首页> 外文期刊>Journal of physical chemistry letters >Electron Spin Polarization Transfer to ortho-H-2 by Interaction of para-H-2 with Paramagnetic Species: A Key to a Novel para -> ortho Conversion Mechanism
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Electron Spin Polarization Transfer to ortho-H-2 by Interaction of para-H-2 with Paramagnetic Species: A Key to a Novel para -> ortho Conversion Mechanism

机译:对位H-2与顺磁性物质相互作用将电子自旋极化转移至邻位H-2:新颖的对位>邻位转化机制的关键

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We report that at ambient temperature and with 100% enriched para-hydrogen (p-H-2) dissolved in organic solvents, paramagnetic spin catalysis of para -> ortho hydrogen conversion is accompanied at the onset by a negative ortho-hydrogen (o-H-2) proton NMR signal. This novel finding indicates an electron spin polarization transfer, and we show here that this can only occur if the H-2 molecule is dissociated upon its transient adsorption by the paramagnetic catalyst. Following desorption, o-H-2 is created until the thermodynamic equilibrium is reached. A simple theory confirms that in the presence of a static magnetic field, the hyperfine coupling between unpaired electrons and nuclear spins is responsible for the observed polarization transfer. Owing to the negative electron gyromagnetic ratio, this explains the experimental results and ascertains an as yet unexplored mechanism for para -> ortho conversion. Finally, we show that the recovery of o-H-2 magnetization toward equilibrium can be simply modeled, leading to the para -> ortho conversion rate.
机译:我们报告说,在环境温度下,当有机溶剂中溶解有100%富集的对氢(pH-2)时,对->原氢转化的顺磁自旋催化作用伴随着负的原氢(oH-2)的发生。质子NMR信号。这个新发现表明了电子自旋极化转移,我们在这里表明只有在H-2分子在顺磁性催化剂的瞬时吸附作用下解离时才会发生。解吸后,生成o-H-2,直到达到热力学平衡。一个简单的理论证实,在存在静磁场的情况下,未配对电子与核自旋之间的超精细耦合是观察到的极化转移的原因。由于负电子回旋磁比,这解释了实验结果并确定了对->原位转化的尚未探索的机理。最后,我们表明可以简单地模拟o-H-2磁化向平衡的恢复,从而导致对位->原位转化率。

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