一种新型造纸施胶增效剂的合成及其应用

:探讨了丙烯酸 -苯乙烯 -甲基丙烯酸甲酯水溶性三元共聚物的合成条件 ,研究了这种水溶性三元共聚物的性质及其在造纸过程中的可能应用。研究发现 ,在适当的条件下 ,丙烯酸 -苯乙烯 -甲基丙烯酸甲酯可以按一定的摩尔比发生共聚合形成能溶于水的共聚物。这种水溶性的共聚物在高温下 (大于 80℃ )发生固化后而形成具有抗水性的膜 ,因而适合于造纸工业作施胶剂 ,但是 ,由于其分子量不高留着率低 ,要与松香配合使用 ,使松香施胶剂发挥更大的效果 ,实验证明 ,可以把乳化松香的施胶效果提高一倍以上     

Additional ent‐Kaurane Diterpenoids from Rubus corchorifolius L. f.

A further chemical investigation of the plant Rubus corchorifolius L. f., collected in Hunan Province, afforded three new ent‐kauranoids 3 – 5 . Their structures were elucidated by various spectroscopic methods.     

Analytical and experimental studies on out-of-plane dynamic instability of shallow circular arch based on parametric resonance

Nonlinear Dynamics - Little research about the out-of-plane dynamic stability of arches under in-plane loading has been reported in the literature hitherto. This paper presents analytical and...     

A facile synthesis of a complex type N-glycan thiazoline as an effective inhibitor against the antibody-deactivating endo-β-N-acetylglucosaminidases

Endo-β-N-acetylglucosaminidases are a class of endoglycosidases that deglycosylate N-glycans from glycoproteins. We describe here a facile synthesis of a complex type N-glycan thiazoline as a new mechanism-based inhibitor for this class of enzymes. The synthesis started with the readily available sialoglycopeptide (SGP) and its conversion into the glycan thiazoline through several enzymatic and chemical reactions. The synthetic glycan thiazoline showed potent inhibitory activity against several endoglycosidases including the two antibody-deactivating enzymes, Endo-S and Endo-S2, from human pathogen Streptococcus pyogenes, which would be useful as tools for structural and functional studies of these enzymes.     

Synthesis and physicochemical characterization of two gadolinium(III) TTDA-like complexes and their interaction with human serum albumin

Two novel derivatives of TTDA (3,6,10-tri(carboxymethyl)-3,6,10-triazadodecanedioic acid), TTDA-BOM and TTDA-N'-BOM, each having a benzyloxymethyl group, were synthesized. (17)O NMR longitudinal and transverse relaxation rates and chemical shifts of aqueous solutions of their Gd(III) complexes were measured at variable temperature with a magnetic field strength of 9.4 T. The water exchange rate (k(ex)(298)) values for [Gd(TTDA-BOM)(H(2)O)](2-) (117 x 10(6) s(-1)) and [Gd(TTDA-N'-BOM)(H(2)O)](2-) (131 x 10(6) s(-1)) are significantly higher than those of [Gd(DTPA)(H(2)O)](2-) (4.1 x 10(6) s(-1)) and [Gd(BOPTA)(H(2)O)](2-) (3.45 x 10(6) s(-1)). The rotational correlation time (tau) values for [Gd(TTDA-BOM)(H(2)O)](2-) (119 ps) and [Gd(TTDA-N'-BOM)(H(2)O)](2-) (125 ps) are higher than those of [Gd(DTPA)(H(2)O)](2-) (103 ps) and [Gd(TTDA)(H(2)O)](2-) (104 ps). The stepwise stoichiometric binding constants of [Gd(TTDA-BOM)(H(2)O)](2)(-) and [Gd(TTDA-N'-BOM)(H(2)O)](2)(-) bound to HSA are obtained by ultrafiltration studies. Fluorescent probe displacement studies exhibit that [Gd(TTDA-BOM)(H(2)O)](2-) and [Gd(TTDA-N'-BOM)(H(2)O)](2-) can displace dansylsarcosine from HSA with inhibition constants (K(i)) of 1900 and 1600 microM, respectively; however, they are not able to displace warfarin. These results indicate that [Gd(TTDA-BOM)(H(2)O)](2-) and [Gd(TTDA-N'-BOM)(H(2)O)](2-) have a weak binding to site II on HSA. In addition, the mean bound relaxivity (r(1b)) and bound relaxivity (r(1)(b)) values for the [Gd(TTDA-BOM)(H(2)O)](2-)/HSA and [Gd(TTDA-N'-BOM)(H(2)O)](2-)/HSA adducts are obtained by ultrafiltration and relaxivity studies, respectively. The bound relaxivity of these adducts values are significantly higher than those of [Gd(BOPTA)(H(2)O)](2-)/HSA and [Gd(DTPA-BOM(3))(H(2)O)](2-)/HSA. These results also suggest that bound relaxivity is site dependent. In binding sites studies of Gd(III) chelates to HSA, a significant decrease of the relaxation rates (R(1obs)) was observed for the [Eu(TTDA-BOM)(H(2)O)](2-) complex which was added to the [Gd(TTDA-N'-BOM)(H(2)O)](2-)/HSA solution, and this indicated that these Gd(III) complexes share the same HSA binding site. Finally, as measured by the Zn(II) transmetalation process, the kinetic stability of these Gd(III) complexes are significantly higher than that of [Gd(DTPA-BMA)(H(2)O)].     

