Enantiomeric analysis of γ(δ)-lactones by reversed phase high performance liquid chromatography using amylose tris(5-chloro-2-methylphenylcarbamate) as stationary phase.

A Chiralpak AY-3R column was investigated for analytical enantiomeric separation of twelve racemic γ(δ)-lactones using reversed phase high performance liquid chromatography. Main influence factors, including organic modifier, flow rate and column temperature, were optimized. Five kinds of γ(δ)-lactones were successfully enantioseparated using the established method: γ-nonanolactone, δ-decalactone, δ-undecalactone, δ-dodecalactone and δ-tetradecalactone. Under optimized conditions, enantiomeric peak resolution (Rs) for the five γ(δ)-lactones reached more than 1.09, 1.08, 1.54, 1.43, and 1.11, respectively. Their chromatographic elution behavior was investigated using Van't Hoff equation and Van Deemter equation. It was found that an exothermic process occurred during enantiomeric separation of γ(δ)-lactones using this chromatographic column, and it showed a typical Van Deemter curve. Finally, this method was applied in enantiomeric ratio analysis of γ(δ)-lactones contents for purchased butter samples, and results confirmed the predominant content of the (R)-configuration of δ-dodecalactone in natural animal butter, while in margarine, an equal proportion of (R/S)-configuration of δ-dodecalactone was detected.

Recent progress on chiral extractants for enantioselective liquid-liquid extraction.

As the demand for enantiopure compounds increases, chiral separation has become increasingly important in many fields. Enantioselective liquid-liquid extraction is an up-and-coming technology for enantiomeric separation because it is highly efficient and easy to be scaled up. The key factor for enantioselective liquid-liquid extraction is the development of novel chiral extractants with high enantiorecognition performance. With successful studies on catalytically active metal complexes as chiral extractants, novel chiral extractants can be screened and designed from the field of asymmetric catalysis. Chiral ionic liquids, sulfobutylether-ß-cyclodextrins bonded magnetic nanoparticles and 2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol (SPINOL) based phosphoric acid host show unique potential ability in enantioselective liquid-liquid extraction and they deserve further study. Brief principles, extraction equipment and solvent systems in enantioselective liquid-liquid extraction are presented in the present paper, and recent progress in development of new chiral extractants in the past decade is mainly reviewed, including metal complexes, cyclodextrins, ionic liquids, tartrate acids and crown ethers.

Retention correlation and orthogonality between reversed phase countercurrent chromatography and liquid chromatography based on solvent strength.

Correlation of elution performance between reversed phase countercurrent chromatography and liquid chromatography was investigated using five selected natural components. Theoretical guidance for orthogonality of two-dimensional countercurrent chromatography and liquid chromatography was proposed. The difference in retention behavior between countercurrent chromatography and liquid chromatography was studied when the mobile phase was composed of methanol and water by measuring the partition behavior of five selected compounds in two typical biphasic solvent systems composed of n-hexane-ethyl acetate-methanol-water and chloroform-methanol-water. An orthogonal diagram between countercurrent chromatography and liquid chromatography was obtained by normalized treatment of the measured partition coefficients and capacity factors. The experimental results showed that each biphasic solvent system used for countercurrent chromatography had a high orthogonality with liquid chromatography when a specific volume ratio was used.

Impacts of combined water-saving irrigation and controlled-release urea on CH4 emission and its associated microbial communities and function.

Water-saving irrigation and controlled-release nitrogen fertilizer are used in rice farming. The aim of this study was to understand the effects of water-saving irrigation and controlled-release urea on methane (CH4) emission and its associated microbial communities and function. A field experiment was conducted with two nitrogen treatments (NU 100% normal urea, CU 60% normal urea and 40% controlled-release urea, total N amount was the same) and three irrigation modes (CI continuous flooding irrigation, AI alternate wetting and drying irrigation, RI ridge irrigation). CH4 fluxes, organic acid contents and enzyme activities were measured, and soil microbial communities and function were investigated by whole-genome shotgun sequencing analysis, and then their relationships were analyzed by Spearman correlation analysis, redundancy analysis and mantel test. Compared to CI, AI and RI decreased cumulative CH4 emissions by 43.5% and 25.8% in NU, and 64.9% and 13.3% in CU, respectively. Among all treatments, AICU had the lowest CH4 emission and reduced it by 72.2% compared to CINU. AI and RI had higher contents of some organic acids than CI. Compared to CINU, AICU decreased the relative abundance of Methanosarcina barkeri and associated genes in the CO2-reduction methanogenesis pathway by 83.4% and 91.0%. Both abundance of methanogens and associated genes in the CO2-reduction methanogenesis pathway were positively correlated with cumulative CH4 emission, but negatively correlated with most soil organic acids. Thus AICU can mitigate CH4 emission by decreasing the abundance of methanogens and associated genes in the CO2-reduction methanogenesis pathway.

Core-shell structure, biodegradation, and drug release behavior of poly(lactic acid)/poly(ethylene glycol) block copolymer micelles tuned by macromolecular stereostructure.

Poly(ethylene glycol)-b-poly(L-lactic acid)-b-poly(D-lactic acid) (PEG-b-PLLA-b-PDLA) stereoblock copolymers were synthesized by sequential ring-opening polymerization. Their micelle formation, precise micelle structure, biodegradation, and drug release behavior were systematically investigated and compared with the PEG-b-poly(lactic acid) (PEG-b-PLA) diblock copolymers with various PLA stereostructures and PEG-b-PLLA/PEG-b-PDLA enantiomeric mixture. Stereoblock copolymers having comparable PLLA and PDLA block lengths and enantiomerically-mixed copolymers assemble into the stereocomplexed core-shell micelles, while the isotactic and atactic PEG-b-PLA copolymers formed the homocrystalline and amorphous micelles, respectively. The PLA segments in stereoblock copolymer micelles show smaller crystallinity than those in the isotactic and enantiomerically-mixed ones, attributed to the short block length and presence of covalent junction between PLLA and PDLA blocks. As indicated by the synchrotron radiation small-angle X-ray scattering results, the stereoblock copolymer micelles have larger size, micellar aggregation number, core radius, smaller core density, and looser packing of core-forming segments than the isotactic and enantiomerically-mixed copolymer micelles. These unique structural characteristics cause the stereoblock copolymer micelles to possess higher drug loading content, slower degradation, and drug release rates.