2008
DOI: 10.1016/j.carres.2008.06.014
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A structural and thermal investigation of the inclusion of parabens in heptakis(2,6-di-O-methyl)cyclomaltoheptaose

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Cited by 11 publications
(3 citation statements)
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“…14 Cyclodextrin (CD) has been extensively applied in analytical elds for its enantioselective properties, 15 as a modier in capillary electrophoresis, 16 as a chirality selector 17 and as a co-modier in mobile phase techniques. 18 The fact that parabens can form an inclusion complex with b-cyclodextrin (b-CD), [19][20][21] led us to choose to investigate the efficiency of b-CD as a modier in IL-ATPS to determine parabens in environmental water samples.…”
Section: Introductionmentioning
confidence: 99%
“…14 Cyclodextrin (CD) has been extensively applied in analytical elds for its enantioselective properties, 15 as a modier in capillary electrophoresis, 16 as a chirality selector 17 and as a co-modier in mobile phase techniques. 18 The fact that parabens can form an inclusion complex with b-cyclodextrin (b-CD), [19][20][21] led us to choose to investigate the efficiency of b-CD as a modier in IL-ATPS to determine parabens in environmental water samples.…”
Section: Introductionmentioning
confidence: 99%
“…The methods to identify crystal structure or polymorph were not limited to the above examples. Other reported technologies includes thermal gravimetric analysis (TGA) [87], nuclear magnetic resonance (NMR) [86], ultraviolet Spectrophotometer (US) [88], and Atomic-force microscopy (AFM) [89][90][91][92][93][94][95], together with other technologies listed in Table 2. Figure 11 Microscope and SEM images of BP sandwich crystals and the pores inside crystals [56,77]…”
Section: Crystal Structures and Polymorphismmentioning
confidence: 99%
“…The crystal structures of BPN (CSD refcode: UDOMIL) (Yang & Rasmuson, 2013) and its clathrate hydrate (CSD refcode: VOFKIL) have been reported in the literature (de Vries & Caira, 2008). In UDOMIL, the BPN molecule exhibits a planar conformation except for the terminal ethyl moiety of butyl ester group which is in a cis orientation with respect to the ester group.…”
Section: Database Surveymentioning
confidence: 99%