Recyclable LaF·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids

Herein we prepared the novel LaF 3 ·Pd nanocatalyst characterized by XRD and TEM analysis. The nanocatalyst was applied in Suzuki coupling reaction for the synthesis of biaryls in aqueous medium from readily available aryl halides (bromides and iodides) and substituted phenylboronic acids in the pre...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:RSC advances 2024-07, Vol.14 (3), p.21269-21276
Hauptverfasser: Panda, Smitabala, Patra, Sagarika, Acharya, Swadhin Swaraj, Phaomei, Ganngam, Parida, Bibhuti Bhusan
Format: Artikel
Sprache:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 21276
container_issue 3
container_start_page 21269
container_title RSC advances
container_volume 14
creator Panda, Smitabala
Patra, Sagarika
Acharya, Swadhin Swaraj
Phaomei, Ganngam
Parida, Bibhuti Bhusan
description Herein we prepared the novel LaF 3 ·Pd nanocatalyst characterized by XRD and TEM analysis. The nanocatalyst was applied in Suzuki coupling reaction for the synthesis of biaryls in aqueous medium from readily available aryl halides (bromides and iodides) and substituted phenylboronic acids in the presence of K 2 CO 3 as the base at 70 °C. The present method is capable of giving the C-C coupled product in good to excellent yields (up to 97%). The reactions were conducted under green conditions in aqueous medium and the nanocatalyst used in this study was recyclable. The recyclability and reusability of the catalyst was checked for seven consecutive cycles without significant loss in reactivity. A green and sustainable approach has been developed using a recyclable and reusable LaF 3 ·Pd nanocatalyst. This catalyst has been applied in the synthesis of biaryls in good to excellent yields via Suzuki coupling in aqueous medium.
doi_str_mv 10.1039/d4ra00686k
format Article
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_d4ra00686k</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>d4ra00686k</sourcerecordid><originalsourceid>FETCH-rsc_primary_d4ra00686k3</originalsourceid><addsrcrecordid>eNqFj7FqAkEURYeAEFGb9ML7AZPZVQdNGyIWKSTay9vZt-7o-GaZtxsYf8w-XxYLIaW3OcWBA1epl0y_Znq6fCtnEbU2C3N6Uv1cz8wk12b5rEYiR32bmWe5yfrq55tssh4LT_CFq9_rpgRGDhZb9ElacAzb7tKdHNjQNd7x4R0OkYhBErc1iRMIFRQOY_ICVQxnqNEHjMQkgFxCUxMnX4QY2FlA60oZql6FXmh050CNV5-7j_Ukit030Z1vtf3_h-kj_wclyU8-</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Recyclable LaF·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids</title><source>DOAJ Directory of Open Access Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Panda, Smitabala ; Patra, Sagarika ; Acharya, Swadhin Swaraj ; Phaomei, Ganngam ; Parida, Bibhuti Bhusan</creator><creatorcontrib>Panda, Smitabala ; Patra, Sagarika ; Acharya, Swadhin Swaraj ; Phaomei, Ganngam ; Parida, Bibhuti Bhusan</creatorcontrib><description>Herein we prepared the novel LaF 3 ·Pd nanocatalyst characterized by XRD and TEM analysis. The nanocatalyst was applied in Suzuki coupling reaction for the synthesis of biaryls in aqueous medium from readily available aryl halides (bromides and iodides) and substituted phenylboronic acids in the presence of K 2 CO 3 as the base at 70 °C. The present method is capable of giving the C-C coupled product in good to excellent yields (up to 97%). The reactions were conducted under green conditions in aqueous medium and the nanocatalyst used in this study was recyclable. The recyclability and reusability of the catalyst was checked for seven consecutive cycles without significant loss in reactivity. A green and sustainable approach has been developed using a recyclable and reusable LaF 3 ·Pd nanocatalyst. This catalyst has been applied in the synthesis of biaryls in good to excellent yields via Suzuki coupling in aqueous medium.</description><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/d4ra00686k</identifier><ispartof>RSC advances, 2024-07, Vol.14 (3), p.21269-21276</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27903,27904</link.rule.ids></links><search><creatorcontrib>Panda, Smitabala</creatorcontrib><creatorcontrib>Patra, Sagarika</creatorcontrib><creatorcontrib>Acharya, Swadhin Swaraj</creatorcontrib><creatorcontrib>Phaomei, Ganngam</creatorcontrib><creatorcontrib>Parida, Bibhuti Bhusan</creatorcontrib><title>Recyclable LaF·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids</title><title>RSC advances</title><description>Herein we prepared the novel LaF 3 ·Pd