On the public citation graph
Chemiluminogenic Properties of 10-Methyl-9-(phenoxycarbonyl)acridinium Cations in Organic Environments
0 signed · 59 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/1522-7243(200007/08)15:4<239::aid-bio587>3.0.co;2-wopenalex-snapshot
Stable and versatile active acridinium esters I
inferredcites →https://doi.org/10.1002/1522-7243(200007/08)15:4<245::aid-bio588>3.0.co;2-3openalex-snapshot
Stable and versatile active acridinium esters II
inferredcites →https://doi.org/10.1002/9780470186596.ch10openalex-snapshot
Chemiluminescent Reactions of Acridines
inferredcites →https://doi.org/10.1007/978-1-4615-8660-9_5openalex-snapshot
The Influence of the Solvent on Organic Reactivity
inferredcites →https://doi.org/10.1007/978-1-4757-3061-6_6openalex-snapshot
Solvent Effects on Emission Spectra
inferredcites →https://doi.org/10.1007/s10973-009-0154-9openalex-snapshot
Thermochemistry and crystal lattice energetics of phenyl acridine-9-carboxylates and 9-phenoxycarbonyl-10-methylacridinium trifluoromethanesulphonates
inferredcites →https://doi.org/10.1007/s10973-010-0789-6openalex-snapshot
Lattice energetics and thermochemistry of phenyl acridine-9-carboxylates and 9-phenoxycarbonyl-10-methylacridinium trifluoromethanesulphonates
inferredcites →https://doi.org/10.1016/0022-1759(96)00047-6openalex-snapshot
Enhanced sensitivity of a two-site acridinium ester based immunochemiluminometric assay for rat growth hormone-releasing hormone using simple modifications in assay procedure
inferredcites →https://doi.org/10.1016/0040-4039(96)01980-6openalex-snapshot
Synthesis and properties of new luminescent 10-carboxymethylacridinium derivatives
inferredcites →https://doi.org/10.1016/1010-6030(91)80025-dopenalex-snapshot
Synthesis and chemiluminescent evaluation of a series of phenyl N-alkylacridinium 9-carboxylates
inferredcites →https://doi.org/10.1016/1010-6030(95)04203-2openalex-snapshot
Spectral properties and dynamics of the excited state structural relaxation of the ortho analogues of POPOP — Effective abnormally large Stokes shift luminophores
inferredcites →https://doi.org/10.1016/b978-0-12-524140-3.x5001-1openalex-snapshot
Time-Correlated Single Photon Counting
inferredcites →https://doi.org/10.1016/j.aca.2003.11.032openalex-snapshot
Addition of nucleophiles to the 9-cyano-10-methylacridinium cation: utilization in their chemiluminescent assay
inferredcites →https://doi.org/10.1016/j.envint.2004.10.003openalex-snapshot
Measuring the antioxidant activity of olive oil mill wastewater using chemiluminescence
inferredcites →https://doi.org/10.1016/j.jphotochem.2008.12.020openalex-snapshot
Synthesis and properties of novel chemiluminescent biological probes: 2- and 3-(2-Succinimidyloxycarbonylethyl)phenyl acridinium esters
inferredcites →https://doi.org/10.1016/j.marchem.2005.07.001openalex-snapshot
Hydrogen peroxide method intercomparision study in seawater
inferredcites →https://doi.org/10.1016/j.saa.2007.10.045openalex-snapshot
Spectral features of substituted 9-(phenoxycarbonyl)-acridines and their protonated and methylated cation derivatives
inferredcites →https://doi.org/10.1016/s0003-2670(03)00809-2openalex-snapshot
Clinical applications of chemiluminescence
inferredcites →https://doi.org/10.1016/s0022-2860(02)00073-xopenalex-snapshot
1 H and 13 C NMR spectroscopy of 9-acridinones
inferredcites →https://doi.org/10.1016/s0039-9140(99)00294-5openalex-snapshot
Chemiluminescence as diagnostic tool. A review
inferredcites →https://doi.org/10.1016/s1010-6030(00)00209-4openalex-snapshot
Synthesis and properties of novel chemiluminescent biological probes: substituted 4-(2-succinimidyloxycarbonylethyl)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulphonate
inferredcites →https://doi.org/10.1016/s1386-1425(02)00195-6openalex-snapshot
Theoretical interpretation of electronic absorption and emission transitions in 9-acridinones
inferredcites →https://doi.org/10.1021/ac062228wopenalex-snapshot
Flow Injection Analysis of H 2 O 2 in Natural Waters Using Acridinium Ester Chemiluminescence: Method Development and Optimization Using a Kinetic Model
inferredcites →https://doi.org/10.1021/cr020750mopenalex-snapshot
Quantitative Measures of Solvent Polarity
inferredcites →https://doi.org/10.1021/ja00764a046openalex-snapshot
Chemiluminescent reaction of 9-carboxy-N-methylacridinium chloride with potassium peroxydisulfate
inferredcites →https://doi.org/10.1021/jo01022a002openalex-snapshot
Chemiluminescence from the Reaction of 9-Chlorocarbonyl-10-methylacridinium Chloride with Aqueous Hydrogen Peroxide1
inferredcites →https://doi.org/10.1021/jo0354387openalex-snapshot
Origin of Chemiluminescence Accompanying the Reaction of the 9-Cyano-10-methylacridinium Cation with Hydrogen Peroxide
inferredcites →https://doi.org/10.1021/jo970202mopenalex-snapshot
Characterization of Acridancarboxylic Acid Derivatives as Chemiluminescent Peroxidase Substrates
inferredcites →https://doi.org/10.1021/jo980566uopenalex-snapshot
Toward an Understanding of the Chemiluminescence Accompanying the Reaction of 9-Carboxy-10-methylacridinium Phenyl Ester with Hydrogen Peroxide
inferredcites →https://doi.org/10.1039/b811947copenalex-snapshot
Development and application of a novel acridinium ester for use as a chemiluminescent emitter in nucleic acid hybridisation assays using chemiluminescence quenching
inferredcites →https://doi.org/10.1080/13547500600742169openalex-snapshot
Acridinium ester conjugated to lectin as chemiluminescent histochemistry marker
inferredcites →https://doi.org/10.1093/clinchem/35.8.1588openalex-snapshot
Assay formats involving acridinium-ester-labeled DNA probes.
