Study on the stability of molecular chirality and the configuration protection of dihydromyricetin in vine tea.

This study aims to investigate the impact of four key factors, namely, temperature, water source, metal ion, and pH, on the stability of molecular chirality of dihydromyricetin (DMY) and proposed effective strategies for configuration protection. The findings reveal that temperatures exceeding 80°C could accelerate the racemization process of DMY, with a significant increase in racemization observed at 100°C. In addition, DMY exhibited heightened stability in ultrapure water as compared to various water sources, including pure water-1, pure water-2, mineral water, and running water. Notably, the presence of Fe2+ displayed an inhibitory effect on the racemization of DMY, whereas Mg2+, Ca2+, and Mn2+ showed a substantial promotional effect. Additionally, acidic conditions (pH < 5.0) were found to be protective for maintaining the stability of DMY, whereas alkaline conditions (pH > 9.0) were observed to be detrimental. Meanwhile, we first identified the presence of another pair of DMY isomers in this work.

Cyclodextrin-dendrimers nanocomposites functionalized high performance liquid chromatography stationary phase for efficient separation of aromatic compounds.

In this work, novel cyclodextrin-dendrimers nanocomposites functionalized high performance liquid chromatography stationary phases were developed for efficient separation of aromatic compounds. ß-cyclodextrin was grafted onto the surface of silica gel matrix with poly (amidoamine) dendrimers as spacers. Scanning electron microscope, fourier transform infrared spectroscopy, element analysis and Brunner-Emmet-Teller measurement proved the successful grafting of cyclodextrin-dendrimers nanocomposites. The obtained stationary phases showed satisfactory separation effects for alkylbenzenes and benzenesulfonic acid substituents in reverse phase liquid chromatography mode. Weak hydrophilic and ion exchange interactions were also confirmed at the same time. Meanwhile, the effects of dendrimers and cyclodextrin on the chromatography performance were discussed. Separation mechanism of the stationary phases were verified by two-dimensional nuclear magnetic resonance technology, and the result implied that the proposed cyclodextrin-dendrimers nanocomposites functionalized stationary phases have significant prospects for separation and determination of more aromatic compounds in future.

Determination of tautomeric preference of fenobam in solution by high-resolution NMR spectroscopy.

In this work, tautomeric preference of fenobam in solution was investigated by homonuclear and heteronuclear solution nuclear magnetic resonance (NMR) spectroscopy. 1 H-1 H nuclear Overhauser effect spectroscopy (NOESY) spectrum revealed that fenobam in liquid state exists exclusively in one of the two possible tautomeric structures, which was confirmed by 1 H-13 C HSQC and heteronuclear multiple bond correlation (HMBC) spectra. Moreover, difference between the two tautomeric structures was studied by theoretical calculations, which further proved the result obtained by the NMR experiments.