MacArthur R, Sucheta A, Chong F F, Einarsdóttir O
Department of Chemistry and Biochemistry, University of California, Santa Cruz, 95064, USA.
Proc Natl Acad Sci U S A. 1995 Aug 29;92(18):8105-9. doi: 10.1073/pnas.92.18.8105.
Upon photolysis at 355 nm, dioxygen is released from a (mu-peroxo)(mu-hydroxo)bis[bis(bipyridyl)cobalt-(III)] complex in aqueous solutions and at physiological pH with a quantum yield of 0.04. The [Co(bpy)2(H2O)2]2+ (bpy = bipyridyl) photoproduct was generated on a nanosecond or faster time scale as determined by time-resolved optical absorption spectroscopy. A linear correspondence between the spectral changes and the oxygen production indicates that O2 is released on the same time scale. Oxyhemoglobin was formed from deoxyhemoglobin upon photodissociation of the (mu-peroxo) (mu-hydroxo)bis[bis(bipyridyl)cobalt(III)] complex, verifying that dioxygen is a primary photoproduct. This complex and other related compounds provide a method to study fast biological reactions involving O2, such as the reduction of dioxygen to water by cytochrome oxidase.
在355nm光解时,二氧从水溶液中及生理pH条件下的(μ-过氧)(μ-羟基)双[双(联吡啶)钴(III)]配合物中释放出来,量子产率为0.04。通过时间分辨光吸收光谱测定,[Co(bpy)2(H2O)2]2+(bpy = 联吡啶)光产物在纳秒或更快的时间尺度上生成。光谱变化与氧气产生之间的线性对应关系表明O2在相同的时间尺度上释放。(μ-过氧)(μ-羟基)双[双(联吡啶)钴(III)]配合物光解离后,脱氧血红蛋白形成了氧合血红蛋白,证实二氧是主要光产物。该配合物及其他相关化合物提供了一种研究涉及O2的快速生物反应的方法,例如细胞色素氧化酶将二氧还原为水的反应。