Polycyclic aromatic hydrocarbons (PAHs) and their heterocyclic analogs possessing curved π-conjugated architectures (e.g., saddle- or bowl-shaped) attract substantial attention of the broad scientific community due to their unparalleled properties and potential application in the field of organic electronics1,2,3,4,5,6. Seminal publications on the synthesis of corannulene reported by Scott7 and Siegel8,9 encouraged chemists all over the world to pursue the goal of bottom-up synthesis of fullerene and carbon nanotubes10. Indeed, truly enthralling architectures have been synthesized over the recent years11,12,13,14. Displacement from planarity in π-extended systems usually requires harsh reaction conditions, which heterocycles rarely tolerate. Incorporation of heteroatoms into polycyclic aromatic frameworks, however, should drastically change their intrinsic optoelectronic properties15,16,17,18. Synthesis of nitrogen-embedded corannulene analogs is a challenging task. Only recently, two groups independently reported preparation of such conjugates19,20.

Serendipitous discovery made in our laboratory in 2013 on the one-pot, multicomponent synthesis for 1,2,4,5-tetraarylpyrrolo[3,2-b]pyrroles (TAPPs) opens up the possibilities for the formation of previously unknown π-expanded aza-analogs of PAHs21,22,23. A particularly suitable feature of this methodology is the fact that sterically congested ortho-substituted benzaldehydes give products in high yields, which makes this approach a powerful tool for the construction of highly conjugated molecules comprising pyrrolo[3,2-b]pyrrole (PP) units24,25,26,27,28. Conversely, presence of two fused pentagonal rings in the center makes the pursuit of circularly conjugated species particularly complex, since it requires thermodynamically demanding closure of two heptagonal rings. In this regard, modern on-surface chemistry serves as a powerful synthetic tool toward bottom-up fabrication of complex nanostructures unattainable via solution chemistry29. Many challenging syntheses of carbon-based nanostructures have been realized through this approach including atomically precise graphene nanoribbons30, single-chirality single-walled carbon nanotubes31, longest to-date acenes32 and periacenes33, and embedment of non-hexagonal rings in PAHs34.

Here we report a concise preparation of the first fully conjugated buckybowl based on the PP scaffold. Our synthetic pathway encompasses a combination of in-solution and on-surface chemistry. In particular, on-surface cyclodehydrogenation of suitably designed precursor molecules on a Au(111) surface was the crucial step toward formation of the nitrogen-embedded buckybowl. Bond-resolved scanning tunneling microscopy (STM) unequivocally confirms the structure of the final molecule. In addition, scanning tunneling spectroscopy (STS) in combination with density functional theory (DFT) calculations further lend support to the synthesis of the final product. Notably, the core of the buckybowl contains a unique combination of pentagonal and heptagonal rings: the inverse Stone–Thrower–Wales (ISTW) topology, a topological defect in graphene that remains challenging to obtain experimentally. As a consequence of this unique topology, the nitrogen-doped buckybowl adopts a dome-shaped bowl-opening-down conformation on the surface—a property unprecedented for isolated buckybowls on surface.


Design and synthesis of precursor molecules

Our previous studies indicated that scrupulous design of TAPPs bearing bromine atoms and aryl rings in ortho position with respect to the central core facilitates smooth expansion of the π-system by means of intramolecular direct arylation and oxidative aromatic coupling, respectively25,27. Highly conjugated molecules based on the PP core adopt nonplanar architecture due to the close spatial vicinity of adjacent benzene rings.

Our initial assumption was that the naked analog 6a (lacking any bulky groups at the peripheries) might serve as a precursor for the on-surface cyclodehydrogenation. We thus began with the synthesis of the parent TAPP 4a bearing bromine atoms and phenyl rings in suitable ortho positions with respect to the central core (Fig. 1, left panel). One-pot multicomponent condensation between 2-bromo-6-phenylbenzaldehyde (1a), aniline (2a) and butane-2,3-dione (3) gives 4a in 36% yield. Subjecting 4a to palladium-catalyzed intramolecular direct arylation leads smoothly to the formation of two new carbon–carbon bonds around the core and hence to the planar derivative 5a obtained in 80% yield. In the final step we employed oxidative aromatic coupling utilizing iron(III) chloride. As a result, the central core is connected with two peripheral benzene rings leading to the nonplanar compound 6a produced in 90% yield. Subjecting 6a prepared in this way to subsequent traditional oxidation methods, such as DDQ/TfOH, MoCl5, etc., however, does not give the desired compound 8.

