竹岡 裕子

Third-order optical nonlinearity of regioregular head-to-tail coupled poly(3-hexylthiophene)(HT-PHT) was measured using degenerate four wave mixing (DFWM), and the dispersion spectrum of \X-(3)\ around the exciton absorption peak was obtained. In addition, the relaxation process of the excitons was measured using the transient grating method. The resultant decay time was less than 2 ps and consisted of two components.

Third-order optical nonlinearity of regioregular head-to-tail coupled poly(3-hexylthiophene)(HT-PHT) was measured using degenerate four wave mixing (DFWM), and the dispersion spectrum of |χ(3)| around the exciton absorption peak was obtained. In addition, the relaxation process of the excitons was measured using the transient grating method. The resultant decay time was less than 2 ps and consisted of two components.

The effect of NaCl concentration on the redox potential of alpha-ferrocenylundecyl-omega-hydroxy-polyoxyethylene (FPEG) micelles has been studied in aqueous solutions. With increasing NaCl concentration, the anodic half-wave potentials E-1/2 of cyclic voltammograms of the aqueous solutions shift to higher potential, and the peak currents of the cyclic voltammograms decrease. The results are discussed in terms of thermodynamics of the micelle formation. An equation which interprets the correlation between the E-1/2, the salt concentration, diffusion coefficient of the micelle D-M, and the aggregation number m, has been derived. The changes in D-M and m with NaCl concentration do not explain the change in the value of E-1/2. The decrease in the equilibrium constant for the micelle-disruption K-d with increasing NaCl concentration affects the redox-potential of the FPEG micellar solutions. (C) 1997 Elsevier Science S.A.

We measured the third-order optical nonlinearity of regioregular head-to-tail coupled poly (3-hexylthiophene) (HT-PHT) and regiorandom poly (3-hexylthiophene) (R-PHT) around exciton resonance using degenerate four wave mixing. The observed value of |χ⁽³⁾| at the exciton resonance peak of HT-PHT is in the order of 10^-9 esu which is approximately three-fold larger than that of R-PHT. We observed for the first time the enhancement in optical nonlinearity that occurs through the control of regularity of the polymeric structure. Response time of the nonlinearity was also measured using the transient grating method. The decay time of the transient grating in R-PHT and HT-PHT was less than 2 ps.

The dissolved states of redox-active non-ionic surfactant (FPEG) in the swollen state of N-isopropyl acrylamide (NIPA) hydrogel have been studied by using a gel-modified electrode. The pronounced decrease in the peak current and the negative shift in the formal potential of CV at the gel-modified electrode, as compared with the normal GC electrode, was observed in the micelle-solution; this indicates that the diffusive FPEG molecules which form the micelle hardly penetrate into the NIPA gel. This result suggests that there exists all interaction between FPEG molecules and the NIFA gel in the vicinity of the surface of the NIPA gel in the micelle-solution. However, this also indicates that a small amount of FPEG molecules which can form micelles exist in the NIPA gel. (C) 1997 Elsevier Science Ltd.

The conductive ultra thin films were fabricated from mixed monolayers containing stearic acid and Head-to-Tail poly(3-alkylthiophene). These films exhibited well-defined layered structures as determined by optical absorption and X-ray diffraction measurements. The UV-Vis absorption spectra of these films showed lower energy absorption shifts of 48 nm from that of the random poly(3-alkylthiophene)/stearic acid LB films. The blue shift of absorption maximum of the LB film is attributed to the increase of pi-conjugation length caused by no steric hindrance of alkyl side chains. The conductivity of the Head-to-Tail poly(3-hexylthiophene)/stearic acid LB films was greatly improved in the range of 67-100 S/cm.

A non-ionic redox active surfactant, alpha-ferrocenylundecyl-omega-hydroxy-oligo(ethylene oxide), exhibits high ability to form polymer complexes with poly(acrylic acid) at a micelle forming concentration, in spite of the low molecular weight of the oligo(ethylene oxide) site. The fraction of carboxyls associated with ether oxygens (theta) between them has a high value (ca. 0.8) which is independent of the concentration of poly(acrylic acid). The complex formation seemed to be caused by hydrogen bonding and hydrophobic interactions. The complex formation influenced on electrochemical reactions of the redox active surfactant.