On the public citation graph
Aromaticity, the Hückel 4 n+2 Rule and Magnetic Current
0 signed · 162 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-987x(19960115)17:1<49::aid-jcc5>3.0.co;2-0openalex-snapshot
Using redundant internal coordinates to optimize equilibrium geometries and transition states
inferredcites →https://doi.org/10.1002/1521-3765(20021018)8:20<4693::aid-chem4693>3.0.co;2-bopenalex-snapshot
Structures, Bond Energies, Heats of Formation, and Quantitative Bonding Analysis of Main-Group Metallocenes [E(Cp)2] (E=Be–Ba, Zn, Si–Pb) and [E(Cp)] (E=Li–Cs, B–Tl)
inferredcites →https://doi.org/10.1002/chem.200500376openalex-snapshot
An Energetic Measure of Aromaticity and Antiaromaticity Based on the Pauling–Wheland Resonance Energies
inferredcites →https://doi.org/10.1002/chem.200601674openalex-snapshot
Aromaticity in Metallabenzenes
inferredcites →https://doi.org/10.1002/chem.200700154openalex-snapshot
Double Aromaticity in Monocyclic Carbon, Boron, and Borocarbon Rings Based on Magnetic Criteria
inferredcites →https://doi.org/10.1002/chem.201001392openalex-snapshot
Aromaticity in Group 14 Homologues of the Cyclopropenylium Cation
inferredcites →https://doi.org/10.1002/chem.201403889openalex-snapshot
Distortions of π‐Coordinated Arenes with Anionic Character
inferredcites →https://doi.org/10.1002/jcc.20543openalex-snapshot
Unicorns in the world of chemical bonding models
inferredcites →https://doi.org/10.1002/jcc.21824openalex-snapshot
A dissected ring current model for assessing magnetic aromaticity: A general approach for both organic and inorganic rings
inferredcites →https://doi.org/10.1002/qua.560090204openalex-snapshot
Møller–Plesset theory for atomic ground state energies
inferredcites →https://doi.org/10.1002/qua.560140503openalex-snapshot
Electron correlation theories and their application to the study of simple reaction potential surfaces
inferredcites →https://doi.org/10.1002/qua.560140504openalex-snapshot
Many‐body perturbation theory, coupled‐pair many‐electron theory, and the importance of quadruple excitations for the correlation problem
inferredcites →https://doi.org/10.1007/bf01339530openalex-snapshot
Quantentheoretische Beitr�ge zum Benzolproblem
inferredcites →https://doi.org/10.1007/s00214-015-1617-7openalex-snapshot
Is NICS a reliable aromaticity index for transition metal clusters?
inferredcites →https://doi.org/10.1016/0009-2614(90)87031-lopenalex-snapshot
Non-iterative fifth-order triple and quadruple excitation energy corrections in correlated methods
inferredcites →https://doi.org/10.1016/0009-2614(92)86093-wopenalex-snapshot
A comparison of the efficiency and accuracy of the quadratic configuration interaction (QCISD), coupled cluster (CCSD), and Brueckner coupled cluster (BCCD) methods
inferredcites →https://doi.org/10.1016/j.cplett.2003.11.048openalex-snapshot
Overlap populations, bond orders and valences for ‘fuzzy’ atoms
inferredcites →https://doi.org/10.1016/j.jorganchem.2006.01.038openalex-snapshot
Nucleus-independent chemical shift (NICS) profiles in a series of monocyclic planar inorganic compounds
inferredcites →https://doi.org/10.1016/s0009-2614(89)87395-6openalex-snapshot
A fifth-order perturbation comparison of electron correlation theories
inferredcites →https://doi.org/10.1021/cr030088+openalex-snapshot
Nucleus-Independent Chemical Shifts (NICS) as an Aromaticity Criterion
