Gulshat A. Masyagutova, Alexander V. Mamykin, Sergey L. Khursan
{"title":"乙腈溶液中 Eu(FOD)3 与二氟化氙相互作用过程中 Eu(III) 的配体辅助激发","authors":"Gulshat A. Masyagutova, Alexander V. Mamykin, Sergey L. Khursan","doi":"10.1016/j.jfluchem.2024.110270","DOIUrl":null,"url":null,"abstract":"<div><p>The interaction of <em>tris</em>(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)europium(III), (Eu(FOD)<sub>3</sub>), with xenon difluoride in acetonitrile solution was found to be accompanied by chemiluminescence (CL). The kinetic curve of CL at a ratio of reagents Eu<sup>3+</sup>/XeF<sub>2</sub> of 1:2 has a complex form; an initial rapid decrease is replaced by an increase in CL intensity, the maximum of which is reached approximately 10 min after the start of the reaction. Next, an exponential decay of the CL intensity is observed over several tens of minutes. The CL spectrum is located in the wavelength range 400–750 nm and corresponds to the emission of an electronically excited europium (III) ion coordinated with FOD and fluoride ion. Spectral methods were used to identify the reaction products – europium (III) fluoride in the sediment and oxygen difluoride in the gas phase. A mechanism for chemiexcitation of europium(III) has been proposed, including: 1) acceptance of fluorine anion from the XeF<sub>2</sub> molecule by europium ion with the formation of active intermediate XeF<sup>+</sup>; 2) oxidative fluorination of the ligand, which is initiated by the interaction of oxygen atom of the FOD ligand with XeF<sup>+</sup> cation and ends with the formation of oxygen difluoride and the electronically excited product P*, presumably a fluorinated ketone; 3) non-radiative transfer of excitation energy from P* to the europium ion within its coordination sphere, followed by its radiative deactivation.</p></div>","PeriodicalId":357,"journal":{"name":"Journal of Fluorine Chemistry","volume":"275 ","pages":"Article 110270"},"PeriodicalIF":1.7000,"publicationDate":"2024-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ligand-assisted excitation of Eu(III) during interaction of Eu(FOD)3 with xenon difluoride in acetonitrile solution\",\"authors\":\"Gulshat A. Masyagutova, Alexander V. Mamykin, Sergey L. Khursan\",\"doi\":\"10.1016/j.jfluchem.2024.110270\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The interaction of <em>tris</em>(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)europium(III), (Eu(FOD)<sub>3</sub>), with xenon difluoride in acetonitrile solution was found to be accompanied by chemiluminescence (CL). The kinetic curve of CL at a ratio of reagents Eu<sup>3+</sup>/XeF<sub>2</sub> of 1:2 has a complex form; an initial rapid decrease is replaced by an increase in CL intensity, the maximum of which is reached approximately 10 min after the start of the reaction. Next, an exponential decay of the CL intensity is observed over several tens of minutes. The CL spectrum is located in the wavelength range 400–750 nm and corresponds to the emission of an electronically excited europium (III) ion coordinated with FOD and fluoride ion. Spectral methods were used to identify the reaction products – europium (III) fluoride in the sediment and oxygen difluoride in the gas phase. A mechanism for chemiexcitation of europium(III) has been proposed, including: 1) acceptance of fluorine anion from the XeF<sub>2</sub> molecule by europium ion with the formation of active intermediate XeF<sup>+</sup>; 2) oxidative fluorination of the ligand, which is initiated by the interaction of oxygen atom of the FOD ligand with XeF<sup>+</sup> cation and ends with the formation of oxygen difluoride and the electronically excited product P*, presumably a fluorinated ketone; 3) non-radiative transfer of excitation energy from P* to the europium ion within its coordination sphere, followed by its radiative deactivation.</p></div>\",\"PeriodicalId\":357,\"journal\":{\"name\":\"Journal of Fluorine Chemistry\",\"volume\":\"275 \",\"pages\":\"Article 110270\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-03-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Fluorine Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022113924000319\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fluorine Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022113924000319","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Ligand-assisted excitation of Eu(III) during interaction of Eu(FOD)3 with xenon difluoride in acetonitrile solution
The interaction of tris(1,1,1,2,2,3,3-heptafluoro-7,7-dimethyl-4,6-octanedionato)europium(III), (Eu(FOD)3), with xenon difluoride in acetonitrile solution was found to be accompanied by chemiluminescence (CL). The kinetic curve of CL at a ratio of reagents Eu3+/XeF2 of 1:2 has a complex form; an initial rapid decrease is replaced by an increase in CL intensity, the maximum of which is reached approximately 10 min after the start of the reaction. Next, an exponential decay of the CL intensity is observed over several tens of minutes. The CL spectrum is located in the wavelength range 400–750 nm and corresponds to the emission of an electronically excited europium (III) ion coordinated with FOD and fluoride ion. Spectral methods were used to identify the reaction products – europium (III) fluoride in the sediment and oxygen difluoride in the gas phase. A mechanism for chemiexcitation of europium(III) has been proposed, including: 1) acceptance of fluorine anion from the XeF2 molecule by europium ion with the formation of active intermediate XeF+; 2) oxidative fluorination of the ligand, which is initiated by the interaction of oxygen atom of the FOD ligand with XeF+ cation and ends with the formation of oxygen difluoride and the electronically excited product P*, presumably a fluorinated ketone; 3) non-radiative transfer of excitation energy from P* to the europium ion within its coordination sphere, followed by its radiative deactivation.
期刊介绍:
The Journal of Fluorine Chemistry contains reviews, original papers and short communications. The journal covers all aspects of pure and applied research on the chemistry as well as on the applications of fluorine, and of compounds or materials where fluorine exercises significant effects. This can include all chemistry research areas (inorganic, organic, organometallic, macromolecular and physical chemistry) but also includes papers on biological/biochemical related aspects of Fluorine chemistry as well as medicinal, agrochemical and pharmacological research. The Journal of Fluorine Chemistry also publishes environmental and industrial papers dealing with aspects of Fluorine chemistry on energy and material sciences. Preparative and physico-chemical investigations as well as theoretical, structural and mechanistic aspects are covered. The Journal, however, does not accept work of purely routine nature.
For reviews and special issues on particular topics of fluorine chemistry or from selected symposia, please contact the Regional Editors for further details.