The absolute molecular weight of polyaniline in the pernigraniline, emeraldine, and leucoemeraldine oxidation states has been measured by light scattering and the exact number of aniline repeat units determined for the first time. Using potential-time profiling to monitor the chemical oxidative polymerization of aniline using ammonium peroxydisulfate oxidant, all three oxidation states of polyaniline can be synthesized in one step and the evolution of polymer molecular weight monitored. The pernigraniline intermediate formed during the chemical oxidative polymerization of aniline increases by 17-20% when it is converted to emeraldine, which is consistent with a two-step polymerization mechanism. These findings establish a solid experimental framework to chemically synthesize block copolymers of polyaniline by using different monomers to intercept the reaction at the pernigraniline oxidation state. 相似文献
Pyrolysis–gas chromatography/mass spectrometry (Py–CG/MS) has been applied to study and compare the composition of two electrochemically synthesized polyaniline (PANI) forms: fully reduced leucoemeraldine (LE) and intermediately oxidized emeraldine (EM). The different PANI forms were electrochemically synthesized using cyclic voltammetry. They were dedoped by stirring for 24 h in ammoniacal solutions. Leucoemeraldine and emeraldine pyrograms presented differences in the relative intensity of their fragment signals. Emeraldine pyrograms presented a higher relative intensity of the signals associated to oxidized fragments (i.e. quinone imine) than leucoemeraldine pyrograms. On the other hand, polymer samples synthesized under different anodic potentials showed small differences, consistent with a higher degree of crosslinking at higher anodic potentials. The results obtained indicate that Py–GC/MS may be used for identification among different oxidation states in aryl amine polymers. 相似文献
The aniline dimer, N-(4-aminophenyl)aniline has been polymerized cleanly under mild conditions to obtain an emeraldine base form of polyaniline using [MeB(3-(Mes)Pz)3]CuCl as the catalyst and H2O2 as the oxidant, while the subsequent acidification of the emeraldine base gives the conducting emeraldine salt form of polyaniline. 相似文献
The fully oxidized state of polyaniline (PANI), pernigraniline (PN), was synthesizedby oxidation of the emeraldine base form of PANI dissolved in NMP solvent with m-chloroperoxybenzoic acid. The resulted PN was characterized by FTIR and UV-Visiblespectra. The third-order nonlinear optical properties of PN in concentrated sulfuric acid(PN/H_2SO_4) were measured by a degenerated four wave mixing (DFWM) method. The re-sults obtained suggest that the soliton-pair intermediate state associated with thedegenerated state does not play a major role in the third order nonlinear optical prop-erties of PANI. 相似文献
Polyanilines doped with (HCl+KCl) and (HCl+CoCl2) were prepared by co-doping method, respectively. For comparison, polyaniline emeraldine salt (ES) by doping with HCl and its emeraldine base (EB) form were also synthesized. The co-doped polyanilines, ES and EB samples were all characterized by Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy aiming to understand the transformations in the different doping status. The results show that the doping degree of K+ ions is considerably higher than that of Co2+ ions under the same co-doping conditions possibly due to different pseudoprotonation constants of EB with K+ ions and Co2+ ions. Moreover, morphology difference of polyaniline co-doped with alkaline metal ions or transition meal ions may arise from different coordination geometry of metal ions. Nevertheless, there are similar chemical transformations of quinoid units to benzenoid ones on polyaniline backbones for the ES and both co-doped samples. And the polyaniline backbones co-doped with H+ and metal cations are found to attain weaker charge delocalization than the ES which is doped solely with H+. 相似文献
A 3D array of organic semiconductors was assembled using a DNA scaffold. An octameric aniline molecule (“octaniline”) was incorporated into a DNA building block based on a dimeric tensegrity triangle. The construct self-assembled to form a 3D crystal. Reversible redox conversion between the pernigraniline and leucoemeraldine states of the octaniline is retained in the crystal. Protonic doping gave emeraldine salt at pH 5, corresponding to the conductive form of polyaniline. Redox cycling within the crystal was visualized by color changes and Raman microscopy. The ease of conversion between the octaniline states suggests that it is a viable electronic switch within a unique 3D structure. 相似文献
Raman spectroelectrochemical study has been done with electrochemically prepared films of polyaniline and a copolymer of polyaniline and metanilic acid using a green laser excitation (532 nm). The experimental variables included solutions of different pH between 0.5 and 9.0, and varying electrode potential between 0.0 and 0.8 V versus Ag/AgCl. Raman bands within the wavenumber limits of 500–1700 cm−1 have been analysed, and their changes, proceeding with varying of electrode potential and solution pH, have been interpreted. It has been stressed that the spectral changes of polymer films proceed continuously rather than stepwise by changing the electrode potential. Considering leucoemeraldine and pernigraniline forms of polyaniline as fully reduced and oxidised structures, respectively, it could be concluded that many different redox forms can exist between these two limiting forms, rather than the only possible emeraldine form. 相似文献
Here the redox‐driven switch between the wrinkled and dewrinkled states on polyaniline (PANI) film is reported. This switch is derived from the reversible transition in different intrinsic redox states of polyaniline (e.g., between emeraldine salt (ES) and leucoemeraldine base (LEB) or between ES and pernigraniline base (PB)) that are involved in the redox reaction, coupled with the corresponding volume expansion/shrinkage. Interestingly, the as‐wrinkled ES film becomes deswollen and dewrinkled when reduced to the LEB state or oxidized to the PB state. Conversely, oxidation of the LEB film or reduction of the PB film into the swollen ES film leads to the reoccurrence of surface wrinkling. Furthermore, the reducibility of the dewrinkled LEB film and the oxidizability of the dewrinkled PB film are well utilized respectively to yield various wrinkled PANI‐based composite films.
Dispersion of carbon nanotubes into solvents affects their surface chemistries, electronic structures, and subsequent functionalization. In this Communication, a water-soluble self-doped polyaniline nanocomposite was fabricated by in situ polymerization of the 3-aminophenylboronic acid monomers in the presence of single-stranded DNA dispersed- and functionalized-single-walled carbon nanotubes. For the first time, we found that the carbon nanotubes became novel active stabilizers owing to the DNA functionalization. The nanotubes reduced the polyaniline backbone from the unstable, degradable, fully oxidized pernigraniline state to the stable, conducting emeraldine state because of their reductive ability, which could improve the chemical stability of the self-doped polyaniline. Electrical measurements demonstrate that the conductivity of the nanocomposite was much higher than that of the pure self-doped polyaniline in both acidic and neutral solutions. 相似文献