Greber T, Sljivancanin Z, Schillinger R, Wider J, Hammer B
Physik Institut, Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.
Phys Rev Lett. 2006 Feb 10;96(5):056103. doi: 10.1103/PhysRevLett.96.056103. Epub 2006 Feb 9.
Two distinct non-mirror-symmetric conformations of D- and L-cysteine were found after adsorption on Au(17 11 9)S. This demonstrates chiral heterorecognition, i.e., enantioselectivity of S kinks on vicinal Au(111). The structures as determined by angle scanned x-ray photoelectron diffraction agree well with those from density functional theory calculations. The calculations predict adsorption energies of approximately 2 eV where D-cysteine binds 140 meV stronger than L-cysteine. The classical three point contact model for molecular recognition fails to explain these findings.
在吸附于Au(17 11 9)S后,发现了D-和L-半胱氨酸的两种不同的非镜像对称构象。这证明了手性异质识别,即邻位Au(111)上S扭结的对映选择性。通过角度扫描X射线光电子衍射确定的结构与密度泛函理论计算的结构非常吻合。计算预测吸附能约为2 eV,其中D-半胱氨酸的结合比L-半胱氨酸强140 meV。分子识别的经典三点接触模型无法解释这些发现。