Novel adamantane substituted polythiophenes as competitors to Poly (3-Hexylthiophene)
Identifikátory výsledku
Kód výsledku v 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>
Výsledek na webu
<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>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Novel adamantane substituted polythiophenes as competitors to Poly (3-Hexylthiophene)
Popis výsledku v původním jazyce
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.
Název v anglickém jazyce
Novel adamantane substituted polythiophenes as competitors to Poly (3-Hexylthiophene)
Popis výsledku anglicky
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.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10400 - Chemical sciences
Návaznosti výsledku
Projekt
<a href="/cs/project/GA21-01057S" target="_blank" >GA21-01057S: Nové organické polovodiče pro budoucí bioelektronické zařízení pro regenerativní medicínu</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2022
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Polymer
ISSN
0032-3861
e-ISSN
1873-2291
Svazek periodika
258
Číslo periodika v rámci svazku
23.8.2022
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
12
Strana od-do
125274-125286
Kód UT WoS článku
000862163500005
EID výsledku v databázi Scopus
2-s2.0-85138102531