Reactivity of the nitro-group of a π-conjugated polymer upon the interface formation with chromium:: a photoelectron spectroscopy investigation

被引:8
作者
Iucci, G
Polzonetti, G
Altamura, P
Paolucci, G
Goldoni, A
D'Amato, R
Russo, MV
机构
[1] Univ Roma Tre, Dept Phys E Amaldi, I-00146 Rome, Italy
[2] Univ Roma Tre, INFM, I-00146 Rome, Italy
[3] Sincrotrone Trieste, SCpA SS, I-34012 Trieste, Italy
[4] Univ Rome La Sapienza, Dept Chem, I-00185 Rome, Italy
关键词
organometallic polymers; polymer/metal interfaces; X-ray photoelectron spectroscopy; synchrotron radiation;
D O I
10.1016/S0169-4332(99)00333-5
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
X-ray photoelectron spectroscopy was used in order to investigate the interface formation between chromium and thin films of a newly synthesised pi-conjugated polymer P(PA-pNO(2)PA); the investigated material is a block copolymer consisting of phenylacetylene (PA) and para-nitro phenylacetylene (pNO(2)PA) units {[-(CH=C-R)(n)-(CH=C-R')(m)-](N); R = C6H5, R' = C6H4NO2}. Chromium was evaporated stepwise in situ onto the polymer surface and the XPS spectra of the substrate polymer and of the metal overlayer were studied as a function of increasing chromium thickness. In the early stages of the interface formation, chromium was found to interact mainly with the nitrogen atoms of the -NO2 groups, that are reduced to nitride-like species; the N-O bond is broken, as evidenced by the modifications occurring in the N1s and O1s spectra. The changes in the C1s spectra upon increasing metal deposition suggest the formation of a chromium-arene pi-complex at low chromium coverage and of carbide-like species at higher chromium thickness. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:10 / 18
页数:9
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