A sustainable approach for nickel nanoparticles synthesis: expeditious access to N-heterocycles under heterogeneous condition and photophysical studies
A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC 2 O 4 ·2H 2 O-NPs) using Portulaca oleracea (purslane) leaf extract has been disclosed for the first time. The phytochemicals found in Portulaca oleracea leaf extract were found to serve as a reducing a...
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Veröffentlicht in: | New journal of chemistry 2023-05, Vol.47 (17), p.8268-8276 |
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container_title | New journal of chemistry |
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creator | Hegde, Rajeev V Ghosh, Arnab Limaye, Akshay S Rode, Haridas B Sridhar, Balasubramanian Dateer, Ramesh B |
description | A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC
2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time. The phytochemicals found in
Portulaca oleracea
leaf extract were found to serve as a reducing agent and subsequently act as a stabilizing agent. The various analytical and spectroscopic techniques confirm the formation of Ni-NPs. The catalytic potential of Ni-NPs was investigated to achieve cost-effective, sustainable, atom and step economic synthesis of pharmaceutically important quinazoline, 2-aminoquinoline, and
N
-(alkyl amino) quinoline
via
hydrogen auto transfer and acceptorless dehydrogenative annulation without the aid of external ligand and additives. Importantly, the photophysical property studies of the synthesized N-heterocycles are deliberated and gram-scale synthesis was achieved. Moreover, catalyst recyclability, control experiments, and mechanistic elucidation were elaborated.
A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC
2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time. |
doi_str_mv | 10.1039/d3nj00988b |
format | Article |
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2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time. The phytochemicals found in
Portulaca oleracea
leaf extract were found to serve as a reducing agent and subsequently act as a stabilizing agent. The various analytical and spectroscopic techniques confirm the formation of Ni-NPs. The catalytic potential of Ni-NPs was investigated to achieve cost-effective, sustainable, atom and step economic synthesis of pharmaceutically important quinazoline, 2-aminoquinoline, and
N
-(alkyl amino) quinoline
via
hydrogen auto transfer and acceptorless dehydrogenative annulation without the aid of external ligand and additives. Importantly, the photophysical property studies of the synthesized N-heterocycles are deliberated and gram-scale synthesis was achieved. Moreover, catalyst recyclability, control experiments, and mechanistic elucidation were elaborated.
A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC
2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/d3nj00988b</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Additives ; Aminoquinolines ; Chemical reactions ; Chemical synthesis ; Dehydrogenation ; Nanoparticles ; Quinoline ; Recyclability ; Reducing agents ; Stabilizers (agents)</subject><ispartof>New journal of chemistry, 2023-05, Vol.47 (17), p.8268-8276</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c281t-789cbca6de513602bcb9d0816a87c7c44053ecab0aa4a97845a145d67479c5503</citedby><cites>FETCH-LOGICAL-c281t-789cbca6de513602bcb9d0816a87c7c44053ecab0aa4a97845a145d67479c5503</cites><orcidid>0009-0006-7283-775X ; 0000-0001-6025-7826 ; 0009-0008-5975-4460 ; 0009-0001-5781-1811 ; 0000-0002-1573-5259</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Hegde, Rajeev V</creatorcontrib><creatorcontrib>Ghosh, Arnab</creatorcontrib><creatorcontrib>Limaye, Akshay S</creatorcontrib><creatorcontrib>Rode, Haridas B</creatorcontrib><creatorcontrib>Sridhar, Balasubramanian</creatorcontrib><creatorcontrib>Dateer, Ramesh B</creatorcontrib><title>A sustainable approach for nickel nanoparticles synthesis: expeditious access to N-heterocycles under heterogeneous condition and photophysical studies</title><title>New journal of chemistry</title><description>A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC
2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time. The phytochemicals found in
Portulaca oleracea
leaf extract were found to serve as a reducing agent and subsequently act as a stabilizing agent. The various analytical and spectroscopic techniques confirm the formation of Ni-NPs. The catalytic potential of Ni-NPs was investigated to achieve cost-effective, sustainable, atom and step economic synthesis of pharmaceutically important quinazoline, 2-aminoquinoline, and
N
-(alkyl amino) quinoline
via
hydrogen auto transfer and acceptorless dehydrogenative annulation without the aid of external ligand and additives. Importantly, the photophysical property studies of the synthesized N-heterocycles are deliberated and gram-scale synthesis was achieved. Moreover, catalyst recyclability, control experiments, and mechanistic elucidation were elaborated.
