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References from Atom-precise construction of fully conjugated curved carbon nanostructures. Local targets link to admitted publications; unresolved targets remain external evidence.
C60: Buckminsterfullerene
10.1038/318162a0 · 1985 · External reference
Helical microtubules of graphitic carbon
10.1038/354056a0 · 1991 · External reference
Diamond from graphite
10.1038/352762a0 · 1991 · External reference
10.1007/978-3-642-50665-9
10.1007/978-3-642-50665-9 · External reference
Energetics of negatively curved graphitic carbon
10.1038/355333a0 · 1992 · External reference
Magnetism in all-carbon nanostructures with negative Gaussian curvature
10.1103/physrevlett.91.237204 · 2003 · External reference
Personal perspectives on graphene: New graphene-related materials on the horizon
10.1557/mrs.2012.278 · 2012 · External reference
Negatively curved carbon as the anode for lithium ion batteries
10.1016/j.carbon.2013.08.033 · 2014 · External reference
Schwarzites for natural gas storage: A grand-canonical Monte Carlo study
10.1557/adv.2018.190 · 2018 · External reference
Molecular hydrogen sorption capacity of P216-schwarzite: PM6-D3, MP2 and QTAIM approaches
10.1016/j.commatsci.2022.111410 · 2022 · External reference
Solid C60: A new form of carbon
10.1038/347354a0 · 1990 · External reference
High-yield synthesis, separation, and mass-spectrometric characterization of fullerenes C60 to C266
10.1021/ja00020a008 · 1991 · External reference
Topologically unique molecular nanocarbons
10.1021/acs.accounts.9b00402 · 2019 · External reference
Functional fullerenes for organic photovoltaics
10.7312/li--16274-023 · 2012 · External reference
Fullerene-based antioxidants and neurodegenerative disorders
10.1016/s1353-8020(00)00064-x · 2001 · External reference
Fullerene on non-iron cluster-matrix co-catalysts promotes collaborative H2 and N2 activation for ammonia synthesis
10.1038/s41557-024-01626-6 · 2024 · External reference
Fullerenes make copper catalysis better
10.1126/science.abo3155 · 2022 · External reference
Cyclocarbon coalescence: Mechanisms for tailor-made fullerene formation
10.1126/science.259.5101.1594 · 1993 · External reference
Precursors to endohedral metal fullerene complexes: Synthesis and X-ray structure of a flexible acetylenic cyclophane C60H18
10.1021/ja9606384 · 1996 · External reference
[16.16.16](1,3,5)Cyclophanetetracosayne (C60H6): A precursor to C60 fullerene
10.1021/ja9803308 · 1998 · External reference
Polyethynylated cyclic π-systems: Scaffoldings for novel two and three-dimensional carbon networks
10.1039/a708900g · 1999 · External reference
Corannulene bowl-to-bowl inversion is rapid at room temperature
10.1021/ja00031a079 · 1992 · External reference
Synthesis and dynamics of the corannulene nucleus
10.1021/ja00031a080 · 1992 · External reference
Buckybowls: Synthesis and ab initio calculated structure of the first semibuckminsterfullerene
10.1021/ja00096a054 · 1994 · External reference
Novel syntheses of three C30H12 bowl-shaped polycyclic aromatic hydrocarbons
10.1002/anie.199704061 · 1997 · External reference
“Locking” the bowl-shaped geometry of corannulene: Cyclopentacorannulene
10.1021/ja00060a073 · 1993 · External reference
Circumtrindene: A geodesic dome of molecular dimensions. Rational synthesis of 60 of C601
10.1021/ja993028n · 2000 · External reference
Synthesis and characterization of a C36H12 fullerene subunit
10.1021/ja9621511 · 1996 · External reference
Buckybowls 2. Toward the total synthesis of buckminsterfullerene (C60): Benz[5,6]-as-indaceno[3,2,1,8,7-mnopqr]indeno[4,3,2,1-cdef]chrysene
10.1021/ja00128a052 · 1995 · External reference
Crystallographic characterization of the molecular structure and solid state packing of the fullerene-shaped hydrocarbon C36H12
10.1021/ja970845j · 1997 · External reference
Groundwork for a rational synthesis of C60: Cyclodehydrogenation of a C60H30 polyarene
10.1126/science.1064250 · 2001 · External reference
