Catecholase activity investigations using in situ copper complexes with pyrazole and pyridine based ligands
[Display omitted] ► All copper complexes formed in situ catalyze the oxidation reaction of catechol. ► Oxidation reaction rate depends on four parameters. ► The highest rate activity is given by L4 [Cu(CH3COO)2]. The in situ copper (II) complexes of six pyrazole and pyridine based ligands: 1-[5-meth...
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Veröffentlicht in: | Applied catalysis. A, General General, 2013-03, Vol.454, p.93-99 |
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description | [Display omitted]
► All copper complexes formed in situ catalyze the oxidation reaction of catechol. ► Oxidation reaction rate depends on four parameters. ► The highest rate activity is given by L4 [Cu(CH3COO)2].
The in situ copper (II) complexes of six pyrazole and pyridine based ligands: 1-[5-methyl-1-pyridin-2-yl-1H-pyrazol-3-yl] methanol L1, 2-(3,5-dimethyl-pyrazol-1-yl)-pyridine L2, (5-methyl-3-pyridin-2-yl-1H-pyrazol-1-yl) ethyl acetate L3, 1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-ethyl carboxylat L4, (1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-yl) methanol L5, and 5,5′-diphenyl-3,3′-bipyrazole L6, are reported and studied for their catecholase activities at ambient conditions, the reaction rate depends on four parameters: The nature of the carbonic chain bounded to the pyrazole ring, the nature of counter anion, the concentration of ligand and the nature of solvent. The highest rate activity is given by complex resulting from one equivalent of ligand L4 and two equivalents of Cu(CH3COO)2 in methanol, which equal to 4.440μmolL−1min−1. |
doi_str_mv | 10.1016/j.apcata.2013.01.011 |
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► All copper complexes formed in situ catalyze the oxidation reaction of catechol. ► Oxidation reaction rate depends on four parameters. ► The highest rate activity is given by L4 [Cu(CH3COO)2].
The in situ copper (II) complexes of six pyrazole and pyridine based ligands: 1-[5-methyl-1-pyridin-2-yl-1H-pyrazol-3-yl] methanol L1, 2-(3,5-dimethyl-pyrazol-1-yl)-pyridine L2, (5-methyl-3-pyridin-2-yl-1H-pyrazol-1-yl) ethyl acetate L3, 1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-ethyl carboxylat L4, (1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-yl) methanol L5, and 5,5′-diphenyl-3,3′-bipyrazole L6, are reported and studied for their catecholase activities at ambient conditions, the reaction rate depends on four parameters: The nature of the carbonic chain bounded to the pyrazole ring, the nature of counter anion, the concentration of ligand and the nature of solvent. The highest rate activity is given by complex resulting from one equivalent of ligand L4 and two equivalents of Cu(CH3COO)2 in methanol, which equal to 4.440μmolL−1min−1.</description><identifier>ISSN: 0926-860X</identifier><identifier>EISSN: 1873-3875</identifier><identifier>DOI: 10.1016/j.apcata.2013.01.011</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Catalysis ; Catechol ; Chemistry ; Copper ; Equivalence ; Exact sciences and technology ; General and physical chemistry ; Ligands ; Methyl alcohol ; Nitrogen heterocycles ; Oxidation reaction ; Pyrazole ; Pyridines ; Pyridylpyrazole ; Solvents ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><ispartof>Applied catalysis. A, General, 2013-03, Vol.454, p.93-99</ispartof><rights>2013 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-3e5d6800aa1d78f23229c3f9312808cdcc94701c932efda3792ce276ce6e4bf93</citedby><cites>FETCH-LOGICAL-c406t-3e5d6800aa1d78f23229c3f9312808cdcc94701c932efda3792ce276ce6e4bf93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0926860X13000380$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27216331$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Mouadili, A.</creatorcontrib><creatorcontrib>Attayibat, A.</creatorcontrib><creatorcontrib>Kadiri, S. El</creatorcontrib><creatorcontrib>Radi, S.</creatorcontrib><creatorcontrib>Touzani, R.</creatorcontrib><title>Catecholase activity investigations using in situ copper complexes with pyrazole and pyridine based ligands</title><title>Applied catalysis. A, General</title><description>[Display omitted]
► All copper complexes formed in situ catalyze the oxidation reaction of catechol. ► Oxidation reaction rate depends on four parameters. ► The highest rate activity is given by L4 [Cu(CH3COO)2].
