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To What Extent Can Aromaticity Be Defined Uniquely?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Global and Local Aromaticity in Porphyrins: An Analysis Based on Molecular Geometries and Nucleus-Independent Chemical Shifts
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An Alternative Approach to the Nomenclature of Cyclic Conjugated Polyolefins, together with some Observations on the Use of the Term “Aromatic”
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Nucleus-Independent Chemical Shifts from Semiempirical Calculations
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Aromatic character of carbocyclic π-electron systems deduced from molecular geometry
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Big Is Beautiful−“Aromaticity” Revisited from the Viewpoint of Macromolecular and Supramolecular Benzene Chemistry
inferredcites →https://doi.org/10.1021/cr990332qopenalex-snapshot
Spherical Aromaticity of Fullerenes
inferredcites →https://doi.org/10.1021/cr990358hopenalex-snapshot
Cyclic Aromatic Systems with Hypervalent Centers
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Antiaromaticity in Monocyclic Conjugated Carbon Rings
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Aromaticity as a quantitative concept. 1. A statistical demonstration of the orthogonality of classical and magnetic aromaticity in five- and six-membered heterocycles
inferredcites →https://doi.org/10.1021/ja00183a003openalex-snapshot
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Theoretical approaches to aromatic electrophilic substitution processes. II. Intermediates in electrophilic fluorination
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Structure of thamnosin. Novel dimeric coumarin system
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Hyperconjugative π-Aromaticity: How To Make Cyclopentadiene Aromatic
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Recent advances in the chemistry of large-ring conjugated systems
inferredcites →https://doi.org/10.5860/choice.32-2145openalex-snapshot
Aromaticity and antiaromaticity: electronic and structural aspects
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inferred← citeshttps://doi.org/10.1002/poc.4463openalex-snapshot
Aromaticity and antiaromaticity in monoheterocyclic three‐membered rings: Application of natural bond orbital theory
inferred← citeshttps://doi.org/10.1002/poc.4612openalex-snapshot
Addition reaction of azoles to acetone‐ d 6 : NMR and computational studies
inferred← citeshttps://doi.org/10.1002/poc.631openalex-snapshot
Aromatic stabilization in heterofullerenes C 48 X 12 (X = N, P, B, Si)
inferred← citeshttps://doi.org/10.1002/poc.658openalex-snapshot
Aromaticity and antiaromaticity: what role do ionic configurations play in delocalization and induction of magnetic properties?
inferred← citeshttps://doi.org/10.1002/poc.666openalex-snapshot
Non‐additivity of the static correlation energy of π‐electrons in planar molecules as a manifestation of anti/aromaticity
inferred← citeshttps://doi.org/10.1002/poc.674openalex-snapshot
Tadeusz Marek Krygowski—from aromaticity through X‐ray crystallography to interpretative structural Chemistry
inferred← citeshttps://doi.org/10.1002/poc.70024openalex-snapshot
Assessing the Aromaticity of Fluorinated Benzene Derivatives Using New Descriptors Based on the Distributed Multipole Analysis (DMA) Partition of the Electron Density
inferred← citeshttps://doi.org/10.1002/poc.728openalex-snapshot
Mutual relationships between magnetic aromaticity indices of heterocyclic compounds
inferred← citeshttps://doi.org/10.1002/poc.756openalex-snapshot
Solvolysis of aromatic benzoyl chlorides: how is the π‐electron stabilization of the aromatic acyl chlorides and acylium cations related to the π‐electron delocalization?
inferred← citeshttps://doi.org/10.1002/poc.843openalex-snapshot
Aromaticity and stability of furofurans and thienothiophenes
inferred← citeshttps://doi.org/10.1002/poc.938openalex-snapshot
Assessment of Clar's aromatic π‐sextet rule by means of PDI, NICS and HOMA indicators of local aromaticity
inferred← citeshttps://doi.org/10.1002/poc.960openalex-snapshot
Relation between resonance energy and substituent resonance effect in P‐phenols
inferred← citeshttps://doi.org/10.1002/qua.20071openalex-snapshot
Analysis of electronic delocalization in buckminsterfullerene (C60)
inferred← citeshttps://doi.org/10.1002/qua.21325openalex-snapshot
Planar mono‐, di‐ aza‐ and phospha‐naphthalene: Structure and aromaticity
inferred← citeshttps://doi.org/10.1002/qua.22271openalex-snapshot
The substitution effect on heavy versions of cyclobutadiene
inferred← citeshttps://doi.org/10.1002/qua.22349openalex-snapshot
Novel metal‐[metal oxide]‐nonmetal sandwich‐like superalkali compounds Li3OMC5H5 (M = Be, Mg, and Ca): How to increase the aromaticity of Li ring?
