as-Indaceno[3,2,1,8,7,6-ghijklm]terrylene as a near-infrared absorbing C70-fragment

Abstract

Carbon and hydrogen are fundamental components of organic molecules and a fascinating plethora of functions can be generated using these two elements. Yet, realizing attractive electronic structures only by using carbon and hydrogen remains challenging. Herein, we report the synthesis and properties of the C70 fragment as-indaceno[3,2,1,8,7,6-ghijklm]terrylene, which exhibits near-infrared (NIR) absorption (up to ca. 1300 nm), even though this molecule consists of only 34 carbon and 14 hydrogen atoms. A remarkably small highest occupied molecular orbital–lowest unoccupied molecular orbital (HOMO–LUMO) gap is confirmed by electrochemical measurement and theoretical calculations. Furthermore, as-indacenoterrylene is stable despite the absence of peripheral substituents, which contrasts with the cases of other NIR-absorbing hydrocarbons such as diradicaloids and antiaromatic molecules. The results of this study thus offer fundamental insights into the design of hydrocarbons with a small band gap.

Introduction

Bowl-shaped aromatic hydrocarbons have been actively explored in modern organic chemistry1,2,3,4,5,6,7,8. Owing to their structural nonplanarity, these molecules exhibit intriguing characteristics such as high solubility, structural flexibility9,10,11,12,13,14, unique host–guest recognition15,16,17,18 and high electronic conductivity19,20. Hence, endowing bowl-shaped aromatic hydrocarbons with unique electronic structures can be considered a promising approach to realize intriguing functions. Recently, Cao and co-workers21 have reported indene-fused corannulene derivative 1, which exhibits a narrow highest occupied molecular orbital–lowest unoccupied molecular orbital (HOMO–LUMO) gap due to its diradical nature (Fig. 1a). Such a nonplanar hydrocarbon with a small HOMO–LUMO gap is attractive with regard to potential applications including near-infrared (NIR)-absorbing dyes and ambipolar organic semiconductors22,23,24.

Fig. 1: NIR-absorbing bowl-shaped (anti)aromatic hydrocarbons 1–3.
figure1

a Indene-fused corannulene derivative 1. b Dicyclopenta[4,3,2,1-ghi:4′,3′,2′,1′-pqr]perylene (2). c as-Indaceno[3,2,1,8,7,6-ghijklm]terrylene (3).

During the past three decades, studies on bowl-shaped aromatic hydrocarbons have been related to C60-fullerene fragments and their π-extended derivatives25,26,27,28,29,30. C60 adopts a sphere-like structure with high symmetry (Ih), while C70-fullerene shows lower symmetry (D5h). Consequently, C70 fragments are inherently diverse, albeit that the hitherto reported C70 fragments remain limited31,32,33,34,35,36,37,38,39,40,41. Among these, especially dicyclopenta[4,3,2,1-ghi:4′,3′,2′,1′-pqr]perylene (2), synthesized by Wu and co-workers,41 is worth mentioning, as 2 exhibits distinct antiaromaticity and a narrow HOMO–LUMO gap (Fig. 1b). Considering that antiaromatic compounds are relatively rare42,43,44,45, this result highlights that the construction of C70-fragments may offer a good opportunity to access unique bowl-shaped hydrocarbons with fascinating electronic structures.

Herein, we disclose the synthesis and properties of C70 fragment as-indaceno[3,2,1,8,7,6-ghijklm]terrylene (3) (Fig. 1c). Surprisingly, 3 exhibits NIR absorption tailing to ca. 1300 nm although it contains only 34 carbons and 14 hydrogen atoms. as-Indacenoterrylene 3 is stable enough even without any peripheral substituents. This feature is contrasting with other NIR-absorbing hydrocarbons such as singlet diradicaloids and antiaromatic molecules.

Results

Synthesis of as-indacenoterrylene 3

The synthesis of as-indacenoterrylene 3 is shown in Fig. 2a. The synthetic approach is based on the incorporation of sp3-hybridized carbon atoms into the fused π-system to generate the curved structure. The bromine–lithium exchange reaction between 1-bromonaphthalene and butyllithium, followed by the addition of 1,4,5,8-tetrachloroanthraquinone (4), afforded the corresponding dinaphthylated diols. The crude mixture was methylated with iodomethane in the presence of sodium hydride, which provided a mixture of cis-adduct 5 and trans-adduct 6 in 22% and 64% yield (over two steps), respectively. These isomers exhibit different solubility in CH2Cl2 and were separated by filtration. The cis-isomer 5 engaged in a Pd-catalysed intramolecular C–H/C–Cl coupling17 to provide methoxy-substituted as-indacenoterrylene 7 in 21% yield, wherein the two five-membered rings are located on the same side. Another isomer, in which the two five-membered rings are located on the opposite side, was not detected. The methoxy group in 7 was transformed to hydrogen using triethylsilane (HSiEt3) and trifluoromethanesulfonic acid (TfOH)46, which afforded 8 in 90% yield. The 1H nuclear magnetic resonance (NMR) signal of the internal hydrogens was observed at 5.91 ppm (Supplementary Fig. 5), which is comparable to that of hydrofullerene C60H2 (5.93 ppm)47. Finally, abstraction of hydrogen from 8 using 1,4-dichloro-2,6-dicyano-p-benzoquinone (DDQ) furnished as-indacenoterrylene 3 in 73% yield. Although 3 exhibits very low solubility in most common organic solvents, it slightly dissolved in CH2Cl2/CS2, o-dichlorobenzene and N-methylpyrrolidone. The attempted reductive aromatization of 7 with SnCl2 and HCl resulted in decomposition without the formation of any isolable products. In addition, no fully fused product was detected in the reaction mixture when trans-adduct 6 was subjected to the intramolecular C–H/C–Cl coupling. This result could be due to the large structural distortion of the expected product having oppositely directed sp3 carbons.