Determination of DL-tetrahydropalmatine in Corydalis yanhusuo by L-tetrahydropalmatine imprinted monolithic column coupling with reversed-phase high performance liquid chromatography

A method for direct determination of DL-tetrahydropalmatine (DL-THP) in Corydalis yanhusuo, a traditional Chinese herb, by L-THP imprinted monolithic precolumn on-line/off-line coupling with reversed-phase high performance liquid chromatography (RP-HPLC) was developed. The L-THP imprinted monolithic column has been prepared by in situ polymerization using methacrylic acid (MAA) and ethylene dimethacrylate (EDMA) as functional monomer and cross-linker, respectively. With the optimization of chromatographic conditions, such as mobile phase composition, flow rate, column temperature and sample loading, for the separation of enantiomer, DL-THP was base-line separated on the MIP. The imprinted monolithic column was used as a precolumn for fractionation of the C. yanhusuo extract. Both the non-retained and retained fractions were separated by RP-HPLC. Meanwhile, the D-THP and L-THP can be detected in the non-retained and retained fractions, respectively. Additionally, direct determination of L-THP using molecularly imprinted monolith on-line coupling with a reversed-phase column was acquired.     

Aggregation of quaternary ammonium gemini surfactants C12-s-C12.2Br in n-heptane/n-hexanol solution: effect of the spacer chains on the critical reverse micelle concentrations

The critical reverse micelle concentrations of C(12)-s-C(12).2Br (s=2,3,4,5,6,8,12) in n-heptane/n-hexanol solutions, cmc(I)s, have been determined by absorption spectrum method using iodine as probe. The values of cmc(I)s are smaller than those of the critical micelle concentrations (cmc(aq)s) in aqueous solution and reach a maximum at s=4, which is similar to the variation of cmc(aq) with s. The variation of cmc(I) with s is attributed to the alteration in the spacer chain conformation, i.e. when the spacer is short enough, it may adopt stretch configuration and when the spacer is long, it tends to bend towards the continuous oil phase to achieve a more densely packing of the quaternary ammonium heads on the surface of the core.     

A sugar-quinoline fluorescent chemosensor for selective detection of Hg2+ ion in natural water

A selective and sensitive fluorescent sensor for detection of Hg2+ in natural water was achieved by incorporating the well-known fluorophore quinoline group and a water-soluble D-glucosamine group within one molecule.     

Ionic liquid buffers: a new class of chemicals with potential for controlling pH in non-aqueous media

Ionic liquids with buffering characteristics, synthesized by the reaction of [RMIM]OH base moieties with phthalic and tartaric acid, respectively, are potential reagents for controlling pH in non-aqueous media; remarkable [Base]/[Acid] molar ratio dependence of the catalytic activities has been observed in the hydrogenation of olefins with [RuCl2(PPh3)3] complex in DMF and [BMIM][BF4].