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Ultra-Fast Molecular Rotors within Porous Organic Cages.


ABSTRACT: Using variable temperature 2 H static NMR spectra and 13 C spin-lattice relaxation times (T1 ), we show that two different porous organic cages with tubular architectures are ultra-fast molecular rotors. The central para-phenylene rings that frame the "windows" to the cage voids display very rapid rotational rates of the order of 1.2-8×106 ?Hz at 230?K with low activation energy barriers in the 12-18?kJ?mol-1 range. These cages act as hosts to iodine guest molecules, which dramatically slows down the rotational rates of the phenylene groups (5-10×104 ?Hz at 230?K), demonstrating potential use in applications that require molecular capture and release.

SUBMITTER: Hughes AR 

PROVIDER: S-EPMC5813266 | biostudies-literature | 2017 Dec

REPOSITORIES: biostudies-literature

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Ultra-Fast Molecular Rotors within Porous Organic Cages.

Hughes Ashlea R AR   Brownbill Nick J NJ   Lalek Rachel C RC   Briggs Michael E ME   Slater Anna G AG   Cooper Andrew I AI   Blanc Frédéric F  

Chemistry (Weinheim an der Bergstrasse, Germany) 20171122 68


Using variable temperature <sup>2</sup> H static NMR spectra and <sup>13</sup> C spin-lattice relaxation times (T<sub>1</sub> ), we show that two different porous organic cages with tubular architectures are ultra-fast molecular rotors. The central para-phenylene rings that frame the "windows" to the cage voids display very rapid rotational rates of the order of 1.2-8×10<sup>6</sup>  Hz at 230 K with low activation energy barriers in the 12-18 kJ mol<sup>-1</sup> range. These cages act as hosts  ...[more]

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