THE CORRELATION STATES OF FURAN AND THIOPHENE BY HIGH-RESOLUTION SYNCHROTRON PHOTOELECTRON-SPECTROSCOPY

被引:33
作者
BAWAGAN, ADO
OLSSON, BJ
TAN, KH
CHEN, JM
YANG, BX
机构
[1] UNIV WESTERN ONTARIO, DEPT CHEM, LONDON N6A 5B7, ONTARIO, CANADA
[2] UNIV WISCONSIN, CANADIAN SYNCHROTRON RADIAT FACIL, STOUGHTON, WI 53589 USA
[3] UNIV WESTERN ONTARIO, CTR CHEM PHYS, LONDON N6A 5B7, ONTARIO, CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1016/0301-0104(92)87151-X
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The high resolution synchrotron photoelectron spectra (PES) of furan and thiophene are obtained at 90-200 eV photon energy. Several ionization peaks attributed to inner valence orbitals and correlation (satellite) states are resolved for the first time. By using the photon energy dependence of the ionization cross sections of the valence orbitals and the correlation states, significant insight into the dominant character of the valence orbitals and correlation states of furan and thiophene is attained. Two classes of a1-type molecular orbitals in furan, two classes of b2-type molecular orbitals in furan and two types of correlation (satellite) states in thiophene are distinguished by the present procedure. Some limitations of the photon energy dependence of molecular photoionization cross sections are also discussed.
引用
收藏
页码:283 / 304
页数:22
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