National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui 230029, P.R. China.
Rapid Commun Mass Spectrom. 2009 Dec;23(24):3994-4002. doi: 10.1002/rcm.4339.
The absolute photoionization cross-sections of aromatics and aromatic derivatives including toluene, ethylbenzene, n-propylbenzene, o-xylene, m-xylene, p-xylene, 1,3,5-trimethylbenzene, styrene, phenylacetylene, indene, indane, 1-methylnaphthalene, benzyl alcohol and benzaldehyde were measured at the photon energy range from ionization thresholds to 11.7 eV. The experiments were performed by tunable synchrotron vacuum ultraviolet (VUV) photoionization mass spectrometry. Benzene was chosen as a calibration standard, since its photoionization cross-section is well known. Binary liquid mixtures of the investigated molecules and benzene were used in the measurements. Photo-induced fragments from the molecules were also observed, and their photoionization cross-sections are also presented.
芳香族和芳香族衍生物(包括甲苯、乙苯、正丙苯、邻二甲苯、间二甲苯、对二甲苯、1,3,5-三甲苯、苯乙烯、苯乙炔、茚、茚满、1-甲基萘、苄醇和苯甲醛)的绝对光电子电离截面在从电离阈值到 11.7 eV 的光子能量范围内进行了测量。实验是通过可调谐同步辐射真空紫外(VUV)光电子电离质谱法进行的。选择苯作为校准标准,因为其光电子电离截面是已知的。在所研究的分子和苯的二元液体混合物中进行了测量。还观察到了分子的光致碎片,并且也给出了它们的光电子电离截面。