On the public citation graph

Fullerenes

https://doi.org/10.1039/9781849732956
0 signed · 52 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4349259openalex-extracted
inferred← citeshttps://doi.org/10.1002/9781118742952.ch34openalex-snapshot
Metal Catalysis in Fullerene Chemistry
inferred← citeshttps://doi.org/10.1002/9781118858981.ch10openalex-snapshot
Indenofluorenes and Related Structures
inferred← citeshttps://doi.org/10.1002/chem.201803596openalex-snapshot
Exfoliation of Graphene by Dendritic Water‐Soluble Zinc Phthalocyanine Amphiphiles in Polar Media
inferred← citeshttps://doi.org/10.1002/chem.202404418openalex-snapshot
Synthesis, Photophysical, and Chemiexcitation Properties of Luminol‐Fullerene Dyads: Toward Chemiexcitation Electron Transfer
inferred← citeshttps://doi.org/10.1002/cjoc.202300094openalex-snapshot
Stereoselective Synthesis of Nontethered trans‐4 Bis(aziridino)[60]fullerene Derivatives†
inferred← citeshttps://doi.org/10.1002/cphc.70467openalex-snapshot
Entropic Effects Distinguishing the Reactivity of Fullerenes in Diels–Alder Cycloadditions
inferred← citeshttps://doi.org/10.1002/ejoc.201701626openalex-snapshot
Understanding the Reactivity of Fullerenes Through the Activation Strain Model
inferred← citeshttps://doi.org/10.1002/ejoc.202100571openalex-snapshot
Regioselective Preparation of Fullerene Bis‐adducts from Cleavable Macrocyclic Bis‐malonates
inferred← citeshttps://doi.org/10.1002/ejoc.202100572openalex-snapshot
Regioselective Synthesis of Fullerene Tris‐adducts for the Preparation of Clickable Fullerene [3:3]‐Hexa‐adduct Scaffolds
inferred← citeshttps://doi.org/10.1002/pssb.201700170openalex-snapshot
Towards Rational Synthesis of Non‐IPR Fullerenes Via Tandem Cyclodehydrofluorination of Fluoroarene‐Based Precursors
inferred← citeshttps://doi.org/10.1002/qua.25645openalex-snapshot
Fulfilling the 2(N+1)2 Hirsch rule in smaller hollow fullerenes. Evaluation of long‐range magnetic behavior and NMR patterns of C28, , C24N4, and C28H4
inferred← citeshttps://doi.org/10.1002/tcr.201402081openalex-snapshot
The Impact of Copper‐Catalyzed Alkyne–Azide 1,3‐Dipolar Cycloaddition in Fullerene Chemistry
inferred← citeshttps://doi.org/10.1007/12_2017_7openalex-snapshot
Rational Synthesis of Fullerenes, Buckybowls, and Single-Walled Carbon Nanotubes by a Surface-Assisted Approach
inferred← citeshttps://doi.org/10.1007/978-3-642-36199-9_332-1openalex-snapshot
Exohedral Fullerenes
inferred← citeshttps://doi.org/10.1007/978-3-642-36199-9_338-1openalex-snapshot
New Synthetic Carbon Allotropes
inferred← citeshttps://doi.org/10.1007/s00419-025-02794-8openalex-snapshot
Static analysis of a hemispherical nanoshell under uniform pressure based on MCST: a comparison of FEM and GDQ solutions
inferred← citeshttps://doi.org/10.1007/s11224-017-1031-yopenalex-snapshot
Stabilization of boron clusters with classical fullerene structures by combined doping effect: a quantum chemical study
inferred← citeshttps://doi.org/10.1016/j.diamond.2023.110031openalex-snapshot
Decomposition of solid C60–indene adducts by retro Diels Alder reaction – A kinetic and thermodynamic study
inferred← citeshttps://doi.org/10.1021/acs.joc.1c03116openalex-snapshot
Successive Diels–Alder Cycloadditions of Cyclopentadiene to [10]CPP⊃C60: A Computational Study
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00340openalex-snapshot
Synthesis and Characterization of Two Unsymmetrical Indenofluorene Analogues: Benzo[5,6]-s-indaceno[1,2-b]thiophene and Benzo[5,6]-s-indaceno[2,1-b]thiophene
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02424openalex-snapshot
Predicting and Understanding the Reactivity of Aza[60]fullerenes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00218openalex-snapshot
Rationalizing the Regioselectivity of the Diels–Alder Biscycloaddition of Fullerenes
inferred← citeshttps://doi.org/10.1021/acs.jpca.0c04732openalex-snapshot
Fullerene Thermochemical Stability: Accurate Heats of Formation for Small Fullerenes, the Importance of Structural Deformation on Reactivity, and the Special Stability of C 60
inferred← citeshttps://doi.org/10.1021/acs.jpca.4c08287openalex-snapshot
Diels–Alder Cycloaddition of Cyclopentadiene to C60 and Si60 and Their Endohedral Li+ Counterparts
inferred← citeshttps://doi.org/10.1021/acs.jpcc.8b02419openalex-snapshot
Induced Magnetic Field of Fullerenes: Role of σ- and π- Contributions to Spherical Aromatic, Nonaromatic, and Antiaromatic Character in C60q (q = +10, 0, −6, −12), and Related Alkali-Metal Decorated Building Blocks, Li12C60 and Na6C60
