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Thematische Bibliographien / Tetraalkylammonium / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Tetraalkylammonium“

Autor: Grafiati

Veröffentlicht am 18. Mai 2024

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1

Schwendt, P., J. Chrappová und K. Lišcák. „Tetraalkylammonium fluorooxoperoxovanadates“. Monatshefte für Chemie Chemical Monthly 128, Nr. 4 (April 1997): 317–22. http://dx.doi.org/10.1007/bf00810768.

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2

Kulapina, E. G., E. S. Pogorelova, N. M. Makarova und L. A. Bazhanova. „Physicochemical properties of tetraalkylammonium tetraphenylborates and tetraalkylammonium dodecylsulfates“. Russian Journal of Inorganic Chemistry 58, Nr. 1 (Januar 2013): 112–16. http://dx.doi.org/10.1134/s0036023613010129.

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3

Perez-Tejeda, P., A. Maestre, P. Delgado-Cobos und J. Burgess. „Single-ion Setschenow coefficients for several hydrophobic non-electrolytes in aqueous electrolyte solutions“. Canadian Journal of Chemistry 68, Nr. 2 (01.02.1990): 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 into 1,2-dichloroethane. Keywords: solubilities, aqueous salt solutions, Setschenow coefficients.

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4

Anastasio, Paola, Tiziana Del Giacco, Raimondo Germani, Nicoletta Spreti und 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, Nr. 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 TiO₂photocatalyzed degradation of Alizarin Red-S under UV light irradiation.

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5

Duan, Erhong, Peng Zhang, Kun Yang, Weizhao Liang, Meiting Yu, Sheng Wang und Jianrui Niu. „Effect of alkyl and halide moieties on the absorption and stratification of SO2 in tetrabutylammonium halide aqueous solutions“. RSC Advances 6, Nr. 60 (2016): 55401–5. http://dx.doi.org/10.1039/c6ra05677f.

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To explore the interactions between SO₂ and tetraalkylammonium halide, the effects of temperature, concentration, length of alkyl chain, and halide anion on the solubility of SO₂ in tetraalkylammonium halide aqueous solutions were investigated.

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6

Rowland, Clare E., Mercouri G. Kanatzidis und L. Soderholm. „Tetraalkylammonium Uranyl Isothiocyanates“. Inorganic Chemistry 51, Nr. 21 (16.10.2012): 11798–804. http://dx.doi.org/10.1021/ic301741u.

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7

Rybakova, I. A., R. I. Shekhtman und E. N. Prilezhaeva. „Synthesis of tetraalkylammonium thiolates“. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, Nr. 9 (September 1991): 1903–5. http://dx.doi.org/10.1007/bf00960427.

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8

Haldar, Purushottam, und Bijan Das. „Conductometric Study of Some Tetraalkylammonium Bromides in 2-Ethoxyethanol in the Temperature Range 35–50 °C“. Zeitschrift für Physikalische Chemie 218, Nr. 9 (01.09.2004): 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 also been estimated. Appreciable ionic association was observed for all of these electrolytes in 2-ethoxyethanol. The tetraalkylammonium ions (R4N+) were found to remain scarcely solvated in the present solvent medium within the temperature range investigated here. The solvation of the bromide ion in these tetraalkylammonium bromide is found to be weakened as soon as the ion-pairs are formed. An increase in the temperature results in a lower level of ion-pairing for each of these salts.

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9

Haldar, Purushottam, und 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, Nr. 5 (01.05.2005): 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 activation for viscous flow of the solution. The viscosity of the solvent is found to be greatly modified by the presence of all of the tetraalkylammonium ions investigated. Moreover, the tetraalkylammonium ions are found to be unsolvated in 2-ethoxyethanol solutions, they behave neither as structure-breaker nor as structure-maker and the formation of the transition state is made less favorable in their presence.Key words: viscosity, electrolytes, tetraalkylammonium ion, 2-ethoxyethanol, ionic contribution, solvation, transition-state treatment.

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10

Holba, Vladislav. „Activity Coefficients and Gibbs Energies of Transfer of Tetraalkylammonium Dianilinetetraisothiocyanatochromates(III)“. Collection of Czechoslovak Chemical Communications 59, Nr. 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

Anand, Hardeep, und 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, Nr. 5 (27.05.2019): 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 Jones-Dole equation are positive in all salts. The A coefficients are in reasonable good agreement with the limiting theoretical values (Aη) calculated using Falkenhagen-Vernon equation. The variation of the ionic B± coefficients as well as the actual solvated radii (ri) with solvent composition in DMSO + MeOH mixtures show the preferential solvation of tetraalkylammonium ions by MeOH and MeOH-rich region of the mixtures. The tetraalkylammonium ions exhibit solvation in the order Me4N+ > Et4N+ > Pr4N+ > Bu4N+.

