<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>40</viewCount><searchCount>0</searchCount></scores><additional><submitter>Zhang K</submitter><funding>Dutch Research Council (NWO)</funding><funding>MESA+ Institute for Nanotechnology, University of Twente</funding><pagination>10029-10035</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5538755</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>139(29)</volume><pubmed_abstract>We report on the synthesis and structure-property relations of a novel, dual-responsive organometallic poly(ionic liquid) (PIL), consisting of a poly(ferrocenylsilane) backbone of alternating redox-active, silane-bridged ferrocene units and tetraalkylphosphonium sulfonate moieties in the side groups. This PIL is redox responsive due to the presence of ferrocene in the backbone and also exhibits a lower critical solution temperature (LCST)-type thermal responsive behavior. The LCST phase transition originates from the interaction between water molecules and the ionic substituents and shows a concentration-dependent, tunable transition temperature in aqueous solution. The PIL's LCST-type transition temperature can also be influenced by varying the redox state of ferrocene in the polymer main chain. As the polymer can be readily cross-linked and is easily converted into hydrogels, it represents a new dual-responsive materials platform. Interestingly, the as-formed hydrogels display an unusual, strongly hysteretic volume-phase transition indicating useful thermal memory properties. By employing the dispersing abilities of this cationic PIL, CNT-hydrogel composites were successfully prepared. These hybrid conductive composite hydrogels showed bi-stable states and tunable resistance in heating-cooling cycles.</pubmed_abstract><journal>Journal of the American Chemical Society</journal><pubmed_title>Hydrogels with a Memory: Dual-Responsive, Organometallic Poly(ionic liquid)s with Hysteretic Volume-Phase Transition.</pubmed_title><pmcid>PMC5538755</pmcid><funding_grant_id>728.011.205</funding_grant_id><funding_grant_id>700.56.322</funding_grant_id><pubmed_authors>Vancso GJ</pubmed_authors><pubmed_authors>Zhang K</pubmed_authors><pubmed_authors>Feng X</pubmed_authors><pubmed_authors>Ye C</pubmed_authors><pubmed_authors>Hempenius MA</pubmed_authors><view_count>40</view_count></additional><is_claimable>false</is_claimable><name>Hydrogels with a Memory: Dual-Responsive, Organometallic Poly(ionic liquid)s with Hysteretic Volume-Phase Transition.</name><description>We report on the synthesis and structure-property relations of a novel, dual-responsive organometallic poly(ionic liquid) (PIL), consisting of a poly(ferrocenylsilane) backbone of alternating redox-active, silane-bridged ferrocene units and tetraalkylphosphonium sulfonate moieties in the side groups. This PIL is redox responsive due to the presence of ferrocene in the backbone and also exhibits a lower critical solution temperature (LCST)-type thermal responsive behavior. The LCST phase transition originates from the interaction between water molecules and the ionic substituents and shows a concentration-dependent, tunable transition temperature in aqueous solution. The PIL's LCST-type transition temperature can also be influenced by varying the redox state of ferrocene in the polymer main chain. As the polymer can be readily cross-linked and is easily converted into hydrogels, it represents a new dual-responsive materials platform. Interestingly, the as-formed hydrogels display an unusual, strongly hysteretic volume-phase transition indicating useful thermal memory properties. By employing the dispersing abilities of this cationic PIL, CNT-hydrogel composites were successfully prepared. These hybrid conductive composite hydrogels showed bi-stable states and tunable resistance in heating-cooling cycles.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jul</publication><modification>2024-11-05T18:57:59.156Z</modification><creation>2019-03-27T02:52:19Z</creation></dates><accession>S-EPMC5538755</accession><cross_references><pubmed>28654756</pubmed><doi>10.1021/jacs.7b04920</doi></cross_references></HashMap>