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Functionalisation of conjugated macrocycles with type I and II concealed antiaromaticity via cross-coupling reactions

https://doi.org/10.1039/d3me00045a
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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/anie.198006241openalex-snapshot
Dianion and Tetraanion of [24] Paracyclophanetetraene—New Unusual Perimeter Systems
inferredcites →https://doi.org/10.1002/anie.201006198openalex-snapshot
Conjugated Macrocycles: Concepts and Applications
inferredcites →https://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
inferredcites →https://doi.org/10.1002/anie.202212623openalex-snapshot
Squarephaneic Tetraanhydride: A Conjugated Square‐Shaped Cyclophane for the Synthesis of Porous Organic Materials**
inferredcites →https://doi.org/10.1002/ejoc.202100352openalex-snapshot
Visualisation of Chemical Shielding Tensors (VIST) to Elucidate Aromaticity and Antiaromaticity**
inferredcites →https://doi.org/10.1021/ja00061a018openalex-snapshot
Synthesis and properties of optically active helical metallocene oligomers
inferredcites →https://doi.org/10.1021/ja00336a035openalex-snapshot
Diatropic cyclophane dianions
inferredcites →https://doi.org/10.1021/ja00769a025openalex-snapshot
Quantum organic photochemistry. II. Resonance and aromaticity in the lowest 3.pi..pi.* state of cyclic hydrocarbons
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/jacs.0c05611openalex-snapshot
Controlling the S1 Energy Profile by Tuning Excited-State Aromaticity
inferredcites →https://doi.org/10.1021/jacs.9b12435openalex-snapshot
Strategies for Design of Potential Singlet Fission Chromophores Utilizing a Combination of Ground-State and Excited-State Aromaticity Rules
inferredcites →https://doi.org/10.1021/jp8037335openalex-snapshot
Ground- and Excited-State Aromaticity and Antiaromaticity in Benzene and Cyclobutadiene
inferredcites →https://doi.org/10.1038/nchem.1518openalex-snapshot
Exciting excited-state aromaticity
inferredcites →https://doi.org/10.1038/ncomms12094openalex-snapshot
Light-melt adhesive based on dynamic carbon frameworks in a columnar liquid-crystal phase
inferredcites →https://doi.org/10.1038/nnano.2012.37openalex-snapshot
Observation of quantum interference in molecular charge transport
inferredcites →https://doi.org/10.1039/b104847nopenalex-snapshot
Four- and two-electron rules for diatropic and paratropic ring currents in monocyclic π systems
inferredcites →https://doi.org/10.1039/c3cp53866dopenalex-snapshot
Cross-conjugation and quantum interference: a general correlation?
inferredcites →https://doi.org/10.1039/c7tc01533jopenalex-snapshot
Flapping viscosity probe that shows polarity-independent ratiometric fluorescence
inferredcites →https://doi.org/10.1039/d1qo00901jopenalex-snapshot
Functional group introduction and aromatic unit variation in a set of π-conjugated macrocycles: revealing the central role of local and global aromaticity
inferredcites →https://doi.org/10.1055/s-2001-18060openalex-snapshot
An Efficient Method for the Preparation of Benzylic Bromides
inferredcites →https://doi.org/10.1063/1.1558471openalex-snapshot
Natural transition orbitals
inferredcites →https://doi.org/10.1063/1.4885819openalex-snapshot
New tools for the systematic analysis and visualization of electronic excitations. I. Formalism
inferredcites →https://doi.org/10.12688/openreseurope.13723.2openalex-snapshot
[2.2.2.2]Paracyclophanetetraenes (PCTs): cyclic structural analogues of poly(p‑phenylene vinylene)s (PPVs)
inferredcites →https://doi.org/10.12688/openreseurope.19690.1openalex-snapshot
Concealed antiaromaticity
inferredcites →https://doi.org/10.3390/chemistry3020038openalex-snapshot
Exploitation of Baird Aromaticity and Clar’s Rule for Tuning the Triplet Energies of Polycyclic Aromatic Hydrocarbons
inferredcites →https://doi.org/10.3891/acta.chem.scand.29b-0138openalex-snapshot
A Simple Synthesis of [2.2.2.2]-Paracyclophane-1,9,17,25-tetraene by a Wittig Reaction.
inferredcites →https://doi.org/10.3891/acta.chem.scand.30b-0369openalex-snapshot
Synthesis of [2.2](3,6)Phenanthrenophanediene.
inferredcites →https://doi.org/10.3891/acta.chem.scand.31b-0135openalex-snapshot
A New Synthesis of [2.2.2.2]Cyclophanetetraenes.
inferredcites →https://doi.org/10.3891/acta.chem.scand.37b-0589openalex-snapshot
Photocyclisations of Unsaturated [2(4)]Paracyclophanes.

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/10.1016/j.mser.2025.100974openalex-snapshot
Designing organic mixed ionic-electronic conductors with low environmental footprint for bioelectronics and energy storage
inferred← citeshttps://doi.org/10.1016/j.susmat.2024.e00835openalex-snapshot
Biomimetic nucleotide-graphene hybrids for electrocatalytic oxygen conversion: Quantifying biomolecule mass loading
inferred← citeshttps://doi.org/10.1039/d3fd00145hopenalex-snapshot
Reducing undesired solubility of squarephaneic tetraimide for use as an organic battery electrode material
inferred← citeshttps://doi.org/10.1039/d4sc06439aopenalex-snapshot
Reversible formation of tetraphenylpentalene, a room temperature stable antiaromatic hydrocarbon
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