The in situ copper (II) complexes of six pyrazole and pyridine based ligands: 1-[5-methyl-1-pyridin-2-yl-1H-pyrazol-3-yl] methanol L1, 2-(3,5-dimethyl-pyrazol-1-yl)-pyridine L2, (5-methyl-3-pyridin-2-yl-1H-pyrazol-1-yl) ethyl acetate L3, 1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-ethyl carboxylat L4, (1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-yl) methanol L5, and 5,5′-diphenyl-3,3′-bipyrazole L6, are reported and studied for their catecholase activities at ambient conditions, the reaction rate depends on four parameters: The nature of the carbonic chain bounded to the pyrazole ring, the nature of counter anion, the concentration of ligand and the nature of solvent. The highest rate activity is given by complex resulting from one equivalent of ligand L4 and two equivalents of Cu(CH3COO)2 in methanol, which equal to 4.440μmolL−1min−1.</description><subject>Catalysis</subject><subject>Catechol</subject><subject>Chemistry</subject><subject>Copper</subject><subject>Equivalence</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Ligands</subject><subject>Methyl alcohol</subject><subject>Nitrogen heterocycles</subject><subject>Oxidation reaction</subject><subject>Pyrazole</subject><subject>Pyridines</subject><subject>Pyridylpyrazole</subject><subject>Solvents</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><issn>0926-860X</issn><issn>1873-3875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kE1rGzEQhkVpoW6Sf9CDLoVe1tXXancvhWL6BYFeGuhNTEazidy1divJbt1fHxmHHAMDwwzPvC_zMvZWirUU0n7YrmFBKLBWQuq1kLXkC7aSfacb3XftS7YSg7JNb8Wv1-xNzlshhDJDu2K_N1AI7-cJMnHAEg6hHHmIB8ol3EEJc8x8n0O8q0ueQ9lznJeFUm27ZaJ_lPnfUO75ckzwf56qSPSnIfgQid9WWc-nqhR9vmSvRpgyXT32C3bz5fPPzbfm-sfX75tP1w0aYUujqfW2FwJA-q4flVZqQD0OWqpe9OgRB9MJiYNWNHrQ3aCQVGeRLJnbyl2w92fdJc1_9vURtwsZaZog0rzPThprWjOYvq2oOaOY5pwTjW5JYQfp6KRwp2zd1p2zdadsnZC1ZD179-gAGWEaE0QM-elWdUparU_cxzNH9d1DoOQyBopIPiTC4vwcnjd6AAq_k4c</recordid><startdate>20130315</startdate><enddate>20130315</enddate><creator>Mouadili, A.</creator><creator>Attayibat, A.</creator><creator>Kadiri, S. El</creator><creator>Radi, S.</creator><creator>Touzani, R.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130315</creationdate><title>Catecholase activity investigations using in situ copper complexes with pyrazole and pyridine based ligands</title><author>Mouadili, A. ; Attayibat, A. ; Kadiri, S. El ; Radi, S. ; Touzani, R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-3e5d6800aa1d78f23229c3f9312808cdcc94701c932efda3792ce276ce6e4bf93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Catalysis</topic><topic>Catechol</topic><topic>Chemistry</topic><topic>Copper</topic><topic>Equivalence</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Ligands</topic><topic>Methyl alcohol</topic><topic>Nitrogen heterocycles</topic><topic>Oxidation reaction</topic><topic>Pyrazole</topic><topic>Pyridines</topic><topic>Pyridylpyrazole</topic><topic>Solvents</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mouadili, A.</creatorcontrib><creatorcontrib>Attayibat, A.</creatorcontrib><creatorcontrib>Kadiri, S. El</creatorcontrib><creatorcontrib>Radi, S.</creatorcontrib><creatorcontrib>Touzani, R.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied catalysis. A, General</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mouadili, A.</au><au>Attayibat, A.</au><au>Kadiri, S. El</au><au>Radi, S.</au><au>Touzani, R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catecholase activity investigations using in situ copper complexes with pyrazole and pyridine based ligands</atitle><jtitle>Applied catalysis. A, General</jtitle><date>2013-03-15</date><risdate>2013</risdate><volume>454</volume><spage>93</spage><epage>99</epage><pages>93-99</pages><issn>0926-860X</issn><eissn>1873-3875</eissn><abstract>[Display omitted]
► All copper complexes formed in situ catalyze the oxidation reaction of catechol. ► Oxidation reaction rate depends on four parameters. ► The highest rate activity is given by L4 [Cu(CH3COO)2].
The in situ copper (II) complexes of six pyrazole and pyridine based ligands: 1-[5-methyl-1-pyridin-2-yl-1H-pyrazol-3-yl] methanol L1, 2-(3,5-dimethyl-pyrazol-1-yl)-pyridine L2, (5-methyl-3-pyridin-2-yl-1H-pyrazol-1-yl) ethyl acetate L3, 1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-ethyl carboxylat L4, (1′,5,5′-trimethyl-1′H-1,3′-bipyrazol-3-yl) methanol L5, and 5,5′-diphenyl-3,3′-bipyrazole L6, are reported and studied for their catecholase activities at ambient conditions, the reaction rate depends on four parameters: The nature of the carbonic chain bounded to the pyrazole ring, the nature of counter anion, the concentration of ligand and the nature of solvent. The highest rate activity is given by complex resulting from one equivalent of ligand L4 and two equivalents of Cu(CH3COO)2 in methanol, which equal to 4.440μmolL−1min−1.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcata.2013.01.011</doi><tpages>7</tpages></addata></record> |
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subjects | Catalysis Catechol Chemistry Copper Equivalence Exact sciences and technology General and physical chemistry Ligands Methyl alcohol Nitrogen heterocycles Oxidation reaction Pyrazole Pyridines Pyridylpyrazole Solvents Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Catecholase activity investigations using in situ copper complexes with pyrazole and pyridine based ligands |
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