<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bobrova EA</submitter><funding>Ministry of Science and Higher Education of the Russian Federation</funding><funding>Russian Science Foundation</funding><pagination>124</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12844271</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>An efficient synthetic method for the preparation of self-assembling conjugated organic materials with a silazane anchor group based on direct hydrosilylation reaction is reported. A novel organic semiconductor molecule, &lt;b>NH(Si-Und-BTBT-Hex)&lt;sub>2&lt;/sub>&lt;/b>, consisting of a polar silazane anchor group linked through undecylenic (Und) aliphatic spacers to conjugated blocks based on benzothieno[3,2-b][1]benzothiophene (BTBT) and solubilizing hexyl (Hex) end groups, was synthesized. Its self-organization on the air-water interface and solid substrates into ultrathin layers obtained by the Langmuir-Schaefer or Langmuir-Blodgett methods was investigated. Monolayer organic field-effect transistors manufactured from &lt;b>NH(Si-Und-BTBT-Hex)&lt;sub>2&lt;/sub>&lt;/b> showed operation in the &lt;i>p&lt;/i>-type mo</pubmed_abstract><journal>Nanomaterials (Basel, Switzerland)</journal><pubmed_title>Self-Assembling Conjugated Organic Materials with a Silazane Anchor Group: Synthesis, Self-Organization, and Semiconductor Properties.</pubmed_title><pmcid>PMC12844271</pmcid><funding_grant_id>FFSM-2024-0003</funding_grant_id><funding_grant_id>19-73-30028</funding_grant_id><pubmed_authors>Skorotetсky MS</pubmed_authors><pubmed_authors>Ponomarenko SA</pubmed_authors><pubmed_authors>Bobrova EA</pubmed_authors><pubmed_authors>Gaidarzhi VP</pubmed_authors><pubmed_authors>Trul AA</pubmed_authors><pubmed_authors>Agina EV</pubmed_authors><pubmed_authors>Kuleshov BS</pubmed_authors><pubmed_authors>Borshchev OV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Self-Assembling Conjugated Organic Materials with a Silazane Anchor Group: Synthesis, Self-Organization, and Semiconductor Properties.</name><description>An efficient synthetic method for the preparation of self-assembling conjugated organic materials with a silazane anchor group based on direct hydrosilylation reaction is reported. A novel organic semiconductor molecule, &lt;b>NH(Si-Und-BTBT-Hex)&lt;sub>2&lt;/sub>&lt;/b>, consisting of a polar silazane anchor group linked through undecylenic (Und) aliphatic spacers to conjugated blocks based on benzothieno[3,2-b][1]benzothiophene (BTBT) and solubilizing hexyl (Hex) end groups, was synthesized. Its self-organization on the air-water interface and solid substrates into ultrathin layers obtained by the Langmuir-Schaefer or Langmuir-Blodgett methods was investigated. Monolayer organic field-effect transistors manufactured from &lt;b>NH(Si-Und-BTBT-Hex)&lt;sub>2&lt;/sub>&lt;/b> showed operation in the &lt;i>p&lt;/i>-type mo</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-09T03:17:28.503Z</modification><creation>2026-06-09T03:11:43.129Z</creation></dates><accession>S-EPMC12844271</accession><cross_references><pubmed>41591041</pubmed><doi>10.3390/nano16020124</doi></cross_references></HashMap>