Chiral separation of halogenated amino acids by ligand-exchange capillary electrophoresis

The chiral separation of halogenated amino acids by ligand-exchange CE is described. Halogenated amino acids attracted increasing interest in recent years because of their physiological activities. Different chiral selectors, as there are L-4-hydroxyproline, L-histidine, and N-alkyl derivatives of L-4-hydroxyproline in form of their copper(II) complexes, are compared for their chiral recognition ability for halogenated amino acids. The influence of various parameters, such as selector concentration, pH, organic modifier, and field strength, on the resolution was investigated. All halogenated amino acids investigated were baseline-separated under optimized conditions.     

Efficient algorithms for the recognition of topologically conjugate gradient-like diffeomorhisms

It is well known that the topological classification of structurally stable flows on surfaces as well as the topological classification of some multidimensional gradient-like systems can be reduced to a combinatorial problem of distinguishing graphs up to isomorphism. The isomorphism problem of general graphs obviously can be solved by a standard enumeration algorithm. However, an efficient algorithm (i. e., polynomial in the number of vertices) has not yet been developed for it, and the problem has not been proved to be intractable (i. e., NPcomplete). We give polynomial-time algorithms for recognition of the corresponding graphs for two gradient-like systems. Moreover, we present efficient algorithms for determining the orientability and the genus of the ambient surface. This result, in particular, sheds light on the classification of configurations that arise from simple, point-source potential-field models in efforts to determine the nature of the quiet-Sun magnetic field.     

Natural specimen of triple solid solution ettringite–thaumasite–chromate-ettringite

Three natural minerals of ettringite group were investigated by TG to refine their chemical composition. Two samples are ettringite Ca_5.97Mg_0.01Sr_0.02Al_1.99Cr_0.01(SO₄)₃(OH)₁₂·23.7H₂O and bentorite Ca_5.99Mg_0.01Cr_1.95Al_0.01Si_0.03(SO₄)_2.82·(CO₃)_0.20(OH)₁₂·19.4H₂O, but the third one Ca_5.99Na_0.01Al_1.38Si_0.62(SO₄)_2.49·(CrO₄)_0.36·(CO₃)_0.46(OH)₁₂·15.8H₂O has found to be a solid solution among ettringite, thaumasite, and chromate-ettringite, not registered yet as a new mineral species. Similar phase is well known in concrete formed with Cr⁶⁺ admixture, but is found for the first time as a natural compound. X-ray single-crystal investigation allowed us to refine the structure and support substitution (SO₄)^2? ? (CrO₄)^2? in natural minerals of ettringite group.     

Synthesis of H (type 4) trisaccharide,key structural fragment of globo-H and fucosyl-GM1 cancer-associated antigens

A convenient synthesis of Fucα1-2Galβ1-3GalNAcβ-OCH₂CH₂CH₂NH₂ (trisaccharide H type 4) is described. This glycan is the terminal part of glycosphingolipids globo-H and fucosyl-GM1 known as cancer-associated carbohydrate antigens.     

Sterically Hindered o‐Quinone Annulated with Dithiete: A Molecule Comprising Diolate and Dithiolate Coordination Sites

A new stable sterically hindered o‐quinone annelated with a 1,2‐dithiete ring was prepared by using mild conditions. The skeleton of the compound comprises diolate and dithiolate functions that have the potential to bind metals leading to the corresponding complexes. The reactivity of this compound as a ligand with respect to both coordination sites was studied. Reactions with metals indicate that the o‐quinone function is reduced in the first stage to give semiquinonate and catecholate complexes. The dithiolate coordination site was involved in the reaction in a few cases only after diolate was bound. A trinuclear manganese complex with coordination on both sites was obtained and characterized by EPR spectroscopy. The electrochemical study of this quinone fused with dithiete is reported.