Fig. 2: Syntheses and X-ray crystal structures.
figure2

a Synthesis of as-indacenoterrylene 3. b X-ray crystal structures of internally methoxy-substituted as-indacenoterrylene 7 (left) and internally hydrogenated as-indacenoterrylene 8 (right). Thermal ellipsoids are drawn at 50% probability and all hydrogen atoms except for the internal hydrogen atoms of 8 are omitted for clarity. c Synthesis of 2-mesityl-as-indacenoterrylene 9.

The structures of methoxy-substituted as-indacenoterrylene 7 and hydrogenated as-indacenoterrylene 8 were unequivocally determined by single-crystal X-ray diffraction analysis (Fig. 2b). Both 7 and 8 adopt a bowl-shaped structure with two sp3-hybridized carbon atoms in the central six-membered ring. Notably, 7 and 8 can be regarded as internally functionalized bowl-shaped aromatics, which have been rarely explored48,49,50. The methoxy groups of 7 are aligned perpendicular to the π-surface, which shows a bowl-depth of 2.10 Å. Unfortunately, the crystal data of 8 are insufficient for a detailed structural analysis due to severe disorder.

The 1H NMR spectrum of as-indacenoterrylene 3 in CDCl3/CS2 exhibited seven signals in the range of 7.21–6.78 ppm, supporting a Cs-symmetric structure (Supplementary Fig. 7). These signals are upfield-shifted by ca. 1 ppm compared to those of other C70 fragments, except for antiaromatic dicyclopentaperylene 2 (refs. 31,32,33,34,35,36,37,38,39,40,41). The upfield-shifted 1H NMR signals are characteristic for π-conjugated systems with narrow HOMO–LUMO gaps as theoretical studies suggest that, in such systems, the quantum-chemical perturbation of excited states to the ground state results in the increase of paratropic ring current51,52. The high-resolution atmospheric pressure chemical ionization time-of-flight (APCI-TOF) mass spectrum of 3 showed a parent ion peak at m/z = 423.1184 (calcd for C34H14, m/z = 423.1168 [M + H]+), which is in accordance with the expected molecular composition.

As the low solubility of as-indacenoterrylene 3 hampered a detailed investigation of the physical properties, we synthesized 2-mesityl-as-indacenoterrylene 9 (Fig. 2c). The iridium-catalysed C–H borylation53 of 7 with bis(pinacolato)diboron furnished 2-borylated 10. A subsequent Suzuki–Miyaura cross-coupling reaction with 2-bromomesitylene and 1-bromo-3,5-di-tert-butylbenzene afforded the arylated products 11 and 12, respectively. The structure of 12 was determined by a single-crystal X-ray diffraction analysis (Supplementary Fig. 21). Mesityl-substituted derivative 11 was further transformed to 2-mesityl-as-indacenoterrylene 9, which exhibits high solubility in common organic solvents including CH2Cl2, toluene and tetrahydrofuran.

Bowl-to-bowl inversion

Variable-temperature 1H NMR spectra of 9 were recorded in CDCl3 (Supplementary Fig. 22). At 0 °C, the signals that arise from the ortho-methyl groups of the mesityl substituent were observed as a pair of singlets. At 35 °C, these singlets coalesced to a single singlet at 2.08 ppm. A plot of the experimental ln(k/T) values versus 1/T was fitted by the Eyring equation54, affording the activation enthalpy ΔH and entropy ΔS of 16.9 kcal mol–1 and 4.08 cal K–1 mol–1, respectively (Supplementary Fig. 23). Density functional theory (DFT) calculations at the CAM-B3LYP/6–311+G(d,p)//B3LYP/6–31G(d) level of theory suggest that the bowl-to-bowl inversion passes through a planar transition state (TS) with the activation barrier of 15.1 kcal mol–1 (Supplementary Fig. 24). This value is smaller than the calculated rotation barrier of the peripheral mesityl group (26.1 kcal mol–1) (Supplementary Fig. 25). Hence, the observed temperature dependence of NMR spectra can be interpreted in terms of an inversion of the bowl-shaped structure.

