Heteroatom-Doped Nanographenes with Structural Precision.

Nanographenes, which are defined as nanoscale (1-100 nm) graphene cutouts, include quasi-one-dimensional graphene nanoribbons (GNRs) and quasi-zero-dimensional graphene quantum dots (GQDs). Polycyclic aromatic hydrocarbons (PAHs) larger than 1 nm can be viewed as GQDs with atomically precise molecular structures and can thus be termed nanographene molecules. As a result of quantum confinement, nanographenes are promising for next-generation semiconductor applications with finite band gaps, a significant advantage compared with gapless two-dimensional graphene. Similar to the atomic doping strategy in inorganic semiconductors, incorporation of heteroatoms into nanographenes is a viable way to tune their optical, electronic, catalytic, and magnetic properties. Such properties are highly dependent not only on the molecular size and edge structure but also on the heteroatom type, doping position, and concentration. Therefore, reliable synthetic methods are required to precisely control these structural features. In this regard, bottom-up organic synthesis provides an indispensable way to achieve structurally well-defined heteroatom-doped nanographenes. Polycyclic heteroaromatic compounds have attracted great attention of organic chemists for decades. Research in this direction has been further promoted by modern interest in supramolecular chemistry and organic electronics. The rise of graphene in the 21st century has endowed large polycyclic heteroaromatic compounds with a new role as model systems for heteroatom-doped graphene. Heteroatom-doped nanographene molecules are in their own right promising materials for photonic, optoelectronic, and spintronic applications because of the extended π conjugation. Despite the significant advances in polycyclic heteroaromatic compounds, heteroatom-doped nanographene molecules with sizes of over 1 nm and their relevant GNRs are still scarce. In this Account, we describe the synthesis and properties of large heteroatom-doped nanographenes, mainly summarizing relevant advances in our group in the past decade. We first present several examples of heteroatom doping based on the prototypical nanographene molecule, i.e., hexa-peri-hexabenzocoronene (HBC), including nitrogen-doped HBC analogues by formal replacement of benzene with other heterocycles (e.g., aromatic pyrimidine and pyrrole and antiaromatic pyrazine) and sulfur-doped nanographene molecules via thiophene annulation. We then introduce heteroatom-doped zigzag edges and a variety of zigzag-edged nanographene molecules incorporating nitrogen, boron, and oxygen atoms. We finally summarize heteroatom-doped GNRs based on the success in the molecular cases. We hope that this Account will further stimulate the synthesis and applications of heteroatom-doped nanographenes with a combined effort from different disciplines.

Introduction

Since the isolation of single graphene layers by Geim and Novoselov,[1] graphene has opened up tremendous opportunities for materials science because of its extraordinary properties and broad applications.[2−5] In particular, the ultrahigh charge-carrier mobility of graphene is extremely appealing for electronic devices; however, the use of graphene as the active layer in field-effect transistors (FETs) is hindered by the lack of an electronic band gap because the devices cannot be switched off.[6] This disadvantage can be overcome by reduction in the dimensionality of graphene, generating quasi-zero-dimensional graphene quantum dots (GQDs) and quasi-one-dimensional graphene nanoribbons (GNRs) (Figure ).[5,7] Because of quantum confinement, these nanoscale graphenes (nanographenes) are promising for next-generation semiconductor applications with finite band gaps.[8,9] The fabrication of nanographenes is often accomplished through top-down methods such as “cutting” of graphene and carbon nanotubes.[5] The applications of nanographenes, for example, in electronic devices, catalysis, bioimaging and sensing, have also been demonstrated.[8,10] However, the top-down approach cannot accurately control the size and edge structure, which are highly relevant to the physical and chemical properties of nanographenes. Therefore, control of the nanographene structure at the atomic level is required to achieve reliable structure–property correlations and desired functions.[5] This goal can be realized through bottom-up syntheses starting with molecular precursors, and this approach illustrates how organic chemists can contribute to the materials science of nanographenes, providing atomically precise GQDs (e.g., nanographene molecules) and GNRs.[11,12] The capability to precisely control nanographene structures further promotes the creation of emergent materials such as magnetic GNRs and topological insulators by rational molecular design.[13−15]

Figure 1

Schematic illustration of graphene and its nanoscale subunits (i.e., nanographenes), including nanographene molecules (atomically precise graphene quantum dots) and graphene nanoribbons.

