Literature DB >> 34145711

Iodine(III)-Based Halogen Bond Donors: Properties and Applications.

Raphaël Robidas1, Dominik L Reinhard2, Claude Y Legault1, Stefan M Huber2.   

Abstract

Halogen bonding, the non-covalent interaction of Lewis bases with an electron-deficient region of halogen substituents, received increased attention recently. Consequently, the design and evaluation of numerous halogen-containing species as halogen bond donors have been subject to intense research. More recently, organoiodine compounds at the iodine(III) state have been receiving growing attention in the field. Due to their electronic and structural properties, they provide access to unique binding modes. For this reason, our groups have been involved in the development of such compounds, in the quantification of their halogen bonding strength (through the evaluation of their Lewis acidities), as well as in the evaluation of their activities as catalysts in several model reactions. This account will describe these contributions.
© 2021 The Authors. Published by The Chemical Society of Japan & Wiley-VCH GmbH.

Entities:  

Keywords:  Diaryliodonium; Halogen bonding; Hypervalent iodine; Iodolium; Lewis acidity

Year:  2021        PMID: 34145711     DOI: 10.1002/tcr.202100119

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  2 in total

1.  Orbital analysis of bonding in diarylhalonium salts and relevance to periodic trends in structure and reactivity.

Authors:  Shubhendu S Karandikar; Avik Bhattacharjee; Bryan E Metze; Nicole Javaly; Edward J Valente; Theresa M McCormick; David R Stuart
Journal:  Chem Sci       Date:  2022-05-19       Impact factor: 9.969

2.  Pushing the Limits of Characterising a Weak Halogen Bond in Solution.

Authors:  Stefan Peintner; Máté Erdélyi
Journal:  Chemistry       Date:  2021-12-13       Impact factor: 5.020

  2 in total

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