| Literature DB >> 25044629 |
Michael C Young1, Lauren R Holloway, Amber M Johnson, Richard J Hooley.
Abstract
A combination of self-complementary hydrogen bonding and metal-ligand interactions allows stereocontrol in the self-assembly of prochiral ligand scaffolds. A unique, non-tetrahedral M4L6 structure is observed upon multicomponent self-assembly of 2,7-diaminofluorenol with 2-formylpyridine and Fe(ClO4)2. The stereochemical outcome of the assembly is controlled by self-complementary hydrogen bonding between both individual ligands and a suitably sized counterion as template. This hydrogen-bonding-mediated stereoselective metal-ligand assembly allows the controlled formation of nonsymmetric discrete cage structures from previously unexploited ligand scaffolds.Entities:
Keywords: diastereoselectivity; hydrogen bonding; ligand effects; self-assembly; supramolecular chemistry
Year: 2014 PMID: 25044629 DOI: 10.1002/anie.201405242
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336