Szyczewski A, Krzyminiewski R, Hafez A M, Pietrzak J
Int J Radiat Biol Relat Stud Phys Chem Med. 1986 Nov;50(5):841-52. doi: 10.1080/09553008614551261.
The molecular structure of free radicals formed in gamma-irradiated monoclinic and orthorhombic single crystals of hydrated testosterone were investigated by EPR spectroscopy. Two different types of radical were observed. In the monoclinic form, the radical arises by the loss of a hydrogen atom from the carbon atom C(2), whereas, in the orthorhombic form, it arises by addition of a hydrogen atom to the oxygen atom O(3). The hyperfine spectrum of the radical formed in the monoclinic single crystal originates from the interaction of the unpaired electron with one alpha-proton in position 2 and two non equivalent beta-protons in position 1. In the orthorhombic single crystal, we observed interaction of the unpaired electron, which is delocalized on the carbons C(3), C(4) and C(5) with one alpha-proton in position 4 and with four nonequivalent beta-protons connected with the carbon atoms C(2) and C(6). The hyperfine tensors of the coupling and the g-tensor of the radicals are given.
通过电子顺磁共振光谱研究了γ辐照的水合睾酮单斜晶体和正交晶体中形成的自由基的分子结构。观察到两种不同类型的自由基。在单斜晶型中,自由基是由碳原子C(2)上的氢原子损失产生的,而在正交晶型中,它是由氢原子加到氧原子O(3)上产生的。单斜单晶中形成的自由基的超精细光谱源于未成对电子与位置2处的一个α-质子以及位置1处的两个不等价β-质子的相互作用。在正交单晶中,我们观察到未成对电子(其离域在碳原子C(3)、C(4)和C(5)上)与位置4处的一个α-质子以及与连接碳原子C(2)和C(6)的四个不等价β-质子之间的相互作用。给出了自由基的耦合超精细张量和g张量。