C?C Bond Formation via C?H Activation and C?N Bond Formation via Oxidative Amination Catalyzed by Palladium‐ Polyoxometalate Nanomaterials Using Dioxygen as the Terminal Oxidant

An efficient heterogeneous palladium‐polyoxometalate catalyst with the formula Pd‐H₆PV₃Mo₉O₄₀/C has been successfully developed for carbon‐carbon (C C) bond formation via carbon‐hydrogen (C H) activation and carbon‐nitrogen (C N) bond formation via oxidative amination using oxygen as the terminal oxidant. The coupling processes are simple, and use relatively mild conditions to form the desired products. In addition, less waste is generated as no additional reagents such as organic/inorganic oxidants are required, and water is the only by‐product generated.     

Exploring the Biocatalytic Scope of Alditol Oxidase from Streptomyces coelicolor

The substrate scope of the flavoprotein alditol oxidase (AldO) from Streptomyces coelicolor A3(2), recombinantly produced in Escherichia coli, was explored. While it has been established that AldO efficiently oxidizes alditols to D ‐aldoses, this study revealed that the enzyme is also active with a broad range of aliphatic and aromatic alcohols. Alcohols containing hydroxy groups at the C‐1 and C‐2 positions like 1,2,4‐butanetriol (K_m=170 mM, k_cat=4.4 s⁻¹), 1,2‐pentanediol (K_m=52 mM, k_cat=0.85 s⁻¹) and 1,2‐hexanediol (K_m=97 mM, k_cat=2.0 s⁻¹) were readily accepted by AldO. Furthermore, the enzyme was highly enantioselective for the oxidation of 1,2‐diols [e.g., for 1‐phenyl‐1,2‐ethanediol the (R)‐enantiomer was preferred with an E‐value of 74]. For several diols the oxidation products were determined by GC‐MS and NMR. Interestingly, for all tested 1,2‐diols the products were found to be the α‐hydroxy acids instead of the expected α‐hydroxy aldehydes. Incubation of (R)‐1‐phenyl‐1,2‐ethanediol with ¹⁸O‐labelled water (H₂¹⁸O) revealed that a second enzymatic oxidation step occurs via the hydrate product intermediate. The relaxed substrate specificity, excellent enantioselectivity, and independence of coenzymes make AldO an attractive enzyme for the preparation of optically pure 1,2‐diols and α‐hydroxy acids.     

Boronic Acid‐Catalyzed Selective Oxidation of 1,2‐Diols to α‐Hydroxy Ketones in Water

The activation of 1,2‐diols through formation of boronate esters was found to enhance the selective oxidation of 1,2‐diols to their corresponding α‐hydroxy ketones in aqueous medium. The oxidation step was accomplished using dibromoisocyanuric acid (DBI) as a terminal chemical oxidant or an electrochemical process. The electrochemical process was based on the use of platinum electrodes, methylboronic acid [MeB(OH)₂] as a catalyst and bromide ion as a mediator. Electro‐generated OH⁻ ions (EGB) at the cathode acted as a base and “Br⁺” ion generated at the anode acted as an oxidant. Various cyclic and acyclic 1,2‐diols as substrates were selectively oxidized to the corresponding α‐hydroxy ketones via their boronate esters by the two oxidative methods in good to excellent yields.

     

A Mild Catalytic Oxidation System: Ruthenium Porphyrin and 2,6‐Dichloropyridine N‐Oxide Applied for Alkene Dihydroxylation

A new method was developed to transform alkenes into three types of functional molecules, including epoxides, aldehydes and 1,2‐diols by using dichlororuthenium(IV) meso‐tetrakis(2,6‐dichlorophenyl)porphyrin [Ru(IV)(TDCPP)Cl₂] as catalyst and 2,6‐dichloropyridine N‐oxide (Cl₂pyNO) as the oxidant, in which the 1,2‐diols were afforded via “one‐pot” reactions in moderate yields.     

Combined Effects of Sb-Doping and of Preparation via Lacunary Precursor for P/Mo-Based, Keggin-Type Polyoxometalates, Catalysts for the Selective Oxidation of Isobutane to Methacrylic Acid

