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Synthesis and Characterization of [5]Cycloparaphenylene
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Tightening of the Nanobelt upon Multielectron Reduction
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Conjugated Belts and Nanorings with Radially Oriented p Orbitals
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New Strategies for Synthesizing Short Sections of Carbon Nanotubes
inferredcites →https://doi.org/10.1002/anie.200902617openalex-snapshot
Selective Synthesis of [12]Cycloparaphenylene
inferredcites →https://doi.org/10.1002/anie.200905659openalex-snapshot
Synthesis of [8]Cycloparaphenylene from a Square‐Shaped Tetranuclear Platinum Complex
inferredcites →https://doi.org/10.1002/anie.201005734openalex-snapshot
A Modular and Size‐Selective Synthesis of [n]Cycloparaphenylenes: A Step toward the Selective Synthesis of [n,n] Single‐Walled Carbon Nanotubes
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Conjugated Macrocycles: Concepts and Applications
inferredcites →https://doi.org/10.1002/anie.201007232openalex-snapshot
Concise Synthesis and Crystal Structure of [12]Cycloparaphenylene
inferredcites →https://doi.org/10.1002/anie.201102302openalex-snapshot
Size‐Selective Encapsulation of C60 by [10]Cycloparaphenylene: Formation of the Shortest Fullerene‐Peapod
inferredcites →https://doi.org/10.1002/anie.201108167openalex-snapshot
Synthesis, Characterization, and Crystal Structure of [6]Cycloparaphenylene
inferredcites →https://doi.org/10.1002/anie.201301226openalex-snapshot
Tightening of the Nanobelt upon Multielectron Reduction
inferredcites →https://doi.org/10.1002/anie.201306881openalex-snapshot
Isolation and Characterization of the Cycloparaphenylene Radical Cation and Dication
inferredcites →https://doi.org/10.1002/chem.201302694openalex-snapshot
Size‐ and Orientation‐Selective Encapsulation of C70 by Cycloparaphenylenes
inferredcites →https://doi.org/10.1002/cphc.201300144openalex-snapshot
Enhancement of the Quinoidal Character for Smaller [n]Cycloparaphenylenes Probed by Raman Spectroscopy
inferredcites →https://doi.org/10.1002/tcr.201300035openalex-snapshot
Organoplatinum‐Mediated Synthesis of Cyclic π‐Conjugated Molecules: Towards a New Era of Three‐Dimensional Aromatic Compounds
inferredcites →https://doi.org/10.1007/bfb0025270openalex-snapshot
Belt-, ball-, and tube-shaped molecules
inferredcites →https://doi.org/10.1016/0022-328x(92)83232-7openalex-snapshot
Mechanism of CC coupling reactions of aromatic halides, promoted by Ni(COD)2 in the presence of 2,2′-bipyridine and PPh3, to give biaryls
inferredcites →https://doi.org/10.1016/j.carbon.2013.09.082openalex-snapshot
Raman spectroscopy of carbon nanohoops
inferredcites →https://doi.org/10.1016/j.cplett.2010.04.067openalex-snapshot
Progress and challenges for the bottom-up synthesis of carbon nanotubes with discrete chirality
inferredcites →https://doi.org/10.1016/s0079-6565(00)00022-4openalex-snapshot
NMR studies of cyclophanes
inferredcites →https://doi.org/10.1021/ar300055xopenalex-snapshot
Synthesis of Cycloparaphenylenes and Related Carbon Nanorings: A Step toward the Controlled Synthesis of Carbon Nanotubes
inferredcites →https://doi.org/10.1021/cr0509657openalex-snapshot
Ball-, Bowl-, and Belt-Shaped Conjugated Systems and Their Complexing Abilities: Exploration of the Concave−Convex π−π Interaction
inferredcites →https://doi.org/10.1021/ja00074a066openalex-snapshot
Electrochemically-reversible, single-electron oxidation of C60 and C70
inferredcites →https://doi.org/10.1021/ja00180a036openalex-snapshot
