L'influence du temps dans les solutions statiques

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Alkaloide

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Noncovalent cross-links in context with other structural and functional elements of proteins

Proteins are heteropolymers with evolutionary selected native sequences of residues. These native sequences code for unique and stable 3D structures indispensable for biochemical activity and for proteolysis resistance, the latter which guarantees an appropriate lifetime for the protein in the protease rich cellular environment. Cross-links between residues close in space but far in the primary structure are required to maintain the folded structure of proteins. Some of these cross-links are covalent, most frequently disulfide bonds, but the majority of the cross-links are sets of cooperative noncovalent long-range interactions. In this paper we focus on special clusters of noncovalent long-range interactions: the Stabilization Centers (SCs). The relation between the SCs and secondary structural elements as well as the relation between SCs and functionally important regions of proteins are presented to show a detailed picture of these clusters, which are believed to be primarily responsible for major aspects of protein stability.     

The Volterra Operator is not Supercyclic

It is shown that the classical Volterra operator, which is cyclic, is not supercyclic on any of the spaces L^p[0, 1], 1 p < . This solves a question posed by Héctor Salas. This contrasts with the fact that the derivative operator, the left inverse of the Volterra operator, although unbounded, is hypercyclic on L^p[0, 1].     

Isolation and characterisation of the mixed-metal alkyl amide [(TMEDA)Na(mu-Bu)(mu-TMP)Mg(TMP)], an unexpected chelate-trapped intermediate in the formation of inverse crowns

Only two-fold amination occurs when 3 molar equivalents of TMPH are offered to a 1:1 BuNa-Bu2Mg mixture; adding TMEDA gives the mixed alkyl amide [(TMEDA)Na(mu-Bu)(mu-TMP)Mg(TMP)], which itself affords the phenyl-bridged analogue when reacted with benzene.     

HPLC separation of diastereomers of Ln(III)-ethylenepropylene-triamine-pentaacetate complexes. Direct assessment of their water exchange rate

The diastereomers of two Ln(III)-EPTPA derivatives have been separated by reversed-phase HPLC, and the water exchange rate on their Gd(III) complexes has been directly determined by 17O NMR (H5EPTPA = ethylenepropylene-triamine-pentaacetic acid).     

A unique series of dinuclear transition metal-polyradical complexes with a m-phenylenediamine spacer and their catalytic reactivity

A series of dinuclear transition metal complexes with either six or four iminosemiquinone radicals, in which the metal centres are separated by a distance of approximately 6.8 A, together with their catalytic reactivity is reported.     

Dioxygen activation by an osmium-dihydride: preparation and characterization of a d4 square-planar complex

Exposure of OsH2Cl2(PiPr3)2 to air or bubbling with pure O2 affords the dioxo-Os(VI) compound OsO2Cl2(PiPr3)2 as result of a direct O=O double bond activation reaction. This Os(VI) species is reduced in the presence of n-BuLi to the novel dioxo-Os(IV) derivative OsO2(PiPr3)2, a rare example of a d4 square-planar compound.