A rational chemical synthesis of C60
10.1126/science.1068427 · 2002 · External reference
Bowls, hoops, and saddles: Synthetic approaches to curved aromatic molecules
10.1002/anie.201807004 · 2019 · External reference
Anisotropic electron transport properties in sumanene crystal
10.1021/ja805997v · 2009 · External reference
Pentaindenocorannulene and tetraindenocorannulene: New aromatic hydrocarbon π systems with curvatures surpassing that of C60
10.1021/ja067487h · 2007 · External reference
Fullerenes from aromatic precursors by surface-catalysed cyclodehydrogenation
10.1038/nature07193 · 2008 · External reference
Single-shell carbon nanotubes of 1-nm diameter
10.1038/363603a0 · 1993 · External reference
Cobalt-catalysed growth of carbon nanotubes with single-atomic-layer walls
10.1038/363605a0 · 1993 · External reference
Carbon nanotubes: Synthesis, integration, and properties
10.1021/ar0101640 · 2002 · External reference
Carbon nanotubes: Present and future commercial applications
10.1126/science.1222453 · 2013 · External reference
Recent development of carbon nanotube transparent conductive films
10.1021/acs.chemrev.6b00179 · 2016 · External reference
Horizontally aligned carbon nanotube arrays: Growth mechanism, controlled synthesis, characterization, properties and applications
10.1039/c7cs00104e · 2017 · External reference
Chirality-controlled synthesis and applications of single-wall carbon nanotubes
10.1021/acsnano.6b06900 · 2017 · External reference
Narrow (n,m)-distribution of single-walled carbon nanotubes grown using a solid supported catalyst
10.1021/ja036622c · 2003 · External reference
Atomic-resolution imaging of the nucleation points of single-walled carbon nanotubes
10.1002/smll.200500200 · 2005 · External reference
Control the chirality of carbon nanotubes by epitaxial growth
10.1016/j.cplett.2006.01.110 · 2006 · External reference
Preferential growth of single-walled carbon nanotubes with metallic conductivity
10.1126/science.1177599 · 2009 · External reference
Arrays of horizontal carbon nanotubes of controlled chirality grown using designed catalysts
10.1038/nature21051 · 2017 · External reference
Chirality-specific growth of single-walled carbon nanotubes on solid alloy catalysts
10.1038/nature13434 · 2014 · External reference
Growing zigzag (16,0) carbon nanotubes with structure-defined catalysts
10.1021/jacs.5b04403 · 2015 · External reference
Water-assisted preparation of high-purity semiconducting (14,4) carbon nanotubes
10.1021/acsnano.6b06890 · 2017 · External reference
Selective growth of chirality-enriched semiconducting carbon nanotubes by using bimetallic catalysts from salt precursors
10.1039/c7nr07855b · 2018 · External reference
A short, rigid, structurally pure carbon nanotube by stepwise chemical synthesis
10.1021/ja209461g · 2012 · External reference
Initiation of carbon nanotube growth by well-defined carbon nanorings
10.1038/nchem.1655 · 2013 · External reference
Controlled synthesis of single-chirality carbon nanotubes
10.1038/nature13607 · 2014 · External reference
Nearly exclusive growth of small diameter semiconducting single-wall carbon nanotubes from organic chemistry synthetic end-cap molecules
10.1021/nl504066f · 2015 · External reference
Synthesis, characterization, and theory of [9]-, [12]-, and [18]cycloparaphenylene: Carbon nanohoop structures
10.1021/ja807126u · 2008 · External reference
Selective synthesis of [12]cycloparaphenylene
10.1002/anie.200902617 · 2009 · External reference
Synthesis of [8]cycloparaphenylene from a square-shaped tetranuclear platinum complex
10.1002/anie.200905659 · 2010 · External reference
A Macrocyclic gold(I)-biphenylene complex: Triangular molecular structure with twisted Au2(diphosphine) corners and reductive elimination of [6]Cycloparaphenylene
10.1002/anie.202005482 · 2020 · External reference
Aromatic hydrocarbon belts
10.1038/s41557-021-00671-9 · 2021 · External reference
Strategy for the synthesis of tube-shaped molecules
