Mei Wen, Robert Medel, Pavel V. Zasimov and Sebastian Riedel*,
{"title":"具有As = B双键特征的arsinborene F2B-As = BF的基质分离","authors":"Mei Wen, Robert Medel, Pavel V. Zasimov and Sebastian Riedel*, ","doi":"10.1021/acs.inorgchem.4c0541810.1021/acs.inorgchem.4c05418","DOIUrl":null,"url":null,"abstract":"<p >We report on the generation of F<sub>2</sub>B–As═BF, an arsinoborene (boranylidenearsane) with a genuine As═B double bond, where both the As and B atoms are two-coordinate. It was obtained from the reaction of AsF<sub>3</sub> with laser-ablated boron atoms under cryogenic conditions in neon and argon matrices. In addition, the single-bonded arsenic–boron radicals FB–AsF<sub>2</sub> and F<sub>2</sub>B–AsF were characterized. These species were identified by infrared spectroscopy and <sup>10/11</sup>B isotope substitution in conjunction with quantum-chemical calculations at the B3LYP and CCSD(T) levels of theory. The isomerization from FB–AsF<sub>2</sub> to F<sub>2</sub>B–AsF can be triggered by irradiation with ultraviolet light (λ = 275 nm) in argon. This discovery of the arsinoborene F<sub>2</sub>B–As═BF further extends the series of multiple-bonded systems between heavy main group elements and boron.</p><p >The arsinoborene F<sub>2</sub>B−As═BF features two-coordinate arsenic and boron atoms and a genuine As═B double bond. Additionally, the photolysis behavior of new boron−arsenic compounds upon irradiation with ultraviolet (UV) light of λ = 275 nm enabled the spectroscopic identification of FB−AsF<sub>2</sub> and F<sub>2</sub>B−AsF.</p>","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":"64 10","pages":"5105–5112 5105–5112"},"PeriodicalIF":4.7000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.inorgchem.4c05418","citationCount":"0","resultStr":"{\"title\":\"Matrix Isolation of the Arsinoborene F2B–As═BF with an As═B Double Bond Character\",\"authors\":\"Mei Wen, Robert Medel, Pavel V. Zasimov and Sebastian Riedel*, \",\"doi\":\"10.1021/acs.inorgchem.4c0541810.1021/acs.inorgchem.4c05418\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We report on the generation of F<sub>2</sub>B–As═BF, an arsinoborene (boranylidenearsane) with a genuine As═B double bond, where both the As and B atoms are two-coordinate. It was obtained from the reaction of AsF<sub>3</sub> with laser-ablated boron atoms under cryogenic conditions in neon and argon matrices. In addition, the single-bonded arsenic–boron radicals FB–AsF<sub>2</sub> and F<sub>2</sub>B–AsF were characterized. These species were identified by infrared spectroscopy and <sup>10/11</sup>B isotope substitution in conjunction with quantum-chemical calculations at the B3LYP and CCSD(T) levels of theory. The isomerization from FB–AsF<sub>2</sub> to F<sub>2</sub>B–AsF can be triggered by irradiation with ultraviolet light (λ = 275 nm) in argon. This discovery of the arsinoborene F<sub>2</sub>B–As═BF further extends the series of multiple-bonded systems between heavy main group elements and boron.</p><p >The arsinoborene F<sub>2</sub>B−As═BF features two-coordinate arsenic and boron atoms and a genuine As═B double bond. Additionally, the photolysis behavior of new boron−arsenic compounds upon irradiation with ultraviolet (UV) light of λ = 275 nm enabled the spectroscopic identification of FB−AsF<sub>2</sub> and F<sub>2</sub>B−AsF.</p>\",\"PeriodicalId\":40,\"journal\":{\"name\":\"Inorganic Chemistry\",\"volume\":\"64 10\",\"pages\":\"5105–5112 5105–5112\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-03-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acs.inorgchem.4c05418\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.inorgchem.4c05418\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.inorgchem.4c05418","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Matrix Isolation of the Arsinoborene F2B–As═BF with an As═B Double Bond Character
We report on the generation of F2B–As═BF, an arsinoborene (boranylidenearsane) with a genuine As═B double bond, where both the As and B atoms are two-coordinate. It was obtained from the reaction of AsF3 with laser-ablated boron atoms under cryogenic conditions in neon and argon matrices. In addition, the single-bonded arsenic–boron radicals FB–AsF2 and F2B–AsF were characterized. These species were identified by infrared spectroscopy and 10/11B isotope substitution in conjunction with quantum-chemical calculations at the B3LYP and CCSD(T) levels of theory. The isomerization from FB–AsF2 to F2B–AsF can be triggered by irradiation with ultraviolet light (λ = 275 nm) in argon. This discovery of the arsinoborene F2B–As═BF further extends the series of multiple-bonded systems between heavy main group elements and boron.
The arsinoborene F2B−As═BF features two-coordinate arsenic and boron atoms and a genuine As═B double bond. Additionally, the photolysis behavior of new boron−arsenic compounds upon irradiation with ultraviolet (UV) light of λ = 275 nm enabled the spectroscopic identification of FB−AsF2 and F2B−AsF.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.