Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction
In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The pr...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Patil, Seema P. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2023 |
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| Schlagwörter: |
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| Anmerkung: |
© Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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| Übergeordnetes Werk: |
Enthalten in: Chemical papers - Wien : Springer Vienna, 1947, 77(2023), 9 vom: 16. Juni, Seite 5555-5569 |
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| Übergeordnetes Werk: |
volume:77 ; year:2023 ; number:9 ; day:16 ; month:06 ; pages:5555-5569 |
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| DOI / URN: |
10.1007/s11696-023-02885-2 |
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| Katalog-ID: |
SPR052764508 |
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| 520 | |a In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract | ||
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| 650 | 4 | |a LDH |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Suzuki–Miyaura coupling |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Recyclability |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Jadhav, Sanjay N. |4 aut | |
| 700 | 1 | |a Inamdar, Firoz A. |4 aut | |
| 700 | 1 | |a Ameen, Mohd Aatif |4 aut | |
| 700 | 1 | |a Rode, Chandrashekhar V. |4 aut | |
| 700 | 1 | |a Rajmane, Archana S. |4 aut | |
| 700 | 1 | |a Kumbhar, Arjun S. |0 (orcid)0000-0001-5927-3482 |4 aut | |
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10.1007/s11696-023-02885-2 doi (DE-627)SPR052764508 (SPR)s11696-023-02885-2-e DE-627 ger DE-627 rakwb eng Patil, Seema P. verfasserin aut Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract PdNPs (dpeaa)DE-He213 LDH (dpeaa)DE-He213 Suzuki–Miyaura coupling (dpeaa)DE-He213 Recyclability (dpeaa)DE-He213 Jadhav, Sanjay N. aut Inamdar, Firoz A. aut Ameen, Mohd Aatif aut Rode, Chandrashekhar V. aut Rajmane, Archana S. aut Kumbhar, Arjun S. (orcid)0000-0001-5927-3482 aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 77(2023), 9 vom: 16. Juni, Seite 5555-5569 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:77 year:2023 number:9 day:16 month:06 pages:5555-5569 https://dx.doi.org/10.1007/s11696-023-02885-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 77 2023 9 16 06 5555-5569 |
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10.1007/s11696-023-02885-2 doi (DE-627)SPR052764508 (SPR)s11696-023-02885-2-e DE-627 ger DE-627 rakwb eng Patil, Seema P. verfasserin aut Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract PdNPs (dpeaa)DE-He213 LDH (dpeaa)DE-He213 Suzuki–Miyaura coupling (dpeaa)DE-He213 Recyclability (dpeaa)DE-He213 Jadhav, Sanjay N. aut Inamdar, Firoz A. aut Ameen, Mohd Aatif aut Rode, Chandrashekhar V. aut Rajmane, Archana S. aut Kumbhar, Arjun S. (orcid)0000-0001-5927-3482 aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 77(2023), 9 vom: 16. Juni, Seite 5555-5569 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:77 year:2023 number:9 day:16 month:06 pages:5555-5569 https://dx.doi.org/10.1007/s11696-023-02885-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 77 2023 9 16 06 5555-5569 |
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10.1007/s11696-023-02885-2 doi (DE-627)SPR052764508 (SPR)s11696-023-02885-2-e DE-627 ger DE-627 rakwb eng Patil, Seema P. verfasserin aut Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract PdNPs (dpeaa)DE-He213 LDH (dpeaa)DE-He213 Suzuki–Miyaura coupling (dpeaa)DE-He213 Recyclability (dpeaa)DE-He213 Jadhav, Sanjay N. aut Inamdar, Firoz A. aut Ameen, Mohd Aatif aut Rode, Chandrashekhar V. aut Rajmane, Archana S. aut Kumbhar, Arjun S. (orcid)0000-0001-5927-3482 aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 77(2023), 9 vom: 16. Juni, Seite 5555-5569 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:77 year:2023 number:9 day:16 month:06 pages:5555-5569 https://dx.doi.org/10.1007/s11696-023-02885-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 77 2023 9 16 06 5555-5569 |
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10.1007/s11696-023-02885-2 doi (DE-627)SPR052764508 (SPR)s11696-023-02885-2-e DE-627 ger DE-627 rakwb eng Patil, Seema P. verfasserin aut Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract PdNPs (dpeaa)DE-He213 LDH (dpeaa)DE-He213 Suzuki–Miyaura coupling (dpeaa)DE-He213 Recyclability (dpeaa)DE-He213 Jadhav, Sanjay N. aut Inamdar, Firoz A. aut Ameen, Mohd Aatif aut Rode, Chandrashekhar V. aut Rajmane, Archana S. aut Kumbhar, Arjun S. (orcid)0000-0001-5927-3482 aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 77(2023), 9 vom: 16. Juni, Seite 5555-5569 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:77 year:2023 number:9 day:16 month:06 pages:5555-5569 https://dx.doi.org/10.1007/s11696-023-02885-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 77 2023 9 16 06 5555-5569 |