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12

Clough, Matthew T., Karolin Geyer, Patricia A. Hunt, Alastair J. S. McIntosh, Rebecca Rowe, Tom Welton und Andrew J. P. White. „Azoniaspiro salts: towards bridging the gap between room-temperature ionic liquids and molten salts“. Physical Chemistry Chemical Physics 18, Nr. 4 (2016): 3339–51. http://dx.doi.org/10.1039/c5cp07209c.

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13

Epand, Richard M., Robert J. B. Chen und Kelli S. Robinson. „Tetraalkylammonium salts and phospholipid polymorphism“. Journal of the American Chemical Society 111, Nr. 17 (August 1989): 6833–35. http://dx.doi.org/10.1021/ja00199a052.

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14

Jansson, Mikael, Angela Jönsson, Puyong Li und 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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15

Yushina, Irina, Boris Rudakov, Igor Krivtsov und Ekaterina Bartashevich. „Thermal decomposition of tetraalkylammonium iodides“. Journal of Thermal Analysis and Calorimetry 118, Nr. 1 (23.07.2014): 425–29. http://dx.doi.org/10.1007/s10973-014-3944-7.

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16

Kariv-Miller, Essie, und Vesna Svetličić. „Stoichiometry of a tetraalkylammonium “amalgam”“. Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 205, Nr. 1-2 (Juni 1986): 319–22. http://dx.doi.org/10.1016/0022-0728(86)90243-3.

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17

Kariv-Miller, Essie, und Phillip B. Lawin. „Tetraalkylammonium-lead: electrogeneration and stoichiometry“. Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 247, Nr. 1-2 (Juni 1988): 345–49. http://dx.doi.org/10.1016/0022-0728(88)80156-6.

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18

Stellwagen, Earle, und Nancy Stellwagen. „Interaction of Tetraalkylammonium+ and DNA“. Biophysical Journal 110, Nr. 3 (Februar 2016): 562a—563a. http://dx.doi.org/10.1016/j.bpj.2015.11.3009.

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19

Marin-Montesinos, I., J. C. Paniagua, M. Vilaseca, A. Urtizberea, F. Luis, M. Feliz, F. Lin, S. Van Doorslaer und M. Pons. „Self-assembled trityl radical capsules – implications for dynamic nuclear polarization“. Physical Chemistry Chemical Physics 17, Nr. 8 (2015): 5785–94. http://dx.doi.org/10.1039/c4cp05225k.

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20

Lieffrig, Julien, Arnode G. Niassy, Olivier Jeannin und Marc Fourmigué. „Halogen-bonded halide networks from chiral neutral spacers“. CrystEngComm 17, Nr. 1 (2015): 50–57. http://dx.doi.org/10.1039/c4ce01935k.

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21

Emami, Marzieh, Katarzyna Anna Ślepokura, Monika Trzebiatowska, Nader Noshiranzadeh und Vasyl Kinzhybalo. „Oxyanion clusters with antielectrostatic hydrogen bonding (AEHB) in tetraalkylammonium hypodiphosphates“. CrystEngComm 20, Nr. 35 (2018): 5209–19. http://dx.doi.org/10.1039/c8ce00880a.

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22

Rahman, Shofiur, Ahmed Zein, Louise N. Dawe, Grigory Shamov, Pall Thordarson und 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, Nr. 68 (2015): 54848–52. http://dx.doi.org/10.1039/c5ra07802d.

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23

Boudesocque, S., A. Mohamadou, L. Dupont, A. Martinez und I. Déchamps. „Use of dicyanamide ionic liquids for extraction of metal ions“. RSC Advances 6, Nr. 109 (2016): 107894–904. http://dx.doi.org/10.1039/c6ra18991a.

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24

Verma, Meenakshi, Kultar Singh und Mandeep Singh Bakshi. „Surface active magnetic iron oxide nanoparticles for extracting metal nanoparticles across an aqueous–organic interface“. Journal of Materials Chemistry C 7, Nr. 34 (2019): 10623–34. http://dx.doi.org/10.1039/c9tc03109j.

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25

Dunwell, M., Junhua Wang, Y. Yan und B. Xu. „Surface enhanced spectroscopic investigations of adsorption of cations on electrochemical interfaces“. Physical Chemistry Chemical Physics 19, Nr. 2 (2017): 971–75. http://dx.doi.org/10.1039/c6cp07207k.

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26

Li, Jiaye, Haijin Zhu, Xiaoen Wang, Douglas R. MacFarlane, Michel Armand und Maria Forsyth. „Increased ion conduction in dual cation [sodium][tetraalkylammonium] poly[4-styrenesulfonyl(trifluoromethylsulfonyl)imide-co-ethylacrylate] ionomers“. Journal of Materials Chemistry A 3, Nr. 39 (2015): 19989–95. http://dx.doi.org/10.1039/c5ta04407c.

