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Quenching of Metal-Catalyzed Living Radical Polymerization with Silyl Enol Ethers

Quenching of naphthalene by iotfide in . Revised and repriaied, with p raission, fromRel 109, Copyright 9 1990, American Chemical Soeieiy.

Quenching of PBAC

Quenching of PET processes between A and D by secondary electron transfer A electron acceptor D

Quenching of photocurrent by electron transfer via surface states.

Quenching of photoexcitation at a metal electrode. On photoexcitation of a sensitiser molecule S at the metal surface . The order of steps 2 and 3 may be reversed but the effect is still rapidly to quench S.

Quenching of protolysis products by carbon monoxide.

Quenching of Ru

Quenching of SFA fluorescence chromatograms with addition of Cu. Post-column reagent concentration of Cu is listed above corresponding chromatogram. Conditions are the same as listed in figure 1.

Quenching of the C60 emission in exTTF-oPPE -C60 9b, 9c upon excitation at 355 nm with matching optical density at 355 nm in THF

Quenching of the coherent vibrational oscillations of MDMO-PPV upon photoinduced charge transfer. The AT T dynamics for pure MDMO-PPV and for MDMO-PPV PCBM 1

Quenching of the di- and tetra-anions of 1,2-dianthrylethane with protons.

Quenching of the fluorescence of the receptors 10 and 12 on binding the substrate 1, exc 420 nm, em 654 nm. Graph top, overlayed fluorescence emission spectra of host 12 with increasing added concentrations of p-carotene 1 graph bottom, relative fluorescence intensities of aqueous solutions of 12 as a function of added p-carotene concentration. was

Quenching of the fluorescence spectrum of MeUmbG2 by CBH II from Trichoderma reesei is added. When correction is made for dilution, spectrum E is equivalent to spectrum A. Curves F said G represent buffer and protein blanks, respectively. Spectra were measured at pH 5.0 and 6.6 C.

Quenching of the relative fluorescence intensity of T-AT versus the quantity of polymer added. Adsorption of T-AT onto

Quenching of the relative fluorescence intensity of T-AT versus the quantity of polymer added. In the absence of heparin, adsorption of T-AT onto 0 PSSO2GIU, o PSSO3.

Quenching of the triplet state of the sensitizer by the cis allyl phosphate, c s-1, generates the triplet state, T , of the 1,2-biradical 2. The 1,2-biradical is trapped by the phosphorus atom to afford the triplet state, TP, of the spirophosphoranyl 1,3-biradical 3. Then, inter-system crossing generates the

Quenching of the tryptophan fluorescence of or -acid glycoprotein . Photochemistry and Photobiology, 69,22-26, with permission of the American Society for Photobiology.

Quenching of the tyrosine fluorescence of p-lactoglobulin. Spectra were recorded in the absence . Parameters

Quenching of thionine fluorescence by mononucleotides and polynucleotides. . A.f 623 nm. 2x10 M.

Quenching of traits- cis isomerization of compounds . Reprinted by permission of the American Chemical Society.

Quenching of trans - cis isomerization of compound 89 Reprinted by permission of the American Chemical Society.

Quenching of trans- cis isomerization of compounds . 89 Reprinted by permission of the American Chemical Society.

Quenching of triplet state of a substrate, 3S, by 02 generating lOs by exchange mechanism.

Quenching of triplet state of a substrate, 3S, by generating JOs by exchange mechanism.



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