cesium bismuth iodide (Cs<sub>3</sub>Bi<sub>2</sub>I<sub>9</sub>) were prepared by a facile sonication-assisted method using a green solvent. The photoluminescence properties were tuned by anion exchange with tetraalkylammonium halides.

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