Krouse Ian H, Wenthold Paul G
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, USA.
Inorg Chem. 2003 Jul 14;42(14):4293-8. doi: 10.1021/ic034301w.
This study focuses upon the Lewis acid reactivity of XeF(+) with various bases in the gas phase and the determination of the bond dissociation energy of XeF(+). The bond dissociation energy of XeF(+) has been measured by using energy-resolved collision-induced dissociation with neon, argon, and xenon target gases. Experiments with neon target yield a 298 K bond dissociation enthalpy of 2.81 +/- 0.09 eV, and those with argon target give a similar value at 2.83 +/- 0.12 eV. When using a xenon target, a significantly lower value of 1.95 +/- 0.16 eV was observed, which corresponds closely with previous measurements and theoretical predictions. It is proposed that the lighter target gases give inefficient excitation of the XeF(+) vibration leading to dissociation at energies higher than the BDE. Novel xenon-base adducts have been prepared in a flowing afterglow mass spectrometer by termolecular addition to XeF(+) and by reaction of base with XeF(+)(H(2)O). New species have been characterized qualitatively by CID, and it is found that the products formed reflect the relative ionization energies of the fragments. Among the new xenon-containing species that have been prepared are the first examples of xenon carbonyls.
本研究聚焦于XeF(+)在气相中与各种碱的路易斯酸反应活性以及XeF(+)键解离能的测定。通过使用与氖、氩和氙靶气体的能量分辨碰撞诱导解离来测量XeF(+)的键解离能。以氖为靶气体的实验得到298 K时的键解离焓为2.81±0.09 eV,以氩为靶气体的实验得到类似值为2.83±0.12 eV。当使用氙为靶气体时,观察到显著更低的值为1.95±0.16 eV,这与先前的测量和理论预测密切相符。有人提出,较轻的靶气体对XeF(+)振动的激发效率较低,导致在高于键解离能的能量下发生解离。通过在流动余辉质谱仪中使XeF(+)进行三分子加成以及使碱与XeF(+)(H₂O)反应,制备了新型的氙 - 碱加合物。通过碰撞诱导解离对新物种进行了定性表征,发现形成的产物反映了碎片的相对电离能。在已制备的新型含氙物种中,有首例羰基氙。