Electronic structures

The ultraviolet (UV)/vis/NIR absorption spectra of 3, 7 and fullerene C70 are shown in Fig. 3a. Methoxy-substituted 7 exhibits weak absorption bands in the range of 400–520 nm, and the presence of vibrational bands implies structural rigidity. The absorption of 7 is blueshifted compared to that of fullerene C70 due to the disrupted conjugation on account of the central sp3-hybridized carbon atoms. In sharp contrast, as-indacenoterrylene 3 displays a significantly redshifted absorption with a peak top at 952 nm and a tail to ca. 1300 nm. The optical HOMO–LUMO gap is 1.30 eV. The extinction coefficient of the broad absorption band (4.1 × 103 cm–1 M–1) is considerable in comparison to those of the forbidden absorption of indene-fused corannulene derivative 1 (ref. 21) and dicyclopentaperylene 2 (ref. 41). As the forbidden S0–S1 transition is a diagnostic feature of antiaromatic molecules42,43,44,45, the allowed nature of the low-energy absorption of 3 cannot be explained in terms of a potential contribution of antiaromaticity. Interestingly, the absorption tail of 3 is even comparable to that of quarteranthene55, which is a zigzag-edge nanocarbon that consists of 56 carbon atoms. The NIR absorption band of 3 obeys the Lambert–Beer’s law and was matched with that of mesityl-substituted derivative 9 (Supplementary Fig. 26). These results clearly suggest a negligible effect of aggregation on the NIR absorption.

Fig. 3: Narrow HOMO–LUMO gap of as-indacenoterrylenes.
figure3

a UV/vis/NIR absorption spectra of 3 (red), 7 (blue), and fullerene C70 (black) in o-dichlorobenzene (λ: wavelength; ε: extinction coefficient). Noise was generated at 900 nm by switching detectors. b Cyclic voltammogram of 2-mesityl-as-indacenoterrylene 9 (solvent: CH2Cl2; supporting electrolyte: 0.1 M [Bu4N][PF6]; reference electrode: Ag/AgNO3). The second oxidation potential was determined by differential pulse voltammetry.

The electrochemical properties of 2-mesityl-as-indacenoterrylene 9 were studied by cyclic voltammetry (Fig. 3b), using the ferrocene/ferrocenium couple as an external reference, which revealed one reversible oxidation wave at 0.17 V as well as two reversible reduction waves at –1.16 and –1.45 V. The electrochemical HOMO–LUMO gap (ΔE = 1.33 eV) is in good agreement with the optical HOMO–LUMO gap. Indene-fused corannulene derivative 1 exhibited redox potentials Eox1 and Ered1 at 0.33 and –0.81 V, respectively21. Dicyclopentaperylene 2 displayed redox potentials Eox1 and Ered1 at 0.33 and –0.96 V, respectively41. The ΔE value of 9 is slightly wider than that of 1 and comparable to that of 2. The redox potentials of 9 are by ca. 0.2–0.3 V positively shifted relative to those of 1 and 2, which is indicative of a higher electron-donating ability.

To evaluate the electronic structure of 3, DFT calculations were conducted at the CAM-B3LYP/6–311+G(d,p) level of theory (Supplementary Figs. 27 and 29). Time-dependent (TD)-DFT calculations predicted the presence of the HOMO–LUMO transition at 820 nm with an oscillator strength of 0.1226, which is in good agreement with the experimental absorption spectrum (Supplementary Fig. 28, Supplementary Table 1). The calculated HOMOs and LUMOs of 3 and its fragments, as-indacenopyrene and terrylene, are shown in Fig. 4a and Supplementary Fig. 31. The HOMO of 3 is delocalized along the longitudinal axis, whose distribution and energy level are almost identical to those of the HOMO of terrylene rather than those of HOMO of as-indacenopyrene. In contrast, the LUMO of 3 is mainly located at the centre of the molecule, which resembles the LUMO of as-indacenopyrene and energetically much lower than the LUMO of terrylene by 0.7 eV. The high electron-deficiency of as-indacenopyrene can be attributed to the incorporated non-alternant hydrocarbon segments56.

Fig. 4: Computational results for the electronic structure of as-indacenoterrylene 3.
figure4

a HOMO and LUMO of 3. Inset: HOMO of terrylene and LUMO of as-indacenopyrene. b NICS values of 3. c ACID plot of 3.

Nucleus-independent chemical shift (NICS)57,58,59 calculations and anisotropy of the induced current density (ACID)60 calculations were conducted for as-indacenoterrylene 3 at the B3LYP/6–31G(d) level (Fig. 4c, d). The NICS(0)iso values, except for that at the five-membered ring, fall in the range –3.9 to 6.4 ppm. An essentially similar trend was also observed for the NICS(1)zz values (Fig. 4c, Supplementary Table 2)59. The ACID plot indicates a negligible contribution of the macrocyclic ring current. Besides, the ACID calculations predict counter-clockwise ring current at the five-membered rings, which accord with the positively large NICS values. Although the exact reason remains unclear, this observation can be accounted for by the local antiaromaticity at the five-membered rings, which could be due to the cyclopentadienyl cation-like electronic contribution associated with the electron-deficient character of as-indacenopyrene segment. These results suggest that the overall electronic structure of 3 cannot be rationalized satisfactorily in term of antiaromaticity.

