<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wiesner T</submitter><funding>China Scholarship Council</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>National Natural Science Foundation of China</funding><funding>Julius-Maximilians-Universität Würzburg</funding><pagination>e202201919</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10092590</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(69)</volume><pubmed_abstract>Tetraiodotetraazapentacene I&lt;sub>4&lt;/sub> TAP, the last missing derivative in the series of halogenated silylated tetraazapentacenes, was synthesized via condensation chemistry from a TIPS-ethynylated diaminobenzothiadiazol in three steps. Single and double reduction furnished its air-stable monoanion and relatively air-stable dianion, both of which were characterized by crystallography. All three species are structurally and spectroscopically compared to non-halogenated TAP and Br&lt;sub>4&lt;/sub> TAP. I&lt;sub>4&lt;/sub> TAP is an n-channel material in thin-film transistors with average electron mobilities exceeding 1 cm&lt;sup>2&lt;/sup> (Vs)&lt;sup>-1&lt;/sup> .</pubmed_abstract><journal>Chemistry (Weinheim an der Bergstrasse, Germany)</journal><pubmed_title>The Radical Anion, Dianion and Electron Transport Properties of Tetraiodotetraazapentacene.</pubmed_title><pmcid>PMC10092590</pmcid><funding_grant_id>22101130</funding_grant_id><funding_grant_id>PhD scholarship</funding_grant_id><pubmed_authors>Wiesner T</pubmed_authors><pubmed_authors>Moos M</pubmed_authors><pubmed_authors>Ji L</pubmed_authors><pubmed_authors>Reiss H</pubmed_authors><pubmed_authors>Lambert C</pubmed_authors><pubmed_authors>Friedrich A</pubmed_authors><pubmed_authors>Freudenberg J</pubmed_authors><pubmed_authors>Dreuw A</pubmed_authors><pubmed_authors>Marder TB</pubmed_authors><pubmed_authors>Rudin B</pubmed_authors><pubmed_authors>Bunz UHF</pubmed_authors><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Braunschweig H</pubmed_authors><pubmed_authors>Rominger F</pubmed_authors><pubmed_authors>Tverskoy O</pubmed_authors><pubmed_authors>Krummenacher I</pubmed_authors><pubmed_authors>Han J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Radical Anion, Dianion and Electron Transport Properties of Tetraiodotetraazapentacene.</name><description>Tetraiodotetraazapentacene I&lt;sub>4&lt;/sub> TAP, the last missing derivative in the series of halogenated silylated tetraazapentacenes, was synthesized via condensation chemistry from a TIPS-ethynylated diaminobenzothiadiazol in three steps. Single and double reduction furnished its air-stable monoanion and relatively air-stable dianion, both of which were characterized by crystallography. All three species are structurally and spectroscopically compared to non-halogenated TAP and Br&lt;sub>4&lt;/sub> TAP. I&lt;sub>4&lt;/sub> TAP is an n-channel material in thin-film transistors with average electron mobilities exceeding 1 cm&lt;sup>2&lt;/sup> (Vs)&lt;sup>-1&lt;/sup> .</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-05-28T11:49:25.149Z</modification><creation>2025-04-07T03:21:56.827Z</creation></dates><accession>S-EPMC10092590</accession><cross_references><pubmed>35916326</pubmed><doi>10.1002/chem.202201919</doi></cross_references></HashMap>