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Chemiluminogenic Features of 10-Methyl-9-(phenoxycarbonyl)acridinium Trifluoromethanesulfonates Alkyl Substituted at the Benzene Ring in Aqueous Media
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Stable and versatile active acridinium esters II
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Chemiluminescent Reactions of Acridines
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Nucleophilic addition to the 9 position of 9‐phenylcarboxylate‐10‐methylacridinium protects against hydrolysis of the ester
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Substituent Constants for Correlation Analysis in Chemistry and Biology.
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Density Functional Methods in Chemistry
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The influence of polarization functions on molecular orbital hydrogenation energies
inferredcites →https://doi.org/10.1007/bf01242430openalex-snapshot
Acridinium ester chemiluminescence: pH dependent hydrolysis of reagents and flow injection analysis of hydrogen peroxide and glutamate
inferredcites →https://doi.org/10.1007/s00216-010-4157-yopenalex-snapshot
DNA sensor by using electrochemiluminescence of acridinium ester initiated by tripropylamine
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
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Frontier Orbitals and Organic Chemical Reactions
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Synthesis and properties of new luminescent 10-carboxymethylacridinium derivatives
inferredcites →https://doi.org/10.1016/0076-6879(86)33080-5openalex-snapshot
[31] Immunoassays using acridinium esters
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Time-Correlated Single Photon Counting
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Enhanced immunoassay sensitivity using chemiluminescent acridinium esters with increased light output
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.cccn.2005.03.021openalex-snapshot
Novel biotinylated acridinium derivatives: New reagents for fluorescence immunoassays and proteomics
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.molstruc.2008.11.001openalex-snapshot
9-[(Mesityloxy)carbonyl]-10-methylacridinium trifluoromethanesulphonate and its derivative mesityl 9-methoxy-10-methyl-9,10-dihydroacridine-9-carboxylate: Structural and physicochemical features
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/j.saa.2010.02.014openalex-snapshot
Vibrational spectra of phenyl acridine-9-carboxylates and their 10-methylated cations: A theoretical and experimental study
inferredcites →https://doi.org/10.1016/j.saa.2010.10.029openalex-snapshot
1H and 13C NMR spectra, structure and physicochemical features of phenyl acridine-9-carboxylates and 10-methyl-9-(phenoxycarbonyl)acridinium trifluoromethanesulphonates – alkyl substituted in the phenyl fragment
inferredcites →https://doi.org/10.1016/s0003-2670(02)00254-4openalex-snapshot
Electrochemiluminescence assay for the detection of acridinium esters
inferredcites →https://doi.org/10.1016/s0003-2670(03)00809-2openalex-snapshot
Clinical applications of chemiluminescence
inferredcites →https://doi.org/10.1016/s0022-328x(00)99651-7openalex-snapshot
Ab initio molecular orbital theory
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/10.1016/s1570-0232(03)00364-7openalex-snapshot
Derivatization of biomolecules for chemiluminescent detection in capillary electrophoresis
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/ar50107a003openalex-snapshot
Ab initio molecular orbital theory
inferredcites →https://doi.org/10.1021/cr00031a013openalex-snapshot
Molecular Interactions in Solution: An Overview of Methods Based on Continuous Distributions of the Solvent
inferredcites →https://doi.org/10.1021/ja00466a012openalex-snapshot
Ground states of molecules. 44. MINDO/3 calculations of absolute heat capacities and entropies of molecules without internal rotations
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/je049947xopenalex-snapshot
Octanol/Water Partition Coefficient of Selected Herbicides: Determination Using Shake-Flask Method and Reversed-Phase High-Performance Liquid Chromatography
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/jo1013405openalex-snapshot
Experimental Evidence of the Occurrence of Intramolecular Electron Transfer in Catalyzed 1,2-Dioxetane Decomposition
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/10.1021/jo9917487openalex-snapshot
Kinetics of Two Pathways in Peroxyoxalate Chemiluminescence
inferredcites →https://doi.org/10.1021/jp104253fopenalex-snapshot
Chemiluminogenic Properties of 10-Methyl-9-(phenoxycarbonyl)acridinium Cations in Organic Environments
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/10.1039/b813330aopenalex-snapshot
Using acridinium ester as the sonochemiluminescent probe for labeling of protein
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1063/1.474671openalex-snapshot
A new definition of cavities for the computation of solvation free energies by the polarizable continuum model
inferredcites →https://doi.org/10.1080/13547500600742169openalex-snapshot
Acridinium ester conjugated to lectin as chemiluminescent histochemistry marker
inferredcites →https://doi.org/10.1093/clinchem/29.8.1474openalex-snapshot
Acridinium esters as high-specific-activity labels in immunoassay.
inferredcites →https://doi.org/10.1093/hesc/9780198847816.001.0001openalex-snapshot
Atkins’ Physical Chemistry
inferredcites →https://doi.org/10.1103/physreva.38.3098openalex-snapshot
Density-functional exchange-energy approximation with correct asymptotic behavior
inferredcites →https://doi.org/10.1103/physrevb.37.785openalex-snapshot
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
inferredcites →https://doi.org/10.1107/s0108270104030537openalex-snapshot
2-Ethylphenyl acridine-9-carboxylate and 2,5-dimethylphenyl acridine-9-carboxylate
inferredcites →https://doi.org/10.1107/s1600536806000377openalex-snapshot
2-Methylphenyl acridine-9-carboxylate
inferredcites →https://doi.org/10.1107/s1600536806002340openalex-snapshot
10-Methyl-9-(2-methylphenoxycarbonyl)acridinium trifluoromethanesulfonate
inferredcites →https://doi.org/10.1107/s1600536807052002openalex-snapshot
9-(2-tert-Butylphenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferredcites →https://doi.org/10.1107/s1600536810008950openalex-snapshot
9-(2-Ethylphenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferredcites →https://doi.org/10.1107/s1600536810009979openalex-snapshot
10-Methyl-9-phenoxycarbonylacridinium trifluoromethanesulfonate monohydrate
inferredcites →https://doi.org/10.1107/s1600536810016302openalex-snapshot
9-(4-Methylphenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferredcites →https://doi.org/10.1107/s160053681003953xopenalex-snapshot
10-Methyl-9-[2-(propan-2-yl)phenoxycarbonyl]acridinium trifluoromethanesulfonate
inferredcites →https://doi.org/10.1107/s1600536810041449openalex-snapshot
9-(2,6-Dimethylphenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferredcites →https://doi.org/10.1111/j.1751-1097.2007.00140.xopenalex-snapshot
Development of a Quantitative Bio/Chemiluminescence Spectrometer Determining Quantum Yields: Re‐examination of the Aqueous Luminol Chemiluminescence Standard
inferredcites →https://doi.org/10.1351/pac197024030611openalex-snapshot
The chemiluminescence of organic compounds
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/10.2116/analsci.25.587openalex-snapshot
Chemiluminescence Platforms in Immunoassay and DNA Analyses
inferredcites →https://doi.org/10.2174/1385272023374625openalex-snapshot
Potential of Chemiluminescence and Bioluminescence in Organic Analysis
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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