期刊
JOURNAL OF ORGANOMETALLIC CHEMISTRY
卷 713, 期 -, 页码 96-103出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2012.04.025
关键词
Ferrocene functionalized polyester dendrimer; Grafting rate; Electron transfer; Catalytic performance; Ammonium perchlorate; Thermal decomposition
资金
- National Natural Science Foundation of China [10876004]
- Natural Science Foundation of Hebei Province [B2010001055]
A novel ferrocene functionalized polyester dendrimer (PEDr-Fc) containing 6, 12 and 24 peripheral ferrocene moieties were obtained using the esterification reaction between ferrocene carboxylic and polyester dendrimer (PEDr). The H-1 NMR, C-13 NMR, MALDI-TOF mass spectra and elemental analysis techniques confirmed the structure of PEDr-Fc and provided evidences of the successful functionalization of PEDr by ferrocene with high yield over 92% and high grafting rate (more than 91%) of ferrocene on the terminals of dendrimer. The cyclic voltammogram measurements were carried out to analyze the redox properties of PEDr-Fcs. The catalytic performances for thermal decomposition of ammonium perchlorate (AP) were investigated by DSC techniques. The kinetic parameters were computed by the Kissinger method. PEDr-Fcs maintained the special redox properties by electron transfer of ferrocene/ferrocenium in ferrocene groups and all the redox centers were equivalent with no interaction between them. The electrode reactions of PEDr-Fcs were diffusion-controlled redox processes. PEDr-Fc presented an efficient catalytic effect on the thermal degradation of AP and the catalytic reactions were characterized by decreased activation energy and increased rate constant of thermal decomposition. The possible catalytic mechanism was that the electron transfer between Fe2+ and Fe3+ in ferrocene oxidized by AP and reduced by NH3 produced by the degradation of AP accelerated decomposition reaction below 300 degrees C, and the formation of iron clusters with large surface areas might cause the rupture of the chemical bond in AP at high temperature. (C) 2012 Elsevier B.V. All rights reserved.
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