Global Aromaticity and Antiaromaticity in Porphyrin Nanoring Anions Martin D. Peeks, Michael Jirasek, Timothy D. W. Claridge and Harry L. Anderson* Abstract: Doping, through oxidation or reduction, is often used to structure, e.g. by oxidation or excitation. The removal of two modify the properties of π-conjugated oligomers. In most cases, the electrons from [8]CPP leads to global aromaticity (30 - resulting charge distribution is difficult to determine. If the oligomer is electrons).[9] Removal of 4 or 6 electrons from the six-porphyrin cyclic and doping establishes global aromaticity or antiaromaticity, nanoring c-P6∙T6 leads to macrocyclic global antiaromaticity (80 then it is certain that the charge is fully delocalized over the entire -electrons) or aromaticity (78 -electrons), respectively.[13] perimeter of the ring. Here we show that reduction of a six-porphyrin Electronic excitation can lead to excited state aromaticity,[4,14] and nanoring using decamethylcobaltocene results in global aromaticity molecules such as c-P6 are aromatic in their lowest excited (in the 6– state; [90 π]) and antiaromaticity (in the 4– state; [88 π]), states.[15] Many other macrocycles with emergent global consistent with Hückel’s rules. Aromaticity is assigned by NMR aromaticity in the neutral, cationic and excited states have been spectroscopy and density-functional theory calculations. reported recently.[16-21] Aromaticity is one of the oldest concepts in chemistry, and it is widely used to predict the properties of unsaturated cyclic molecules.[1] In essence, aromaticity describes the anomalous stability of certain molecules, and their peculiarly large anisotropic diamagnetic susceptibilities.[2] This unusual diamagnetism results from the tendency of aromatic molecules to sustain a ring current when placed in a magnetic field. This effect is easily detected by NMR spectroscopy, but aromatic ring currents were first postulated by Pauling and Lonsdale before NMR spectroscopy had been invented.[3] While the earliest aromatic molecules were flat symmetric carbocyclic -systems, the concept has been extended to -bonded systems, metal clusters, excited states, twisted molecules, and so on.[4-6] Figure 1. Examples of π-conjugated macrocycles: [n]-cycloparaphenylenes Hückel’s calculations predict that an annulene (CnHn) with a ([n]CPPs), and a six-porphyrin nanoring, c-P6∙T6 (template T6 in blue; [7] conjugated circuit of [4n+2] -electrons will be aromatic. Breslow conjugated circuit in orange). extended this rule to state that annulenes with [4n] -electrons are antiaromatic, with reduced stability and the opposite ring currents (paratropic rather than diatropic).[8] Although Hückel’s original Porphyrin oligomers have an exceptionally wide range of calculations were restricted to the all-carbon, monocyclic accessible oxidation states; for example c-P6∙T6 can be annulenes, the rules also apply to a wide range of heterocyclic reversibly oxidized up to the 12+ state and reduced to the 6– and polycyclic molecules. However, there are many macrocyclic state.[13,22] Here we demonstrate that global ring currents can also π-conjugated rings with [4n+2] or [4n] -electrons that do not be established by reduction. We show that the tetraanion is display global aromatic or antiaromatic ring currents. For antiaromatic (88 -electrons), and the hexaanion is aromatic (90 example, cycloparaphenylenes ([n]CPPs, Figure 1) have [4n] - -electrons). The chemical reduction of annulenes was widely electrons in their circumferential conjugation path, yet are non- explored during the 1980s,[23] but there are few recent examples aromatic in their electronically neutral ground states.[9] Similarly, of macrocycles that become aromatic in anionic reduced butadiyne-linked porphyrin nanorings such as c-P6∙T6 do not states,[19] and it was not clear whether this strategy could be used exhibit global (anti)aromaticity in their neutral states.[10-12] These in complex heterocyclic macrocycles such as porphyrin macrocycles consist of aromatic subunits, and the local nanorings. aromaticity of the subunit dominates in the neutral ground states. We began this study by using computational techniques to (Anti)aromaticity can be induced by perturbing the electronic predict the (anti)aromaticity in reduced states of c-P6∙T6. The nucleus-independent chemical shift (NICS),[24] which evaluates the chemical shift at a point in space, was calculated using density [*] Dr. M. D. Peeks, M. Jirasek, Prof. T. D. W. Claridge, Prof. H. L. functional theory (DFT, B3LYP/6-31+G*). The diatropic ring Anderson currents of aromatic molecules generate an induced field that Department of Chemistry, University of Oxford opposes the external magnetic field inside the ring, leading to a Chemistry Research Laboratory, Oxford, OX1 3TA, UK Email: [email protected] shielding effect and lower chemical shifts. Outside the ring, the Homepage: http://hla.chem.ox.ac.uk/ induced field reinforces the applied field, leading to NMR Dr. M. D. Peeks deshielding. The paratropic ring currents of antiaromatic School of Chemistry, University of New South Wales, Sydney NSW molecules have the opposite NMR effects. Therefore a negative 2052, Australia NICS inside the nanoring indicates aromaticity and a positive Supporting information for this article is given via a link at the end of NICS indicates antiaromaticity. the document. 