2010
DOI: 10.1016/j.chroma.2009.11.052
|View full text |Cite
|
Sign up to set email alerts
|

Characterization of 1,3-alternate calix[4]arene-silica bonded stationary phases and their comparison to selected commercial columns by using principal component analysis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2

Citation Types

0
17
0

Year Published

2010
2010
2015
2015

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 24 publications
(17 citation statements)
references
References 29 publications
0
17
0
Order By: Relevance
“…With increasing electron deficiency in the phenyl rings as a consequence of the presence of electron-withdrawing groups like Cl, NO 2 and F, the aromatic selectivity parameters increased. As a general behavior, hydrophobic retention capacity of the studied stationary phases was found to be lower than that of C18 [70]. In another study of the same research group, retention behavior of some polyaromatic hydrocarbons was studied on some of the above mentioned 1,3-alternate calix [4]arene-silica bonded stationary phases.…”
Section: High Performance Liquid Chromatographymentioning
confidence: 93%
See 1 more Smart Citation
“…With increasing electron deficiency in the phenyl rings as a consequence of the presence of electron-withdrawing groups like Cl, NO 2 and F, the aromatic selectivity parameters increased. As a general behavior, hydrophobic retention capacity of the studied stationary phases was found to be lower than that of C18 [70]. In another study of the same research group, retention behavior of some polyaromatic hydrocarbons was studied on some of the above mentioned 1,3-alternate calix [4]arene-silica bonded stationary phases.…”
Section: High Performance Liquid Chromatographymentioning
confidence: 93%
“…The results, again, emphasized the importance of the chemistry of the functionalities on the studied calixarene. However, it is difficult to relate the retention behavior of the studied analyte on the studied calixarenebonded stationary phases with a unique interaction mechanism [70].…”
Section: High Performance Liquid Chromatographymentioning
confidence: 99%
“…They showed that naphthylamines and naphthols gave comparatively weaker retention on the ODS than on the calixarene columns. This means that there were additional interactions with the exception of the hydrophobic Sliwka-Kaszynska et al [127] used six aspects, including surface coverage, hydrophobic selectivity, aromatic selectivity, shape selectivity, hydrogen bonding capacity and ion-exchange capacity, to study 12 calix [4]arene stationary phases (Fig. 8), which had been synthesized before by them.…”
Section: Lc Stationary Phases For Molecular Recognitionmentioning
confidence: 99%
“…The calixarene phases had significant differences in hydrogen bonding capacities, which did not correspond to the degree of their surface coverage. CalixBn, CalixBzF 5 , CalixBph and CalixBnOMe columns exhibited the highest total silanol activity among calixarene phases [127].…”
Section: Lc Stationary Phases For Molecular Recognitionmentioning
confidence: 99%
See 1 more Smart Citation