inferredcites →https://doi.org/10.1021/cr990363lopenalex-snapshot
A Different Story of π-DelocalizationThe Distortivity of π-Electrons and Its Chemical Manifestations
inferredcites →https://doi.org/10.1021/ct100098copenalex-snapshot
Not All That Has a Negative NICS Is Aromatic: The Case of the H-Bonded Cyclic Trimer of HF
inferredcites →https://doi.org/10.1021/ct4007184openalex-snapshot
All-Metal Aromaticity: Revisiting the Ring Current Model among Transition Metal Clusters
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/jp0467696openalex-snapshot
Exploration of C6H6 Potential Energy Surface: A Computational Effort to Unravel the Relative Stabilities and Synthetic Feasibility of New Benzene Isomers
inferredcites →https://doi.org/10.1021/jp0609176openalex-snapshot
Electron Delocalization and Aromaticity in Linear Polyacenes: Atoms in Molecules Multicenter Delocalization Index
inferredcites →https://doi.org/10.1021/jp0716132openalex-snapshot
Properties of Aromaticity Indices Based on the One-Electron Density Matrix
inferredcites →https://doi.org/10.1021/ol016217vopenalex-snapshot
Dissected Nucleus-Independent Chemical Shift Analysis of π-Aromaticity and Antiaromaticity
inferredcites →https://doi.org/10.1021/ol0529546openalex-snapshot
Which NICS Aromaticity Index for Planar π Rings Is Best?
inferredcites →https://doi.org/10.1039/b002009popenalex-snapshot
Multicenter bond indices as a measure of aromaticity
inferredcites →https://doi.org/10.1039/b508541aopenalex-snapshot
Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy
inferredcites →https://doi.org/10.1039/b605086gopenalex-snapshot
Electron sharing indexes at the correlated level. Application to aromaticity calculations
inferredcites →https://doi.org/10.1039/b606835aopenalex-snapshot
Direct estimate of conjugation and aromaticity in cyclic compounds with the EDA method
inferredcites →https://doi.org/10.1039/b903677fopenalex-snapshot
Efficiency of the NICSzz-scan curves to probe the antiaromaticity of organic and inorganic rings/cages
inferredcites →https://doi.org/10.1039/c5cp05222jopenalex-snapshot
Unification of ground-state aromaticity criteria – structure, electron delocalization, and energy – in light of the quantum chemical topology
inferredcites →https://doi.org/10.1039/c5cs00004aopenalex-snapshot
Aromaticity of metallabenzenes and related compounds
inferredcites →https://doi.org/10.1039/c6cp00671jopenalex-snapshot
10-π-Electron arenes à la carte: structure and bonding of the [E–(C n H n )–E] n−6 (E = Ca, Sr, Ba; n = 6–8) complexes
inferredcites →https://doi.org/10.1051/jphysrad:01937008010039700openalex-snapshot
Théorie quantique des courants interatomiques dans les combinaisons aromatiques
inferredcites →https://doi.org/10.1063/1.1646354openalex-snapshot
Energy partitioning for “fuzzy” atoms
inferredcites →https://doi.org/10.1063/1.1749766openalex-snapshot
The Diamagnetic Anisotropy of Aromatic Molecules
inferredcites →https://doi.org/10.1063/1.443164openalex-snapshot
A full coupled-cluster singles and doubles model: The inclusion of disconnected triples
inferredcites →https://doi.org/10.1063/1.463096openalex-snapshot
Fully optimized contracted Gaussian basis sets for atoms Li to Kr
inferredcites →https://doi.org/10.1063/1.464480openalex-snapshot
Coupled-cluster methods with noniterative triple excitations for restricted open-shell Hartree–Fock and other general single determinant reference functions. Energies and analytical gradients
