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Diels−Alder Reactivity of Polycyclic Aromatic Hydrocarbon Bay Regions: Implications for Metal-Free Growth of Single-Chirality Carbon Nanotubes

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What this work says

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

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1,1,8,8‐Tetramethyl[8](2,11)teropyrenophane: Half of an Aromatic Belt and a Segment of an (8,8) Single‐Walled Carbon Nanotube
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New Strategies for Synthesizing Short Sections of Carbon Nanotubes
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Selective Synthesis of [12]Cycloparaphenylene
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Liquid‐Crystalline and Electron‐Deficient Coronene Oligocarboxylic Esters and Imides By Twofold Benzogenic Diels–Alder Reactions on Perylenes
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The kinetics of the Diels–Alder addition of cyclopentadiene to acetylene and the decomposition of norbornadiene
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Mit rationaler Synthese zu Kohlenstoff‐Nanotubes
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Circumacenes versus periacenes: HOMO–LUMO gap and transition from nonmagnetic to magnetic ground state with size
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Steps toward the synthesis of a geodesic C60H12 end cap for a C3v carbon [6,6]nanotube
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Kekulé structures and resonance energies of benzenoid hydrocarbons
inferredcites →https://doi.org/10.1021/ja00782a026openalex-snapshot
Stereochemistry of the noncatalytic addition of molecular deuterium to cyclopentadiene
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/ja809142xopenalex-snapshot
Transition State Distortion Energies Correlate with Activation Energies of 1,4-Dihydrogenations and Diels−Alder Cycloadditions of Aromatic Molecules
inferredcites →https://doi.org/10.1021/ja9031852openalex-snapshot
Aromatic π-Systems More Curved Than C 60 . The Complete Family of All Indenocorannulenes Synthesized by Iterative Microwave-Assisted Intramolecular Arylations
inferredcites →https://doi.org/10.1021/jo00829a095openalex-snapshot
Photochemical preparation of 4,11-diphenylbisanthene
inferredcites →https://doi.org/10.1039/j19690001734openalex-snapshot
Thermal decomposition of cyclohexa-1,4-dienes. Part IV. cis-3,6-Dimethyl-, trans-3,6-dimethyl- and 3,3,6,6-tetramethyl-cyclohexa-1,4-diene
inferredcites →https://doi.org/10.1039/jr9570004616openalex-snapshot
927. Syntheses of coronene and 1 : 2-7 : 8-dibenzocoronene
inferredcites →https://doi.org/10.1080/00268970902784918openalex-snapshot
On the aromatic stabilization energy of the 4N π electron pyrene

What points at this work

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

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One‐Step Conversion of Aromatic Hydrocarbon Bay Regions into Unsubstituted Benzene Rings: A Reagent for the Low‐Temperature, Metal‐Free Growth of Single‐Chirality Carbon Nanotubes
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Heteroatom Cycloaddition at the (BN) 2 Bay Region of Dibenzoperylene
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Towards the Highly Efficient Synthesis and Selective Methylation of C(sp3)‐Bridged [6]Cycloparaphenylenes from Fluoren[3]arenes
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Annulative π‐Extension by Rhodium(III)‐Catalyzed Ketone‐Directed C−H Activation: Rapid Access to Pyrenes and Related Polycyclic Aromatic Hydrocarbons (PAHs)
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inferred← citeshttps://doi.org/10.1021/acs.jpcc.7b06210openalex-snapshot
Can HCCH/HBNH Break B═N/C═C Bonds of Single-Wall BN/Carbon Nanotubes at Their Surface?
