Spiro-fused bis-hexa- peri -hexabenzocoronene †

A spiro-fused hexa- peri -hexabenzocoronene dimer was synthe-sized, and its physicochemical properties were studied by UV-Vis absorption and emission spectroscopy as well as cyclic voltammetry. Chemical oxidation of SB-HBC aﬀorded its radical cation and dication derivatives, which could be reversibly reduced to the neutral state.

high intrinsic charge-carrier mobility. 25,26 There are numerous planar HBC derivatives in the literature, but there has been only a limited number of reports on the incorporation of HBC into 3D scaffolds, [27][28][29] despite the intriguing properties demonstrated for smaller PAHs arranged in 3D structures, such as intrinsic chirality, 30,31 amorphous aggregation 1 and unique packing modes. 32,33 Herein, we report an efficient synthesis of a novel 3,4,5,6-annulated SBF derivative, bearing two spiro-linked HBC units (spiro-bis-HBC, SB-HBC, Scheme 1). Its robust orthogonally arranged structure was confirmed by X-ray crystallography. The photophysical and electrochemical properties of SB-HBC were investigated in comparison with the parent HBC, revealing largely enhanced absorptivity and two-electron oxidation. Moreover, chemical oxidation and reduction were shown to be reversible.
Single crystals of SB-HBC were grown by slowly diffusing pentane vapor into its tetrahydrofuran solution. As shown in Fig. 2, the SB-HBC molecule revealed a nearly orthogonal spiroshaped structure with the dihedral angle of 87.01 between the two fused five-membered rings. This is close to the reported torsion angle of SBF (ca. 89.01) 35 and also in good agreement with the value of 88.71 calculated for the gas phase by density functional theory (DFT) at the B3LYP/6-31G(d,p) level (Fig. S2, ESI †). The HBC subunits in SB-HBC are slightly bent, with the largest distance of 0.48 Å between the outermost carbons and the plane of the central benzene ring. This is attributed to the concurrent effects of the steric interactions among tert-butyl groups and the strains induced by the five-membered rings. It is noteworthy that adjacent SB-HBC molecules are stacked by p-p overlap of the HBC subunits along the c-axis, forming one-dimensional arrays (Fig. 2c). The intermolecular p-p stacking distances are in the range of 3.42 to 3.63 Å. This molecular stacking mode is similar to that of previously reported spirobiphenalenyl neutral radicals, which show longrange one-dimensional charge-transporting properties. 36,37 The optoelectronic behavior of SB-HBC was initially investigated by UV-Vis absorption spectroscopy in comparison with 2,5,8,11,14,17-hexa-tert-butyl-HBC (HBC-tBu). 38,39 As displayed in Fig. 3a, SB-HBC exhibits a similar but less structured absorption pattern. The significantly enhanced absorption behavior of SB-HBC relative to HBC-tBu can be clearly disclosed from the nearly two-fold enhancement of the maximum molar extinction coefficient (e max (SB-HBC) at 363 nm: B3.1 Â 10 5 L mol À1 cm À1 and e max (HBC-tBu) at 359 nm: B1.8 Â 10 5 L mol À1 cm À1 ). The slightly red-shifted absorption maximum of SB-HBC implied the spiro-conjugation effect between two spiro-fused HBC moieties, which has been previously observed in other spirocyclic fused aromatics. 24 Further lower-energy absorption bands for SB-HBC were observed at 432 nm (e: B6.0 Â 10 3 L mol À1 cm À1 ) with a shoulder at 442 nm and at 464 nm (e: B6.3 Â 10 3 L mol À1 cm À1 ), which are more pronounced compared with the corresponding   peaks from HBC-tBu (inset Fig. 3a). Excitation spectrum of SB-HBC is well consistent with the absorption with distinct long-wavelength excitation bands at 438, 446 and 465 nm (Fig. S6, ESI †). Notably, compared to HBC-tBu, SB-HBC showed an extremely sharp emission band at 467 nm assignable to the 0-0 vibronic transition (Fig. 2a), which is attributed to a reduced symmetry of SB-HBC. 40 Furthermore, the fluorescence quantum yield of SB-HBC was determined to be 0.063, which is higher than the reported values of HBC-tBu (F F = 0.030) and other alkyl substituted HBC derivatives. 41 In contrast to the doubly degenerated HOMO and LUMO of unsubstituted HBC, DFT calculations demonstrated the non-degenerate frontier molecular orbitals (HOMO and LUMO) of SB-HBC, with the electron density shared over the spiro bridge (Fig. 4). On the basis of the time-dependent DFT (TD-DFT) method, HBC shows a symmetry-forbidden low-energy transition at 429 nm (oscillator strength ( f ) = 0.000) (Fig. S4 and Table S1, ESI †), which was previously assigned to the a-band. 42 In contrast, the low-energy transition at 432 nm of SB-HBC is partially symmetry allowed with f = 0.023 ( Fig. S5 and Table S2, ESI †), which is in line with the experimental observations. When studied by cyclic voltammetry, SB-HBC presented reversible two-electron oxidation in the range of 0-1.5 V as evidenced by differential pulse voltammetry (DPV) curves in contrast to the one-electron oxidation process of HBC-tBu (Fig. 3b). The onset oxidation potentials of SB-HBC and HBC-tBu were close to each other (SB-HBC: 0.95 V, HBC-tBu: 0.92 V), which implied their comparable electron-donating abilities.
We also undertook chemical oxidation of SB-HBC using antimony chloride (SbCl 5 ) as the oxidant, which were monitored by UV-Vis-NIR absorption spectroscopy and electron paramagnetic resonance (EPR) measurements. Upon incremental addition of a solution of SbCl 5 in DCM, the light yellow solution of SB-HBC turned red with the appearance of a sharp absorption band at 548 nm and a broad band from 600 to 1000 nm centered at 815 nm (red lines in Fig. 5a). We assign these new absorption bands to the radical cation of SB-HBC (SB-HBC + ), also based on the observation of an intensive EPR signal (g = 2.0033) (inset of Fig. 5a and Fig. S8, S9, ESI †). Excess amounts of SbCl 5 were necessary for this oxidation process (Fig. S7, ESI †). Nevertheless, loss of degeneracy in the HOMO of SB-HBC, as predicted by the DFT calculation (Fig. 4), precludes the formation of bis(radical cation) species.
Further oxidation of the red SB-HBC + with an increasing amount of SbCl 5 afforded a green solution with a broad absorption band centered at 756 nm (green lines in Fig. 5a). These spectral and color changes coincided with the disappearance of the EPR signal (inset of Fig. 5a), suggesting the formation of diamagnetic SB-HBC dication (SB-HBC 2+ ). This is in agreement with the loss of degeneracy of the HOMO mentioned above and in contrast to oxidation of coronene which can form a paramagnetic diradical dication due to the two-fold degenerate HOMOs. 43 It is noteworthy that the green SB-HBC 2+ could be reversibly reduced to the neutral state by adding tin(II) chloride (SnCl 2 ). A stepwise color change was observed from green to red and then to light yellow, which was accompanied by simultaneous changes of the absorption and EPR spectra, demonstrating the recovery of SB-HBC + and then of the neutral SB-HBC (Fig. 5b). The reversible redox property of SB-HBC indicated the good stability of its oxidized species.
In summary, we have demonstrated the efficient synthesis of a spiro-fused bis-HBC (SB-HBC), representing a novel PAH with a robust spiro-linkage. The orthogonally arranged p-system of SB-HBC was proven by X-ray crystallography, with the adjacent molecules stacking by the marked one-dimensional p-p  overlapping pattern. The chemical oxidation of SB-HBC into the stable oxidized species and reversible reduction process are demonstrated. Our result sheds light on p-extended SBF with modulated optical and electronic properties, and can become a starting point for the investigation of other spiro-fused nanographene structures.
We acknowledge the financial support from the Max Planck Society and the European Commission through the FET-Proactive Project ''MoQuaS'' (No. 610449) and Graphene Flagship (No. CNECT-ICT-604391). Open Access funding provided by the Max Planck Society.

Conflicts of interest
There are no conflicts to declare.