A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC
2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time.</description><subject>Additives</subject><subject>Aminoquinolines</subject><subject>Chemical reactions</subject><subject>Chemical synthesis</subject><subject>Dehydrogenation</subject><subject>Nanoparticles</subject><subject>Quinoline</subject><subject>Recyclability</subject><subject>Reducing agents</subject><subject>Stabilizers (agents)</subject><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpFkU2P1DAMhiMEEsPAhTtSJG4rFZJJ-sVtd_nWaLjAuXJdD81Qkm6cSttfwt-lM13ByZb1-LXe10K81OqNVqZ-2xl_UqquqvaR2GhT1Fm9K_TjpdfWZiq3xVPxjHlhtC4LvRF_riVPnMB5aAeSMI4xAPbyGKL0Dn_RID34MEJMDgdiybNPPbHjd5LuR-pccmFiCYjELFOQh6ynRDHgfOEn31GU6-gneTrDGPxlz0vwnRz7kMLYz-wQBslp6hzxc_HkCAPTi4e6FT8-fvh--znbf_v05fZ6n-Gu0ikrqxpbhKKjfHGrdi22dacqXUBVYonWqtwQQqsALNRlZXPQNu-K0pY15rkyW_F61V18303EqTmFKfrlZLOrFqHSWGsW6mqlMAbmSMdmjO43xLnRqjkH37w3h6-X4G8W-NUKR8Z_3P_HmL_O74Qg</recordid><startdate>20230502</startdate><enddate>20230502</enddate><creator>Hegde, Rajeev V</creator><creator>Ghosh, Arnab</creator><creator>Limaye, Akshay S</creator><creator>Rode, Haridas B</creator><creator>Sridhar, Balasubramanian</creator><creator>Dateer, Ramesh B</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>H9R</scope><scope>JG9</scope><scope>KA0</scope><orcidid>https://orcid.org/0009-0006-7283-775X</orcidid><orcidid>https://orcid.org/0000-0001-6025-7826</orcidid><orcidid>https://orcid.org/0009-0008-5975-4460</orcidid><orcidid>https://orcid.org/0009-0001-5781-1811</orcidid><orcidid>https://orcid.org/0000-0002-1573-5259</orcidid></search><sort><creationdate>20230502</creationdate><title>A sustainable approach for nickel nanoparticles synthesis: expeditious access to N-heterocycles under heterogeneous condition and photophysical studies</title><author>Hegde, Rajeev V ; Ghosh, Arnab ; Limaye, Akshay S ; Rode, Haridas B ; Sridhar, Balasubramanian ; Dateer, Ramesh B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c281t-789cbca6de513602bcb9d0816a87c7c44053ecab0aa4a97845a145d67479c5503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Additives</topic><topic>Aminoquinolines</topic><topic>Chemical reactions</topic><topic>Chemical synthesis</topic><topic>Dehydrogenation</topic><topic>Nanoparticles</topic><topic>Quinoline</topic><topic>Recyclability</topic><topic>Reducing agents</topic><topic>Stabilizers (agents)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hegde, Rajeev V</creatorcontrib><creatorcontrib>Ghosh, Arnab</creatorcontrib><creatorcontrib>Limaye, Akshay S</creatorcontrib><creatorcontrib>Rode, Haridas B</creatorcontrib><creatorcontrib>Sridhar, Balasubramanian</creatorcontrib><creatorcontrib>Dateer, Ramesh B</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Illustrata: Natural Sciences</collection><collection>Materials Research Database</collection><collection>ProQuest Illustrata: Technology Collection</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hegde, Rajeev V</au><au>Ghosh, Arnab</au><au>Limaye, Akshay S</au><au>Rode, Haridas B</au><au>Sridhar, Balasubramanian</au><au>Dateer, Ramesh B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A sustainable approach for nickel nanoparticles synthesis: expeditious access to N-heterocycles under heterogeneous condition and photophysical studies</atitle><jtitle>New journal of chemistry</jtitle><date>2023-05-02</date><risdate>2023</risdate><volume>47</volume><issue>17</issue><spage>8268</spage><epage>8276</epage><pages>8268-8276</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC
2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time. The phytochemicals found in
Portulaca oleracea
leaf extract were found to serve as a reducing agent and subsequently act as a stabilizing agent. The various analytical and spectroscopic techniques confirm the formation of Ni-NPs. The catalytic potential of Ni-NPs was investigated to achieve cost-effective, sustainable, atom and step economic synthesis of pharmaceutically important quinazoline, 2-aminoquinoline, and
N
-(alkyl amino) quinoline
via
hydrogen auto transfer and acceptorless dehydrogenative annulation without the aid of external ligand and additives. Importantly, the photophysical property studies of the synthesized N-heterocycles are deliberated and gram-scale synthesis was achieved. Moreover, catalyst recyclability, control experiments, and mechanistic elucidation were elaborated.
A sustainable and environmentally benign biogenic technique for one-step synthesis of Ni-NPs (NiC
2
O
4
·2H
2
O-NPs) using
Portulaca oleracea
(purslane) leaf extract has been disclosed for the first time.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d3nj00988b</doi><tpages>9</tpages><orcidid>https://orcid.org/0009-0006-7283-775X</orcidid><orcidid>https://orcid.org/0000-0001-6025-7826</orcidid><orcidid>https://orcid.org/0009-0008-5975-4460</orcidid><orcidid>https://orcid.org/0009-0001-5781-1811</orcidid><orcidid>https://orcid.org/0000-0002-1573-5259</orcidid></addata></record> |
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identifier | ISSN: 1144-0546 |
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language | eng |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Additives Aminoquinolines Chemical reactions Chemical synthesis Dehydrogenation Nanoparticles Quinoline Recyclability Reducing agents Stabilizers (agents) |
title | A sustainable approach for nickel nanoparticles synthesis: expeditious access to N-heterocycles under heterogeneous condition and photophysical studies |
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