Supra-Amphiphilic Porphyrin Based on Thermoresponsive Poly(N-Isopropylacrylamide-co-2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium) Hydrogels: Synthesis, Characterization and Catalytic Applications

The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly call...

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Veröffentlicht in:Catalysis letters 2023-11, Vol.153 (11), p.3342-3356
Hauptverfasser: Maddahzadeh-Darini, Nastaran, Ghorbanloo, Massomeh
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description The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly called p(NIPAM- co-Na AMPS)‐[Mn(TMPyP)]. Free-radical polymerization at ambient temperature was employed to construct this catalytic system. To prepare this temperature-sensitive catalyst, “smart” poly(N-isopropylacrylamide- co -NaAMPS) was axially grafted onto the metal centers of the Mn III composite. Dynamic light scattering was used to determine the temperature-responsiveness of the catalyst and the hydrodynamic radii of the constructed compounds. In order to identify the amounts of metals in prepared compound, atomic absorption spectroscopy (AAS) was utilized. The results indicated that p(NIPAM- co-Na AMPS)‐[Mn(TMPyP)] had the potential to efficiently catalyze olefin oxidation with high selectivity in the solid–liquid biphasic reaction system. Furthermore, the catalytic activities of styrene, α -methyl-styrene, cis -cyclooctene, indene oxidation by the reaction-controlled phase transfer catalyst system were compared in the presence of hydrogen peroxide (H 2 O 2 ) and tert -Butyl hydroperoxide (TBHP), as oxidants, in a biphasic environment. It was found that functioning as a nanoreactor, the prepared catalyst system facilitated the epoxidation of un-functionalized olefins in water, leading to the substantial acceleration of catalytic reaction rates. After the completion of the catalytic activity, the catalyst could be separated easily from the reaction media by manipulating temperature and reused without any activity loss. In effect, the quality of the catalyst remained the same for eight cycles. In a similar vein, the FT-IR spectra and atomic absorption spectroscopy confirmed the great recyclability, durability, and leaching resistance of the catalyst. Graphical Abstract The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly called P(NIPAM- co-Na AMPS)‐[Mn(TMPyP)].
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Free-radical polymerization at ambient temperature was employed to construct this catalytic system. To prepare this temperature-sensitive catalyst, “smart” poly(N-isopropylacrylamide- co -NaAMPS) was axially grafted onto the metal centers of the Mn III composite. Dynamic light scattering was used to determine the temperature-responsiveness of the catalyst and the hydrodynamic radii of the constructed compounds. In order to identify the amounts of metals in prepared compound, atomic absorption spectroscopy (AAS) was utilized. The results indicated that p(NIPAM- co-Na AMPS)‐[Mn(TMPyP)] had the potential to efficiently catalyze olefin oxidation with high selectivity in the solid–liquid biphasic reaction system. Furthermore, the catalytic activities of styrene, α -methyl-styrene, cis -cyclooctene, indene oxidation by the reaction-controlled phase transfer catalyst system were compared in the presence of hydrogen peroxide (H 2 O 2 ) and tert -Butyl hydroperoxide (TBHP), as oxidants, in a biphasic environment. It was found that functioning as a nanoreactor, the prepared catalyst system facilitated the epoxidation of un-functionalized olefins in water, leading to the substantial acceleration of catalytic reaction rates. After the completion of the catalytic activity, the catalyst could be separated easily from the reaction media by manipulating temperature and reused without any activity loss. In effect, the quality of the catalyst remained the same for eight cycles. In a similar vein, the FT-IR spectra and atomic absorption spectroscopy confirmed the great recyclability, durability, and leaching resistance of the catalyst. Graphical Abstract The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly called P(NIPAM- co-Na AMPS)‐[Mn(TMPyP)].</description><identifier>ISSN: 1011-372X</identifier><identifier>EISSN: 1572-879X</identifier><identifier>DOI: 10.1007/s10562-022-04241-7</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Absorption spectroscopy ; Acceleration ; Alkenes ; Ambient temperature ; Anabolic steroids ; Atomic absorption analysis ; Atomic properties ; Butyl hydroperoxide ; Catalysis ; Catalytic activity ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Epoxidation ; Free radical polymerization ; Hydrogels ; Hydrogen peroxide ; Indene ; Industrial Chemistry/Chemical Engineering ; Infrared spectroscopy ; Isopropylacrylamide ; Leaching ; Manganese ; Olefins ; Organometallic Chemistry ; Oxidation ; Oxidizing agents ; Peroxides ; Phase transfer catalysts ; Photon correlation spectroscopy ; Physical Chemistry ; Polymerization ; Porphyrins ; Sodium ; Spectrum analysis ; Styrenes</subject><ispartof>Catalysis letters, 2023-11, Vol.153 (11), p.3342-3356</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022. 