نتایج جستجو برای: anthracene derivatives

تعداد نتایج: 108664  

Journal: :Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 2014
Alberto Moscatelli Elena Sartori Marco Ruzzi Steffen Jockusch Xuegong Lei Igor Khudyakov Nicholas Turro

Time-resolved electron paramagnetic resonance spectroscopy, transient absorption, and phosphorescence spectroscopy were used to investigate the spin polarization of a nitroxide free radical induced by interaction with singlet oxygen ((1)O2). The latter was generated by photolysis of endoperoxides of two anthracene derivatives. Although both anthracene endoperoxides are structurally similar, opp...

Journal: :Chemosphere 2011
Marian Asantewah Nkansah Alfred A Christy Tanja Barth

Polycyclic aromatic hydrocarbons are very stable compounds and tend to bioaccumulate in the environment due to their high degree of conjugation and aromaticity. Hydrous pyrolysis is explored as a technique for the treatment of industrial water containing PAH, using anthracene as a model compound. The reactivity of anthracene under a range of temperatures and durations are studied in this paper....

2011
Y. L. N. MURTHY B. VIJAYA CH. V. V. SATYANARAYANA MURTHY K. SRIHARI VARMA

Literature survey reveal that a good number of Anthracene and substituted Anthracene are potential lasing organic compounds. As per mit suo meada66 9,10-dimethyl and 9,10-diphenyl Anthracenes exhibit lasing properties, around 435-450 nm (ethanol). In continuation of our studies in this lab, our objective is to synthesize new lasing organic dyes, in particular, new Anthracene derivatives and stu...

2008
ZHONGFA WANG

Theoretical studies on anthracene and a series of its derivatives were performed using the AM1 method and DFT. Based on B3LYP/6-31G(d) optimized geometries, the electronic, IR and NMR spectra of anthracene oligomers were calculated using the Indo/Cis, AM1 and B3LYP/6-31G(d) methods, respectively. The energy gaps of the oligomers decreased and the main absorptions in the electronic spectra of th...

Journal: :Cancer research 1978
W M Baird R Chemerys C J Chern L Diamond

Secondary cultures of hamster embryo cells exposed to 0.5 nmol [G-3H]7,12-dimethylbenz(a)anthracene (DMBA) per ml medium metabolized more than 90% of the DMBA within 48 hr. Samples of medium were extracted with chloroform, methanol, and water. The chloroform phases contained about one-third of the DMBA metabolites; the major chloroform-extractable metabolite was 8,9-dihydro-8,9-dihydroxy-7,12-d...

Journal: :The Journal of organic chemistry 2008
Emanuela Berni Christel Dolain Brice Kauffmann Jean-Michel Léger Chuanlang Zhan Ivan Huc

The synthesis of various 1,8-diaza-4,5-dialkoxy-2,7-anthracene dicarboxylic acid derivatives and their incorporation into cyclic and helically folded aromatic oligoamides are reported. The ability of the diaza-anthracene monomers to undergo photoaddition or head-to-tail photodimerization was investigated in the solid state and in solution. Quantitative conversion of a monomer diester to the cor...

Journal: :Applied and environmental microbiology 1982
D F Liberman R C Fink F L Schaefer R J Mulcahy A A Stark

The mutagenicity of anthracene, anthraquinone, and four structurally similar compounds of each was evaluated in the Ames/Salmonella microsome assay. Anthraquinone was shown to be mutagenic for strains TA1537, TA1538, and TA98 in the absence of rat liver homogenate. The four anthraquinone derivatives tested were mutagenic for TA1537 exclusively. None of the anthracenes exhibited mutagenic activity.

Crude oils and source rocks from the northern and offshore Niger Delta basin, Nigeria, have been characterized by gas chromatography-mass spectrometry in terms of their origin and thermal maturity based on the distribution of chrysene and its derivatives. The crude oils and source rocks were characterized by the dominance of chrysene over benzo[a]anthracene. 3-methylchrysene predominated over o...

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