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dc.contributor.authorParambath, Mithun
dc.contributor.authorHanley, Quentin S.
dc.contributor.authorMartin-Martinez, Francisco J.
dc.contributor.authorGiesa, Tristan
dc.contributor.authorBuehler, Markus J.
dc.contributor.authorPerry, Carole C.
dc.date.accessioned2016-03-04T16:26:53Z
dc.date.available2016-03-04T16:26:53Z
dc.date.issued2015-12
dc.date.submitted2015-08
dc.identifier.issn1463-9076
dc.identifier.issn1463-9084
dc.identifier.urihttp://hdl.handle.net/1721.1/101600
dc.description.abstractPDMPO (2-(4-pyridyl)-5-((4-(2-dimethylaminoethylaminocarbamoyl)methoxy)phenyl)oxazole), has unique silica specific fluorescence and is used in biology to understand biosilicification. This ‘silicaphilic’ fluorescence is not well understood nor is the response to local environmental variables like solvent and pH. We investigated PDMPO in a range of environments: using UV-vis and fluorescence spectroscopy supported by computational data, (SPARC, molecular dynamics simulations, density functional theory calculations), dynamic light scattering and zeta potential measurements to understand the PDMPO–silica interaction. From absorption data, PDMPO exhibited a pK[subscript a] of 4.20 for PDMPOH[2+ over 2] to PDMPOH[superscript +]. Fluorescence emission measurements revealed large shifts in excited state pK[* over a] values with different behaviour when bound to silica (pK[* over a] of 10.4). PDMPO bound to silica particles is located in the Stern layer with the dye exhibiting pH dependent depolarising motion. In aqueous solution, PDMPO showed strong chromaticity with correlation between the maximum emission wavelength for PDMPOH[superscript +*] and dielectric constant (4.8–80). Additional chromatic effects were attributed to changes in solvent accessible surface area. Chromatic effects were also observed for silica bound dye which allow its use as a direct probe of bulk pH over a range far in excess of what is possible for the dye alone (3–5.2). The unique combination of chromaticity and excited state dynamics allows PDMPO to monitor pH from 3 to 13 while also reporting on surface environment opening a new frontier in the quantitative understanding of (bio)silicification.en_US
dc.description.sponsorshipUnited States. Air Force Office of Scientific Research (FA9550-11-1-0199)en_US
dc.description.sponsorshipUnited States. Office of Naval Research. Presidential Early Career Awards for Scientists and Engineers (N00014-10-1-0562)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c5cp05105cen_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/en_US
dc.sourceRoyal Society of Chemistryen_US
dc.titleThe nature of the silicaphilic fluorescence of PDMPOen_US
dc.typeArticleen_US
dc.identifier.citationParambath, Mithun, Quentin S. Hanley, Francisco J. Martin-Martinez, Tristan Giesa, Markus J. Buehler, and Carole C. Perry. “The Nature of the Silicaphilic Fluorescence of PDMPO.” Phys. Chem. Chem. Phys. 18, no. 8 (2016): 5938–5948. © 2015 Royal Society of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Civil and Environmental Engineeringen_US
dc.contributor.mitauthorMartin-Martinez, Francisco J.en_US
dc.contributor.mitauthorGiesa, Tristanen_US
dc.contributor.mitauthorBuehler, Markus J.en_US
dc.relation.journalPhysical Chemistry Chemical Physicsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsParambath, Mithun; Hanley, Quentin S.; Martin-Martinez, Francisco J.; Giesa, Tristan; Buehler, Markus J.; Perry, Carole C.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-4173-9659
dc.identifier.orcidhttps://orcid.org/0000-0001-7149-5512
dc.identifier.orcidhttps://orcid.org/0000-0002-6601-9199
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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