inferred← citeshttps://doi.org/10.1021/acs.jpclett.0c01349openalex-snapshot
On-Surface Synthesis of All-cis Standing Phenanthrene Polymers upon Selective C–H Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.jpclett.5b00880openalex-snapshot
Toward Controlled Growth of Helicity-Specific Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02746openalex-snapshot
Bay-Region Annulative π-Extension of o-Iodobiphenyls with Aliphatic Anhydrides Catalyzed by Pd(OAc)2
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03443openalex-snapshot
Annulative π-Extension by Cp*Co(III)-Catalyzed Ketone-Directed peri-Annulation: An Approach to Access Fused Arenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02487openalex-snapshot
Lewis Acid Assisted Diels–Alder Reaction with Regio- and Stereoselectivity: Anti-1,4-Adducts with Rigid Scaffolds and Their Application in Explosives Sensing
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00904openalex-snapshot
Syntheses and Structures of Functionalized [9]Cycloparaphenylenes as Carbon Nanohoops Bearing Carbomethoxy and N-Phenylphthalimido Groups
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01071openalex-snapshot
Light-Driven EDA–APEX Approach: A One-Pot Access to Phenanthrenes and Naphthalenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02055openalex-snapshot
From Planar Macrocycle to Cylindrical Molecule: Synthesis and Properties of a Phenanthrene-Based Coronal Nanohoop as a Segment of [6,6]Carbon Nanotube
inferred← citeshttps://doi.org/10.1021/acsapm.2c01763openalex-snapshot
Preparation and Characterization of Polyethylene Copolymers with PAH Side Groups as Carbon Fiber Precursors
inferred← citeshttps://doi.org/10.1021/ar200302gopenalex-snapshot
Chemistry at the Dirac Point: Diels–Alder Reactivity of Graphene
inferred← citeshttps://doi.org/10.1021/ar300055xopenalex-snapshot
Synthesis of Cycloparaphenylenes and Related Carbon Nanorings: A Step toward the Controlled Synthesis of Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/ar5004253openalex-snapshot
Syntheses of the Smallest Carbon Nanohoops and the Emergence of Unique Physical Phenomena
inferred← citeshttps://doi.org/10.1021/ja209461gopenalex-snapshot
A Short, Rigid, Structurally Pure Carbon Nanotube by Stepwise Chemical Synthesis
inferred← citeshttps://doi.org/10.1021/ja3023626openalex-snapshot
Polyaromatic Ribbons from Oligo-Alkynes via Selective Radical Cascade: Stitching Aromatic Rings with Polyacetylene Bridges
inferred← citeshttps://doi.org/10.1021/ja3054354openalex-snapshot
Curved Polycyclic Aromatic Molecules That Are π-Isoelectronic to Hexabenzocoronene
inferred← citeshttps://doi.org/10.1021/ja305769vopenalex-snapshot
Single-walled Carbon Nanotube Growth from Chiral Carbon Nanorings: Prediction of Chirality and Diameter Influence on Growth Rates
inferred← citeshttps://doi.org/10.1021/ja307373ropenalex-snapshot
Synthesis, Characterization, and Computational Studies of Cycloparaphenylene Dimers
inferred← citeshttps://doi.org/10.1021/ja509880vopenalex-snapshot
All-Benzene Carbon Nanocages: Size-Selective Synthesis, Photophysical Properties, and Crystal Structure
inferred← citeshttps://doi.org/10.1021/jacs.1c04037openalex-snapshot
Scalable, Divergent Synthesis of a High Aspect Ratio Carbon Nanobelt
inferred← citeshttps://doi.org/10.1021/jacs.4c16328openalex-snapshot
Molten Metal Synthesis of Nanographenes
inferred← citeshttps://doi.org/10.1021/jacs.5b02952openalex-snapshot
Quantum Chemical Simulation of Carbon Nanotube Nucleation on Al2O3 Catalysts via CH4 Chemical Vapor Deposition
inferred← citeshttps://doi.org/10.1021/jacs.6b04092openalex-snapshot
Synthesis of Stable Nanographenes with OBO-Doped Zigzag Edges Based on Tandem Demethylation-Electrophilic Borylation
inferred← citeshttps://doi.org/10.1021/jacs.7b02258openalex-snapshot
Heteroatom-Doped Perihexacene from a Double Helicene Precursor: On-Surface Synthesis and Properties
inferred← citeshttps://doi.org/10.1021/jacs.8b03711openalex-snapshot
Toward Full Zigzag-Edged Nanographenes: peri-Tetracene and Its Corresponding Circumanthracene
inferred← citeshttps://doi.org/10.1021/jacs.8b09232openalex-snapshot
Polycyclic Arene Synthesis by Annulative π-Extension
