Frunzi Michael, Cross R James, Saunders Martin
Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, USA.
J Am Chem Soc. 2007 Oct 31;129(43):13343-6. doi: 10.1021/ja075568n. Epub 2007 Oct 9.
Solutions containing 3He@C60, 129Xe@C60, and varying amounts of 9,10-dimethylanthracene (DMA) were allowed to reach equilibrium, and the 3He and 129Xe NMR spectra were taken at the same temperature. Each spectrum showed peaks for the unreacted X@C60 and for the monoadduct. The ratios of the peak heights show that the included xenon atom substantially changes the equilibrium constant. This change is temperature dependent, meaning that the xenon atom changes both DeltaH and DeltaS for the reaction. DMA is more reactive with He@C60 at low temperatures and with Xe@C60 at higher temperatures. The difference in chemical shift between the monoadduct and the unreacted X@C60 is more than twice as large for Xe than for He and in the opposite direction. Calculations show that the electron density in Xe@C60 is higher than that in empty C60 on the outside of the cage.
含有3He@C60、129Xe@C60以及不同量9,10 - 二甲基蒽(DMA)的溶液达到平衡后,在相同温度下采集3He和129Xe的核磁共振谱。每个谱图都显示了未反应的X@C60和单加合物的峰。峰高比表明所包含的氙原子显著改变了平衡常数。这种变化与温度有关,意味着氙原子改变了反应的ΔH和ΔS。DMA在低温下与He@C60反应性更强,而在高温下与Xe@C60反应性更强。单加合物与未反应的X@C60之间的化学位移差异,氙的情况比氦的大两倍多,且方向相反。计算表明,笼外Xe@C60中的电子密度高于空C60中的电子密度。