Lin Mingzhang, Katsumura Yosuke, Hata Kuniki, Muroya Yusa, Nakagawa Keichi
Advanced Science Research Center, Japan Atomic Energy Agency, 2-4 Shirakata Shirane, Tokaimura, Nakagun, Ibaraki 319-1195, Japan.
J Photochem Photobiol B. 2007 Nov 12;89(1):36-43. doi: 10.1016/j.jphotobiol.2007.08.001. Epub 2007 Aug 7.
The reactions between edaravone and various one-electron oxidants such as ()OH, N(3)(), Br(2)(-), and SO(4)(-), have been studied by pulse radiolysis techniques. The transient species produced by the reaction of edaravone with ()OH radical shows an absorption band with lambda(max)=320 nm, while the oxidation by N(3)(), Br(2)(-), SO(4)(-) and CCl(3)OO() results in an absorption band with lambda(max)=345 nm. Different from the previous reports, the main transient species by the reaction of edaravone with ()OH radical in the absence of O(2) is attributed to OH-adducts. At neutral condition (pH 7), the rate constants of edaravone reacting with ()OH, N(3)(), SO(4)(-), CCl(3)OO(*), and e(aq)(-) are estimated to be 8.5x10(9), 5.8x10(9), 6x10(8), 5.0x10(8) and 2.4x10(9)dm(3)mol(-1)s(-1), respectively. From the pH dependence on the formation of electron adducts and on the rate constant of edaravone with hydrated electron, the pK(a) of edaravone is estimated to be 6.9+/-0.1.
通过脉冲辐解技术研究了依达拉奉与各种单电子氧化剂如()OH、N₃()、Br₂(-)和SO₄(-)之间的反应。依达拉奉与()OH自由基反应产生的瞬态物种在λ(max)=320nm处有一个吸收带,而被N₃()、Br₂(-)、SO₄(-)和CCl₃OO()氧化则导致在λ(max)=345nm处出现一个吸收带。与先前的报道不同,在没有O₂的情况下,依达拉奉与()OH自由基反应产生的主要瞬态物种归因于OH加合物。在中性条件(pH 7)下,依达拉奉与()OH、N₃()、SO₄(-)、CCl₃OO(*)和e(aq)(-)反应的速率常数分别估计为8.5×10⁹、5.8×10⁹、6×10⁸、5.0×10⁸和2.4×10⁹dm³mol⁻¹s⁻¹。根据pH对电子加合物形成以及依达拉奉与水合电子反应速率常数的依赖性估计,依达拉奉的pKₐ为6.9±0.1。