Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, 1001, Ta-Hsueh Road, Hsinchu 30010, Taiwan.
J Chem Phys. 2012 Apr 21;136(15):154304. doi: 10.1063/1.3703502.
We use protonated benzene (C(6)H(7)(+)) and cyclohexadienyl radical (c-C(6)H(7)) to demonstrate a new method that has some advantages over other methods currently used. C(6)H(7)(+) and c-C(6)H(7) were produced on electron bombardment of a mixture of benzene (C(6)H(6)) and para-hydrogen during deposition onto a target at 3.2 K. Infrared (IR) absorption lines of C(6)H(7)(+) decreased in intensity when the matrix was irradiated at 365 nm or maintained in the dark for an extended period, whereas those of c-C(6)H(7) increased in intensity. Observed vibrational wavenumbers, relative IR intensities, and deuterium isotopic shifts agree with those predicted theoretically. This method, providing a wide spectral coverage with narrow lines and accurate relative IR intensities, can be applied to larger protonated polyaromatic hydrocarbons and their neutral species which are difficult to study with other methods.
我们使用质子化苯(C(6)H(7)(+))和环己二烯基自由基(c-C(6)H(7))来展示一种新方法,该方法相对于目前使用的其他方法具有一些优势。在 3.2 K 时,将苯(C(6)H(6))和仲氢的混合物沉积到靶上,通过电子轰击产生 C(6)H(7)(+)和 c-C(6)H(7)。当基质在 365nm 下照射或在暗处长时间保持时,C(6)H(7)(+)的红外(IR)吸收线的强度会降低,而 c-C(6)H(7)的强度会增加。观察到的振动波数、相对 IR 强度和氘同位素位移与理论预测相符。这种方法提供了宽的光谱覆盖范围、窄的谱线和准确的相对 IR 强度,可以应用于更大的质子化多环芳烃及其中性物种,这些物种很难用其他方法研究。