Fig. 1
figure 1

Synthetic route to the nitrogen-embedded buckybowl 8. (Left panel) Solution-synthetic routes to precursor molecules 6a and 6b. (Right panel) Subsequent on-surface synthetic route to partially closed species 7a, 7b and the fully conjugated nitrogen-embedded buckybowl 8. Crucial rings formed in the final steps are marked in colors (via oxidative aromatic coupling—yellow, via on-surface cyclodehydrogenation—blue)

Previous success in the formation of highly π-extended species by surface-assisted techniques motivated us to apply this approach to compound 6a. In this case, on-surface cyclodehydrogenation effectively leads to the formation of half-closed species with only one heptagonal ring, 7a (Fig. 1, right panel). Conversely, the targeted fully conjugated compound containing two heptagons is not formed.

This partial success prompted us to design an alternative precursor 6b, which possesses two preformed heptagonal rings. In this approach, additional benzene rings originate from aniline derivatives. Indeed, condensation between 2-bromobenzaldehyde (1b), 2-aminobiphenyl (2b), and butane-2,3-dione (3) gives TAPP 4b in 33% yield (Fig. 1, left panel). Analogous to the previous synthesis, subjecting TAPP 4b to palladium-catalyzed intramolecular direct arylation produces planar π-extended derivative 5b in 80% yield. Compound 5b undergoes efficient oxidation with iron(III) chloride in dichloroethane at 80 °C giving 6b in 60% yield. This reaction leads to the formation of two new C–C bonds and results in a highly distorted π-extended PP derivative possessing two heptagons in its structure.

Unlike 6a, cyclodehydrogenation of 6b requires the closure of two hexagonal instead of two heptagonal rings to obtain the fully conjugated target species 8. Opportunely, precursor 6b proves to be viable for on-surface cyclodehydrogenation. Annealing this compound to 320 °C under ultra-high vacuum (UHV) conditions on a Au(111) substrate effectively leads to the formation of the desired nitrogen-embedded buckybowl 8 (Fig. 1, right panel).

On-surface synthesis of nitrogen-embedded buckybowls

After sublimation of precursor 6a under UHV conditions onto an atomically clean Au(111) surface held at room temperature, large-scale STM images (Fig. 2a) acquired at 5 K show the presence of self-assembled chains that follow the Au(111) herringbone reconstruction, along with sporadically distributed individual molecules. Figure 2b shows a representative high-resolution STM image of the predominant species on the surface (95% of 170 molecules), which presents two bright lobes of 2.5 Å in height (measured at a sample bias of −1 V). The experimental features are well reproduced by the DFT-optimized geometry of 6a on a Au(111) surface (Fig. 2d, e), which shows that 6a adopts a twisted conformation on the surface. In addition, the corresponding STM simulation (Fig. 2c) agrees well with the experimental STM image.

Fig. 2
figure 2

On-surface reaction of 6a on Au(111). a Overview STM topography image of the surface after room temperature deposition of 6a, revealing the coexistence of predominant chains running along fcc domains, and isolated molecules (V = −1 V, I = 10 pA, scale bar: 5 nm). b High-resolution STM image (V = −0.1 V, I = 50 pA, scale bar: 1 nm) and c DFT-simulated STM image (V = −0.2 V, scale bar: 1 nm) of 6a. The colored dots serve as a guide to the eye for comparing the intramolecular features in experimental and simulated STM images. d, e Top and side views of the DFT equilibrium geometry of 6a. f Overview STM topography image of the surface after annealing to 280 °C (V = −1 V, I = 10 pA, scale bar: 5 nm). The white circle highlights the half-closed species 7a, presenting only one lobe. g High-resolution STM image of 7a acquired with a CO tip (V = 10 mV, I = 50 pA, scale bar: 0.5 nm). The blue rectangle marks the acquisition area of the UHR-STM image. h Corresponding UHR-STM image of 7a (open feedback parameters: V = 5 mV, I = 50 pA; Δz = −50 pm; scale bar: 0.5 nm). The red arrow indicates the heptagonal ring formed after this annealing step. i, j Top and side views of the DFT equilibrium geometry of 7a. The newly formed bond at this annealing step is highlighted in red