inferredcites →https://doi.org/10.1080/00268979909483052openalex-snapshot
Electric and magnetic properties of hexaethynylbenzene
inferredcites →https://doi.org/10.1093/oso/9780198551683.001.0001openalex-snapshot
Atoms in Molecules
inferredcites →https://doi.org/10.1098/rspa.1929.0081openalex-snapshot
The structure of the benzene ring in C6 (CH3)6
inferredcites →https://doi.org/10.1098/rspa.1937.0064openalex-snapshot
Magnetic anisotropy and electronic structure of aromatic molecules
inferredcites →https://doi.org/10.1098/rstl.1825.0022openalex-snapshot
XX. On new compounds of carbon and hydrogen, and on certain other products obtained during the decomposition of oil by heat
inferredcites →https://doi.org/10.1103/physrev.46.618openalex-snapshot
Note on an Approximation Treatment for Many-Electron Systems
inferredcites →https://doi.org/10.1103/physreva.38.3098openalex-snapshot
Density-functional exchange-energy approximation with correct asymptotic behavior
inferredcites →https://doi.org/10.1103/physrevb.33.8822openalex-snapshot
Density-functional approximation for the correlation energy of the inhomogeneous electron gas
inferredcites →https://doi.org/10.2174/1874364101105010079openalex-snapshot
Direct Estimate of Aromaticity with the Energy Decomposition Analysis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.12688/openreseurope.19690.1zenodo-depositor-declared
Concealed antiaromaticity
inferred← citeshttps://doi.org/10.1002/ange.202009638openalex-snapshot
A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi2N‐Ring
inferred← citeshttps://doi.org/10.1002/ange.202206836openalex-snapshot
Reply to the Correspondence on “How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring”**
inferred← citeshttps://doi.org/10.1002/anie.202009638openalex-snapshot
A Neutral Three‐Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four‐Membered BSi2N‐Ring
inferred← citeshttps://doi.org/10.1002/anie.202206836openalex-snapshot
Reply to the Correspondence on “How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring”**
inferred← citeshttps://doi.org/10.1002/anie.202506305openalex-snapshot
Imidazo[1,5‐ a ]pyridines – A Versatile Platform for Structurally Distinct N ‐Heterocyclic Olefins and π‐Extended Heterocycles
inferred← citeshttps://doi.org/10.1002/chem.201702035openalex-snapshot
Usefulness of the σ‐Aromaticity and σ‐Antiaromaticity Concepts for Clusters and Solid‐State Compounds
inferred← citeshttps://doi.org/10.1002/chem.202202264openalex-snapshot
Quest for the Most Aromatic Pathway in Charged Expanded Porphyrins
inferred← citeshttps://doi.org/10.1002/chem.202203748openalex-snapshot
Photochemistry Driven by Excited‐State Aromaticity Gain or Antiaromaticity Relief
inferred← citeshttps://doi.org/10.1002/chem.202400361openalex-snapshot
Effect of Benzo‐Annelation on Triplet State Energies in Polycyclic Conjugated Hydrocarbons
inferred← citeshttps://doi.org/10.1002/chem.202401041openalex-snapshot
Antiaromaticity of Cycloheptatrienyl Anions: Structure, Acidity, and Magnetic Properties
inferred← citeshttps://doi.org/10.1002/chem.202401282openalex-snapshot
Can Aromaticity Be Evaluated Using Atomic Partitions Based on the Hilbert‐Space?
inferred← citeshttps://doi.org/10.1002/chem.202402970openalex-snapshot
The Possible Aromatic Conjugation via the Different Edges of (Car)Borane Clusters: Can the Relationship Between 3D and 2D Aromatic Systems Be Reconciled?
