<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>49</viewCount><searchCount>0</searchCount></scores><additional><submitter>Tebikachew BE</submitter><funding>Carlsbergfondet</funding><funding>Natur og Univers, Det Frie Forskningsr???d</funding><funding>Stiftelsen f???r Strategisk Forskning</funding><funding>European Research Council</funding><funding>U.S. Department of Defense</funding><funding>National Science Foundation</funding><pagination>7094-7100</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5385524</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>121(13)</volume><pubmed_abstract>Integrating functional molecules into single-molecule devices is a key step toward the realization of future computing machines based on the smallest possible components. In this context, photoswitching molecules that can make a transition between high and low conductivity in response to light are attractive candidates. Here we present the synthesis and conductance properties of a new type of robust molecular photothermal switch based on the norbornadiene (NB)-quadricyclane (QC) system. The transport through the molecule in the ON state is dominated by a pathway through the π-conjugated system, which is no longer available when the system is switched to the OFF state. Interestingly, in the OFF state we find that the same pathway contributes only 12% to the transport properties. We attribute this observation to the strained tetrahedral geometry of the QC. These results challenge the prevailing assumption that current will simply flow through the shortest through-bond path in a molecule.</pubmed_abstract><journal>The journal of physical chemistry. C, Nanomaterials and interfaces</journal><pubmed_title>Effect of Ring Strain on the Charge Transport of a Robust Norbornadiene-Quadricyclane-Based Molecular Photoswitch.</pubmed_title><pmcid>PMC5385524</pmcid><funding_grant_id>337221</funding_grant_id><funding_grant_id>ERC StG SIMONE</funding_grant_id><pubmed_authors>Hihath J</pubmed_authors><pubmed_authors>Li HB</pubmed_authors><pubmed_authors>Solomon GC</pubmed_authors><pubmed_authors>Borjesson K</pubmed_authors><pubmed_authors>Moth-Poulsen K</pubmed_authors><pubmed_authors>Tebikachew BE</pubmed_authors><pubmed_authors>Pirrotta A</pubmed_authors><view_count>49</view_count></additional><is_claimable>false</is_claimable><name>Effect of Ring Strain on the Charge Transport of a Robust Norbornadiene-Quadricyclane-Based Molecular Photoswitch.</name><description>Integrating functional molecules into single-molecule devices is a key step toward the realization of future computing machines based on the smallest possible components. In this context, photoswitching molecules that can make a transition between high and low conductivity in response to light are attractive candidates. Here we present the synthesis and conductance properties of a new type of robust molecular photothermal switch based on the norbornadiene (NB)-quadricyclane (QC) system. The transport through the molecule in the ON state is dominated by a pathway through the π-conjugated system, which is no longer available when the system is switched to the OFF state. Interestingly, in the OFF state we find that the same pathway contributes only 12% to the transport properties. We attribute this observation to the strained tetrahedral geometry of the QC. These results challenge the prevailing assumption that current will simply flow through the shortest through-bond path in a molecule.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Apr</publication><modification>2024-11-21T10:02:05.708Z</modification><creation>2019-03-27T02:40:47Z</creation></dates><accession>S-EPMC5385524</accession><cross_references><pubmed>28408968</pubmed><doi>10.1021/acs.jpcc.7b00319</doi></cross_references></HashMap>