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Novel adamantane substituted polythiophenes as competitors to Poly (3-Hexylthiophene)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26310%2F22%3APU146352" target="_blank" >RIV/00216305:26310/22:PU146352 - isvavai.cz</a>

  • Result on the web

    <a href="https://reader.elsevier.com/reader/sd/pii/S0032386122007625?token=7C7A0246313C6AFE21AA1CFFCB403CE2DA5A6DEB2D1E0B8A4728AC590EB85896349D008FF761D8F13B091209AA0B2225&originRegion=eu-west-1&originCreation=20221129081953" target="_blank" >https://reader.elsevier.com/reader/sd/pii/S0032386122007625?token=7C7A0246313C6AFE21AA1CFFCB403CE2DA5A6DEB2D1E0B8A4728AC590EB85896349D008FF761D8F13B091209AA0B2225&originRegion=eu-west-1&originCreation=20221129081953</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.polymer.2022.125274" target="_blank" >10.1016/j.polymer.2022.125274</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Novel adamantane substituted polythiophenes as competitors to Poly (3-Hexylthiophene)

  • Original language description

    The investigation of poly(3-alkylthiophenes) (P3ATs) has gained great attention in the last decades. Here, we present the synthesis, experimental and theoretical study of the novel regioregular poly(3-adamantylmethylthiophene) (PMAT) and poly(3-adamantylethylthiophene) (PEAT), characterised by a bulky adamantane side group. The prepared compounds are solution-processable in common organic solvents, possess excellent thermal stability up to 491 degrees C and have unique chemical endurance. The molecular ordering of the polymers was investigated by the GIWAXS technique, and PMAT was found to have the higher content of crystalline phase. The experimental absorption and fluorescence spectra of investigated polymers indicate a higher rigidity of the adamantane side group with respect to torsional rotation in solutions and in thin layers. Electrical measurements exhibit charge carrier mobilities comparable to poly(3-hexylthiophene) (P3HT). In contrast to P3HT, adamantyl-substituted polymers show quasi-reversible reduction alongside the expected quasi -reversible oxidation, which in theory supports the ability to transport both types of electric charges. The newly synthetized regioregular adamantane substituted polythiophenes are serious competitors for a wide range of applications in electronics and optoelectronics.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10400 - Chemical sciences

Result continuities

  • Project

    <a href="/en/project/GA21-01057S" target="_blank" >GA21-01057S: Novel organic semiconductors for future bioelectronics devices for regenerative medicine</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Polymer

  • ISSN

    0032-3861

  • e-ISSN

    1873-2291

  • Volume of the periodical

    258

  • Issue of the periodical within the volume

    23.8.2022

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    125274-125286

  • UT code for WoS article

    000862163500005

  • EID of the result in the Scopus database

    2-s2.0-85138102531