Bent acenes. Synthesis and molecular structure of [6](1,4)naphthalenophane and [6](1,4)anthracenophane
inferredcites →https://doi.org/10.1021/ja00786a066openalex-snapshot
Electron nuclear double resonance of bacteriochlorophyll free radical in vitro and in vivo
inferredcites →https://doi.org/10.1021/ja2020668openalex-snapshot
Selective and Random Syntheses of [n]Cycloparaphenylenes (n = 8–13) and Size Dependence of Their Electronic Properties
inferredcites →https://doi.org/10.1021/ja205606popenalex-snapshot
Selective Synthesis of Strained [7]Cycloparaphenylene: An Orange-Emitting Fluorophore
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/jo3011667openalex-snapshot
Selective Syntheses of [7]–[12]Cycloparaphenylenes Using Orthogonal Suzuki–Miyaura Cross-Coupling Reactions
inferredcites →https://doi.org/10.1021/jo302186hopenalex-snapshot
Bending Benzene: Syntheses of [n]Cycloparaphenylenes
inferredcites →https://doi.org/10.1021/jp9074674openalex-snapshot
Optoelectronic Properties of Carbon Nanorings: Excitonic Effects from Time-Dependent Density Functional Theory
inferredcites →https://doi.org/10.1021/jz2012534openalex-snapshot
Anomalous Optoelectronic Properties of Chiral Carbon Nanorings…and One Ring to Rule Them All
inferredcites →https://doi.org/10.1021/jz3014826openalex-snapshot
Excited States in Cycloparaphenylenes: Dependence of Optical Properties on Ring Length
inferredcites →https://doi.org/10.1021/ol301242topenalex-snapshot
Selective Synthesis and Crystal Structure of [10]Cycloparaphenylene
inferredcites →https://doi.org/10.1021/om00023a078openalex-snapshot
Nickel-Complex-Promoted Carboxylation of Haloarenes Involving Insertion of CO2 into NiII-C Bonds
inferredcites →https://doi.org/10.1038/nchem.1655openalex-snapshot
Initiation of carbon nanotube growth by well-defined carbon nanorings
inferredcites →https://doi.org/10.1039/b904087kopenalex-snapshot
Synthetic approaches to aromatic belts: building up strain in macrocyclic polyarenes
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/c2ob25199jopenalex-snapshot
Combined experimental and theoretical studies on the photophysical properties of cycloparaphenylenes
inferredcites →https://doi.org/10.1039/c2sc20343jopenalex-snapshot
Size-selective synthesis of [9]–[11] and [13]cycloparaphenylenes
inferredcites →https://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
inferredcites →https://doi.org/10.1039/c3cc48683dopenalex-snapshot
Selective synthesis of [7]- and [8]cycloparaphenylenes
inferredcites →https://doi.org/10.1055/s-0031-1290360openalex-snapshot
Overcoming Molecular Strain: Synthesis of [7]Cycloparaphenylene
inferredcites →https://doi.org/10.1246/cl.130188openalex-snapshot
Selective Synthesis of [6]-, [8]-, and [10]Cycloparaphenylenes
inferredcites →https://doi.org/10.1246/cl.2011.423openalex-snapshot
[9]Cycloparaphenylene: Nickel-mediated Synthesis and Crystal Structure
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Die präzise Synthese von Phenylen‐erweiterten cyclischen Hexa‐peri‐hexabenzocoronenen ausgehend von polyarylierten [n]Cycloparaphenylenen mithilfe der Scholl‐Reaktion
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Versatile Design Principles for Facile Access to Unstrained Conjugated Organoborane Macrocycles
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Curved Oligophenylenes as Donors in Shape‐Persistent Donor–Acceptor Macrocycles with Solvatofluorochromic Properties
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Regioselective Synthesis and Characterization of Multinuclear Convex‐Bound Ruthenium‐[n]Cycloparaphenylene (n=5 and 6) Complexes
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Design und Synthese von Kohlenstoffnanoröhrensegmenten
