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ChemInform Abstract: Tetracyclic Derivatives of Acridine. Heterofused Acridines
ChemInform, 1997AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
J.‐P. GALY +3 more
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Tetrahedron, 2014
Abstract Oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines were synthesized through nucleophilic additions and aromatization reactions of arynes with 2-aminoaryl ketones or 2-aminoaryl aldehydes in good yields at room temperature.
Jie Zhang +6 more
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Abstract Oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines were synthesized through nucleophilic additions and aromatization reactions of arynes with 2-aminoaryl ketones or 2-aminoaryl aldehydes in good yields at room temperature.
Jie Zhang +6 more
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Excited state characteristics of acridine dyes: acriflavine and acridine orange
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2003The magnitude of the Stokes shift (frequency shifts in absorption and fluorescence spectra) is observed on changing the solvents and further has been used to calculate experimentally the dipole moments (ground state and excited state) of acriflavine and acridine orange dye molecules. Theoretically, dipole moments are calculated using PM 3 Model.
Vijay K, Sharma +4 more
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2-Ethylphenyl acridine-9-carboxylate and 2,5-dimethylphenyl acridine-9-carboxylate
Acta Crystallographica Section C Crystal Structure Communications, 2004The title compounds, 2-ethylphenyl acridine-9-carboxylate, C22H17NO2, (I), and 2,5-dimethylphenyl acridine-9-carboxylate, C22H17NO2, (II), form triclinic and monoclinic crystals, respectively. Related by a centre of symmetry, adjacent molecules of (I) are linked in the lattice via a network of C-H...pi and non-specific dispersive interactions.
Artur, Sikorski +3 more
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Applied Spectroscopy, 2013
A fluorescence quenching method was used to determine the equilibrium binding constants for the association of acridine, acridine orange, and acridine yellow G to humic acid. The fluorescence of each polycyclic aromatic nitrogen heterocycle (PANH) was monitored as aliquots of humic acid were added, and a Stern–Volmer plot was produced in which the ...
Jake T, Herb, Bruce D, Anderson
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A fluorescence quenching method was used to determine the equilibrium binding constants for the association of acridine, acridine orange, and acridine yellow G to humic acid. The fluorescence of each polycyclic aromatic nitrogen heterocycle (PANH) was monitored as aliquots of humic acid were added, and a Stern–Volmer plot was produced in which the ...
Jake T, Herb, Bruce D, Anderson
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Australian Journal of Chemistry, 2018
The quantitative determination of the products of bromination of acridine in concentrated sulfuric acid and glacial acetic acid is described. In both cases, the only monobromo products were the 2- and 4-substituted compounds. With sulfuric acid, the 4-isomer predominates whereas in acetic acid, the 2-isomer is predominant.
Graham S. Chandler, Wolfgang H. F. Sasse
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The quantitative determination of the products of bromination of acridine in concentrated sulfuric acid and glacial acetic acid is described. In both cases, the only monobromo products were the 2- and 4-substituted compounds. With sulfuric acid, the 4-isomer predominates whereas in acetic acid, the 2-isomer is predominant.
Graham S. Chandler, Wolfgang H. F. Sasse
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Electrochemiluminescence of Acridines
Electroanalysis, 2016AbstractAcridines play an important role in various fields of sciences. Besides their application for treatment of a number of infections, cancer, viral and prion diseases, they have been extensively used in chemiluminescence. Electrochemiluminescence (ECL) is a unique kind of chemiluminescence with the precise temporal and spatial control of light ...
Saadat Majeed +4 more
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Tetracyclic derivatives of acridine. Heterofused acridines
Journal of Heterocyclic Chemistry, 1996Galy, Jean‐pierre +3 more
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