Catalysts for the selective oxidation of isobutane to methacrylic acid, based on ammonium salts of phosphorus/molybdenum Keggin-type polyoxometalates, were prepared by precipitation of a lacunary precursor at pH 4.0, and by calcination of the precipitate at 350 °C in air. The thermal treatment led to the transformation of the lacunary polyoxometalate into (NH₄)₃PMo₁₂ O₄₀. This procedure yielded a catalyst that was active, but poorly selective, from the beginning of its reaction time, since the active sites were generated during the calcination, and thus during the transformation of the lacunary precursor into the Keggin compound. Nevertheless, for the reaction under isobutane-rich conditions, the catalyst exhibited an initial period during which the progressive reduction of the polyoxometalate led to an improvement of the selectivity to methacrylic acid. An alternative method to develop a partially reduced compound was by preparation of a Sb³⁺-doped polyoxometalate. A solid-state redox reaction between Sb³⁺ and Mo⁶⁺ occurred in the Keggin framework during the calcination of the precursor. With this procedure, a catalyst was obtained, which did not require the preliminary equilibration, and which therefore was active and selective from the beginning of its reaction time. Furthermore, the catalyst was found to be surprisingly very active under isobutane-lean conditions.     

Continuous‐Flow Asymmetric Hydrogenation of the β‐Keto Ester Methyl Propionylacetate in Ionic Liquid–Supercritical Carbon Dioxide Biphasic Systems

A continuous‐flow process for the asymmetric hydrogenation of methyl propionylacetate as a prototypical β‐keto ester in a biphasic system of ionic liquid and supercritical carbon dioxide (scCO₂) is presented. An established ruthenium/2,2′‐bis(diphenylphosphino)‐1,1′‐binaphthyl (BINAP) catalyst was immobilised in an imidazolium‐based ionic liquid while scCO₂ was used as mobile phase transporting reactants in and products out of the reactor. The use of acidic additives led to significantly higher reaction rates and enhanced catalyst stability albeit at slightly reduced enantioselectivity. High single pass conversions (>90%) and good enantioselectivity (80–82% ee) were achieved in the first 80 h. The initial catalyst activity was retained to 91% after 100 h and to 69% after 150 h time‐on‐stream, whereas the enantioselectivity remained practically constant during the entire process. A total turnover number of ∼21,000 and an averaged space‐time yield (STY_av) of 149 g L⁻¹ h⁻¹ were reached in a long‐term experiment. No ruthenium and phosphorus contaminants could be detected via inductively coupled plasma optical emission spectrometry (ICP‐OES) in the product stream and almost quantitative retention by the analysis of the stationary phase was confirmed. A comparison between batch‐wise and continuous‐flow operation on the basis of these data is provided.     

Copper Catalysts for Selective C?C Bond Cleavage of β‐O‐4 Lignin Model Compounds

The reactivity of homogeneous copper catalysts towards the selective C C bond cleavage of both phenolic and non‐phenolic arylglycerol β‐aryl ether lignin model compounds has been explored. Several copper precursors, nitrogen ligands, and solvents were evaluated in order to optimize the catalyst system. Using the optimized catalyst system, copper(I) trifluoromethanesulfonate [Cu(OTf)]/L/TEMPO (L=2,6‐lutidine, TEMPO=2,2,6,6‐tetramethyl‐piperidin‐1‐yl‐oxyl), aerobic oxidation of the non‐phenolic β‐O‐4 lignin model compound proceeded with good selectivity for C_α C_β bond cleavage, affording 3,5‐dimethoxybenzaldehyde as the major product. Aerobic oxidation of the corresponding phenolic β‐O‐4 lignin model proceeded with different selectivity, affording 2,6‐dimethoxybenzoquinone and α,β‐unsaturated aldehyde products resulting from cleavage of the C_α C_aryl bond. At low catalyst concentrations, however, a change in selectivity was observed as oxidation of the benzylic secondary alcohol predominated with both substrates.

     

Palladium‐Catalyzed Carbonylation of Diols to Cyclic Carbonates

The catalytic alkoxycarbonylation of 1,2‐diols by (neocuproine)palladium(II) acetate (neocuproine=2,9‐dimethyl‐1,10‐phenanthroline) or palladium(II) acetate/(−)‐sparteine using N‐chlorosuccinimide as the oxidant affords cyclic carbonates. The oxidative carbonylation of diols proceeds under mild conditions, requiring only 1 atm of carbon monoxide, and produces cyclic carbonates in moderate to good yields. Both 1,2‐ and 1,3‐diols can be carbonylated using (neocuproine)Pd(OAc)₂ and sodium dichloroisocyanuric acid, which serves as a competent oxidant and base for this system, to yield 5‐ and 6‐membered cyclic carbonates.     

Stabilization of Palladium Nanoparticles by Polyoxometalates Appended with Alkylthiol Tethers and their Use as Binary Catalysts for Liquid Phase Aerobic Oxydehydrogenation

A polyoxometalate with two alkyl thiol appendages, Q₄[SiW₁₁O₄₀(SiCH₂CH₂CH₂SH)₂] (Q=ammonium salt) stabilized the formation of palladium nanoparticles. This tethered polyoxometalate–palladium binary catalyst was effective for the aerobic oxydehydrogenation of vinylcyclohexene and vinylcyclohexane to styrene as the major product via activation of the allylic, tertiary carbon‐hydrogen bond.     