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Flow‐Assisted Synthesis of [10]Cycloparaphenylene through Serial Microreactions under Mild Conditions
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Pentagon‐Embedded Cycloarylenes with Cylindrical Shapes
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Bromination of Cycloparaphenylenes: Strain‐Induced Site‐Selective Bis‐Addition and Its Application for Late‐Stage Functionalization
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Strain‐Induced Double Carbon–Carbon Bond Activations of Cycloparaphenylenes by a Platinum Complex: Application to the Synthesis of Cyclic Diketones
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A Macrocyclic Gold(I)–Biphenylene Complex: Triangular Molecular Structure with Twisted Au2(diphosphine) Corners and Reductive Elimination of [6]Cycloparaphenylene
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Ultrafast Exciton Self‐Trapping and Delocalization in Cycloparaphenylenes: The Role of Excited‐State Symmetry in Electron‐Vibrational Coupling
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Ultrafast Nuclear Rearrangement Governs Excited‐State Radial π‐Conjugation and Electron Transfer Dynamics in Organic Nanoring
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inferred← citeshttps://doi.org/10.1002/anie.201409389openalex-snapshot
Thiophene‐Based, Radial π‐Conjugation: Synthesis, Structure, and Photophysical Properties of Cyclo‐1,4‐phenylene‐2′,5′‐thienylenes
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Versatile Design Principles for Facile Access to Unstrained Conjugated Organoborane Macrocycles
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Curved Oligophenylenes as Donors in Shape‐Persistent Donor–Acceptor Macrocycles with Solvatofluorochromic Properties
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Flow‐Assisted Synthesis of [10]Cycloparaphenylene through Serial Microreactions under Mild Conditions
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Bromination of Cycloparaphenylenes: Strain‐Induced Site‐Selective Bis‐Addition and Its Application for Late‐Stage Functionalization
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[Sc©[3]CPP]+: A Viable Metal-Centered [3]Cycloparaphenylene
inferred← citeshttps://doi.org/10.1021/acs.jctc.7b00166openalex-snapshot
Indirect Intersystem Crossing (S1 → T3/T2 → T1) Promoted by the Jahn–Teller Effect in Cycloparaphenylenes
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02507openalex-snapshot
Electrostatic Potential for Exploring Electron Delocalization in Infinitenes, Circulenes, and Nanobelts
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00485openalex-snapshot
Preparation of a Cyclic Polyphenylene Array for a Zigzag-Type Carbon Nanotube Segment
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00339openalex-snapshot
“Planetary Orbit” Systems Composed of Cycloparaphenylenes
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00425openalex-snapshot
Tetracyclo(2,7-carbazole)s: Diatropicity and Paratropicity of Inner Regions of Nanohoops
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00085openalex-snapshot
Synthesis, Structures, and Assembly of Geodesic Phenine Frameworks with Isoreticular Networks of [n]Cyclo-para-phenylenes
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02742openalex-snapshot
Cycloparaphenylene Lemniscates and Trefoils
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02844openalex-snapshot
Selective and Gram-Scale Synthesis of [8]Cycloparaphenylene
inferred← citeshttps://doi.org/10.1021/acs.jpca.5b01189openalex-snapshot