inferred← citeshttps://doi.org/10.1002/qua.22731openalex-snapshot
Quantitative structure property relationships to evaluate the photosensitizing capability in porphyrins and chlorins
inferred← citeshttps://doi.org/10.1002/slct.201601384openalex-snapshot
Aromaticity in Pericyclic Transition State Structures? A Critical Rationalisation Based on the Topological Analysis of Electron Density
inferred← citeshttps://doi.org/10.1002/slct.202203958openalex-snapshot
Synthesis of Quinoline‐Pyrene Derivatives and Theoretical Investigation of Their Fluorescence and Electronic Properties
inferred← citeshttps://doi.org/10.1002/slct.202501788openalex-snapshot
A Computational Investigation on the Characteristic Electron Delocalization of Symmetrical Squaraine Dyes
inferred← citeshttps://doi.org/10.1002/slct.202506584openalex-snapshot
Exploring Triplet Aromaticity in Azaboracyclooctatetraenes Using New Descriptors Based on Electron Density Partitioning
inferred← citeshttps://doi.org/10.1002/wcms.1270openalex-snapshot
Calculations of magnetically induced current densities: theory and applications
inferred← citeshttps://doi.org/10.1002/wcms.72openalex-snapshot
Homodesmotic reactions for thermochemistry
inferred← citeshttps://doi.org/10.1002/zaac.201700460openalex-snapshot
Chromium Bis(anthracene‐η6) Complexes – A DFT Study
inferred← citeshttps://doi.org/10.1007/3-540-46100-0_4openalex-snapshot
Transient Nitrilium Phosphanylid Complexes — New Versatile Building Blocks in Phosphorus Chemistry
inferred← citeshttps://doi.org/10.1007/7081_2008_1openalex-snapshot
How Aromaticity Affects the Chemical and Physicochemical Properties of Heterocycles: A Computational Approach
inferred← citeshttps://doi.org/10.1007/7081_2008_2openalex-snapshot
Aromaticity of Six-Membered Rings with One Heteroatom
inferred← citeshttps://doi.org/10.1007/978-3-540-68343-8_2openalex-snapshot
Aromatic Phosphorus Heterocycles
inferred← citeshttps://doi.org/10.1007/978-3-540-68343-8_4openalex-snapshot
How Aromaticity Affects the Chemical and Physicochemical Properties of Heterocycles: A Computational Approach
inferred← citeshttps://doi.org/10.1007/978-3-540-68343-8_5openalex-snapshot
Aromaticity of Six-Membered Rings with One Heteroatom
inferred← citeshttps://doi.org/10.1007/978-3-642-28974-3_8openalex-snapshot
Competitive Solvation and Chemisorption in Silver Colloidal Suspensions
inferred← citeshttps://doi.org/10.1007/978-3-642-45149-2_5openalex-snapshot
Aromaticity of Organic and Inorganic Heterocycles
inferred← citeshttps://doi.org/10.1007/978-94-007-2076-3_29openalex-snapshot
Delocalization Effects in Pristine and Oxidized Graphene Substrates
inferred← citeshttps://doi.org/10.1007/978-981-15-5451-3_15openalex-snapshot
Creation of Molecularly Integrated Multi-responsive Photochromic Systems
inferred← citeshttps://doi.org/10.1007/bf02704362openalex-snapshot
Relationship between electrophilicity index, Hammett constant and nucleus-independent chemical shift
inferred← citeshttps://doi.org/10.1007/s00214-006-0123-3openalex-snapshot
Conformational Analysis of 2,2′-bifuran: Correlated High-level Ab initio and DFT Results
inferred← citeshttps://doi.org/10.1007/s00214-006-0128-yopenalex-snapshot
CHIH-DFT Determination of the Molecular Structure and Infrared and Ultraviolet Spectra of Azathiophenes
inferred← citeshttps://doi.org/10.1007/s00214-006-0211-4openalex-snapshot
Magnetotropicity of five-membered heterocyclic molecules
inferred← citeshttps://doi.org/10.1007/s00214-007-0247-0openalex-snapshot
Magnetotropicity of phosphole and its arsenic analogue
inferred← citeshttps://doi.org/10.1007/s00214-009-0692-zopenalex-snapshot
Theoretical basis for the correlation between energetic, magnetic, and electron density criteria of aromaticity: definition of molecular circuit electric conductance
inferred← citeshttps://doi.org/10.1007/s00214-010-0794-7openalex-snapshot
How to properly compute the resonance energy within the ab initio valence bond theory: a response to the ZHJVL paper
inferred← citeshttps://doi.org/10.1007/s00214-013-1391-3openalex-snapshot
Concurrent loss of aromaticity and onset of superexchange in Mg3Na2 with an increasing Na–Mg3 distance
inferred← citeshttps://doi.org/10.1007/s00214-015-1617-7openalex-snapshot
Is NICS a reliable aromaticity index for transition metal clusters?