1 Table 1. Nucleus-independent chemical shifts for c-P6 as a function of oxidation assignment of neutral c-P6∙T6 (Figure 3a). The protons of the state, at B3LYP/6-31+G* solubilizing trihexylsilyl groups (THSi and THSo for those pointing inside and outside the ring, respectively) give rise to a broad neutral 4– 6– 4+[a] 6+[a] overlapping set of peaks around 1 ppm. The porphyrin -pyrrole protons (labelled a and b in Figure 3) resonate at 9.6 and 8.8 ppm, n e– 84 88 90 80 78 respectively, and the protons of the meso-aryl groups (labelled oo, NICS(0)iso –1.5 88.7 –13 101 –13 oi and p) appear in the expected region for aromatic signals (8.1– 8.4 ppm). In contrast, the template protons (, , and ) are [a] Data from ref [13]. substantially (up to 6 ppm) shielded by their axial coordination to the porphyrin subunits, which are each locally aromatic. The results of NICS calculations (Figure 2 and Table 1) are The global ring current around the nanoring can be evaluated consistent with predictions from Hückel’s rule: the 4− state is by comparing the shielding inside and outside the nanoring (i.e. antiaromatic (NICS(0)iso = 89 ppm) and the 6− state is aromatic THSi vs. THSo and oi vs. oo). The template protons (, , and ) (NICS(0)iso = −13 ppm). These NICS values are similar to those in c-P6∙T66− are easily identified by comparison with the spectrum [13] calculated previously for the 4+ and 6+ oxidation states. The of template-free c-P66−, revealing their signals at ~4–5 ppm (SI prediction of aromaticity in the 6− state is consistent across other Figure S8). The meso-aryl protons (oi, oo and p) are each related functionals (M06-2X and B97XD, see SI Table S1). The 4− state by a 4J scalar coupling, and so exhibit a characteristic coupling undergoes symmetry-breaking from D6h to approximate C2v pattern in the 1H TOCSY spectrum (SI Figure S9). NOE symmetry, reflecting the pseudo-Jahn-Teller distortion common to correlations between the template protons and oi permit the antiaromatic molecules. The functionals M06-2X and B97XD assignment of the latter, and further NOE correlations to the THS predict greater ellipticity than B3LYP (SI Table S2), and manifold centred around −0.5 ppm confirm its assignment as THSi corresponding lower NICS values (SI Table S1). Calculations of (SI Figure S11). THSo and oo are related by NOE correlations, and the anisotropy of the induced current density (ACID) confirm the p can then be assigned by elimination. Although the THSi [25] conclusions from the NICS calculations (SI Figure S3). resonance is shielded by the global aromatic ring current, the The square-wave voltammetry of c-P6∙T6 reveals six THSo resonance is at the same chemical shift as for the neutral reversible reductions in the window −1.30 V to −1.80 V (vs. ring because these protons sit at the border between the shielding + [22] Fc/Fc ). There are few reducing agents available in this and deshielding regions of the chemical shift anisotropy cone (SI [26] potential range. Alkali metals are strong reducing agents, but it Figure S2). The chemical shift difference between resonances on is difficult to titrate them to avoid over- or under-reduction. Therien the inside and outside of the nanoring, , gives a measure of and coworkers used decamethylcobaltocene (CoCp*2) to prepare 6– global (anti)aromaticity. For c-P6•T6 , o = –3.35 ppm, and [27] radical anions of linear porphyrin oligomers. CoCp*2 is a THS,CH3 = –1.18 ppm. These values are approximately 1.75 convenient reducing agent because it is sufficiently soluble in times higher than those for the aromatic hexacation, c-P6•T66+,[13] + [26] THF, and it has a reduction potential of −1.84 V vs. Fc/Fc , suggesting that the hexaanion has a stronger global diatropic ring making it strong enough to access the 6− oxidation state of c- current than the hexacation. P6∙T6. Addition of excess CoCp*2 to a solution of c-P6∙T6 in d8-THF results in a red-brown solution with a fairly well resolved 1H NMR 6− spectrum corresponding to c-P6∙T6 . Addition of d5-pyridine (5% by volume of solvent) results in a slightly sharper spectrum (Figure 3c). Reduction is reversible and addition of ferrocenium hexafluorophosphate cleanly regenerates c-P6∙T6 (SI Figure S7). Addition of 4 equivalents of CoCp*2 to neutral c-P6∙T6 gives the 4− state, characterized by a broad chemical-shift dispersion (signals up to 18 ppm, Figure 3b).