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Quenching from 475 , reannealing and quenching in water .

Quenching from 475 , reannealing followed by very slow cooling .

Quenching from 475 , reannealing, followed by cooling in air .

Quenching has to be associated to the complexation of the Cu centre by the tetramine subunit. This is confirmed by the appearance in the absorption spectrum of a band centred at 520 nm

Quenching mechanism of the complex CuAu n in donor solvents.

Quenching of 2 by the added coreactant S20g.

Quenching of a hot casting shortly after heat treatment 237, HUT, 2003

Quenching of a hot casting shortly after heat treatment.91

Quenching of a radical intermediate in the synthesis of FK-506.

Quenching of acridinium cation fluorescence in SDS micelles by iodide anion anions

Quenching of an excited molecule through sequential electron transfer. Here an ion pair is formed in the first place, within which back electron transfer leads to overall deactivation of the excited energy donor

Quenching of benzophenone triplet by 0.24-mM melatonin in acetonitrile, monitored at 600 nm following 355-nm laser excitation. Each point is derived from a trace such as that shown in

Quenching of benzophenone triplet by 0.24-mM melatonin in acetonitrile, monitored at 600 nm following 355-nm laser excitation. The spectrum was recorded at room temperature, under a nitrogen atmosphere.

Quenching of counurinC 20 by the nucleosides uridine . The sample was exdt at the isosbesdc point at 360 nm, Revised and r irinted. with pennluioA. firom Ref. 19. Copyri O 1996. Anedcan Chemical Sod e y.

Quenching of Cu

Quenching of cyclo-octatetraene with tetrabromoneopentane.

Quenching of ethidium bromide fluorescence by amsacrine in the presence of poly .

Quenching of fluorescence of a solution of naphthalene

Quenching of fluorescence of PP solution in benzene. Quenchers

Quenching of fluorescence of tumor necrosis factor . Parameters

Quenching of free radical reaction in ozonation of Polyazo dye AZ5 82

Quenching of free radical reaction in ozonation of Polyazo dye AZ5 was added to the reaction mixture.

Quenching of HDAC metabolite ML by chemical derivatization.

Quenching of higher-level emission by cross relaxation. Left-hand side Eu the D emission on ion I is quenched by transferring the energy difference D - Do to ion 2 which is promoted to the F3 level. Right-hand side the D3 emission on ion I is quenched by transferring the energy difference D3- D4 to ion 2 which is promoted 10 the Fo level

Quenching of HSA by caffeine at three temperatures. Revised from Ref. 59.



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