Structures of glycine, enantiopure alanine, and racemic alanine adlayers on Cu(110) and Cu(100) surfaces

被引:92
作者
Rankin, RB [1 ]
Sholl, DS [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
关键词
D O I
10.1021/jp0535700
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have determined the structures of dense adlayers of glycine and alanine on the Cu(110) and Cu(100) surfaces using plane wave density functional theory. These calculations resolve several experimental controversies regarding these structures. Glycine exists on Cu(1 10) as a single adlayer structure, while on Cu(100) two distinct glycine adlayers coexist. The glycine structures serve as useful starting points for constructing alanine adlayer structures. We considered separately the adsorption of enantiopure alanine and racemic alanine on each surface. Adlayers of enantiopure alanine are found to be closely related to the adlayers observed for glycine. Racemic alanine adlayers on Cu(I 10) are structurally analogous to those observed for glycine on this surface and adopt a pseudo-racemate ordering. On Cu(100), in contrast to glycine, racemic alanine is found to adopt a single adlayer structure that is an ordered racemate. Spontaneous segregation of molecular enantiomers does not occur in racemic adsorbed mixtures on either surface. Consideration of the orientationally distinct domains that may exist for each adlayer on these surfaces provides important information for the interpretation of the adlayer domain boundaries that are commonly observed in scanning tunneling microscopy images of amino acid adlayers. Examining this set of amino acid adlayers provides useful insight into the range of subtle behaviors that can arise in these and related systems where chiral molecules form ordered adlayers on flat metal surfaces.
引用
收藏
页码:16764 / 16773
页数:10
相关论文
共 77 条
[1]   Electrochemical studies of enantioselectivity at chiral metal surfaces [J].
Attard, GA .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (16) :3158-3167
[2]   Temperature effects in the enantiomeric electro-oxidation of D- and L-glucose on Pt{643}S [J].
Attard, GA ;
Ahmadi, A ;
Feliu, J ;
Rodes, A ;
Herrero, E ;
Blais, S ;
Jerkiewicz, G .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (09) :1381-1385
[3]  
BAIKER A, 1997, HDB HETEROGENEOUS CA, V5, P2422
[4]  
BARLOW S, IN PRESS SURF SCI
[5]   A study of glycine adsorption on a Cu{110} surface using reflection absorption infrared spectroscopy [J].
Barlow, SM ;
Kitching, KJ ;
Haq, S ;
Richardson, NV .
SURFACE SCIENCE, 1998, 401 (03) :322-335
[6]   Bonding, organization, and dynamical growth behavior of tripeptides on a defined metal surface: Tri-L-alanine and tri-L-leucine on Cu{100} [J].
Barlow, SM ;
Haq, S ;
Raval, R .
LANGMUIR, 2001, 17 (11) :3292-3300
[7]   Chemisorption and diffusion of hydrogen on surface and subsurface sites of flat and stepped nickel surfaces [J].
Bhatia, B ;
Sholl, DS .
JOURNAL OF CHEMICAL PHYSICS, 2005, 122 (20)
[8]   ENANTIOSELECTIVE HYDROGENATION OF ETHYL PYRUVATE - KINETIC MODELING OF THE MODIFICATION OF PT CATALYSTS BY CINCHONA ALKALOIDS [J].
BLASER, HU ;
GARLAND, M ;
JALLET, HP .
JOURNAL OF CATALYSIS, 1993, 144 (02) :569-578
[9]   Determination of the local structure of glycine adsorbed on Cu(110) [J].
Booth, NA ;
Woodruff, DP ;
Schaff, O ;
Giessel, T ;
Lindsay, R ;
Baumgartel, P ;
Bradshaw, AM .
SURFACE SCIENCE, 1998, 397 (1-3) :258-269
[10]   Enantioselective hydrogenation of 2-methyl-2-pentenoic acid over cinchonidine-modified Pd/alumina [J].
Borszeky, K ;
Mallat, T ;
Baiker, A .
CATALYSIS LETTERS, 1996, 41 (3-4) :199-202