inferred← citeshttps://doi.org/10.1002/chem.71596openalex-snapshot
Exploring the Boundaries of Aromaticity in Complex Structures and Excited States Through Computational Analysis
inferred← citeshttps://doi.org/10.1002/cmtd.202500064openalex-snapshot
Exploring Aromaticity in Expanded Porphyrins: A Multidimensional Approach to Structure–Property Relationships
inferred← citeshttps://doi.org/10.1002/cphc.201800364openalex-snapshot
Why is Benzene Unique? Screening Magnetic Properties of C 6 H 6 Isomers
inferred← citeshttps://doi.org/10.1002/cptc.202300291openalex-snapshot
Intra and interatomic energy contributions in the photophysical relaxation of small aromatic molecules
inferred← citeshttps://doi.org/10.1002/ejic.201800339openalex-snapshot
Aromaticity of [M3(µ‐X)3X6]0/2– (M = Re and Tc, X = Cl, Br, I) Clusters Confirmed by Ring Current Analysis and Induced Magnetic Field
inferred← citeshttps://doi.org/10.1002/ejoc.202201008openalex-snapshot
Quantifying Vertical Resonance Energy in Aromatic Systems with Natural Bond Orbitals
inferred← citeshttps://doi.org/10.1002/jcc.24805openalex-snapshot
The role of the long‐range exchange corrections in the description of electron delocalization in aromatic species
inferred← citeshttps://doi.org/10.1002/jcc.26018openalex-snapshot
Vorticity: Simplifying the analysis of the current density
inferred← citeshttps://doi.org/10.1002/jcc.27214openalex-snapshot
On the aromaticity and stability of benzynes in the ground and lowest‐lying triplet excited states
inferred← citeshttps://doi.org/10.1002/jcc.27304openalex-snapshot
Unraveling the effect of aromaticity for the dynamics of excited states of single benzene fluorophores
inferred← citeshttps://doi.org/10.1002/open.201900014openalex-snapshot
Electron Delocalization in Planar Metallacycles: Hückel or Möbius Aromatic?
inferred← citeshttps://doi.org/10.1002/poc.4447openalex-snapshot
In the quest of Hückel–Hückel and Hückel–Baird double aromatic tropylium (tri)cation and anion derivatives
inferred← citeshttps://doi.org/10.1002/poc.4455openalex-snapshot
Azaboracyclooctatetraenes reveal that the different aspects of triplet state Baird‐aromaticity are nothing but different
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/qua.25848openalex-snapshot
The vorticity of the current density tensor and 3D‐aromaticity
inferred← citeshttps://doi.org/10.1002/slct.201901557openalex-snapshot
6π, 8π and 10π Six Membered Sulfur Nitrogen Compounds: A Comparative Study with Organic Analogues
inferred← citeshttps://doi.org/10.1002/wcms.1404openalex-snapshot
Connecting and combining rules of aromaticity. Towards a unified theory of aromaticity
inferred← citeshttps://doi.org/10.1007/s00214-024-03116-xopenalex-snapshot
Investigation of solvent effects on the aromaticity of hydroxybenzenes, considering magnetically induced current densities in adducts with explicit water molecules
inferred← citeshttps://doi.org/10.1007/s00214-026-03342-5openalex-snapshot
A brief journey through aromaticity indices
inferred← citeshttps://doi.org/10.1007/s11227-026-08347-2openalex-snapshot
Mathematical quantification of nanostructures using degree-based reduced reverse indices
inferred← citeshttps://doi.org/10.1016/b978-0-12-822723-7.00002-9openalex-snapshot
Overview of the computational methods to assess aromaticity
inferred← citeshttps://doi.org/10.1016/b978-0-12-822723-7.00006-6openalex-snapshot
Quantifying aromaticity according to the energetic criterion
inferred← citeshttps://doi.org/10.1016/b978-0-12-822723-7.00008-xopenalex-snapshot
The electron density of delocalized bonds (EDDBs) as a measure of local and global aromaticity
inferred← citeshttps://doi.org/10.1016/b978-0-323-90891-7.00009-8openalex-snapshot
Scalar and vector fields derived from magnetically induced current density
inferred← citeshttps://doi.org/10.1016/j.chempr.2026.103265openalex-snapshot
