Covalent Template-Directed Synthesis of a Spoked 18-Porphyrin Nanoring.

Rings of porphyrins mimic natural light-harvesting chlorophyll arrays and offer insights into electronic delocalization, providing a motivation for creating larger nanorings with closely spaced porphyrin units. Here, we demonstrate the first synthesis of a macrocycle consisting entirely of 5,15-linked porphyrins. This porphyrin octadecamer was constructed using a covalent six-armed template, made by cobalt-catalyzed cyclotrimerization of an H-shaped tolan with porphyrin trimer ends. The porphyrins around the circumference of the nanoring were linked together by intramolecular oxidative meso-meso coupling and partial ß-ß fusion, to give a nanoring consisting of six edge-fused zinc(II) porphyrin dimer units and six un-fused nickel(II) porphyrins. STM imaging on a gold surface confirms the size and shape of the spoked 18-porphyrin nanoring (calculated diameter: 4.7 nm).

Altering the Properties of Spiropyran Switches Using Coordination Cages with Different Symmetries.

Molecular confinement effects can profoundly alter the physicochemical properties of the confined species. A plethora of organic molecules were encapsulated within the cavities of supramolecular hosts, and the impact of the cavity size and polarity was widely investigated. However, the extent to which the properties of the confined guests can be affected by the symmetry of the cage─which dictates the shape of the cavity─remains to be understood. Here we show that cage symmetry has a dramatic effect on the equilibrium between two isomers of the encapsulated spiropyran guests. Working with two Pd-based coordination cages featuring similarly sized but differently shaped hydrophobic cavities, we found a highly selective stabilization of the isomer whose shape matches that of the cavity of the cage. A Td-symmetric cage stabilized the spiropyrans' colorless form and rendered them photochemically inert. In contrast, a D2h-symmetric cage favored the colored isomer, while maintaining reversible photoswitching between the two states of the encapsulated spiropyrans. We also show that the switching kinetics strongly depend on the substitution pattern on the spiropyran scaffold. This finding was used to fabricate a time-sensitive information storage medium with tunable lifetimes of the encoded messages.

Organoboron Complexes in Edge-Sharing Macrocycles: The Triphyrin(2.1.1)-Tetraphyrin(1.1.1.1) Hybrid.

The formation of a precisely designed environment predefined for stabilizing electron-deficient atoms, such as boron(III), is an important approach for optimizing the properties of a chromophore. A triphyrin(2.1.1) motif built on the extended π-system of a tetraphyrin(1.1.1.1) skeleton creates a new coordination environment, with a CNN set of donors confined in a limited space predefined for binding small cations. The entrapment of boron(III) in the triphyrin(2.1.1) sector, with formation of a direct B-C bond, significantly changes the optical response and the global aromatic character of the compound, leading to an extension of the π-delocalisation.

The anti-aromatic dianion and aromatic tetraanion of [18]annulene.

π-Conjugated macrocycles behave differently from analogous linear chains because their electronic wavefunctions resemble a quantum particle on a ring, leading to aromaticity or anti-aromaticity. [18]Annulene, (CH)18, is the archetypal non-benzenoid aromatic hydrocarbon. Molecules with circuits of 4n + 2 π electrons, such as [18]annulene (n = 4), are aromatic, with enhanced stability and diatropic ring currents (magnetic shielding inside the ring), whereas those with 4n π electrons, such as the dianion of [18]annulene, are expected to be anti-aromatic and exhibit the opposite behaviour. Here we use 1H NMR spectroscopy to re-evaluate the structure of the [18]annulene dianion. We also show that it can be reduced further to an aromatic tetraanion, which has the same shape as the dianion. The crystal structure of the tetraanion lithium salt confirms its geometry and reveals a metallocene-like sandwich, with five Li+ cations intercalated between two [18]annulene tetraanions. We also report a heteroleptic sandwich, with [18]annulene and corannulene tetraanion decks.

Porphyrin-fused graphene nanoribbons.