Radical Ions of Cyclopyrenylene: Comparison of Spectral Properties with Cycloparaphenylene
inferred← citeshttps://doi.org/10.1021/acs.jpca.5b04404openalex-snapshot
Carbon Nanohoops: Excited Singlet and Triplet Behavior of Aza[8]CPP and 1,15-Diaza[8]CPP
inferred← citeshttps://doi.org/10.1021/acs.jpca.5c01409openalex-snapshot
Supramolecular Nanostructures of Boron–Nitrogen-Embedded Cycloparaphenylene Triradicals: Tuning Charge Transfer and Nonlinear Optical Properties
inferred← citeshttps://doi.org/10.1021/acs.jpca.8b03105openalex-snapshot
Near-Infrared Fluorescence from In-Plane-Aromatic Cycloparaphenylene Dications
inferred← citeshttps://doi.org/10.1021/acs.jpca.9b03334openalex-snapshot
Size-Dependent Relaxation Processes of Photoexcited [n]Cycloparaphenylenes (n = 5–12): Significant Contribution of Internal Conversion in Smaller Rings
inferred← citeshttps://doi.org/10.1021/acs.jpcc.0c03031openalex-snapshot
New Structure-Nonlinear Optical Property Correlation in “Russian Doll” Complexes Formed by Nested Pd(II) Nanorings
inferred← citeshttps://doi.org/10.1021/acs.jpcc.6b05781openalex-snapshot
Theoretical Determination of Interaction and Cohesive Energies of Weakly Bound Cycloparaphenylene Molecules
inferred← citeshttps://doi.org/10.1021/acs.jpclett.4c03432openalex-snapshot
The Unexploring Optoelectronic Features in Organic Trans-Dimensional Materials of Gridofluorenes at the Nanoscale
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01102openalex-snapshot
A Non-Cross-Coupling Approach to Arene-Bridged Macrocycles: Synthesis, Structure, and Direct, Regioselective Functionalization of a Cycloparaphenylene Fragment
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00430openalex-snapshot
Investigating the Reactivity of 1,4-Anthracene-Incorporated Cycloparaphenylene
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.6b01536openalex-snapshot
A Macrocyclic 1,4-Diketone Enables the Synthesis of a p-Phenylene Ring That Is More Strained than a Monomer Unit of [4]Cycloparaphenylene
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02702openalex-snapshot
Synthesis, Structure, and Reactivity of a Cylinder-Shaped Cyclo[12]orthophenylene[6]ethynylene: Toward the Synthesis of Zigzag Carbon Nanobelts
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01231openalex-snapshot
Synthesis of [8]Cycloparaphenylene-octacarboxylates via Rh-Catalyzed Stepwise Cross-Alkyne Cyclotrimerization
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03134openalex-snapshot
Synthesis, Optoelectronic, and Supramolecular Properties of a Calix[4]arene–Cycloparaphenylene Hybrid Host
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01563openalex-snapshot
Size-Selective Synthesis of Large Cycloparaphenyleneacetylene Carbon Nanohoops Using Alkyne Metathesis
inferred← citeshttps://doi.org/10.1021/acsomega.3c07294openalex-snapshot
Computation of Neighborhood M-Polynomial of Cycloparaphenylene and Its Variants
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/ct500524yopenalex-snapshot
Quantum Dynamics Simulations Reveal Vibronic Effects on the Optical Properties of [ n ]Cycloparaphenylenes
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/ja511320fopenalex-snapshot
In-Plane Aromaticity in Cycloparaphenylene Dications: A Magnetic Circular Dichroism and Theoretical Study
inferred← citeshttps://doi.org/10.1021/ja511951xopenalex-snapshot
Highly Strained Nonclassical Nanotube End-caps. A Single-Step Solution Synthesis from Strain-Free, Non-Macrocyclic Precursors
inferred← citeshttps://doi.org/10.1021/ja512271popenalex-snapshot