Calculations of 3 at the CASSCF(2,2)/6–31G level of theory furnished a diradical index (y = 0.05) that is comparable to that of bisanthene (y = 0.07) and much smaller than that of teranthene (y = 0.54)55. The increase of the calculation level (CASSCF(4,6)/6–31G(d)) again provided a relatively small diradical index of y = 0.07. In addition, the closed-shell (CS) singlet, open-shell (OS) singlet and triplet states of 3 were optimized at the (U)CAM-B3LYP/6–311+G(d,p) level (Supplementary Tables 35). The OS singlet state is structurally almost identical with the CS singlet state, being slightly more stable than the CS singlet state by 0.9 kcal mol–1 with the small diradical index of y = 0.03. The triplet state is energetically unfavourable with the energy gap ΔEST of 6.7 kcal mol–1. These results suggest the non-dominant contribution of an OS diradical state, which will be due to a small energetical gain given by the formation of one Clar’s sextet in its resonance structure (Supplementary Fig. 36)61. This assumption has been supported by the experimental fact that heating an o-dichlorobenzene solution of 3 at 100 °C for 12 h in air resulted in no distinct spectral change of the absorption, indicating that 3 is remarkably stable despite the absence of peripheral substituents (Supplementary Fig. 35).

The above-mentioned studies indicate that the electronic structure of as-indacenoterrylene 3 cannot be satisfactorily explained in terms of its antiaromaticity and diradical character. One plausible description could be the coexistence of as-indacenopyrene- and terrylene units, which are moderately merged together without diminishing the individual electronic character. TD-DFT calculations predict that, while the S0–S1 transition of terrylene is allowed (oscillator strength = 0.8363) with a large gap of 2.52 eV, that of as-indacenopyrene is forbidden (oscillator strength = 0.0118) with a small gap of 0.97 eV (Supplementary Figs. 33 and 34). The oscillator strength and energy gap of 3 (0.1226 and 1.51 eV) lie between those of terrylene and as-indacenopyrene. Importantly, the transition dipoles of 3, as-indacenopyrene and terrylene are directed in the same molecular axis, which could be the origin of the moderate mixing of the transitions. Because of the coexistence of electron-accepting and electron-donating segments62, the S0–S1 transition of 3 could include some contribution of the charge-transfer (CT) character. Indeed, the electrostatic potential maps suggest that the S0–S1 transition associates with the change of orbital- and charge-distributions (Supplementary Figs. 30 and 32). The ill-defined absorption feature of 3 and 9 with the absence of vibrational bands in the NIR region is reminiscent of CT character.

Discussion

We have synthesized the C70 fragment as-indaceno[3,2,1,8,7,6-ghijklm]terrylene 3. The synthetic concept is based on the generation of curvature by incorporation of sp3-hybridized carbon atoms in the fused π-system. The structure was assigned based on NMR spectroscopy and mass spectrometry. The physical properties were probed by UV/vis/NIR absorption spectroscopy, cyclic voltammetry, temperature-dependent NMR analysis, and theoretical calculations. Even though 3 contains only 34 carbon and 14 hydrogen atoms, it absorbs in the NIR region up to ca. 1300 nm. The absorption tail of 3 is comparable to organic diradicaloid 1 and antiaromatic hydrocarbon 2. However, as-indacenoterrylene 3 exhibits outstanding stability despite the absence of peripheral substituents, which stands in sharp contrast to the behaviour of other NIR-absorbing hydrocarbons such as diradicaloids and antiaromatic molecules. The current study thus offers effective design guidelines for aromatic hydrocarbons with narrow HOMO–LUMO gaps.

Methods

Materials and characterization

1H NMR (500 MHz) and 13C NMR (126 MHz) spectra were recorded on a Bruker AVANCE III HD spectrometer. Chemical shifts were reported as the delta scale in ppm relative to CDCl3 (δ = 7.26) for 1H NMR and CDCl3 (δ = 77.16 ppm) for 13C NMR. The 1H and 13C NMR spectra of structurally novel chemical compounds are shown in Supplementary Figs. 117. Mass spectra were recorded using a Bruker microTOF by APCI methods. UV/vis/NIR absorption spectra were recorded on a Shimadzu UV-2550 or JASCO V670 spectrometer. X-ray data were obtained using a Rigaku CCD diffractometer (Saturn 724 with MicroMax-007) with Varimax Mo optics using graphite monochromated Mo-Kα radiation (λ = 0.71075 Å). The crystal structures of 5, 7, 8 and 12 are shown in Supplementary Figs. 1821. Redox potentials were measured by the cyclic voltammetry method on an ALS electrochemical analyzer model 612C. Unless otherwise noted, materials obtained from commercial suppliers were without further purification.

Synthesis

Selected procedures are shown below. Other procedures as well as compound data are described in the Supplementary Methods.

Dimethoxy-substituted dihydro-as-indaceno[3,2,1,8,7,6-ghijklm]terrylene (7). A Schlenk tube containing 5 (100 mg, 0.154 mmol), Pd(OPiv)2 (36.8 mg, 0.119 mmol), PCy3•HBF4 (87.6 mg, 0.238 mmol) and K2CO3 (220 mg, 1.59 mmol) was evacuated and then refilled with N2. To the tube, dry and degassed N,N-dimethylacetamide (DMA) (6.0 ml) was added. The mixture was stirred at 130 °C for 2 h and then poured into CH2Cl2. The mixture was passed through Celite. After removing the solvent, the purification by silica-gel column chromatography (CH2Cl2 as eluent) afforded 7 in 21% yield (16.5 mg, 34.0 μmol) as a yellow solid.