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27

Thielemann, Gabi, und Stefan Spange. „Polarity of tetraalkylammonium-based ionic liquids and related low temperature molten salts“. New Journal of Chemistry 41, Nr. 16 (2017): 8561–67. http://dx.doi.org/10.1039/c7nj00443e.

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28

Pérez-Pérez, Jovana, Uvaldo Hernández-Balderas, Diego Martínez-Otero und Vojtech Jancik. „Bifunctional silanol-based HBD catalysts for CO2 fixation into cyclic carbonates“. New Journal of Chemistry 43, Nr. 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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29

Cougnon, Charles, und Jacques Simonet. „Are tetraalkylammonium cations inserted into palladium cathodes? Formation of new palladium phases involving tetraalkylammonium halides“. Journal of Electroanalytical Chemistry 507, Nr. 1-2 (Juli 2001): 226–33. http://dx.doi.org/10.1016/s0022-0728(01)00431-4.

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30

Molina-Muriel, Ricardo, J. Ramón Romero, Yifan Li, Gemma Aragay und Pablo Ballester. „The effect of solvent on the binding of anions and ion-pairs with a neutral [2]rotaxane“. Organic & Biomolecular Chemistry 19, Nr. 45 (2021): 9986–95. http://dx.doi.org/10.1039/d1ob01845k.

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31

Matsumoto, Kazuhiko, Ukyo Harinaga, Ryo Tanaka, Akira Koyama, Rika Hagiwara und 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, Nr. 43 (2014): 23616–26. http://dx.doi.org/10.1039/c4cp03391d.

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32

Fernandez-Maestre, R., C. Wu und 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, Nr. 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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33

Dib, Eddy, Antoine Gimenez, Tzonka Mineva und Bruno Alonso. „Preferential orientations of structure directing agents in zeolites“. Dalton Transactions 44, Nr. 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)₃N⁺ cations that adopt preferential orientations at the crossing between channels.

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34

Yamada, Shinji, Azusa Iwaoka, Yuka Fujita und Seiji Tsuzuki. „Tetraalkylammonium-Templated Stereoselective Norrish–Yang Cyclization“. Organic Letters 15, Nr. 23 (13.11.2013): 5994–97. http://dx.doi.org/10.1021/ol4028732.

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35

Abramov, Alexander A., Magomed S. A. Dzhigirkhanov, Yurii I. Matyunin und Boris Z. Iofa. „Extraction of oxoanions by tetraalkylammonium salts“. Mendeleev Communications 11, Nr. 3 (Januar 2001): 121–22. http://dx.doi.org/10.1070/mc2001v011n03abeh001443.

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36

Manin, N. G., A. V. Kustov und O. A. Antonova. „Heat capacities of crystalline tetraalkylammonium salts“. Russian Journal of Physical Chemistry A 86, Nr. 5 (04.04.2012): 878–80. http://dx.doi.org/10.1134/s0036024412050226.

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37

Gittleman, C. S., S. S. Lee, A. T. Bell und C. J. Radke. „Zeolite synthesis from tetraalkylammonium silicate gels“. Microporous Materials 3, Nr. 4-5 (Januar 1995): 511–30. http://dx.doi.org/10.1016/0927-6513(94)00062-z.

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38

Su, Yuan, Debra J. Searles und 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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39

German, K. E., S. V. Krjuchkov, L. I. Belyaeva und V. I. Spitsyn. „Ion association in tetraalkylammonium pertechnetate solutions“. Journal of Radioanalytical and Nuclear Chemistry Articles 121, Nr. 2 (April 1988): 515–21. http://dx.doi.org/10.1007/bf02041440.

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40

Shirakawa, Seiji, Shiyao Liu, Shiho Kaneko, Yusuke Kumatabara, Airi Fukuda, Yumi Omagari und Keiji Maruoka. „Tetraalkylammonium Salts as Hydrogen-Bonding Catalysts“. Angewandte Chemie International Edition 54, Nr. 52 (13.11.2015): 15767–70. http://dx.doi.org/10.1002/anie.201508659.

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41

Shirakawa, Seiji, Shiyao Liu, Shiho Kaneko, Yusuke Kumatabara, Airi Fukuda, Yumi Omagari und Keiji Maruoka. „Tetraalkylammonium Salts as Hydrogen-Bonding Catalysts“. Angewandte Chemie 127, Nr. 52 (13.11.2015): 15993–96. http://dx.doi.org/10.1002/ange.201508659.