η6-Cycloparaphenylene Transition Metal Complexes: Synthesis, Structure, Photophysical Properties, and Application to the Selective Monofunctionalization of Cycloparaphenylenes
inferred← citeshttps://doi.org/10.1021/ja513102mopenalex-snapshot
Cyclic 2,12-Porphyrinylene Nanorings as a Porphyrin Analogue of Cycloparaphenylenes
inferred← citeshttps://doi.org/10.1021/jacs.1c01329openalex-snapshot
1,3-Diradicals Embedded in Curved Paraphenylene Units: Singlet versus Triplet State and In-Plane Aromaticity
inferred← citeshttps://doi.org/10.1021/jacs.4c01347openalex-snapshot
Tethered Helical Ladder-Type Aromatic Lactams
inferred← citeshttps://doi.org/10.1021/jacs.5b00291openalex-snapshot
Synthesis, Structures, and Photophysical Properties of π-Expanded Oligothiophene 8-mers and Their Saturn-Like C60 Complexes
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/jacs.5c11812openalex-snapshot
Strain-Induced Quinoidal Character in a Carbon Nanoring Embedding Anthracene Units
inferred← citeshttps://doi.org/10.1021/jacs.6b00538openalex-snapshot
Overcoming Strain-Induced Rearrangement Reactions: A Mild Dehydrative Aromatization Protocol for Synthesis of Highly Distorted p -Phenylenes
inferred← citeshttps://doi.org/10.1021/jacs.6b02240openalex-snapshot
Iterative Reductive Aromatization/Ring-Closing Metathesis Strategy toward the Synthesis of Strained Aromatic Belts
inferred← citeshttps://doi.org/10.1021/jacs.6b05474openalex-snapshot
Macrocyclization in the Design of Organic n-Type Electronic Materials
inferred← citeshttps://doi.org/10.1021/jacs.6b07673openalex-snapshot
Synthesis of Oligoparaphenylene-Derived Nanohoops Employing an Anthracene Photodimerization–Cycloreversion Strategy
inferred← citeshttps://doi.org/10.1021/jacs.6b12658openalex-snapshot
An Operationally Simple and Mild Oxidative Homocoupling of Aryl Boronic Esters To Access Conformationally Constrained Macrocycles
inferred← citeshttps://doi.org/10.1021/jacs.6c05318openalex-snapshot
Cyclo- para -azulenes: Segments of Metallic Nonalternant Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/jacs.7b00359openalex-snapshot
2,2′-Bipyridyl-Embedded Cycloparaphenylenes as a General Strategy To Investigate Nanohoop-Based Coordination Complexes
inferred← citeshttps://doi.org/10.1021/jacs.7b11526openalex-snapshot
Gram-Scale Syntheses and Conductivities of [10]Cycloparaphenylene and Its Tetraalkoxy Derivatives
inferred← citeshttps://doi.org/10.1021/jacs.8b06565openalex-snapshot
Influence of Molecular Conformation on Electron Transport in Giant, Conjugated Macrocycles
inferred← citeshttps://doi.org/10.1021/jacs.8b06842openalex-snapshot
Synthesis and Size-Dependent Properties of [12], [16], and [24]Carbon Nanobelts
inferred← citeshttps://doi.org/10.1021/jacs.8b10699openalex-snapshot
Solid-State Order and Charge Mobility in [5]- to [12]Cycloparaphenylenes
inferred← citeshttps://doi.org/10.1021/jacs.9b01797openalex-snapshot
Lemniscular [16]Cycloparaphenylene: A Radially Conjugated Figure-Eight Aromatic Molecule
inferred← citeshttps://doi.org/10.1021/jacs.9b08584openalex-snapshot
Highly Strained, Radially π-Conjugated Porphyrinylene Nanohoops
inferred← citeshttps://doi.org/10.1021/jp504689qopenalex-snapshot
Properties of Triplet-Excited [n]Cycloparaphenylenes (n = 8–12): Excitation Energies Lower than Those of Linear Oligomers and Polymers
inferred← citeshttps://doi.org/10.1021/jp5129657openalex-snapshot
Nature of Noncovalent Interactions in the [n]Cycloparaphenylene⊃C70 (n = 10, 11, and 12) Host–Guest Complexes: A Theoretical Insight into the Shortest C70–Carbon Nanotube Peapod
inferred← citeshttps://doi.org/10.1021/jz5009054openalex-snapshot
Radical Ions of Cycloparaphenylenes: Size Dependence Contrary to the Neutral Molecules