Annealing the surface to 280 °C brings about notable changes in the surface topography. Large-scale STM images (Fig. 2f) show an absence of chains, with isolated molecules present on the surface. Majority of the species have a two-lobed appearance (38% of 100 molecules) and presumably did not undergo cyclodehydrogenation. Notably, there is appearance of a new species (15% of 100 molecules) that present only one lobe of much lower apparent height compared to 6a (highlighted with a white circle in Fig. 2f). While it could be speculated that appearance of only one lobe hints at partial intramolecular cyclodehydrogenation and concomitant planarization of one lobe, it is rather difficult to conclusively identify the exact chemical structure of this product via STM imaging alone, which fundamentally probes the local density of states (LDOS) near the Fermi energy. To circumvent this limitation, we functionalize our tip by a CO molecule that helps us probe the sample in the regime of the onset of Pauli repulsion, thereby allowing to visualize the chemical structure of the molecule. It has been shown that STM tips functionalized with single atoms or molecules can serve as a nanoscale transducer, converting atomic-scale forces exerted by the sample on the tip functional moiety to conductance variations in the tunneling junction35,36. Our choice of CO as the tip functional moiety is governed by its facile manipulation on metal or insulating substrates and its rigid bonding to the metal tip, yielding images of high fidelity36. Figure 2g shows a high-resolution STM image of the one-lobed species acquired with a CO-functionalized tip. While only weak intramolecular contrast can be discerned, it is nevertheless clear that this species adsorbs flat on the surface except for a sharp ridge around the position of the lobe. Furthermore, at the expected position of the second lobe in 6a, we instead find a smooth bay indicating a possible bond closure. Finally, an ultra-high-resolution STM (UHR-STM) image (Fig. 2h) of the bottom part of the molecule (highlighted with a blue rectangle in Fig. 2g) clearly shows formation of a heptagonal ring at the aforementioned bay position (indicated with a red arrow), which leads us to conclude that at this temperature, partial intramolecular cyclodehydrogenation occurs to form the half-closed species 7a. Figure 2i, j show the DFT-optimized structure of 7a on Au(111), which correctly reproduces the experimental features—i.e., the out-of-plane bending of a benzenoid ring corresponding to a single lobe in the STM images, and the otherwise planar adsorption geometry of the molecule on the surface.

Finally, we anneal the surface upwards of 350 °C in an attempt to induce full ring closure. Unfortunately, it was seen that for higher temperatures, intermolecular covalent coupling and side reactions dominate and full ring closure is not observed (see Supplementary Fig. 21). It is worth to mention that we systematically tried to induce ring closure on more catalytically active coinage metal surfaces—i.e., Ag(111) and Cu(111). On Ag(111) (see Supplementary Fig. 19) half-closure to form 7a does take place, but the molecules start to decompose upwards of 300 °C without full ring closure. On the most active Cu(111) surface (see Supplementary Fig. 20), we observe neither half- nor fully-closed species, with widespread intermolecular coupling and decomposition upwards of 260 °C. Thus, with precursor 6a, while intramolecular cyclodehydrogenation to form one heptagonal ring is feasible (on Au(111) and Ag(111) surfaces), closure of the second heptagonal ring, however, is not favored.

