English  |  正體中文  |  简体中文  |  Items with full text/Total items : 6469/11641
Visitors : 19124026      Online Users : 310
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Adv. Search
LoginUploadHelpAboutAdminister

Please use this identifier to cite or link to this item: http://ir.ncue.edu.tw/ir/handle/987654321/10049

Title: Density Functional Calculation of the Inner-Shell Spectra for two stable Enol Tautomers: Acetylacetone and Malonaldehyde
Authors: Chong, D. P.;Hu, Ching-Han
Contributors: 化學系
Date: 1998-06
Issue Date: 2012-05-03T06:16:26Z
Publisher: Elsevier
Abstract: In this paper we report results from our theoretical studies on two P-diketones which exist as stable enol tautomers: acetylacetone and malonaldehyde. We found that density functional theory (DFT) with Becke's exchange functional and Perdew's correlation functional can accurately predict the core-electron binding energies (CEBEs) of both molecules. The oxygen 1s --> pi* inner-shell excitation spectra (ISES) of both tautomers have also been studied using our DFT procedure. The CEBEs for the corresponding carbons and oxygens of the C=O and C-OH groups of malonaldehyde are larger than those of acetylacetone, The first term values corresponding to a core-hole on the carbonyl oxygen were found to be larger than those with a core-hole on the enol oxygen. The observation indicates that the effect of a core-hole in the proximity of pi*: orbital has a stronger effect on increasing the electron affinity of the core-ionized cation.
Relation: J. Elect. Spectr. Rel. Phenom., 94(1-2): 181-185
Appears in Collections:[化學系] 期刊論文

Files in This Item:

File SizeFormat
index.html0KbHTML379View/Open


All items in NCUEIR are protected by copyright, with all rights reserved.

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback