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Toward an Understanding of the Chemiluminescence Accompanying the Reaction of 9-Carboxy-10-methylacridinium Phenyl Ester with Hydrogen Peroxide
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1099-1271(199601)11:1<23::aid-bio400>3.0.co;2-aopenalex-snapshot
Competitive Chemiluminescent Immunoassay for Estradiol Using anN-Functionalized Acridinium Ester
inferredcites →https://doi.org/10.1002/jcc.540070402openalex-snapshot
An algorithm for the location of transition states
inferredcites →https://doi.org/10.1002/jcc.540100209openalex-snapshot
Optimization of parameters for semiempirical methods II. Applications
inferredcites →https://doi.org/10.1002/jcc.540110404openalex-snapshot
Atomic charges derived from semiempirical methods
inferredcites →https://doi.org/10.1007/bf00128336openalex-snapshot
MOPAC: A semiempirical molecular orbital program
inferredcites →https://doi.org/10.1007/bf00533485openalex-snapshot
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/10.1016/0022-2860(79)80172-6openalex-snapshot
Frontier Orbitals and Organic Chemical Reactions
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(93)80188-fopenalex-snapshot
Chemiluminescence of N,N′-dialkyl-9,9′-biacridinium nitrates in aqueous and non-aqueous systems
inferredcites →https://doi.org/10.1016/s0003-2670(00)82338-7openalex-snapshot
Optimal labelling of proteins with acridinium ester
inferredcites →https://doi.org/10.1016/s0003-2670(00)82640-9openalex-snapshot
Chemiluminogenic labels, old and new
inferredcites →https://doi.org/10.1016/s0003-2670(00)82648-3openalex-snapshot
Flow-Injection immunoassays with acridinium ester-based chemiluminescence detection
inferredcites →https://doi.org/10.1016/s0040-4039(00)76969-3openalex-snapshot
A novel chemiluminescence from the reaction of 9-arylmethylene-10-methyl-9,10-dihydroacridines and dimethyldioxirane
inferredcites →https://doi.org/10.1021/ac00175a005openalex-snapshot
Fiber-optic sensor for the determination of glucose using micellar enhanced chemiluminescence of the peroxyoxalate reaction
inferredcites →https://doi.org/10.1021/ar50026a003openalex-snapshot
Chemiluminescence of organic hydrazides
inferredcites →https://doi.org/10.1021/ar50102a001openalex-snapshot
Chemical mechanisms in bioluminescence
inferredcites →https://doi.org/10.1021/j100091a024openalex-snapshot
Comparison of Density Functional and MP2 Calculations on the Water Monomer and Dimer
inferredcites →https://doi.org/10.1021/ja00114a029openalex-snapshot
Theoretical Studies on the Structure, Stability, Ability To Undergo Internal Transformations, and Tautomerization, as Well as Reactivity, of H2PPH2 and HPPH3 Molecules
inferredcites →https://doi.org/10.1021/ja00251a024openalex-snapshot
Chemiluminescence involving acidic and ambident ion light emitters. The chemiluminescence of 9-acridinepercarboxylate anion
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/ja00482a030openalex-snapshot
Chemiluminescence of diphenoyl peroxide. Chemically initiated electron exchange luminescence. A new general mechanism for chemical production of electronically excited states
inferredcites →https://doi.org/10.1021/ja00516a005openalex-snapshot
Cyclic peroxides. 81. Fluorescer-enhanced chemiluminescence of .alpha.-peroxylactones via electron exchange
inferredcites →https://doi.org/10.1021/ja00531a026openalex-snapshot
Structural effects on the intramolecular electron transfer induced decomposition of a series of 1,2-dioxetanes derived from 9-alkylidene-10-methylacridans
inferredcites →https://doi.org/10.1021/ja00725a029openalex-snapshot
Thermochemistry of 1,2-dioxetane and its methylated derivatives. Estimate of activation parameters
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/jo950917uopenalex-snapshot
The Transformation Mechanism of 3,4,6-Tri-O-acetyl-1,5-anhydro-2-deoxy- d -arabino-hex-1-enitol in Water
inferredcites →https://doi.org/10.1021/jp961555copenalex-snapshot
Hartree−Fock and Density Functional Methods and IR and NMR Spectroscopies in the Examination of Tautomerism and Features of Neutral 9-Acridinamine in Gaseous and Condensed Media
inferredcites →https://doi.org/10.1038/279646a0openalex-snapshot
A stable chemiluminescent-labelled antibody for immunological assays
inferredcites →https://doi.org/10.1039/c39770000946openalex-snapshot
Alternative mechanism for dioxetan decomposition
inferredcites →https://doi.org/10.1039/f29726801839openalex-snapshot
Molecular orbital theory for the excited states of transition metal complexes
inferredcites →https://doi.org/10.1039/f29848000227openalex-snapshot
Location of transition states in reaction mechanisms
inferredcites →https://doi.org/10.1039/p29930000799openalex-snapshot
COSMO: a new approach to dielectric screening in solvents with explicit expressions for the screening energy and its gradient
inferredcites →https://doi.org/10.1039/p29950000569openalex-snapshot
CGC, MS and theoretical studies on the transformation mechanism of 3,4-di-O-acetyl-1,5-anhydro-2-deoxy- D -threo-pent-1-enitol in aqueous solutions
inferredcites →https://doi.org/10.1063/1.444267openalex-snapshot
Self-consistent molecular orbital methods. XXIII. A polarization-type basis set for second-row elements
inferredcites →https://doi.org/10.1063/1.464913openalex-snapshot
Density-functional thermochemistry. III. The role of exact exchange
inferredcites →https://doi.org/10.1093/clinchem/29.8.1474openalex-snapshot
Acridinium esters as high-specific-activity labels in immunoassay.