inferred← citeshttps://doi.org/10.1021/acs.jpclett.8b00968openalex-snapshot
Physicochemical Phenomena and Application in Solar Cells of Perovskite:Fullerene Films
inferred← citeshttps://doi.org/10.1021/cr300143vopenalex-snapshot
Functionalizing Nanoparticles with Biological Molecules: Developing Chemistries that Facilitate Nanotechnology
inferred← citeshttps://doi.org/10.1021/ja306105bopenalex-snapshot
Switching the Stereoselectivity: (Fullero)Pyrrolidines “a la Carte”
inferred← citeshttps://doi.org/10.1021/jacs.4c12819openalex-snapshot
Twenty Years of Graphene: From Pristine to Chemically Engineered Nano-Sized Flakes
inferred← citeshttps://doi.org/10.1021/jacs.7b08670openalex-snapshot
Mediating Reductive Charge Shift Reactions in Electron Transport Chains
inferred← citeshttps://doi.org/10.1021/jacs.9b02207openalex-snapshot
Pd(II) Coordination Sphere Engineering: Pyridine Cages, Quinoline Bowls, and Heteroleptic Pills Binding One or Two Fullerenes
inferred← citeshttps://doi.org/10.1021/ol400318zopenalex-snapshot
Indeno[2,1-c]fluorene: A New Electron-Accepting Scaffold for Organic Electronics
inferred← citeshttps://doi.org/10.1038/nchem.2422openalex-snapshot
Sweet fullerenes vanquish viruses
inferred← citeshttps://doi.org/10.1039/c8cp07626jopenalex-snapshot
Decomposition of the electronic activity in competing [5,6] and [6,6] cycloaddition reactions between C 60 and cyclopentadiene
inferred← citeshttps://doi.org/10.1039/c8mh01130copenalex-snapshot
Supramolecular fluorescent hydrogelators as bio-imaging probes
inferred← citeshttps://doi.org/10.1039/c8ra08334gopenalex-snapshot
A new family of fullerene derivatives: fullerene-curcumin conjugates for biological and photovoltaic applications
inferred← citeshttps://doi.org/10.1039/c9cp04223gopenalex-snapshot
Double aromaticity of the B 40 fullerene: induced magnetic field analysis of π and σ delocalization in the boron cavernous structure
inferred← citeshttps://doi.org/10.1039/c9cp06977aopenalex-snapshot
When is the Bell–Evans–Polanyi principle fulfilled in Diels–Alder reactions of fullerenes?
inferred← citeshttps://doi.org/10.1039/d0cp02475aopenalex-snapshot
On the formation of spherical aromatic endohedral buckminsterfullerene. Evaluation of M@C 60 (M = Cr, Mo, W) from relativistic DFT calculations
inferred← citeshttps://doi.org/10.1039/d1ra03944jopenalex-snapshot
Selective formation of dihydrofuran fused [60] fullerene derivatives by TEMPO mediated [3 + 2] cycloaddition of medium chain β-keto esters to C 60
inferred← citeshttps://doi.org/10.1039/d2sd00182aopenalex-snapshot
Diagnosis of cancer using carbon nanomaterial-based biosensors
inferred← citeshttps://doi.org/10.1039/d4cp03238aopenalex-snapshot
Deep learning-driven prediction of chemical addition patterns for carboncones and fullerenes
inferred← citeshttps://doi.org/10.1063/1.4704896openalex-snapshot
Nanosecond simulations of the dynamics of C60 excited by intense near-infrared laser pulses: Impulsive Raman excitation, rearrangement, and fragmentation
inferred← citeshttps://doi.org/10.1134/s1070363225606210openalex-snapshot
Role of Perylene Substructure in the Stability of Fullerenes
inferred← citeshttps://doi.org/10.1140/epjd/e2018-90121-0openalex-snapshot
Low-energy electron scattering from fullerenes and heavy complex atoms: negative ions formation
inferred← citeshttps://doi.org/10.1140/epjd/e2018-90229-1openalex-snapshot
The model of the fullerene C60 and its ions C60+, C60− pseudopotentials for molecular dynamics purposes
inferred← citeshttps://doi.org/10.2174/0113852728278635231127111522openalex-snapshot
Influence of Dispersion Interactions in the Diels-Alder Reaction of Cyclopentadiene, Anthracene and Tetracene with C60: A DFT Examination
inferred← citeshttps://doi.org/10.3390/molecules25112506openalex-snapshot
Non-Functionalized Fullerenes and Endofullerenes in Aqueous Dispersions as Superoxide Scavengers
inferred← citeshttps://doi.org/10.3390/molecules27196522openalex-snapshot
Fullerene-Perylenediimide (C60-PDI) Based Systems: An Overview and Synthesis of a Versatile Platform for Their Anchor Engineering
inferred← citeshttps://doi.org/10.3846/mma.2019.017openalex-snapshot
NUMERICAL SIMULATION OF CHARGED FULLERENE SPECTRUM
inferred← citeshttps://doi.org/10.5772/intechopen.73251openalex-snapshot
Rational Synthesis of Fullerenes
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.