journal article·2000-03-01

Lewis Acid Doped Polyaniline. Part II: Spectroscopic Studies of Emeraldine Base and Emeraldine Hydrochloride Complexation with FeCl3

Françoise Genoud, Irena Kulszewicz-Bajer, Alexandre Bedel, Jean Louis Oddou, Claudine Jeandey, Adam Pron

Chemistry of Materials· Volume 12· Issue 3
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Abstract

It is demonstrated that Lewis acid doping of polyaniline in the oxidation state of emeraldine can be conveniently monitored by 57 Fe Mössbauer spectroscopy if FeCl 3 is used as the dopant. The spectrum of doped polyaniline consists of two doublets with distinctly different Mössbauer parameters which can be unequivocally ascribed to two types of complexing sites (amine and imine nitrogens). From the temperature dependence of the isomer shift and the recoil free absorption, we have calculated Mössbauer lattice temperature ϑ m ‘ as probed by both complexing sites, which were 83 K for the amine and 126 K for the imine sites. These low values of ϑ m ‘ imply significant mobility of the dopant at temperatures close to room temperature, which is typical of small molecules inserted into polymer matrices. FeCl 3 -doped polyaniline is soluble in nitromethane, and acetonitrile and films cast from these solvents show conductivity of 0.2 S/cm. FeCl 3 -doped polyaniline is also a strong near-infrared absorber.
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Research context

OpenAlex topics: Conducting polymers and applications · Analytical Chemistry and Sensors · Electrochemical sensors and biosensors

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Affiliations

Laboratoire des Métaux Synthétiques, UMR 5819, DRFMC-CEA Grenoble, 38054 Grenoble Cedex 9, France; Université Joseph Fourier, Grenoble, France; Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00664 Warszawa, Poland; and Laboratoire de Chimie de Coordination, URA 1194, DRFMC-CEA Grenoble, 38054 Grenoble Cedex 9, France

References (19)

Show source-provided references
1. Pron A. · J. Chem. Soc., Chem. Commun. · 1981 · 78310.1039/C39810000783 ↗
2. Pron A. · Mater. Res. Bull. · 1982 · 14 · 150510.1016/0025-5408(82)90205-7 ↗
3. Kitao S. · J. Phys. Soc. Jpn. · 1997 · 66 · 119510.1143/JPSJ.66.1195 ↗
4. Kulszewicz-Bajer I. · Chem. Mater. · 1999 · 11 · 55210.1021/cm980727a ↗
5. For · 1997 · 2 · 505
6. Huang W. S. · J. Chem. Soc., Chem. Commun. · 1987 · 178410.1039/c39870001784 ↗
7. Huang W. S. · J. Chem. Soc., Faraday Trans. 1 · 1987 · 82 · 238510.1039/f19868202385 ↗
8. Kang E. T. · 1997 · 3 · 121
9. Pron A. · Synth. Met. · 1988 · 24 · 19310.1016/0379-6779(88)90257-3 ↗
10. Tomala K. · Solid State Commun. · 1977 · 24 · 85710.1016/0038-1098(77)91230-3 ↗
11. Greenwood N. N. · 197110.1007/978-94-009-5697-1 ↗
12. Reiff W. M. · Hyperfine Interact. · 1990 · 56 · 172310.1007/BF02405502 ↗
13. Herber R. H. · Physica · 1980 · 99 · 352
14. MacDiarmid A. G. · J. Synth. Met. · 1987 · 18 · 28510.1016/0379-6779(87)90893-9 ↗
15. Zuo F. · J. Phys. Rev. B · 1987 · 36 · 347510.1103/PhysRevB.36.3475 ↗
16. Houzé E. · Phys. Rev. B · 1996 · 53 · 1430910.1103/PhysRevB.53.14309 ↗
17. Houzé E. · Phys. Rev. B · 1997 · 5 · 1226310.1103/PhysRevB.56.12263 ↗
18. Xia Y. · J. Chem. Mater. · 1995 · 7 · 44310.1021/cm00051a002 ↗
19. Rannou P. · Macromolecules · 1998 · 31 · 300710.1021/ma971365f ↗