Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II)
The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocate...
Ausführliche Beschreibung
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Deutsch |
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1982 |
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8 Ill. ; 3 Tab. 12 |
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Wiley InterScience Backfile Collection 1832-2000 |
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in: Helvetica Chimica Acta - New York, NY : Wiley-VCH, 65(1982) vom: Juni, Seite 1929-1940 |
Übergeordnetes Werk: |
volume:65 ; year:1982 ; month:06 ; pages:1929-1940 ; extent:12 |
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520 | |a The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. | ||
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(DE-627)NLEJ162645627 DE-627 ger DE-627 rakwb ger Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) 1982 8 Ill. 3 Tab. 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. Wiley InterScience Backfile Collection 1832-2000 Plancherel, Dominique oth von Zelewsky, Alex oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 65(1982) vom: Juni, Seite 1929-1940 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:65 year:1982 month:06 pages:1929-1940 extent:12 http://dx.doi.org/10.1002/hlca.19820650627 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 65 1982 6 1929-1940 12 |
spelling |
(DE-627)NLEJ162645627 DE-627 ger DE-627 rakwb ger Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) 1982 8 Ill. 3 Tab. 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. Wiley InterScience Backfile Collection 1832-2000 Plancherel, Dominique oth von Zelewsky, Alex oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 65(1982) vom: Juni, Seite 1929-1940 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:65 year:1982 month:06 pages:1929-1940 extent:12 http://dx.doi.org/10.1002/hlca.19820650627 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 65 1982 6 1929-1940 12 |
allfields_unstemmed |
(DE-627)NLEJ162645627 DE-627 ger DE-627 rakwb ger Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) 1982 8 Ill. 3 Tab. 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. Wiley InterScience Backfile Collection 1832-2000 Plancherel, Dominique oth von Zelewsky, Alex oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 65(1982) vom: Juni, Seite 1929-1940 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:65 year:1982 month:06 pages:1929-1940 extent:12 http://dx.doi.org/10.1002/hlca.19820650627 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 65 1982 6 1929-1940 12 |
allfieldsGer |
(DE-627)NLEJ162645627 DE-627 ger DE-627 rakwb ger Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) 1982 8 Ill. 3 Tab. 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. Wiley InterScience Backfile Collection 1832-2000 Plancherel, Dominique oth von Zelewsky, Alex oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 65(1982) vom: Juni, Seite 1929-1940 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:65 year:1982 month:06 pages:1929-1940 extent:12 http://dx.doi.org/10.1002/hlca.19820650627 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 65 1982 6 1929-1940 12 |
allfieldsSound |
(DE-627)NLEJ162645627 DE-627 ger DE-627 rakwb ger Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) 1982 8 Ill. 3 Tab. 12 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. Wiley InterScience Backfile Collection 1832-2000 Plancherel, Dominique oth von Zelewsky, Alex oth in Helvetica Chimica Acta New York, NY : Wiley-VCH 65(1982) vom: Juni, Seite 1929-1940 (DE-627)NLEJ159071178 (DE-600)1475013-2 0018-019X nnns volume:65 year:1982 month:06 pages:1929-1940 extent:12 http://dx.doi.org/10.1002/hlca.19820650627 text/html Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-WIS GBV_NL_ARTICLE AR 65 1982 6 1929-1940 12 |
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Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) |
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Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) |
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Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) |
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Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) |
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photon-triggered complex formation: radical complexes of o-benzosemiquinone, dopa, dopamine and adrenaline formed by electron-transfer reaction from excited tris (2,2′-bipyridyl)ruthenium (ii) |
title_auth |
Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) |
abstract |
The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. |
abstractGer |
The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. |
abstract_unstemmed |
The pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier. |
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Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II) |
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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">NLEJ162645627</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20210707094451.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">070201s1982 xx |||||o 00| ||ger c</controlfield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ162645627</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">ger</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Photon-Triggered Complex Formation: Radical Complexes of o-Benzosemiquinone, Dopa, Dopamine and Adrenaline Formed by Electron-Transfer Reaction from Excited Tris (2,2′-bipyridyl)ruthenium (II)</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1982</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="b">8 Ill.</subfield><subfield code="b">3 Tab.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">12</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 pyrocatechol derivatives, dopamine (2), adrenaline (3) and L-dopa (4) form in their semiquinoid oxidation states complexes with several closed-shell metal ions like Zn2+, Cd2+ and Y3+. This complex formation can be triggered by visible light via a one-electron transfer reaction from the pyrocatechol derivative to (3CT)Ru(bpy)32+, which is thereby reduced (Schemes 1 and 2), The quenching of the triplet charge-transfer state, (3CT)Ru(bpy)32+ cannot be measured by conventional methods (Stern-Volmer plot), because the bimolecular electron-transfer rate is too slow (kq < 10-7 M-1 s-1). ESR. spectroscopy shows, however, clearly the paramagnetic reaction products. The concentration of these paramagnetic species is strongly enhanced by complex formation.The hindered rotation of the side chain in L-dopa and in its Y3+-complex is described within a two-jump model, which gives best agreement between calculated and measured spectra assuming an energy of 37 kJmol-1 for the rotational barrier.</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">Plancherel, Dominique</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">von Zelewsky, Alex</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">in</subfield><subfield code="t">Helvetica Chimica Acta</subfield><subfield code="d">New York, NY : Wiley-VCH</subfield><subfield code="g">65(1982) vom: Juni, Seite 1929-1940</subfield><subfield code="w">(DE-627)NLEJ159071178</subfield><subfield code="w">(DE-600)1475013-2</subfield><subfield code="x">0018-019X</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:65</subfield><subfield code="g">year:1982</subfield><subfield code="g">month:06</subfield><subfield code="g">pages:1929-1940</subfield><subfield code="g">extent:12</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1002/hlca.19820650627</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">65</subfield><subfield code="j">1982</subfield><subfield code="c">6</subfield><subfield code="h">1929-1940</subfield><subfield code="g">12</subfield></datafield></record></collection>
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