Nauser Thomas, Koppenol Willem H, Pelling Jill, Schöneich Christian
Laboratory for Inorganic Chemistry, ETH Zürich, CH-8093 Zürich, Switzerland.
Chem Res Toxicol. 2004 Sep;17(9):1227-35. doi: 10.1021/tx049862u.
Laser flash photolysis at 266 nm of 3-nitrotyrosine and N-acetyl-3-nitrotyrosine ethyl ester generates an oxidizing species, which shows all of the characteristics of a hydroxyl radical. This species reacts with Br(-) to yield Br(2).-, via an intermediate, that is kinetically identified as HOBr.-. Moreover, the formation of Br(2).- can be suppressed by methanol; competition kinetics yield relative rate constants for the reaction of the reactive species with Br(-) and methanol that are similar to those for the hydroxyl radical. Parallel time-resolved UV/vis spectroscopy suggests the formation of phenoxyl radicals, consistent with the formation of hydroxyl radicals. Laser flash photolysis at 355 nm also generates reactive intermediates that oxidize Br(-) to Br(2).- but appear not to be hydroxyl radicals.
用266nm激光闪光光解3-硝基酪氨酸和N-乙酰基-3-硝基酪氨酸乙酯会产生一种氧化物种,该物种具有羟基自由基的所有特征。该物种与Br(-)反应生成Br(2).-,通过一种动力学上被确定为HOBr.-的中间体。此外,甲醇可以抑制Br(2).-的形成;竞争动力学得出反应性物种与Br(-)和甲醇反应的相对速率常数,与羟基自由基的相似。平行的时间分辨紫外/可见光谱表明苯氧基自由基的形成,这与羟基自由基的形成一致。355nm激光闪光光解也会产生将Br(-)氧化为Br(2).-的反应性中间体,但似乎不是羟基自由基。