Organizational Structure and Electronic Decoupling of Surface Bound Chiral Domains and Biomolecules
Santagata, N.M.
Pengshun Luo
Lakhani, A.M.
DeWitt, D.J.
Day, B.S.
Norton, M.L.
Pearl, T.P.
Dept. of Chem., North Carolina State Univ., Raleigh, NC;
This paper appears in: Sensors Journal, IEEE
Publication Date: June 2008
Volume: 8,
Issue: 6
On page(s): 758-766
ISSN: 1530-437X
INSPEC Accession Number: 10003339
Digital Object Identifier: 10.1109/JSEN.2008.923187
Current Version Published: 2008-05-23
Abstract
For the development of reagentless biological and chemical species detection at the single molecule level using external fields, including terahertz radiation, it is paramount to study model systems that uncover how intermolecular and molecule-surface interactions dictate monolayer ordering and electronic properties. This paper addresses two types of molecule-surface interactions and two distinct molecular systems, both of which impact our fundamental understanding of confined molecular domains and single molecule detection. We will first discuss the ordering and electronic characteristics of a chiral molecule, tartaric acid , weakly bound to an achiral metal surface, Ag(111), as studied with low temperature scanning tunneling microscopy (STM). This particular molecule-surface system contains many key elements, including hydrogen bonding interactions and stereochemical features, that would be common to other functional detection schemes. This paper will also treat the characterization of isolated, thiolated DNA molecules chemically bound to Au(111) terraces. Ambient STM and atomic force microscopy (AFM) measurements of both short and long DNA structures in both single and double strand configurations will be discussed with particular attention paid to imaging mechanisms involved. These results are particularly relevant to systems involving biomolecules anchored to inert metal surfaces, such as those used in external field-based assays.
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