2915-83-5Relevant academic research and scientific papers
A supramolecular sorting hat: Stereocontrol in metal-ligand self-assembly by complementary hydrogen bonding
Young, Michael C.,Holloway, Lauren R.,Johnson, Amber M.,Hooley, Richard J.
, p. 9832 - 9836,5 (2014)
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. Abracadabra: The stereoselective self-assembly of an unsymmetrical metal-ligand cage can be controlled by self-complementary hydrogen bonding between alcohol-containing ligands as well as between ligands and suitable anion guests.
METHODS FOR PRODUCING DIAMINOFLUORENOL
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Paragraph 0120-0125, (2020/09/08)
The present invention relates to a method for producing diaminofluorenol, and more particularly, to a 2,7-diamino-9H-fluoren-9-ol compound and a method for producing the same. According to the present invention, it is possible to provide a diaminofluorenol-based compound that can be favorably used as an intermediate important for the synthesis of diaminofluorenol compounds of various embodiments in a high yield and simple synthesis process. The compound is represented by chemical formula 1.COPYRIGHT KIPO 2020