Atomic doping is a common strategy to tune the properties of inorganic materials, for instance, in silicon-based semiconductor industry: doping of silicon with group III or group V elements can achieve p-doped or n-doped semiconductors, respectively. The atomic doping strategy is also essential to nanographene materials through incorporation of heteroatoms into the graphenic carbon network, effectively modulating the electronic, magnetic, and catalytic properties.[16] Again, the bottom-up method is indispensable to achieve atomic precision not only in terms of the size and edge structure but also with regard to the heteroatom type, doping position, and concentration. This accuracy is an indispensable tool for controlling the physical properties and revealing structure–property relationships.[11,12] In addition, structurally well-defined heteroatom-doped nanographenes are intriguing semiconducting materials. The heteroatoms in the nanographene framework provide more opportunities for materials development (i) by modulating the band gap and thus the photophysical properties, (ii) by offering rich electrochemical activities, (iii) by installing coordinating sites for metals, and (iv) by stabilizing charges and spins in the carbon skeleton.[16] Nevertheless, large nanographene molecules and GNRs incorporating various heteroatoms (e.g., B,[17] N,[18,19] O,[20] S,[21] and P[22]) are still scarce.[16]

Our group has been working on the synthesis, characterization, and application of nanographenes during the past decades. In 1995 we reported the synthesis of alkyl-substituted hexa-peri-hexabenzocoronene (HBC) 1b,[23] which has a diameter of over 1 nm and can thus be regarded as a nanographene molecule (Figure a).[5,7] Since this seminal work, we have synthesized various HBC derivatives and other larger nanographene molecules by means of a general synthetic strategy, namely, cyclodehydrogenation of polyphenylene precursors (e.g., hexaphenylbenzene 2, Figure a) to afford planarized products.[24] The alkyl substituents not only impart solubility and solution processability to the disc-shaped nanographene molecules but also induce the formation of columnar liquid-crystalline mesophases (Figure b).[24] Charges can therefore be transported through the columnar π–π stacking channel, which is a special concept for FETs and photovoltaic devices.[25−27] We have further extended the synthetic strategy to achieve atomically precise GNRs through conventional solution chemistry and modern on-surface syntheses.[28] These advances have been reviewed in our previous contributions.[5,7,11,12,24,28] In this Account, we focus on our works toward heteroatom-doped nanographenes, which have yet been comprehensively summarized. In the following, we will discuss the design, synthesis, properties, and future opportunities of the research on heteroatom-doped nanographene molecules and GNRs.

Figure 2

(a) Synthesis of HBCs from the corresponding hexaphenylbenzene precursors via cyclodehydrogenation. (b) Columnar self-assembly of disc-shaped nanographene molecules. Reproduced from ref (24). Copyright 2007 American Chemical Society.

From HBC to Heteroatom-Doped HBC Derivatives

Nitrogen-Doped Nanographene Molecules

Following the synthetic strategy of HBCs, it is easy to imagine the possibility of incorporating heteroatoms into the HBC skeleton by replacing the outer phenyl groups with other heteroaromatic rings in the hexaarylbenzene precursor (Figure a). Indeed, Draper et al. synthesized the first N-doped HBC 4 in 2002 through cyclodehydrogenation of the corresponding pyrimidine-substituted precursor 3 (Figure b).[29] The incorporation of pyrimidine rings endowed the nanographene molecule with electron-accepting properties compared with the parent HBC. Furthermore, the N atoms in the bay region served as a coordinating site with transition metals (e.g., PdII and RuII).[30] Not surprisingly, such metal complexes displayed profoundly changed absorption and emission features.

Figure 3

(a) General synthetic route to heteroatom-doped HBC analogues. (b) Synthesis of N-doped HBC 4 incorporating pyrimidine rings. (c) Synthesis of hexapyrrolohexaazacoronenes 6 incorporating pyrrole rings. (d) Several N-doped HBC analogues with a mixture of benzene and pyrrole rings. (e, f) Extensions of the hexapyrrolohexaazacoronene family, as exemplified by compounds 10–14.

To develop electron-donating HBC analogues, in 2007 our group reported the synthesis and properties of hexapyrrolohexaazacoronenes 6 through oxidative cyclodehydrogenation of hexapyrrolylbenzene precursors 5 (Figure c).[31] The peripheral benzene rings were formally replaced with six pyrroles, providing a π skeleton isoelectronic to that of HBC. The interior nitrogens played an important role in stabilizing the oxidation states, and thereby, the dication of 6c was generated by chemical oxidation and isolated under ambient conditions. Later on, together with Takase, Nishinaga, and co-workers, we extended the family of pyrrole-fused HBC analogues by incorporating a mixture of phenyl and pyrrolyl groups in the hexaarylbenzene precursors (Figure d).[32] This unique class of molecules has attracted great interest from other groups. For example, Takase, Uno, and co-workers made further modifications by changing the peripheral aryl moieties (compounds 10 and 11) or by extending the benzene core to naphthalene (compound 12) (Figure e).[33−35] Stępień et al. reported disc-shaped naphthalene monoimide-fused hexapyrrolohexaazacoronene 13 as well as an interesting derivative 14 containing five-, six-, and seven-membered rings, obtained from an indole-containing precursor (Figure f).[36,37]

As pyrimidine and pyrrole are both 6π aromatic heterocycles, incorporation of these rings into nanographene molecules does not change the aromatic nature because the number of π electrons is unchanged. From a chemistry perspective, we were interested in designing a new class of nanographene molecules involving antiaromatic rings that would lead to low energy gaps between the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) as well as excellent redox properties.[38] In 2017, together with Auwärter, Barth, Palma, and co-workers, we conceived an azomethine ylide homocoupling strategy to achieve the synthesis of pyrazine-embedded HBC 15, which possessed an 8π central ring through the introduction of a pyrazine core instead of a benzene core (Figure a).[39] After deprotonation of dibenzo-9a-azaphenalene salts 16, polycyclic azomethine ylides (PAMYs) 17 were generated in situ with several existing resonance structures, including the zwitterionic and diradical forms (Figure d). The PAMYs were highly reactive and underwent dimerization in solution upon heating to afford “dimers” 18. Oxidative dehydrogenation of 18b in a sealed NMR tube under exclusion of air gave N-doped hexabenzoperylene 19, but further cyclodehydrogenation in solution was unsuccessful. Nevertheless, the on-surface method enabled the synthesis of the fully fused N-doped HBC 15 through dimerization and concomitant cyclodehydrogenation on Ag(111) under ultrahigh vacuum (UHV) using dibenzo-9a-azaphenalene salt 16a as the precursor. The chemical structure of 15 was unambiguously characterized by high-resolution scanning tunneling microscopy (STM) and noncontact atomic force microscopy (nc-AFM) with a CO-functionalized tip (Figure b,c). Density functional theory (DFT) calculations at the B3LYP/6-311G(d,p) level revealed a significantly narrowed HOMO–LUMO gap of 15 (2.06 eV) compared with that of the pristine HBC 1a (3.57 eV), suggesting that the introduction of antiaromatic rings could be an effective way to tune the HOMO–LUMO gap and develop low-energy-gap nanographene materials.

Figure 4

(a) Chemical structures of aromatic HBC 1a and antiaromatic pyrazine-embedded HBC 15. (b) STM and (c) nc-AFM images of 15. Scale bars: 2 Å. A molecular model is partially superimposed on the STM image, and a white arrow pointing to the N atoms indicates the molecular symmetry axis. Reproduced with permission from ref (39). Published by Springer Nature. (d) Synthetic route to 15. TBA, tri-n-butylamine; DMSO, dimethyl sulfoxide; DDQ, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone.

Sulfur-Doped Nanographene Molecules

Incorporation of thiophene rings into the polyphenylene precursors results in S-doped nanographene molecules after cyclodehydrogenation. In 2007 we synthesized tribenzothiophene-fused HBC 21a as the first example of S-doped nanographene molecules through cyclodehydrogenation of the C3-symmetric precursor 20a (Figure a).[40] Recently, the tribenzothiophene-fused HBC core of 21a was derivatized by attaching alkoxy and alkyl chains (21b and 21c) to ensure good solubility and to tune their HOMO and LUMO levels.[41] Remarkably, the electron-rich thiophene rings in the alkyl-substituted tribenzothiophene-fused HBC 21c could be oxidized into electron-deficient thiophene-S,S-dioxide moieties, greatly lowering both the HOMO and LUMO levels by about 0.5 eV and representing an appealing feature of thiophene incorporation. In 2011, Draper et al. described another way of introducing thiophene rings in S-doped HBC analogue 24 (Figure b).[42] During the oxidative cyclodehydrogenation, dimerization of 24 was also observed via intermolecular oxidative coupling at the thiophene α-position.

Figure 5

Syntheses of S-doped nanographene molecules. m-CPBA, m-chloroperoxybenzoic acid.