10.1002/anie.199105751 · 1991 · External reference
10.1002/9781118011263.ch12
10.1002/9781118011263.ch12 · External reference
Synthesis of a carbon nanobelt
10.1126/science.aam8158 · 2017 · External reference
Synthesis and size-dependent properties of [12], [16], and [24]carbon nanobelts
10.1021/jacs.8b06842 · 2018 · External reference
Synthesis of armchair and chiral carbon nanobelts
10.1016/j.chempr.2019.01.004 · 2019 · External reference
Synthesis of triple stranded porphyrin nanobelts
10.1126/science.adz8900 · 2025 · External reference
Molecular orbitals in homologen reihen mehrkerniger aromatischer kohlenwasserstoffe: I. Die eigenwerte yon LCAO-MO’s in homologen reihen
10.1002/hlca.19540370336 · 1954 · External reference
Molecular belts and collars in the making: A hexaepoxyoctacosahydro[12]cyclacene derivative
10.1002/anie.198708921 · 1987 · External reference
Macrocyclic cyclophane belts via double Diels–Alder cycloadditions: Macroannulation of bisdienes by bisdienophiles. Synthesis of a key precursor to an [8]cyclacene
10.1016/0040-4039(96)00263-8 · 1996 · External reference
Transformations of a macrocyclic cyclophane belt into advanced [8]cyclacene and [8]cyclacene triquinone precursors
10.1016/0040-4039(96)00264-x · 1996 · External reference
Synthesis, structure, and reactivity of a cylinder-shaped cyclo[12]orthophenylene[6]ethynylene: Toward the synthesis of zigzag carbon nanobelts
10.1021/acs.orglett.6b02702 · 2016 · External reference
Toward the synthesis of a highly strained hydrocarbon belt
10.1021/jacs.0c00112 · 2020 · External reference
Synthesis of a zigzag carbon nanobelt
10.1038/s41557-020-00627-5 · 2021 · External reference
Synthesis of a sidewall fragment of a (12,0) carbon nanotube
10.1002/anie.202012651 · 2021 · External reference
Synthesis of fully π-conjugated non-alternant carbon nanobelts
10.1038/s44160-025-00797-5 · 2025 · External reference
Mechanical properties of hypothetical graphene foams: Giant schwarzites
10.1016/j.carbon.2015.10.040 · 2016 · External reference
Negatively curved spongy carbon
10.1063/1.1516635 · 2002 · External reference
Generating carbon schwarzites via zeolite-templating
10.1073/pnas.1805062115 · 2018 · External reference
Atomistic structures of zeolite-templated carbon
10.1021/acs.chemmater.0c00535 · 2020 · External reference
Lanthanum-catalysed synthesis of microporous 3D graphene-like carbons in a zeolite template
10.1038/nature18284 · 2016 · External reference
Toward negatively curved carbons
10.1021/acs.accounts.8b00140 · 2018 · External reference
Structurally uniform and atomically precise carbon nanostructures
10.1038/natrevmats.2015.2 · 2016 · External reference
Molecular carbons: How far can we go
10.1021/acsnano.3c07970 · 2023 · External reference
Synthesis and characterization of [7]circulene
10.1021/ja00362a025 · 1983 · External reference
Tetrabenzo[8]circulene: Aromatic saddles from negatively curved graphene
10.1021/ja407842z · 2013 · External reference
Synthesis, structural analysis, and properties of [8]circulenes
10.1002/anie.201303875 · 2013 · External reference
A grossly warped nanographene and the consequences of multiple odd-membered-ring defects
10.1038/nchem.1704 · 2013 · External reference
Aromatic saddles containingtwoheptagons
10.1021/jacs.5b00403 · 2015 · External reference
A twisted nanographene consisting of 96 carbon atoms
10.1002/anie.201703754 · 2017 · External reference
A highly warped heptagon-containing sp2 carbon scaffold via vinylnaphthyl π-extension
10.1002/anie.201909975 · 2019 · External reference
A negatively curved nanographene with four embedded heptagons
10.1021/jacs.4c09185 · 2024 · External reference
A key fragment in carbon schwarzite unit cells and its triple [6]helicene precursor
10.1002/anie.202501169 · 2025 · External reference
Semitubular aromatic fragment of schwarzite P192: A conserved structural motif with two embedded octagons
10.1021/jacs.5c13263 · 2025 · External reference