Abdurakhmanova, NasibaFloris, AndreaTseng, Tzu-ChunComisso, AlessioStepanow, SebastianDe Vita, AlessandroKern, Klaus2013-02-272013-02-272013-02-27201210.1038/ncomms1942https://infoscience.epfl.ch/handle/20.500.14299/89778WOS:000306995000012Controlling supramolecular self-assembly is a fundamental step towards molecular nanofabrication, which involves a formidable reverse engineering problem. It is known that a variety of structures are efficiently obtained by assembling appropriate organic molecules and transition metal atoms on well-defined substrates. Here we show that alkali atoms bring in new functionalities compared with transition metal atoms because of the interplay of local chemical bonding and long-range forces. Using atomic-resolution microscopy and theoretical modelling, we investigate the assembly of alkali (Cs) and transition metals (Mn) co-adsorbed with 7,7,8,8-tetracyanoquinodimethane (TCNQ) molecules, forming chiral superstructures on Ag(100). Whereas Mn-TCNQ(4) domains are achiral, Cs-TCNQ(4) forms chiral islands. The specific behaviour is traced back to the different nature of the Cs- and Mn-TCNQ bonding, opening a novel route for the chiral design of supramolecular architectures. Moreover, alkali atoms provide a means to modify the adlayer electrostatic properties, which is important for the design of metal-organic interfaces.Stereoselectivity and electrostatics in charge-transfer Mn- and Cs-TCNQ(4) networks on Ag(100)text::journal::journal article::research article