An appealing feature of molecular electronics is the possibility of inducing changes in the orbital structure through external stimuli. This can provide functionality on the single-molecule level that can be employed for sensing or switching purposes if the associated conductance changes are sizable upon application of the stimuli. Here, we show that the room-temperature conductance of a spring-like molecule can be mechanically controlled up to an order of magnitude by compressing or elongating it. Quantum-chemistry calculations indicate that the large conductance variations are the result of destructive quantum interference effects between the frontier orbitals that can be lifted by applying either compressive or tensile strain to the molecule. When periodically modulating the electrode separation, a conductance modulation at double the driving frequency is observed, providing a direct proof for the presence of quantum interference. Furthermore, oscillations in the conductance occur when the stress built up in the molecule is high enough to allow the anchoring groups to move along the surface in a stick–slip-like fashion. The mechanical control of quantum interference effects results in the largest-gauge factor reported for single-molecule devices up to now, which may open the door for applications in, e.g., a nanoscale mechanosensitive sensing device that is functional at room temperature.

We introduce a design principle to stabilize helically chiral structures from an achiral tetrasubstituted [2.2]­paracyclophane by integrating it into a macrocycle. The [2.2]­paracyclophane introduces a three-dimensional perturbation into a nearly planar macrocyclic oligothiophene. The resulting helical structure is stabilized by two bulky substituents installed on the [2.2]­paracyclophane unit. The increased enantiomerization barrier enabled the separation of both enantiomers. The synthesis of the target helical macrocycle 1 involves a sequence of halogenation and cross-coupling steps and a high-dilution strategy to close the macrocycle. Substituents tuning the energy of the enantiomerization process can be introduced in the last steps of the synthesis. The chiral target compound 1 was fully characterized by NMR spectroscopy and mass spectrometry. The absolute configurations of the isolated enantiomers were assigned by comparing the data of circular dichroism spectroscopy with TD-DFT calculations. The enantiomerization dynamics was studied by dynamic HPLC and variable-temperature 2D exchange spectroscopy and supported by quantum-chemical calculations.

[2.2]Paracyclophane is the prototypical layered hydrocarbon and has been essential for investigations of through‐space electronic interactions. Over the last years more examples of tetrasubstituted derivatives have been reported. This minireview discusses the synthetic approaches towards various substitution patterns and provides a survey over different approaches used to achieve and derivatize symmetric tetrasubstitution. The first two sections of this work present homo‐tetrasubstituted derivatives, while the third section gives insight into symmetrically hetero‐tetrasubstituted analogues. These approaches are briefly discussed, the resulting structures are presented in detail, and their specific properties resulting from the incorporation of [2.2]paracyclophane are elucidated.

A macrocyclic oligothiophene with an integrated pseudo‐para substituted [2.2]paracyclophane has been achieved. The synthetic sequence relies on alternating steps of halogenation‐ and Suzuki‐coupling conditions. By employing a modified Eglinton reaction under high dilution conditions, the macrocycle is closed and the obtained diacetylene is efficiently transferred to the corresponding thiophene. The molecule is fully characterized and its dynamic racemization is analyzed by variable temperature NMR experiments. The racemization barrier hints with 38 kJ/mol at rapid enantiomerization at room temperature by Mislow’s ‘Euclidian rubber glove’ enantiomerization process. Macrocycle formation results in red‐shifted absorption and emission spectra, hinting at increased conjugation through the oligothiophene versus the trough space conjugation through the [2.2]paracyclophane.

The bowl-shaped, 3-fold interlinked porphyrin dimer 2 was obtained in respectable yields during macrocyclization attempts. Its bicyclic structure, consisting of a macrocycle made of a pair of acetylene interlinked tetraphenylporphyrins which are additionally linked by a C−C bond interlinking two pyrrole subunits, has been confirmed spectroscopically (2D-NMR, UV/vis, HR-MALDI-ToF MS). Late-stage functionalization provided the structural analogue 1 with acetylprotected terminal thiol anchor groups enabling single molecule transport investigations in a mechanically controlled break junction experiment. The formation of single-molecule junctions was observed, displaying large variations in the observed conductance values pointing at a rich diversity in the molecular junctions.

The Front Cover shows the regioselective functionalization of already doubly substituted [2.2]paracyclophanes, resulting in symmetrical fourfold substituted three dimensional building blocks. The variety of synthetic accesses to these structures is summarized in the minireview entitled: “Beyond Simple Substitution Patterns – Symmetrically Tetrasubstituted [2.2]Paracyclophanes as 3D Functional Materials”. More information can be found in the Minireview by M. Mayor et al.

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