We next investigate the on-surface reaction of an alternative precursor 6b, which requires closure of two hexagonal rings (instead of two heptagonal rings as in 6a), with preformed heptagonal rings. When 6b is sublimed under UHV conditions onto an atomically clean Au(111) surface held at room temperature, large-scale STM images (Fig. 3a) show presence of predominantly discrete quasi-rectangular structures with two centrally located bright lobes of roughly 3.5 Å in height (measured at a sample bias of −1 V), in contrast to the long chains seen in case of 6a (c.f. Fig. 2a). High-resolution STM imaging (Fig. 3b) reveals the intramolecular features in more detail, where it is seen that apart from the two prominent central lobes, additional lobes of weaker contrast are present at the terminus. In addition, we also find the occasional species with only one prominent lobe on one side and two lobes of weaker contrast on the opposite side (indicated with the white arrow in Fig. 3b). Evidently, the quasi-rectangular species are, in fact, non-covalently bonded, self-assembled dimers of the isolated species which we assign to be 6b. The rather nontrivial conformation of 6b presenting only one prominent lobe is elucidated by theoretical calculations, wherein its DFT-optimized structure (Fig. 3d, e) on Au(111) shows that, unlike 6a, 6b adopts neither twisted nor folded conformation, but a peculiar conformation in which two benzenoid rings are bent out-of-plane as in a folded conformation (magenta rings in Fig. 3d, e), giving rise to the two weak lobes in STM images; while one of the terminal benzenoid rings is strongly bent out-of-plane (violet ring in Fig. 3d, e), leading to the appearance of one prominent lobe in STM images. Furthermore, the STM image simulated for this conformation (Fig. 3c) agrees well with the experimental one, concluding the structural assignment of 6b on the Au(111) surface.

Fig. 3
figure 3

On-surface reaction of 6b on Au(111). a Overview STM topography image of the surface after room temperature deposition of 6b, showing the predominant presence of self-assembled dimers (V = −1 V, I = 50 pA, scale bar: 5 nm). b High-resolution STM image of the highlighted area in a, consisting of a dimer, and an isolated molecule indicated with the white arrow (V = −1 V, I = 70 pA, scale bar: 1 nm). c DFT-simulated STM image of 6b corroborating the experimentally observed features (V = −1 V, scale bar: 1 nm). The colored dots serve as a guide to the eye for comparing the intramolecular features in experimental and simulated STM images. d, e Top and side views of the DFT equilibrium geometry of 6b. Rings highlighted in violet and magenta colors show an out-of-plane bending contributing to the distinguishing features in the STM images. f Overview STM topography image of the surface after annealing to 270 °C (V = −1 V, I = 40 pA, scale bar: 5 nm). The white circle highlights the half-closed species 7b. The white arrow indicates a still-present 6b on the surface. g High-resolution STM image of 7b (V = 10 mV, I = 50 pA, scale bar: 0.5 nm). h Corresponding UHR-STM image of 7b (open feedback parameters: V = −5 mV, I = 50 pA; Δz = −40 pm; scale bar: 0.5 nm). The red arrow indicates the hexagonal ring formed after this annealing step. i, j Top and side views of the DFT equilibrium geometry of 7b. The newly formed bond at this annealing step is highlighted in red

Having clarified the structure of 6b, we anneal the sample to 270 °C. Figure 3f shows a large-scale STM image of the surface after annealing, where there is a considerable decrease in the number of dimers with a concomitant increase in individual species presenting one prominent lobe (highlighted with a white circle in Fig. 3f). STM images show that these one-lobed species (referred to as 7b), however, are different from 6b, evidenced by a lack of two weaker lobes present at the molecule terminus. Whether isolated or present as dimers, 7b constitutes the predominant species on surface (82% of 141 molecules), while only 7% is present as 6b (the white arrow in Fig. 3f indicates an isolated 6b). Figure 3g, h show a high-resolution STM image and the corresponding UHR-STM image of 7b, respectively. Formation of a hexagonal ring (indicated with a red arrow) is evident in Fig. 3h, allowing us to conclude that 7b results from partial intramolecular cyclodehydrogenation of 6b, where one of the two hexagonal rings have formed. Its DFT-optimized structure on Au(111) (Fig. 3i, j) is in line with experimental observations, where the out-of-plane bent benzenoid ring is responsible for the bright lobe in STM/UHR-STM images, while the rest of the molecule adopts an almost planar geometry on the surface.

After further annealing the surface to 320 °C, large-scale STM images show appearance of a new species (31% of 181 molecules, referred to as 8) with apparent hexagonal shape and no prominent lobes (Fig. 4a, highlighted with the white circles). Furthermore, concomitant with the appearance of 8 is a decrease in the amount of half-closed species 7b on the surface (42% of 181 molecules). Figure 4b shows a high-resolution STM image of 8 acquired with a CO tip, where the presence of six bays at the periphery of molecules clearly hints toward complete ring closure. Finally, the UHR-STM image of 8 (Fig. 4c) unambiguously proves the structure of the intended nitrogen-embedded buckybowl. We note that current state-of-the-art scanning probe techniques used for chemical structure visualization, i.e., noncontact atomic force microscopy and UHR-STM, show no appreciable contrast between carbon and nitrogen atoms evident through previous structural studies employing these techniques on nitrogen-doped graphene nanostructures37,38. This is reflected in the UHR-STM image of 8 where the presence of nitrogen atoms is not apparent. However, any ambiguity regarding the loss of nitrogen atoms from the framework of 8 is alleviated by the fact that Au(111) is a relatively mild substrate for catalyzing on-surface reactions, and previous works on synthesis of nitrogen-doped graphene nanostructures on Au(111), with temperatures similar to or higher than those reported in our work, have shown no loss of heteroatoms from the corresponding organic frameworks39,40. DFT calculations suggest that the molecule adopts a dome-shaped bowl-opening-down conformation on the surface (Fig. 4e, f; also see Supplementary Figs. 25 and 26 for bowl-inversion energetics of 8 in the gas-phase and on Au(111), respectively), which is further confirmed by the excellent agreement between the experimental and simulated STM images (c.f. Fig. 4b, d). The computed bowl depth of the buckybowl on Au(111) amounts to 1.2 Å (bowl depth in the gas-phase amounts to 1.4 Å, see Supplementary Fig. 25). In this respect, the UHR-STM technique is evidently advantageous to gain chemical structure information on geometrically corrugated systems, such as 8. Surface-adsorbed buckybowls are known to show a preference for a bowl-opening-up conformation as a consequence of maximizing the van der Waals interaction between the molecule and the underlying surface. So far, bowl-inversion of surface-adsorbed buckybowls to adopt a bowl-opening-down conformation has been reported to occur either as a result of interplay between intermolecular and molecule–substrate interaction in an ensemble of buckybowls41, or locally due to perturbation with the STM tip42. Similar bidirectional conformational switching has also been observed in supramolecular assemblies of surface-supported porphyrin derivatives43. Interestingly, coronene molecules were also shown to adopt a dome-shaped conformation after complete dehydrogenation on a Ir(111) surface44. However, to the best of our knowledge, we show here the unprecedented case of isolated surface-adsorbed buckybowls with a preferential bowl-opening-down conformation (see Supplementary Fig. 27 for a discussion pertaining to the origin of the bowl-opening-down conformation of 8 on the surface). This class of bowl-opening-down buckybowls may provide a template to intercalate atomic species underneath such structures, allowing for atomic-scale tuning of their chemical or electronic properties, and potential application in emerging fields, such as spintronics45. It is worth to mention that coexistent with the majority bowl-opening-down buckybowls, a minor species (referred to as 8′) is also present on the surface. Our analysis suggests that these minority species are actually the bowl-opening-up form of 8 (see Supplementary Fig. 22 and accompanying text). Finally, after annealing the sample to 350 °C (see Supplementary Fig. 21), most of the molecules undergo intermolecular coupling, with 8 as the predominant species on the surface (60% of 75 molecules). At this juncture, a comment regarding the markedly different efficiencies of 6a and 6b in obtaining 8 is imperative. From a DFT-based structural analysis, 6a and 6b exhibit similar distances of ~3 Å between neighboring uncyclized carbon atoms (Figs. 2d and 3d). Compared to the respective precursor molecules, 7a and 7b feature an increase in the distance between corresponding carbon atoms which remain uncyclized, it being 3.3 Å for 7a and 3.1 Å for 7b (Figs. 2i and 3i). The 0.2 Å larger C–C distance in 7a compared to 7b may explain the unfeasibility of 7a to yield 8 at our reaction conditions, as a larger C–C distance would imply the need for higher temperatures to attempt ring closure, and other competing reaction pathways may dominate at higher temperatures.