Apart from the above-mentioned method through cyclodehydrogenation of suitable precursors to incorporate thiophene rings, we have also developed a postfunctionalization strategy to fuse thiophenes onto the HBC core based on edge-perchlorinated HBC 26.[43] A thiolation reaction was performed to provide trithiophene-annelated HBCs 27 in 35–50% yield and dithiophene-annelated products 28 in 1.5–3% yield (Figure ).[44] Furthermore, Tan, Zheng, and co-workers employed 27a as hole-transporting material (HTM) in perovskite solar cells, providing the best efficiency of 12.8%, which could be improved to 14.0% through further device optimization.[45] Further studies indicated that 27a endowed the devices with enhanced stability compared with the well-established HTM 2,2′,7,7′-tetrakis[N,N-bis(4-methoxyphenyl)amino]-9,9′-spirobifluorene (Spiro-OMeTAD). In addition, together with Wu, Feng, and co-workers, we used nanographene molecule 27a as a precursor to fabricate ultrathin S-doped graphene films, which were found to be applicable to ultrahigh-rate microsupercapacitors.[46]

Figure 6

Synthesis of S-doped nanographene molecules 27 and 28 via postfunctionalization of perchlorinated HBC 26. DMI, 1,3-dimethyl-2-imidazolidinone. The single-crystal structure of perchlorinated HBC 26 was reproduced with permission from ref (43). Copyright 2013 Macmillan Publishers Ltd.

Intrigued by the beautiful structure of contorted hexa-cata-hexabenzocoronene (29) (Figure a)[47] as well as its partially thiophene-substituted analogues such as dibenzotetrathienocoronenes 30 (Figure b) reported by Nuckolls et al.,[48] we synthesized two fully thiophene-fused coronenes, that is, hexathienocoronenes (HTCs) 31 and 32a–c (Figure c,d).[49] HTCs 31 and 32a–c exhibited almost identical absorption features and a highly electron-rich nature with higher HOMO levels compared with 30. Single-crystal X-ray analysis revealed a columnar π-stacking structure of HTC 32b. A discotic liquid-crystalline phase was observed for HTC 32c with longer dodecyl chains. Together with Chen et al., we employed the backbone of HTC 32a to form a gemini-type amphiphile by attaching hydrophobic and hydrophilic side chains on opposite sides of the aromatic core.[50] The obtained amphiphilic molecule 32d self-assembled into nanofibers in solution. After chemical oxidation with nitrosonium tetrafluoroborate (NOBF4), the nanofibers became electroconductive with a resistivity of 1.1 MΩ, which is lower than the value for the amphiphilic HBC nanotubes (2.5 MΩ).[51]

Figure 7

Chemical structures of (a, b) hexa-cata-hexabenzocoronene (29) and dibenzotetrathienocoronenes 30 as well as (c, d) hexathienocoronenes 31 and 32.

Heteroatom Doping on the Zigzag Edges

The edge topologies of nanographene molecules, such as armchair and zigzag structures (Figure ), are essential to their chemical and physical properties.[12] The majority of bottom-up-synthesized nanographene molecules have armchair edges, as represented by HBC and its derivatives. Although relatively rare, zigzag-edged nanographene molecules are particularly appealing, as they often have low HOMO–LUMO gaps and an open-shell ground state with long zigzag peripheries.[52] Despite the appealing characteristics of zigzag-edged nanographene molecules, their syntheses and characterizations are largely hampered by their instability under ambient conditions. On the one hand, replacement of the all-carbon zigzag edges with isostructural heteroatoms provides new access to stable nanographene molecules featuring zigzag architectures. On the other hand, heteroatom-doped zigzag edges are often theoretically considered as active sites in electrochemical catalysts for the oxygen reduction and hydrogen evolution reactions.[53,54] The synthesis of nanographene molecules having such edge structures can thus provide atomically precise models for investigating the electrocatalytic mechanism.

Figure 8

Schematic illustration of armchair and zigzag edge structures of nanographene molecules.

Inspired by the high performance of N-doped graphene-based materials for electrocatalysis, we synthesized dibenzo-9a-azaphenalene 35 as a model compound to study the catalytic activity of N-doped zigzag edges. Although we could not demonstrate a reasonable activity of 35 in electrocatalysis, we further achieved the synthesis of the linearly extended “dimer” 38 (Figure ), indicating the potential of further extension toward the corresponding GNRs.[55] The PAMY unit in 35 was highly reactive, stemming from its diradical and zwitterionic resonance structures (Figure d). Therefore, compounds 35 and 38 were generated only under inert conditions by deprotonation of their charged precursors 34 and 37. In addition, because of the extremely high chemical reactivity of the N-doped zigzag edges, the dibenzo-9a-azaphenalene-based PAMY offered a new entry to internally N-doped nanographene molecules through 1,3-dipolar cycloaddition with dipolarophiles.[56] This chemical reactivity was also independently exploited by Ito, Tokimaru, and Nozaki[57] and used for syntheses of azapentabenzocorannulene derivatives.[58,59]

Figure 9

Synthesis of N-doped zigzag peripheries 35 and 38.

We have also considered the incorporation of multiple heteroatoms to obtain stable heteroatom-doped zigzag edges and deeper insights into the effects of doping on the chemical and physical properties. Together with Zhang, Feng, and co-workers, we conceived nitrogen–boron–nitrogen (NBN)-doped zigzag peripheries based on 1,9-diaza-9a-boraphenalene as the next structural motif.[60] Both monomers 40 and the linearly fused “dimer” 45 were synthesized through electrophilic borylation (Figure ). The NBN-doped zigzag edges exhibited high chemical stability, allowing for electrophilic bromination of 40b and further modifications through cross-coupling reactions to give 42 (Figure a). Furthermore, chemical oxidation of monomers 40 led to σ dimers 43 connected at the positions para to the N atoms. To avoid such a dimerization reaction during oxidation, the active positions were protected by additional phenyl substituents (i.e., compound 42). Clean single-electron oxidation of the NBN-doped zigzag peripheries to afford radical cation 42•+ was demonstrated by in situ spectroelectrochemistry, shedding light on the photophysical perperties of its isoelectronic dibenzophenalenyl radical.

Figure 10

Synthesis of NBN-doped zigzag peripheries based on the 1,9-diaza-9a-boraphenalene motif. (a) Synthetic route to monomers 40 and further derivatizations. (b) Synthetic route to “dimer” 45. NBS, N-bromosuccinimide; o-DCB, o-dichlorobenzene.

In parallel to the studies on heteroatom-doped nanographene molecules, we also tried to tackle the syntheses of peri-acenes (e.g., peri-tetracene[61,62] and peri-pentacene[63]), which comprise two acenes laterally fused at all of the peri positions and can be viewed as segments of full zigzag GNRs (Figure ). It was thus a logical extension to consider the synthesis of heteroatom-doped peri-acenes as the next targets. Our initial attempts to make NBN-doped peri-tetracene turned out to be challenging, and we are still working on different routes to synthesize it, but we were successful in installing oxygen–boron–oxygen (OBO) segments on the zigzag peripheries of peri-acenes. More specifically, we developed a tandem demethylation–borylation method to construct OBO-fused tetrabenzo[a,f,j,o]perylenes 48 by simple heating of precursors 47 with BBr3 in o-dichlorobenzene (Figure a).[64] Further cyclodehydrogenation of 48 provided the first heteroatom-doped peri-tetracenes 49 in 2016, before the all-carbon peri-tetracenes were achieved in 2018.[65,66] The OBO-doped peri-tetracene exhibited excellent ambient stability, blue fluorescence, and a large HOMO–LUMO gap with a low-lying HOMO level compared with pristine peri-tetracene. The incorporation of OBO units drastically changed the properties of peri-tetracene, and therefore, isoelectronic heteroatom doping would be important to maintain the open-shell character of peri-tetracene while improving its stability for potential applications. It is noteworthy that Hatakeyama et al. independently reported compound 48a obtaind by a different method (Figure b), in which a precursor containing two extra iodo groups was used to generate 48a in 55% yield.[67] Our method gives higher yields (>90%) and is simpler since it is based on direct C–H borylation without the need for iodo groups in the precursor. It must be noted that Hatakeyama et al. also independently reported the use of the direct C–H borylation method to synthesize heteroatom-doped benzo[fg]tetracene structures with OBO, NBN, and SBS substitution on the zigzag peripheries.[68]

Figure 11

Schematic representations of peri-acenes and heteroatom-doped peri-acene-type nanographene molecules as a segment of full zigzag GNRs.

Figure 12

(a) Synthesis of OBO-doped peri-tetracenes 49. (b) Another method to synthesize the uncyclized precursor 48a and an isomer of 48b with different substituent positions (compound 51). TfOH, trifluoromethanesulfonic acid.

