<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(30)</volume><submitter>An C</submitter><pubmed_abstract>Two naphthalene diimide (NDI)-benzothiadiazole (BT) based conjugated polymers with high molecular weight, P1 and P2, were synthesized by introducing F atoms to modulate the electron-donating ability of the BT moiety. 3-Decyl-pentadecyl branched alkyl side chains were employed and expected to improve the molecular organization and device performance. Both polymers have excellent solubility in common organic solvents. UV-vis-NIR absorption and cyclic voltammetry indicate that the maximum absorption wavelength of P2 is blue-shifted and the HOMO energy level of P2 is decreased in comparison with P1. Two dimensional wide angle X-ray scattering of thin films revealed a similar organization of both polymers. A less balanced transport in field-effect transistors with increased electron mobility of 0.258 cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup> and lowered hole transport of 2.4 × 10&lt;sup>-3&lt;/sup> cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup> was found for P2. Polymer devices of P1 exhibited a balanced ambipolar transport, with a hole mobility of 0.073 cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup> and electron mobility of 0.086 cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup>.</pubmed_abstract><journal>RSC advances</journal><pagination>16464-16469</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9080245</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effect of fluorination of naphthalene diimide-benzothiadiazole copolymers on ambipolar behavior in field-effect transistors.</pubmed_title><pmcid>PMC9080245</pmcid><pubmed_authors>Baumgarten M</pubmed_authors><pubmed_authors>Marszalek T</pubmed_authors><pubmed_authors>Duan R</pubmed_authors><pubmed_authors>Pisula W</pubmed_authors><pubmed_authors>Hu B</pubmed_authors><pubmed_authors>An C</pubmed_authors><pubmed_authors>Makowska H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of fluorination of naphthalene diimide-benzothiadiazole copolymers on ambipolar behavior in field-effect transistors.</name><description>Two naphthalene diimide (NDI)-benzothiadiazole (BT) based conjugated polymers with high molecular weight, P1 and P2, were synthesized by introducing F atoms to modulate the electron-donating ability of the BT moiety. 3-Decyl-pentadecyl branched alkyl side chains were employed and expected to improve the molecular organization and device performance. Both polymers have excellent solubility in common organic solvents. UV-vis-NIR absorption and cyclic voltammetry indicate that the maximum absorption wavelength of P2 is blue-shifted and the HOMO energy level of P2 is decreased in comparison with P1. Two dimensional wide angle X-ray scattering of thin films revealed a similar organization of both polymers. A less balanced transport in field-effect transistors with increased electron mobility of 0.258 cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup> and lowered hole transport of 2.4 × 10&lt;sup>-3&lt;/sup> cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup> was found for P2. Polymer devices of P1 exhibited a balanced ambipolar transport, with a hole mobility of 0.073 cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup> and electron mobility of 0.086 cm&lt;sup>2&lt;/sup> V&lt;sup>-1&lt;/sup> s&lt;sup>-1&lt;/sup>.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 May</publication><modification>2025-04-19T12:53:18.426Z</modification><creation>2025-04-19T12:53:18.426Z</creation></dates><accession>S-EPMC9080245</accession><cross_references><pubmed>35540535</pubmed><doi>10.1039/c8ra02915f</doi></cross_references></HashMap>