Synthesis and Properties of Open Fullerenes Encapsulating Ammonia and Methane.

Synthesis and Properties of Open Fullerenes Encapsulating Ammonia and Methane.
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DOI:
10.1002/cphc.201701212
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发表时间:
2018-02-05
期刊:
Chemphyschem : a European journal of chemical physics and physical chemistry
影响因子:
--
通讯作者:
Whitby RJ
Whitby RJ
中科院分区:
其他
文献类型:
--
作者:
Bloodworth S;Gräsvik J;Alom S;Kouřil K;Elliott SJ;Wells NJ;Horsewill AJ;Mamone S;Jiménez-Ruiz M;Rols S;Nagel U;Rõõm T;Levitt MH;Whitby RJ

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We describe the synthesis and characterisation of open fullerene (1) and its reduced form (2) in which CH4 and NH3 are encapsulated, respectively. The 1H NMR resonance of endohedral NH3 is broadened by scalar coupling to the quadrupolar 14 n nucleus, which relaxes rapidly. This broadening is absent for small satellite peaks, which are attributed to natural abundance 15N. The influence of the scalar relaxation mechanism on the linewidth of the 1H ammonia resonance is probed by variable temperature NMR. A rotational correlation time of τc=1.5 ps. is determined for endohedral NH3, and of τc=57±5 ps. for the open fullerene, indicating free rotation of the encapsulated molecule. IR spectroscopy of NH3@2 at 5 K identifies three vibrations of NH3 (ν 1, ν 3 and ν 4) redshifted in comparison with free NH3, and temperature dependence of the IR peak intensity indicates the presence of a large number of excited translational/ rotational states. Variable temperature 1H NMR spectra indicate that endohedral CH4 is also able to rotate freely at 223 K, on the NMR timescale. Inelastic neutron scattering (INS) spectra of CH4@1 show both rotational and translational modes of CH4. Energy of the first excited rotational state (J=1) of CH4@1 is significantly lower than that of free CH4.
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