Dihydro-as-indaceno[3,2,1,8,7,6-ghijklm]terrylene (8). A 50 mL two-necked round-bottom flask containing 7 (33.4 mg, 68.9 mmol) was evacuated and then refilled with N2. To the tube, CH2Cl2 (40 mL, dried and degassed) and triethylsilane (414 mg, 3.56 mmol) were added. After stirring, trifluoromethanesulfonic acid (51.6 mg, 0.344 mmol) was added. The mixture was stirred at room temperature for 1.5 h. The reaction was quenched with NEt3 (25.3 mg, 0.250 mmol). The mixture was passed through short silica-gel (CH2Cl2 as an eluent). The solvent was removed by rotary evaporator. Washing the residue with MeOH and hexane afforded 8 in 90% yield (26.2 mg, 61.7 mmol) as a yellow solid.

as-Indaceno[3,2,1,8,7,6-ghijklm]terrylene (3). To a 50 ml round-bottom flask, 8 (11.7 mg, 27.6 μmol), CH2Cl2 (15 mL) and CS2 (15 mL) were added. After stirring, a solution of DDQ in CH2Cl2 (6.21 mM, 8.30 mL) was added. The mixture was stirred at room temperature for 30 min. Saturated NaHCO3 aq. was added to the mixture. The reaction mixture was extracted with CH2Cl2/CS2 (1/1). The combined organic layers were dried over Na2SO4 and passed through short silica-gel (CH2Cl2 as an eluent). After removing the solvent, the purification by washing with hexane, MeOH and CHCl3 afforded 3 in 73% yield (8.50 mg, 20.1 μmol) as a dark red solid.

Theoretical calculations

All calculations were carried out using the Gaussian 09 program63. Initial geometry of 3 was obtained from the X-ray structure of 7. The gas phase S0- and S1-geometries of 3 were optimized with the DFT method at the CAM-B3LYP/6–311+G(d,p) level64. Molecular orbitals were calculated at the CAM-B3LYP/6–311+G(d,p) level. The oscillator strengths of 3 were computed by the TD-DFT formalism at the CAM-B3LYP/6–311+G(d,p) level. The NICS and ACID calculations were conducted at the B3LYP/6–31G(d) level.

For the calculations of the possible diradical contribution, the geometries of 3 with the CS singlet, OS singlet and triplet states were optimized at the (U)CAM-B3LYP/6–311+G(d,p) level. The stability analysis was conducted to check the stability of the OS singlet solution. The diradical index y was obtained on the basis of the natural orbital occupation number (NOON) calculation. We also conducted CASSCF calculations at the CS optimized structure to determine y at the CASSCF(2,2)/6–31G and CASSCF(4,6)/6–31G(d) levels.

The TS geometry and intrinsic reaction coordinate were calculated at the B3LYP/6–31G(d) level by using the GRRM17 program65. The energy and freq calculations of the TS and ground state geometries were conducted at the CAM-B3LYP/6–311+G(d,p) level.

Data availability

Crystallographic data (CIF files) for 5, 7, 8 and 12 have been deposited with the Cambridge Crystallographic Data Centre as supplementary publications. CCDC 2004717 (5), CCDC 2004720 (7), CCDC 2004719 (8) and CCDC 2004718 (12) contain the supplementary crystallographic data. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via [www.ccdc.cam.ac.uk/data_request/cif]. All other data supporting the findings of this study are available within the article and its Supplementary Information.

References

  1. 1.

    Scott, L. T. Methods for the chemical synthesis of fullerenes. Angew. Chem. Int. Ed. 43, 4994–5007 (2004).

    CAS  Google Scholar 

  2. 2.

    Kawase, T. & Kurata, H. Ball-, bowl-, and belt-shaped conjugated systems and their complexing abilities: exploration of the concave−convex π−π interaction. Chem. Rev. 106, 5250–5273 (2006).

    CAS  PubMed  Google Scholar 

  3. 3.

    Tsefrikas, V. M. & Scott, L. T. Geodesic polyarenes by flash vacuum pyrolysis. Chem. Rev. 106, 4868–4884 (2006).

    CAS  PubMed  Google Scholar 

  4. 4.

    Wu, Y.-T. & Siegel, J. S. Aromatic molecular-bowl hydrocarbons: synthetic derivatives, their structures, and physical properties. Chem. Rev. 106, 4843–4867 (2006).

    CAS  PubMed  Google Scholar 

  5. 5.

    Segawa, Y., Yagi, A., Matsui, K. & Itami, K. Design and synthesis of carbon nanotube segments. Angew. Chem. Int. Ed. 55, 5136–5158 (2016).

    CAS  Google Scholar 

  6. 6.

    Saito, M., Shinokubo, H. & Sakurai, H. Figuration of bowl-shaped π-conjugated molecules: properties and functions. Mater. Chem. Front. 2, 635–661 (2018).

    CAS  Google Scholar 

  7. 7.

    Majewski, M. A. & Stępień, M. Bowls, hoops, and saddles: synthetic approaches to curved aromatic molecules. Angew. Chem. Int. Ed. 58, 86–116 (2019).

    CAS  Google Scholar 

  8. 8.

