New water soluble and luminescent platinum(II) compounds, vapochromic behavior of [K(H2O)][Pt(bzq)(CN)2], new examples of the influence of the counterion on the photophysical properties of d8 square-planar complexes

This work describes the synthesis of compounds [Pt(C=N)(NCMe) 2]ClO 4 (C=N = 7,8-benzoquinolinato (bzq), 2-phenylpyridinato (ppy)) and their use as precursors for the preparation of the cyanido complexes [Pt(C=N)(CN) 2] (-), which were isolated as the potassium, [K(H 2O)][Pt(C=N)(CN) 2] [C=N = bzq ( 3a), ppy ( 4a)], and the tetrabutylammonium, NBu 4[Pt(C=N)(CN) 2] [C=N = bzq ( 5), ppy ( 6)], salts. The difference in the cation has an influence on the solubility, color, and emission properties of these compounds. Compounds 5 and 6 are yellow and soluble in organic solvents, while the potassium salts are also soluble in water and exhibit two forms: the water-containing [K(H 2O)][Pt(C=N)(CN) 2] [C=N = bzq ( 3a), ppy ( 4a)] complexes and the anhydrous ones K[Pt(C=N)(CN) 2] [C=N = bzq ( 3b), ppy ( 4b)], the former being strongly colored [red ( 3a) or purple ( 4a)] and the latter being yellow. Compounds 3a and 4a transform reversibly into the yellow, 3b and 4b, compounds upon desorption/ reabsorption of water molecules from the environment. The red solid, 3a, also exhibits vapochromic behavior when it is exposed to volatile organic compounds, the shortest response times being those observed for methanol and ethanol. UV-vis and emission spectra of all compounds were recorded both in solution and in the solid state. In methanol solution, the difference in the cation causes no differences in the absorption nor in the emission spectra, which is as expected for the monomer species. However, in the solid state, the differences are notable. For both the red ( 3a) and purple ( 4a) compounds, a prominent absorption, which has maxima at about 550 nm and is responsible for their intense colors, as well as a structureless emission at lambda > 700 nm that suffers a significant red-shift upon cooling, are due to (1,3)MMLCT (= metal-metal-to-ligand charge transfer) [dsigma*(Pt) --> pi*(C=N)] transitions characteristic of linear-chain platinum complexes with short Pt...Pt contacts. Time-dependent density-functional theory calculations on complex 5 and the X-ray diffraction study on compound [K(OCMe 2) 2][Pt(ppy)(CN) 2] ( 4c) are also included.     

Convenient route to enantiopure fmoc-protected morpholine-3-carboxylic acid

Enantiopure Fmoc-protected morpholine-3-carboxylic acid was synthesized from dimethoxyacetaldehyde and serine methyl ester through a short and practical synthetic route. The preparation consisted of a five-step process based on reductive amination, intramolecular acetalization, and concomitant elimination of the anomeric methoxy substituent, followed by hydrogenation of the double bond and final acidic ester hydrolysis. The optical purity of both enantiomers of the title amino acid was demonstrated by HPLC analysis of the corresponding amide derivatives obtained from coupling with chiral (S)-(-)-1-phenylethylamine. Moreover, the synthesis of a model tripeptide showed full compatibility of the title Fmoc-amino acid with solid-phase peptide synthesis, thus allowing the application of Fmoc-morpholine-3-carboxylic acid in peptidomimetic chemistry on the solid phase.     

A comparison of neptunyl(V) and neptunyl(VI) solution coordination: the stability of cation-cation interactions

The solution coordination environments of pentavalent and hexavalent Np are studied by high-energy X-ray scattering. Np5+ and Np6+ both exist as the neptunyl moiety coordinated with five equatorial waters at Np-O distances of 2.46(2) and 2.37(2) A, respectively. NpO2(2+) also has a second coordination sphere of 6-10 waters at 4.37(3) A. The NpO2+ scattering is complicated by the presence of scattering at about 4.2 A that is attributed to Np-Np cation-cation interactions. The analysis of changing intensity of this peak as a function of Np concentration is used to determine a stability constant of Keq=0.74(9) M(-1) for the dimeric complex.     

Fluoropolymer based on a polyaspartamide containing 1,2,4-oxadiazole units: a potential artificial oxygen (O2) carrier

In this preliminary work we have prepared a fluorinated polymer capable of solubilizing an appreciable amount of O(2) and, at the same time, maintaining a higher water solubility than perfluoroalkanes investigated as injectable O(2) carriers. In particular, we describe the synthesis and characterization of a new macromolecular conjugate obtained by derivatization of alpha,beta-poly(N-2-hydroxyethyl)-DL-aspartamide (PHEA) with 5-pentafluorophenyl-3-perfluoroheptyl-1,2,4-oxadiazole, called PHEA-F. This new water soluble fluoropolymer was prepared in high yield using a simple procedure. It was characterized by FT-IR and UV-vis spectrophotometry, (19)F-NMR and SEC measurements. O(2) solubility studies on PHEA-F aqueous solutions were carried out at 25 degrees C and 37 degrees C at atmospheric pressure and showed that PHEA-F conjugate, despite its low degree of derivatization in fluorine containing groups (2.60 mol-%), is capable of dissolving 13-15% more O(2) than non-fluorinated PHEA. Moreover, O(2) release in simulated physiological conditions is faster for PHEA-F than for PHEA. The biocompatibility of this conjugate has been evaluated by performing an in vitro viability assay on human chronic myelogenous leukaemia cells (K-562) chosen as a model cell line and in vitro haemolysis experiments on human RBCs. All these properties suggest the potential use of PHEA-F as an artificial O(2) carrier.     

