Generation, characterization, and electrochemical behavior of the palladium-hydride cluster [Pd3(dppm)3(mu3-CO)(mu3-H)]+ (dppm=Bis(diphenylphosphinomethane)

Addition of formate on the dicationic cluster [Pd(3)(dppm)(3)(mu(3)-CO)](2+) (dppm=bis(diphenylphosphinomethane) affords quantitatively the hydride cluster [Pd(3)(dppm)(3)(mu(3)-CO)(mu(3)-H)](+). This new palladium-hydride cluster has been characterised by (1)H NMR, (31)P NMR and UV/Vis spectroscopy and MALDI-TOF mass spectrometry. The unambiguous identification of the capping hydride was made from (2)H NMR spectroscopy by using DCO(2) (-) as starting material. The mechanism of the hydride complex formation was investigated by UV/Vis stopped-flow methods. The kinetic data are consistent with a two-step process involving: 1) host-guest interactions between HCO(2) (-) and [Pd(3)(dppm)(3)(mu(3)-CO)](2+) and 2) a reductive elimination of CO(2). Two alternatives routes to the hydride complex were also examined : 1) hydride transfer from NaBH(4) to [Pd(3)(dppm)(3)(mu(3)-CO)](2+) and 2) electrochemical reduction of [Pd(3)(dppm)(3)(mu(3)-CO)](2+) to [Pd(3)(dppm)(3)(mu(3)-CO)](0) followed by an addition of one equivalent of H(+). Based on cyclic voltammetry, evidence for a dual mechanism (ECE and EEC; E=electrochemical (one-electron transfer), C=chemical (hydride dissociation)) for the two-electron reduction of [Pd(3)(dppm)(3)(mu(3)-CO)(mu(3)-H)](+) to [Pd(3)(dppm)(3)(mu(3)-CO)](0) is provided, corroborated by digital simulation of the experimental results. Geometry optimisations of the [Pd(3)(H(2)PCH(2)PH(2))(3)(mu(3)-CO)(mu(3)-H)](n) model clusters were performed by using DFT at the B3 LYP level. Upon one-electron reductions, the Pd--Pd distance increases from a formal single bond (n=+1), to partially bonding (n=0), to weak metal-metal interactions (n=-1), while the Pd--H bond length remains relatively the same.     

Nicotine: on the potential role of ionic liquids for its processing and purification

Marked solubility differences of nicotine in the ionic liquids [C(2)mim][NTf(2)], [C(2)mim][EtOSO(3)], and [C(n)mim]Cl, 6 相似文献   

Ultrasonication Improves Solid Phase Synthesis of Peptides Specific for Fibroblast Growth Factor Receptor and for the Protein-Protein Interface RANK-TRAF6

Considering our interest in the use of peptides as potential target-specific drugs or as delivery vectors of metallodrugs for various biomedical applications, it is crucial to explore improved synthetic methodologies to accomplish the highest peptide crude purity in the shortest time possible. Therefore, we compared “classical” fluorenylmethoxycarbonyl (Fmoc)-solid phase peptide synthesis (SPPS) with ultrasound(US)-assisted SPPS based on the preparation of three peptides, namely the fibroblast growth factor receptor 3(FGFR3)-specific peptide Pep1 (VSPPLTLGQLLS-NH₂) and the novel peptides Pep2 (RQMATADEA-NH₂) and Pep3 (AAVALLPAVLLALLAPRQMATADEA-NH₂), which are being developed aimed at interfering with the intracellular protein-protein interaction(PPI) RANK-TRAF6. Our results demonstrated that US-assisted SPPS led to a 14-fold (Pep1) and 4-fold time reduction (Pep2) in peptide assembly compared to the “classical” method. Interestingly, US-assisted SPPS yielded Pep1 in higher purity (82%) than the “classical” SPPS (73%). The significant time reduction combined with high crude peptide purity attained prompted use to apply US-assisted SPPS to the large peptide Pep3, which displays a high number of hydrophobic amino acids and homooligo-sequences. Remarkably, the synthesis of this 25-mer peptide was attained during a “working day” (347 min) in moderate purity (approx. 49%). In conclusion, we have reinforced the importance of using US-SPPS towards facilitating the production of peptides in shorter time with increased efficacy in moderate to high crude purity. This is of special importance for long peptides such as the case of Pep3.     

电感耦合等离子体原子发射光谱法测定马奶酒中的多种元素

电感耦合等离子体原子发射光谱法测定马奶酒中的多种元素嘎日迪,乌地（内蒙古师范大学化学系,配位化学研究所,呼和浩特,０１００２２）关键词电感耦合等离子体原子发射光谱,马奶酒,微量金属元素蒙古民族喜爱的传统饮料──马奶酒（蒙语“策格”）是用鲜马奶为原料发...     