inferredcites →https://doi.org/10.1103/physrevb.37.785openalex-snapshot
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
inferredcites →https://doi.org/10.1351/pac197024030611openalex-snapshot
The chemiluminescence of organic 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/10.1002/0470862769.ch16openalex-snapshot
Chemiluminescence of Organic Peroxides
inferred← citeshttps://doi.org/10.1002/1097-0231(20001130)14:22<2112::aid-rcm139>3.0.co;2-uopenalex-snapshot
Evidence of nucleophilic addition to chemiluminescentN-Sulfonylacridinium-9-carboxamides from electrospray ionization mass spectrometry
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0362openalex-snapshot
Chemiluminescence of Organic Peroxides
inferred← citeshttps://doi.org/10.1002/bio.2643openalex-snapshot
Chemiluminescence accompanied by the reaction of acridinium ester and manganese (II)
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/elps.201300314openalex-snapshot
A highly sensitive CE‐chemiluminescence method for the determination of sympathomimetic drugs in urine samples by a facile precolumn derivatization using acridinium ester
inferred← citeshttps://doi.org/10.1007/s00216-011-5342-3openalex-snapshot
Chemiluminescent reductive acridinium triggering (CRAT)—mechanism and applications
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s10973-010-0789-6openalex-snapshot
Lattice energetics and thermochemistry of phenyl acridine-9-carboxylates and 9-phenoxycarbonyl-10-methylacridinium trifluoromethanesulphonates
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/j.ab.2010.07.025openalex-snapshot
Enhanced immunoassay sensitivity using chemiluminescent acridinium esters with increased light output
inferred← citeshttps://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
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/10.1016/j.marchem.2005.07.001openalex-snapshot
Hydrogen peroxide method intercomparision study in seawater
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.molstruc.2015.10.041openalex-snapshot
Structural considerations on acridine/acridinium derivatives: Synthesis, crystal structure, Hirshfeld surface analysis and computational studies
inferred← citeshttps://doi.org/10.1016/j.saa.2007.10.045openalex-snapshot
Spectral features of substituted 9-(phenoxycarbonyl)-acridines and their protonated and methylated cation derivatives
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.tet.2003.08.040openalex-snapshot
Synthesis of 3,7-dihydroimidazo[1,2a]pyrazine-3-ones and their chemiluminescent properties
inferred← citeshttps://doi.org/10.1016/j.theochem.2003.09.006openalex-snapshot
Theoretical studies of the mechanism of the Brönsted-acid-catalyzed glycosidation of α- and β-d-glucofuranurono-6,3-lactone
inferred← citeshttps://doi.org/10.1016/s0022-2860(02)00073-xopenalex-snapshot
1 H and 13 C NMR spectroscopy of 9-acridinones
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00624-9openalex-snapshot
Modulation of the chemiluminescent signal from N10-(3-sulfopropyl)-N-sulfonylacridinium-9-carboxamides
inferred← citeshttps://doi.org/10.1016/s0924-2031(01)00129-1openalex-snapshot
Infrared and Raman spectroscopy of 9-acridinones
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02748openalex-snapshot
Strongly Chemiluminescent Acridinium Esters under Neutral Conditions: Synthesis, Properties, Determination, and Theoretical Study
inferred← citeshttps://doi.org/10.1021/jo0354387openalex-snapshot
Origin of Chemiluminescence Accompanying the Reaction of the 9-Cyano-10-methylacridinium Cation with Hydrogen Peroxide
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/jp014539aopenalex-snapshot
Structure, Properties, Thermodynamics, and Isomerization Ability of 9-Acridinones
inferred← citeshttps://doi.org/10.1021/jp104253fopenalex-snapshot
Chemiluminogenic Properties of 10-Methyl-9-(phenoxycarbonyl)acridinium Cations in Organic Environments
inferred← citeshttps://doi.org/10.1023/b:jtan.0000005179.91819.6dopenalex-snapshot