    Muzammil, E. M., Halilovic, D. & Stuparu, M. C. Synthesis of corannulene-based nanographenes. Commun. Chem. 2, 58 (2019).

    Google Scholar 

  9. 9.

    Scott, L. T., Hashemi, M. M. & Bratcher, M. S. Corannulene bowl-to-bowl inversion is rapid at room temperature. J. Am. Chem. Soc. 114, 1920–1921 (1992).

    CAS  Google Scholar 

  10. 10.

    Seiders, T. J., Baldridge, K. K., Grube, G. H. & Siegel, J. S. Structure/energy correlation of bowl depth and inversion barrier in corannulene derivatives: combined experimental and quantum mechanical analysis. J. Am. Chem. Soc. 123, 517–525 (2001).

    CAS  PubMed  Google Scholar 

  11. 11.

    Amaya, T., Sakane, H., Muneishi, T. & Hirao, T. Bowl-to-bowl inversion of Sumanene derivatives. Chem. Commun. 84, 765–767 (2008).

  12. 12.

    Mizyed, S. et al. Embracing C60 with multiarmed geodesic partners. J. Am. Chem. Soc. 123, 12770–12774 (2001).

    CAS  PubMed  Google Scholar 

  13. 13.

    Cheung, K. Y., Chan, C. K., Liu, Z. & Miao, Q. A twisted nanographene consisting of 96 carbon atoms. Angew. Chem. Int. Ed. 56, 9003–9007 (2017).

    CAS  Google Scholar 

  14. 14.

    Fernández-García, J. M. et al. π-Extended corranulene-based nanographenes: selective formation of negative curvature. J. Am. Chem. Soc. 140, 17188–17196 (2018).

    PubMed  Google Scholar 

  15. 15.

    Sygula, A., Fronczek, F. R., Sygula, R., Rabideau, P. W. & Olmstead, M. M. A double concave hydrocarbon buckycatcher. J. Am. Chem. Soc. 129, 3842–3843 (2007).

    CAS  PubMed  Google Scholar 

  16. 16.

    Gallego, M. et al. Electron transfer in a supramolecular associate of a fullerene fragment. Angew. Chem. Int. Ed. 53, 2170–2175 (2014).

    CAS  Google Scholar 

  17. 17.

    Yokoi, H. et al. Nitrogen-embedded buckybowl and its assembly with C60. Nat. Commun. 6, 8215 (2015).

    ADS  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Takeda, M. et al. Azabuckybowl-based molecular tweezers as C60 and C70 receptors. J. Am. Chem. Soc. 140, 6336–6342 (2018).

    CAS  PubMed  Google Scholar 

  19. 19.

    Amaya, T. et al. Anisotropic electron transport properties in Sumanene crystal. J. Am. Chem. Soc. 131, 408–409 (2009).

    CAS  PubMed  Google Scholar 

  20. 20.

    Schmidt, B. M. et al. Electronic properties of trifluoromethylated corannulenes. Angew. Chem. Int. Ed. 51, 11385–11388 (2012).

    ADS  CAS  Google Scholar 

  21. 21.

    Lu, R.-Q. et al. Stable diindeno-fused corannulene regioisomers with open-shell singlet ground states and large diradical characters. Angew. Chem. Int. Ed. 58, 7600–7605 (2019).

    CAS  Google Scholar 

  22. 22.

    Ma, J. et al. A stable saddle-shaped polycyclic hydrocarbon with an open-shell singlet ground state. Angew. Chem. Int. Ed. 56, 3280–3284 (2017).

    ADS  CAS  Google Scholar 

  23. 23.

    Hsieh, Y.-C et al. 5,14-Diaryldiindeno[2,1-f:1',2'-j]Picene: a new stable [7]Helicene with a partial biradical character. J. Am. Chem. Soc. 140, 14357–14366 (2018).

    CAS  PubMed  Google Scholar 

  24. 24.

    Ma, J. et al. Wave-shaped polycyclic hydrocarbons with controlled aromaticity. Chem. Sci. 10, 4025–4031 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Barth, W. E. & Lawton, R. G. Dibenzo[ghi,mno]fluoranthene. J. Am. Chem. Soc. 88, 380–381 (1966).

    CAS  Google Scholar 

  26. 26.

    Rabideau, P. W. et al. Buckybowls: synthesis and ab initio calculated structure of the first semibuckminsterfullerene. J. Am. Chem. Soc. 116, 7891–7892 (1994).

    CAS  Google Scholar 

  27. 27.

    Sakurai, H., Daiko, T. & Hirao, T. A synthesis of Sumanene, a fullerene fragment. Science 301, 1878–1878 (2003).

    CAS  PubMed  Google Scholar 

  28. 28.

    Petrukhina, M. A., Andreini, K. W., Peng, L. & Scott, L. T. Hemibuckminsterfullerene C30H12: X-ray crystal structures of the parent hydrocarbon and of the two-dimensional organometallic network {[Rh2(O2CCF3)4]3·(C30H12)}. Angew. Chem. Int. Ed. 43, 5477–5481 (2004).

    CAS  Google Scholar 

  29. 29.

    Steinberg, B. D. et al. Aromatic π-systems more curved than C60. The complete family of all indenocorannulenes synthesized by iterative microwave-assisted intramolecular arylations. J. Am. Chem. Soc. 131, 10537–10545 (2009).

