Micrometer-Sized Water Droplets Induce Spontaneous ReductionHighly Cited Paper
DC Field | Value | Language |
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dc.contributor.author | Jae Kyoo Lee. | - |
dc.contributor.author | Devleena Samanta | - |
dc.contributor.author | Hong Gil Nam | - |
dc.contributor.author | Richard N. Zare | - |
dc.date.available | 2019-10-22T07:38:42Z | - |
dc.date.created | 2019-08-20 | - |
dc.date.issued | 2019-07 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/6372 | - |
dc.description.abstract | Bulk water serves as an inert solvent for many chemical and biological reactions. Here, we report a striking exception. We observe that in micrometer-sized water droplets (microdroplets), spontaneous reduction of several organic molecules occurs, pyruvate to lactate, lipoic acid to dihydrolipoic acid, fumarate to succinate, and oxaloacetate to malate. This reduction proceeds in microdroplets without any added electron donors or acceptors and without any applied voltage. In three of the four cases, the reduction efficiency is 90% or greater when the concentration of the dissolved organic species is less than 0.1 μM. None of these reactions occurs spontaneously in bulk water. One example demonstrating the possible broad application of reduction in water microdroplets to organic molecules is the reduction of acetophenone to form 1-phenylethanol. Taken together, these results show that microdroplets provide a new foundation for green chemistry by rendering water molecules to be highly electrochemically active without any added reducing agent or applied potential. In this manner, aqueous microdroplets might have provided a route for abiotic reduction reactions in the prebiotic era, thereby providing organic molecules with a reducing power before the advent of biotic reducing machineries. © 2019 American Chemical Society | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | Micrometer-Sized Water Droplets Induce Spontaneous Reduction | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000475533500003 | - |
dc.identifier.scopusid | 2-s2.0-85069330281 | - |
dc.identifier.rimsid | 69316 | - |
dc.contributor.affiliatedAuthor | Hong Gil Nam | - |
dc.identifier.doi | 10.1021/jacs.9b03227 | - |
dc.identifier.bibliographicCitation | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.141, no.27, pp.10585 - 10589 | - |
dc.citation.title | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | - |
dc.citation.volume | 141 | - |
dc.citation.number | 27 | - |
dc.citation.startPage | 10585 | - |
dc.citation.endPage | 10589 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |