Determination of sets of solute descriptors from chromatographic measurements.
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Determination of Abraham model solute descriptors for the monomeric and dimeric forms of trans-cinnamic acid using measured solubilities from the Open Notebook Science ChallengeQuantitative structure-property relationships for predicting sorption of pharmaceuticals to sewage sludge during waste water treatment processesEasy and accurate calculation of programmed temperature gas chromatographic retention times by back-calculation of temperature and hold-up time profiles."Retention projection" enables reliable use of shared gas chromatographic retention data across laboratories, instruments, and methods.Partition of compounds from water and from air into amidesThe biological and toxicological activity of gases and vaporsComparing linear free energy relationships for organic chemicals in soils: effects of soil and solute properties.Could linear solvation energy relationships give insights into chiral recognition mechanisms? 2. Characterization of macrocyclic glycopeptide stationary phases.Hydrogen bonding between solutes in solvents octan-1-ol and water.Modeling and predicting competitive sorption of organic compounds in soilWhat experimental factors influence the accuracy of retention projections in gas chromatography-mass spectrometry?A practical methodology to measure unbiased gas chromatographic retention factor vs. temperature relationships.A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. Application of quantitative structure activity/selectivity relationships.An algorithm for 353 odor detection thresholds in humansConcentration-detection functions for the odor of homologous n-acetate estersIonic liquid stationary phases for gas chromatography.Totally organic biphasic solvent systems for extraction and descriptor determinations.GC for flavonoids analysis: Past, current, and prospective trends.Main interactions and influences of the chromatographic parameters in HILIC separations.Multidimensional gas chromatography beyond simple volatiles separation.Chromatographic methods enabling the characterization of stationary phases and retention prediction in high-performance liquid chromatography and supercritical fluid chromatography.Use and practice of achiral and chiral supercritical fluid chromatography in pharmaceutical analysis and purification.Advances in immobilized artificial membrane (IAM) chromatography for novel drug discovery.Metabolomic Strategies Involving Mass Spectrometry Combined with Liquid and Gas Chromatography.PCDD/F and PCB water column partitioning examination using natural organic matter and black carbon partition coefficient models.Is there an intramolecular hydrogen bond in 2-halophenols? A theoretical and spectroscopic investigation.Descriptors for Pentane-2,4-dione and Its Derivatives.Evaluation of an amide-based stationary phase for supercritical fluid chromatography.Descriptors for the Prediction of Partition Coefficients and Solubilities of Organophosphorus Compounds.Using water-solvent systems to estimate in vivo blood-tissue partition coefficients.An insight into the use of dimethylphenyl carbamate cyclofructan 7 chiral stationary phase in supercritical fluid chromatography: the basic comparison with HPLC.The Evaluation of Pro-Cognitive and Antiamnestic Properties of Berberine and Magnoflorine Isolated from Barberry Species by Centrifugal Partition Chromatography (CPC), in Relation to QSAR Modelling.Baseline toxicity and ion-trapping models to describe the pH-dependence of bacterial toxicity of pharmaceuticals.Quantitative structure/eluent-retention relationships in reversed-phase high-performance liquid chromatography based on the solvatochromic method.Development of polyparameter linear free energy relationship models for octanol-air partition coefficients of diverse chemicals.The prediction of blood-tissue partitions, water-skin partitions and skin permeation for agrochemicals.The hydrogen bond properties of water from 273 K to 573 K; equations for the prediction of gas-water partition coefficients.Predicting the partitioning of biological compounds between room-temperature ionic liquids and water by means of the solvation-parameter model.Prediction of biomagnification factors for some organochlorine compounds using linear free energy relationship parameters and artificial neural networks.Partition of Neutral Molecules and Ions from Water to o-Nitrophenyl Octyl Ether and of Neutral Molecules from the Gas Phase to o-Nitrophenyl Octyl Ether.
P2860
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P2860
Determination of sets of solute descriptors from chromatographic measurements.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Determination of sets of solute descriptors from chromatographic measurements.
@ast
Determination of sets of solute descriptors from chromatographic measurements.
@en
type
label
Determination of sets of solute descriptors from chromatographic measurements.
@ast
Determination of sets of solute descriptors from chromatographic measurements.
@en
prefLabel
Determination of sets of solute descriptors from chromatographic measurements.
@ast
Determination of sets of solute descriptors from chromatographic measurements.
@en
P1476
Determination of sets of solute descriptors from chromatographic measurements
@en
P2093
Adam Ibrahim
Michael H Abraham
P356
10.1016/J.CHROMA.2003.12.004
P407
P577
2004-05-01T00:00:00Z