nanocatalyst characterized by XRD and TEM analysis. The nanocatalyst was applied in Suzuki coupling reaction for the synthesis of biaryls in aqueous medium from readily available aryl halides (bromides and iodides) and substituted phenylboronic acids in the presence of K 2 CO 3 as the base at 70 °C. The present method is capable of giving the C-C coupled product in good to excellent yields (up to 97%). The reactions were conducted under green conditions in aqueous medium and the nanocatalyst used in this study was recyclable. The recyclability and reusability of the catalyst was checked for seven consecutive cycles without significant loss in reactivity. A green and sustainable approach has been developed using a recyclable and reusable LaF 3 ·Pd nanocatalyst. This catalyst has been applied in the synthesis of biaryls in good to excellent yields via Suzuki coupling in aqueous medium.</description><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj7FqAkEURYeAEFGb9ML7AZPZVQdNGyIWKSTay9vZt-7o-GaZtxsYf8w-XxYLIaW3OcWBA1epl0y_Znq6fCtnEbU2C3N6Uv1cz8wk12b5rEYiR32bmWe5yfrq55tssh4LT_CFq9_rpgRGDhZb9ElacAzb7tKdHNjQNd7x4R0OkYhBErc1iRMIFRQOY_ICVQxnqNEHjMQkgFxCUxMnX4QY2FlA60oZql6FXmh050CNV5-7j_Ukit030Z1vtf3_h-kj_wclyU8-</recordid><startdate>20240705</startdate><enddate>20240705</enddate><creator>Panda, Smitabala</creator><creator>Patra, Sagarika</creator><creator>Acharya, Swadhin Swaraj</creator><creator>Phaomei, Ganngam</creator><creator>Parida, Bibhuti Bhusan</creator><scope/></search><sort><creationdate>20240705</creationdate><title>Recyclable LaF·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids</title><author>Panda, Smitabala ; Patra, Sagarika ; Acharya, Swadhin Swaraj ; Phaomei, Ganngam ; Parida, Bibhuti Bhusan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d4ra00686k3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Panda, Smitabala</creatorcontrib><creatorcontrib>Patra, Sagarika</creatorcontrib><creatorcontrib>Acharya, Swadhin Swaraj</creatorcontrib><creatorcontrib>Phaomei, Ganngam</creatorcontrib><creatorcontrib>Parida, Bibhuti Bhusan</creatorcontrib><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panda, Smitabala</au><au>Patra, Sagarika</au><au>Acharya, Swadhin Swaraj</au><au>Phaomei, Ganngam</au><au>Parida, Bibhuti Bhusan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recyclable LaF·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids</atitle><jtitle>RSC advances</jtitle><date>2024-07-05</date><risdate>2024</risdate><volume>14</volume><issue>3</issue><spage>21269</spage><epage>21276</epage><pages>21269-21276</pages><eissn>2046-2069</eissn><abstract>Herein we prepared the novel LaF 3 ·Pd nanocatalyst characterized by XRD and TEM analysis. The nanocatalyst was applied in Suzuki coupling reaction for the synthesis of biaryls in aqueous medium from readily available aryl halides (bromides and iodides) and substituted phenylboronic acids in the presence of K 2 CO 3 as the base at 70 °C. The present method is capable of giving the C-C coupled product in good to excellent yields (up to 97%). The reactions were conducted under green conditions in aqueous medium and the nanocatalyst used in this study was recyclable. The recyclability and reusability of the catalyst was checked for seven consecutive cycles without significant loss in reactivity. A green and sustainable approach has been developed using a recyclable and reusable LaF 3 ·Pd nanocatalyst. This catalyst has been applied in the synthesis of biaryls in good to excellent yields via Suzuki coupling in aqueous medium.</abstract><doi>10.1039/d4ra00686k</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier EISSN: 2046-2069
ispartof RSC advances, 2024-07, Vol.14 (3), p.21269-21276
issn 2046-2069
language
recordid cdi_rsc_primary_d4ra00686k
source DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; PubMed Central Open Access
title Recyclable LaF·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T16%3A14%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Recyclable%20LaF%C2%B7Pd%20nanocatalyst%20in%20Suzuki%20coupling:%20green%20synthesis%20of%20biaryls%20from%20haloarenes%20and%20phenylboronic%20acids&rft.jtitle=RSC%20advances&rft.au=Panda,%20Smitabala&rft.date=2024-07-05&rft.volume=14&rft.issue=3&rft.spage=21269&rft.epage=21276&rft.pages=21269-21276&rft.eissn=2046-2069&rft_id=info:doi/10.1039/d4ra00686k&rft_dat=%3Crsc%3Ed4ra00686k%3C/rsc%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true