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Sr-Centered Monocyclic Carbon Ring Sr@C14: A Newly Stable Cluster

https://doi.org/10.2139/ssrn.4684339
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inferredcites →https://doi.org/10.1002/anie.201107379openalex-extracted
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inferredcites →https://doi.org/10.1002/anie.202105222openalex-extracted
Endocircular Li Carbon Rings
inferredcites →https://doi.org/10.1002/asia.202000528openalex-extracted
Achieving Adaptive Aromaticity in Cyclo[10]carbon by Screening Cyclo[n]carbon (n=8−24)
inferredcites →https://doi.org/10.1002/jcc.21135openalex-extracted
Chemical bonding in view of electron charge density and kinetic energy density descriptors
inferredcites →https://doi.org/10.1002/jcc.22885openalex-extracted
Multiwfn: A multifunctional wavefunction analyzer
inferredcites →https://doi.org/10.1002/wcms.1327openalex-extracted
Software update: the ORCA program system, version 4.0
inferredcites →https://doi.org/10.1016/0009-2614(83)80005-0openalex-extracted
Charge, bond order and valence in the AB initio SCF theory
inferredcites →https://doi.org/10.1016/0263-7855(96)00018-5openalex-extracted
VMD: Visual molecular dynamics
inferredcites →https://doi.org/10.1016/j.carbon.2015.09.092openalex-extracted
When is 6 less than 5? Penta- to hexa-graphene transition
inferredcites →https://doi.org/10.1016/j.carbon.2018.09.027openalex-extracted
Three-dimensional honeycomb carbon: Junction line distortion and novel emergent fermions
inferredcites →https://doi.org/10.1016/j.carbon.2020.04.099openalex-extracted
An sp-hybridized all-carboatomic ring, cyclo[18]carbon: Bonding character, electron delocalization, and aromaticity
inferredcites →https://doi.org/10.1016/j.carbon.2021.11.005openalex-extracted
Potential optical molecular switch: Lithium@cyclo[18]carbon complex transforming between two stable configurations
inferredcites →https://doi.org/10.1016/j.cplett.2021.139221openalex-extracted
Magnesium dimer entrapped in cyclo[18]carbon: Mg2@C18
inferredcites →https://doi.org/10.1016/s0166-1280(00)00477-2openalex-extracted
Chemical content of the kinetic energy density
inferredcites →https://doi.org/10.1021/acs.inorgchem.1c03341openalex-extracted
12-Membered Ring Carbides with Stabilization of Actinide Atoms
inferredcites →https://doi.org/10.1021/acs.jctc.7b00118openalex-extracted
A Robust and Accurate Tight-Binding Quantum Chemical Method for Structures, Vibrational Frequencies, and Noncovalent Interactions of Large Molecular Systems Parametrized for All spd-Block Elements ( Z = 1–86)
inferredcites →https://doi.org/10.1021/acs.jpca.0c09692openalex-extracted
Aromaticity of Even-Number Cyclo[ n ]carbons ( n = 6–100)
inferredcites →https://doi.org/10.1021/acs.jpclett.9b02815openalex-extracted
Cyclo[18]carbon: Insight into Electronic Structure, Aromaticity, and Surface Coupling
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Anisotropy of the Induced Current Density (ACID), a General Method To Quantify and Visualize Electronic Delocalization
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Lanthanum complexes of spheroidal carbon shells
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Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
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Extractions of Y@C 60 , Ba@C 60 , La@C 60 , Ce@C 60 , Pr@C 60 , Nd@C 60 , and Gd@C 60 with Aniline
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Comparison of the AIM Delocalization Index and the Mayer and Fuzzy Atom Bond Orders
inferredcites →https://doi.org/10.1038/318162a0openalex-extracted
C60: Buckminsterfullerene
inferredcites →https://doi.org/10.1038/354056a0openalex-extracted
Helical microtubules of graphitic carbon
inferredcites →https://doi.org/10.1038/nchem.828openalex-extracted
Synthesis of polyynes to model the sp-carbon allotrope carbyne
inferredcites →https://doi.org/10.1038/s41467-018-04681-zopenalex-extracted
On-surface synthesis of poly(p-phenylene ethynylene) molecular wires via in situ formation of carbon-carbon triple bond
inferredcites →https://doi.org/10.1038/s41557-018-0067-yopenalex-extracted
Polyyne formation via skeletal rearrangement induced by atomic manipulation
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On-surface synthesis of a doubly anti-aromatic carbon allotrope
inferredcites →https://doi.org/10.1038/s41586-023-06741-xopenalex-extracted
On-surface synthesis of aromatic cyclo[10]carbon and cyclo[14]carbon
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Gas-phase electronic spectrum of the C 14 ring
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C72: gaudiene, a hollow and aromatic all-carbon molecule
inferredcites →https://doi.org/10.1039/c9cc08399eopenalex-extracted
Cyclo[18]carbon: the smallest all-carbon electron acceptor
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Potential molecular semiconductor devices: cyclo-C n ( n = 10 and 14) with higher stabilities and aromaticities than acknowledged cyclo-C 18
inferredcites →https://doi.org/10.1039/d0cp01252aopenalex-extracted
Induced magnetic field in sp-hybridized carbon rings: analysis of double aromaticity and antiaromaticity in cyclo[2 N ]carbon allotropes
inferredcites →https://doi.org/10.1039/d0cp06256aopenalex-extracted
Antiaromaticity–aromaticity transition of cyclo[16]carbon upon metal encapsulation
inferredcites →https://doi.org/10.1039/d1ra05367aopenalex-extracted
Metal-centered monocyclic carbon wheel clusters with record coordination numbers in planar species
inferredcites →https://doi.org/10.1063/1.2408420openalex-extracted
Canonical sampling through velocity rescaling
inferredcites →https://doi.org/10.1063/1.2838200openalex-extracted
CCSD calculations on C14, C18, and C22 carbon clusters
inferredcites →https://doi.org/10.1126/science.1102896openalex-extracted
Electric Field Effect in Atomically Thin Carbon Films
inferredcites →https://doi.org/10.1126/science.aay1914openalex-extracted
An sp-hybridized molecular carbon allotrope, cyclo[18]carbon
inferredcites →https://doi.org/10.21203/rs.3.rs-3411934/v1openalex-extracted
On-surface synthesis and characterization of anti-aromatic cyclo[20]carbon
inferredcites →https://doi.org/10.21203/rs.3.rs-3411973/v1openalex-extracted
On-surface synthesis of anti-aromatic cyclo[12]carbon and aromatic cyclo[6]carbon
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On the Endocircular Li@C16 System
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