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Reactivity of the convex and concave surfaces of single-walled carbon nanotubes (SWCNTs) towards addition reactions: dependence on the carbon-atom pyramidalization.Bond-order discrimination by atomic force microscopy.Sphere currents of Buckminsterfullerene.Adsorption of Cu(II) on oxidized multi-walled carbon nanotubes in the presence of hydroxylated and carboxylated fullerenes.The topology of fullerenes.A geometric constraint, the head-to-tail exclusion rule, may be the basis for the isolated-pentagon rule in fullerenes with more than 60 verticesProbing the electronic properties and structural evolution of anionic gold clusters in the gas phase.The role of aromaticity in determining the molecular structure and reactivity of (endohedral metallo)fullerenes.Quantum-mechanical calculations on molecular substructures involved in nanosystems.Th(IV) Adsorption onto Oxidized Multi-Walled Carbon Nanotubes in the Presence of Hydroxylated Fullerene and Carboxylated Fullerene.Capillary electrophoresis and nanomaterials - Part I: Capillary electrophoresis of nanomaterials.Molecular structures of M2N2(2-) (M and N = B, Al, and Ga) clusters using the gradient embedded genetic algorithm.Behavior of Halogen Bonds of the Y-X⋅⋅⋅π Type (X, Y=F, Cl, Br, I) in the Benzene π System, Elucidated by Using a Quantum Theory of Atoms in Molecules Dual-Functional Analysis.Cyclic π-electron delocalization in non-planar linear acenes.Solubilization of aromatic and hydrophobic moieties by arginine in aqueous solutions.Inside a superatom: the M7q (M=Cu, Ag, q=1+, 0, 1-) case.Analysis of anisotropic effects in trinuclear metal carbonyl compounds by visualization of through-space NMR shielding.Indan-C60: from a crystalline molecule to photovoltaic application.Selecting boron fullerenes by cage-doping mechanisms.Conformational analysis of alternariol on the quantum level.Synthesis, structure, and reactivity of Lewis base stabilized plumbacyclopentadienylidenes.Evaluation of bonding, electron affinity, and optical properties of M@C28 (M = Zr, Hf, Th, and U): Role of d- and f-orbitals in endohedral fullerenes from relativistic DFT calculations.The nature of structure and bonding between transition metal and mixed Si-Ge tetramers: A 20-electron superatom system.Magnetic response properties of gaudiene - a cavernous and aromatic carbocage.C72: gaudiene, a hollow and aromatic all-carbon molecule.Reduction-triggered aromatic to aromatic electronic structure switching in tribenzotetraazachlorin-fullerene conjugates.Aromaticity and antiaromaticity of substituted fulvene derivatives: perspectives from the information-theoretic approach in density functional reactivity theory.Regioselective Diels-Alder reaction to open-cage ketolactam derivatives of C60.Evaluation of Hollow Golden Icosahedrons: Bonding and Spherical Aromatic Properties of [Au11 E]3- Superatoms (E=Se and Te) from Relativistic DFT calculations, Persistent Structures?Is C50 a superaromat? Evidence from electronic structure and ring current calculations.