English  |  正體中文  |  简体中文  |  Items with full text/Total items : 62805/95882 (66%)
Visitors : 3880796      Online Users : 273
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/80542

    Title: Photo-physical Properties of N-methyl-3,4-fulleropyrrolidine and Its Derivatives: A DFT and TD-DFT Investigation
    Authors: Tai, Chin-Kuen;Hsieh, Wei-Yi;Yeh, Pao-Ling;Chiu, Houn-Lin;Wang, Bo-Cheng
    Contributors: 淡江大學化學學系
    Keywords: NMFP derivatives;Substituted effect;Electron-donating ability;Resonance energy;DFT/B3LYP;TD-DFT/B3LYP
    Date: 2013-03
    Issue Date: 2013-01-31 10:32:00 (UTC+8)
    Publisher: Oxford: Wiley-Blackwell Publishing Ltd
    Abstract: A series of N-methyl-3,4-fulleropyrrolidine (NMFP) derivatives were designed by selecting different π-conjugated linkers and electron-donating groups as D-π-A and D-A systems. The optimised structures and photo-physical properties of NMFP and its derivatives have been determined using density functional theory (DFT) and time-dependent density functional theory (TD-DFT) methods with the B3LYP functional and the 6-31G basis set. According to the computation analysis, both the π-conjugated linkers and the electron-donating groups can influence the electronic and photo-physical properties of the NMFP derivatives. Our calculated results demonstrated that the electron-donating groups, with significant electron-donating ability, had the tendency to increase the highest occupied molecular orbital (HOMO) energy. The π-conjugated linkers with lower resonance energy decreased the lowest occupied molecular orbital (LUMO) energy and caused a significant decrease in the energy gap (Eg) between the EHOMO and ELUMO. A Natural Bond Orbital (NBO) analysis examines the effect of the electron-donating group, π conjugated linker, and electron-withdrawing group for these NMFP derivatives. For the NMFP derivatives, a projected density of state (PDOS) analysis demonstrated that the electron density of HOMO and LUMO are concentrated on the electron-donating group and the π-conjugated linker, respectively. A TD-DFT/B3LYP calculation was performed to calculate the electronic absorption spectra of these NMFP derivatives. Both the electron-donating group and the π-conjugated linker contribute to the major absorption peaks, which are assigned as HOMO to LUMO transitions and are red-shifted relative to those of non-substituted NMFP.
    Relation: Journal of the Chinese Chemical Society 60(3), pp.235–344
    DOI: 10.1002/jccs.201200247
    Appears in Collections:[Graduate Institute & Department of Chemistry] Journal Article

    Files in This Item:

    File Description SizeFormat

    All items in 機構典藏 are protected by copyright, with all rights reserved.

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