Abstract
Qirui Long, Ming-Wei Wang, Zhaohui Wang
Abstract
Authors
Institutions
No ROR-resolved institution is linked to this work yet.
Provenance
crossref
Confidence 100%
unpaywall
Confidence 95%
datacite
Confidence 0%
No local reference links have been materialized yet.
No local citing links have been materialized yet.
C60: Buckminsterfullerene
10.1038/318162a0 · 1985
Helical microtubules of graphitic carbon
10.1038/354056a0 · 1991
Diamond from graphite
10.1038/352762a0 · 1991
10.1007/978-3-642-50665-9
10.1007/978-3-642-50665-9
Energetics of negatively curved graphitic carbon
10.1038/355333a0 · 1992
Magnetism in all-carbon nanostructures with negative Gaussian curvature
10.1103/physrevlett.91.237204 · 2003
Personal perspectives on graphene: New graphene-related materials on the horizon
10.1557/mrs.2012.278 · 2012
Negatively curved carbon as the anode for lithium ion batteries
10.1016/j.carbon.2013.08.033 · 2014
Schwarzites for natural gas storage: A grand-canonical Monte Carlo study
10.1557/adv.2018.190 · 2018
Molecular hydrogen sorption capacity of P216-schwarzite: PM6-D3, MP2 and QTAIM approaches
10.1016/j.commatsci.2022.111410 · 2022
Solid C60: A new form of carbon
10.1038/347354a0 · 1990
High-yield synthesis, separation, and mass-spectrometric characterization of fullerenes C60 to C266
10.1021/ja00020a008 · 1991
Topologically unique molecular nanocarbons
10.1021/acs.accounts.9b00402 · 2019
Functional fullerenes for organic photovoltaics
10.7312/li--16274-023 · 2012
Fullerene-based antioxidants and neurodegenerative disorders
10.1016/s1353-8020(00)00064-x · 2001
Fullerene on non-iron cluster-matrix co-catalysts promotes collaborative H2 and N2 activation for ammonia synthesis
10.1038/s41557-024-01626-6 · 2024
Fullerenes make copper catalysis better
10.1126/science.abo3155 · 2022
Cyclocarbon coalescence: Mechanisms for tailor-made fullerene formation
10.1126/science.259.5101.1594 · 1993
Precursors to endohedral metal fullerene complexes: Synthesis and X-ray structure of a flexible acetylenic cyclophane C60H18
10.1021/ja9606384 · 1996
[16.16.16](1,3,5)Cyclophanetetracosayne (C60H6): A precursor to C60 fullerene
10.1021/ja9803308 · 1998
Polyethynylated cyclic π-systems: Scaffoldings for novel two and three-dimensional carbon networks
10.1039/a708900g · 1999
Corannulene bowl-to-bowl inversion is rapid at room temperature
10.1021/ja00031a079 · 1992
Synthesis and dynamics of the corannulene nucleus
10.1021/ja00031a080 · 1992
Buckybowls: Synthesis and ab initio calculated structure of the first semibuckminsterfullerene
10.1021/ja00096a054 · 1994
Novel syntheses of three C30H12 bowl-shaped polycyclic aromatic hydrocarbons
10.1002/anie.199704061 · 1997
“Locking” the bowl-shaped geometry of corannulene: Cyclopentacorannulene
10.1021/ja00060a073 · 1993
Circumtrindene: A geodesic dome of molecular dimensions. Rational synthesis of 60 of C601
10.1021/ja993028n · 2000
Synthesis and characterization of a C36H12 fullerene subunit
10.1021/ja9621511 · 1996
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
Crystallographic characterization of the molecular structure and solid state packing of the fullerene-shaped hydrocarbon C36H12
10.1021/ja970845j · 1997
Groundwork for a rational synthesis of C60: Cyclodehydrogenation of a C60H30 polyarene
10.1126/science.1064250 · 2001
A rational chemical synthesis of C60
10.1126/science.1068427 · 2002
Bowls, hoops, and saddles: Synthetic approaches to curved aromatic molecules
10.1002/anie.201807004 · 2019
Anisotropic electron transport properties in sumanene crystal
10.1021/ja805997v · 2009
Pentaindenocorannulene and tetraindenocorannulene: New aromatic hydrocarbon π systems with curvatures surpassing that of C60
10.1021/ja067487h · 2007
Fullerenes from aromatic precursors by surface-catalysed cyclodehydrogenation
10.1038/nature07193 · 2008
Single-shell carbon nanotubes of 1-nm diameter
10.1038/363603a0 · 1993
Cobalt-catalysed growth of carbon nanotubes with single-atomic-layer walls
10.1038/363605a0 · 1993
Carbon nanotubes: Synthesis, integration, and properties
10.1021/ar0101640 · 2002
Carbon nanotubes: Present and future commercial applications
