Templating effect of carbon nanoforms on highly cross‐linked imidazolium network: Catalytic activity of the resulting hybrids with Pd nanoparticles

Two different carbon nanoforms (CNFs), namely multi‐walled carbon nanotubes (MWCNTs) and carbon nanohorns (CNHs), have been chosen as support for the direct polymerization of a bis‐vinylimidazolium salt. Transmission electron microscopy analyses revealed a templating effect of the CNFs on the growth of the polymeric network, which perfectly covers their whole surfaces creating a cylindrical or spherical coating for MWCNTs and CNHs, respectively. Subsequently, the CNFs‐polyimidazolium have been used as stabilizers for Pd nanoparticles (Pd NPs), and the obtained materials have been characterized by means of analytical and spectroscopic techniques and then employed as easily recoverable and recyclable catalysts for Suzuki and Heck reactions. Quantitative conversions have been obtained in almost all the explored reactions, even employing low loading of catalyst (down to 0.007 mol%). Suzuki reactions were carried out in pure water under aerobic conditions. Both materials showed excellent activity and recyclability for the investigated C‐C coupling reactions, with the CNHs‐based material resulting slightly more active than the MWCNTs‐based one due to a higher superficial exposure of Pd NPs.     

Recent Reviews. 41

Reviews are listed in order of appearance in the sources indicated. In multidisciplinary review journals, only those reviews which fall within the scope of this Journal are included. Sources are listed alphabetically in three categories: regularly issued review journals and series volumes, contributed volumes, and other monographs. Titles are numbered serially, and these numbers are used for reference in the index. Major English-language sources of critical reviews are covered. Encyclopedic treatises, annual surveys such as Specialist Periodical Reports, and compilations of symposia proceedings are omitted. This installment of Recent Reviews covers principally the early part of the 1996 literature. Previous installment: J. Org. Chem. 1996, 61(7), 2572-80. These Recent Review articles are now also available in a database form on the ACS Organic Division WWW site http://www.organic.emory.edu/acsorg/index.html.     

Regioselective Alkylation of Lithium Enolates Derived from 2-Heptanone

The benzylation and $\text{u}$-butylation of the kinetic enolate mixture derived from 2-heptanone has been studied in DME in the absence and in the presence of lithium ion complexing agents (triglyme, benzo-14-crown-4, DMF (neat), DMF, and HMPA).     

Ceria-Zirconia Nanostructured Materials for Catalytic Applications: Textural Characteristics and Redox Properties

Highly dispersed solid solutions of ceria-zirconia with nominal composition Ce_0.6Zr_0.4O₂ were prepared by sol-gel technique and the influence of the gel aging time (1 day–3 weeks) on the morphological and textural properties of the materials was investigated. The samples were calcined at 923 K for 8 h, then characterized by XRD, BET surface area and pore size measurements by gas adsorption and by mercury porosimetry. DTA, TEM and SEM analyses were also carried out. The aging of the gel seems to have a remarkable influence on the morphology of the materials, whose surface area and porosity increase by increasing aging time. The phase composition of the solid solutions of ceria-zirconia, as determined by XRD analysis, seems to be independent from the synthetic procedure; in any case a cubic phase (space group Fm-3m) was identified as the main component. XRD and TEM characterizations show the presence of highly dispersed crystallites, with diameters in the range 60–80 Å. The redox properties and hydrogen chemisorption capacity have been studied by TPR/TPD/TPO experiments. Oxygen storage capacity measurements were carried out by a pulse technique, to determine the overall reducibility of the solid, OSCC (Oxygen storage capacity complete). OBC (Oxygen buffering capacity) measurement were also performed to determine the ability of the ceria-zirconia oxides to attenuate fast oscillations (0.1 Hz) of oxygen partial pressure. The correlation between textural, structural and redox properties of the oxides is discussed.     

Synthesis of 1-deoxysphingosine derivatives with conformationally restricted pyrrolidinediol head groups

[structure: see text] A family of cyclic 1-deoxysphingolipid derivatives of structure 4 has been designed and synthesized, which may serve as tumorigenesis suppressors for various cancers. Compound 4 is a second-generation analogue developed from sphingosine (1), in which a hydroxyl substituent is moved from C1 to C5 and a methylene is added for conformational rigidity between the C2-nitrogen substituent and C4. The synthetic chemistry for pyrrolidine ring closure at C3-C4 features ring-closing metathesis followed by hydroboration-oxidation.     

Systematics of proton emission

A very simple formula is presented that relates the logarithm of the half-life, corrected by the centrifugal barrier, with the Coulomb parameter in proton decay processes. The corresponding experimental data lie on two straight lines which appear as a result of a sudden change in the nuclear shape marking two regions of deformation independently of the angular momentum of the outgoing proton. This feature provides a powerful tool to assign experimentally quantum numbers in proton emitters.     

Benign coupling of reactions and separations with reversible ionic liquids

Reversible ionic liquids are a novel class of solvents that combine an effective medium where reactions occur with a ‘built-in’ separation ability for facile recovery of the products and catalysts, making the solvent available for recycle. We report the utility of these solvents in a number of reactions (Claisen-Schmidt condensation, Heck C-C coupling, and CO₂ capture) and discuss the effectiveness of the separation. We also provide insight into the challenges and limitations of using these unique solvent systems to couple reactions and separations.     

Screening for pharmaco‐toxicologically relevant compounds in biosamples using high‐resolution mass spectrometry: a ‘metabolomic’ approach to the discrimination between isomers

High‐resolution mass spectrometry (HRMS) enables the identification of a chemical formula of small molecules through the accurate measurement of mass and isotopic pattern. However, the identification of an unknown compound starting from the chemical formula requires additional tools: (1) a database associating chemical formulas to compound names and (2) a way to discriminate between isomers. The aim of this present study is to evaluate the ability of a novel ‘metabolomic’ approach to reduce the list of candidates with identical chemical formula. Urine/blood/hair samples collected from real positive cases were submitted to a screening procedure using ESI‐MS‐TOF (positive‐ion mode) combined with either capillary electrophoresis or reversed phase liquid chromatography (LC). Detected peaks were searched against a Pharmaco/Toxicologically Relevant Compounds database (ca 50 500 compounds and phase I and phase II metabolites) consisting of a subset of PubChem compounds and a list of candidates was retrieved. Then, starting from the mass of unknown, mass shifts corresponding to pre‐defined biotransformations (e.g. demethylation, glucuronidation, etc.) were calculated and corresponding mass chromatograms were extracted from the total ion current (TIC) in order to search for metabolite peaks. For each candidate, the number of different functional groups in the molecule was automatically calculated using E‐Dragon software (Talete srl, Milan, Italy). Then, the presence of metabolites in the TIC was matched with functional groups data in order to exclude candidates with structures not compatible with observed biotransformations (e.g. loss of methyl from a structure not bearing methyls). The procedure was tested on 108 pharmaco‐toxicologically relevant compounds (PTRC) and their phase I metabolites were detected in real positive samples. The mean list length (MLL) of candidates retrieved from the database was 7.01 ± 4.77 (median, 7; range, 1–28) before the application of the ‘metabolomic’ approach, and after the application it was reduced to 4.08 ± 3.11 (median 3, range 1–17). HRMS allows a much broader screening for PTRC than other screening approaches (e.g. library search on mass spectra databases). The ‘metabolomic’ approach enables the reduction of the list of candidate isomers. Copyright © 2009 John Wiley & Sons, Ltd.