Halogen bonded associates of iodonium salts with 18-crown-6: does structural flexibility or structural rigidity of the σ-hole donor provide efficient substrate ligation?-Reference-Cited by-同舟云学术

Halogen bonded associates of iodonium salts with 18-crown-6: does structural flexibility or structural rigidity of the σ-hole donor provide efficient substrate ligation?

Published:2024 Issue:29 Volume:48 Page:12929-12935
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Sysoeva Alexandra A.¹^ORCID,Novikov Alexander S.¹²^ORCID,Il’in Mikhail V.¹^ORCID,Bolotin Dmitrii S.¹^ORCID

Affiliation:

1. Institute of Chemistry, Saint Petersburg State University, Universitetskaya Nab. 7/9, Saint Petersburg, 199034, Russian Federation

2. Peoples’ Friendship University of Russia (RUDN University), Miklukho-Maklaya Str. 6, 117198 Moscow, Russian Federation

Abstract

An acyclic diphenyliodonium cation forms stronger interactions with a bulky Lewis base than a cyclic dibenziodolium cation.

Funder

Saint Petersburg State University

RUDN University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D4NJ02105C

Reference44 articles.

1. Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications

2. Diaryliodonium salts as efficient Lewis acid catalysts for direct three component Mannich reactions

3. A Bidentate Iodine(III)‐Based Halogen‐Bond Donor as a Powerful Organocatalyst**

4. Diaryliodoniums as Hybrid Hydrogen- and Halogen-Bond-Donating Organocatalysts for the Groebke–Blackburn–Bienaymé Reaction

5. Influence of Coordination to Silver(I) Centers on the Activity of Heterocyclic Iodonium Salts Serving as Halogen‐Bond‐Donating Catalysts

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