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How to Prepare Kinetically Stable Self‐assembled Pt 12 L 24 Nanocages while Circumventing Kinetic Traps
Author(s) -
Bobylev Eduard O.,
Poole David A.,
Bruin Bas,
Reek Joost N. H.
Publication year - 2021
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202101931
Subject(s) - nanocages , palladium , platinum , chemistry , supramolecular chemistry , ligand (biochemistry) , catalysis , metal , self assembly , nanotechnology , combinatorial chemistry , crystallography , materials science , organic chemistry , crystal structure , biochemistry , receptor
Supramolecular coordination‐based self‐assembled nanostructures have been widely studied, and currently various applications are being explored. For several applications, the stability of the nanostructure is of key importance, and this strongly depends on the metal used in the self‐assembly process. Herein, design strategies and synthetic protocols to access desirable kinetically stable Pt 12 L 24 nanospheres are reported, and it is demonstrated that these are stable under conditions under which the palladium counterparts decompose. Descriptors previously used for palladium nanospheres are insufficient for platinum analogues, as the stronger metal–ligand bond results in a mixture of kinetically trapped structures. We report that next to the dihedral angle, the rigidity of the ditopic ligand is also a key parameter for the controlled formation of Pt 12 L 24 nanospheres. Catalytic amounts of coordinating additives to labilise the platinum‐pyridyl bond to some extent are needed to selectively form Pt 12 L 24 assemblies. The formed Pt 12 L 24 nanospheres were demonstrated to be stable in the presence of chloride, amines and acids, unlike the palladium analogues.