Thin lead sheets in the decorative features in Pavia Charterhouse

The facade of the church of the Pavia Charterhouse, built at the end of the 15th century, shows outstanding decorative features made of different stone materials, such as marbles, breccias and sandstones. Magnificent ornamental elements are made of thin lead sheets, and some marble slabs are inlaid with them. Metal elements are shaped in complex geometric and phytomorphic design, to form a Greek fret in black contrasting with the white Carrara marble. Lead pins were fixed to the back of the thin lead sheets with the aim of attaching the metal elements to the marble; in so doing the pins and the lead sheets constitute a single piece of metal. In some areas, lead elements have been lost, and they have been substituted with a black plaster, matching the colour of the metal. To the authors' knowledge, this kind of decorative technique is rare, and confirms the refinement of Renaissance Lombard architecture. This work reports on the results of an extensive survey of the white, orange and yellowish layers, which are present on the external surface of the lead. The thin lead sheets have been characterized and their state of conservation has been studied with the aid of Optical Microscopy, SEM-EDS, FTIR and Raman analyses. Lead sulphate, lead carbonates and oxides have been identified as decay products.     

Assessment of protein folding potentials with an evolutionary method

Many different protein folding potentials have been developed in the last decades, based upon knowledge of experimentally determined protein structures. Decoy-based techniques are frequently used to assess these force fields, but other methods can explore different features in the performance of the interaction schemes, thus helping in their evaluation. Here, we propose an evolutionary strategy to efficiently assess folding potentials. We apply it to three potentials with different characteristics, taken from the bibliography. A search for minimum energy protein topologies, treated as arrangements of rigid protein fragments, is performed. The method, applied to a set of helix bundle proteins, shows the different behavior of the studied potentials, providing a reasonably fast tool to evaluate their advantages and limitations.     

Synthesis of 1,3-dihydrobenzo[c]furans from ortho-lithiated aryloxiranes

A general method for the synthesis of hydroxyalkyl 1,3-dihydrobenzo[c]furans from ortho-lithiated aryloxiranes and carbonyl compounds is described.     

Assessing the instability of the isoelectric focusing patterns of erythropoietin in urine

IEF can be used to differentiate human urinary erythropoietin (uEPO), recombinant human erythropoietin or epoetin (rEPO) and darbepoetin (novel erythropoiesis stimulating protein (NESP)). This is the basis of the method currently used to detect misuse of rEPO and NESP by elite athletes. Recently, an unknown activity has been attributed to some urine samples (denominated 'unstable' urine by the World Anti-Doping Agency; WADA). This activity has shown to give rise to artefactual profiles for both rEPO and NESP when incubated with such urine and, thus, raised concerns with respect to doping control. We have evaluated which charges produce the characteristic IEF profiles of uEPO, rEPO and NESP and how these profiles respond to distinct enzymatic reactions. From sialidase digestions it became evident that only uEPO contains charges different from sialic acid, and a comparison of all substances after complete de-N-glycosylation localized these charges in the carbohydrate moiety. Partial desialylation, or digestion with arylsulfatase from Helix pomatia yielded profiles for recombinants species similar to those observed for unstable urine samples. The contributions from our studies to the anti-doping problem include: (i) protocols that may corroborate the potential misuse of rEPO or NESP based on the particular enzymatic activity of an arylsulfatase preparation, or a broad-specificity sialidase; (ii) assurance that the instability observed in some urine samples may only result from false-negatives, but not from false-positive testing; and (iii) a simple remedy to prevent an unstable urine from altering the IEF profile by adding selective competitive substrates.     

Full counting statistics with spin-sensitive detectors reveals spin singlets

We study the full counting statistics of electric current to several drain terminals with spin-dependent entrance conductances. We show that the statistics of charge transfers can be interpreted in terms of single electrons and spin-singlet pairs coming from the source. If the source contains transport channels of high transparency, a significant fraction of electrons comes in spin-singlet pairs.     

On the mod cohomology of

We study the mod  cohomology of the classifying space of the projective unitary group . We first prove that conjectures due to J.F. Adams and Kono and Yagita (1993) about the structure of the mod  cohomology of the classifying space of connected compact Lie groups hold in the case of . Finally, we prove that the classifying space of the projective unitary group is determined by its mod  cohomology as an unstable algebra over the Steenrod algebra for 3$">, completing previous work by Dwyer, Miller and Wilkerson (1992) and Broto and Viruel (1998) for the cases .