Tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates

Abstract Recently, the organic functionalization of polyoxometalates (POMs) has drawn increasing interest, and an easy and effective route to achieve organic derivatives is of great importance. Herein, the first reported synthesis of a tosyl ester derivative of the polyoxometalate (Bu4N)2[V6O13{(OCH...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Hongli Jia, Qi Li, Aruuhan Bayaguud, Shan She, Yichao Huang, Kun Chen, Yongge Wei
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/be4ee172b75447ee874ef889c196bfdc
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:be4ee172b75447ee874ef889c196bfdc
record_format dspace
spelling oai:doaj.org-article:be4ee172b75447ee874ef889c196bfdc2021-12-02T15:05:55ZTosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates10.1038/s41598-017-12633-82045-2322https://doaj.org/article/be4ee172b75447ee874ef889c196bfdc2017-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-12633-8https://doaj.org/toc/2045-2322Abstract Recently, the organic functionalization of polyoxometalates (POMs) has drawn increasing interest, and an easy and effective route to achieve organic derivatives is of great importance. Herein, the first reported synthesis of a tosyl ester derivative of the polyoxometalate (Bu4N)2[V6O13{(OCH2)3CCH2SO3C7H4}2]·2.5CH3CN (compound 1) was performed by using DMAP as an activating reagent and triethylamine as an HCl scavenger. The tosyl ester was transformed into an azide or halide group by using sodium azide or sodium bromide, respectively, as the nucleophilic agent. Two derivatives of POMs, (Bu4N)2[V6O13{(OCH2)3CCH2N3}2]·4CH3CN (compound 2) and (Bu4N)2[V6O13{(OCH2)3CCH2Br}2] (compound 3), were easily obtained. All the compounds were structurally and compositionally characterized by single-crystal X-ray diffraction, elemental analysis, IR spectroscopy, NMR spectroscopy, ESI-MS, UV-Vis spectroscopy and TGA. This work provides a new route for the functional group transformation of organic derivatives of polyoxometalates.Hongli JiaQi LiAruuhan BayaguudShan SheYichao HuangKun ChenYongge WeiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hongli Jia
Qi Li
Aruuhan Bayaguud
Shan She
Yichao Huang
Kun Chen
Yongge Wei
Tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates
description Abstract Recently, the organic functionalization of polyoxometalates (POMs) has drawn increasing interest, and an easy and effective route to achieve organic derivatives is of great importance. Herein, the first reported synthesis of a tosyl ester derivative of the polyoxometalate (Bu4N)2[V6O13{(OCH2)3CCH2SO3C7H4}2]·2.5CH3CN (compound 1) was performed by using DMAP as an activating reagent and triethylamine as an HCl scavenger. The tosyl ester was transformed into an azide or halide group by using sodium azide or sodium bromide, respectively, as the nucleophilic agent. Two derivatives of POMs, (Bu4N)2[V6O13{(OCH2)3CCH2N3}2]·4CH3CN (compound 2) and (Bu4N)2[V6O13{(OCH2)3CCH2Br}2] (compound 3), were easily obtained. All the compounds were structurally and compositionally characterized by single-crystal X-ray diffraction, elemental analysis, IR spectroscopy, NMR spectroscopy, ESI-MS, UV-Vis spectroscopy and TGA. This work provides a new route for the functional group transformation of organic derivatives of polyoxometalates.
format article
author Hongli Jia
Qi Li
Aruuhan Bayaguud
Shan She
Yichao Huang
Kun Chen
Yongge Wei
author_facet Hongli Jia
Qi Li
Aruuhan Bayaguud
Shan She
Yichao Huang
Kun Chen
Yongge Wei
author_sort Hongli Jia
title Tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates
title_short Tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates
title_full Tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates
title_fullStr Tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates
title_full_unstemmed Tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates
title_sort tosylation of alcohols: an effective strategy for the functional group transformation of organic derivatives of polyoxometalates
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/be4ee172b75447ee874ef889c196bfdc
work_keys_str_mv AT honglijia tosylationofalcoholsaneffectivestrategyforthefunctionalgrouptransformationoforganicderivativesofpolyoxometalates
AT qili tosylationofalcoholsaneffectivestrategyforthefunctionalgrouptransformationoforganicderivativesofpolyoxometalates
AT aruuhanbayaguud tosylationofalcoholsaneffectivestrategyforthefunctionalgrouptransformationoforganicderivativesofpolyoxometalates
AT shanshe tosylationofalcoholsaneffectivestrategyforthefunctionalgrouptransformationoforganicderivativesofpolyoxometalates
AT yichaohuang tosylationofalcoholsaneffectivestrategyforthefunctionalgrouptransformationoforganicderivativesofpolyoxometalates
AT kunchen tosylationofalcoholsaneffectivestrategyforthefunctionalgrouptransformationoforganicderivativesofpolyoxometalates
AT yonggewei tosylationofalcoholsaneffectivestrategyforthefunctionalgrouptransformationoforganicderivativesofpolyoxometalates
_version_ 1718388667976777728