In our pursuit of longer peri-acene-type nanographene molecules, we synthesized OBO-doped peri-hexacene as the longest peri-acene analogue.[69] We first tried to furnish the OBO-fused precursor 54 by our tandem demethylation–borylation method from 1,2,4,5-tetrakis(3-methoxynaphthalen-2-yl)benzene (52) (Figure a), but the reaction was not successful, probably because of the high reactivity of naphthalene α-positions during the electrophilic borylation. Therefore, we adopted Hatakeyama’s method by introducing iodo groups on the central benzene to synthesize 1,4-diiodo-2,3,5,6-tetrakis(3-methoxynaphthalen-2-yl)benzene (53). After lithiation and reaction with BBr3, the OBO-fused precursor 54 was obtained in 43% yield (Figure a). However, oxidative cyclodehydrogenation of 54 in solution did not provide the planarized product after attempts under different conditions. We thus employed on-surface synthesis in collaboration with Fasel et al. and achieved the OBO-doped perihexacene 55 on Au(111) by heating precursor 54 at 380 °C under UHV (Figure a). The structure of 55 was unambiguously characterized by STM and nc-AFM (Figure b,c). Furthermore, OBO-doped peri-hexacene 55 formed two kinds of 1D superstructures via intermolecular hydrogen bonding and metal coordination with the OBO segments on the zigzag edges (Figure b,d), demonstrating a potential edge-doping strategy for engineering self-assembled structures of graphene nanoarchitectures.

Figure 13

(a) Synthetic route to OBO-doped peri-hexacene 55. (b) STM and (c) nc-AFM images of 55 on a Au(111) surface. (d) Schematic illustration of molecular assembly via metal coordination and O···H hydrogen bonding. Reproduced from ref (69). Copyright 2017 American Chemical Society.

The OBO-fused precursor 54 featured a double [5]helicene substructure, which underwent a conformational change upon interactions with the surface.[69] On the other hand, in the crystal structure of double [5]helicene 48a, we observed a pair of (P,P) and (M,M) enantiomers in one unit cell.[64] Hatakeyama et al. separated the enantiomers of such a double [5]helicene through the incorporation of bulky tert-butyl groups (compound 51) to increase the isomerization energy barrier.[67] The interesting properties of double helicenes inspired us to further push the limit of double helicene synthesis and to explore their chiroptical properties. By adjusting the connectivity of the naphthalene rings, we synthesized the first double [7]helicene 57 (Figure a),[70] which is an isomer of the π-extended OBO-fused double [5]helicene 54. Compound 57 was obtained in 7% yield through a tandem demethylation–borylation reaction of 1,2,4,5-tetrakis(2-methoxynaphthalen-1-yl)benzene (56). The isolated yield is apparently lower than those of compounds 48 (over 90%), presumably because of the high strain built up during the ring closure. Single-crystal X-ray diffraction revealed substantial π overlap between the terminal benzene rings (Figure b). Compound 57 exhibited excellent chiral stability, which facilitated the optical resolution of the enantiomers by chiral HPLC. The separated (P,P) and (M,M) isomers displayed opposite responses in circular dichroism spectra (Figure c). The successful synthesis of the first double [7]helicene with OBO incorporation demonstrated the efficacy of the tandem demethylation–borylation method in the synthesis of even strained architectures, stimulating more efforts toward longer double helicenes and opening up a new avenue to chiral synthetic nanographenes.

Figure 14

(a) Synthetic route to OBO-fused double [7]helicene 57. (b) Single-crystal structures of the (M,M) and (P,P) isomers. (c) Circular dichroism spectra of the (M,M) and (P,P) isomers. Reproduced from ref (70). Copyright 2016 American Chemical Society.

To examine the scope of the tandem demethylation–borylation reaction, we tested the direct C–H borylation reactivity toward the chemically inert 2- and 7-positions of pyrene (Figure ).[71] We found that the tandem reaction readily occurred under typical conditions, generating a new kind of oxaborin-annelated pyrene-based chromophores (60 and 63) in excellent yields (>95%). The singly annelated compound 60 displayed strong blue fluorescence (λmax = 442 nm, ΦF = 70%), whereas the doubly annelated product 63b resembled perylene diimide (PDI) dyes in terms of bright green fluorescence (λmax = 525 nm, ΦF = 84%) and strong aggregation tendency in solution. The tandem demethylation–borylation reaction thus provided a new method for π extension of pyrene to obtain novel photonic and optoelectronic materials.

