Results 161 to 170 of about 40,002 (209)

(Acridine)trimethylgallium–Acridine (2/1)

Acta Crystallographica Section C Crystal Structure Communications, 1996
The reaction of excess trimethylgallium with acridine in diethyl ether gave the title layer inclusion compound, [Ga(CH 3 ) 3 (C 13 H 9 N)].0.5C 13 H 9 N. The Ga-N bond length is 2.203 (3) A.
Sun, HS, Wang, XM, Sun, XZ, You, XZ, Wang, JZ   +4 more
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Acridines

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Prager, Rolf Herman, Williams, C M
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The genetic toxicology of acridines

Mutation Research/Reviews in Genetic Toxicology, 1991
Acridine and its derivatives are planar polycyclic aromatic molecules which bind tightly but reversibly to DNA by intercalation, but do not usually covalently interact with it. Acridines have a broad spectrum of biological activities, and a number of derivatives are widely used as antibacterial, antiprotozoal and anticancer drugs. Simple acridines show
L R, Ferguson, W A, Denny
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Synthesis and characterization of oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines

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, Yali Chen, Xuanming Chen, Xiaoxing Zheng, Weiguo Cao, Jie Chen, Min 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, 2003
The 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, P D, Sahare, Ramesh C, Rastogi, S K, Ghoshal, D, Mohan   +4 more
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Investigating the Binding of Acridine, Acridine Orange, and Acridine Yellow G to Humic Acid through Fluorescence Quenching

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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Bromination of Acridine*

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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Solvent and Isotopic Effects on Acridine and Deuterated Acridine Polymorphism

Crystal Growth & Design, 2012
The influence of pure solvents (p.a.) and impure solvents (techn. quality) on the crystallization of polymorphic forms of non-, partial-, and per-deuterated acridine from solution was investigated. Remarkably different crystallization behavior of acridine and deuterated acridine related to the used solvents was observed, especially shown in the case of
A. Kupka, V. Vasylyeva, D. W. M. Hofmann, Kirill V. Yusenko, K. Merz   +4 more
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Electrochemiluminescence of Acridines

Electroanalysis, 2016
AbstractAcridines 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, Wenyue Gao, Yuriy Zholudov, Kateryna Muzyka, Guobao Xu   +4 more
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ChemInform Abstract: Tetracyclic Derivatives of Acridine. Heterofused Acridines

ChemInform, 1997
AbstractChemInform 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, S. MOREL, G. BOYER, J. ELGUERO   +3 more
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