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Oxidative fluorination with Selectfluor: A convenient procedure for preparing hypervalent iodine(V) fluorides

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journal contribution
posted on 2024-09-05, 15:11 authored by Samuel MG Dearman, Xiang Li, Yang Li, Kuldip Singh, Alison M Stuart
The ability to investigate hypervalent iodine(V) fluorides has been limited primarily by their difficult preparation traditionally using harsh fluorinating reagents such as trifluoromethyl hypofluorite and bromine trifluoride. Here, we report a mild and efficient route using Selectfluor to deliver hypervalent iodine(V) fluorides in good isolated yields (72–90%). Stability studies revealed that bicyclic difluoro(aryl)-λ5-iodane 6 was much more stable in acetonitrile-d3 than in chloroform-d1, presumably due to acetonitrile coordinating to the iodine(V) centre and stabilising it via halogen bonding.

History

Author affiliation

College of Science & Engineering Chemistry

Version

  • VoR (Version of Record)

Published in

Beilstein Journal of Organic Chemistry

Volume

20

Pagination

1785 - 1793

Publisher

Beilstein Institut

issn

1860-5397

eissn

1860-5397

Copyright date

2024

Available date

2024-09-05

Spatial coverage

Germany

Language

en

Deposited by

Dr Alison Stuart

Deposit date

2024-08-15

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