Diversiform Nanostructures Constructed from Tetraphenylethene and Pyrene-Based Acid/Base Controllable Molecular Switching Amphiphilic [2]Rotaxanes with Tunable Aggregation-Induced Static Excimers

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Distinct Nanostructures and Organogel Driven by Reversible Molecular Switching of a Tetraphenylethene-Involved Calix[4]arene-Based Amphiphilic [2 ]Rotaxane

Artificial Molecular Machines. - Abstract - Europe PMC

Construction of anisotropic nanostructures by self-assembly of aggregation- induced emission driven from tris-branched [2]rotaxane based molecular zipper - ScienceDirect

Acid–base controllable nanostructures and the fluorescence detection of H 2 PO 4 − by the molecular shuttling of tetraphenylethene-based [2]rotaxanes - Journal of Materials Chemistry C (RSC Publishing) DOI:10.1039/D0TC05358A

Full article: Proposed modification to a muscle-like acid-base switchable [2 ](2)rotaxane for improved force delivery

Diversiform Nanostructures Constructed from Tetraphenylethene and Pyrene-Based Acid/Base Controllable Molecular Switching Amphiphilic [2]Rotaxanes with Tunable Aggregation-Induced Static Excimers

Acid–base controllable nanostructures and the fluorescence detection of H 2 PO 4 − by the molecular shuttling of tetraphenylethene-based [2]rotaxanes - Journal of Materials Chemistry C (RSC Publishing) DOI:10.1039/D0TC05358A

1 H NMR spectra of E to Z isomerisation of the molecule 1.

Diversiform Nanostructures Constructed from Tetraphenylethene and Pyrene-Based Acid/Base Controllable Molecular Switching Amphiphilic [2]Rotaxanes with Tunable Aggregation-Induced Static Excimers

Controlled Sol–Gel and Diversiform Nanostructure Transitions by Photoresponsive Molecular Switching of Tetraphenylethene- and Azobenzene-Functionalized Organogelators

Diversiform Nanostructures Constructed from Tetraphenylethene and Pyrene-Based Acid/Base Controllable Molecular Switching Amphiphilic [2]Rotaxanes with Tunable Aggregation-Induced Static Excimers

Molecular Dynamics Simulation of Amphiphilic Bistable [2]Rotaxane Langmuir Monolayers at the Air/Water Interface

Fig. S1 TGA thermograms of TPE-cored luminogens recorded under nitrogen

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