Fig. 4
figure 4

Structural and electronic properties of the nitrogen-embedded buckybowl 8. a Overview STM topography image of the surface after an annealing step to 320 °C, showing the presence of mostly half-closed species (7b), and the fully closed buckybowls (8) highlighted by the white circles (V = −1.2 V, I = 20 pA, scale bar: 5 nm). b High-resolution STM image of 8 acquired with a CO tip (V = −0.1 V, I = 50 pA, scale bar: 0.5 nm). c Corresponding UHR-STM image of 8, evidencing complete ring closure and presence of the ISTW topology at the core (open feedback parameters: V = 5 mV, I = 50 pA; Δz = −50 pm; scale bar: 0.5 nm). d DFT-simulated STM image of 8 (V = −0.3 V, scale bar: 0.5 nm). e Top (upper panel) and side (lower panel) views of the DFT equilibrium geometry of 8. The out-of-plane buckling of the buckybowl to assume the bowl-opening-down conformation is evident. f STS spectra on 8 showing differential conductance peaks at −1.15 V and +2.70 V corresponding to the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO). A reference spectrum on Au(111) is shown in gray and serves as marker for the tip quality. The spectra are vertically shifted for clarity. Inset: STM topography image of 8 with overlaid DFT-optimized molecular model. The red and blue circles mark the positions at which the corresponding STS spectra were acquired. g, i Experimental dI/dV maps at the energies of HOMO and LUMO; and h, j corresponding DFT-simulated dI/dV maps at a tip-sample distance of 5 Å. (Open feedback parameters for the STS spectra: V = −1.6 V, I = 50 pA, Vrms = 20 mV, f= 860 Hz. Open feedback parameters for the experimental dI/dV maps: d V = −1.15 V, I = 40 pA, Vrms = 20 mV, f= 860 Hz; i V = 2.70 V, I = 40 pA, Vrms = 20 mV, f= 860 Hz.) All scale bars: 0.5 nm

We also performed STS measurements on 8 to probe its detailed electronic structure. The right panel of Fig. 4 shows the result of STS measurements. Voltage-dependent differential conductance spectra (dI/dV vs. V) show strong peaks in the density of states at −1.15 V and +2.70 V (Fig. 4f and Supplementary Fig. 24), which are assigned to the positive and negative ion resonances deriving from the highest occupied and lowest unoccupied molecular orbitals (HOMO and LUMO) of 8, respectively. Figure 4g, i show corresponding constant-height dI/dV maps at the energetic positions of HOMO and LUMO. The conductance feature associated with the HOMO appears elliptical in shape and has maximum intensity at the center of the molecule, with its long axis oriented approximately along the heptagonal rings. The LUMO appears as two bright lobes of high intensity around the center, with additional features of weaker intensity at the bay positions of the molecule. Interpretation of these dI/dV maps is facilitated via DFT-calculated LDOS maps of HOMO and LUMO for 8 on Au(111) surface (Fig. 4h, j), evaluated at a height of 5 Å above the molecule to account for a realistic comparison to experimental conditions. Indeed, the calculated LDOS maps show excellent agreement with the experimental dI/dV maps, reinforcing the chemical identity of the molecule and allowing us to conclude that features present in the experimental dI/dV maps in Fig. 4g, i can indeed be correlated with the spatial distribution of frontier orbital wavefunctions. Regarding the appearance of dI/dV maps, it must be mentioned that the experimentally observed limited spatial extension of frontier orbitals in or around the center of the molecule should not be interpreted as a localized conductance feature. We rather attribute this feature to a combined effect of the geometrical corrugation of the buckybowl (as revealed by DFT calculations in Fig. 4e), where the STM tip that scans at a constant height above the Au(111) surface will be significantly closer to the central part of the buckybowl than the peripheral part; and the joint effect of the tip-sample distance and the parity of sample orbital wavefunctions, as has been shown previously in STS investigations on graphene nanoribbons46. These factors, taken together, may explain our observation of a weaker dI/dV signal at the periphery and comparatively stronger signal in or around the central part of the buckybowl. In fact, the DFT-calculated frontier orbital wavefunctions of 8 are found to be delocalized over the entire molecule (see Supplementary Fig. 23).