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.</rights><rights>COPYRIGHT 2023 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-dab47922680141f159598b1034dcb88448e14f24ee67f81dfd726cd3353b03f23</citedby><cites>FETCH-LOGICAL-c386t-dab47922680141f159598b1034dcb88448e14f24ee67f81dfd726cd3353b03f23</cites><orcidid>0000-0002-2224-0975 ; 0000-0003-2399-1559</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10562-022-04241-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10562-022-04241-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27933,27934,41497,42566,51328</link.rule.ids></links><search><creatorcontrib>Maddahzadeh-Darini, Nastaran</creatorcontrib><creatorcontrib>Ghorbanloo, Massomeh</creatorcontrib><title>Supra-Amphiphilic Porphyrin Based on Thermoresponsive Poly(N-Isopropylacrylamide-co-2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium) Hydrogels: Synthesis, Characterization and Catalytic Applications</title><title>Catalysis letters</title><addtitle>Catal Lett</addtitle><description>The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly called p(NIPAM- co-Na AMPS)‐[Mn(TMPyP)]. Free-radical polymerization at ambient temperature was employed to construct this catalytic system. To prepare this temperature-sensitive catalyst, “smart” poly(N-isopropylacrylamide- co -NaAMPS) was axially grafted onto the metal centers of the Mn III composite. Dynamic light scattering was used to determine the temperature-responsiveness of the catalyst and the hydrodynamic radii of the constructed compounds. In order to identify the amounts of metals in prepared compound, atomic absorption spectroscopy (AAS) was utilized. The results indicated that p(NIPAM- co-Na AMPS)‐[Mn(TMPyP)] had the potential to efficiently catalyze olefin oxidation with high selectivity in the solid–liquid biphasic reaction system. Furthermore, the catalytic activities of styrene, α -methyl-styrene, cis -cyclooctene, indene oxidation by the reaction-controlled phase transfer catalyst system were compared in the presence of hydrogen peroxide (H 2 O 2 ) and tert -Butyl hydroperoxide (TBHP), as oxidants, in a biphasic environment. It was found that functioning as a nanoreactor, the prepared catalyst system facilitated the epoxidation of un-functionalized olefins in water, leading to the substantial acceleration of catalytic reaction rates. After the completion of the catalytic activity, the catalyst could be separated easily from the reaction media by manipulating temperature and reused without any activity loss. In effect, the quality of the catalyst remained the same for eight cycles. In a similar vein, the FT-IR spectra and atomic absorption spectroscopy confirmed the great recyclability, durability, and leaching resistance of the catalyst. Graphical Abstract The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly called P(NIPAM- co-Na AMPS)‐[Mn(TMPyP)].</description><subject>Absorption spectroscopy</subject><subject>Acceleration</subject><subject>Alkenes</subject><subject>Ambient temperature</subject><subject>Anabolic steroids</subject><subject>Atomic absorption analysis</subject><subject>Atomic properties</subject><subject>Butyl hydroperoxide</subject><subject>Catalysis</subject><subject>Catalytic activity</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Epoxidation</subject><subject>Free radical polymerization</subject><subject>Hydrogels</subject><subject>Hydrogen peroxide</subject><subject>Indene</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Infrared spectroscopy</subject><subject>Isopropylacrylamide</subject><subject>Leaching</subject><subject>Manganese</subject><subject>Olefins</subject><subject>Organometallic Chemistry</subject><subject>Oxidation</subject><subject>Oxidizing agents</subject><subject>Peroxides</subject><subject>Phase transfer catalysts</subject><subject>Photon correlation spectroscopy</subject><subject>Physical Chemistry</subject><subject>Polymerization</subject><subject>Porphyrins</subject><subject>Sodium</subject><subject>Spectrum