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Near-Infrared Fluorescence from In-Plane-Aromatic Cycloparaphenylene Dications

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Outgoing claims: the papers this work cites, builds on, or argues with.

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The Remarkable Stable Emerald Green C60F15[CBr(CO2Et)2]3: The First [60]Fullerene That Is also the First [18]Trannulene
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Synthesis and Structure of the Highly Chlorinated [60]Fullerene C60Cl30 with a Drum‐Shaped Carbon Cage
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Selective Synthesis of [12]Cycloparaphenylene
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Synthesis of [8]Cycloparaphenylene from a Square‐Shaped Tetranuclear Platinum Complex
inferredcites →https://doi.org/10.1002/anie.201108167openalex-snapshot
Synthesis, Characterization, and Crystal Structure of [6]Cycloparaphenylene
inferredcites →https://doi.org/10.1002/anie.201306881openalex-snapshot
Isolation and Characterization of the Cycloparaphenylene Radical Cation and Dication
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A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP)
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Photophysical properties of benzoannelated metal-free phthalocyanines
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Magnetic Circular Dichroism of Porphyrins Containing M = Ca, Ni, and Zn. A Computational Study Based on Time-Dependent Density Functional Theory
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Magnetic Circular Dichroism of Phthalocyanine (M = Mg, Zn) and Tetraazaporphyrin (M = Mg, Zn, Ni) Metal Complexes. A Computational Study Based on Time-Dependent Density Functional Theory
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Observation of fluorescence emission from solutions of C60 and C70 fullerenes and measurement of their excited-state lifetimes
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An intermediate neglect of differential overlap technique for spectroscopy of transition-metal complexes. Ferrocene
inferredcites →https://doi.org/10.1021/ja044409qopenalex-snapshot
Intense Near-Infrared Optical Absorbing Emerald Green [60]Fullerenes
inferredcites →https://doi.org/10.1021/ja205606popenalex-snapshot
Selective Synthesis of Strained [7]Cycloparaphenylene: An Orange-Emitting Fluorophore
inferredcites →https://doi.org/10.1021/ja413214qopenalex-snapshot
Synthesis and Characterization of [5]Cycloparaphenylene
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/ja807126uopenalex-snapshot
Synthesis, Characterization, and Theory of [9]-, [12]-, and [18]Cycloparaphenylene: Carbon Nanohoop Structures
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/ja9810437openalex-snapshot
From Dodecahedrapentaene to the “[n]Trannulenes”. A New In-Plane Aromatic Family
inferredcites →https://doi.org/10.1021/jacs.5b10855openalex-snapshot
Synthesis and Characterization of [n]CPP (n = 5, 6, 8, 10, and 12) Radical Cation and Dications: Size-Dependent Absorption, Spin, and Charge Delocalization
inferredcites →https://doi.org/10.1021/jo00373a006openalex-snapshot
In-plane aromaticity and trishomoaromaticity: a computational evaluation
inferredcites →https://doi.org/10.1021/jo3011667openalex-snapshot
Selective Syntheses of [7]–[12]Cycloparaphenylenes Using Orthogonal Suzuki–Miyaura Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/jp060522mopenalex-snapshot
Electronic Structure and Spectroscopic Studies of D3d-C60Cl30, a Chlorofullerene with a [18]Trannulene Ring, and Its Relation to Other [18]Trannulenes
inferredcites →https://doi.org/10.1021/jz200978fopenalex-snapshot
Unique Ultralow 18π-Trannulenyl HOMO–LUMO Energy Gap of Photostable Emerald-Green D3d-2-Methylmalonato[60]fullerenes
inferredcites →https://doi.org/10.1021/nl072014+openalex-snapshot
Fluorescence Efficiency of Individual Carbon Nanotubes
inferredcites →https://doi.org/10.1021/nl503133eopenalex-snapshot
Self-Trapping of Excitons, Violation of Condon Approximation, and Efficient Fluorescence in Conjugated Cycloparaphenylenes
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Electronic Response Properties of Carbon Nanotubes in Magnetic Fields
inferredcites →https://doi.org/10.1038/nchem.1888openalex-snapshot
Efficient room-temperature synthesis of a highly strained carbon nanohoop fragment of buckminsterfullerene
inferredcites →https://doi.org/10.1039/c2cp42712eopenalex-snapshot
Size-dependent fluorescence properties of [n]cycloparaphenylenes (n = 8–13), hoop-shaped π-conjugated molecules
inferredcites →https://doi.org/10.1039/c4sc01996bopenalex-snapshot
Exploring the ring current of carbon nanotubes by first-principles calculations
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Application of magnetically perturbed time-dependent density functional theory to magnetic circular dichroism: Calculation of B terms
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Application of magnetically perturbed time-dependent density functional theory to magnetic circular dichroism. II. Calculation of A terms
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A new mixing of Hartree–Fock and local density-functional theories
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Density-functional thermochemistry. III. The role of exact exchange
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The energy gap law for radiationless transitions in large molecules
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.37.785openalex-snapshot
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
inferredcites →https://doi.org/10.1246/cl.130188openalex-snapshot
Selective Synthesis of [6]-, [8]-, and [10]Cycloparaphenylenes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Synthesis of theoretically interesting molecules
inferred← citeshttps://doi.org/10.1016/j.comptc.2024.114790openalex-snapshot
Theoretical predictions on In-Plane aromaticity in double hydrogen transfer reactions between ethane and ethylene
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00581openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.0c08926openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acsnano.1c05105openalex-snapshot
Single-Molecule Magnet with Thermally Activated Delayed Fluorescence Based on a Metallofullerene Integrated by Dysprosium and Yttrium Ions
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A dodecamethoxy[6]cycloparaphenylene consisting entirely of hydroquinone ethers: unveiling in-plane aromaticity through a rotaxane structure
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Visible and near-infrared photoluminescence of a supramolecular complex constructed from a cycloparaphenylene nanoring and an erbium metallofullerene
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Electronic delocalization in charged macrocycles is associated with global aromaticity
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Charge delocalization and aromaticity of doubly reduced double-walled carbon nanohoops
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Multistage organic redox systems. Aromaticity as a guiding principle for materials chemistry
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Stable cationic nanobelts synthesized by chemical oxidation of methylene-bridged [6]cycloparaphenylene
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Electron-injection-induced global aromaticity enables stable open-shell nanopillars with intense mid-infrared magnetic circular dichroism
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Revealing the vibronic coupling effects in the size-dependent optical properties of cycloparaphenylene dications
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