Electrochemistry of catechol terminated monolayers with Cu(II), Ni(II) and Fe(III) cations : a model for the marine adhesive interface

The redox electrochemistry of hydroquinone and Cu2+-, Ni2+-, and Fe3+-hydroquinone complexes immobilized at the SAM interface has been studied in aqueous solutions with pH 5 to 12 using cyclic voltammetry. Self-assembled monolayers were constructed with terminal hydroquinone residues designed to mod...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1991. - 24(2008), 16 vom: 19. Aug., Seite 9074-81
1. Verfasser: Brooksby, Paula A (VerfasserIn)
Weitere Verfasser: Schiel, David R, Abell, Andrew D
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2008
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Adhesives Alkanes Catechols Cations Sulfhydryl Compounds Copper 789U1901C5 Nickel mehr... 7OV03QG267 Iron E1UOL152H7 catechol LF3AJ089DQ
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245 1 0 |a Electrochemistry of catechol terminated monolayers with Cu(II), Ni(II) and Fe(III) cations  |b a model for the marine adhesive interface 
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520 |a The redox electrochemistry of hydroquinone and Cu2+-, Ni2+-, and Fe3+-hydroquinone complexes immobilized at the SAM interface has been studied in aqueous solutions with pH 5 to 12 using cyclic voltammetry. Self-assembled monolayers were constructed with terminal hydroquinone residues designed to model marine adhesive proteins that use the DOPA (3,4-dihydroxyphenylalanine) moiety. Coordination of metal to the hydroquinone group results in a shift to the ligand oxidation potential, with the value for Delta E p,a dependent on the solution pH and identity of the metal. Cu2+ shifts the hydroquinone oxidation by -285 mV (pH 8.8), and Ni2+ by -194 mV (pH 9.16). The hydroquinone oxidation was shifted by -440 mV at pH 5 for Fe3+ solutions examined up to pH 7. By contrast, reduction of the quinone is unperturbed by the presence of Cu2+, Ni2+, and Fe3+ ions. Implications of these results to the mechanism of marine adhesion are discussed 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Adhesives  |2 NLM 
650 7 |a Alkanes  |2 NLM 
650 7 |a Catechols  |2 NLM 
650 7 |a Cations  |2 NLM 
650 7 |a Sulfhydryl Compounds  |2 NLM 
650 7 |a Copper  |2 NLM 
650 7 |a 789U1901C5  |2 NLM 
650 7 |a Nickel  |2 NLM 
650 7 |a 7OV03QG267  |2 NLM 
650 7 |a Iron  |2 NLM 
650 7 |a E1UOL152H7  |2 NLM 
650 7 |a catechol  |2 NLM 
650 7 |a LF3AJ089DQ  |2 NLM 
700 1 |a Schiel, David R  |e verfasserin  |4 aut 
700 1 |a Abell, Andrew D  |e verfasserin  |4 aut 
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