Evolution from out-of-plane to in-plane metallo-annulenes: Theoretical investigations of putative planar transition metallo-annulenes
inferred← citeshttps://doi.org/10.1016/j.cplett.2020.138065openalex-snapshot
Towards understanding metal aromaticity in different spin states: A density functional theory and information-theoretic approach analysis
inferred← citeshttps://doi.org/10.1016/j.cplett.2023.140370openalex-snapshot
Effect of benzo-annelation on magnetically induced current density
inferred← citeshttps://doi.org/10.1016/j.jmgm.2017.12.026openalex-snapshot
Comparison of effects of charge delocalization and π-electron delocalization on the stability of monocyclic compounds
inferred← citeshttps://doi.org/10.1016/j.jmgm.2025.109184openalex-snapshot
Optimizing OLED efficiency through thermally activated delayed fluorescence: Computational insights into position isomers of BN-perylenes
inferred← citeshttps://doi.org/10.1016/j.jmgm.2026.109546openalex-snapshot
Closed-form connection-number-based topological indices for porphyrazine and tetrakis-porphyrazine networks
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c03139openalex-snapshot
From (Sub)Porphyrins to (Sub)Phthalocyanines: Aromaticity Signatures in the UV–Vis Absorption Spectra
inferred← citeshttps://doi.org/10.1021/acs.jcim.9b00909openalex-snapshot
Database of Nuclear Independent Chemical Shifts (NICS) versus NICSZZ of Polycyclic Aromatic Hydrocarbons (PAHs)
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01167openalex-snapshot
Hückel Molecular Orbital Analysis for Stability and Instability of Stacked Aromatic and Stacked Antiaromatic Systems
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01807openalex-snapshot
Magnetic Antiaromaticity─Paratropicity─Does Not Necessarily Imply Instability
inferred← citeshttps://doi.org/10.1021/acs.jpca.0c08926openalex-snapshot
Triplet State Baird Aromaticity in Macrocycles: Scope, Limitations, and Complications
inferred← citeshttps://doi.org/10.1021/acs.jpca.2c00346openalex-snapshot
On Aromaticity of the Aromatic α-Amino Acids and Tuning of the NICS Indices to Find the Aromaticity Order
inferred← citeshttps://doi.org/10.1021/acs.jpca.3c05784openalex-snapshot
Antiaromatic Molecules as Magnetic Couplers: A Computational Quest
inferred← citeshttps://doi.org/10.1021/acs.jpca.4c02580openalex-snapshot
The n ,π* States of Heteroaromatics: When are They the Lowest Excited States and in What Way Can They Be Aromatic or Antiaromatic?
inferred← citeshttps://doi.org/10.1021/acs.jpca.5c00817openalex-snapshot
Assessing Aromaticity in Ions: Evaluating Induced Ring Current and UV–Vis Spectrum-Based Criteria
inferred← citeshttps://doi.org/10.1021/acs.jpca.5c05498openalex-snapshot
Dynamic Four-Membered Rings with 2π Aromaticity
inferred← citeshttps://doi.org/10.1021/acs.jpca.7b07607openalex-snapshot
Relation Between Ring Currents and Hydrogenation Enthalpies for Assessing the Degree of Aromaticity
inferred← citeshttps://doi.org/10.1021/acs.jpca.9b09056openalex-snapshot
Electrostatic Topographical Viewpoint of π-Conjugation and Aromaticity of Hydrocarbons
inferred← citeshttps://doi.org/10.1021/acs.jpcc.0c04673openalex-snapshot
Effect of Heteroaromaticity on Adsorption of Pyrazine on the Ge(100)-2×1 Surface
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01147openalex-snapshot
Synthesis of Planar meso-Aryl Rosarins: A Reversible Antiaromatic/Aromatic Interconversion
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01374openalex-snapshot
Unveiling the True Identity of Carborane-Fused Phosphorus Heterocycles
inferred← citeshttps://doi.org/10.1021/acsomega.9b00916openalex-snapshot
Effect of Exocyclic Substituents and π-System Length on the Electronic Structure of Chichibabin Diradical(oid)s
inferred← citeshttps://doi.org/10.1021/jacs.1c13478openalex-snapshot
Three-Dimensional Fully π-Conjugated Macrocycles: When 3D-Aromatic and When 2D-Aromatic-in-3D?
