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A Covalent Organic Cage Compound Acting as a Supramolecular Shadow Mask for the Regioselective Functionalization of C60

05 June 2020, Version 1
Working Paper
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

A trigonal-bipyramidal covalent organic cage compound serves as an efficient host to form stable 1:1-complexes with C60 and C70. Fullerene encapsulation has been comprehensively studied by NMR and UV/Vis spectroscopy, mass spectrometry as well as single-crystal X-ray diffraction. Exohedral functionalization of encapsulated C60 via threefold Prato reaction revealed high selectivity for the symmetry-matched all-trans-3 addition pattern.

Keywords

covalent organic cage compounds
fullerenes
Prato reaction
regioselectivity

Supplementary materials

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Description
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Title
2020 06 Leonhardt ESI ChemRxiv
Description
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Title
C60 1 complex
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Now Published

A covalent organic cage compound acting as a supramolecular shadow mask for the regioselective functionalization of C60 [opens in a new tab]
Viktoria Leonhardt, Stefanie Fimmel, Ana-Maria Krause, Florian Beuerle journal article
Chemical Science , Volume 11, Issue 32
Online publication date: 2020

Version History

Jun 05, 2020 Version 1

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The content is available under CC BY NC ND 4.0 [opens in a new tab]

DOI

10.26434/chemrxiv.12424664.v1
D O I: 10.26434/chemrxiv.12424664.v1 [opens in a new tab]

Funding

Deutsche Forschungsgemeinschaft (BE4808/2-1)
Collaborative Research Network “Solar Technologies Go Hybrid” of the Bavarian Ministry of Science, Research and the Arts

Author’s competing interest statement

There are no conflicts to declare.

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