| Literature DB >> 26485442 |
Peumie L Abeyratne Kuragama1, Frank R Fronczek2, Andrzej Sygula1.
Abstract
Bis-corannulene receptors 4 and 5 with Klärner's tethers prepared by the Diels-Alder cycloaddition form inclusion complexes with C60 and C70, as evidenced by (1)H NMR titration. While 4 exhibits affinity toward fullerenes comparable to the previously reported corannulene-based receptors, 5 exceeds the performance of the former systems by ca. 2 orders of magnitude and, in addition, shows an enhanced preference for C70 over C60. The X-ray crystal structure of C60@5 and DFT calculations indicate that the tether in 5 not only preorganizes the pincers into a proper topology of the host but also contributes to the dispersion-based binding with the fullerene guests.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26485442 DOI: 10.1021/acs.orglett.5b02666
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005