inferred← citeshttps://doi.org/10.1021/ol500194sopenalex-snapshot
Synthesis of Substituted [8]Cycloparaphenylenes by [2 + 2 + 2] Cycloaddition
inferred← citeshttps://doi.org/10.1021/ol500643copenalex-snapshot
Synthesis and Dimerization of Chloro[10]cycloparaphenylene: A Directly Connected Cycloparaphenylene Dimer
inferred← citeshttps://doi.org/10.1021/ol5007604openalex-snapshot
A Strain Induced Change of Mechanism from a [2 + 2 + 2] to a [2 + 1 + 2 + 1] Cycloaddition Reaction
inferred← citeshttps://doi.org/10.1021/ol500904xopenalex-snapshot
Functionalized Carbon Nanohoops: Synthesis and Structure of a [9]Cycloparaphenylene Bearing Three 5,8-Dimethoxynaphth-1,4-diyl Units
inferred← citeshttps://doi.org/10.1038/s41467-018-04246-0openalex-snapshot
Hollow organic capsules assemble into cellular semiconductors
inferred← citeshttps://doi.org/10.1038/s41467-025-59934-5openalex-snapshot
Cycloparaazine, a full-azine carbon nanoring
inferred← citeshttps://doi.org/10.1038/s41570-019-0140-0openalex-snapshot
Emerging applications of carbon nanohoops
inferred← citeshttps://doi.org/10.1038/s44160-025-00965-7openalex-snapshot
Customized cycloparaphenylene skeletons prepared via the intramolecular coupling of extended biphen[n]arenes
inferred← citeshttps://doi.org/10.1039/9781788019279-00174openalex-snapshot
Carbon Nanotube Synthesis and Applications
inferred← citeshttps://doi.org/10.1039/c4cs00366gopenalex-snapshot
Cycloparaphenylenes and related nanohoops
inferred← citeshttps://doi.org/10.1039/c4cs00531gopenalex-snapshot
Optical chirality sensing using macrocycles, synthetic and supramolecular oligomers/polymers, and nanoparticle based sensors
inferred← citeshttps://doi.org/10.1039/c4fd00103fopenalex-snapshot
Chameleon-like behaviour of cyclo[n]paraphenylenes in complexes with C 70 : on their impressive electronic and structural adaptability as probed by Raman spectroscopy
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/c5cp02882eopenalex-snapshot
Theoretical exploration of the nanoscale host–guest interactions between [n]cycloparaphenylenes (n = 10, 8 and 9) and fullerene C 60 : from single- to three-potential well
inferred← citeshttps://doi.org/10.1039/c5cs00143aopenalex-snapshot
The dynamic, size-dependent properties of [5]–[12]cycloparaphenylenes
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/c6cp03376hopenalex-snapshot
Cyclotetrahalo-p-phenylenes: simulations of halogen substituted cycloparaphenylenes and their interaction with C 60
inferred← citeshttps://doi.org/10.1039/c6ob01941bopenalex-snapshot
Chemoselective reduction of quinols as an alternative to Sonogashira coupling: synthesis of polysubstituted benzofurans
inferred← citeshttps://doi.org/10.1039/c6qo00828copenalex-snapshot
From tetrabenzoheptafulvalene to sp 2 carbon nano-rings
inferred← citeshttps://doi.org/10.1039/c6sc00011hopenalex-snapshot
High yielding synthesis of 2,2′-bipyridine macrocycles, versatile intermediates in the synthesis of rotaxanes
inferred← citeshttps://doi.org/10.1039/c6sc00092dopenalex-snapshot
Cycloparaphenylene as a molecular porous carbon solid with uniform pores exhibiting adsorption-induced softness
inferred← citeshttps://doi.org/10.1039/c6sc00765aopenalex-snapshot
The Raman fingerprint of cyclic conjugation: the case of the stabilization of cations and dications in cycloparaphenylenes
inferred← citeshttps://doi.org/10.1039/c6sc04048aopenalex-snapshot
Synthesis and properties of [8]-, [10]-, [12]-, and [16]cyclo-1,4-naphthylenes
inferred← citeshttps://doi.org/10.1039/c7cc07370dopenalex-snapshot
Facile three-step synthesis and photophysical properties of [8]-, [9]-, and [12]cyclo-1,4-naphthalene nanorings via platinum-mediated reductive elimination
