TY  - JOUR
AB  - Molecular self-assembly on insulating surfaces, despite being highly relvant to many applications, generally suffers from the weak moleculesurface interactions present on dielectric surfaces, especially when benchmarked against metallic substrates. Therefore, to fully exploit the potential of molecular self-assembly, increasing the influence of the substrate constitutes an essential prerequisite. Upon deposition of terephthalic acid and trimesic acid onto the natural cleavage plane of calcite, extended hydrogen-bonded networks are formed, which wet the substrate. The observed structural complexity matches the variety realized on metal surfaces. A detailed analysis of the molecular structures observed on calcite reveals a significant influence of the underlying substrate, clearly indicating a substantial templating effect of the surface on the resulting molecular networks. This work demonstrates that choosing suitable molecule/substrate systems allows for tuning the balance between intermolecular and moleculesurface interactions even in the case of typically weakly interacting insulating surfaces. This study, thus, provides a strategy for deliberately exploiting substrate templating to increase the structural variety in molecular self-assembly on a bulk insulator at room temperature.
DA  - 2012
DO  - 10.1002/smll.201200681
KW  - self-assembly
KW  - templating
KW  - bulk insulator
KW  - calcite
KW  - atomic force
KW  - microscopy
LA  - eng
IS  - 19
M2  - 2969
PY  - 2012
SN  - 1613-6810
SP  - 2969-2977
T2  - Small
TI  - Substrate Templating upon Self-Assembly of Hydrogen-Bonded Molecular Networks on an Insulating Surface
UR  - https://nbn-resolving.org/urn:nbn:de:0070-pub-29138094
Y2  - 2024-11-22T02:08:22
ER  -