Abstract

AbstractI obtained colorless, transparent, metallically conductive polymer films by anion exchange in the microcrystals of (BO)2.4I3 [BO = bis(ethylenedioxytetrathiafulvalene)], forming the conductive network in surface‐conducting reticulate‐doped polycarbonate (PC) films. Strongly absorbing I3− anions were replaced by I− or Br− anions, showing weaker absorption in visible light. Interestingly, this transformation proceeded without deterioration of the continuity of the network, and even the shape of the microcrystals was preserved. Particularly, the salt (BO)2.4I3 could be transformed to (BO)2Br(H2O)3 or to (BO)2I(H2O)x. I achieved this by immersing strongly colored PC/(BO)2.4I3 films in the KBr solution or by contact with a Cu plate in KI solution. Depending on the conditions of the ion‐exchange reaction, colorless films showing metallic conductivity down to helium temperatures or showing semiconducting behavior below 100 K were obtained. Electrical properties of some systems are very sensitive to the partial pressure of water. The (BO)2Br(H2O)3 and (BO)2I(H2O)x microcrystals could reversibly change their water content, as shown by comparative X‐ray diffraction and electrical studies performed under reduced pressure or dry atmosphere and under ambient conditions. The controlled anion exchange presented in this article can be considered as a new effective way of modifying the polycrystalline networks of (BO)2.4I3 and other similar salts. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1465–1472, 2002

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.