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Journal articles on the topic 'Fluorinated stationary phases'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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1

Yang, Shenyuan, Lisa F. Resotko Kruk, and Morteza G. Khaledi. "Fluorinated bonded stationary phases in micellar liquid chromatography." Journal of Chromatography A 664, no. 1 (1994): 1–11. http://dx.doi.org/10.1016/0021-9673(94)80622-5.

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2

Pomaville, Rena M., and Colin F. Poole. "Thermally stable, highly fluorinated stationary phases for gas chromatography." Analytica Chimica Acta 200 (1987): 151–69. http://dx.doi.org/10.1016/s0003-2670(00)83766-6.

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3

Pesek, Joseph J., Maria T. Matyska, and Kavita V. Prajapati. "Synthesis and evaluation of silica hydride-based fluorinated stationary phases." Journal of Separation Science 33, no. 19 (2010): 2908–16. http://dx.doi.org/10.1002/jssc.201000302.

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4

Bacalum, Elena, and Mihaela Cheregi. "Recent analytical applications of fluorinated hydrocarbon-based stationary phases in HPLC." Journal of Liquid Chromatography & Related Technologies 40, no. 2 (2017): 59–68. http://dx.doi.org/10.1080/10826076.2017.1284676.

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5

de Miguel, I., S. Exbrayat, and D. Samain. "Study of the selective retention of fluorinated compounds on perfluorinated stationary phases." Chromatographia 24, no. 1 (1987): 849–53. http://dx.doi.org/10.1007/bf02688597.

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6

Krafft, Marie Pierre, Francois Jeannaux, Maurice Le Blanc, Jean G. Riess, and Alain Berthod. "Highly fluorinated stationary phases for analysis for polyfluorinated solutes by reversed-phase high-performance liquid chromatography." Analytical Chemistry 60, no. 18 (1988): 1969–72. http://dx.doi.org/10.1021/ac00169a026.

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7

Regalado, Erik L., Alexey A. Makarov, Ray McClain, Matthew Przybyciel, and Christopher J. Welch. "Search for improved fluorinated stationary phases for separation of fluorine-containing pharmaceuticals from their desfluoro analogs." Journal of Chromatography A 1380 (February 2015): 45–54. http://dx.doi.org/10.1016/j.chroma.2014.12.025.

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8

Berthod, A., J. Serpinet, M. Traore, et al. "Preparation and evaluation of highly fluorinated stationary phases in the HPLC analysis of poly- or perfluorinated derivatives." Journal of Fluorine Chemistry 35, no. 1 (1987): 261. http://dx.doi.org/10.1016/0022-1139(87)95202-x.

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9

Scully, Norma M., Liam O. Healy, Tom O’Mahony, Jeremy D. Glennon, Benjamin Dietrich, and Klaus Albert. "Effect of silane reagent functionality for fluorinated alkyl and phenyl silica bonded stationary phases prepared in supercritical carbon dioxide." Journal of Chromatography A 1191, no. 1-2 (2008): 99–107. http://dx.doi.org/10.1016/j.chroma.2008.02.052.

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10

Shearer, Justin W., Lunhan Ding, and Susan V. Olesik. "Solvation parameter models for retention on perfluorinated and fluorinated low temperature glassy carbon stationary phases in reversed-phase liquid chromatography." Journal of Chromatography A 1141, no. 1 (2007): 73–80. http://dx.doi.org/10.1016/j.chroma.2006.12.003.

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11

Lajkó, Gyula, Tímea Orosz, Lóránd Kiss та ін. "High-performance liquid chromatographic enantioseparation of fluorinated cyclicβ3-amino acid derivatives on polysaccharide-based chiral stationary phases. Comparison with nonfluorinated counterparts". Biomedical Chromatography 30, № 9 (2016): 1441–48. http://dx.doi.org/10.1002/bmc.3702.

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12

Peluso, Paola, Alessandro Dessì, Roberto Dallocchio, et al. "Enantioseparation of 5,5′-Dibromo-2,2′-dichloro-3-selanyl-4,4′-bipyridines on Polysaccharide-Based Chiral Stationary Phases: Exploring Chalcogen Bonds in Liquid-Phase Chromatography." Molecules 26, no. 1 (2021): 221. http://dx.doi.org/10.3390/molecules26010221.

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Abstract:
The chalcogen bond (ChB) is a noncovalent interaction based on electrophilic features of regions of electron charge density depletion (σ-holes) located on bound atoms of group VI. The σ-holes of sulfur and heavy chalcogen atoms (Se, Te) (donors) can interact through their positive electrostatic potential (V) with nucleophilic partners such as lone pairs, π-clouds, and anions (acceptors). In the last few years, promising applications of ChBs in catalysis, crystal engineering, molecular biology, and supramolecular chemistry have been reported. Recently, we explored the high-performance liquid ch
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13

Boichenko, Alexander P., Natalia Govorukhina, Ate G. J. van der Zee, and Rainer Bischoff. "Multidimensional separation of tryptic peptides from human serum proteins using reversed-phase, strong cation exchange, weak anion exchange, and fused-core fluorinated stationary phases." Journal of Separation Science 36, no. 21-22 (2013): 3463–70. http://dx.doi.org/10.1002/jssc.201300750.

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14

Ciogli, Alessia, Patrizia Simone, Claudio Villani, et al. "Revealing the Fine Details of Functionalized Silica Surfaces by Solid-State NMR and Adsorption Isotherm Measurements: The Case of Fluorinated Stationary Phases for Liquid Chromatography." Chemistry - A European Journal 20, no. 26 (2014): 8138–48. http://dx.doi.org/10.1002/chem.201304330.

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15

Jankech, Timotej, Dominika Pindjakova, Jiri Kos, Milan Hutta, and Josef Jampilek. "Preparation and Hydro-Lipophilic Properties of Novel Fluorinated Benzyl Carbamates of 4-Aminosalicylanilides." Chemistry Proceedings 3, no. 1 (2020): 32. http://dx.doi.org/10.3390/ecsoc-24-08094.

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A series of seven fluorinated benzyl carbamates of 4-aminosalicylanilides and unsubstituted benzyl [3-hydroxy-4-(phenylcarbamoyl)phenyl]carbamate designed as agents with the expected anticholinesterase and anti-inflammatory activity were prepared and characterized. As lipophilicity significantly influences the biological activity of compounds, the hydro-lipophilic properties of these mono-, di-, and tri-substituted carbamates were investigated in this study. All the discussed derivatives of 4-{[(benzyloxy)carbonyl]amino}-2-hydroxybenzoic acid were analyzed using reversed-phase high performance
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16

Sudarkova, Svetlana M., Viktor E. Khinevich, Ilya N. Ioffe, Martin Quick, and Sergey A. Kovalenko. "Substitution pattern dependent behavior of the singlet excited states in symmetrically fluorinated biphenyls." Physical Chemistry Chemical Physics, 2021. http://dx.doi.org/10.1039/d1cp03560f.

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We report stationary and ultrafast solution-phase spectra for symmetric biphenyls: pristine biphenyl (bP0), 4,4'-difluorobiphenyl (bP2), 2,3,5,6,2',3',5',6'-octafluorobiphenyl (bP8), and perfluorobiphenyl (bP10). Initial excitation to the S3 state in bP0 and bP2,...
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