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In this work, we study the influence of the PEDOT to PSS ratio on the optical properties of PEDOT:PSS thin solid films using spectroscopic ellipsometry and UV-vis spectrometry. In the data analysis, we develop a consisted composition dependent optical model of PEDOT:PSS. This enabled us to account for contributions from PSS part within the Tauc-Lorentz optical model and from PEDOT part within the Drude-Lorentz optical model. Moreover, we relate the optical properties of PEDOT:PSS thin solid films to their electrical specific conductivities in the frame of the generalized effective medium theory. Determined in this manner electrical conductivities of five commercially available water dispersions of PEDOT:PSS are compared with their nominal values.

A series of model compounds from 4‐benzoyl‐1,8‐naphthalene anhydride and aromatic amines and diamines has been synthesized. The influence of the reaction conditions on the structure of the compounds obtained has been investigated to explain the high‐temperature polycondensation reaction mechanism. It was found that at high‐temperature polycondensation of 1,8‐naphthalene‐type anhydrides with aromatic amines, isoimides with cis and and trans structures are formed instead of amic acids. The only trans isoimides may isomerize to imide structure. © 1995 John Wiley & Sons, Inc.

Optical properties of polymer/fullerene blend films upon thermal annealing are investigated by spectroscopic ellipsometry and described consistently within an optical model of the blend film. The optical model developed in this work treats both components, polymer and fullerene, as mixtures of reference materials, that is, their optically ordered and disordered phase. Then, the polymer/fullerene blend layer is also described as a mixture of these two components. In this manner, we extend an existing optical model, which accounts for the optical order within the polymer phases, on cases where the optically ordered PCBM phase occurs, too. Determination of the dielectric functions of all four reference materials allows for a unique quantitative characterization of a polymer/fullerene blend film by assigning to it thickness and the polymer to fullerene volume fraction of its layers as well as corresponding volume fractions of theirs optically ordered and disordered polymer and fullerene phases. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2018, 56, 1094–1100

The paper presents a synthesis of poly(l-lactide) with bacteriostatic properties. This polymer was obtained by ring-opening polymerization of the lactide initiated by selected low-toxic zinc complexes, Zn[(acac)(L)H2O], where L represents N-(pyridin-4-ylmethylene) tryptophan or N-(2-pyridin-4-ylethylidene) phenylalanine. These complexes were obtained by reaction of Zn[(acac)2 H2O] and Schiff bases, , the products of the condensation of amino acids and 4-pyridinecarboxaldehyde. The composition, structure, and geometry of the synthesized complexes were determined by NMR and FTIR spectroscopy, elemental analysis, and molecular modeling. Both complexes showed the geometry of a distorted trigonal bipyramid. The antibacterial and antifungal activities of both complexes were found to be much stronger than those of the primary Schiff bases. The present study showed a higher efficiency of polymerization when initiated by the obtained zinc complexes than when initiated by the zinc(II) acetylacetonate complex. The synthesized polylactide showed antibacterial properties, especially the product obtained by polymerization initiated by a zinc(II) complex with a ligand based on l-phenylalanine. The polylactide showed a particularly strong antimicrobial effect against Pseudomonas aeruginosa, Staphylococcus aureus, and Aspergillus brasiliensis. At the same time, this polymer does not exhibit fibroblast cytotoxicity.

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A series of polymers from dinaphthalene dianhydrides and aromatic diamines has been synthesized using one‐step high‐temperature polycondensation. The influence of the monomers structure on the polymers properties has been investigated. © 1997 John Wiley & Sons, Inc.