<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Miao Z</submitter><funding>H2020 Marie Sklodowska-Curie Actions</funding><funding>University of Southern California</funding><funding>Division of Materials Research</funding><pagination>8331-8338</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9614958</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(20)</volume><pubmed_abstract>Relationships between chemical structure and conductivity in ordered polymers (OPs) are difficult to probe using bulk samples. We propose that conductance measurements of appropriate molecular-scale models can reveal trends in electronic coupling(s) between repeat units that may help inform OP design. Here, we apply the scanning tunneling microscope-based break-junction (STM-BJ) method to study transport through single-molecules comprising OP-relevant imine, imidazole, diazaborole, and boronate ester dynamic covalent chemical bridges. Notably, solution-stable boron-based compounds dissociate &lt;i>in situ&lt;/i> unless measured under a rigorously inert glovebox atmosphere. We find that junction conductance negatively correlates with the electronegativity difference between bridge atoms, and corr</pubmed_abstract><journal>Nano letters</journal><pubmed_title>Charge Transport Across Dynamic Covalent Chemical Bridges.</pubmed_title><pmcid>PMC9614958</pmcid><funding_grant_id>DMR-2044552</funding_grant_id><funding_grant_id>898657</funding_grant_id><pubmed_authors>Parr JM</pubmed_authors><pubmed_authors>Inkpen MS</pubmed_authors><pubmed_authors>Czyszczon-Burton TM</pubmed_authors><pubmed_authors>Rotthowe N</pubmed_authors><pubmed_authors>Liu ZF</pubmed_authors><pubmed_authors>Quainoo T</pubmed_authors><pubmed_authors>Miao Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Charge Transport Across Dynamic Covalent Chemical Bridges.</name><description>Relationships between chemical structure and conductivity in ordered polymers (OPs) are difficult to probe using bulk samples. We propose that conductance measurements of appropriate molecular-scale models can reveal trends in electronic coupling(s) between repeat units that may help inform OP design. Here, we apply the scanning tunneling microscope-based break-junction (STM-BJ) method to study transport through single-molecules comprising OP-relevant imine, imidazole, diazaborole, and boronate ester dynamic covalent chemical bridges. Notably, solution-stable boron-based compounds dissociate &lt;i>in situ&lt;/i> unless measured under a rigorously inert glovebox atmosphere. We find that junction conductance negatively correlates with the electronegativity difference between bridge atoms, and corr</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-04T09:42:07.613Z</modification><creation>2025-04-04T09:42:07.613Z</creation></dates><accession>S-EPMC9614958</accession><cross_references><pubmed>36215246</pubmed><doi>10.1021/acs.nanolett.2c03288</doi></cross_references></HashMap>