Gas-Phase Synthesis of the C40 Nano Bowl

Combined molecular beam and computational investigations reveal the gas-phase formation of benzocorannulene and onward to the C40 nanobowl through an aryl radical mediated benzannulation and cyclodehydrogenation framework.
Published in Chemistry
Gas-Phase Synthesis of the C40 Nano Bowl

Share this post

Choose a social network to share with, or copy the shortened URL to share elsewhere

This is a representation of how your post may appear on social media. The actual post will vary between social networks

Nanobowls, which belong to an extended family of curved (three-dimensional) polycyclic aromatic hydrocarbons (PAHs) with the prototype species being the smallest bowl-shaped corannulene (C20H10) molecule, represent vital molecular building blocks of fullerenes and nanotubes as detected in combustion systems and in deep space (Fig. 1). However, synthesis of nanobowls more complex than corannulene, such as C40 (C40H10) and C50 (C50H10), have remained a fundamental challenge. Whereas the formation and isolation of these nanobowls is interesting by itself from the synthetic chemistry viewpoint, the ultimate goal is to exploit these nanostructures as transitional templates to direct the synthesis of the closed icosahedral C60–fullerene structure and to employ them as end-caps of nanotubes. While there have been synthetic routes preparing mono- to pentabenzocorannulenes (C40H20), they do not rationalize the pathways to naturally prepared fullerenes detected in combustion flames, in meteorites such as Allende and Murchison, and in the planetary nebula TC-1. Consequently, hitherto elusive high temperature chemical routes for the synthesis of fullerenes along with their nanobowls must exist either from the bottom up or the top down.

Figure 1. The smallest nanobowl, corannulene [1], as well as the C40 nanobowl [2] emphasized as a molecular building block of Buckminsterfullerene (C60) [3], rugbyballene (C70) [4], and end-capped (5,5) armchair nanotubes [5]. The C40 nanobowl carbons are black, the remaining carbons are grey, and hydrogens are white.

By merging molecular beam experiments with electronic structure calculations, we reveal a complex chain of reactions initiated through the gas-phase preparation of benzocorannulene (C24H12) via ring annulation of the corannulenyl radical (C20H9) by vinylacetylene (C4H4). The experiments were conducted at the Swiss Light Source (SLS) utilizing a chemical microreactor coupled to a molecular beam apparatus operated with a double velocity map imaging (VMI) photoelectron photoion coincidence (PEPICO) spectrometer. Combining this setup with incident vacuum ultraviolet (VUV) synchrotron radiation, we obtained a product molecular formula (C24H12) using mass spectrometry and verified the benzocorannulene structural isomer via photo­ioni­zation efficiency curves (PIEs) and photoion mass-selected threshold photoelectron spectra (ms-TPES) (Fig. 2).

Figure 2. PIE curves at (a) m/z = 300 (C24H12) and (b) m/z = 301 (13CC23H12) as well as ms-TPES at (c) m/z = 300. Black: experimental curves; blue: benzocorannulene curves; red: benzocorannulene Franck-Condon (FC) stick spectrum; green: calculated ionization onset and FC spectrum for trans-4-(1-buten-3-yne)corannulene; orange: calculated ionization onset and FC spectrum for cis-4-(3-buten-1-yne)corannulene; magenta: calculated ionization energies of 8.152, 8.184, and 8.453 eV corresponding to the 22Aʺ, 12Aʹ, and 32Aʺ electronic excited states of the benzocorannulene cation. The overall error bars (gray area) consist of two parts: 1 σ error of the PIE curve averaged over the individual scans and ±10% based on the accuracy of the photodiode.

Exploiting benzocorannulene (C24H12) as a benchmark, we further expose in silico that the benzannulation mechanism can be expanded up to pentabenzocorannulene (C40H20) followed by successive cyclodehydrogenation to the C40 nanobowl (C40H10) (Figs. 3 and 4). The exploitation of linearly scaling coupled cluster method for electronic structure calculations of molecules as large as C40H20 opens a previously unavailable avenue for accurate exploration of potential energy diagrams of complex molecules with chemical accuracy allowing to obtain detailed information on energies of metastable states/products, barriers, and chemical pathways complementary to experimental data. This high-temperature route opens up a facile, isomer-selective bottom up pathway to nanobowls via resonantly stabilized free-radical intermediates and ring annulation in combustion flames and in planetary nebulae, which may act as precursors to buckminsterfullerene (C60) thus changing our conception of the formation of complex carbon nanostructures in our Galaxy.

Figure 3. Calculated potential energy diagram for the most important channels of the [C36H17] plus vinylacetylene reaction. Relative energies of various species calculated at the DLPNO-CCSD(T)/cc-pVDZ level of theory are given in kJ mol−1 with respect to the initial reactants.
Figure 4. Calculated potential energy diagrams for the conversion of pentabenzocorannulene (C40H20) to C40H18 (a) and C40H12 to the C40 nanobowl (C40H10) (b) via a hydrogen abstraction – cyclodehydrogenation mechanism. Relative energies of various species calculated at the DLPNO-CCSD(T)/cc-pVDZ level of theory are given in kJ mol−1 with respect to the initial reactants.

Please sign in or register for FREE

If you are a registered user on Research Communities by Springer Nature, please sign in

Subscribe to the Topic

Physical Sciences > Chemistry

Related Collections

With collections, you can get published faster and increase your visibility.

Materials and devices for separation, sensing, and protection

In this Collection, the editors of Nature Communications and Communications Materials welcome the submission of primary research articles that highlight the development and application of functional materials in the areas of separation, sensing, and protection.

Publishing Model: Open Access

Deadline: Jun 30, 2024

Applied Sciences

This collection highlights research and commentary in applied science. The range of topics is large, spanning all scientific disciplines, with the unifying factor being the goal to turn scientific knowledge into positive benefits for society.

Publishing Model: Open Access

Deadline: Ongoing