Journal Article

Amplification of chirality in two-dimensional enantiomorphous lattices

Ernst, Karl-Heinz, Fasel, Roman, Parschau, Manfred

2006

Overview

The concept of chirality dates back to 1848, when Pasteur manually separated left-handed from right-handed sodium ammonium tartrate crystals 1 . Crystallization is still an important means for separating chiral molecules into their two different mirror-image isomers (enantiomers) 2 , yet remains poorly understood 3 . For example, there are no firm rules to predict whether a particular pair of chiral partners will follow the behaviour of the vast majority of chiral molecules and crystallize together as racemic crystals 4 , or as separate enantiomers. A somewhat simpler and more tractable version of this phenomenon is crystallization in two dimensions, such as the formation of surface structures by adsorbed molecules. The relatively simple spatial molecular arrangement of these systems makes it easier to study the effects of specific chiral interactions 5 ; moreover, chiral assembly and recognition processes can be observed directly and with molecular resolution using scanning tunnelling microscopy 6 , 7 , 8 , 9 . The enantioseparation of chiral molecules in two dimensions is expected to occur more readily because planar confinement excludes some bulk crystal symmetry elements and enhances chiral interactions 10 , 11 ; however, many surface structures have been found to be racemic 12 , 13 , 14 , 15 , 16 , 17 , 18 . Here we show that the chiral hydrocarbon heptahelicene on a Cu(111) surface does not undergo two-dimensional spontaneous resolution into enantiomers 19 , but still shows enantiomorphism on a mesoscopic length scale that is readily amplified. That is, we observe formation of racemic heptahelicene domains with non-superimposable mirror-like lattice structures, with a small excess of one of the heptahelicene enantiomers suppressing the formation of one domain type. Similar to the induction of homochirality in achiral enantiomorphous monolayers 20 by a chiral modifier, a small enantiomeric excess suffices to ensure that the entire molecular monolayer consists of domains having only one of two possible, non-superimposable, mirror-like lattice structures.

• Publisher: Nature Publishing Group UK,Nature Publishing,Nature Publishing Group
• Subject: Ammonium / Atomic and molecular physics / Chemistry / Crystal lattices / Crystallization / Crystals / Exact sciences and technology / Humanities and Social Sciences / Hydrocarbons / letter / Microscopy / Molecular properties and interactions with photons / Molecular structure / multidisciplinary / Optical activity and dichroism; magnetooptical and electrooptical spectra / Optical activity, optical rotation; circular dichroism / Physics / Science / Science (multidisciplinary) / Sodium