    CAS  PubMed  Google Scholar 

  30. 30.

    Scott, L. T. et al. A short, rigid, structurally pure carbon nanotube by stepwise chemical synthesis. J. Am. Chem. Soc. 134, 107–110 (2012).

    CAS  PubMed  Google Scholar 

  31. 31.

    Wegner, H. A. et al. Oligoindenopyrenes: a new class of polycyclic aromatics. J. Org. Chem. 71, 9080–9087 (2006).

    CAS  PubMed  Google Scholar 

  32. 32.

    Wu, T.-C., Hsin, H.-J., Kuo, M.-Y., Li, C.-H. & Wu, Y.-T. Synthesis and structural analysis of a highly curved buckybowl containing corannulene and sumanene fragments. J. Am. Chem. Soc. 133, 16319–16321 (2011).

    CAS  PubMed  Google Scholar 

  33. 33.

    Wu, T.-C., Chen, M.-K., Lee, Y.-W., Kuo, M.-Y. & Wu, Y.-T. Bowl-shaped fragments of C70 or higher fullerenes: synthesis, structural analysis, and inversion. Dyn. Angew. Chem. Int. Ed. 52, 1289–1293 (2013).

    CAS  Google Scholar 

  34. 34.

    Chen, M.-K. et al. Highly curved bowl-shaped fragments of fullerenes: synthesis, structural analysis, and physical properties. Chem. Eur. J. 20, 598–608 (2014).

    CAS  PubMed  Google Scholar 

  35. 35.

    Stöckl, Q. S., Hsieh, Y.-C., Mairena, A., Wu, Y.-T. & Ernst, K.-H. Aggregation of C70-fragment buckybowls on surfaces: π–H and π–π bonding in bowl up-side-down ensembles. J. Am. Chem. Soc. 138, 6111–6114 (2016).

    PubMed  Google Scholar 

  36. 36.

    Liu, J. et al. Fused dibenzo[a,m]Rubicene: a new bowl-shaped subunit of C70 containing two pentagons. J. Am. Chem. Soc. 138, 8364–8367 (2016).

    CAS  PubMed  Google Scholar 

  37. 37.

    Papaianina, O. et al. Synthesis of rationally halogenated buckybowls by chemoselective aromatic C–F bond activation. Angew. Chem. Int. Ed. 56, 4834–4838 (2017).

    CAS  Google Scholar 

  38. 38.

    Hishikawa, S. et al. Synthesis of a C70 fragment buckybowl C28H14 from a C60 fragment Sumanene. Chem. Lett. 46, 1556–1559 (2017).

    CAS  Google Scholar 

  39. 39.

    Huang, J.-L. et al. Dicyclopenta[ghi,pqr]Perylene as a structural motif for bowl-shaped hydrocarbons: synthetic and conformational studies. Org. Lett. 21, 2504–2508 (2019).

    CAS  PubMed  Google Scholar 

  40. 40.

    Gao, G. et al. Rational functionalization of a C70 buckybowl to enable a C70: buckybowl cocrystal for organic semiconductor applications. J. Am. Chem. Soc. 142, 2460–2470 (2020).

    CAS  PubMed  Google Scholar 

  41. 41.

    Zou, Y. et al. Dicyclopenta[4,3,2,1-ghi:4',3',2',1'-pqr]Perylene: a bowl-shaped fragment of fullerene C70 with global antiaromaticity. J. Am. Chem. Soc. 141, 7266–7270 (2019).

  42. 42.

    Nishinaga, T., Ohmae, T. & Iyoda, M. Recent studies on the aromaticity and antiaromaticity of planar cyclooctatetraene. Symmetry 2, 76–97 (2010).

    CAS  Google Scholar 

  43. 43.

    Braunschweig, H. & Kupfer, T. Recent developments in the chemistry of antiaromatic boroles. Chem. Commun. 47, 10903 (2011).

    CAS  Google Scholar 

  44. 44.

    Sung, Y. M. et al. Control and switching of aromaticity in various all-aza-expanded porphyrins: spectroscopic and theoretical analyses. Chem. Rev. 117, 2257–2312 (2017).

    CAS  PubMed  Google Scholar 

  45. 45.

    Frederickson, C. K., Rose, B. D. & Haley, M. M. Explorations of the indenofluorenes and expanded quinoidal analogues. Acc. Chem. Res. 50, 977–987 (2017).

    CAS  PubMed  Google Scholar 

  46. 46.

    Miyamoto, N. et al. Synthesis of 9,10-diarylanthracenes via Mg(TMP)2·2LiCl-mediated benzyne generation/[4+2] cycloaddition and deoxygenation of 9,10-epoxyanthracene intermediates. Synlett. 29, 513–518 (2018).

    CAS  Google Scholar 

  47. 47.

    Henderson, C. C. & Cahill, P. A. C60H2: synthesis of the simplest C60 hydrocarbon derivative. Science 259, 1885–1887 (1993).

    ADS  CAS  PubMed  Google Scholar 

  48. 48.

    Bronstein, H. E. & Scott, L. T. Fullerene-like chemistry at the interior carbon atoms of an alkene-centered C26H12 geodesic polyarene. J. Org. Chem. 73, 88–93 (2008).

