We achieved optical resolution of 4,7,12,15-tetrasubstituted [2.2]paracyclophane and subsequent transformation to planar chiral building blocks. An optically active propeller-shaped macrocyclic compound containing a planar chiral cyclophane core was synthesized, showing excellent chiroptical properties such as high fluorescence quantum efficiency and a large circularly polarized luminescence dissymmetry factor
International audienceChiral, π-conjugated 3,4-butano-1-phenyl-2,5-bis(2-pyridyl)phosphole derivativ...
New types of [2.2]paracyclophane derivatives, g-BNMe2-Cp and m-BNMe2-Cp, in which electron-donating...
We introduce a design principle to stabilize helically chiral structures from an achiral tetrasubsti...
We achieved optical resolution of 4,7,12,15-tetrasubstituted [2.2]paracyclophane and subsequent tra...
International audienceIn this article, we report the preparation of a series of [2.2]paracyclophane-...
In this article, we report the preparation of a series of [2.2]paracyclophane-fused coumarin system...
Here, we report an approach to the synthesis of highly charged enantiopure cyclophanes by the insert...
International audienceAbstract Here, we report an approach to the synthesis of highly charged enanti...
Optically active π-conjugated oligo(<i>p</i>-phenylene ethynylene) dimers with a planar chiral 4,7,...
International audienceWe describe the synthesis and photophysical characterization of differently su...
Novel BN-doped compounds based on chiral, tetrasubstituted [2.2]paracyclophane and NBN-benzo[f,g]tet...
The synthetic access to macrocyclic molecular topologies with interesting photophysical properties h...
A versatile method for converting various fluorescent polycyclic aromatic hydrocarbons into circular...
Abstract An optically active π-stacked molecule was synthesized incorporating planar chiral [2.2]par...
The synthetic access to macrocyclic molecular topologies with interesting photophysical properties h...
International audienceChiral, π-conjugated 3,4-butano-1-phenyl-2,5-bis(2-pyridyl)phosphole derivativ...
New types of [2.2]paracyclophane derivatives, g-BNMe2-Cp and m-BNMe2-Cp, in which electron-donating...
We introduce a design principle to stabilize helically chiral structures from an achiral tetrasubsti...
We achieved optical resolution of 4,7,12,15-tetrasubstituted [2.2]paracyclophane and subsequent tra...
International audienceIn this article, we report the preparation of a series of [2.2]paracyclophane-...
In this article, we report the preparation of a series of [2.2]paracyclophane-fused coumarin system...
Here, we report an approach to the synthesis of highly charged enantiopure cyclophanes by the insert...
International audienceAbstract Here, we report an approach to the synthesis of highly charged enanti...
Optically active π-conjugated oligo(<i>p</i>-phenylene ethynylene) dimers with a planar chiral 4,7,...
International audienceWe describe the synthesis and photophysical characterization of differently su...
Novel BN-doped compounds based on chiral, tetrasubstituted [2.2]paracyclophane and NBN-benzo[f,g]tet...
The synthetic access to macrocyclic molecular topologies with interesting photophysical properties h...
A versatile method for converting various fluorescent polycyclic aromatic hydrocarbons into circular...
Abstract An optically active π-stacked molecule was synthesized incorporating planar chiral [2.2]par...
The synthetic access to macrocyclic molecular topologies with interesting photophysical properties h...
International audienceChiral, π-conjugated 3,4-butano-1-phenyl-2,5-bis(2-pyridyl)phosphole derivativ...
New types of [2.2]paracyclophane derivatives, g-BNMe2-Cp and m-BNMe2-Cp, in which electron-donating...
We introduce a design principle to stabilize helically chiral structures from an achiral tetrasubsti...