Light-stable silver N-Heterocyclic carbene catalysts for the alkynylation of ketones in air

The authors gratefully acknowledge the Royal Society (University Research Fellowship to C.S.J.C) for funding.N-Heterocyclic carbene (NHC) silver(I) complexes were efficiently employed in the alkynylation of ketones. These cationic complexes were found highly active and efficient under mild conditions without the need of additive, and in air. The mechanism of this transformation was investigated. Experiments suggest the formation of a silver-acetylide key intermediate and the release of one ligand from the silver centre enabling the transformation.PostprintPeer reviewe

Influence of the Solvent Quality on Ring Polymer Dimensions

We present a systematic investigation of well-characterized, experimentally pure polystyrene (PS) rings with molar mass of 161 000 g/mol in dilute solutions. We measure the ring form factor at θ - and good-solvent conditions as well as in a polymeric solvent (linear PS of roughly comparable molar mass) by means of small-angle neutron scattering (SANS). Additional dynamic light scattering (DLS) measurements support the SANS data and help elucidate the role of solvent quality and solution preparation. The results indicate the increase of ring dimensions as the solvent quality improves. Furthermore, the experimental form factors in both θ -solvent and linear matrix behave as ideal rings and are fully superimposable. The nearly Gaussian conformations of rings in a melt of linear chains provide evidence of threading of linear chains through rings. The latter result has implications for the dynamics of ring-linear polymer mixtures

Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO₃)₂ or imidazole as catalysts

A new method for the direct synthesis of primary and secondary amides from carboxylic acids is described using Mg(NO3)2·6H2O or imidazole as a low-cost and readily available catalyst, and urea as a stable, and easy to manipulate nitrogen source. This methodology is particularly useful for the direct synthesis of primary and methyl amides avoiding the use of ammonia and methylamine gas which can be tedious to manipulate. Furthermore, the transformation does not require the employment of coupling or activating agents which are commonly required

Magnetite and Metal-Impregnated Magnetite Catalysts in Organic Synthesis: A Very Old Concept with New Promising Perspectives

Magnetite is a well-known material, with the impregnation of transition metals onto its surface being a very old protocol for preparing catalysts. However, only recently, the combination of both, magnetite and impregnation protocols, have been recognized as a powerful methodology to prepare catalysts. The impregnation protocol, of nearly all transition metals in the magnetite surface, has rendered the first generation of catalysts. These simple catalysts have been used in a very broad range of organic transformations. Thus, simple imine derivative formation or unknown reactions such as the direct cross β-alkylation of primary alcohols, through dehydrogenation, oxidation, addition, hydrogen autotransfer, and multicomponent reactions has been accomplished using these catalysts. In most cases, these catalysts could be just isolated by magnetic decantation and reused several times without a detrimental effect on the initial results. In some cases, the study of the surface of the catalyst by means of several surface characterization techniques has permitted to determine the real species involved in the process and their structural changes within the reaction cycles. Furthermore, the post-modification of the catalysts by reduction or oxidation of the immobilized metal, or by the addition of ligands, has enlarged the applicability of this type of catalysts.This work was supported by the current Spanish Ministerio de Economía y Competitividad (CTQ2011-24151) and by the University of Alicante