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Mark R. Anderson

Self-assembled monolayers

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Full-Text Articles in Physical Sciences and Mathematics

Potential Driven Deposition Of Polyelectrolytes Onto The Surface Of Cysteine Monolayers Assembled On Gold, Wesley Sanders, Mark Anderson Feb 2010

Potential Driven Deposition Of Polyelectrolytes Onto The Surface Of Cysteine Monolayers Assembled On Gold, Wesley Sanders, Mark Anderson

Mark R. Anderson

Electrochemical impedance spectroscopy and the quartz crystal microbalance measurements are used to examine the ability of potential applied to a substrate to create, in situ, conditions favorable for the electrostatic deposition of polyelectrolytes onto a gold substrate modified by the self-assembly of cysteine. Cysteine is a zwitterionic compound that, when confined to a substrate, has the ability to establish either a net positive or a net negative interfacial charge, depending on the conditions. As such, cysteine modified interfaces could possibly be used as a versatile substrate for deposition of either cationic or anionic polyelectrolytes. The potential of zero charge of …


Reductivedesorption Of 11-Mercaptoundecanoic Acid Monolayers Modified By Covalent Attachment Of 1,3- And 1,4-Phenylenediamine, Mark Anderson, Richard Baltzersen Jul 2003

Reductivedesorption Of 11-Mercaptoundecanoic Acid Monolayers Modified By Covalent Attachment Of 1,3- And 1,4-Phenylenediamine, Mark Anderson, Richard Baltzersen

Mark R. Anderson

1,3- and 1,4-phenylenediamine were covalently attached to a self-assembled monolayer of 11-mercaptoundecanoic acid by formation of an amide bond. Bonding of the phenylenediamine isomers was confirmed by the presence of infrared features attributable to ring vibrational modes, the amide I vibration, and the amide II vibration in the reflection–absorption infrared spectrum of the modified interface. Reductivedesorption peak potentials were shifted by 120 mV for the monolayer modified by 1,4-phenylenediamine and by 90 mV for the monolayer modified by 1,3-phenylenediamine relative to the desorption potential of the unmodified 11-mercaptoundecanoic acid monolayer. These potential shifts represent 23 and 17 kJ/mol stabilization of …