Effect of W on PtSn/C catalysts for ethanol electrooxidation

Binary and ternary Pt-based catalysts were prepared by the Pechini–Adams modified method on carbon Vulcan XC-72, and different nominal compositions were characterized by TEM and XRD. XRD showed that the electrocatalysts consisted of the Pt displaced phase, suggesting the formation of a solid solution between the metals Pt/W and Pt/Sn. Electrochemical investigations on these different electrode materials were carried out as a function of the electrocatalyst composition, in acid medium (0.5 mol dm⁻³ H₂SO₄) and in the presence of ethanol. The results obtained at room temperature showed that the PtSnW/C catalyst display better catalytic activity for ethanol oxidation compared to PtW/C catalyst. The reaction products (acetaldehyde, acetic acid and carbon dioxide) were analyzed by HPLC and identified by in situ infrared reflectance spectroscopy. The latter technique also allowed identification of the intermediate and adsorbed species. The presence of linearly adsorbed CO and CO₂ indicated that the cleavage of the C–C bond in the ethanol substrate occurred during the oxidation process. At 90 °C, the Pt₈₅Sn₈W₇/C catalyst gave higher current and power performances as anode material in a direct ethanol fuel cell (DEFC).     

Mechanistic Study of Carbon Oxidation with NO2 and O2 in the Presence of a Ru/Na‐Y Catalyst

The oxidation of model soot by NO₂ and O₂ in the presence of a Ru/Na‐Y catalyst under conditions close to automotive exhaust gas after‐treatment systems is investigated. Isothermal oxidation experiments of a physical mixture of carbon black and catalyst were performed in a temperature range of 300–400 °C. A remarkable increase of the oxidation rate by NO₂ and O₂ in the presence of the Ru/Na‐Y catalyst was observed. An overall mechanism involving oxygen transfer from the Ru catalyst to the carbon surface leading to an increase of C(O) complexes is proposed. These C(O) complexes are destabilized in the presence of NO₂ increasing the carbon oxidation rate.     

Enantioselective Biooxidation of Racemic trans‐Cyclic Vicinal Diols: One‐Pot Synthesis of Both Enantiopure (S,S)‐Cyclic Vicinal Diols and (R)‐α‐Hydroxy Ketones

Highly regio‐ and enantioselective alcohol dehydrogenases BDHA (2,3‐butanediol dehydrogenase from Bacillus subtilis BGSC1A1), CDDHPm (cyclic diol dehydrogenase from Pseudomonas medocina TA5), and CDDHRh (cyclic diol dehydrogenase from Rhodococcus sp. Moj‐3449) were discovered for the oxidation of racemic trans‐cyclic vicinal diols. Recombinant Escherichia coli expressing BDHA was engineered as an efficient whole‐cell biocatalyst for the oxidation of (±)‐1,2‐cyclopentanediol, 1,2‐cyclohexanediol, 1,2‐cycloheptane‐diol, and 1,2‐cyclooctanediol, respectively, to give the corresponding (R)‐α‐hydroxy ketones in >99% ee and (S,S)‐cyclic diols in >99% ee at 50% conversion in one pot. Escherichia coli (BDHA‐LDH) co‐expressing lactate dehydrogenase (LDH) for intracellular regeneration of NAD⁺ catalyzed the regio‐ and enantioselective oxidation of (±)‐1,2‐dihydroxy‐1,2,3,4‐tetrahydronaphthalene to produce the corresponding (R)‐α‐hydroxy ketone in >99% ee and (S,S)‐cyclic diol in 96% ee at 49% conversion. Preparative biotransformations were also demonstrated. Thus, a novel and useful method for the one‐pot synthesis of both vicinal diols and α‐hydroxy ketones in high ee was developed via highly regio‐ and enantioselective oxidations of the racemic vicinal diols.

