2014
DOI: 10.1007/s10337-014-2675-z
|View full text |Cite
|
Sign up to set email alerts
|

Separation of Isomers on Nematic Liquid Crystal Stationary Phases in Gas Chromatography: A Review

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
13
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 19 publications
(13 citation statements)
references
References 44 publications
0
13
0
Order By: Relevance
“…To date, a large number of LCSPs have been synthesized, and the structural requirements for giving liquid crystalline phases have generally been well understood [25][26][27][28].…”
Section: Development Of Nematic Liquidmentioning
confidence: 99%
See 1 more Smart Citation
“…To date, a large number of LCSPs have been synthesized, and the structural requirements for giving liquid crystalline phases have generally been well understood [25][26][27][28].…”
Section: Development Of Nematic Liquidmentioning
confidence: 99%
“…Recently, we have reviewed a comparative analytical study for the separation of isomers on nematic LCSPs [28].…”
Section: Separation Techniquementioning
confidence: 99%
“…It is known that terminally substituted compounds exhibited more stable mesophase compared to unsubstituted mesogenic compounds and that a para-substituted phenyl ring ensures that the molecules have structural linearity and large molecular polarizability [43]. The effect of terminal substituents on mesophase stability and analytical behaviors has been studied quite extensively for nematic liquid crystals [31,35,36]. Terminal substituents are many and varied, including either a small polar substituent (cyano, nitro, halogen, etc.)…”
Section: Introductionmentioning
confidence: 99%
“…These unique solvent properties of liquid crystals were reported for the first time by Kelker [7] and by Dewar and Schroeder [8,9] and were initially applied to the separation of the positional isomers of various disubstituted benzenes. Since this pioneering work, a large number of publications describe the analytical performance of liquid crystals [10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26] and several reviews outlining the fundamentals and applications of liquid crystal stationary phases (LCSPs) in both packed and capillary columns are available [27][28][29][30][31][32][33][34][35][36]. Up to now, the results of the studies on LCSPs indicate that the chromatographic behavior of liquid crystals is basically dependent on its molecular structure in which a slight change in the molecular geometry brings about considerable change in its thermal and analytical properties.…”
Section: Introductionmentioning
confidence: 99%
“…Since the introduction of their use in gas chromatography (GC) [1], liquid-crystalline (mesogenic) materials have been widely studied and used in various research fields [2]. Their applications as stationary phases in chromatographic analyses (GC and high-performance liquid chromatography) have attracted much attention, and they have been used in the separation of toxic isomers of compounds in the environment [3][4][5].…”
Section: Introductionmentioning
confidence: 99%