Transition metal-mediated oxidations utilizing monomeric iodosyl- and iodylarene species

Several transition metal-mediated oxidations using hypervalent iodine species are reported. A convenient procedure for preparation of iodylarenes via RuCl₃-catalyzed oxidation of iodoarenes has been developed. This procedure allows the generation of highly reactive monomeric iodine(V) species, which are excellent oxidants toward alcohols and hydrocarbons in situ. A broad range of substrates can be oxidized to carbonyl compounds by a tandem catalytic system based on the Ru(III)-catalyzed reoxidation of ArIO to ArIO₂ using Oxone^® as oxidant. It was shown that electrophilic iodine(III) species, originating from oligomeric iodosylbenzene sulfate (PhIO)₃SO₃, are efficient oxygenating agents in catalytic oxidation of aromatic hydrocarbons in the presence of metalloporphyrin complexes.     

Multiarm Star-Shaped Polydimethylsiloxanes with a Dendritic Branching Center

New multiarm stars have been synthesized based on polylithium derivatives of high-generation carbosilane dendrimers. In the synthesis of multiarm stars based on the eighth-generation dendrimer, steric hindrances were observed even during the synthesis of a polylithium initiator. Subsequently, this led to chain transfer reactions between growing arms, as well as other side effects. As a result, dense nanogel formations with a higher tendency of ordering than in classical objects of this type were isolated from the reaction mixture. The study of the rheology of multiarm stars based on sixth-generation dendrimers made it possible to determine the activation energies of viscous flow in these objects, which makes it possible to consider them as objects with a macromolecular nature and a reptation flow mechanism.     

A mass spectrometric study of halogenated beryllium μ4-oxohexa-μ-acetates

The electron impact mass spectra of Be₄O(CHal₃CO₂)₆ (Hal = F, Cl) are reported. The compounds give two series of fragment ions, [Be₄OL_x]⁺ and [Be₄OL₊]⁺, where L is an intact ligand or its fragmentation product. The major ligand dissociation path is the elimination of CHal₂CO₂ with halogen transfer to the metal. Other processes of importance are the loss of acid anhydride fragments, CF₂ with fluorine shift to the carboxyl group carbon atom, and halogens. Trinuclear ions also undergo decarboxylation, e.g. to give [Be₂O(CHal₃CO₂)₂(CHal₃)]⁺. Both spectra contain comparatively intense peaks of double-charged ions. The fragmentation patterns are rationalized by stereochemical considerations.     

Preparation and chemistry of phosphoranyl-derived iodanes

The preparation and chemistry of novel phosphoranyl-derived lambda(3)-iodanes is reported. The phosphoranyl-derived phenyliodonium sulfonates were prepared in good yields by the reaction of stabilized phosphonium ylides [1-triphenylphosphoranylidene-2-propanone, methyl(triphenylphosphoranylidene)acetate, (triphenylphosphoranylidene)acetaldehyde, and (triphenylphosphoranylidene)acetonitrile] with the pyridinium complex of iodobenzene ditriflate or with [hydroxy(tosyloxy)iodo]benzene under mild conditions. These compounds represent a potentially useful class of reagents that combine in one molecule synthetic advantages of a phosphonium ylide and an iodonium salt. Specifically, phosphorane-derived phenyliodonium tosylates can react with soft nucleophiles, such as iodide, bromide, benzenesulfinate, and thiophenolate anions, with a selective formation of the respective alpha-functionalized phosphonium ylides, which can be further converted to alkenes by the Wittig reaction with benzaldehyde. The phosphoranyl-derived benziodoxoles can be prepared by the reaction of 1-acetoxybenziodoxole with stabilized phosphonium ylides. An unusual ligand exchange on the iodine(III) center resulting in the substitution of a carbon ligand with an oxygen ligand was observed in the reaction of these compounds with strong acids.     

Catalytic, asymmetric synthesis of α,α-disubstituted amino acids

Copper(salen) complex 1 has been found to catalyse the asymmetric alkylation of enolates derived from a variety of amino acids. There is a clear relationship between the size of the side chain in the substrate and the enantioselectivity of the process, so that the enantioselectivity decreases in the order alanine>aminobutyric acid>allylglycine>leucine>phenylalanine>valine. A transition state model which accounts for the influence of the size of the side chain on the enantioselectivity of the reactions is presented.     

A general strategy for the synthesis of difluoromethyl-containing pyrazoles, pyridines and pyrimidines

Difluoromethyl-containing heteroannulated pyridines, pyrimidines and pyrazoles are prepared by a two step method. The regioselective cyclizations of electron-excessive aminoheterocycles, hydrazines and amidines with CF₂Cl-substituted 1,3-dicarbonyl compounds provide the corresponding CF₂Cl-substituted heterocycles. Subsequent radical reactions with trimethylstannane or allyltrimethylstannane gave difluoromethyl-containing heteroannulated pyridines, pyrimidines and pyrazoles, respectively.     

Determination of carbon in solidified sodium coolant using new ICP-OES methods

New methods for the determination of carbon in sodium using laser ablation inductively coupled plasma optical emission spectrometry (LA-ICP-OES) and ICP-OES with pneumatic nebulisation (PN-ICP-OES) were developed. The determination was required for the study of the carbon dioxide reaction with molten sodium at high temperatures (300–600°C). After exposition to CO₂, the solidified sodium sample was subjected to direct solid analysis by LA-ICP-OES and to solution analysis. For the determination of carbon in the sodium sample surface layer by LA-ICP-OES, three different matrices containing sodium were tested (NaCl, NaF, and Na₂B₄O₇ · 10H₂O) as calibration pellets. The calibration dependences were improved using sodium as the internal standard. Average carbon content in the sodium bulk sample was determined by PN-ICP-OES after the sample dissolution by water vapour.