     

Highly stable Fe/γ‐Al2O3 catalyst for catalytic wet peroxide oxidation

BACKGROUND: A highly stable Fe/γ‐Al₂O₃ catalyst for catalytic wet peroxide oxidation has been studied using phenol as target pollutant. The catalyst was prepared by incipient wetness impregnation of γ‐Al₂O₃ with an aqueous solution of Fe(NO₃)₃· 9H₂O. The influence of pH, temperature, catalyst and H₂O₂ doses, as well as the initial phenol concentration has been analyzed. RESULTS: The reaction temperature and initial pH significantly affect both phenol conversion and total organic carbon removal. Working at 50 °C, an initial pH of 3, 100 mg L^?1 of phenol, a dose of H₂O₂ corresponding to the stoichiometric amount and 1250 mg L^?1 of catalyst, complete phenol conversion and a total organic carbon removal efficiency close to 80% were achieved. When the initial phenol concentration was increased to 1500 mg L^?1, a decreased efficiency in total organic carbon removal was observed with increased leaching of iron that can be related to a higher concentration of oxalic acid, as by‐product from catalytic wet peroxide oxidation of phenol. CONCLUSION: A laboratory synthesized γ‐Al₂O₃ supported Fe has shown potential application in catalytic wet peroxide oxidation of phenolic wastewaters. The catalyst showed remarkable stability in long‐term continuous experiments with limited Fe leaching, < 3% of the initial loading. Copyright © 2010 Society of Chemical Industry     

Hydrogen-Atom Transfer Oxidation with H2O2 Catalyzed by [FeII(1,2-bis(2,2′-bipyridyl-6-yl)ethane(H2O)2]2+: Likely Involvement of a (μ-Hydroxo)(μ-1,2-peroxo)diiron(III) Intermediate

The iron(II) triflate complex ( 1 ) of 1,2-bis(2,2′-bipyridyl-6-yl)ethane, with two bipyridine moieties connected by an ethane bridge, was prepared. Addition of aqueous 30 % H₂O₂ to an acetonitrile solution of 1 yielded 2 , a green compound with λ_max=710 nm. Moessbauer measurements on 2 showed a doublet with an isomer shift (δ) of 0.35 mm/s and a quadrupole splitting (ΔE_Q) of 0.86 mm/s, indicative of an antiferromagnetically coupled diferric complex. Resonance Raman spectra showed peaks at 883, 556 and 451 cm⁻¹ that downshifted to 832, 540 and 441 cm⁻¹ when 1 was treated with H₂¹⁸O₂. All the spectroscopic data support the initial formation of a (μ-hydroxo)(μ-1,2-peroxo)diiron(III) complex that oxidizes carbon-hydrogen bonds. At 0 °C 2 reacted with cyclohexene to yield allylic oxidation products but not epoxide. Weak benzylic C−H bonds of alkylarenes were also oxidized. A plot of the logarithms of the second order rate constants versus the bond dissociation energies of the cleaved C−H bond showed an excellent linear correlation. Along with the observation that oxidation of the probe substrate 2,2-dimethyl-1-phenylpropan-1-ol yielded the corresponding ketone but no benzaldehyde, and the kinetic isotope effect, k_H/k_D, of 2.8 found for the oxidation of xanthene, the results support the hypothesis for a metal-based H-atom abstraction mechanism. Complex 2 is a rare example of a (μ-hydroxo)(μ-1,2-peroxo)diiron(III) complex that can elicit the oxidation of carbon-hydrogen bonds.     

Electrocatalytic oxidation of ethanol on Sn<Subscript>(1−<Emphasis Type="Italic">x</Emphasis>)</Subscript>Ir<Subscript>(<Emphasis Type="Italic">x</Emphasis>)</Subscript>O<Subscript>2</Subscript> electrodes in acid medium

The electrochemical oxidation of ethanol at Sn_(1−x)Ir _x O₂ electrodes (with x = 0.01, 0.05, 0.1 and 0.3) was studied in 0.1 mol L⁻¹ HClO₄ solution. Electrolysis experiments were carried out and the reaction products were analyzed by Liquid Chromatography. It was found that the amounts of the reaction products depended on the composition of the electrode. In situ infrared reflectance spectroscopy measurements were performed to identify the adsorbed intermediates and to postulate a reaction mechanism for ethanol electrooxidation on these electrode materials. As evidence, acetaldehyde and acetic acid were formed through a successive reaction process. Carbon dioxide was also identified as the end product, showing that the cleavage of the carbon–carbon bond occurred. These results indicate that the synthesized catalysts are able to lead to the total combustion of organic compounds. Analysis of the water bending band at different potentials illustrated its role at the electrode interface.     