Figure 15

Synthetic routes to oxaborin-annelated pyrene derivatives 60 and 63 and their solutions in CHCl3 under UV light (365 nm). Images were reproduced with permission from ref (71). Copyright 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Toward Heteroatom-Doped Graphene Nanoribbons

The studies of the nanographene molecules have paved the way to heteroatom-doped GNRs by offering model cases. For example, when we established the surface-assisted synthesis of atomically precise GNRs together with Fasel et al. in 2010, we fabricated chevron-type GNR 65 from 6,11-dibromo-1,2,3,4-tetraphenyltriphenylene precursor 64 (Figure a,b).[72] The chevron-type GNR comprises HBC units that are fused side by side. Therefore, considering the many heteroatom-doped HBC analogues as described previously, one could easily imagine synthesizing heteroatom-doped chevron-type GNRs by modifying the triphenylene-based molecular precursors. Among the various possibilities, N doping is particularly interesting, as it can effectively lower the valence and conduction bands to afford n-type semiconductors. In 2013, Bronner, Hecht, Tegeder, and co-workers synthesized N-doped chevron-type GNRs 67 by replacing one or two phenyl rings with 4-pyridinyl groups in the monomers (Figure c).[73] Compared with the pristine chevron-type GNR 65, the introduction of N atoms simultaneously lowered the valence and conduction bands, leaving the band gaps nearly unchanged. In 2014, together with Du, Gao, and co-workers, our group reported N-doped GNR 67b fabricated on Au(111) under UHV and investigated its structure by high-resolution STM.[74] Different from its all-carbon counterpart 65, the N-doped GNR 67b exhibited a side-by-side alignment due to the inter-ribbon N···H interactions (Figure d). In the same year, together with Fasel et al., we reported the on-surface synthesis of GNR heterojunction 69 comprising alternating pristine and N-doped GNR segments (Figure e–g).[75] The incorporation of N atoms was accomplished by replacing two phenyl groups with 5-pyrimidinyl rings in the triphenylene-based precursor to give monomer 68. The resulting GNR heterojunction 69 displayed a band offset of about 0.5 eV, representing the first GNR-based p–n junction and indicating great potential for future applications in nanoelectronics.

Figure 16

(a) Surface-assisted synthesis of chevron-type GNR 65. (b) STM image of GNR 65 on a Au(111) surface. Reproduced with permission from ref (72). Copyright 2010 Macmillan Publishers Ltd. (c) Surface-assisted synthesis of N-doped chevron-type GNRs 67. (d) High-resolution STM image of GNR 67b, displaying a side-by-side alignment due to inter-ribbon N···H interactions. Reproduced with permission from ref (74). Copyright 2014 AIP Publishing LLC. (e) Surface-assisted synthesis of GNR heterojunction 69. (f, g) STM images of GNR heterojuction 69, with N-doped and pristine GNR segments highlighted in blue and light-gray dashed lines, respectively. Reproduced with permission from ref (75). Copyright 2014 Macmillan Publishers Ltd.

N-doping of GNRs in the form of pyridine and pyrimidine rings lowers the energies of the valence and conduction bands, whereas the band gap is nearly unaffected because the lone pair of N atoms is not conjugated with the GNR π system. In this regard, S doping in the form of thiophene incorporation is supposed to involve the lone pair in the π conjugation of GNRs and thus can effectively modulate the electronic structures and band gaps. Recently, together with Du, Gao, and co-workers, our group described the on-surface synthesis of S-doped GNR 71 by employing 6,11-dibromo-1,4-diphenyl-2,3-bis(thien-3-yl)triphenylene (70) as the monomer (Figure a), that is, by replacing two phenyl rings with 3-thienyl groups in the typical triphenylene-based monomer.[76] Different from the N-doped chevron-type GNRs, the rotation of the single bonds connecting thienyl rings and the triphenylene core led to different isomers when the precursor was deposited on the Au(111) surface (Figure b). After polymerization and cyclodehydrogenation at 450 °C, different S-doped GNR segments were obtained (Figure c–e), giving rise to a sequence of tunable band gaps (1.28–1.78 eV), as confirmed by experimental STM and scanning tunneling spectroscopy (STS) as well as theoretical calculations. Through molecular engineering of the triphenylene-based monomers, Fischer et al. further achieved heteroatom-doped chevron-type GNRs with trigonal-planar S-, N-, and O-dopant atoms.[77]

Figure 17

(a) Surface-assisted synthesis of S-doped GNR 71. (b) Distinct isomers of 70 due to restriction of thienyl group rotation on Au(111). (c) Schematic illustration of GNR 71 on Au(111). (d) Large-area STM image of GNR 71. (e) High-resolution STM image of GNR 71 with an overlaid chemical structure. Reproduced with permission from ref (76). Copyright 2017 Tsinghua University Press and Springer-Verlag GmbH Germany.