inferred← citeshttps://doi.org/10.1021/jacs.9b00384openalex-snapshot
Regioselective Hydrogenation of a 60-Carbon Nanographene Molecule toward a Circumbiphenyl Core
inferred← citeshttps://doi.org/10.1021/jacs.9b01267openalex-snapshot
Benzo-Fused Periacenes or Double Helicenes? Different Cyclodehydrogenation Pathways on Surface and in Solution
inferred← citeshttps://doi.org/10.1021/jacs.9b10358openalex-snapshot
A Long π-Conjugated Poly( para -Phenylene)-Based Polymeric Segment of Single-Walled Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/jacs.9b10957openalex-snapshot
Synthesis of Circumpyrene by Alkyne Benzannulation of Brominated Dibenzo[ hi , st ]ovalene
inferred← citeshttps://doi.org/10.1021/jo100132vopenalex-snapshot
Synthesis of a Basket-Shaped C56H38 Hydrocarbon as a Precursor toward an End-Cap Template for Carbon [6,6]Nanotubes
inferred← citeshttps://doi.org/10.1021/jo301024gopenalex-snapshot
Synthesis of Tetraphenyl-Substituted [12]Cycloparaphenylene: Toward a Rationally Designed Ultrashort Carbon Nanotube
inferred← citeshttps://doi.org/10.1021/jo3011667openalex-snapshot
Selective Syntheses of [7]–[12]Cycloparaphenylenes Using Orthogonal Suzuki–Miyaura Cross-Coupling Reactions
inferred← citeshttps://doi.org/10.1021/jp107964ropenalex-snapshot
Intense and Tunable Electrochemiluminescence of Corannulene
inferred← citeshttps://doi.org/10.1021/nl1010178openalex-snapshot
Cap Formation Engineering: From Opened C60 to Single-Walled Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/nl402259kopenalex-snapshot
Chirality-Dependent Vapor-Phase Epitaxial Growth and Termination of Single-Wall Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/nl504066fopenalex-snapshot
Nearly Exclusive Growth of Small Diameter Semiconducting Single-Wall Carbon Nanotubes from Organic Chemistry Synthetic End-Cap Molecules
inferred← citeshttps://doi.org/10.1021/ol1006168openalex-snapshot
Theoretical Studies on the Structures and Strain Energies of Cycloparaphenylenes
inferred← citeshttps://doi.org/10.1021/ol200730mopenalex-snapshot
Synthesis and Racemization Process of Chiral Carbon Nanorings: A Step toward the Chemical Synthesis of Chiral Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/ol202987eopenalex-snapshot
Reactivity of Long Conjugated Systems: Selectivity of Diels–Alder Cycloaddition in Oligofurans
inferred← citeshttps://doi.org/10.1021/ol3005112openalex-snapshot
Synthesis and Properties of Cycloparaphenylene-2,5-pyridylidene: A Nitrogen-Containing Carbon Nanoring
inferred← citeshttps://doi.org/10.1038/natrevmats.2015.2openalex-snapshot
Structurally uniform and atomically precise carbon nanostructures
inferred← citeshttps://doi.org/10.1038/nchem.464openalex-snapshot
Diels–Alder delivers
inferred← citeshttps://doi.org/10.1038/ncomms11160openalex-snapshot
Growth of semiconducting single-wall carbon nanotubes with a narrow band-gap distribution
inferred← citeshttps://doi.org/10.1038/ncomms1896openalex-snapshot
Enantioselective synthesis of a chiral nitrogen-doped buckybowl
inferred← citeshttps://doi.org/10.1038/ncomms2205openalex-snapshot
Chirality-controlled synthesis of single-wall carbon nanotubes using vapour-phase epitaxy
inferred← citeshttps://doi.org/10.1038/ncomms7251openalex-snapshot
One-shot K-region-selective annulative π-extension for nanographene synthesis and functionalization
inferred← citeshttps://doi.org/10.1038/nnano.2010.9openalex-snapshot
Growth potential
inferred← citeshttps://doi.org/10.1038/pj.2013.55openalex-snapshot
The efficient synthesis of N-fused coronene analogs and a related polyimide with near-infrared absorption
inferred← citeshttps://doi.org/10.1038/s41467-023-39086-0openalex-snapshot
Trichalcogenasupersumanenes and its concave-convex supramolecular assembly with fullerenes
inferred← citeshttps://doi.org/10.1038/s41557-021-00671-9openalex-snapshot
Aromatic hydrocarbon belts
inferred← citeshttps://doi.org/10.1038/s42004-026-01946-3openalex-snapshot
Diels-Alder reaction affords circumpyrene tetracarboxydiimide with excited state intramolecular charge transfer character
inferred← citeshttps://doi.org/10.1039/b904087kopenalex-snapshot
Synthetic approaches to aromatic belts: building up strain in macrocyclic polyarenes