σ-Aromatic cyclic M3(+) (M = Cu, Ag, Au) clusters and their complexation with dimethyl imidazol-2-ylidene, pyridine, isoxazole, furan, noble gases and carbon monoxide.The studies on the aromaticity of fullerenes and their holmium endohedral compounds.Fluxional and aromatic behavior in small magic silicon clusters: a full ab initio study of Si(n), Si(n) (1-), Si(n) (2-), and Si(n) (1+), n=6, 10 clusters.Open-shell spherical aromaticity: the 2N2 + 2N + 1 (with S = N + ½) ruleMaximum Aromaticity as a Guiding Principle for the Most Suitable Hosting Cages in Endohedral MetallofullerenesAromatic stabilization in heterofullerenes C48X12(X = N, P, B, Si)Structures and magnetic properties of mono-doped fullerenes C59X n and C59X(6−n)− (X=B−, N+, P+, As+, Si): isoelectronic analogues of C60 and C60 6−Oxa- and thia-fullerenes (C59O, C59S): Closed or opened cages?Endohedral 1H NMR Chemical Shifts of H2-, H2O- and NH3-Encapsulated Fullerene Compounds: Accurate Calculation and PredictionSoluble fullerene derivatives: The effect of electronic structure on transistor performance and air stability
P2860
Q34178774-64099581-AC44-4276-8651-1D3C3510C3BFQ34300097-E77ED999-3638-49F6-B854-68362CE7BDC2Q34393427-4BED58CB-AF69-4461-8EEA-F555B8C0A408Q34979541-B3AF2D91-7A66-4A9F-914A-55E2DCC28ABAQ35037552-884001F4-37B9-4E9C-8C8B-35127F227F2DQ37039437-2A454155-A588-40B7-86A6-CE2F1DC45C20Q38003916-A57D160B-4054-49EA-985F-CD410E92A926Q38211982-1DC62D71-77FC-4711-A8F1-80C5EAD2A999Q38255209-8BC533CF-EAB5-4489-85F0-239343B5288CQ38634234-A0216C94-96E7-4473-9792-D2B2035233BDQ39407054-4F424509-B856-4F3B-9FB8-8957A58EDAD4Q39550646-B67DFD44-5FC0-45FA-9B9A-8CB360E74A99Q39813900-5C972254-2C99-430E-8589-6EA39981AA52Q40030677-34DFA494-536D-4C01-A3B9-BD02745D6C26Q42938322-F4006FA9-5B9D-45E3-9CA6-961E54BC1BC0Q43193471-4EDD1106-6360-4EE1-9032-621808958246Q44702184-9250F02A-262B-4BB2-B7DE-24794F55D613Q45048346-E2FDBD5C-651A-4AE4-B007-B04B1CE1070CQ46048614-F66CE9F6-A5C3-47B1-8AC0-61B70886B667Q46086537-8D92D2E0-E3E8-473E-801E-6117E3468C56Q46468655-B5C997AD-9925-45B8-9E8A-F6AEA17113DBQ46472477-8C851DBB-9C8B-48E3-BFA1-DBF143B57929Q46511945-F277A780-0A23-401A-8295-72ED3F0FD320Q46526145-C7C55AF1-30C0-4A2A-96F5-362E1B99E063Q46560883-B083CCD4-2A4B-49B6-8A3F-3AF21CE3599EQ46829346-1AFD03D9-8129-41E9-9A57-73195683FFFAQ47942574-90DF13CB-EDFF-4F6F-94FD-9572ECC7F688Q48161155-3310D738-8740-402F-A443-6041E556518FQ48942955-88D178A2-AF77-4B7E-BB5D-7659E2138B42Q49108134-7BB23B8C-55AD-4BCE-8054-46B22BE5C09DQ50206745-0F01211C-6AF0-403F-9B6D-87F5B861BE2BQ51700064-5F8B8799-E0DB-4571-984A-D902AB1EB0BAQ51910494-CDB960C4-3235-41FF-AB62-977882D18607Q56442808-AB9B5DAF-9FC7-4C0C-ADEC-032F3400D919Q56880592-6EB7B9CC-0131-417E-920B-E68911A96797Q57398039-5EC605A8-8F2D-42FC-A1C5-D37805AF2DD5Q57398065-3ABA4F53-0315-490A-A803-8F143C53557CQ57398072-B9B43BD5-C40D-4BFD-AE28-3A5A426DB518Q57614666-CBE1121D-AAF6-4D92-B5B6-B167395B6546Q57746084-044ED084-3C9C-4160-9D72-20595637D52C
P2860
description
im Mai 2001 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 May 2001
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в травні 2001
@uk
name
Spherical Aromaticity of Fullerenes
@en
Spherical Aromaticity of Fullerenes
@nl
type
label
Spherical Aromaticity of Fullerenes
@en
Spherical Aromaticity of Fullerenes
@nl
prefLabel
Spherical Aromaticity of Fullerenes
@en
Spherical Aromaticity of Fullerenes
@nl
P356
P1433
P1476
Spherical aromaticity of fullerenes
@en
P2093
P304
P356
10.1021/CR990332Q
P577
2001-05-01T00:00:00Z