Topologically, the core of 8 consists of a pair of joined pentagonal rings in between a pair of heptagonal rings, identified as the ISTW defect in graphene. The ISTW defect differs in the topology of the non-hexagonal rings from the more prevalent STW defect, which consists of a pair of joined heptagonal rings in between a pair of pentagonal rings47,48,49,50. So far, the ISTW defect has been experimentally demonstrated to occur on single layer graphene under a transmission electron microscope (TEM) either via high-energy electron irradiation, causing removal of atoms and subsequent reconstruction of the carbon lattice around vacancies51, or low-energy landing of carbon atom(s) and their subsequent incorporation as dimers in the sp2 framework52. While promising, the short lifetime of such defects under the electron beam of a TEM and the random nature of generation with no control over spatial location precludes their application in nanoscale defect engineering of graphene for device applications. We demonstrate here the first controllable synthesis of the ISTW topology embedded in a buckybowl. The possibility of tailoring the chemical and electronic properties of graphene53,54 and carbon nanotubes55,56 by such topological defects has been theoretically discussed. We expect that our combined solution/surface synthetic approach will provide future avenues toward fabrication of such exotic non-hexagonal ring topologies with atomic precision, with the possibility of heteroatom substitution to further tailor their properties; and provide precise control over their spatial location in graphene flakes and extended graphenic structures. It is interesting to note that the dome-shaped conformation of the synthesized buckybowl agrees with the theoretical prediction of the out-of-plane buckling of a graphene sheet due to the strain imposed by the ISTW topology, creating nanoscale “blisters”54. As an outlook, we propose to incorporate the ISTW topology in two-dimensional graphenic sheets via on-surface Ullmann-like coupling of suitably designed precursor molecules to create designer graphene supracrystals57. Finally, a short discourse regarding the merits and shortcomings of on-surface synthetic methodology is appropriate. It is evident that on-surface synthesis provides for a powerful synthetic toolbox to fabricate complex nanostructures, which are otherwise difficult or impossible to achieve in solution phase. Furthermore, this approach allows for a detailed structural and electronic characterization at the atomic scale via scanning probe microscopies. However, submonolayer coverage of products obtained on the surface and the difficulty of post-synthetic transfer of products to insulating substrates or organic solvents poses challenges toward device fabrication and employment of bulk characterization techniques. Thus, while on-surface synthesis opens new avenues in the fabrication and characterization of novel materials with great potential, its limited scalability currently stands as a challenge toward device applications. Nevertheless, recent progress in post-synthetic transfer techniques for surface to device translation holds great promise in this regard58.


We developed a concise synthetic pathway to the first buckybowl containing the PP core. Starting from the parent TAPP, the nitrogen-embedded buckybowl was obtained via successive ring-closing steps through in-solution oxidative aromatic coupling and on-surface cyclodehydrogenation on Au(111). The buckybowl represents the first discrete molecule possessing the ISTW topology, leading to the unprecedented case of isolated surface-adsorbed buckybowls with a preferential bowl-opening-down conformation. The electron-rich fully fused nitrogen-embedded buckybowl assuming curved bowl-like architecture may serve as an ideal candidate for a host-guest study and may play a role as a foundation for further π-extension. This work shows the potential of on-surface synthesis toward the formation of unprecedented π-extended aza-analogs of graphene and atomically precise incorporation of challenging non-hexagonal ring topologies as a route to tailor the electronic and chemical properties of graphenic structures and provide a ground for new functionalities.



