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dc.creatorKang, B
dc.creatorYang, W
dc.creatorLee, S
dc.creatorMukherjee, S
dc.creatorForstater, J
dc.creatorKim, H
dc.creatorGoh, B
dc.creatorKim, TY
dc.creatorVoelz, VA
dc.creatorPang, Y
dc.creatorSeo, J
dc.date.accessioned2021-01-28T22:16:12Z
dc.date.available2021-01-28T22:16:12Z
dc.date.issued2017-12-01
dc.identifier.issn2045-2322
dc.identifier.issn2045-2322
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/5108
dc.identifier.other28684782 (pubmed)
dc.identifier.urihttp://hdl.handle.net/20.500.12613/5126
dc.description.abstract© 2017 The Author(s). The energy flow during natural photosynthesis is controlled by maintaining the spatial arrangement of pigments, employing helices as scaffolds. In this study, we have developed porphyrin-peptoid (pigment-helix) conjugates (PPCs) that can modulate the donor-acceptor energy transfer efficiency with exceptional precision by controlling the relative distance and orientation of the two pigments. Five donor-acceptor molecular dyads were constructed using zinc porphyrin and free base porphyrin (Zn(i + 2)-Zn(i + 6)), and highly efficient energy transfer was demonstrated with estimated efficiencies ranging from 92% to 96% measured by static fluorescence emission in CH2Cl2 and from 96.3% to 97.6% using femtosecond transient absorption measurements in toluene, depending on the relative spatial arrangement of the donor-acceptor pairs. Our results suggest that the remarkable precision and tunability exhibited by nature can be achieved by mimicking the design principles of natural photosynthetic proteins.
dc.format.extent4786-
dc.language.isoen
dc.relation.haspartScientific Reports
dc.relation.isreferencedbySpringer Science and Business Media LLC
dc.rightsCC BY
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBiomimetics
dc.subjectEnergy Transfer
dc.subjectMetalloporphyrins
dc.subjectMethylene Chloride
dc.subjectMolecular Structure
dc.subjectPeptoids
dc.subjectPhotosynthesis
dc.subjectPorphyrins
dc.subjectToluene
dc.subjectUltraviolet Rays
dc.titlePrecisely tuneable energy transfer system using peptoid helix-based molecular scaffold
dc.typeArticle
dc.type.genreJournal Article
dc.relation.doi10.1038/s41598-017-04727-0
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.creator.orcidVoelz, Vincent|0000-0002-1054-2124
dc.date.updated2021-01-28T22:16:07Z
refterms.dateFOA2021-01-28T22:16:13Z


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