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Flexible C−C Bonds: Reversible Expansion, Contraction, Formation, and Scission of Extremely Elongated Single Bonds
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Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
The 48 checked references that resolve
resolves10.1002/anie.201807004
Bowls, Hoops, and Saddles: Synthetic Approaches to Curved Aromatic Molecules
resolves10.1002/ange.201807004
Schalen, Reifen und Sattel: Methoden zur Synthese gebogener aromatischer Moleküle
resolves10.1039/C7QM00593H
Figuration of bowl-shaped π-conjugated molecules: properties and functions
resolves10.1021/jacs.7b07113
Synthesis, Structures, and Properties of Hexapole Helicenes: Assembling Six [5]Helicene Substructures into Highly Twisted Aromatic Systems
resolves10.1021/jacs.8b09825
Synthesis of a Helical Analogue of Kekulene: A Flexible π-Expanded Helicene with Large Helical Diameter Acting as a Soft Molecular Spring
resolves10.1021/jacs.9b05610
π-Extended Pyrene-Fused Double [7]Carbohelicene as a Chiral Polycyclic Aromatic Hydrocarbon
resolves10.1126/science.aav5021
Topological molecular nanocarbons: All-benzene catenane and trefoil knot
resolves10.1038/s41557-019-0399-2
3D global aromaticity in a fully conjugated diradicaloid cage at different oxidation states
resolves10.1002/anie.201915509
Synthesis of a Hemispherical Geodesic Phenine Framework by a Polygon Assembling Strategy
resolves10.1002/ange.201915509
Synthesis of a Hemispherical Geodesic Phenine Framework by a Polygon Assembling Strategy
resolves10.1021/jacs.0c01117
Exploration of the Solid-State Sorption Properties of Shape-Persistent Macrocyclic Nanocarbons as Bulk Materials and Small Aggregates
resolves10.1038/nature10367
Overcoming lability of extremely long alkane carbon–carbon bonds through dispersion forces
resolves10.1002/anie.199717571
[2+2] Cycloaddition Products of Tetradehydrodianthracene: Experimental and Theoretical Proof of Extraordinary Long CC Single Bonds
resolves10.1002/ange.19971091625
[2+2]‐Cycloaddukte von Tetradehydrodianthracen: experimenteller und theoretischer Nachweis außergewöhnlich langer C‐C‐Einfachbindungen
resolves10.1016/S0040-4020(01)00249-6
Preparation and structural study of naphtho- and anthrocyclobutene derivatives which have extremely long C–C bonds
resolves10.1016/j.chempr.2018.01.011
Longest C–C Single Bond among Neutral Hydrocarbons with a Bond Length beyond 1.8 Å
resolves10.1002/anie.201812555
Exceptionally Long C−C Single Bonds in Diamino‐<i>o</i>‐carborane as Induced by Negative Hyperconjugation
resolves10.1002/ange.201812555
Exceptionally Long C−C Single Bonds in Diamino‐<i>o</i>‐carborane as Induced by Negative Hyperconjugation
resolves10.1021/jacs.9b09646
Photo- and Thermal Interconversion of Multiconfigurational Strained Hydrocarbons Exhibiting Completely Switchable Oxidation to Stable Dicationic Dyes
resolves10.1021/cr500249p
Photochromism of Diarylethene Molecules and Crystals: Memories, Switches, and Actuators
resolves10.1021/jacs.8b09523
Shining New Light on the Spiropyran Photoswitch: A Photocage Decides between <i>cis</i>–<i>trans</i> or Spiro-Merocyanine Isomerization
resolves10.1039/C9CC08545A
Reversible tricolour luminescence switching based on a piezochromic iridium(
<scp>iii</scp>
) complex
resolves10.1021/jacs.9b06104
Nitrogen Bridged Diazocines: Photochromes Switching within the Near-Infrared Region with High Quantum Yields in Organic Solvents and in Water
resolves10.1039/C9CC09081A
Reversible single-crystal-to-single-crystal conversion of a photoreactive coordination network for rewritable optical memory storage
resolves10.1002/anie.199316141
Crystallographic Study of a Single Crystal to Single Crystal Photodimerization and Its Thermal Reverse Reaction
resolves10.1002/ange.19931051115
Kristallographische Untersuchung einer Einkristall‐zu‐Einkristall‐Photodimerisierung und ihrer thermischen Rückreaktion
resolves10.1002/anie.201306746
Reversible Single‐Crystal‐to‐Single‐Crystal Photochemical Formation and Thermal Cleavage of a Cyclobutane Ring
resolves10.1002/ange.201306746
Reversible Single‐Crystal‐to‐Single‐Crystal Photochemical Formation and Thermal Cleavage of a Cyclobutane Ring
resolves10.1039/C8CC02743A
Covalent switching, involving divinylbenzene ligands within 3D coordination polymers, indicated by changes in fluorescence
resolves10.1039/C9CC04765D
A reversible photochemical solid-state transformation in an interpenetrated 3D metal–organic framework with mechanical softness
resolves10.1021/jacs.9b05961
A Multistimulus Responsive Porous Coordination Polymer: Temperature-Mediated Control of Solid-State [2+2] Cycloaddition
resolves10.1039/C9CC05227E
Light-controlled efficient photoluminescence based on an europium β-diketonate complex with single-crystal-to-single-crystal [2+2] cycloaddition
resolves10.3390/molecules22111900
9,10-Dihydrophenanthrene with Two Spiro(dibenzocycloheptatriene) Units: A Highly Strained Caged Hydrocarbon Exhibiting Reversible Electrochromic Behavior
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