Self-Assembled Monolayers Formed using Zero Net Curvature Norbornylogous Bridges: The Influence of Potential on Molecular Orientation

被引:13
作者
Eggers, Paul K. [1 ,2 ]
Da Silva, Paulo [2 ]
Darwish, Nadim A. [2 ]
Zhang, Yi [1 ]
Tong, Yujin [1 ]
Ye, Shen [1 ,3 ]
Paddon-Row, Michael N. [2 ]
Gooding, J. Justin [2 ]
机构
[1] Hokkaido Univ, Catalysis Res Ctr, Sapporo, Hokkaido 0010021, Japan
[2] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
[3] Japan Sci & Technol Agcy JST, PRESTO, Tokyo, Japan
基金
澳大利亚研究理事会; 日本科学技术振兴机构;
关键词
SCANNING ELECTROCHEMICAL MICROSCOPY; ELECTRON-TRANSFER PROCESSES; IN-SITU; ALKANETHIOLATE MONOLAYERS; TRIRUTHENIUM CLUSTER; CHARGE SEPARATION; THIOL MONOLAYERS; REDOX REACTION; FERROCENE; GOLD;
D O I
10.1021/la101590b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new class of electroactive norbornylogous bridges, with no net curvature, that form self-assembled monolayers on gold electrodes were studied by electrochemistry and in situ infrared spectroscopy. The influence of the electrode potential on the structure and conformation of the self-assembled monolayers (SAMs) was investigated. This was performed using two different lengths of rigid norbornylogous bridges with terminal ferrocene moieties and omega-hydroxyalkanethiols. It was found that single component monolayers of the rigid norbornylogous bridges changed their tilt angle with their transition from the ferrocene to ferricinium. However, when the norbornylogous SAMs were diluted with omega-hydroxyalkanethiols the tilt angle remained unchanged upon oxidation of ferrocene to ferricinium. It was also observed that the tilt angle of the diluent, omega-hydroxyalkanethiols changed at potentials exceeding 500 mV.
引用
收藏
页码:15665 / 15670
页数:6
相关论文
共 39 条
[1]   Charge transfer on the nanoscale: Current status [J].
Adams, DM ;
Brus, L ;
Chidsey, CED ;
Creager, S ;
Creutz, C ;
Kagan, CR ;
Kamat, PV ;
Lieberman, M ;
Lindsay, S ;
Marcus, RA ;
Metzger, RM ;
Michel-Beyerle, ME ;
Miller, JR ;
Newton, MD ;
Rolison, DR ;
Sankey, O ;
Schanze, KS ;
Yardley, J ;
Zhu, XY .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (28) :6668-6697
[2]   Length dependence of charge transport in nanoscopic molecular junctions incorporating a series of rigid thiol-terminated norbornylogs [J].
Beebe, JM ;
Engelkes, VB ;
Liu, JQ ;
Gooding, J ;
Eggers, PK ;
Jun, Y ;
Zhu, XY ;
Paddon-Row, MN ;
Frisbie, CD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (11) :5207-5215
[3]   FREE-ENERGY AND TEMPERATURE-DEPENDENCE OF ELECTRON-TRANSFER AT THE METAL-ELECTROLYTE INTERFACE [J].
CHIDSEY, CED .
SCIENCE, 1991, 251 (4996) :919-922
[4]   Self-Assembled Carbon Nanotube Electrode Arrays: Effect of Length of the Linker between Nanotubes and Electrode [J].
Chou, Alison ;
Eggers, Paul K. ;
Paddon-Row, Michael N. ;
Gooding, J. Justin .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (08) :3203-3211
[5]   Silicon (100) Electrodes Resistant to Oxidation in Aqueous Solutions: An Unexpected Benefit of Surface Acetylene Moieties [J].
Ciampi, Simone ;
Eggers, Paul K. ;
Le Saux, Guillaume ;
James, Michael ;
Harper, Jason B. ;
Gooding, J. Justin .
LANGMUIR, 2009, 25 (04) :2530-2539
[6]  
Colthup N. B., 1990, Introduction to Infrared and Raman Spectroscopy, V3
[7]   Structure and Properties of Redox Active Self-Assembled Monolayers Formed from Norbornylogous Bridges [J].
Eggers, Paul K. ;
Zareie, Hadi M. ;
Paddon-Row, Michael N. ;
Gooding, J. Justin .
LANGMUIR, 2009, 25 (18) :11090-11096
[8]   The Effect of Surface Polarity on the Electrochemical Double Layer and Its Influence on the Measurement of the Standard Rate Constant of Electron Transfer [J].
Eggers, Paul K. ;
Hibbert, D. Brynn ;
Paddon-Row, Michael N. ;
Gooding, J. Justin .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (20) :8964-8971
[9]   ELECTRON-TRANSFER KINETICS IN ORGANIZED THIOL MONOLAYERS WITH ATTACHED PENTAAMMINE(PYRIDINE)RUTHENIUM REDOX CENTERS [J].
FINKLEA, HO ;
HANSHEW, DD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (09) :3173-3181
[10]  
Frisch M., 2004, GAUSSIAN 03 REVISION, DOI DOI 10.1016/J.MOLSTRUC.2017.03.014