inferredcites →https://doi.org/10.1351/pac198557030523openalex-snapshot
Chemiluminescence immunoassay
inferredcites →https://doi.org/10.1590/s0103-50532008000100025openalex-snapshot
Determination of the pKa values of some biologically active and inactive hydroxyquinones
inferredcites →https://doi.org/10.3987/rev-93-455openalex-snapshot
The Reactivity of Acridinium Salts and Related Compounds
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.4751208openalex-extracted
Aromatic Acridinium Thioesters as New Chemiluminescence Indicators In The Analysis of Biological Antioxidants
inferred← citeshttps://doi.org/10.1002/chem.201802030openalex-snapshot
A Novel Linking Strategy of Using 9,10‐Dihydroacridine to Construct Efficient Host Materials for Red Phosphorescent Organic Light‐Emitting Diodes
inferred← citeshttps://doi.org/10.1002/chem.201901498openalex-snapshot
Synergistic Catalysis: Highly Enantioselective Cascade Reaction for the Synthesis of Dihydroacridines
inferred← citeshttps://doi.org/10.1002/cphc.202200166openalex-snapshot
Solvent Effect on the Chemiluminescence of Acridinium Thioester: A Computational Study
inferred← citeshttps://doi.org/10.1002/jemt.22837openalex-snapshot
Dimethyl‐2‐[(acridin‐9‐yl)methylidene]‐malonate as fluorescent probe for histochemical analysis
inferred← citeshttps://doi.org/10.1007/s10973-017-6306-4openalex-snapshot
Lattice energetics and thermochemistry of acridine derivatives and substituted acridinium trifluoromethanesulphonates
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.04.004openalex-snapshot
Recent Advances in the Chemistry of Acridines
inferred← citeshttps://doi.org/10.1016/j.dyepig.2015.11.016openalex-snapshot
A new synthesis strategy for acridine derivatives to constructing novel host for phosphorescent organic light-emitting diodes
inferred← citeshttps://doi.org/10.1016/j.jlumin.2017.02.068openalex-snapshot
Chemiluminogenic acridinium salts: A comparison study. Detection of intermediate entities appearing upon light generation
inferred← citeshttps://doi.org/10.1016/j.jlumin.2024.120745openalex-snapshot
Aromatic acridinium thioesters–a new class of chemiluminogenic compounds and their interactions with some biological antioxidants
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01856openalex-snapshot
Photoinduced Regioselective Decarbonylative and Decarboxylative C–O Bond Functionalizations: Approach toward Chemoselective Scissions of Isatoic Anhydride and Unraveling the Enroutes through Control Experiments and DFT Studies
inferred← citeshttps://doi.org/10.1021/jo1020882openalex-snapshot
Chemiluminogenic Features of 10-Methyl-9-(phenoxycarbonyl)acridinium Trifluoromethanesulfonates Alkyl Substituted at the Benzene Ring in Aqueous Media
inferred← citeshttps://doi.org/10.1021/ol202609aopenalex-snapshot
Palladium-Catalyzed Decarboxylative Coupling of Isatoic Anhydrides with Arylboronic Acids
inferred← citeshttps://doi.org/10.1039/c1ob05543gopenalex-snapshot
Effect of surfactants on the chemiluminescence of acridinium dimethylphenyl ester labels and their conjugates
inferred← citeshttps://doi.org/10.1039/c4ob02528hopenalex-snapshot
A comparison of chemiluminescent acridinium dimethylphenyl ester labels with different conjugation sites
inferred← citeshttps://doi.org/10.1039/c4ra02516dopenalex-snapshot
Effect of branching in remote substituents on light emission and stability of chemiluminescent acridinium esters
inferred← citeshttps://doi.org/10.1039/c4ra06061jopenalex-snapshot
Synthesis of a borylated boron–dibenzopyrromethene dye enabling the visual detection of H 2 O 2 vapor
inferred← citeshttps://doi.org/10.1039/c5ob01798jopenalex-snapshot
Effective chemiluminogenic systems based on acridinium esters bearing substituents of various electronic and steric properties
inferred← citeshttps://doi.org/10.1039/c5ra00334bopenalex-snapshot
Synthesis and properties of chemiluminescent acridinium esters with different N-alkyl groups
inferred← citeshttps://doi.org/10.1039/c6nj00725bopenalex-snapshot
Structure, formation, thermodynamics and interactions in 9-carboxy-10-methylacridinium-based molecular systems
inferred← citeshttps://doi.org/10.1039/d1ob00027fopenalex-snapshot
Ruthenium( ii )-catalyzed decarbonylative and decarboxylative coupling of isatoic anhydrides with salicylaldehydes: access to aryl 2-aminobenzoates
inferred← citeshttps://doi.org/10.3390/ijms24119468openalex-snapshot
What Other Than Acridinium Esters? Computational Search for New Acridinium-Based Chemiluminogens
inferred← citeshttps://doi.org/10.3390/molecules31061041openalex-snapshot
Acridinium Chemiluminogenic Labels—Synthesis, Analytical Performance, and Mechanism of Light Generation—A Comparison in View of Biomedical Diagnostics
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.