Gao Yunlong, Kispert Lowell D, van Tol Johan, Brunel Louis-Claude
Key Lab of Analytical Chemistry for Life Science, Department of Chemistry, Nanjing University, Nanjing, 210093, People's Republic of China.
J Phys Chem B. 2005 Oct 6;109(39):18289-92. doi: 10.1021/jp052550v.
Perdeuterated all-trans beta-carotene imbedded in activated Cu-MCM-41 was examined by electron paramagnetic resonance (EPR) and electron spin-echo envelope modulation (ESEEM) spectroscopies. The EPR study showed that complexation and electron transfer between Cu2+ and deuterated beta-carotene occurs. The interaction was confirmed by detecting the spin-echo modulation of deuterium in the ESEEM spectra of Cu2+. Ratio analysis of ESEEM was used to determine the number of deuterons which interact with Cu2+ and the distance between deuteron(s) and Cu2+. The bonding site of beta- carotene determined by ESEEM and pulse electron nuclear double resonance is the C15=C15' double bond.
通过电子顺磁共振(EPR)和电子自旋回波包络调制(ESEEM)光谱对嵌入活化Cu-MCM-41中的全氘代全反式β-胡萝卜素进行了研究。EPR研究表明,Cu2+与氘代β-胡萝卜素之间发生了络合和电子转移。通过检测Cu2+的ESEEM光谱中氘的自旋回波调制,证实了这种相互作用。利用ESEEM的比率分析来确定与Cu2+相互作用的氘核数量以及氘核与Cu2+之间的距离。通过ESEEM和脉冲电子核双共振确定的β-胡萝卜素的结合位点是C15=C15'双键。