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Reversible redox switching between local and global aromaticity for core-modified expanded carbaisophlorinoids
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajoc.201402157openalex-snapshot
Synthesis, Characterization, and Electron‐Transport Properties of a π‐Conjugated Heteromacrocycle: A Selenium‐Bridged Neutral Annulene
inferredcites →https://doi.org/10.1002/ange.19600721803openalex-snapshot
Totalsynthese des Chlorophylls
inferredcites →https://doi.org/10.1002/anie.198916511openalex-snapshot
The Thiophene Analogue of Porphyrin: Tetrathiaporphyrin Dication
inferredcites →https://doi.org/10.1002/anie.200702854openalex-snapshot
A Core‐Modified Rubyrin with meso‐Aryl Substituents and Phenanthrene‐Fused Pyrrole Rings: A Highly Conjugated Near‐Infrared Dye and Hg2+ Probe
inferredcites →https://doi.org/10.1002/anie.201207987openalex-snapshot
Antiaromatic Supramolecules: F⋅⋅⋅S, F⋅⋅⋅Se, and F⋅⋅⋅π Intermolecular Interactions in 32 π Expanded Isophlorins
inferredcites →https://doi.org/10.1002/anie.201403372openalex-snapshot
Reversible Redox Reaction Between Antiaromatic and Aromatic States of 32π‐Expanded Isophlorins
inferredcites →https://doi.org/10.1002/anie.201406893openalex-snapshot
An Amphoteric Switch to Aromatic and Antiaromatic States of a Neutral Air‐Stable 25π Radical
inferredcites →https://doi.org/10.1002/anie.201905763openalex-snapshot
Cyclobis(7,8‐(para‐quinodimethane)‐4,4′‐triphenylamine) and Its Cationic Species Showing Annulene‐Like Global (Anti)Aromaticity
inferredcites →https://doi.org/10.1007/bf01339530openalex-snapshot
Quantentheoretische Beitr�ge zum Benzolproblem
inferredcites →https://doi.org/10.1016/s0040-4020(99)00979-5openalex-snapshot
Aromaticity: a Theoretical Concept of Immense Practical Importance
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00544openalex-snapshot
Isophlorinoids: The Antiaromatic Congeners of Porphyrinoids
inferredcites →https://doi.org/10.1021/acs.orglett.7b02317openalex-snapshot
Oxidative Transformation of a Tetrathia S-Confused Isophlorin into Porphyrin Cation
inferredcites →https://doi.org/10.1021/cr0300901openalex-snapshot
Anisotropy of the Induced Current Density (ACID), a General Method To Quantify and Visualize Electronic Delocalization
inferredcites →https://doi.org/10.1021/cr990367qopenalex-snapshot
Antiaromaticity in Monocyclic Conjugated Carbon Rings
inferredcites →https://doi.org/10.1021/ja00861a028openalex-snapshot
Unsaturated Macrocyclic Compounds. XXI.1 The Synthesis of a Series of Fully Conjugated Macrocyclic Polyene-polyynes (Dehydro-annulenes) from 1,5-Hexadiyne
inferredcites →https://doi.org/10.1021/ja017852zopenalex-snapshot
Tetraphenyl-p-benziporphyrin: A Carbaporphyrinoid with Two Linked Carbon Atoms in the Coordination Core
inferredcites →https://doi.org/10.1021/ja053723xopenalex-snapshot
Dithiadiazuliporphyrin: Facile Generation of Carbaporphyrinoid Cation Radical and Dication
inferredcites →https://doi.org/10.1021/ja511320fopenalex-snapshot
In-Plane Aromaticity in Cycloparaphenylene Dications: A Magnetic Circular Dichroism and Theoretical Study
inferredcites →https://doi.org/10.1021/ja906290dopenalex-snapshot
Aromatic Expanded Isophlorins: Stable 30π Annulene Analogues with Diverse Structural Features
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/jo7015218openalex-snapshot
Dioxadiazuliporphyrin: A Near-IR Redox Switchable Chromophore
inferredcites →https://doi.org/10.1021/jo980407aopenalex-snapshot
Preparation and Structures of Crystalline Aromatic Cation-Radical Salts. Triethyloxonium Hexachloroantimonate as a Novel (One-Electron) Oxidant
inferredcites →https://doi.org/10.1021/ol062359jopenalex-snapshot
Cyclic Oligofurans: One-Pot Synthesis of 30π and 40π Expanded Porphyrinoids
inferredcites →https://doi.org/10.1039/b715553kopenalex-snapshot
π-Conjugated macrocycles from thiophenes and benzenes
inferredcites →https://doi.org/10.1039/c0cc03974hopenalex-snapshot
New sulfur bridged neutral annulenes. Structure, physical properties and applications in organic field-effect transistors
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.202400780openalex-snapshot
Breaking Global Diatropic Current to Tame Diradicaloid Character: Thiele's Hydrocarbon Under Macrocyclic Constraints
inferred← citeshttps://doi.org/10.1002/anie.202400780openalex-snapshot
Breaking Global Diatropic Current to Tame Diradicaloid Character: Thiele's Hydrocarbon Under Macrocyclic Constraints
inferred← citeshttps://doi.org/10.1002/chem.202300477openalex-snapshot
Design, Synthesis and Aromaticity of an Alternating Cyclo[4]Thiophene[4]Furan
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