inferred← citeshttps://doi.org/10.1021/jacs.4c14515openalex-snapshot
Unraveling the Bonding and Aromaticity of Pentazole, Pentaphosphole, and Cyclopentadiene Anions: A Comprehensive Study
inferred← citeshttps://doi.org/10.1038/s41467-018-03368-9openalex-snapshot
Studying an antiaromatic polycyclic hydrocarbon adsorbed on different surfaces
inferred← citeshttps://doi.org/10.1038/s41467-024-46853-0openalex-snapshot
Ultra-photostable small-molecule dyes facilitate near-infrared biophotonics
inferred← citeshttps://doi.org/10.1038/s41570-024-00617-yopenalex-snapshot
On the aromaticity of actinide compounds
inferred← citeshttps://doi.org/10.1038/s41586-021-04319-zopenalex-snapshot
[{Th(C8H8)Cl2}3]2− is stable but not aromatic
inferred← citeshttps://doi.org/10.1038/s41598-017-00867-5openalex-snapshot
Chemical Bonding and σ-Aromaticity in Charged Molecular Alloys: [Pd2As14]4− and [Au2Sb14]4− Clusters
inferred← citeshttps://doi.org/10.1038/s41598-017-10739-7openalex-snapshot
The novel link between planar möbius aromatic and third order nonlinear optical properties of metal–bridged polycyclic complexes
inferred← citeshttps://doi.org/10.1039/c7cp03544fopenalex-snapshot
Aromaticity and antiaromaticity of substituted fulvene derivatives: perspectives from the information-theoretic approach in density functional reactivity theory
inferred← citeshttps://doi.org/10.1039/c7cp06114eopenalex-snapshot
The electron density of delocalized bonds (EDDB) applied for quantifying aromaticity
inferred← citeshttps://doi.org/10.1039/c7cp07581bopenalex-snapshot
New electron delocalization tools to describe the aromaticity in porphyrinoids
inferred← citeshttps://doi.org/10.1039/c7cp07965fopenalex-snapshot
On the regioselectivity of the Diels–Alder cycloaddition to C 60 in high spin states
inferred← citeshttps://doi.org/10.1039/c8cp03737jopenalex-snapshot
The electronic structure and stability of germanium tubes Ge 30 H 12 and Ge 33 H 12
inferred← citeshttps://doi.org/10.1039/c9cp00117dopenalex-snapshot
Delocalization energy retrieved from the current density tensor
inferred← citeshttps://doi.org/10.1039/d0cp04502kopenalex-snapshot
Are all planar and quasi-planar boron clusters aromatic? Counter examples of island or global π antiaromaticity from chemical bonding analysis
inferred← citeshttps://doi.org/10.1039/d1cc00593fopenalex-snapshot
An unprecedented π-electronic circuit involving an odd number of carbon atoms in a grossly warped non-planar nanographene
inferred← citeshttps://doi.org/10.1039/d1cp02516copenalex-snapshot
Density functional theory studies of boron clusters with exotic properties in bonding, aromaticity and reactivity
inferred← citeshttps://doi.org/10.1039/d1dt04096kopenalex-snapshot
Synthesis, structure and aromaticity of metallapyridinium complexes
inferred← citeshttps://doi.org/10.1039/d1ra06457fopenalex-snapshot
The hidden aromaticity in borazine
inferred← citeshttps://doi.org/10.1039/d2cp04846aopenalex-snapshot
Metallaaromaticity – a protean world
inferred← citeshttps://doi.org/10.1039/d2dt01001aopenalex-snapshot
α-Rhenabenzofuran with nonaromatic T 0 and aromatic S 1 states
inferred← citeshttps://doi.org/10.1039/d2ma00063fopenalex-snapshot
Thermally encapsulated phenothiazine@MWCNT cathode for aqueous zinc ion battery
