Fullertubes: A 30-Year Story of Prediction, Experimental Validation, and Applications for a Long-Missing Family of Soluble Carbon Molecules.

ConspectusDuring the last 30 years, theoretical scientists imagined segmental families of monolayer carbon tubules with fullerene-based end-caps. These fullertube molecules would possess structural features of both fuller enes (hemispherical end-caps) and tubular belts of single-walled carbon nano tubes (SWCNTs). Yet, their experimental verification remained elusive for decades. It was not until 2020-2023 that segmental families of fullertubes were finally confirmed in the lab. The shocking irony is that these fullertubes were unwittingly coproduced alongside fullerenes (e.g., C 60, C 70, C 84 ) in both flame and electric arc soot since the 1990s. Yet, nobody knew these "hidden" families of fullertubes were experimentally present in their extracted soot due to their low abundance and the absence of isolation methodology.This eruption of fullertube discoveries in 2020-2023 was brought to fruition by structural data, both DFT and experimental. This "Treasure Trove" of new molecules during this four-year window occurred with only microgram quantities. Typically, milligram levels of purified samples are required for X-ray crystallography and 13 C NMR structural analysis. The breakthrough for experimentally verifying the missing fullertubes was an aminopropanol reagent to selectively react with and remove spheroidal carbon (e.g., C 60 , C 70 , C 84 ) as hydrophilic derivatives. In contrast, there was suppressed reaction with fullertubes, which remained in organic solvent. It is well established that high symmetry (3-, 5-, and 6-fold) hemispheres for C 60 -I h and other fullerenes and metallofullerenes are prerequisite end-caps for fullertubes. For the case of [5,5] C 130 fullertubes, this requirement results in only eight 3-, 5-, and 6-fold symmetry structural isomers possible from a total of 39,393 possible isolated pentagon rule (IPR) isomers. From this C 130 list of 8 candidate isolated pentagon rule (IPR) high symmetry isomers, surprisingly only one structure matched the DFT polarizability versus chromatographic retention parameter (a new gold standard for isomer identification). The simultaneous emergence of DFT computations of other properties (e.g., total energy, HOMO-LUMO gap, UV-vis) for large carbon molecules provided support for structural determination. Experimental approaches (e.g., mass spectrometry, UV-vis, XPS, Raman, and STEM) provided additional layers of structural elucidation at the microgram level. For the first time, we developed a chemical isolation protocol that would allow the preparation and isolation of soluble pristine fullertubes in the range of C 90 -C 200 . To date, applications of SWCNTs for use in nanoscale computer applications requires purities greater than 99.999%. Although this stringent mandate has not yet been demonstrated using SWCNT samples, this high level of purity appears achievable for metallic [5,5] D 5 d -C 120 and semiconductor [10,0] D 5 h -C 120 [10,766] fullertubes. Moreover, commercial production of pristine fullertubes should easily be feasible by the flame method due to its continuous operation and inexpensive feedstock. For application development, theoretical and electrochemical experimental data show that fullertubes exhibit high catalytic activity in oxygen reduction reactions. In the medical sector, pristine fullertube dispersions exhibit antimicrobial effects on Mycobacterium smegmatis and M. abscessus .