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10.1007/s11696-023-02885-2 doi (DE-627)SPR052764508 (SPR)s11696-023-02885-2-e DE-627 ger DE-627 rakwb eng Patil, Seema P. verfasserin aut Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract PdNPs (dpeaa)DE-He213 LDH (dpeaa)DE-He213 Suzuki–Miyaura coupling (dpeaa)DE-He213 Recyclability (dpeaa)DE-He213 Jadhav, Sanjay N. aut Inamdar, Firoz A. aut Ameen, Mohd Aatif aut Rode, Chandrashekhar V. aut Rajmane, Archana S. aut Kumbhar, Arjun S. (orcid)0000-0001-5927-3482 aut Enthalten in Chemical papers Wien : Springer Vienna, 1947 77(2023), 9 vom: 16. Juni, Seite 5555-5569 (DE-627)518347737 (DE-600)2252770-9 1336-9075 nnns volume:77 year:2023 number:9 day:16 month:06 pages:5555-5569 https://dx.doi.org/10.1007/s11696-023-02885-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_266 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 77 2023 9 16 06 5555-5569 |
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Patil, Seema P. @@aut@@ Jadhav, Sanjay N. @@aut@@ Inamdar, Firoz A. @@aut@@ Ameen, Mohd Aatif @@aut@@ Rode, Chandrashekhar V. @@aut@@ Rajmane, Archana S. @@aut@@ Kumbhar, Arjun S. @@aut@@ |
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Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. 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Patil, Seema P. |
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Patil, Seema P. misc PdNPs misc LDH misc Suzuki–Miyaura coupling misc Recyclability Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction |
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Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction PdNPs (dpeaa)DE-He213 LDH (dpeaa)DE-He213 Suzuki–Miyaura coupling (dpeaa)DE-He213 Recyclability (dpeaa)DE-He213 |
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misc PdNPs misc LDH misc Suzuki–Miyaura coupling misc Recyclability |
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misc PdNPs misc LDH misc Suzuki–Miyaura coupling misc Recyclability |
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misc PdNPs misc LDH misc Suzuki–Miyaura coupling misc Recyclability |
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Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction |
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Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction |
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Patil, Seema P. |
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Patil, Seema P. Jadhav, Sanjay N. Inamdar, Firoz A. Ameen, Mohd Aatif Rode, Chandrashekhar V. Rajmane, Archana S. Kumbhar, Arjun S. |
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Patil, Seema P. |
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recyclable pd nanoparticles immobilized on amine functionalized ldh for the suzuki–miyaura cross-coupling reaction |
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Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction |
| abstract |
In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| abstractGer |
In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| abstract_unstemmed |
In the present work, we invented a Pd nanoparticle immobilized on an amine-functionalized LDH catalyst (PdNP$ NH_{2} $-LDH-Al-MCM-41) for cross-coupling reactions. The palladium was grafted onto the support by treating the Pd(OAc)2 with $ NH_{2} $-LDH-Al-MCM-41 in acetone at room temperature. The prepared catalyst was characterized by FT-IR, SEM, TGA, TEM, and XPS techniques. The TEM characterization of the catalyst showed the uniform distribution of PdNPs with sizes ranging from 3 to 6 nm located inside the mesoporous. The Suzuki–Miyaura cross-coupling reaction was used to demonstrate the catalytic efficiency of the prepared PdNPs@$ NH_{2} $-LDH-Al-MCM-41 catalyst. The prepared and analyzed catalyst showed good to excellent activity in the Suzuki–Miyaura cross-coupling reaction of various aryl bromides with different aryl boronic acids in ethanol at 80 °C. The catalyst showed TON up to ~ 47 and TOF ~ 47 $ h^{−1} $. The catalytic results exhibited that the catalyst is completely recoverable with simple filtration. The catalytic efficiency shows a slight decrease in activity for the Suzuki–Miyaura cross-coupling reactions even after five repeated recycles. TEM images of the freshly prepared and reused catalysts (after five catalytic cycles) showed palladium nanoparticles remain unchanged at the end of the reactions. Graphical abstract © Institute of Chemistry, Slovak Academy of Sciences 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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| container_issue |
9 |
| title_short |
Recyclable Pd nanoparticles immobilized on amine functionalized LDH for the Suzuki–Miyaura cross-coupling reaction |
| url |
https://dx.doi.org/10.1007/s11696-023-02885-2 |
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| author2 |
Jadhav, Sanjay N. Inamdar, Firoz A. Ameen, Mohd Aatif Rode, Chandrashekhar V. Rajmane, Archana S. Kumbhar, Arjun S. |
| author2Str |
Jadhav, Sanjay N. Inamdar, Firoz A. Ameen, Mohd Aatif Rode, Chandrashekhar V. Rajmane, Archana S. Kumbhar, Arjun S. |
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| doi_str |
10.1007/s11696-023-02885-2 |
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2024-07-03T14:37:47.214Z |
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| score |
7.402667 |