On the public citation graph
Effects of Alkoxy Substitution on the Optical Properties of 9,10-Anthraquinone and Anthracene: 2,3,6,7-Tetrapropoxy-substituted vs. 2,6-Dipropoxy-substituted Derivatives
0 signed · 29 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1021/cg9008569openalex-snapshot
Anthracene-Arrangement-Dependent Emissions of Crystals of 9-Anthrylpyrazole Derivatives
inferredcites →https://doi.org/10.1021/jp807684mopenalex-snapshot
Fluorescence Quantum Yield of Aromatic Hydrocarbon Crystals
inferredcites →https://doi.org/10.1021/jz200099popenalex-snapshot
Role of Molecular Packing in Determining Solid-State Optical Properties of π-Conjugated Materials
inferredcites →https://doi.org/10.1039/b418241copenalex-snapshot
A tunable solid-state fluorescence system consisting of organic salts of anthracene-2,6-disulfonic acid with primary amines
inferredcites →https://doi.org/10.1080/15421400701617350openalex-snapshot
Influence of Alkyl Chain Length on the Solid-State Packing and Fluorescence of 1,4,5,8-Tetra(alkyl)anthracenes
inferredcites →https://doi.org/10.1246/cl.2006.1022openalex-snapshot
Preparation, Structure, and Properties of Tris(trimethylsilyl)silyl-substituted Anthracenes: Realization of Ideal Conformation for σ–π Conjugation Involving Eclipse of Si–Si σ-Bond with p-Orbital of Aromatic Ring
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.4772835openalex-extracted
The Influence of Phosphine Ligands on the Redox Properties of 1,4-Divinylanthrylene-Bridged Diruthenium Complexes and a Derived Macrocyclic Analog
inferred← citeshttps://doi.org/10.1002/ange.202414406openalex-snapshot
Synthesis and Structural Characterization of Carbazole‐Tailored Luminescent Triarylmethyl Radical and its Stable Cation
inferred← citeshttps://doi.org/10.1002/anie.202414406openalex-snapshot
Synthesis and Structural Characterization of Carbazole‐Tailored Luminescent Triarylmethyl Radical and its Stable Cation
inferred← citeshttps://doi.org/10.1002/chem.201902812openalex-snapshot
Preparation and Characterisation of a Bis‐μ‐Hydroxo‐Ni III 2 Complex
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110601openalex-snapshot
Synthesis, spectroscopic characterization, one and two-photon absorption properties of β-β linked BODIPY dimers
inferred← citeshttps://doi.org/10.1016/j.dyepig.2025.113329openalex-snapshot
Organic luminescent radicals with blue-green emission for organic light-emitting diodes
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123185openalex-snapshot
The influence of phosphine ligands on the redox properties of 1,4-divinylanthrylene-bridged diruthenium complexes and a derived macrocyclic analog
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2015.08.021openalex-snapshot
Photoinduced processes in macrocyclic isoalloxazine–anthracene systems
inferred← citeshttps://doi.org/10.1016/j.poly.2015.03.021openalex-snapshot
Synthesis, structural features and luminescence properties of a 1-D poly(azolato)-based coordination polymer
inferred← citeshttps://doi.org/10.1016/j.trechm.2026.07.004openalex-snapshot
Evaluating photochemically induced deformation of organic materials
inferred← citeshttps://doi.org/10.1021/acs.chemrev.1c00263openalex-snapshot
Direct Photocatalyzed Hydrogen Atom Transfer (HAT) for Aliphatic C–H Bonds Elaboration
inferred← citeshttps://doi.org/10.1021/acs.langmuir.0c02586openalex-snapshot
9,10-Anthraquinones Disubstituted with Linear Alkoxy Groups: Spectroscopy, Electrochemistry, and Peculiarities of Their 2D and 3D Supramolecular Organizations
inferred← citeshttps://doi.org/10.1021/acs.macromol.4c02691openalex-snapshot
Targeting 2D Nanostructures in Phase-Separated Materials through Molecular Design
inferred← citeshttps://doi.org/10.1039/d2cc06083copenalex-snapshot
Synthesis and structure elucidation of triarylmethyl radicals with anthryl substitution
inferred← citeshttps://doi.org/10.1107/s1600536812033119openalex-snapshot
2,3,6,7-Tetramethoxy-9,10-anthraquinone
inferred← citeshttps://doi.org/10.1107/s1600536812037361openalex-snapshot
2,6-Dimethoxy-9,10-anthraquinone
inferred← citeshttps://doi.org/10.1107/s2056989015011901openalex-snapshot
Crystal structure of 1,4-diethoxy-9,10-anthraquinone
inferred← citeshttps://doi.org/10.1107/s2056989017015973openalex-snapshot
Crystal structures of 1-hydroxy-4-propyloxy-9,10-anthraquinone and its acetyl derivative
inferred← citeshttps://doi.org/10.1107/s2414314616007537openalex-snapshot
4-(3-Bromopropyloxy)-1-hydroxy-9,10-anthraquinone
inferred← citeshttps://doi.org/10.1107/s2414314616009068openalex-snapshot
1,4-Dihydroxy-2,3-dinitro-9,10-anthraquinone
inferred← citeshttps://doi.org/10.1111/cote.12810openalex-snapshot
Chemical profiling and characterisation of anthraquinone‐based polyphenols as biocolourants from Cortinarius semisanguineus
inferred← citeshttps://doi.org/10.1246/bcsj.20140406openalex-snapshot
Solid-State Optical Properties and Crystal Structures of 1,4-Dipropoxy-9,10-anthraquinone Polymorphs
inferred← citeshttps://doi.org/10.2139/ssrn.5429733openalex-snapshot
Organic luminescent radicals with blue-green emission for organic light-emitting diodes
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.