Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity
The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that...
Ausführliche Beschreibung
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Englisch |
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1994 |
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7 Ill. ; 7 Tab. 11 |
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Wiley InterScience Backfile Collection 1832-2000 |
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in: Journal of Polymer Science Part A: Polymer Chemistry - Bognor Regis [u.a.] : Wiley, 32(1994), Seite 2457-2467 |
Übergeordnetes Werk: |
volume:32 ; year:1994 ; month:13 ; pages:2457-2467 ; extent:11 |
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(DE-627)NLEJ164002278 DE-627 ger DE-627 rakwb eng Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity 1994 7 Ill. 7 Tab. 11 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. Wiley InterScience Backfile Collection 1832-2000 Nemoto, Nobukatsu oth Ishii, Hiroji oth Ihara, Manabu oth Takamiya, Nobuo oth Ikeda, Koji oth in Journal of Polymer Science Part A: Polymer Chemistry Bognor Regis [u.a.] : Wiley 32(1994), Seite 2457-2467 (DE-627)NLEJ159071542 (DE-600)1473076-5 0887-624X nnns volume:32 year:1994 month:13 pages:2457-2467 extent:11 http://dx.doi.org/10.1002/pola.1994.080321307 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 32 1994 13 2457-2467 11 |
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(DE-627)NLEJ164002278 DE-627 ger DE-627 rakwb eng Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity 1994 7 Ill. 7 Tab. 11 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. Wiley InterScience Backfile Collection 1832-2000 Nemoto, Nobukatsu oth Ishii, Hiroji oth Ihara, Manabu oth Takamiya, Nobuo oth Ikeda, Koji oth in Journal of Polymer Science Part A: Polymer Chemistry Bognor Regis [u.a.] : Wiley 32(1994), Seite 2457-2467 (DE-627)NLEJ159071542 (DE-600)1473076-5 0887-624X nnns volume:32 year:1994 month:13 pages:2457-2467 extent:11 http://dx.doi.org/10.1002/pola.1994.080321307 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 32 1994 13 2457-2467 11 |
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(DE-627)NLEJ164002278 DE-627 ger DE-627 rakwb eng Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity 1994 7 Ill. 7 Tab. 11 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. Wiley InterScience Backfile Collection 1832-2000 Nemoto, Nobukatsu oth Ishii, Hiroji oth Ihara, Manabu oth Takamiya, Nobuo oth Ikeda, Koji oth in Journal of Polymer Science Part A: Polymer Chemistry Bognor Regis [u.a.] : Wiley 32(1994), Seite 2457-2467 (DE-627)NLEJ159071542 (DE-600)1473076-5 0887-624X nnns volume:32 year:1994 month:13 pages:2457-2467 extent:11 http://dx.doi.org/10.1002/pola.1994.080321307 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 32 1994 13 2457-2467 11 |
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(DE-627)NLEJ164002278 DE-627 ger DE-627 rakwb eng Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity 1994 7 Ill. 7 Tab. 11 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. Wiley InterScience Backfile Collection 1832-2000 Nemoto, Nobukatsu oth Ishii, Hiroji oth Ihara, Manabu oth Takamiya, Nobuo oth Ikeda, Koji oth in Journal of Polymer Science Part A: Polymer Chemistry Bognor Regis [u.a.] : Wiley 32(1994), Seite 2457-2467 (DE-627)NLEJ159071542 (DE-600)1473076-5 0887-624X nnns volume:32 year:1994 month:13 pages:2457-2467 extent:11 http://dx.doi.org/10.1002/pola.1994.080321307 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 32 1994 13 2457-2467 11 |
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(DE-627)NLEJ164002278 DE-627 ger DE-627 rakwb eng Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity 1994 7 Ill. 7 Tab. 11 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. Wiley InterScience Backfile Collection 1832-2000 Nemoto, Nobukatsu oth Ishii, Hiroji oth Ihara, Manabu oth Takamiya, Nobuo oth Ikeda, Koji oth in Journal of Polymer Science Part A: Polymer Chemistry Bognor Regis [u.a.] : Wiley 32(1994), Seite 2457-2467 (DE-627)NLEJ159071542 (DE-600)1473076-5 0887-624X nnns volume:32 year:1994 month:13 pages:2457-2467 extent:11 http://dx.doi.org/10.1002/pola.1994.080321307 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 32 1994 13 2457-2467 11 |
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Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity |
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The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. |
abstractGer |
The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. |
abstract_unstemmed |
The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc. |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ164002278</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230506105403.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070201s1994 xx |||||o 00| ||eng c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ164002278</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Hydroquinone oxidation catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane. II.For Part I, see: Reference 40. Elucidation of factors related to catalytic activity</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1994</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="b">7 Ill.</subfield><subfield code="b">7 Tab.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">11</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">The oxidation of hydroquinone catalyzed by pyridine-Cu(II) complexes attached to polyorganosiloxane was investigated in the mixed solvent of methanol/water (vol. ratio 2/1). The catalytic oxidation followed Michaelis-Menten-like kinetics. The large k2 term related to a turnover number indicated that the present polymeric catalysts have a remarkable effect on the activation process. The methylene number between the side-chain acid amido and pyridyl groups of the polymeric ligand was shown to be closely related to the appearance of hydrophobic effects in both the substrate-binding and the activation processes as deduced from the Michaelis constant and the thermodynamic and activation parameters. The binding parameters for 4-methoxyphenol with pyridyl-functionalized polyorganosiloxanes supported that the flexible backbone is also effective in the oxidation of hydroquinone. The Cu(II) complexes with pyridyl-functionalized polyorganosiloxane would have the structures distorted from square planar formation, which would promote the reduction of Cu(II) to Cu(I), as concluded from ESR spectroscopy and electrochemical measurement. © 1994 John Wiley & Sons, Inc.</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Wiley InterScience Backfile Collection 1832-2000</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Nemoto, Nobukatsu</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ishii, Hiroji</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ihara, Manabu</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Takamiya, Nobuo</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ikeda, Koji</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Journal of Polymer Science Part A: Polymer Chemistry</subfield><subfield code="d">Bognor Regis [u.a.] : Wiley</subfield><subfield code="g">32(1994), Seite 2457-2467</subfield><subfield code="w">(DE-627)NLEJ159071542</subfield><subfield code="w">(DE-600)1473076-5</subfield><subfield code="x">0887-624X</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:32</subfield><subfield code="g">year:1994</subfield><subfield code="g">month:13</subfield><subfield code="g">pages:2457-2467</subfield><subfield code="g">extent:11</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1002/pola.1994.080321307</subfield><subfield code="q">text/html</subfield><subfield code="z">Deutschlandweit zugänglich</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-WIS</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">32</subfield><subfield code="j">1994</subfield><subfield code="c">13</subfield><subfield code="h">2457-2467</subfield><subfield code="g">11</subfield></datafield></record></collection>
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