| Literature DB >> 27001727 |
Wende Xiao1,2, Karl-Heinz Ernst1,3, Krisztian Palotas4, Yuyang Zhang2, Emilie Bruyer5, Lingqing Peng6, Thomas Greber7, Werner A Hofer8, Lawrence T Scott6, Roman Fasel1,9.
Abstract
In biomineralization, inorganic materials are formed with remarkable control of the shape and morphology. Chirality, as present in the biomolecular world, is therefore also common for biominerals. Biomacromolecules, like proteins and polysaccharides, are in direct contact with the mineral phase and act as modifiers during nucleation and crystal growth. Owing to their homochirality--they exist only as one of two possible mirror-symmetric isomers--their handedness is often transferred into the macroscopic shape of the biomineral crystals, but the way in which handedness is transmitted into achiral materials is not yet understood at the atomic level. By using the submolecular resolution capability of scanning tunnelling microscopy, supported by photoelectron diffraction and density functional theory, we show how the chiral 'buckybowl' hemibuckminsterfullerene arranges copper surface atoms in its vicinity into a chiral morphology. We anticipate that such new insight will find its way into materials synthesis techniques.Entities:
Year: 2016 PMID: 27001727 DOI: 10.1038/nchem.2449
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427