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Diatropic cyclophane dianions

https://doi.org/10.1021/ja00336a035
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Concealed antiaromaticity
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The McMurry Coupling and Related Reactions
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π-Conjugated Anions: From Carbon-Rich Anions to Charged Carbon Allotropes
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The Lithium Metal Reduction of π‐Conjugated Hydrocarbons and Fullerenes
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Formation of Alkenes by Elimination
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Formation of Alkenes by Wittig and Related Reactions
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Hydrocarbon Oligomers
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Neue reduktive Umwandlungen cyclischer ungesättigter Kohlenwasserstoffe
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[2.2](1,4)Benzo[g]chrysenoparacyclophan-Dianion, ein neues, paratropes, doppellagiges Carbanion
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Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch
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Inversion Triggered by Protonation—A Rubyrin with Embedded α,β′‐Pyridine Moieties
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Global Aromaticity and Antiaromaticity in Porphyrin Nanoring Anions
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Switching between Local and Global Aromaticity in a Conjugated Macrocycle for High‐Performance Organic Sodium‐Ion Battery Anodes
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New Reductive Transformations of Unsaturated Cyclic Hydrocarbons [New Synthetic Methods (66)]
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[2.2](1,4)Benzo[g]chrysenoparacyclophane Dianion: A Novel, Paratropic, Double‐Layered Carbanion
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Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch
inferred← citeshttps://doi.org/10.1002/anie.201811138openalex-snapshot
Inversion Triggered by Protonation—A Rubyrin with Embedded α,β′‐Pyridine Moieties
inferred← citeshttps://doi.org/10.1002/anie.201909032openalex-snapshot
Global Aromaticity and Antiaromaticity in Porphyrin Nanoring Anions
inferred← citeshttps://doi.org/10.1002/anie.202003386openalex-snapshot
Switching between Local and Global Aromaticity in a Conjugated Macrocycle for High‐Performance Organic Sodium‐Ion Battery Anodes
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Electron Transfer and Conformational Interconversions in 1, n ‐Diphenylpolyenes
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ChemInform Abstract: DIATROPIC CYCLOPHANE DIANIONS
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Macrocyclic Compounds Having Sulfide Moieties Derived from o‐Terphenyl.
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Simple and Effective Identification of Local 6 π ‐ and Global [4 n + 2] Aromaticity of Macrocyclic Conjugated Hydrocarbons by 1 H/ 13 C Chemical Shifts and the Corresponding Ring Current Effect
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Poly(phenylenvinylen); Entwicklung eines elektroaktiven Polymermaterials vom unschmelzbaren Pulver zum transparenten Film
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Radical ions: Where organic chemistry meets materials sciences
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Carbon Rich Cyclophanes with Unusual Properties — an Update
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Ein Beitrag zum Tetrathiaporphycen-Redoxsystem: Elektrochemische Reduktion eines 20?-Cyclophans zum diatropen 22?-Dianion
inferred← citeshttps://doi.org/10.1007/bfb0111256openalex-snapshot
Polycyclic anions: From doubly to highly charged π-conjugated systems
inferred← citeshttps://doi.org/10.1007/s00894-009-0508-zopenalex-snapshot
Macrocyclic conjugation in N-fused porphyrins and related species
inferred← citeshttps://doi.org/10.1016/0040-4039(95)02065-9openalex-snapshot
Synthesis, properties and molecular structure of a new isomer of [2.4]-paracyclophanetetraene:(E,Z,E,Z)-[2.4]-paracyclophanetetraene
inferred← citeshttps://doi.org/10.1016/0166-1280(88)87011-8openalex-snapshot
Characteristic polynomials and eigenvalues of molecular graphs with a greater than twofold axis of symmetry
inferred← citeshttps://doi.org/10.1016/j.cplett.2003.09.114openalex-snapshot
Hückel-like rule of superaromaticity for charged paracyclophanes
inferred← citeshttps://doi.org/10.1016/j.cplett.2004.12.112openalex-snapshot
First hyperpolarizabilities of dipolar, bis-dipolar, and octupolar molecules
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)86066-xopenalex-snapshot
Probing the nature of polycyclic conjugated dianions: from carbocyclic to heterocyclic dianions: NMR studies, π-delocalization and electronic structure
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The dianion of [2.2.2]paracyclophene; a 20 π-perimeter species?
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)88569-xopenalex-snapshot
Multiply charged anions from molecules with extended π-systems
inferred← citeshttps://doi.org/10.1016/s0040-4039(86)80048-xopenalex-snapshot
A sixfold triplet-sensitized Z/E isomerization of a π-perimeter macrocycle
inferred← citeshttps://doi.org/10.1016/s0079-6565(00)00022-4openalex-snapshot
NMR studies of cyclophanes
inferred← citeshttps://doi.org/10.1021/ja017852zopenalex-snapshot
Tetraphenyl-p-benziporphyrin: A Carbaporphyrinoid with Two Linked Carbon Atoms in the Coordination Core
inferred← citeshttps://doi.org/10.1021/jacs.5b06258openalex-snapshot
Strain-Induced Stereoselective Formation of Blue-Emitting Cyclostilbenes
inferred← citeshttps://doi.org/10.1021/jacsau.6c00720openalex-snapshot
Tetrahedral M II4L6 ( M = Fe, Zn) Cages Equipped with Walls Featuring Antiaromatic Pentalene Motifs
inferred← citeshttps://doi.org/10.1021/jp310480dopenalex-snapshot
Validity and Limitations of the Bridged Annulene Model for Porphyrins
inferred← citeshttps://doi.org/10.1021/ol801888dopenalex-snapshot
Synthesis and Guest Recognition Ability of 2,3-Dimethoxy-1,4-phenylene-Containing Porphyrinoids
inferred← citeshttps://doi.org/10.1039/a701906hopenalex-snapshot
Substituted [24]paracyclophanes
inferred← citeshttps://doi.org/10.1039/a909633gopenalex-snapshot
Charged paracyclophanes behave as annulenes with enhanced anisotropy
inferred← citeshttps://doi.org/10.1039/b715553kopenalex-snapshot
π-Conjugated macrocycles from thiophenes and benzenes
inferred← citeshttps://doi.org/10.1039/c2ob25692dopenalex-snapshot
The origin of global and macrocyclic aromaticity in porphyrinoids
inferred← citeshttps://doi.org/10.1039/c6cc06078aopenalex-snapshot
The reductive aromatization of tridecacyclene
inferred← citeshttps://doi.org/10.1039/d2cc05434eopenalex-snapshot
Transformation of π-conjugated macrocycles: from furanophanes to napthalenophanes
inferred← citeshttps://doi.org/10.1039/d3me00045aopenalex-snapshot
Functionalisation of conjugated macrocycles with type I and II concealed antiaromaticity via cross-coupling reactions
inferred← citeshttps://doi.org/10.1039/d3sc04251kopenalex-snapshot
Crystallographic evidence for global aromaticity in the di-anion and tetra-anion of a cyclophane hydrocarbon
inferred← citeshttps://doi.org/10.1039/d5qo00746aopenalex-snapshot
Multistage organic redox systems. Aromaticity as a guiding principle for materials chemistry
inferred← citeshttps://doi.org/10.1246/bcsj.20160237openalex-snapshot
Graph Theory of Aromatic Stabilization
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Macrocyclic Compounds Having Sulfide Moieties Derived from o-Terphenyl
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