1-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dione

Appropriately substituted N-centered urazolyl radicals are capable of generating interesting cage-like structures upon forming N-N bonds. The radicals are generated by the oxidation of the corresponding NH urazole precursors. We synthesized a triurazole precursor that we hoped would dimerize through...

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Main Authors: Gary W. Breton, James Alexander Bowron
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Molbank
Subjects:
Online Access:https://www.mdpi.com/1422-8599/2023/1/M1535
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author Gary W. Breton
James Alexander Bowron
author_facet Gary W. Breton
James Alexander Bowron
author_sort Gary W. Breton
collection DOAJ
description Appropriately substituted N-centered urazolyl radicals are capable of generating interesting cage-like structures upon forming N-N bonds. The radicals are generated by the oxidation of the corresponding NH urazole precursors. We synthesized a triurazole precursor that we hoped would dimerize through the formation of three N-N bonds to afford a large molecular cage. Unfortunately, the attempts at the oxidation of the urazoles to form urazolyl radicals instead only lead to random oligomerization, forming plastic-like materials rather than the desired cages.
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spelling doaj.art-4953018fce2a4e5092c514f0f4d35efe2023-11-17T12:49:05ZengMDPI AGMolbank1422-85992022-12-0120231M153510.3390/M15351-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dioneGary W. Breton0James Alexander Bowron1Department of Chemistry and Biochemistry, Berry College, Mount Berry, GA 30149, USADepartment of Chemistry and Biochemistry, Berry College, Mount Berry, GA 30149, USAAppropriately substituted N-centered urazolyl radicals are capable of generating interesting cage-like structures upon forming N-N bonds. The radicals are generated by the oxidation of the corresponding NH urazole precursors. We synthesized a triurazole precursor that we hoped would dimerize through the formation of three N-N bonds to afford a large molecular cage. Unfortunately, the attempts at the oxidation of the urazoles to form urazolyl radicals instead only lead to random oligomerization, forming plastic-like materials rather than the desired cages.https://www.mdpi.com/1422-8599/2023/1/M1535urazoleradicalsmolecular cages
spellingShingle Gary W. Breton
James Alexander Bowron
1-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dione
Molbank
urazole
radicals
molecular cages
title 1-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dione
title_full 1-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dione
title_fullStr 1-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dione
title_full_unstemmed 1-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dione
title_short 1-(4-{[3,5-<i>bis</i>({[3,5-Dimethyl-4-(4-methyl-3,5-dioxo-1,2,4-triazolidin-1-yl)-phenoxy]methyl})phenyl]methoxy}-2,6-dimethyl-phenyl)-4-methyl-1,2,4-triazolidine-3,5-dione
title_sort 1 4 3 5 i bis i 3 5 dimethyl 4 4 methyl 3 5 dioxo 1 2 4 triazolidin 1 yl phenoxy methyl phenyl methoxy 2 6 dimethyl phenyl 4 methyl 1 2 4 triazolidine 3 5 dione
topic urazole
radicals
molecular cages
url https://www.mdpi.com/1422-8599/2023/1/M1535
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