10.1126/science.1222453 · 2013
Semitubular aromatic fragment of schwarzite P192: A conserved structural motif with two embedded octagons
10.1021/jacs.5c13263 · doi-reference
A key fragment in carbon schwarzite unit cells and its triple [6]helicene precursor
10.1002/anie.202501169 · doi-reference
A negatively curved nanographene with four embedded heptagons
10.1021/jacs.4c09185 · doi-reference
A highly warped heptagon-containing sp2 carbon scaffold via vinylnaphthyl π-extension
10.1002/anie.201909975 · doi-reference
A twisted nanographene consisting of 96 carbon atoms
10.1002/anie.201703754 · doi-reference
Aromatic saddles containingtwoheptagons
10.1021/jacs.5b00403 · doi-reference
A grossly warped nanographene and the consequences of multiple odd-membered-ring defects
10.1038/nchem.1704 · doi-reference
Synthesis, structural analysis, and properties of [8]circulenes
10.1002/anie.201303875 · doi-reference
Tetrabenzo[8]circulene: Aromatic saddles from negatively curved graphene
10.1021/ja407842z · doi-reference
Synthesis and characterization of [7]circulene
10.1021/ja00362a025 · doi-reference
Molecular carbons: How far can we go
10.1021/acsnano.3c07970 · doi-reference
Structurally uniform and atomically precise carbon nanostructures
10.1038/natrevmats.2015.2 · doi-reference
Toward negatively curved carbons
10.1021/acs.accounts.8b00140 · doi-reference
Lanthanum-catalysed synthesis of microporous 3D graphene-like carbons in a zeolite template
10.1038/nature18284 · doi-reference
Atomistic structures of zeolite-templated carbon
10.1021/acs.chemmater.0c00535 · doi-reference
Generating carbon schwarzites via zeolite-templating
10.1073/pnas.1805062115 · doi-reference
Negatively curved spongy carbon
10.1063/1.1516635 · doi-reference
Mechanical properties of hypothetical graphene foams: Giant schwarzites
10.1016/j.carbon.2015.10.040 · doi-reference
Synthesis of fully π-conjugated non-alternant carbon nanobelts
10.1038/s44160-025-00797-5 · doi-reference
Synthesis of a sidewall fragment of a (12,0) carbon nanotube
10.1002/anie.202012651 · doi-reference
Synthesis of a zigzag carbon nanobelt
10.1038/s41557-020-00627-5 · doi-reference
Toward the synthesis of a highly strained hydrocarbon belt
10.1021/jacs.0c00112 · doi-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 · doi-reference
Transformations of a macrocyclic cyclophane belt into advanced [8]cyclacene and [8]cyclacene triquinone precursors
10.1016/0040-4039(96)00264-x · doi-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 · doi-reference
Molecular belts and collars in the making: A hexaepoxyoctacosahydro[12]cyclacene derivative
10.1002/anie.198708921 · doi-reference
Molecular orbitals in homologen reihen mehrkerniger aromatischer kohlenwasserstoffe: I. Die eigenwerte yon LCAO-MO’s in homologen reihen
10.1002/hlca.19540370336 · doi-reference
Synthesis of triple stranded porphyrin nanobelts
10.1126/science.adz8900 · doi-reference
Synthesis of armchair and chiral carbon nanobelts
10.1016/j.chempr.2019.01.004 · doi-reference
Synthesis and size-dependent properties of [12], [16], and [24]carbon nanobelts
10.1021/jacs.8b06842 · doi-reference
Synthesis of a carbon nanobelt
10.1126/science.aam8158 · doi-reference
10.1002/9781118011263.ch12
10.1002/9781118011263.ch12 · doi-reference
Strategy for the synthesis of tube-shaped molecules
10.1002/anie.199105751 · doi-reference
Aromatic hydrocarbon belts
10.1038/s41557-021-00671-9 · doi-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 · doi-reference
Synthesis of [8]cycloparaphenylene from a square-shaped tetranuclear platinum complex
10.1002/anie.200905659 · doi-reference
Selective synthesis of [12]cycloparaphenylene
10.1002/anie.200902617 · doi-reference
Synthesis, characterization, and theory of [9]-, [12]-, and [18]cycloparaphenylene: Carbon nanohoop structures
10.1021/ja807126u · doi-reference
Nearly exclusive growth of small diameter semiconducting single-wall carbon nanotubes from organic chemistry synthetic end-cap molecules
10.1021/nl504066f · doi-reference
Controlled synthesis of single-chirality carbon nanotubes
10.1038/nature13607 · doi-reference