First row transition metal complexes of phthalocyanine are employed as catalysts for the oxidation of cyclohexene and cyclooctene using iodosylbenzene and pentafluoroiodosyl benzene. The catalysis was performed in dichloromethane: methanol:water (80:18:2) solvent mixture.  The products of the catalysis for cyclohexene are epoxycyclohexane, 2-cyclohexene-1-ol and 2-cyclohexene-1-one whereas ...

Oxidation of cyclooctene was studied in presence aqueous hydrogen peroxide (30%, v/v) over nano iron oxide. The catalyst prepared by microemulsion method and characterized using various techniques including XRD, TEM and BET techniques for evaluating phase, structure and morphology and surface area. In this study, we investigated the effects of varying the catalyst content, reaction temperature,...

A 3D porous framework [Co3(μ2-OH)4(I)2]·2H2O (I = hypoxanthine) with two types of 1D channels possess excellent catalytic ability for the selective oxidation of cis-cyclooctene.

There is considerable interest in the use of bioorthogonal covalent chemistry, such as “click” reactions, to label small molecules located on live or fixed cells. Such labeling has been used for the visualization of glycans, activity-based protein profiling, the site-specific tagging of proteins, the detection of DNA and RNA synthesis, investigation of the fate of small molecules in plants, and...

The ability of Au catalysts to effect the challenging task of utilizing molecular oxygen for the selective epoxidation of cyclooctene is fascinating. Although supported nanometre-size Au particles are poorly active, here we show that solubilized atomic Au clusters, present in ng ml-1 concentrations and stabilized by ligands derived from the oxidized hydrocarbon products, are active. They can be...

Detailed kinetic analyses of inverse electron-demand Diels–Alder cycloaddition and nitrilimine-alkene/alkyne 1,3-diploar cycloaddition reactions were conducted and the reactions were applied for rapid protein bioconjugation. When reacted with a tetrazine or a diaryl nitrilimine, strained alkene/alkyne entities including norbornene, trans-cyclooctene, and cyclooctyne displayed rapid kinetics. To...

The molybdenum-based monoaryloxide monopyrrolide (MAP) species, Mo(NAd)(CHCMe(2)Ph)(C(4)H(4)N)(HIPTO) (2a), which contains "small" imido (Ad = 1-adamantyl) and "large" aryloxide (HIPTO = O-2,6(2,4,6-i-Pr(3)C(6)H(2))C(6)H(3)) ligands, catalyzes Z-selective metathesis reactions as a consequence of intermediate metallacyclobutane species not being able to have an (anti) substituent pointing toward...

A (perarylcyclopentadienyl)molybdenum(VI) dioxo complex is shown to catalyse epoxidation of cyclooctene by t-butylhydroperoxide, but decomposition to a much more active non-cyclopentadienyl containing catalyst occurs as the reaction proceeds.

A novel hierarchically ordered porous vanado-silicate nanocomposite with interconnecting macroporous windows and meso-microporous walls containing well dispersed vanadyl species has been fabricated and used as a heterogeneous catalyst for the oxidation of a bulky organic molecule, namely cyclooctene.