Wen Chao, Robert Skog, Benjamin N Frandsen, Gregory H Jones, Kayla T Pham, Mitchio Okumura, Mads P Sulbaek Andersen, Carl J Percival, Frank A F Winiberg
{"title":"ClCO自由基在cl引发的CO氧化催化循环中的紫外可见光谱。","authors":"Wen Chao, Robert Skog, Benjamin N Frandsen, Gregory H Jones, Kayla T Pham, Mitchio Okumura, Mads P Sulbaek Andersen, Carl J Percival, Frank A F Winiberg","doi":"10.1038/s42004-025-01520-3","DOIUrl":null,"url":null,"abstract":"<p><p>In Venus's mesosphere, the observation/model discrepancy of molecular oxygen, O<sub>2</sub>, abundance has been a long-standing puzzle. Chlorine atoms have been proposed as a catalyst to oxidize carbon monoxide through the formation of chloroformyl radicals (ClCO), removing O<sub>2</sub> and ultimately generating CO<sub>2</sub>. However, relevant kinetic studies of this catalytic cycle are scarce and highly uncertain. In this work, we report the spectrum of the ClCO radical between 210-520 nm using a multipass UV-Vis spectrometer coupled to a pulsed-laser photolysis flow reactor at 236-294 K temperature and 50-491 Torr pressure ranges. High-level ab initio calculations were performed to simulate the observed spectrum and to investigate the electronic structure. In addition, we observed the formation of molecular chlorine, Cl<sub>2</sub>, and phosgene, Cl<sub>2</sub>CO, suggesting that both the terminal chlorine and the central carbon in the ClCO radical are reactive towards chlorine atoms. Most importantly, the reported spectrum will enable future measurements of essential kinetic parameters related to ClCO radicals, which are important in regulating the O<sub>2</sub> abundance in Venus's mesosphere.</p>","PeriodicalId":10529,"journal":{"name":"Communications Chemistry","volume":"8 1","pages":"163"},"PeriodicalIF":5.9000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12103620/pdf/","citationCount":"0","resultStr":"{\"title\":\"The UV-Vis spectrum of the ClCO radical in the catalytic cycle of Cl-initiated CO oxidation.\",\"authors\":\"Wen Chao, Robert Skog, Benjamin N Frandsen, Gregory H Jones, Kayla T Pham, Mitchio Okumura, Mads P Sulbaek Andersen, Carl J Percival, Frank A F Winiberg\",\"doi\":\"10.1038/s42004-025-01520-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In Venus's mesosphere, the observation/model discrepancy of molecular oxygen, O<sub>2</sub>, abundance has been a long-standing puzzle. Chlorine atoms have been proposed as a catalyst to oxidize carbon monoxide through the formation of chloroformyl radicals (ClCO), removing O<sub>2</sub> and ultimately generating CO<sub>2</sub>. However, relevant kinetic studies of this catalytic cycle are scarce and highly uncertain. In this work, we report the spectrum of the ClCO radical between 210-520 nm using a multipass UV-Vis spectrometer coupled to a pulsed-laser photolysis flow reactor at 236-294 K temperature and 50-491 Torr pressure ranges. High-level ab initio calculations were performed to simulate the observed spectrum and to investigate the electronic structure. In addition, we observed the formation of molecular chlorine, Cl<sub>2</sub>, and phosgene, Cl<sub>2</sub>CO, suggesting that both the terminal chlorine and the central carbon in the ClCO radical are reactive towards chlorine atoms. Most importantly, the reported spectrum will enable future measurements of essential kinetic parameters related to ClCO radicals, which are important in regulating the O<sub>2</sub> abundance in Venus's mesosphere.</p>\",\"PeriodicalId\":10529,\"journal\":{\"name\":\"Communications Chemistry\",\"volume\":\"8 1\",\"pages\":\"163\"},\"PeriodicalIF\":5.9000,\"publicationDate\":\"2025-05-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12103620/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Communications Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1038/s42004-025-01520-3\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1038/s42004-025-01520-3","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
The UV-Vis spectrum of the ClCO radical in the catalytic cycle of Cl-initiated CO oxidation.
In Venus's mesosphere, the observation/model discrepancy of molecular oxygen, O2, abundance has been a long-standing puzzle. Chlorine atoms have been proposed as a catalyst to oxidize carbon monoxide through the formation of chloroformyl radicals (ClCO), removing O2 and ultimately generating CO2. However, relevant kinetic studies of this catalytic cycle are scarce and highly uncertain. In this work, we report the spectrum of the ClCO radical between 210-520 nm using a multipass UV-Vis spectrometer coupled to a pulsed-laser photolysis flow reactor at 236-294 K temperature and 50-491 Torr pressure ranges. High-level ab initio calculations were performed to simulate the observed spectrum and to investigate the electronic structure. In addition, we observed the formation of molecular chlorine, Cl2, and phosgene, Cl2CO, suggesting that both the terminal chlorine and the central carbon in the ClCO radical are reactive towards chlorine atoms. Most importantly, the reported spectrum will enable future measurements of essential kinetic parameters related to ClCO radicals, which are important in regulating the O2 abundance in Venus's mesosphere.
期刊介绍:
Communications Chemistry is an open access journal from Nature Research publishing high-quality research, reviews and commentary in all areas of the chemical sciences. Research papers published by the journal represent significant advances bringing new chemical insight to a specialized area of research. We also aim to provide a community forum for issues of importance to all chemists, regardless of sub-discipline.