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High-molecular-weight polyaniline

The high reactivity of the 6/Pd-catalyst was exploited in the preparation of high molecular weight polyaniline, Eq. (93) [99]. After thermolytic deprotection of the Boc protecting groups and air oxidation, emeraldine, the conductive form of polyanihne was obtained. [Pg.169]

Introduction Conventional Route for Synthesizing High-Molecular-Weight Polyaniline Improved Route for Synthesizing High-Molecular-Weight Polyaniline Base-Processing Route for the Fabrication of... [Pg.1123]

Synthesis of High-Molecular-Weight Polyaniline for Fiber Spinning... [Pg.1126]

Conventional Route for Synthesizing High-Molecular-Weight Polyaniline... [Pg.1128]

Concentrations of HB and B are measurable by spectroscopy, and pK values of the acids HB" " are well known. Hammett acidity function. Ho, scales are useftil for comparing different acid media for acid strength. Typically, the Hammett acidity functions for the reaction mixtures to synthesize high-molecular-weight polyaniline are in the range —2 < Hq < 0.5. [Pg.1130]

The fibers that are described in the following section were spun from a 12 wt% PANI-AMPSA/DCAA dope solution with the high-molecular-weight polyaniline synthesized in-house (M 280,000 g/mol). [Pg.1156]

MacDiarmid, A.G., S.K. Manohar, and L.H.C. Mattoso. 1996. High molecular weight polyanilines and synthetic methods therefor. US Patent 5,519,111. [Pg.1187]

Adams, P.N., P.J. Laughlin, A.P. Monkman, and A.M. Kenwright. 1996. Low temperature synthesis of high molecular weight polyaniline. Polymer 37 3411. [Pg.1187]

Bowman, D., and B.R. Mattes. 2005. Conductive fibre prepared from ultra-high molecular weight polyaniline for smart fabric and interactive textile applications. Synth Met 154 9. [Pg.1189]

Mattoso, L.H.C., A.G. MacDiarmid, and A.J. Epstein. 1997. Controlled synthesis of high molecular weight polyaniline and poly(o-methoxyaniline). Synth Met 68 1. [Pg.158]

P. N. Adams, A. P. Monkman, Characterization of high molecular weight polyaniline synthesized at —40°C using a 0.25 1 mole ratio of persulfate oxidant to aniline, Synthetic Metals 1997, 87, 165. [Pg.150]

M. Abe, A. Ohtani, Y. Umemoto, S. Akizuki, M. Ezoe, H. Higuchi, K. Nakamoto, A. Okuno, Y. Noda, Soluble and high molecular weight polyaniline, Chemical Communications 1989, 1736. [Pg.210]

Mattoso et al. [1028] polymerized aniline at —40°C in the presence of LiCl and HQ to yield a high-molecular-weight polyaniline. A similar procedure has been applied to prepare poly(o-methor aniline) [1029]. [Pg.33]


See other pages where High-molecular-weight polyaniline is mentioned: [Pg.166]    [Pg.57]    [Pg.1126]    [Pg.1127]    [Pg.1128]    [Pg.1129]    [Pg.1129]    [Pg.1131]    [Pg.1150]    [Pg.1154]    [Pg.94]    [Pg.97]    [Pg.99]    [Pg.99]    [Pg.100]    [Pg.102]    [Pg.121]    [Pg.125]    [Pg.127]    [Pg.118]    [Pg.517]    [Pg.31]    [Pg.155]   
See also in sourсe #XX -- [ Pg.516 ]




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