The synthesis of compounds 4a, 4b, 5a, 5b, 6a, and 6b is described in detail in the Supplementary Information (see Supplementary Methods). For NMR spectra of the compounds reported in this article, see Supplementary Figs. 3-18. For X-ray crystallographic data of compounds 4b and 6c, see Supplementary Figs. 1 and 2.

Sample preparation and STM measurements

STM experiments were performed with a commercial low-temperature STM (T~5 K) from ScientaOmicron operating at base pressure below 1 × 10−10 mbar. Au(111), Ag(111), and Cu(111) single crystal surfaces were prepared by iterated cycles of sputtering with Ar+ ions (p = 6 × 10−6 mbar) and annealing to 750 K for 20 min at pressures below 5 × 10−10 mbar. STM was used to check the quality of the surfaces before deposition of molecules. Precursor molecules 6a and 6b were sublimed at 583 and 603 K, respectively, on the single crystal surfaces held at room temperature. Owing to the large distance between the evaporator and the substrate, only ~2% of the sublimated molecules reach the substrate. All STM images were acquired in constant-current mode, unless otherwise noted. Indicated tunneling bias voltages are given with respect to the sample. Unless otherwise mentioned, gold-coated tungsten tips were used for STM imaging and spectroscopy. Differential conductance spectra and associated maps were measured using the lock-in technique to obtain a signal proportional to dI/dV from the first harmonic of the tunneling current. UHR-STM images were acquired with a CO-terminated tip in constant-height mode, at biases close to the Fermi energy, and the current signal was recorded. Open feedback parameters and subsequent approach distances (Δz) are given in respective figure descriptions. CO-terminated tips were obtained by picking up individual CO molecules from NaCl islands deposited after completion of on-surface reactions. NaCl islands facilitate the identification and pickup of individual CO molecules. All STM and dI/dV images were processed and analyzed with WSxM software59.

Calculation methods

To obtain the equilibrium geometries of the molecules adsorbed on the Au(111) substrate and to compute corresponding STM images, we used the CP2K code60,61 implementing DFT within a mixed Gaussian plane waves approach62. The surface/adsorbate systems were modeled within the repeated slab scheme63, i.e., a simulation cell contained four atomic layers of Au along the [111] direction, a layer of hydrogen atoms to passivate one side of the slab (in order to suppress one of the two Au(111) surface states) and 40 Å of vacuum to decouple the system from its periodic replicas in the direction perpendicular to the surface. The electronic states were expanded with a TZV2P Gaussian basis set64 for C and H species, and a DZVP basis set for N and Au species. A cutoff of 600 Ry was used for the plane wave basis set. Norm-conserving Goedecker–Teter–Hutter65 pseudopotentials were used to represent the frozen core electrons of the atoms. We used the PBE parameterization for the generalized gradient approximation of the exchange correlation functional66. To account for van der Waals interactions we used the scheme proposed by Grimme et al.67. We considered supercells of 41.64 × 41.21 Å corresponding to 224 surface units. To obtain the equilibrium geometries we kept the atomic positions of the bottom two layers of the slab fixed to the ideal bulk positions, all other atoms were relaxed till forces were lower than 0.005 eV/Å.

To obtain simulated STM images68, within the Tersoff–Hamann approximation69, we extrapolated the electronic orbitals to the vacuum region in order to correct the wrong decay of the charge density in vacuum due to the localized basis set. The inversion energy barrier for the molecule in the gas-phase was obtained by means of the nudged elastic band method70, employing nine replicas.

Data availability

X-ray crystallographic data for 4b and 6c can be obtained free of charge from the Cambridge Crystallographic Data Centre (CCDC) with the CCDC numbers 1589417 (4b) and 1589418 (6c) via its website ( All other data that support the findings of this study are available from the corresponding authors upon reasonable request.