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42

Guncheva, Maya, Momtchil Dimitrov, Paula Ossowicz und Ewa Janus. „Tetraalkylammonium acetates and tetraalkylammonium tetrafluoroborates as new templates for room-temperature synthesis of mesoporous silica spheres“. Journal of Porous Materials 25, Nr. 3 (12.09.2017): 935–43. http://dx.doi.org/10.1007/s10934-017-0505-z.

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43

Tayama, Eiji, Noriko Naganuma, Hajime Iwamoto und Eietsu Hasegawa. „Double axial chirality promoted asymmetric [2,3] Stevens rearrangement of N-cinnamyl l-alanine amide-derived ammonium ylides“. Chem. Commun. 50, Nr. 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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44

Lima, Thamires A., Vitor H. Paschoal, Rafael S. Freitas, Luiz F. O. Faria, Zhixia Li, Madhusudan Tyagi, Y. Z und Mauro C. C. Ribeiro. „An inelastic neutron scattering, Raman, far-infrared, and molecular dynamics study of the intermolecular dynamics of two ionic liquids“. Physical Chemistry Chemical Physics 22, Nr. 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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45

Mitsudo, Koichi, Kazuki Yoshioka, Takayuki Hirata, Hiroki Mandai, Koji Midorikawa und Seiji Suga. „1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides“. Synlett 30, Nr. 10 (11.04.2019): 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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46

Nakano, Shu-ichi, Hirofumi Yamashita, Kazuya Tanabe und Naoki Sugimoto. „Bulky cations greatly increase the turnover of a native hammerhead ribozyme“. RSC Advances 9, Nr. 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 Mg²⁺ and TPeA ions.

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47

Ali, Rana Faryad, Irene Andreu und 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, Nr. 11 (2019): 4442–49. http://dx.doi.org/10.1039/c9na00586b.

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Halide perovskite nanocrystals of cesium bismuth iodide (Cs₃Bi₂I₉) 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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48

Popr, Martin, Simona Hybelbauerová und Jindřich Jindřich. „A complete series of 6-deoxy-monosubstituted tetraalkylammonium derivatives of α-, β-, and γ-cyclodextrin with 1, 2, and 3 permanent positive charges“. Beilstein Journal of Organic Chemistry 10 (18.06.2014): 1390–96. http://dx.doi.org/10.3762/bjoc.10.142.

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An efficient synthetic route toward the preparation of a complete series of monosubstituted tetraalkylammonium cyclodextrin (CD) derivatives is presented. Monotosylation of native CDs (α-, β-, γ-) at position 6 gave the starting material. Reaction of monotosylate (mono-Ts-CD) with 45% aqueous trimethylamine gave CDs substituted with one cationic functional group in a single step. Derivatives equipped with a substituent containing two cationic sites separated by an ethylene or a propylene linker were prepared by reacting mono-Ts-CD with neat N,N,N’-trimethylethane-1,2-diamine or N,N,N’-trimethylpropane-1,3-diamine and subsequent methylation by CH3I in good yields. Finally, analogues bearing a moiety with three tetraalkylammonium sites were synthesized by reacting mono-Ts-CD with bis(3-aminopropyl)amine and subsequent methylation. The majority of the presented reactions are very straightforward with a simple work-up, which avoids the need of chromatographic separation. Thus, these reactions are suitable for the multigram-scale production of monosubstituted cationic CDs.

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Журавлев, Олег Евгеньевич, Глеб Сергеевич Юлмасов, Екатерина Сергеевна Суратова, Дарья Валерьевна Горбунова und Людмила Ивановна Ворончихина. „SYNTHESIS OF AMMONIUM IONIC LIQUIDS AND STUDY OF THE ELECTRICAL CONDUCTIVITY OF THEIR SOLUTIONS IN ACETONITRILE“. Вестник Тверского государственного университета. Серия: Химия, Nr. 2(44) (25.06.2021): 123–30. http://dx.doi.org/10.26456/vtchem2021.2.12.

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Авторами работы получены ионные жидкости с катионом тетраалкиламмония и неорганическими анионами. Проведены исследования электропроводности их растворов в ацетонитриле. The authors of the work obtained ionic liquids with tetraalkylammonium cation and inorganic anions. Studies of the electrical conductivity of their solutions in acetonitrile have been carried out.

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Mikhailovskaya, A. P., A. S. Grishchuk, I. V. Elokhin und S. S. Lysova. „SORPTION OF TETRAALKYLAMMONIUM HALIDES ON CELLULOSE CRYSTALLITES“. Izvestiya vysshikh uchebnykh zavedenii Tekhnologiya legkoi promyshlennosti 53, Nr. 3 (2021): 92–95. http://dx.doi.org/10.46418/0021-3489_2021_53_03_20.

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