    CAS  PubMed  Google Scholar 

  49. 49.

    Preda, D. V. & Scott, L. T. Addition of dihalocarbenes to corannulene. A fullerene-type reaction. Tetrahedron Lett. 41, 9633–9637 (2000).

    CAS  Google Scholar 

  50. 50.

    Zabula, A. V., Spisak, S. N., Filatov, A. S., Rogachev, A. Y. & Petrukhina, M. A. A strain-releasing trap for highly reactive electrophiles: structural characterization of bowl-shaped arenium carbocations. Angew. Chem. Int. Ed. 50, 2971–2974 (2011).

    CAS  Google Scholar 

  51. 51.

    McWeeny, R. Ring currents and proton magnetic resonance in aromatic molecules. Mol. Phys. 1, 311–321 (1958).

    ADS  CAS  Google Scholar 

  52. 52.

    Aihara, J.-i. General formulas for evaluating ring currents induced in a polycyclic conjugated system. Bull. Chem. Soc. Jpn 58, 1045–1046 (1985).

    CAS  Google Scholar 

  53. 53.

    Preshlock, S. M. et al. High-throughput optimization of Ir-catalyzed C–H borylation: a tutorial for practical applications. J. Am. Chem. Soc. 135, 7572–7582 (2013).

    CAS  PubMed  Google Scholar 

  54. 54.

    Gasparro, F. P. & Kolodny, N. H. NMR determination of the rotational barrier in N,N-dimethylacetamide. A physical chemistry experiment. J. Chem. Educ. 54, 258 (1977).

    CAS  Google Scholar 

  55. 55.

    Konishi, A. et al. Synthesis and characterization of quarteranthene: elucidating the characteristics of the edge state of graphene nanoribbons at the molecular level. J. Am. Chem. Soc. 135, 1430–1437 (2013).

    CAS  PubMed  Google Scholar 

  56. 56.

    Koper, C., Sarobe, M. & Jenneskens, L. W. Redox properties of non-alternant cyclopenta-fused polycyclic aromatic hydrocarbons: the effect of peripheral pentagon annelation. Phys. Chem. Chem. Phys. 6, 319–327 (2004).

    CAS  Google Scholar 

  57. 57.

    Chen, Z., Wannere, C. S., Corminboeuf, C., Puchta, R. & Schleyer, P. v. R. Nucleus-independent chemical shifts (NICS) as an aromaticity criterion. Chem. Rev. 105, 3842–3888 (2005).

    CAS  PubMed  Google Scholar 

  58. 58.

    Schleyer, P. v. R., Maerker, C., Dransfeld, A., Jiao, H. & van Eikema Hommes, N. J. R. Nucleus-independent chemical shifts: a simple and efficient aromaticity probe. J. Am. Chem. Soc. 118, 6317–6318 (1996).

    CAS  PubMed  Google Scholar 

  59. 59.

    Fallah-Bagher-Shaidaei, H., Wannere, C. S., Corminboeuf, C., Puchta, R. & Schleyer, P. v. R. Which NICS aromaticity index for planar π rings is best? Org. Lett. 8, 863–866 (2006).

    CAS  PubMed  Google Scholar 

  60. 60.

    Geuenich, D., Hess, K., Köhler, F. & Herges, R. Anisotropy of the induced current density (ACID), a general method to quantify and visualize electronic delocalization. Chem. Rev. 105, 3758–3772 (2005).

    CAS  PubMed  Google Scholar 

  61. 61.

    Kubo, T. Recent progress in quinoidal singlet biradical molecules. Chem. Lett. 44, 111–122 (2015).

    Google Scholar 

  62. 62.

    Fukazawa, Y., Aoyagi, M. & Ito, S. Naphtho[1,8-ab:4,5-a'b']diazulene, the first nonalternant isomer of dibenzopyrene. Tetrahedron Lett. 22, 3879–3882 (1981).

    CAS  Google Scholar 

  63. 63.

    Frisch, M. J. et al. Gaussian 09, Revision D.01 (Gaussian, Inc., Wallingford, CT, 2013).

  64. 64.

    Yanai, T., Tew, D. P. & Handy, N. C. A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP). Chem. Phys. Lett. 393, 51–57 (2004).

    ADS  CAS  Google Scholar 

  65. 65.

    Maeda, S. et al. Implementation and performance of the artificial force induced reaction method in the GRRM17 program. J. Comp. Chem. 39, 233–250 (2018).

    CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by JSPS KAKENHI grants JP26102003, JP15K21721, JP17H01190 and JP20K15257.

Author information

Affiliations

Authors

Contributions

H.S. and N.F. designed and conducted the project and prepared the manuscript. Y.T. carried out the synthesis and characterization.

Corresponding authors

Correspondence to Norihito Fukui or Hiroshi Shinokubo.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review information Nature Communications thanks David Casanova, Nazario Martín and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Tanaka, Y., Fukui, N. & Shinokubo, H. as-Indaceno[3,2,1,8,7,6-ghijklm]terrylene as a near-infrared absorbing C70-fragment. Nat Commun 11, 3873 (2020). https://doi.org/10.1038/s41467-020-17684-6

Download citation

Further reading

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing