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Dipolar Molecular Rotors in SURMOFs

Subject Area Solid State and Surface Chemistry, Material Synthesis
Physical Chemistry of Solids and Surfaces, Material Characterisation
Term since 2016
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 316660646
 
In a molecular rotor, one part of the molecule (the rotator) can easily revolve with respect to a fixed portion of the molecule (the stator). When the rotator contains a dipole moment one speaks of a dipolar molecular rotor, and an electric field can be used to apply a torque to the rotator that causes it to align with the external field. Moreover, if many dipolar molecular rotors are brought together into an array their dipole moments interact with one another. Given enough free volume is maintained to allow unhindered rotation, these interactions between dipoles can induce collective behaviour. In this way, long-range ordered patterns of dipoles can spontaneously form. Significant effort notwithstanding, such spontaneous ordering has been observed only in a 2D array on a surface to date. The aim of this proposal is to develop 3D arrays of dipolar rotors, and prototype thin film devices that would modulate light transmission by switching the rotators from a spontaneously-ordered state to a field-aligned state. To do this, we focus on developing dipolar molecular rotors from which surface-anchored metal-organic frameworks can be made. With these molecular rotors, the stator provides the link between adjacent metal centres and the rotator is held halfway between the metal centres (and rotates around the axis defined by the stator). Using such structures to host dipolar rotors is optimal because the free volume necessary for rotation can be achieved while at the same time the nearest neighbour distances are kept short enough that dipole-dipole interactions can be significant. Thus, ideal conditions to induce collective behaviour can be reached, plus the thin-film format of the SURMOF is perfectly-suited for subsequent device fabrication.In the initial funding period of the COORNETs priority programme, we successfully implemented the first generation of dipolar rotor linkers in SURMOFs and demonstrated that therein the barrier to rotation is very small (on the order of kJ/mol). These are very encouraging results, but given the dipole moment of these linkers is moderate (2.6 D), we still do not have conclusive evidence of whether collective states are formed. We have also laid groundwork for dielectric- and optical-characterization, and device fabrication (with a total of seven SPP-related publications in the first three-year of funding). In the second period, we will increase the dipole moments and optical absorption of the linkers, focusing on achieving spontaneous ordering. We will also develop thin-film devices with graphene electrodes contacting the dipolar rotor-SURMOF in order to switch its optical transmission.
DFG Programme Priority Programmes
 
 

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