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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J20-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J20-286
filingDate 2011-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b13893014c16651a3aa670cc58f90e38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6d7aa0b0ba6e845ec11ebfc45922b5cb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e3a2806cf22ecb2cbf67152b207dd64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_377153214ad2fd811f8a25560f1bfaad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c632e9f55592b0b050d87d35b088f070
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4cf279b171d3def59e3779165cf02d77
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a848c70c1b22dce4df5d32cc6bf12fc
publicationDate 2013-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102489275-B
titleOfInvention Phenylalanine-substituted calix [4] arene bonded silica gel stationary phase, preparation method thereof, and application thereof
abstract The invention relates to a phenylalanine-substituted calix [4] arene bonded silica gel stationary phase, a preparation method thereof, and an application thereof. According to the invention, gamma-aminopropyltrimethoxysilane is adopted as a coupling agent; with a catalyst and under the protection of an inert gas, the coupling agent is subject to a reaction with specially prepared silica gel, such that gamma-aminopropyltrimethoxy bonded silica gel is prepared; with a catalyst and under the protection of an inert gas, the gamma-aminopropyltrimethoxy bonded silica gel is subject to a reaction with 25,27-di(L-methyl phenylalanine-N-carbonylmethoxy)-26,28-dihydroxy-p-tert-butyl calix [4] arene, such that the phenylalanine-substituted calix [4] arene bonded silica gel stationary phase is obtained. The bonded stationary phase provided by the invention has high bonding amount, stable performance, and better separation selectivity. The bonded stationary phase has a traditional ODS reversion phase chromatography performance, and can provide various action sites such as inclusion action sites and hydrogen bond action sites. The bonded stationary phase has a certain advantage in separating some specific substances that are hard to separate.
priorityDate 2011-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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