analysis</subject><subject>Styrenes</subject><issn>1011-372X</issn><issn>1572-879X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9UtmKFDEULUTBcfQHfAr4omDGJLWkyreyUWdgXKBHmLeQTm66MlQlmaRKKL_QzzI97YIgkvXenHOXcIriKSVnlBD-KlFSNwwTllfFKor5veKE1pzhlnfX9_OdUIpLzq4fFo9SuiGEdJx2J8X37RKixP0UBpvnaBX67GMY1mgdeiMTaOQduhogTj5CCt4l-xUyZlyff8QXyYfowzpKFfM2WQ1Yecxw_8s-GB9gHtbxAJQO0HYZjXc5T6-sRluv7TK9QOerjn4PY3qNtqubB0g2vUSbQUapZoj2m5xtLkQ6jTZyluM6HyKEkAu-e0mPiwdGjgme_DxPiy_v3l5tzvHlp_cXm_4Sq7JtZqzlruIdY01LaEUNrbu6a3eUlJVWu7atqhZoZVgF0HDTUm00Z43SZVmXO1IaVp4Wz45xcz-3C6RZ3PglupxSsDZ_Ka9pxv5G7eUIwjrj59zIZJMSPW84J13XNRl19g9UHhomq7wDY7P_LwI7ElT0KUUwIkQ7ybgKSsRBCOIoBJGFIO6EIHgmlUdSymC3h_in4v-wfgDgWbkc</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Maddahzadeh-Darini, Nastaran</creator><creator>Ghorbanloo, Massomeh</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><orcidid>https://orcid.org/0000-0002-2224-0975</orcidid><orcidid>https://orcid.org/0000-0003-2399-1559</orcidid></search><sort><creationdate>20231101</creationdate><title>Supra-Amphiphilic Porphyrin Based on Thermoresponsive Poly(N-Isopropylacrylamide-co-2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium) Hydrogels: Synthesis, Characterization and Catalytic Applications</title><author>Maddahzadeh-Darini, Nastaran ; 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Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Catalysis letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maddahzadeh-Darini, Nastaran</au><au>Ghorbanloo, Massomeh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Supra-Amphiphilic Porphyrin Based on Thermoresponsive Poly(N-Isopropylacrylamide-co-2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium) Hydrogels: Synthesis, Characterization and Catalytic Applications</atitle><jtitle>Catalysis letters</jtitle><stitle>Catal Lett</stitle><date>2023-11-01</date><risdate>2023</risdate><volume>153</volume><issue>11</issue><spage>3342</spage><epage>3356</epage><pages>3342-3356</pages><issn>1011-372X</issn><eissn>1572-879X</eissn><abstract>The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly called p(NIPAM- co-Na AMPS)‐[Mn(TMPyP)]. Free-radical polymerization at ambient temperature was employed to construct this catalytic system. To prepare this temperature-sensitive catalyst, “smart” poly(N-isopropylacrylamide- co -NaAMPS) was axially grafted onto the metal centers of the Mn III composite. Dynamic light scattering was used to determine the temperature-responsiveness of the catalyst and the hydrodynamic radii of the constructed compounds. In order to identify the amounts of metals in prepared compound, atomic absorption spectroscopy (AAS) was utilized. The results indicated that p(NIPAM- co-Na AMPS)‐[Mn(TMPyP)] had the potential to efficiently catalyze olefin oxidation with high selectivity in the solid–liquid biphasic reaction system. Furthermore, the catalytic activities of styrene, α -methyl-styrene, cis -cyclooctene, indene oxidation by the reaction-controlled phase transfer catalyst system were compared in the presence of hydrogen peroxide (H 2 O 2 ) and tert -Butyl hydroperoxide (TBHP), as oxidants, in a biphasic environment. It was found that functioning as a nanoreactor, the prepared catalyst system facilitated the epoxidation of un-functionalized olefins in water, leading to the substantial acceleration of catalytic reaction rates. After the completion of the catalytic activity, the catalyst could be separated easily from the reaction media by manipulating temperature and reused without any activity loss. In effect, the quality of the catalyst remained the same for eight cycles. In a similar vein, the FT-IR spectra and atomic absorption spectroscopy confirmed the great recyclability, durability, and leaching resistance of the catalyst. Graphical Abstract The present study aims to introduce a new catalytic system, namely, thermo-responsive amphiphilic manganese porphyrin-paired ionic co -polymeric hydrogel, poly(N-isopropylacrylamide- co -2-acrylamido-2-methylpropane sulfonic acid sodium)-Mn (III) meso tetra(N-methyl-4-pyridyl) porphine, briefly called P(NIPAM- co-Na AMPS)‐[Mn(TMPyP)].</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10562-022-04241-7</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-2224-0975</orcidid><orcidid>https://orcid.org/0000-0003-2399-1559</orcidid></addata></record>
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subjects Absorption spectroscopy
Acceleration
Alkenes
Ambient temperature
Anabolic steroids
Atomic absorption analysis
Atomic properties
Butyl hydroperoxide
Catalysis
Catalytic activity
Chemical synthesis
Chemistry
Chemistry and Materials Science
Epoxidation
Free radical polymerization
Hydrogels
Hydrogen peroxide
Indene
Industrial Chemistry/Chemical Engineering
Infrared spectroscopy
Isopropylacrylamide
Leaching
Manganese
Olefins
Organometallic Chemistry
Oxidation
Oxidizing agents
Peroxides
Phase transfer catalysts
Photon correlation spectroscopy
Physical Chemistry
Polymerization
Porphyrins
Sodium
Spectrum analysis
Styrenes
title Supra-Amphiphilic Porphyrin Based on Thermoresponsive Poly(N-Isopropylacrylamide-co-2-Acrylamido-2-Methylpropane Sulfonic Acid Sodium) Hydrogels: Synthesis, Characterization and Catalytic Applications
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