Oligoynes are archetypical molecular wires due to their 1-D chain of conjugated carbon atoms and ability to transmit charge over long distances by coherent tunneling. However, the stability of the oligoyne can be an issue. Here we address this problem by two stabilization methods, namely sterically shielding endgroups, and rotaxination to produce an insulated molecular wire. We demonstrate the threading of a hexayne within a macrocycle to form a rotaxane and report measurements of the electrical conductance of this single supramolecular assembly within an STM break junction. The macrocycle is retained around the hexayne through the use of 3,5-diphenylpyridine stoppers at both ends of the molecular wire, which also serve as chemisorption contacts to the gold electrodes of the junction. Molecular conductance was measured for both the supramolecular assembly and also for the molecular wire in the absence of the macrocycle. The threaded macrocycle, which at room temperature is mobile along the length of the hexayne between the stoppers, has only a minimal impact on the conductance. However, the probability of molecular junction formation in a given break junction formation cycle is notably lower with the rotaxane. In seeking to understand the conductance behavior, the electronic properties of these molecular assemblies and the electrical behavior of the junctions have been investigated by using DFT-based computational methods.

A 4-ethynylpyridyl derivative with sterically shielding phenyl groups in the 3- and 5-positions has been synthesized and used to terminate a series of polyynes. This approach allows for the synthesis of stable polyynes up to an octayne, twice as long as previous accessible for "unstabilized" pyridyl-endcapped polyynes. The potential of these polyynes as wire-like linkers to metal centers is demonstrated by axial coordination of pyridyl groups to zinc- and ruthenium-metalloporphyrins.

Multidimensional, conjugated building blocks have been formed through the axial coordination of polyynes to the central Ga atom of tetraarylporphyrins.E lectron deficient pentafluorophenyl substituents in the meso-positions provide more stable s-acetylide complexes to Ga than analogous structures with tert-butylphenyl groups.Mono-, di-, and triynes have been used, including ap yridyl endcapped diyne that allows for formation of porphyrin triads through coordination of the pyridyl ligand to aR uporphyrin. Figure 1. a) Porphyrin oligomer formed by Vernier templation. [8] b) Porphyrin dimer as the subunit of amolecularbox. [9] c) Schematic construction perpendiculart oporphyrin plane via metal acetylides, and d) Known axial metal acetylidesw ith pentacoordinate Ga-, In-, and Fe-metalloporphyrins (TPP, R' = C 6 H 5 ,R= H; OEP, R' = H, R = C 2 H 5 ).

A 4‐ethynylpyridyl derivative with sterically shielding phenyl groups in the 3‐ and 5‐positions has been synthesized and used to terminate a series of polyynes. This approach allows for the synthesis of stable polyynes up to an octayne, twice as long as previous accessible for “unstabilized” pyridyl‐endcapped polyynes. The potential of these polyynes as wire‐like linkers to metal centers is demonstrated by axial coordination of pyridyl groups to zinc‐ and ruthenium‐metalloporphyrins.

Multidimensional, conjugated building blocks have been formed through the axial coordination of polyynes to the central Ga atom of tetraarylporphyrins. Electron deficient pentafluorophenyl substituents in the meso‐positions provide more stable σ‐acetylide complexes to Ga than analogous structures with tert‐butylphenyl groups. Mono‐, di‐, and triynes have been used, including a pyridyl endcapped diyne that allows for formation of porphyrin triads through coordination of the pyridyl ligand to a Ru porphyrin.