Performance of H‐ZSM‐5‐supported bimetallic catalysts for the combustion of polluting volatile organic compounds in air

The performance of H‐ZSM‐5‐supported bimetallic catalysts with chromium as the base metal in the combustion of ethyl acetate and benzene is reported. A reactor operated from 100 to 500 °C at a gas hourly space velocity (GHSV) of 32 000 h^?1 was used for study of the activity. A combination of 1.0 wt% chromium and 0.5 wt% copper yielded a catalyst (Cr_1.0Cu_0.5/Z) with improved conversion and carbon dioxide yield. Cr₂O₃ (Cr³⁺) and CuO (Cu²⁺) were the predominant metal species in the catalyst. In agreement with the Mars–van Krevelen model, improved reducibility of Cr³⁺ in the presence of Cu²⁺ led to an improvement in activity. The copper content in Cr_1.0Cu_0.5/Z also favored the formation of deep combustion products. Condensation and subsequent growth of coke precursors in the catalyst pores led to the formation of a softer and less aromatic coke fraction while dehydrogenation activity on acid sites formed a harder and more aromatic coke fraction. The use of Cr_1.0Cu_0.5/Z favored the formation of lower molecular weight intermediates, leading to reduction in formation of softer coke. Copyright © 2005 Society of Chemical Industry     

Cyclohexa‐3,5‐diene‐1,2‐trans‐diols – Synthesis and Application in Target‐Oriented Syntheses

An exhaustive overview of the field of cyclohexa‐3,5‐diene‐1,2‐trans‐diols is given. Early and recent methods for the formation of the compounds are reviewed and the various syntheses in which the title compounds have been applied are presented. Special emphasis is given to naturally occurring epoxides, which have been the dominant target molecules since the 1970s. Finally, recent advances in biotechnology are highlighted; with the increased availability of the enantiomerically pure cyclohexa‐3,5‐diene‐1,2‐trans‐diols, new synthetic endeavours were initiated.     

Polymer‐Based Spherical Activated Carbon as Easy‐to‐Handle Catalyst Support for Hydrogenation Reactions

The application of polymer‐based spherical activated carbon (PBSAC) as catalyst support offers unprecedented advantages in the handling of the catalyst in all stages of its application due to its superior fluid dynamic properties and dust‐free character, minimizing post processing times and facilitating catalyst recycling. The preparation of PBSAC‐based Pd catalysts has been addressed using PBSAC of different particle sizes and degrees of activation. Prior to Pd deposition, the support was oxidized in nitric and sulfuric acidic media under different operating conditions in order to introduce surface charges for the ion exchange. This method was successfully applied as, even for the mildest functionalization conditions, full deposition of Pd was achieved. The synthesized Pd‐PBSAC catalysts were successfully employed in the hydrogenation of cinnamic acid achieving its complete conversion at an optimum effective rate constant of 0.122 m³ kg_Pd^?1 s^?1.     

Effects of Lewis acid catalysts on the cleavage of aliphatic and aryl-aryl linkages in coal-related structures

ZnCl₂ and AlCl₃ catalyse the cleavage of aliphatic linkages between aromatic nuclei but not the cleavage of direct aryl-aryl bonds between such nuclei. The rate of alkyl-aryl bond breakage depends on the Brönsted acidity of the active catalyst (e.g. H⁺(ZnCl₂X)^? or H⁺(AlCl₃X)^?) and the Brönsted basicity of the aromatic portions of the reactant. AlCl₃ is significantly more active than ZnCl₂, and reactants containing hydroxyphenyl or napthyl groups are more reactive than those containing phenyl groups. The distribution of final products is strongly affected by the reactions of the aryl-alkyl carbonium ion formed upon cleavage of an alkyl-aryl bond. If the alkyl portion of the carbonium ion contains three or more carbon atoms, the ion preferentially undergoes an intramolecular reaction to form a hydroaromatic product. With only one or two carbon atoms the carbonium ion reacts via either hydride abstraction or electrophilic substitution, the hydride abstraction producing an alkylaromatic product, which may in turn undergo dealkylation. Reactant and products produced by a Scholl condensation act as the principle sources of hydride ions. Molecular H₂ also contributes some hydride ions. The reaction of carbonium ions by electrophilic substitution leads either to the regeneration of the initial reactant or to the formation of high-molecular-weight tars.     

Bimetallic‐Catalyzed Reduction of Carboxylic Acids and Lactones to Alcohols and Diols

The homogeneously catalyzed reduction of carboxylic acids with hydrogen was studied. Bimetallic catalysts consisting of a group 8 or 9 late transition‐metal and a second group 6 or 7 transition‐metal carbonyl showed a synergistic effect allowing the conversion in good yields under moderate conditions. Besides the effect of different catalyst precursors, the influence of temperature, hydrogen pressure, and catalyst concentration was investigated. An equimolar mixture of [Rh(acac)(CO)₂] and [Mo(CO)₆] showed the highest activity and was therefore applied to the reduction of lactones to diols. The reduction potential of the catalyst was found to be dependent on the ring size of the lactone used. Five‐membered ring lactones were hardly converted to diols whereas six‐ and seven‐ membered ring lactones reacted easily.