Cargando…
Iodine(I) and Silver(I) Complexes Incorporating 3-Substituted Pyridines
[Image: see text] Building upon the first report of a 3-acetaminopyridine-based iodine(I) complex (1b) and its unexpected reactivity toward (t)BuOMe, several new 3-substituted iodine(I) complexes (2b–5b) have been synthesized. The iodine(I) complexes were synthesized from their analogous silver(I) c...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324066/ https://www.ncbi.nlm.nih.gov/pubmed/37426204 http://dx.doi.org/10.1021/acsomega.3c03097 |
_version_ | 1785069068853706752 |
---|---|
author | Rissanen, Kari Ward, Jas S. |
author_facet | Rissanen, Kari Ward, Jas S. |
author_sort | Rissanen, Kari |
collection | PubMed |
description | [Image: see text] Building upon the first report of a 3-acetaminopyridine-based iodine(I) complex (1b) and its unexpected reactivity toward (t)BuOMe, several new 3-substituted iodine(I) complexes (2b–5b) have been synthesized. The iodine(I) complexes were synthesized from their analogous silver(I) complexes (2a–5a) via a silver(I) to iodine(I) cation exchange reaction, incorporating functionally related substituents as 3-acetaminopyridine in 1b; 3-acetylpyridine (3-Acpy; 2), 3-aminopyridine (3-NH(2)py; 3), and 3-dimethylaminopyridine (3-NMe(2)py; 4), as well as the strongly electron-withdrawing 3-cyanopyridine (3-CNpy; 5), to probe the possible limitations of iodine(I) complex formation. The individual properties of these rare examples of iodine(I) complexes incorporating 3-substituted pyridines are also compared to each other and contrasted to their 4-substituted counterparts which are more prevalent in the literature. While the reactivity of 1b toward etheric solvents could not be reproduced in any of the functionally related analogues synthesized herein, the reactivity of 1b was further expanded to a second etheric solvent. Reaction of bis(3-acetaminopyridine)iodine(I) (1b) and (i)Pr(2)O gave [3-acetamido-1-(3-iodo-2-methylpentan-2-yl)pyridin-1-ium]PF(6) (1d), which demonstrated potentially useful C–C and C–I bond formation under ambient conditions. |
format | Online Article Text |
id | pubmed-10324066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-103240662023-07-07 Iodine(I) and Silver(I) Complexes Incorporating 3-Substituted Pyridines Rissanen, Kari Ward, Jas S. ACS Omega [Image: see text] Building upon the first report of a 3-acetaminopyridine-based iodine(I) complex (1b) and its unexpected reactivity toward (t)BuOMe, several new 3-substituted iodine(I) complexes (2b–5b) have been synthesized. The iodine(I) complexes were synthesized from their analogous silver(I) complexes (2a–5a) via a silver(I) to iodine(I) cation exchange reaction, incorporating functionally related substituents as 3-acetaminopyridine in 1b; 3-acetylpyridine (3-Acpy; 2), 3-aminopyridine (3-NH(2)py; 3), and 3-dimethylaminopyridine (3-NMe(2)py; 4), as well as the strongly electron-withdrawing 3-cyanopyridine (3-CNpy; 5), to probe the possible limitations of iodine(I) complex formation. The individual properties of these rare examples of iodine(I) complexes incorporating 3-substituted pyridines are also compared to each other and contrasted to their 4-substituted counterparts which are more prevalent in the literature. While the reactivity of 1b toward etheric solvents could not be reproduced in any of the functionally related analogues synthesized herein, the reactivity of 1b was further expanded to a second etheric solvent. Reaction of bis(3-acetaminopyridine)iodine(I) (1b) and (i)Pr(2)O gave [3-acetamido-1-(3-iodo-2-methylpentan-2-yl)pyridin-1-ium]PF(6) (1d), which demonstrated potentially useful C–C and C–I bond formation under ambient conditions. American Chemical Society 2023-06-21 /pmc/articles/PMC10324066/ /pubmed/37426204 http://dx.doi.org/10.1021/acsomega.3c03097 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Rissanen, Kari Ward, Jas S. Iodine(I) and Silver(I) Complexes Incorporating 3-Substituted Pyridines |
title | Iodine(I) and Silver(I)
Complexes Incorporating 3-Substituted
Pyridines |
title_full | Iodine(I) and Silver(I)
Complexes Incorporating 3-Substituted
Pyridines |
title_fullStr | Iodine(I) and Silver(I)
Complexes Incorporating 3-Substituted
Pyridines |
title_full_unstemmed | Iodine(I) and Silver(I)
Complexes Incorporating 3-Substituted
Pyridines |
title_short | Iodine(I) and Silver(I)
Complexes Incorporating 3-Substituted
Pyridines |
title_sort | iodine(i) and silver(i)
complexes incorporating 3-substituted
pyridines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324066/ https://www.ncbi.nlm.nih.gov/pubmed/37426204 http://dx.doi.org/10.1021/acsomega.3c03097 |
work_keys_str_mv | AT rissanenkari iodineiandsilvericomplexesincorporating3substitutedpyridines AT wardjass iodineiandsilvericomplexesincorporating3substitutedpyridines |