A Ruthenium Olefin Metathesis Catalyst with a Four-Membered N-Heterocyclic Carbene Ligand

The first ruthenium olefin metathesis catalyst bearing a four-membered N-heterocyclic carbene (5) was synthesized and characterized by NMR spectroscopy and X-ray crystallography. The synthesis of a (carbene)carbonylrhodium complex (6) was also reported, allowing the study of the electronic properties of this new carbene ligand. The complex 5 was screened toward different olefin metathesis reactions, and it showed a slow reactivity

A Stable Four-Membered N-Heterocyclic Carbene

The synthesis of the first four-membered N-heterocyclic carbene is described. Depending on the substituents on the nitrogen atoms, it is possible to characterize at room temperature the carbene dimer or the free carbene. Crystallographic analyses are provided for these carbene species

Tuning the formal potential of ferrocyanide over a 2.1 V range

We report the synthesis and characterization of homoleptic borane adducts of hexacyanoferrate(II). Borane coordination blueshifts d–d transitions and CN IR and Raman frequencies. Control over redox properties is established with respect to borane Lewis acidity, reflected in peak anodic potential shifts per borane of +250 mV for BPh_3 and +350 mV for B(C_6F_5)_3. Electron transfer from [Fe(CN-B(C_6F_5)_3)_6]^(4−) to photogenerated [Ru(2,2′-bipyridine)_3]^(3+) is very rapid, consistent with voltammetry data. Coordination by Lewis acids provides an avenue for selective modification of the electronic structures and electrochemical properties of cyanometalates

Reversible 1,2-Alkyl Migration to Carbene and Ammonia Activation in an N-Heterocyclic Carbene–Zirconium Complex

Addition of trimethylphosphine to a bis(phenolate)benzylimidazolylidene(dibenzyl)zirconium complex induces migration of a benzyl ligand from the metal center to the C_(carbine) atom. This process may be reversed, resulting in C_(sp)^3–C_(sp)^3 activation, by abstraction of the phosphine, an example of regulated, reversible alkyl migration. Addition of ammonia to the dibenzyl complex results in migration of one benzyl group and protonolysis of the other to generate a bis(NH_2)-bridged dimer via an NMR-observable intermediate NH_3 adduct

Mechanistic Insights on the Controlled Switch from Oligomerization to Polymerization of 1-Hexene Catalyzed by an NHC-Zirconium Complex

The benzimidazolylidene zirconium complex 1 switches from an oligomerization (without additive) to a polymerization catalyst by addition of an L-type ligand such as trimethylphosphine, while larger phosphines or amines completely inhibit catalysis. On the basis of the regioselectivity of the oligomers/polymers obtained, the time profiles of reactions as a function of added ligand, and the molecular structures of several cationic zirconium complexes, we propose a mechanistic framework for interpreting this complex catalytic behavior

Unexpected rearrangements in the synthesis of an unsymmetrical tridentate dianionic N-heterocyclic carbene

Starting from the same ethylenediamine species, three valuable carbene precursors were synthesized under differing conditions: a tridentate dianionic N-heterocyclic carbene bearing an aniline, a phenol and a central dihydroimidazolium salt, its benzimidazolium isomer by intramolecular rearrangement and a dicationic benzimidazolium-benzoxazolium salt by changing the Brønsted acid from HCl to HBF_4. A DFT study was performed to understand the rearrangement pathway. The structure of a bis[(NCO)carbene] zirconium complex was determined

Silver-Catalyzed C-C Bond Formation between Methane and Ethyl Diazoacetate in Supercritical CO2

Even in the context of hydrocarbons’ general resistance to selective functionalization, methane’s volatility and strong bonds pose a particular challenge. We report here that silver complexes bearing perfluorinated indazolylborate ligands catalyze the reaction of methane (CH4) with ethyl diazoacetate (N2CHCO2Et) to yield ethyl propionate (CH3CH2CO2Et). The use of supercritical carbon dioxide (scCO2) as the solvent is key to the reaction’s success. Although the catalyst is only sparingly soluble in CH4/CO2 mixtures, optimized conditions presently result in a 19% yield of ethyl propionate (based on starting quantity of the diazoester) at 40°C over 14 hours.Ministerio de Ciencia e Innovación (grants CTQ2008-00042-BQU, CTQ2007-65251-BQU, and CTQ2007-30762-E), the European Research Area Chemistry Programme (2nd call “Chemical activation of carbon dioxide and methane” contract no. 1736154), the Consolider Ingenio 2010 (grants CSD2006-003 and CSD2007-00006), the Institut de Chimie of the CNRS, the Junta de Andalucía (P07-FQM-2870), and the Generalitat Velenciana (ACOMP/2010/155).We dedicate this work to Professor Ernesto Carmona. Support for this work was provided by the Ministerio de Ciencia e Innovacion (grants CTQ2008-00042-BQU, CTQ2007-65251-BQU, and CTQ2007-30762-E), the European Research Area Chemistry Programme (2nd call "Chemical activation of carbon dioxide and methane" contract no. 1736154), the Consolider Ingenio 2010 (grants CSD2006-003 and CSD2007-00006), the Institut de Chimie of the CNRS, the Junta de Andalucia (P07-FQM-2870), and the Generalitat Velenciana (ACOMP/2010/155). We thank the Servicio Central de Soporte a la Investigacion Experimental (Universidad de Valencia) for access to the instrumental facilities and J. de la Rosa and A. Sanchez de la Campa (Universidad de Huelva) for ICP-MS analyses

L’Union de la Republique Sud-Africaine et de l'etat libre d'Orange

leyds-70-9194.pdf created from original pamphlet in the WJ Leyds Collection held in the Africana Section of the Stellenbosch University Library and Information Service.Extract from de la "Revue generale de droit international public"

Addition of a phosphine ligand switches an N-heterocyclic carbene-zirconium catalyst from oligomerization to polymerization of 1-hexene

A catalyst for the oligomerization of 1-hexene, generated by the activation of a benzimidazolylidene zirconium dibenzyl complex, switches to a polymerization catalyst on addition of a trialkylphosphine