As we had developed heteroatom-doped zigzag-edged nanographene molecules, we subsequently aimed at synthesizing GNRs with heteroatom-doped zigzag edge topologies. During the past years, although armchair GNRs have been extensively investigated,[79] zigzag GNRs have very rarely been achieved (Figure ).[13] Chiral GNRs with a mixture of armchair and zigzag edges have also attracted great attention, but the bottom-up-synthesized structures have been limited only to (3,1)-GNRs (for the definition of the chiral index, see Figure ) obtained from 9,9′-bianthracene-based monomers,[80] calling for further variations of the chiral edge configurations.

Figure 18

Schematic representation of (a) armchair GNRs, (b) zigzag GNRs, and (c) chiral GNRs. The edge configuration of chiral GNRs in (c) is defined by the translation vector C, described as C = na1 + ma2 = (n, m), where a1 and a2 represent the unit vectors of the graphene lattice. Reproduced from ref (78). Copyright 2018 American Chemical Society.

In 2018, together with Fasel et al., we reported the surface-assisted synthesis of the first heteroatom-doped chiral (4,1)-GNR 74 from the rationally designed monomer 6,16-dibromo-9,10,19,20-tetraoxa-9a,19a-diboratetrabenzo[a,f,j,o]perylene (73) containing both boron and oxygen (Figure a). It should be noted that bottom-up-synthesized GNRs with multiple heteroatom substitution are still scarce.[81] Monomer 73 was synthesized through tandem demethylation–borylation of 1,4-bis(5′-bromo-2′-methoxyphenyl)-2,5-bis(2′-methoxyphenyl)benzene (72) bearing two bromo groups. The structure of the chiral GNRs was characterized by STM and nc-AFM (Figure b–d) as well as Raman spectroscopy. STS studies and theoretical calculations revealed a larger band gap of the OBO-doped (4,1)-GNRs compared with the pristine (4,1)-GNRs. As a result of the OBO units on the edges, lateral assembly of the chiral GNRs was observed, achieving aligned GNR arrays with different homochiral and heterochiral inter-ribbon assembly modes (Figure e,f). The first OBO-doped GNRs suggested that the OBO structures on the edges facilitated lateral alignment of GNRs, which would be of importance for future GNR-based devices.

Figure 19

(a) Surface-assisted synthesis of OBO-doped (4,1)-GNR 74. (b) Large-area STM image and (c) high-resolution STM image of GNR 74 on Au(111). (d) nc-AFM image of GNR 74. (e, f) Theoretically calculated models of inter-ribbon interactions for heterochiral and homochiral assemblies of GNR 74, respectively. Reproduced from ref (78). Copyright 2018 American Chemical Society.

Conclusions and Outlook

We have summarized our works on heteroatom-doped nanographene molecules and GNRs during the past decade. On the basis of the prototypical nanographene molecule HBC, we have explored N doping through the incorporation of aromatic pyrrole and antiaromatic pyrazine rings. We have also developed a series of thiophene-annelated HBC derivatives as S-doped nanographene molecules. These results have promoted heteroatom doping as a powerful method for modulating the energy levels, band gaps, aromaticity, electron densities, and magnetic properties of nanographene molecules. Moreover, being aware of the importance of zigzag-edged nanographene molecules, we have explored heteroatom doping on zigzag edge structures, including generation of the PAMY as well as NBN and OBO incorporation. In particular, the OBO-doped compounds are easy to synthesize and are stable under ambient conditions, thereby representing a new class of nanographene molecules, including stable peri-tetracene and peri-hexacene analogues displaying intermolecular self-assembly tendency on the surface and double [7]helicene with high chiral stability as well as new pyrene-based chromophores. All of these achievements in nanographene molecules have paved the way to heteroatom-doped GNRs, such as N-doped and S-doped chevron-type GNRs with tunable band gaps and OBO-doped chiral (4,1)-GNRs with lateral alignment.

Nanocarbon science has attracted increasing interest in recent years, giving rise to a variety of carbon nanostructures. The incorporation of heteroatoms into the carbon frameworks provides a number of new opportunities to fine-tune the molecular properties. Certainly this process defines grand challenges in synthesis, thereby requesting the development of new and efficient synthetic methods. Convincing cases have been demonstrated in the PAMY chemistry and the tandem demethylation–borylation reaction, both of which have opened up new avenues to various heteroatom-doped nanographenes. Furthermore, the synthesis of heteroatom-doped GNRs is lagging behind that of nanographene molecules. There is much room to explore new structures such as pyrrole- and pyrazine-incorporated GNRs and heteroatom-doped full zigzag GNRs. In any case, close collaborations among chemists, physicists, and engineers are required to realize the applications of GNRs in future nanoelectronic and spintronic devices.