Synthesis of a Homologous Series of Trialkyl Arsines (C3-C12) and Applications of Arsenic Triiodide as a Synthetic Precursor
This work presents some modifications in the post-synthetic processing for a classical arsenic reagent: AsI3. In comparison with the widely used analog, the trichloride, arsenic triiodide presents several advantages such as low toxicity, air stability, and low volatility. It was used as a synthetic...
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Published in | Journal of the Brazilian Chemical Society Vol. 32; no. 4; pp. 912 - 916 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Sociedade Brasileira de Química
01.04.2021
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Abstract | This work presents some modifications in the post-synthetic processing for a classical arsenic reagent: AsI3. In comparison with the widely used analog, the trichloride, arsenic triiodide presents several advantages such as low toxicity, air stability, and low volatility. It was used as a synthetic precursor in the preparation of a variety of arsenic(III) derivatives like arsines, arsenites, and thioarsenites. Besides that, AsI3 was submitted to a diversity-oriented Grignard reaction in the preparation of a homologous series of trialkyl arsines ranging from AsC3H9 to AsC12H27. The series was analyzed by comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry to provide a trialkyl arsines library that can be used for the direct analysis of natural samples. |
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AbstractList | This work presents some modifications in the post-synthetic processing for a classical arsenic reagent: AsI3. In comparison with the widely used analog, the trichloride, arsenic triiodide presents several advantages such as low toxicity, air stability, and low volatility. It was used as a synthetic precursor in the preparation of a variety of arsenic(III) derivatives like arsines, arsenites, and thioarsenites. Besides that, AsI3 was submitted to a diversity-oriented Grignard reaction in the preparation of a homologous series of trialkyl arsines ranging from AsC3H9 to AsC12H27. The series was analyzed by comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry to provide a trialkyl arsines library that can be used for the direct analysis of natural samples. |
Author | Esteves, Pierre Ligiéro, Carolina Gama, Michelle Carbonezi, Carlos Francisco, Marcos Leocadio, Isabela de Souza, Wladmir |
AuthorAffiliation | Universidade Federal do Rio de Janeiro PETROBRAS |
AuthorAffiliation_xml | – name: Universidade Federal do Rio de Janeiro – name: PETROBRAS |
Author_xml | – sequence: 1 givenname: Carolina orcidid: 0000-0002-1944-9030 surname: Ligiéro fullname: Ligiéro, Carolina – sequence: 2 givenname: Marcos surname: Francisco fullname: Francisco, Marcos – sequence: 3 givenname: Michelle surname: Gama fullname: Gama, Michelle – sequence: 4 givenname: Carlos surname: Carbonezi fullname: Carbonezi, Carlos – sequence: 5 givenname: Isabela surname: Leocadio fullname: Leocadio, Isabela – sequence: 6 givenname: Wladmir surname: de Souza fullname: de Souza, Wladmir – sequence: 7 givenname: Pierre orcidid: 0000-0001-6048-4690 surname: Esteves fullname: Esteves, Pierre |
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Keywords | two-dimensional chromatography trialkyl arsines diversity-oriented Grignard arsenic triiodide |
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Title | Synthesis of a Homologous Series of Trialkyl Arsines (C3-C12) and Applications of Arsenic Triiodide as a Synthetic Precursor |
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