inferred← citeshttps://doi.org/10.1039/d2sc03511aopenalex-snapshot
Conjugation between 3D and 2D aromaticity: does it really exist? The case of carborane-fused heterocycles
inferred← citeshttps://doi.org/10.1039/d3cc03464jopenalex-snapshot
Electronic delocalization in charged macrocycles is associated with global aromaticity
inferred← citeshttps://doi.org/10.1039/d3cp00651dopenalex-snapshot
Engineering magic number Au 19 and Au 20 cage structures using electron withdrawing atoms
inferred← citeshttps://doi.org/10.1039/d4nj04433aopenalex-snapshot
Size effects of Möbius carbon nanobelts (MCNBs) from the (7-7)MCNB to the (21-21)MCNB on their aromatic properties and third order nonlinear optical properties
inferred← citeshttps://doi.org/10.1039/d4sc04692gopenalex-snapshot
Proton transfer induced excited-state aromaticity gain for chromophores with maximal Stokes shifts
inferred← citeshttps://doi.org/10.1039/d5cp02697kopenalex-snapshot
Aromaticity and antiaromaticity in the cyclic 6π and 4π molecules of carbon and silicon E 6 H 6 and E 4 H 4 (E = C, Si)
inferred← citeshttps://doi.org/10.1039/d5cp02867aopenalex-snapshot
SD aromaticity index: a new assessment of aromaticity based on Ramsey spin dipolar contribution to NMR spin–spin coupling constants
inferred← citeshttps://doi.org/10.1039/d5cp03929kopenalex-snapshot
The limit of the current aromaticity concept
inferred← citeshttps://doi.org/10.1039/d5cp04577kopenalex-snapshot
Expanding aromaticity tests to include lowest-lying triplet excited states and charged and heterocyclic rings
inferred← citeshttps://doi.org/10.1039/d5cs01502bopenalex-snapshot
Antiaromaticity by on-surface synthesis
inferred← citeshttps://doi.org/10.1039/d5sc02743hopenalex-snapshot
Revisiting aromaticity and stability in the diboron actinide compound Pa 2 B 2
inferred← citeshttps://doi.org/10.1039/d5sc05880eopenalex-snapshot
Taming boroloborinines: toward photostable polycyclic antiaromatic hydrocarbons
inferred← citeshttps://doi.org/10.1080/00268976.2017.1403657openalex-snapshot
Structure, aromaticity and reactivity of corannulene and its analogues: a conceptual density functional theory and density functional reactivity theory study
inferred← citeshttps://doi.org/10.20517/energymater.2024.185openalex-snapshot
Machine learning prediction of small molecule passivators and their impacts on the passivation and photocatalytic performance of organic-inorganic hybrid perovskite interfaces
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-nwgg8openalex-snapshot
Eliminating Fragment Group Orbital (eFGO) Analysis for Deciphering Chemical Bonding in Complex Systems
inferred← citeshttps://doi.org/10.3389/fchem.2017.00022openalex-snapshot
Why Aromaticity Is a Suspicious Concept? Why?
inferred← citeshttps://doi.org/10.3389/fchem.2021.767421openalex-snapshot
Cluster Assembled Silicon-Lithium Nanostructures: A Nanowire Confined Inside a Carbon Nanotube
inferred← citeshttps://doi.org/10.3390/chemistry3020038openalex-snapshot
Exploitation of Baird Aromaticity and Clar’s Rule for Tuning the Triplet Energies of Polycyclic Aromatic Hydrocarbons
inferred← citeshttps://doi.org/10.3390/chemistry6060103openalex-snapshot
py.Aroma: An Intuitive Graphical User Interface for Diverse Aromaticity Analyses
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.