inferred← citeshttps://doi.org/10.1007/s00521-025-11643-2openalex-snapshot
Multidimensional analysis and visualization of aromaticity in five- and six-membered ring compounds
inferred← citeshttps://doi.org/10.1007/s00894-008-0440-7openalex-snapshot
Solvent impact on the aromaticity of benzene analogues: implicit versus explicit solvent approach
inferred← citeshttps://doi.org/10.1007/s00894-010-0806-5openalex-snapshot
Environment influences on the aromatic character of nucleobases and amino acids
inferred← citeshttps://doi.org/10.1007/s00894-010-0844-zopenalex-snapshot
Sigma- and pi- electron structure of aza-azoles
inferred← citeshttps://doi.org/10.1007/s00894-010-0848-8openalex-snapshot
Theoretical studies on nitrogen rich energetic azoles
inferred← citeshttps://doi.org/10.1007/s00894-011-0959-xopenalex-snapshot
Computational design and structure–property relationship studies on heptazines
inferred← citeshttps://doi.org/10.1007/s00894-011-1264-4openalex-snapshot
Aromatic character of heptafulvene and its complexes with halogen atoms
inferred← citeshttps://doi.org/10.1007/s00894-012-1362-yopenalex-snapshot
Theoretical studies on all-metal binuclear sandwich-like complexes M2(η4-E4)2 (M=Al, Ga, In; E=Sb, Bi)
inferred← citeshttps://doi.org/10.1007/s00894-015-2743-9openalex-snapshot
Effect of donor strength of extended alkyl auxiliary groups on optoelectronic and charge transport properties of novel naphtha[2,1-b:6,5-b′]difuran derivatives: simple yet effective strategy
inferred← citeshttps://doi.org/10.1007/s00894-015-2786-yopenalex-snapshot
DFT study of 1-butyl-3-methylimidazolium salicylate: a third-generation ionic liquid
inferred← citeshttps://doi.org/10.1007/s00894-017-3513-7openalex-snapshot
Inorganic benzenes as the noncovalent interaction donor: a study of the π-hole interactions
inferred← citeshttps://doi.org/10.1007/s00894-020-04543-wopenalex-snapshot
Heteroatom effects on aromaticity of five-membered rings in acenaphthylene analogs
inferred← citeshttps://doi.org/10.1007/s00894-020-04650-8openalex-snapshot
The redox potential of flavin derivatives as a mediator in biosensors
inferred← citeshttps://doi.org/10.1007/s10593-014-1586-0openalex-snapshot
Substituent Effect of Nitro Group on Aromaticity of Carbazole Rings
inferred← citeshttps://doi.org/10.1007/s10876-017-1310-1openalex-snapshot
Boosting BeONT Reactivity with HCN by Calcium and Magnesium Doping: A DFT Investigation of Electronic Structure, AIM, NMR, NQR and NBO Analysis
inferred← citeshttps://doi.org/10.1007/s10910-012-0062-2openalex-snapshot
π-Electron currents in fixed π-sextet aromatic benzenoids
inferred← citeshttps://doi.org/10.1007/s10947-008-0169-2openalex-snapshot
Aromatic stability energy studies on five-membered heterocyclic C4H4M (M = O, S, Se, Te, NH, PH, AsH and SbH): DFT calculations
inferred← citeshttps://doi.org/10.1007/s11172-012-0035-4openalex-snapshot
Molecular interaction of H2 and H2O with borthiin: a theoretical study
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