Oligothiophene isocyanides for platinum-based molecular electronic applications

被引:28
作者
Bong, D [1 ]
Tam, I [1 ]
Breslow, R [1 ]
机构
[1] Columbia Univ, Dept Chem, New York, NY 10027 USA
关键词
D O I
10.1021/ja045904p
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Understanding molecular orientation on a metal surface is key to designing molecular electronic device junctions. Though platinum device electrodes are of particular interest as a more stable alternative to the often used gold electrodes, the chemisorption of conducting molecules onto platinum surfaces has not been thoroughly studied. We present herein the first detailed study of the ability and manner in which soluble oligothiophene isocyanides, of lengths ranging from 2 to 7 nm, chemisorb onto platinum surfaces and nanoparticles. It was found that these oligothiophene isocyanides stand at a 41° angle from the platinum surface normal, suggesting their applicability in molecule-bridged platinum electrode devices. Copyright © 2003 American Chemical Society.
引用
收藏
页码:11796 / 11797
页数:2
相关论文
共 35 条
[1]  
[Anonymous], 1999, HDB OLIGO POLYTHIOPH
[2]   Redox states of well-defined π-conjugated oligothiophenes functionalized with poly(benzyl ether) dendrons [J].
Apperloo, JJ ;
Janssen, RAJ ;
Malenfant, PRL ;
Groenendaal, L ;
Fréchet, JMJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (29) :7042-7051
[3]  
BALDWIN JE, 1990, SYNLETT, P603
[4]   Exploration of the Stille coupling reaction for the syntheses of functional polymers [J].
Bao, ZN ;
Chan, WK ;
Yu, LP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (50) :12426-12435
[5]   OLIGOTHIOPHENES - YET LONGER - SYNTHESIS, CHARACTERIZATION, AND SCANNING-TUNNELING-MICROSCOPY IMAGES OF HOMOLOGOUS, ISOMERICALLY PURE OLIGO(ALKYLTHIOPHENE)S [J].
BAUERLE, P ;
FISCHER, T ;
BIDLINGMEIER, B ;
STABEL, A ;
RABE, JP .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (03) :303-307
[6]  
BAUERLE P, 1993, J AM CHEM SOC, V115, P10217
[7]   Contact resistance in metal-molecule-metal junctions based on aliphatic SAMs: Effects of surface linker and metal work function [J].
Beebe, JM ;
Engelkes, VB ;
Miller, LL ;
Frisbie, CD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (38) :11268-11269
[8]   Comparative study of electrochemically directed assembly versus conventional self-assembly of thioacetyl-terminated oligo(phenylene ethynlyene)s on gold and platinum surface [J].
Cheng, L ;
Yang, JP ;
Yao, YX ;
Price, DW ;
Dirk, SM ;
Tour, JM .
LANGMUIR, 2004, 20 (04) :1335-1341
[9]  
Cornil J, 1998, ELECTRONIC MATERIALS: THE OLIGOMER APPROACH, P432
[10]   Synthesis and characterization of conjugated mono- and dithiol oligomers and characterization of their self-assembled monolayers [J].
de Boer, B ;
Meng, H ;
Perepichka, DF ;
Zheng, J ;
Frank, MM ;
Chabal, YJ ;
Bao, ZN .
LANGMUIR, 2003, 19 (10) :4272-4284