Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface

Miniaturized liquid–liquid interfacial reactors offer enhanced surface area and rapid confinement of compounds of opposite solubility, yet they are unable to provide in situ reaction monitoring at a molecular level at the interface. A picoreactor operative at the liquid–liquid interface is described...

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Main Authors: Phan-Quang, Gia Chuong, Lee, Hiang Kwee, Ling, Xing Yi
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2017
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Online Access:https://hdl.handle.net/10356/83780
http://hdl.handle.net/10220/42792
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-837802023-02-28T19:37:20Z Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface Phan-Quang, Gia Chuong Lee, Hiang Kwee Ling, Xing Yi School of Physical and Mathematical Sciences Colloidosomes High Throughput Miniaturized liquid–liquid interfacial reactors offer enhanced surface area and rapid confinement of compounds of opposite solubility, yet they are unable to provide in situ reaction monitoring at a molecular level at the interface. A picoreactor operative at the liquid–liquid interface is described, comprising plasmonic colloidosomes containing Ag octahedra strategically assembled at the water-in-decane emulsion interface. The plasmonic colloidosomes isolate ultrasmall amounts of solutions (<200 pL), allowing parallel monitoring of multiple reactions simultaneously. Using the surface-enhanced Raman spectroscopy (SERS) technique, in situ monitoring of the interfacial protonation of dimethyl yellow (p-dimethylaminoazobenzene (DY)) is performed, revealing an apparent rate constant of 0.09 min−1 for the first-order reaction. The presence of isomeric products with similar physical properties is resolved, which would otherwise be indiscernible by other analytical methods. ASTAR (Agency for Sci., Tech. and Research, S’pore) Accepted version 2017-07-04T05:21:29Z 2019-12-06T15:31:55Z 2017-07-04T05:21:29Z 2019-12-06T15:31:55Z 2016 Journal Article Phan-Quang, G. C., Lee, H. K., & Ling, X. Y. (2016). Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface. Angewandte Chemie International Edition, 55(29), 8304-8308. 1433-7851 https://hdl.handle.net/10356/83780 http://hdl.handle.net/10220/42792 10.1002/anie.201602565 en Angewandte Chemie International Edition © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the author created version of a work that has been peer reviewed and accepted for publication by Angewandte Chemie International Edition, WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1002/anie.201602565]. 37 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Colloidosomes
High Throughput
spellingShingle Colloidosomes
High Throughput
Phan-Quang, Gia Chuong
Lee, Hiang Kwee
Ling, Xing Yi
Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface
description Miniaturized liquid–liquid interfacial reactors offer enhanced surface area and rapid confinement of compounds of opposite solubility, yet they are unable to provide in situ reaction monitoring at a molecular level at the interface. A picoreactor operative at the liquid–liquid interface is described, comprising plasmonic colloidosomes containing Ag octahedra strategically assembled at the water-in-decane emulsion interface. The plasmonic colloidosomes isolate ultrasmall amounts of solutions (<200 pL), allowing parallel monitoring of multiple reactions simultaneously. Using the surface-enhanced Raman spectroscopy (SERS) technique, in situ monitoring of the interfacial protonation of dimethyl yellow (p-dimethylaminoazobenzene (DY)) is performed, revealing an apparent rate constant of 0.09 min−1 for the first-order reaction. The presence of isomeric products with similar physical properties is resolved, which would otherwise be indiscernible by other analytical methods.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Phan-Quang, Gia Chuong
Lee, Hiang Kwee
Ling, Xing Yi
format Article
author Phan-Quang, Gia Chuong
Lee, Hiang Kwee
Ling, Xing Yi
author_sort Phan-Quang, Gia Chuong
title Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface
title_short Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface
title_full Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface
title_fullStr Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface
title_full_unstemmed Isolating Reactions at the Picoliter Scale: Parallel Control of Reaction Kinetics at the Liquid-Liquid Interface
title_sort isolating reactions at the picoliter scale: parallel control of reaction kinetics at the liquid-liquid interface
publishDate 2017
url https://hdl.handle.net/10356/83780
http://hdl.handle.net/10220/42792
_version_ 1759856643136290816