Please use this identifier to cite or link to this item: https://doi.org/10.1002/adfm.201700523
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dc.titleDistinct Bimodal Roles of Aromatic Molecules in Controlling Gold Nanorod Growth for Biosensing
dc.contributor.authorSoh, J.H
dc.contributor.authorLin, Y
dc.contributor.authorThomas, M.R
dc.contributor.authorTodorova, N
dc.contributor.authorKallepitis, C
dc.contributor.authorYarovsky, I
dc.contributor.authorYing, J.Y
dc.contributor.authorStevens, M.M
dc.date.accessioned2020-10-27T10:22:21Z
dc.date.available2020-10-27T10:22:21Z
dc.date.issued2017
dc.identifier.citationSoh, J.H, Lin, Y, Thomas, M.R, Todorova, N, Kallepitis, C, Yarovsky, I, Ying, J.Y, Stevens, M.M (2017). Distinct Bimodal Roles of Aromatic Molecules in Controlling Gold Nanorod Growth for Biosensing. Advanced Functional Materials 27 (29) : 1700523. ScholarBank@NUS Repository. https://doi.org/10.1002/adfm.201700523
dc.identifier.issn1616301X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181257
dc.description.abstractNew aromatic molecule–seed particle interactions are examined and exploited to control and guide seed-mediated gold nanorod (Au NR) growth. This new approach enables better understanding of how small molecules impact the synthesis of metallic nanostructures, catalyzing their use in various biomedical applications, such as plasmonic biosensing. Experimental studies and theoretical molecular simulations using a library of aromatic molecules, making use of the chemical versatility of the molecules with varied spatial arrangements of electron-donating/withdrawing groups, charge, and Au-binding propensity, are performed. Au NR growth is regulated by two principal mechanisms, producing either a red or blue shift in the longitudinal localized surface plasmon resonance (LLSPR) peaks. Aromatic molecules with high redox potentials produce an increase in NR aspect ratio and red shift of LLSPR peaks. In contrast, molecules that strongly bind gold surfaces result in blue shifts, demonstrating a strong correlation between their binding energy and blue shifts produced. Through enzymatic conversion of selected molecules, 4-aminophenylphosphate to 4-aminophenol, opposing growth mechanisms at opposite extremes of target concentration are obtained, and a chemical pathway for performing plasmonic enzyme-linked immunosorbent assays is established. This unlocks new strategies for tailoring substrate design and enzymatic mechanisms for controlling plasmonic response to target molecules in biosensing applications. © 2017 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectAlkalinity
dc.subjectAromatic compounds
dc.subjectAromatization
dc.subjectAspect ratio
dc.subjectBinding energy
dc.subjectBins
dc.subjectMedical applications
dc.subjectMolecules
dc.subjectNanorods
dc.subjectPhosphatases
dc.subjectPlasmons
dc.subjectRedox reactions
dc.subjectSurface plasmon resonance
dc.subjectSynthesis (chemical)
dc.subjectALkaline phosphatase
dc.subjectAnisotropic growth
dc.subjectAromatic additives
dc.subjectGold nanorod
dc.subjectPlasmonic sensing
dc.subjectGold
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/adfm.201700523
dc.description.sourcetitleAdvanced Functional Materials
dc.description.volume27
dc.description.issue29
dc.description.page1700523
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