inferred← citeshttps://doi.org/10.1039/c7cp08323hopenalex-snapshot
Local and global aromaticity in a molecular carbon nanobelt: insights from magnetic response properties in neutral and charged species
inferred← citeshttps://doi.org/10.1039/c7ra06409hopenalex-snapshot
Theoretical studies on the structure and thermochemistry of cyclicparaphenylenediazenes
inferred← citeshttps://doi.org/10.1039/c8cp04860fopenalex-snapshot
Significant structural relaxations of excited [ n ]cycloparaphenylene dications ( n = 5–9)
inferred← citeshttps://doi.org/10.1039/c9cp02625hopenalex-snapshot
Endohedral alkali cations promote charge transfer transitions in complexes of C 60 with [10]cycloparaphenylenes
inferred← citeshttps://doi.org/10.1039/c9ob00763fopenalex-snapshot
Preparation of a large-sized highly flexible carbon nanohoop
inferred← citeshttps://doi.org/10.1039/c9sc00169gopenalex-snapshot
Symmetry breaking and the turn-on fluorescence of small, highly strained carbon nanohoops
inferred← citeshttps://doi.org/10.1039/d0nj02637aopenalex-snapshot
The photophysical properties of cycloparaphenylene-based compounds with figure-eight configurations
inferred← citeshttps://doi.org/10.1039/d0sc03072dopenalex-snapshot
Structural deformation and host–guest properties of doubly-reduced cycloparaphenylenes, [ n ]CPPs 2− ( n = 6, 8, 10, and 12)
inferred← citeshttps://doi.org/10.1039/d0sc03923copenalex-snapshot
Effect of curvature and placement of donor and acceptor units in cycloparaphenylenes: a computational study
inferred← citeshttps://doi.org/10.1039/d1cc04400aopenalex-snapshot
Macrocyclic host molecules with aromatic building blocks: the state of the art and progress
inferred← citeshttps://doi.org/10.1039/d1sc00713kopenalex-snapshot
Stretching [8]cycloparaphenylene with encapsulated potassium cations: structural and theoretical insights into core perturbation upon four-fold reduction and complexation
inferred← citeshttps://doi.org/10.1039/d2cp03667copenalex-snapshot
Enabling dual aromaticity in fused nanobelts: evaluation of the magnetic behavior of fused [10]CPP units
inferred← citeshttps://doi.org/10.1039/d2cp05326hopenalex-snapshot
Switch from local to global aromatic character in Möbius carbon nanobelts upon dioxidation. Evaluation of magnetic behavior in neutral and charged species
inferred← citeshttps://doi.org/10.1039/d2nj01394kopenalex-snapshot
Exploring the photophysical properties of unusual π-conjugated porphyrin nanohoops
inferred← citeshttps://doi.org/10.1039/d3cp00299copenalex-snapshot
Planar π-extended all-armchair edge topological cycloparaphenylenes
inferred← citeshttps://doi.org/10.1039/d3cp00569kopenalex-snapshot
Local and global aromaticity under rotation: analysis of two- and three-dimensional representative carbon nanostructures
inferred← citeshttps://doi.org/10.1039/d3cp01994bopenalex-snapshot
Charge delocalization and aromaticity of doubly reduced double-walled carbon nanohoops
inferred← citeshttps://doi.org/10.1039/d4sc02028fopenalex-snapshot
Contracted porphyrins and calixpyrroles: synthetic challenges and ring-contraction effects
inferred← citeshttps://doi.org/10.1039/d4sc03408bopenalex-snapshot
Nanohoops in membranes: confined supramolecular spaces within phospholipid bilayer membranes
inferred← citeshttps://doi.org/10.1039/d5cc04263aopenalex-snapshot
Synthesis of a highly strained deep cavitand
inferred← citeshttps://doi.org/10.1039/d5qo00746aopenalex-snapshot
Multistage organic redox systems. Aromaticity as a guiding principle for materials chemistry
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