Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Serigne Sarr"'
Autor:
Yan Xie, Amaël Borzée, Kit-Yue Kwan, John MacKinnon, Haichao Zhou, Eric Ameca, Cristian Bonacic, Bo Cai, Topiltzin Contreras-MacBeath, Keith Crandall, Alok Das, Abraham Desalegn, Maximin Djondo, Weidong Li, Gregory Mueller, Serigne Sarr, Meta Sindani, Manfredo Turcios-Casco, Xinquan Zhao
Publikováno v:
Oryx, Vol 58, Pp 154-154 (2024)
Externí odkaz:
https://doaj.org/article/e1c5080bb0594dcc87ab97aec502870e
Publikováno v:
Molecules, Vol 26, Iss 15, p 4568 (2021)
The nature of halogen-bond interactions was scrutinized from the perspective of astatine, potentially the strongest halogen-bond donor atom. In addition to its remarkable electronic properties (e.g., its higher aromaticity compared to benzene), C6At6
Externí odkaz:
https://doaj.org/article/a212f04b259e4031b498fcdfdc3f9cc5
Publikováno v:
Phys.Chem.Chem.Phys.
Phys.Chem.Chem.Phys., 2021, 23 (7), pp.4064-4074. ⟨10.1039/d0cp05840h⟩
Phys.Chem.Chem.Phys., 2021, 23 (7), pp.4064-4074. ⟨10.1039/d0cp05840h⟩
International audience; The ability of organic and inorganic compounds bearing both iodine and astatine atoms to form halogen-bond interactions is theoretically investigated. Upon inclusion of the relativistic spin–orbit interaction, the I-mediated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8b49f3eb1bb8536a12e0964a6549618
https://doi.org/10.1039/d0cp05840h
https://doi.org/10.1039/d0cp05840h
Publikováno v:
Molecules
Molecules, 2021, 26 (15), pp.4568. ⟨10.3390/molecules26154568⟩
Molecules, Vol 26, Iss 4568, p 4568 (2021)
Volume 26
Issue 15
Molecules, MDPI, 2021, 26 (15), pp.4568. ⟨10.3390/molecules26154568⟩
Molecules, 2021, 26 (15), pp.4568. ⟨10.3390/molecules26154568⟩
Molecules, Vol 26, Iss 4568, p 4568 (2021)
Volume 26
Issue 15
Molecules, MDPI, 2021, 26 (15), pp.4568. ⟨10.3390/molecules26154568⟩
The nature of halogen-bond interactions was scrutinized from the perspective of astatine, potentially the strongest halogen-bond donor atom. In addition to its remarkable electronic properties (e.g., its higher aromaticity compared to benzene), C6At6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::900b47112d81a5c2b9a41b984e04b65a
https://pubmed.ncbi.nlm.nih.gov/34361716
https://pubmed.ncbi.nlm.nih.gov/34361716