<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Journal Article</dc:product_type><dc:title>Divalent Metal Cation Optical Sensing Using Single-Walled Carbon Nanotube Corona Phase Molecular Recognition</dc:title><dc:creator>Gong, Xun; Cho, Soo-Yeon; Kuo, Sydney; Ogunlade, Babatunde; Tso, Kathryn; Salem, Daniel P; Strano, Michael S</dc:creator><dc:corporate_author/><dc:editor/><dc:description>Colloidal single-walled carbon nanotubes (SWCNTs) oer a promising platform for the nanoscale engineering of
molecular recognition. Optical sensors have been recently designed through the modification of noncovalent corona phases (CPs) of
SWCNTs through a phenomenon known as corona phase molecular recognition (CoPhMoRe). In CoPhMoRe constructs, DNA
CPs are of great interest due to the breadth of the design space and our ability to control these molecules with sequence specificity at
scale. Utilizing these constructs for metal ion sensing is a natural extension of this technology due to DNA’s well-known
coordination chemistry. Additionally, understanding metal ion interactions of these constructs allows for improved sensor design for
use in complex aqueous environments. In this work, we study the interactions between a panel of 9 dilute divalent metal cations and
35 DNA CPs under the most controlled experimental conditions for SWCNT optical sensing to date. We found that best practices
for the study of colloidal SWCNT analyte responses involve mitigating the eects of ionic strength, dilution kinetics, laser power, and
analyte response kinetics. We also discover that SWCNT with DNA CPs generally oers two unique sensing states at pH 6 and 8.
The combined set of sensors in this work allowed for the dierentiation of Hg2+, Pb2+, Cr2+, and Mn2+. Finally, we implemented
Hg2+ sensing in the context of portable detection within fish tissue extract, demonstrating nanomolar level detection.</dc:description><dc:publisher>Anal. Chem.</dc:publisher><dc:date>2022-11-29</dc:date><dc:nsf_par_id>10631070</dc:nsf_par_id><dc:journal_name>Analytical Chemistry</dc:journal_name><dc:journal_volume>94</dc:journal_volume><dc:journal_issue>47</dc:journal_issue><dc:page_range_or_elocation>16393 to 16401</dc:page_range_or_elocation><dc:issn>0003-2700</dc:issn><dc:isbn/><dc:doi>https://doi.org/10.1021/acs.analchem.2c03648</dc:doi><dcq:identifierAwardId>2124194</dcq:identifierAwardId><dc:subject/><dc:version_number/><dc:location/><dc:rights/><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>