RESEARCH

1. Interfacial Science of Molecular Films

Molecules can be assembled with minute precision at interfaces as can be seen in self-assembled monolayers at metal surfaces or in highly ordered Langmuir-Blodgett and Langmuir-Schaeffer films.

In the case of metal surfaces, we have investigated the effect of molecular structure on packing modes and molecular mobility. Currently, we are focusing on properties of single molecules, either isolated or contained within a film, for use as molecular memory or switching devices.

On the other hand, molecules contained within Langmuir-Blodgett films have the unique feature that they may be manipulated by applying mechanical force (through in situ compression and expansion of the monolayer). Thus, molecular-machine-like functions can be obtained at the nanometric (or smaller!) level through actions performed at the macroscale leading us to coin the term ‘Hand-operated Nanotechnology’.

Molecular Machines at Interfaces

By employing an air water interface it is possible to demonstrate molecular level action through application of a macroscale force, in this case for the capture and release of fluorescent guest molecules. As is shown below, macroscale manipulation of a molecular monolayer at an air-water interface can be used to capture guest molecules in the water subphase since the molecular conformation is coupled with monolayer compression (and expansion – i.e. it is a reversible process).

A researcher prepares a Langmuir-Blodgett film using a Langmuir trough. Macroscale compression/expansion of the monolayer leads respectively to reversible capture and release of molecules in the subphase yielding an on/off response of fluorescence emission.
A researcher prepares a Langmuir-Blodgett film using a Langmuir trough. Macroscale compression/expansion of the monolayer leads respectively to reversible capture and release of molecules in the subphase yielding an on/off response of fluorescence emission.

Chiral Resolution by Applying Macroscale Force

Langmuir-Blodgett monolayer of a cholesterol-substituted cyclen exhibits
Langmuir-Blodgett monolayer of a cholesterol-substituted cyclen exhibits
enantioselectivity of guest binding depending on the applied surface pressure.

Chirality of amino acids can be differentiated using force applied to monolayer films of a cholesterol-substituted cyclen derivative. By varying the pressure applied to this film, enantioselectivity of guest binding was observed.

Nucleoside Differentiation using a Molecular Machine

Subtle structural differences of nucleoside guests can be detected using a cholesterol-substituted triazacyclononane molecular machine operated at an air-water interface. Thus, the single methyl group difference between uridine and 5-methyluridine can be found by mechanical tuning due to monolayer compression.

Cholesterol-armed-TACN for nucleoside differentiation at the air-water interface.
Cholesterol-armed-TACN for nucleoside differentiation at the air-water interface.

Mechanically-controlled Indicator Displacement Assay

Indicator displacement assay has been applied in a Langmuir-Blodgett film to detect carbohydrates using fluorescence resonance energy transfer (FRET).

In a state of low compression FRET does not occur due to separation of the two chromophores dissolved in the subphase. At higher applied surface pressures, FRET begins to occur due to the increasing proximity of the chromophores. If D-glucose is added in the water subphase, indicator is displaced and FRET is returned to an ‘OFF’ state.
In a state of low compression FRET does not occur due to separation of the two chromophores dissolved in the subphase. At higher applied surface pressures, FRET begins to occur due to the increasing proximity of the chromophores. If D-glucose is added  in the water subphase, indicator is displaced and FRET is returned to an ‘OFF’ state.

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