Melting, volatilisation and crystal lattice enthalpies of acridin-9(10H)-ones
inferred← citeshttps://doi.org/10.1039/9781849732024-00051openalex-snapshot
The Nature of Chemiluminescent Reactions
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/c2ob00022aopenalex-snapshot
Chemiluminescence from alkoxy-substituted acridinium dimethylphenyl ester labels
inferred← citeshttps://doi.org/10.1039/c2ob27190gopenalex-snapshot
Synthesis and properties of differently charged chemiluminescent acridinium ester labels
inferred← citeshttps://doi.org/10.1039/c3ra44461aopenalex-snapshot
Use of degradable cationic surfactants with cleavable linkages for enhancing the chemiluminescence of acridinium ester labels
inferred← citeshttps://doi.org/10.1039/c4ob00456fopenalex-snapshot
Synthesis and properties of chemiluminescent acridinium ester labels with fluorous tags
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/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/10.1088/2050-6120/abeed8openalex-snapshot
Acridone and acridinium constructs with red-shifted emission
inferred← citeshttps://doi.org/10.1107/s0108270102000574openalex-snapshot
2-Methylphenyl 2-methoxyacridine-9-carboxylate
inferred← citeshttps://doi.org/10.1107/s0108270102004912openalex-snapshot
9-Cyano-10-methylacridinium hydrogen dinitrate
inferred← citeshttps://doi.org/10.1107/s0108270102017171openalex-snapshot
10-Methyl- and 9,10-dimethylacridinium methyl sulfate
inferred← citeshttps://doi.org/10.1107/s0108270104030537openalex-snapshot
2-Ethylphenyl acridine-9-carboxylate and 2,5-dimethylphenyl acridine-9-carboxylate
inferred← citeshttps://doi.org/10.1107/s0108270105033779openalex-snapshot
9-(2,6-Difluorophenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate and its precursor 2,6-difluorophenyl acridine-9-carboxylate: C—H...O, C—F...π, S—O...π and π–π stacking interactions
inferred← citeshttps://doi.org/10.1107/s1600536805017952openalex-snapshot
9-(2,6-Dibromophenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s1600536805038729openalex-snapshot
2,6-Diiodophenyl acridine-9-carboxylate
inferred← citeshttps://doi.org/10.1107/s1600536806002340openalex-snapshot
10-Methyl-9-(2-methylphenoxycarbonyl)acridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s1600536807068109openalex-snapshot
10-Methyl-9-(2-nitrophenoxycarbonyl)acridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s1600536809007569openalex-snapshot
9-(Biphenyl-4-yloxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s1600536809007570openalex-snapshot
9-[(2,6-Dimethoxyphenoxy)carbonyl]-10-methylacridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s1600536810008950openalex-snapshot
9-(2-Ethylphenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s1600536810009979openalex-snapshot
10-Methyl-9-phenoxycarbonylacridinium trifluoromethanesulfonate monohydrate
inferred← citeshttps://doi.org/10.1107/s1600536810016296openalex-snapshot
9-(4-Bromophenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s1600536810016302openalex-snapshot
9-(4-Methylphenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s160053681003953xopenalex-snapshot
10-Methyl-9-[2-(propan-2-yl)phenoxycarbonyl]acridinium trifluoromethanesulfonate
inferred← citeshttps://doi.org/10.1107/s160053681205129xopenalex-snapshot
2,6-Dimethylphenyl acridine-9-carboxylate
inferred← citeshttps://doi.org/10.1201/9781420041804.ch5openalex-snapshot
Chemiluminescent N-Sulfonylacridinium-9-Carboxamides and Their Application in Clinical Assays
inferred← citeshttps://doi.org/10.3390/ijms21124417openalex-snapshot
Computational Insights on the Mechanism of the Chemiluminescence Reaction of New Group of Chemiluminogens—10-Methyl-9-thiophenoxycarbonylacridinium Cations
inferred← citeshttps://doi.org/10.3390/mi8050149openalex-snapshot
Preparation of an Acridinium Ester-Labeled Antibody and Its Application in GoldMag Nanoparticle-Based, Ultrasensitive Chemiluminescence Immunoassay for the Detection of Human Epididymis Protein 4
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