Surface-controlled reversal of the selectivity of halogen bonds.

Abstract:

:Intermolecular halogen bonds are ideally suited for designing new molecular assemblies because of their strong directionality and the possibility of tuning the interactions by using different types of halogens or molecular moieties. Due to these unique properties of the halogen bonds, numerous areas of application have recently been identified and are still emerging. Here, we present an approach for controlling the 2D self-assembly process of organic molecules by adsorption to reactive vs. inert metal surfaces. Therewith, the order of halogen bond strengths that is known from gas phase or liquids can be reversed. Our approach relies on adjusting the molecular charge distribution, i.e., the σ-hole, by molecule-substrate interactions. The polarizability of the halogen and the reactiveness of the metal substrate are serving as control parameters. Our results establish the surface as a control knob for tuning molecular assemblies by reversing the selectivity of bonding sites, which is interesting for future applications.

journal_name

Nat Commun

journal_title

Nature communications

authors

Tschakert J,Zhong Q,Martin-Jimenez D,Carracedo-Cosme J,Romero-Muñiz C,Henkel P,Schlöder T,Ahles S,Mollenhauer D,Wegner HA,Pou P,Pérez R,Schirmeisen A,Ebeling D

doi

10.1038/s41467-020-19379-4

subject

Has Abstract

pub_date

2020-11-06 00:00:00

pages

5630

issue

1

issn

2041-1723

pii

10.1038/s41467-020-19379-4

journal_volume

11

pub_type

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