Braden Dale A, Parrack Eileen E, Tyler David R
Department of Chemistry, University of Oregon, Eugene, OR 97403-1253, USA.
Photochem Photobiol Sci. 2002 Jun;1(6):418-20. doi: 10.1039/b202112a.
This paper reports the results of a study that used systematic changes in the solvent viscosity to probe the photochemical reactivity of the Cp'2Mo2(CO)6 (Cp' = eta5-C5H4CH3) molecule. The quantum yields for photolysis of Cp'2Mo2(CO)6 in the presence of CCl4 were studied as a function of solvent viscosity. The quantum yields did not decrease to zero with increasing solvent viscosity but rather leveled off at a constant, non-zero value. This result cannot be explained by any of the previously reported radical or Mo-CO dissociation photochemical pathways for this molecule, and therefore an additional photochemical pathway is suggested to be operating in the reaction. The new pathway may involve a reactive isomer of Cp'2Mo2(CO)6 or possibly electron transfer between the excited state of Cp'2Mo2(CO)6 and CCl4.
本文报道了一项研究结果,该研究利用溶剂粘度的系统变化来探究Cp'2Mo2(CO)6(Cp' = η5-C5H4CH3)分子的光化学反应活性。研究了在CCl4存在下,Cp'2Mo2(CO)6光解的量子产率与溶剂粘度的关系。量子产率并未随着溶剂粘度的增加而降至零,而是稳定在一个恒定的非零值。此前报道的该分子的任何自由基或Mo-CO解离光化学途径都无法解释这一结果,因此建议在该反应中存在一条额外的光化学途径。新途径可能涉及Cp'2Mo2(CO)6的一种反应性异构体,或者可能涉及Cp'2Mo2(CO)6的激发态与CCl4之间的电子转移。