Abstract
Mechanically interlocked molecules can exhibit molecular chirality that arises due to the mechanical bond rather than covalent stereogenic units. Developing applications of such systems is made challenging by the absence of techniques for assigning the absolute configuration of products and methods to probe how the mechanical stereogenic unit influences the spatial arrangements of the functional groups in solution. Here we demonstrate for the first time that Vibrational Circular Dichroism (VCD) can be used to not only discriminate between mechanical stereoisomers but also provide detailed information on their (co)conformations. The latter is particularly important as these molecules are now under investigation in catalysis and sensing, both of which rely on the solution phase shape of the interlocked structure. Detailed analysis of the VCD spectra shows that, although many of the signals arise from coupled oscillators isolated in the covalent sub-components, intercomponent coupling between the macrocycle and axle gives rise to several VCD bands.
Original language | English |
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Pages (from-to) | 8469-8475 |
Number of pages | 7 |
Journal | Chemical Science |
Volume | 11 |
Issue number | 32 |
DOIs | |
Publication status | Published - 28 Aug 2020 |
Bibliographical note
Funding Information:MAJK, LV and WJB acknowledge nancial support from NWO in the framework of the Fund New Chemical Innovations (NWO Project No. 731.014.209). VPN acknowledges funding from UEFISCDI (PN-III-P1-1.1-TE-2016-1049, contract nr. 46/2018). SMG thanks the European Research Council (Consolidator Grant Agreement no. 724987), EPSRC (EP/L016621/1) and Lev-erhulme Trust (ORPG-2733) for funding and the Royal Society for a Wolfson Research Fellowship. We furthermore acknowledge useful discussions with Dr Stan van Gisbergen from SCM.
Publisher Copyright:
© The Royal Society of Chemistry.
ASJC Scopus subject areas
- General Chemistry