Alain Vigroux
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Alain Vigroux has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Christophe Laurent
Centre Interuniversitaire de Recherche et d’Ingénierie des Matériaux CIRIMAT, Université de Toulouse, UMR CNRS INP UT 5085, 118 Route de Narbonne, 31062 Toulouse, France
4 shared publications - Isabelle Fabing
Toulouse University, Laboratoire de Synthèse et de Physico-Chimie de Molécules d’Intérêt Biologie (SPCMIB), CNRS (UMR 5068), Toulouse, France
4 shared publications - Pascal Hoffmann
Laboratory of Synthesis and Physicochemistry of Molecules of Biological Interest (LSPCMIB), University of Toulouse, UMR CNRS UT 5068, Toulouse, France
4 shared publications - Christian Lherbet
Laboratoire de Synthèse et Physico-Chimie de Molécules d’Interêt Biologique, LSPCMIB, Université de Toulouse, CNRS, 118 Route de Narbonne, 31062 Toulouse, France
3 shared publications - Marie-Claire Barthelemy
Centre Interuniversitaire de Recherche et d’Ingénierie des Matériaux CIRIMAT, Université de Toulouse, UMR CNRS INP UT 5085, 118 Route de Narbonne, 31062 Toulouse, France
2 shared publications Marie-Claire Barthélémy
CIRIMAT, Université Toulouse 3 Paul Sabatier, UMR CNRS UPS INP 5085, 118 Route de Narbonne, 31062 Toulouse, France
2 shared publications
Latest Publications
- Open Access
A Post-Synthetic Modification Approach to Expand MIL-101-NH2 Functionalization
Considering the importance of organic functionalization of MOFs, we here report a simple, tunable and efficient one-step post-modification procedure for introducing amino and carboxylic groups into the mesoporous metal–organic framework Al- and Cr-MIL-101-NH2 based on its reaction with alkyl bromides. This procedure allows also access to polyfunctionalized MIL-101 decorated with both carboxylic and primary amino groups. Other chemical functions, such as alcohols and alkynes, were also successfully introduced by this method.
Open AccessA Post-Synthetic Modification Approach to Expand MIL-101-NH2 Functionalization
Considering the importance of organic functionalization of MOFs, we here report a simple, tunable and efficient one-step post-modification procedure for introducing amino and carboxylic groups into the mesoporous metal–organic framework Al- and Cr-MIL-101-NH2 based on its reaction with alkyl bromides. This procedure allows also access to polyfunctionalized MIL-101 decorated with both carboxylic and primary amino groups. Other chemical functions, such as alcohols and alkynes, were also successfully introduced by this method.
- Open Access
- 4 February 2025
- Published by MDPI AG in Preprints.org
A Post-Synthetic Modification Approach to Expand MIL-101-NH2 Functionalization
Considering the importance of organic functionalization of MOFs, we here report a simple, tunable and efficient one-step post-modification procedure for introducing amino and carboxylic groups into the mesoporous metal-organic framework Al- and Cr-MIL-101-NH2 based on its reaction with alkyl bromides. This procedure allows also access to polyfunctionnalized MIL-101 decorated with both carboxylic and primary amino groups. Other chemical functions, such as alcohols and alkynes, were also successfully introduced by this method.
- 4 February 2025
- Published by MDPI AG in Preprints.org
Open AccessA Post-Synthetic Modification Approach to Expand MIL-101-NH2 Functionalization
Considering the importance of organic functionalization of MOFs, we here report a simple, tunable and efficient one-step post-modification procedure for introducing amino and carboxylic groups into the mesoporous metal-organic framework Al- and Cr-MIL-101-NH2 based on its reaction with alkyl bromides. This procedure allows also access to polyfunctionnalized MIL-101 decorated with both carboxylic and primary amino groups. Other chemical functions, such as alcohols and alkynes, were also successfully introduced by this method.
- Open Access
- 16 September 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (41) , 26825-26833
A mesoporous metal–organic framework used to sustainably release copper( ii ) into reducing aqueous media to promote the CuAAC click reaction
Cr-MIL-101-NH 2 (MOF1) has been used to encapsulate large amounts of copper sulfate and the resulting loaded material, Cu@MOF1, was successfully used to promote the CuAAC click reaction.
- 16 September 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (41) , 26825-26833
Open AccessA mesoporous metal–organic framework used to sustainably release copper( ii ) into reducing aqueous media to promote the CuAAC click reaction
Cr-MIL-101-NH 2 (MOF1) has been used to encapsulate large amounts of copper sulfate and the resulting loaded material, Cu@MOF1, was successfully used to promote the CuAAC click reaction.
- Open Access
- 1 February 2015
- Published by Elsevier in Inorganica Chimica Acta
- Vol. 426, 15-19
Two new metal–organic framework structures derived from terephthalate and linear trimetallic zinc building units
- 1 February 2015
- Published by Elsevier in Inorganica Chimica Acta
- Vol. 426, 15-19
Open AccessTwo new metal–organic framework structures derived from terephthalate and linear trimetallic zinc building units
- 11 June 2002
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry A
- Vol. 106 (27) , 6521-6526
Reactivity of Phosphate Monoester Monoanions in Aqueous Solution. 2. A Theoretical Study of the Elusive Zwitterion Intermediates RO+(H)PO32-
- 11 June 2002
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry A
- Vol. 106 (27) , 6521-6526
Reactivity of Phosphate Monoester Monoanions in Aqueous Solution. 2. A Theoretical Study of the Elusive Zwitterion Intermediates RO+(H)PO32-