About: Measurement of solution-phase chiral molecular recognition in the gas phase using electrospray ionization-mass spectrometry     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Vysledek, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
Description
  • Development of chiral selectors (SOs) is important both for understanding chiral molecular recognition processes and for their use in the separation of chiral species (selectands). Their evaluation by chromatographic procedures (e.g., as chiral stationary phase) can, however, be time-consuming. In this respect, electrospray ionization-MS (ESI-MS) is tested here as a possible alternative for screening enantioselective binding by SOs. The set of well-characterized cinchona alkaloid SOs are investigated with respect to their enantioselective binding to a set of model enantiomers, dinitrobenzoyl-(R)- and dinitrobenzoyl-(S)-leucine. MS-based enantioselectivity values from normalized gas-phase ion abundances for the diastereomeric complexes are compared empirically to chromatographic (HPLC) enantioselectivity results and shown to be consistent. Investigations into the fundamentals of measuring unbiased enantioselectivity values in the limit of dilute solution by correlation between experimental and modeled
  • Development of chiral selectors (SOs) is important both for understanding chiral molecular recognition processes and for their use in the separation of chiral species (selectands). Their evaluation by chromatographic procedures (e.g., as chiral stationary phase) can, however, be time-consuming. In this respect, electrospray ionization-MS (ESI-MS) is tested here as a possible alternative for screening enantioselective binding by SOs. The set of well-characterized cinchona alkaloid SOs are investigated with respect to their enantioselective binding to a set of model enantiomers, dinitrobenzoyl-(R)- and dinitrobenzoyl-(S)-leucine. MS-based enantioselectivity values from normalized gas-phase ion abundances for the diastereomeric complexes are compared empirically to chromatographic (HPLC) enantioselectivity results and shown to be consistent. Investigations into the fundamentals of measuring unbiased enantioselectivity values in the limit of dilute solution by correlation between experimental and modeled (en)
  • Článek je zaměřen na měření chirálního molekulárního rozpoznávání v plynné fázi s využitím ionizace elektrosprejem v hmotnostní spektrometrii. (cs)
Title
  • Measurement of solution-phase chiral molecular recognition in the gas phase using electrospray ionization-mass spectrometry
  • Měření chirálního molekulárního rozpoznávání v plynné fázi s využitím ionizace elektrosprejem v hmotnostní spektrometrii (cs)
  • Measurement of solution-phase chiral molecular recognition in the gas phase using electrospray ionization-mass spectrometry (en)
skos:prefLabel
  • Measurement of solution-phase chiral molecular recognition in the gas phase using electrospray ionization-mass spectrometry
  • Měření chirálního molekulárního rozpoznávání v plynné fázi s využitím ionizace elektrosprejem v hmotnostní spektrometrii (cs)
  • Measurement of solution-phase chiral molecular recognition in the gas phase using electrospray ionization-mass spectrometry (en)
skos:notation
  • RIV/61989592:15310/05:00002247!RIV06-MSM-15310___
http://linked.open.../vavai/riv/strany
  • 3660-3670
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM6198959216)
http://linked.open...iv/cisloPeriodika
  • 11
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 529226
http://linked.open...ai/riv/idVysledku
  • RIV/61989592:15310/05:00002247
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • PERFORMANCE LIQUID-CHROMATOGRAPHY; EXCHANGE-TYPE SELECTORS; STATIONARY PHASES; BINDING INTERACTIONS; ANION-EXCHANGERS; AMINO-ACIDS; QUANTITATIVE-DETERMINATION; ENANTIOMER DISCRIMINATION; NONCOVALENT INTERACTIONS; PEPTIDE ENANTIOMERS (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [E4F00E788B7B]
http://linked.open...i/riv/nazevZdroje
  • Analytical Chemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 77
http://linked.open...iv/tvurceVysledku
  • Fryčák, Petr
  • Lindner, W.
  • Maier, N. M.
  • Schug, K.
http://linked.open...n/vavai/riv/zamer
issn
  • 0003-2700
number of pages
http://localhost/t...ganizacniJednotka
  • 15310
is http://linked.open...avai/riv/vysledek of
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 58 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software