<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rapp TL</submitter><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><pagination>4942-4947</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6785243</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(9)</volume><pubmed_abstract>Photoresponsive materials afford spatiotemporal control over desirable physical, chemical and biological properties. For advanced applications, there is need for molecular phototriggers that are readily incorporated within larger structures, and spatially-sequentially addressable with different wavelengths of visble light, enabling multiplexing. Here we describe spectrally tunable (λ&lt;sub>max&lt;/sub> = 420-530 nm) ruthenium polypyridyl complexes functionalized with two photolabile nitrile ligands that present terminal alkynes for subsequent crosslinking reactions, including hydrogel formation. Two Ru crosslinkers were incorporated within a PEG-hydrogel matrix, and sequentially degraded by irradiation with 592 nm and 410 nm light.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Designing Photolabile Ruthenium Polypyridyl Crosslinkers for Hydrogel Formation and Multiplexed, Visible-light Degradation.</pubmed_title><pmcid>PMC6785243</pmcid><funding_grant_id>DMR-1720530</funding_grant_id><funding_grant_id>R01 GM-083030</funding_grant_id><funding_grant_id>R01 GM083030</funding_grant_id><funding_grant_id>R35 GM131907</funding_grant_id><pubmed_authors>Dmochowski IJ</pubmed_authors><pubmed_authors>Delessio MA</pubmed_authors><pubmed_authors>Rapp TL</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Gau MR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Designing Photolabile Ruthenium Polypyridyl Crosslinkers for Hydrogel Formation and Multiplexed, Visible-light Degradation.</name><description>Photoresponsive materials afford spatiotemporal control over desirable physical, chemical and biological properties. For advanced applications, there is need for molecular phototriggers that are readily incorporated within larger structures, and spatially-sequentially addressable with different wavelengths of visble light, enabling multiplexing. Here we describe spectrally tunable (λ&lt;sub>max&lt;/sub> = 420-530 nm) ruthenium polypyridyl complexes functionalized with two photolabile nitrile ligands that present terminal alkynes for subsequent crosslinking reactions, including hydrogel formation. Two Ru crosslinkers were incorporated within a PEG-hydrogel matrix, and sequentially degraded by irradiation with 592 nm and 410 nm light.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2024-12-03T17:39:16.681Z</modification><creation>2020-10-29T10:38:33Z</creation></dates><accession>S-EPMC6785243</accession><cross_references><pubmed>31598214</pubmed><doi>10.1039/C8RA09764J</doi></cross_references></HashMap>