Multistep Methods for a Class of Higher Order Differential Problems: Convergence and Error Bounds

In this paper multistep methods for higher order differential systems of the type $Y^{(r)}=f(t,Y)$ are proposed. Such methods permit the numerical solutions of initial value problems for such systems, providing error bounds and avoiding the increase of the computational cost derived from the standard approach based on the consideration of an equivalent extended first order system.     

Plasma-assisted oxidation of Cu(100) and Cu(111)

Oxidized copper surfaces have attracted significant attention in recent years due to their unique catalytic properties, including their enhanced hydrocarbon selectivity during the electrochemical reduction of CO₂. Although oxygen plasma has been used to create highly active copper oxide electrodes for CO₂RR, how such treatment alters the copper surface is still poorly understood. Here, we study the oxidation of Cu(100) and Cu(111) surfaces by sequential exposure to a low-pressure oxygen plasma at room temperature. We used scanning tunnelling microscopy (STM), low energy electron microscopy (LEEM), X-ray photoelectron spectroscopy (XPS), near edge X-ray absorption fine structure spectroscopy (NEXAFS) and low energy electron diffraction (LEED) for the comprehensive characterization of the resulting oxide films. O₂-plasma exposure initially induces the growth of 3-dimensional oxide islands surrounded by an O-covered Cu surface. With ongoing plasma exposure, the islands coalesce and form a closed oxide film. Utilizing spectroscopy, we traced the evolution of metallic Cu, Cu₂O and CuO species upon oxygen plasma exposure and found a dependence of the surface structure and chemical state on the substrate''s orientation. On Cu(100) the oxide islands grow with a lower rate than on the (111) surface. Furthermore, while on Cu(100) only Cu₂O is formed during the initial growth phase, both Cu₂O and CuO species are simultaneously generated on Cu(111). Finally, prolonged oxygen plasma exposure results in a sandwiched film structure with CuO at the surface and Cu₂O at the interface to the metallic support. A stable CuO(111) surface orientation is identified in both cases, aligned to the Cu(111) support, but with two coexisting rotational domains on Cu(100). These findings illustrate the possibility of tailoring the oxidation state, structure and morphology of metallic surfaces for a wide range of applications through oxygen plasma treatments.

A low-pressure oxygen plasma oxidized Cu(100) and Cu(111) surfaces at room temperature. The time-dependent evolution of surface structure and chemical composition is reported in detail for a range of exposure times up to 30 min.     

Evaluation of the Physical-Chemical Properties of Poly(ethylene oxide)-block-Poly(propylene oxide) by Different Characterization Techniques

Summary: A surfactant's efficiency for a given application is dependent on its chemical structure and physical-chemical properties in solution, including surfactant solubility as a function of concentration and temperature as well as adsorption and aggregation behavior. This review work describes the main physical-chemical properties ascertained by means of various characterization techniques, which can be used to study nonionic surfactants based on poly(ethylene oxide)-block-poly(propylene oxide) (PEO-PPO). Among these, some are widely used and others are relatively new for this type of application.     

Lithium bis(2‐phenylphosphidoethyl)phenyl‐phosphine: A reactive phosphorus intermediate

Bis(2‐phenylphosphinoethyl)phenylphosphine, PhP(CH₂CH₂PPh₂)₂, reacts with lithium in tetrahydrofuran to give the corresponding lithium bis(2‐diphenylphosphidoethyl)phenylphosphine, Li₂[PhP(CH₂CH₂PPh)₂]. The lithium diphosphide is identified by NMR spectroscopy and further characterized through arylation with excess brombenzene to reform the starting phosphine, PhP(CH₂CH₂PPh₂)₂. Initial reactivity studies of the diphosphide, PhP(CH₂CH₂PPh), with some alkylhalides are also described. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:675–678, 2007; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20351     

The characteristics of gas/liquid flow in large risers at high pressures

Although most of the work reported on two-phase flows are limited to small pipe diameters, two-phase flow in large risers are increasingly being encountered in the petroleum and nuclear industries. In the present work, a wire mesh sensor was employed to obtain void fraction and bubble size distribution data and visualizations of steam/water flow in a large vertical pipe (194 mm in diameter) at 46 bar. For comparison purposes, measurements were made at similar phase velocities and physical properties to a dataset for nitrogen/naphtha flow in a similar-sized riser. There exist significant differences between both sets of data. Churn-turbulent flow is observed in the present work instead of slug flow, and this differs from the intermittent and semi-annular flow patterns reported for nitrogen/naphtha data. The mean void fraction of the nitrogen/naphtha data is higher than that of the present steam/water data due to the differences in purity in the liquid phases. Furthermore, core peak distributions are observed for the present work in contrast to the flatter profiles deduced for the nitrogen/naphtha using a power law relationship.