Graphene nanoribbons (GNRs), nanometre-wide strips of graphene, are promising materials for fabricating electronic devices. Many GNRs have been reported, yet no scalable strategies are known for synthesizing GNRs with metal atoms and heteroaromatic units at precisely defined positions in the conjugated backbone, which would be valuable for tuning their optical, electronic and magnetic properties. Here we report the solution-phase synthesis of a porphyrin-fused graphene nanoribbon (PGNR). This PGNR has metalloporphyrins fused into a twisted fjord-edged GNR backbone; it consists of long chains (>100 nm), with a narrow optical bandgap (~1.0 eV) and high local charge mobility (>400 cm2 V-1 s-1 by terahertz spectroscopy). We use this PGNR to fabricate ambipolar field-effect transistors with appealing switching behaviour, and single-electron transistors displaying multiple Coulomb diamonds. These results open an avenue to π-extended nanostructures with engineerable electrical and magnetic properties by transposing the coordination chemistry of porphyrins into graphene nanoribbons.

Crystallographic evidence for global aromaticity in the di-anion and tetra-anion of a cyclophane hydrocarbon.

[24]Paracyclophanetetraene is a classic example of a macrocyclic hydrocarbon that becomes globally aromatic on reduction to the di-anion, and switches to globally anti-aromatic in the tetra-anion. This redox activity makes it promising as an electrode material for batteries. Here, we report the solid-state structures of the di- and tetra-anions of this cyclophane, in several coordination environments. The changes in bond length on reduction yield insights into the global aromaticity of the di-anion (26π electrons), and anti-aromaticity of the tetra-anion (28π electrons), that were previously deduced from NMR spectra of species generated in situ. The experimental geometries of the aromatic di-anion and anti-aromatic tetra-anion from X-ray crystallographic data match well with gas-phase calculated structures, and reproduce the low symmetry expected in the anti-aromatic ring. Comparison of coordinated and naked anions confirms that metal coordination has little effect on the bond lengths. The UV-vis-NIR absorption spectra show a sharp intense peak at 878 nm for the di-anion, whereas the tetra-anion gives a broad spectrum typical of an anti-aromatic system.

Strained Porphyrin Tape-Cycloparaphenylene Hybrid Nanorings.

V-Shaped porphyrin dimers, with masked p-phenylene bridges, undergo efficient oxidative coupling to form meso-meso linked cyclic porphyrin oligomers. Reductive aromatization unmasks the p-phenylenes, increasing the strain. Oxidation then fuses the porphyrin dimers, providing a nanoring with curved walls. The strain in this macrocycle bends the p-phenylene and fused porphyrin dimer units (radii of curvature of 11.4 and 19.0 Å, respectively), but it does not significantly alter the electronic structure of the fused porphyrins.

Edge Decoration of Anthracene Switches Global Diatropic Current That Controls the Acene Reactivity.

The 14π-electron system of anthracene has been merged with the unsaturated Z-1,2-difurylethene to form a macrocycle(s) with the retained local conjugation of all incorporated subunits that were substantially modulated with a redox activation, opening a global delocalization involving all integrated aromatics. In addition, the edge modulation of acene via the attachment of a specific isomer of the conjugated system gives steric confinements that are characteristic of small macrocycles, forcing substantially short C(H)···O electrostatic interactions that are documented spectroscopically with the support of X-ray analysis.

Multi-Cation Coordination in Porphyrinoids.

Porphyrinoid macrocycles are unbreakably linked with the coordination of central cations that drastically influence the observed behavior. A specific place has been recorded for structures where more than one cation is entrapped in a single macrocycle. It has been a characteristic feature of expanded porphyrinoids where the increased coordination space allows a multiple coordination. Because of specific steric confinements, an incorporation of more than one cation within regular or contracted porphyrinoids is more demanding but it can be realized on several ways significantly modifying the observed behavior. We will discuss synthetic strategies leading to structures with increased number of cations and the influence on the observed behavior of such modification.

A route to a cyclobutane-linked double-looped system via a helical macrocycle.

Macrocycles built of carbazole and pyridine fragments with alkene/alkane linkers constitute a helical structure as documented structurally and spectroscopically. The 'solid-state' prearrangement observed for two C[double bond, length as m-dash]C bonds leads to unprecedented transformation to a cyclobutane in a head-to-tail (rtct) geometry with two macrocyclic loops in a perpendicular orientation.

meso-N-Pyrrole as a Versatile Substituent Influencing the Optical Properties of Porphyrin.

A meso-N-pyrrole porphyrin converts into a π-extended porphyrin forming an indolizine-3-one motif. The indolizine-3-one frame opens a lactam subunit preserving a six-membered, heterocyclic structure fused with the main macrocycle. The optical properties of formed derivatives follow the structural modifications giving the absorbance and emission eventually modulated by the NH-centered modifications of the fused unit.