6533b7dcfe1ef96bd12727b7
RESEARCH PRODUCT
Self-Sorting Effects in the Self-Assembly of Metallosupramolecular Rhombi from Chiral BINOL-Derived Bis(pyridine) Ligands
Kari RissanenFilip TopićArne LützenGregor SchnakenburgNiklas StruchChristoph GützCaroline StobeRainer Hovorkasubject
Steric effectsAtropisomerEnantiopure drugChemistryStereochemistryOrganic ChemistrySupramolecular chemistrychemistry.chemical_elementSelf-assemblyNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistryPlatinumPalladiumdescription
Four BINOL-based bis(4-pyridyl) ligands were synthesised in enantiopure and racemic form. These ligands form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. In principle, racemic ligands can self-assemble into three stereoisomeric rhombi. The degree of self-sorting in the self-assembly process crucially depends on the substitution pattern and the resulting bend angle of the V-shaped ligands as well as the degree of steric crowding within the assembly when racemic ligands are used. Thus, these processes either lead to homochiral assemblies in a narcissistic self-recognition manner, to heterochiral assemblies in a social self-discriminating manner, or proceed in a nonselective fashion as evidenced by NMR spectroscopy, mass spectrometry and single-crystal X-ray diffraction.
year | journal | country | edition | language |
---|---|---|---|---|
2013-11-04 | European Journal of Organic Chemistry |