Max-Planck-Institut für Bioanorganische Chemie, Stiftstrasse 34-36, D-45470 Mülheim an der Ruhr, Germany.
Phys Chem Chem Phys. 2009 Oct 21;11(39):8680-3. doi: 10.1039/b913635e. Epub 2009 Aug 18.
The light-induced Ni-C to Ni-L transition results in the dissociation of a hydrogenic species, originating from the dihydrogen splitting at the active site. Back conversion in the dark to form Ni-C was investigated by studying the rebinding kinetics of this ligand in protonated (H(2)/H(2)O) and deuterated (D(2)/D(2)O) samples using time resolved FTIR spectroscopy.
光诱导的 Ni-C 到 Ni-L 的转变导致了一种氢化物的离解,该氢化物源自活性位点的氢气分裂。通过使用时间分辨傅里叶变换红外光谱法研究配体在质子化(H(2)/H(2)O)和氘代(D(2)/D(2)O)样品中的复配动力学,研究了在黑暗中向 Ni-C 的逆转化。