Facile preparation of a stable and functionalizable hybrid monolith via ring-opening polymerization for capillary liquid chromatography

Journal of Chromatography A

Volumn 1301, Issue , 2013, Pages 131-138

  Lin, Hui ^a,b   Ou, Junjie ^a   Tang, Shouwan ^c   Zhang, Zhenbin ^a,b   Dong, Jing ^a   Liu, Zhongshan ^a,b   Zou, Hanfa ^a  

^a DALIAN INSTITUTE OF CHEMICAL PHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

^c TAIZHOU UNIVERSITY   (China)

Author keywords

Capillary liquid chromatography; Enantioseparation; Hybrid monolith; Hydrophilic interaction chromatography; Polyhedral oligomeric silsesquioxanes (POSSs)

Indexed keywords

CAPILLARY LIQUID CHROMATOGRAPHY; CELLULOSE TRIS(3 ,5-DIMETHYLPHENYLCARBAMATE); ENANTIOSEPARATIONS; HYBRID MONOLITHS; ORGANIC-INORGANIC HYBRID; POLYHEDRAL OLIGOMERIC SILSESQUIOXANES; REVERSED-PHASE LIQUID CHROMATOGRAPHY; SECONDARY AMINO GROUP;

HYDROPHILICITY; LIQUID CHROMATOGRAPHY; OLIGOMERS; POLYMERIZATION; SEPARATION;

MONOLITHIC INTEGRATED CIRCUITS;

CELLULOSE DERIVATIVE; CELLULOSE TRIS(3,5' DIMETHYLPHENYLCARBAMATE); GAMMA GLUCONOLACTONE; OCTAGLYCIDYLDIMETHYLSILYL POLYHEDRAL OLIGOMERIC SILSESQUIOXANE; POLYETHYLENEIMINE; POLYMER; REAGENT; UNCLASSIFIED DRUG;

ARTICLE; CAPILLARY CHROMATOGRAPHY; CAPILLARY LIQUID CHROMATOGRAPHY; ENANTIOSELECTIVITY; HYBRID; HYDROPHILIC INTERACTION CHROMATOGRAPHY; HYDROPHILICITY; LIQUID CHROMATOGRAPHY; MOLECULAR STABILITY; PHASE TRANSITION; PRIORITY JOURNAL; RING OPENING METATHESIS POLYMERIZATION; SEPARATION TECHNIQUE;

CAPILLARY LIQUID CHROMATOGRAPHY; ENANTIOSEPARATION; HYBRID MONOLITH; HYDROPHILIC-INTERACTION CHROMATOGRAPHY; POLYHEDRAL OLIGOMERIC SILSESQUIOXANES (POSSS);

BENZENE DERIVATIVES; CHROMATOGRAPHY, REVERSE-PHASE; EPOXY COMPOUNDS; GLUCONATES; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; LACTONES; ORGANOSILICON COMPOUNDS; PHARMACEUTICAL PREPARATIONS; PHENOLS; POLYETHYLENEIMINE; POLYMERIZATION; STEREOISOMERISM;

EID: 84879884718     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2013.05.069     Document Type: Article

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