Pd(II) Coordination Sphere Engineering: Pyridine Cages, Quinoline Bowls, and Heteroleptic Pills Binding One or Two Fullerenes
journal contributionposted on 08.05.2019, 00:00 by Bin Chen, Julian J. Holstein, Shinnosuke Horiuchi, Wolf G. Hiller, Guido H. Clever
Fullerenes and their derivatives are of tremendous technological relevance. Synthetic access and application are still hampered by tedious purification protocols, peculiar solubility, and limited control over regioselective derivatization. We present a modular self-assembly system based on a new low-molecular-weight binding motif, appended by two palladium(II)-coordinating units of different steric demands, to either form a [Pd2L14]4+ cage or an unprecedented [Pd2L23(MeCN)2]4+ bowl (with L1 = pyridyl, L2 = quinolinyl donors). The former was used as a selective induced-fit receptor for C60. The latter, owing to its more open structure, also allows binding of C70 and fullerene derivatives. By exposing only a fraction of the bound guests’ surface, the bowl acts as fullerene protecting group to control functionalization, as demonstrated by exclusive monoaddition of anthracene. In a hierarchical manner, sterically low-demanding dicarboxylates were found to bridge pairs of bowls into pill-shaped dimers, able to host two fullerenes. The hosts allow transferring bound fullerenes into a variety of organic solvents, extending the scope of possible derivatization and processing methodologies.
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pill-shaped dimersprocessing methodologiesHeteroleptic Pills BindingPd 2 L 2 3bowl actssterically low-demanding dicarboxylatesL 2L 1Fullerenes Fullerenescontrol functionalizationpurification protocolshoststeric demandsfullerene derivativeslow-molecular-weight binding motifPd 2 L 1 4induced-fit receptorPyridine Cagesself-assembly systemC 70bridge pairsQuinoline Bowlsregioselective derivatizationC 60quinolinyl donorsSynthetic access