Organometallic complexes have long been known to display a wide variety of dynamic stereochemical processes. Classic examples of such processes include the exchange of axial and equatorial environments in trigonal bipyramidal complexes, such as Fe(CO)₅, and the migration of the metal moiety round the periphery of the cyclopentadiene ring in η¹-bound Cp complexes. The systematic study of fluxional processes is of interest because it can not only help provide a detailed, quantitative ‘picture’ of the bonding between the metals and ligands involved, but it can also help to rationalise chemical reactivity patterns. The introduction of chirality into organometallic complexes, usually in the form of a non-racemic chiral ligand, has led to an expl...
Reaction of the chiral amine (<i>S</i>)-<i>N</i>-α-(methylbenzyl)phenylallylamine, [(<i>S</i>)<i>-N...
Enantioselective transition metal catalysis is an area very much at the forefront of contemporary sy...
International audienceFacial selectivity during the π-coordination of pseudo-tetrahedral iridacycles...
Organometallic complexes have long been known to display a wide variety of dynamic stereochemical pr...
International audienceRecent examples of "chiral at metal" complexes and assemblies that are produce...
Labile metal complexes have a useful coordination bond; which is weaker than a covalent C–C bond and...
Transition metal chiral catalysts can feature metal stereocenters in different coordination geometri...
This series offers leading contributions by well-known chemists reviewing the state of the art of th...
While most responsive molecules show a trivial first-order exponential relaxation upon stimulation, ...
Stereogenic sp3-hybridized carbon centres are fundamental building blocks of chiral molecules. Unlik...
Tricarbonylrhenium(I) halide complexes of the non-racemic chiral ligand 2-[(4R),(5R)-dimethyl-1,3-di...
A series of C2-symmetric chiral tetra-dentate ligands were prepared by using [4,5]- or [5,6]-pinene-...
International audienceEnantiopure bimetallic systems containing three different elements of chiralit...
The work described in this thesis is based around attempts to find a system that could use the intri...
The challenging control of the absolute configuration of chiral-at-metal complexes is efficiently ac...
Reaction of the chiral amine (<i>S</i>)-<i>N</i>-α-(methylbenzyl)phenylallylamine, [(<i>S</i>)<i>-N...
Enantioselective transition metal catalysis is an area very much at the forefront of contemporary sy...
International audienceFacial selectivity during the π-coordination of pseudo-tetrahedral iridacycles...
Organometallic complexes have long been known to display a wide variety of dynamic stereochemical pr...
International audienceRecent examples of "chiral at metal" complexes and assemblies that are produce...
Labile metal complexes have a useful coordination bond; which is weaker than a covalent C–C bond and...
Transition metal chiral catalysts can feature metal stereocenters in different coordination geometri...
This series offers leading contributions by well-known chemists reviewing the state of the art of th...
While most responsive molecules show a trivial first-order exponential relaxation upon stimulation, ...
Stereogenic sp3-hybridized carbon centres are fundamental building blocks of chiral molecules. Unlik...
Tricarbonylrhenium(I) halide complexes of the non-racemic chiral ligand 2-[(4R),(5R)-dimethyl-1,3-di...
A series of C2-symmetric chiral tetra-dentate ligands were prepared by using [4,5]- or [5,6]-pinene-...
International audienceEnantiopure bimetallic systems containing three different elements of chiralit...
The work described in this thesis is based around attempts to find a system that could use the intri...
The challenging control of the absolute configuration of chiral-at-metal complexes is efficiently ac...
Reaction of the chiral amine (<i>S</i>)-<i>N</i>-α-(methylbenzyl)phenylallylamine, [(<i>S</i>)<i>-N...
Enantioselective transition metal catalysis is an area very much at the forefront of contemporary sy...
International audienceFacial selectivity during the π-coordination of pseudo-tetrahedral iridacycles...