inferred← citeshttps://doi.org/10.1039/c0jm02517hopenalex-snapshot
Carbon nanotubes from short hydrocarbon templates. Energy analysis of the Diels–Alder cycloaddition/rearomatization growth strategy
inferred← citeshttps://doi.org/10.1039/c0nr00306aopenalex-snapshot
Chemical approaches towards single-species single-walled carbon nanotubes
inferred← citeshttps://doi.org/10.1039/c1nr11112dopenalex-snapshot
Towards nano-organic chemistry: perspectives for a bottom-up approach to the synthesis of low-dimensional carbon nanostructures
inferred← citeshttps://doi.org/10.1039/c1sc00739dopenalex-snapshot
Disc-like 7, 14-dicyano-ovalene-3,4:10,11-bis(dicarboximide) as a solution-processible n-type semiconductor for air stable field-effect transistors
inferred← citeshttps://doi.org/10.1039/c2cc33885hopenalex-snapshot
Diels–Alder cycloaddition of acetylene gas to a polycyclic aromatic hydrocarbon bay region
inferred← citeshttps://doi.org/10.1039/c2ob25208bopenalex-snapshot
Facile air-oxidation of large aromatic hydrocarbon bay regions to bay region quinones: predicted oxygen-sensitivity of hydrogen-terminated carbon nanotubes
inferred← citeshttps://doi.org/10.1039/c2sc20719bopenalex-snapshot
Gram-scale synthesis and crystal structures of [8]- and [10]CPP, and the solid-state structure of C60@[10]CPP
inferred← citeshttps://doi.org/10.1039/c3cs60210aopenalex-snapshot
Preparation of carbon nanomaterials from molecular precursors
inferred← citeshttps://doi.org/10.1039/c3nr02595kopenalex-snapshot
Aligned carbon nanotubes: from controlled synthesis to electronic applications
inferred← citeshttps://doi.org/10.1039/c3py00232bopenalex-snapshot
Diels–Alder reactions for carbon material synthesis and surface functionalization
inferred← citeshttps://doi.org/10.1039/c3sc51447aopenalex-snapshot
One-shot indole-to-carbazole π-extension by a Pd–Cu–Ag trimetallic system
inferred← citeshttps://doi.org/10.1039/c3sc52077copenalex-snapshot
Conjugated macrocycles of phenanthrene: a new segment of [6,6]-carbon nanotube and solution-processed organic semiconductors
inferred← citeshttps://doi.org/10.1039/c4cs00366gopenalex-snapshot
Cycloparaphenylenes and related nanohoops
inferred← citeshttps://doi.org/10.1039/c4ob02383hopenalex-snapshot
Vertically-expanded imidazo[1,2-a]pyridines and imidazo[1,5-a]pyridine via dehydrogenative coupling
inferred← citeshttps://doi.org/10.1039/c5cp02195bopenalex-snapshot
Alternation of aromatic–nonaromatic rings in belt-like structures. The behavior of [6.8] 3 cyclacene in magnetic fields
inferred← citeshttps://doi.org/10.1039/c5cs00143aopenalex-snapshot
The dynamic, size-dependent properties of [5]–[12]cycloparaphenylenes
inferred← citeshttps://doi.org/10.1039/c5cs00183hopenalex-snapshot
New advances in nanographene chemistry
inferred← citeshttps://doi.org/10.1039/c5sc02547hopenalex-snapshot
π-extended [12]cycloparaphenylenes: from a hexaphenylbenzene cyclohexamer to its unexpected C 2 -symmetric congener
inferred← citeshttps://doi.org/10.1039/c5sc04218fopenalex-snapshot
Towards pi-extended cycloparaphenylenes as seeds for CNT growth: investigating strain relieving ring-openings and rearrangements
inferred← citeshttps://doi.org/10.1039/c6cc03002eopenalex-snapshot
A cycloparaphenylene nanoring with graphenic hexabenzocoronene sidewalls
inferred← citeshttps://doi.org/10.1039/c7qm00427copenalex-snapshot
Towards monochiral carbon nanotubes: a review of progress in the sorting of single-walled carbon nanotubes
inferred← citeshttps://doi.org/10.1039/c7qo00290dopenalex-snapshot
A mechanistic study on cationic Li prompted Diels–Alder cycloaddition of cycloparaphenylene
inferred← citeshttps://doi.org/10.1039/c8cy01295dopenalex-snapshot
Heterogeneous catalysis based on supramolecular association
inferred← citeshttps://doi.org/10.1039/c8qo00033fopenalex-snapshot
A novel symmetrically multifunctionalized dodecamethoxy-cycloparaphenylene: synthesis, photophysical, and supramolecular properties
inferred← citeshttps://doi.org/10.1039/c9cc04700jopenalex-snapshot
Precise synthesis and photophysical properties of a small chiral carbon nanotube segment: cyclo[7]paraphenylene-2,6-naphthylene
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