Photochromism of an Organorhodium Dithionite Complex in the Crystalline-State: Molecular Motion of Pentamethylcyclopentadienyl Ligands Coupled to Atom Rearrangement in a Dithionite Ligand

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• 作者：Hidetaka Nakai ; Takashi Nonaka ; Yousuke Miyano ; Motohiro Mizuno ; Yoshiki Ozawa ; Koshiro Toriumi ; Nobuaki Koga ; Takanori Nishioka ; Masahiro Irie ; Kiyoshi Isobe
• 刊名：Journal of the American Chemical Society
• 出版年：2008
• 出版时间：December 31, 2008
• 年：2008
• 卷：130
• 期：52
• 页码：17836-17845
• 全文大小：613K
• 年卷期：v.130,no.52(December 31, 2008)
• ISSN：1520-5126

文摘

In the crystalline state, the rhodium dinuclear complex [(RhCp*)₂(μ-CH₂)₂(μ-O₂SSO₂)] (1) with a photoresponsive dithionite group (μ-O₂SSO₂) and two pentamethylcyclopentadienyl ligands (Cp* = η⁵-C₅Me₅) undergoes a 100% reversible unimolecular type T inverse photochromism upon interconversion to [(RhCp*)₂(μ-CH₂)₂(μ-O₂SOSO)] (2). The photochromism can be followed directly by using stepwise crystal structure analysis (Angew. Chem., Int. Ed. 2006, 45, 6473). In this study, we found that the photoreaction of 1 was triggered by absorption of the 510 nm light (charge transfer band from σ(S−S) to σ*(S−S) and σ*(Rh−Rh) orbitals assigned by DFT calculation) and included two important processes: kinetically controlled oxygen-atom transfer to produce four stereoisomers of 2 and thermodynamically controlled isomerization between the four stereoisomers of 2 to afford the most stable isomer. Although the formation rate of the four stereoisomer products was kinetically controlled and the population of the four stereoisomers produced in the system was thermodynamically controlled, both processes were regulated by the steric hindrance between the μ-O₂SSO₂ or μ-O₂SOSO ligand and the reaction cavity formed by the Cp* ligands. The cooperation of both processes achieved an intriguing stereospecific oxygen-atom rearrangement to produce only one stereoisomer of 2 at the final stage of the photoreaction at room temperature. We also determined the effect of the oxygen-atom rearrangement on the rotational motion of the two crystallographically independent Cp* ligands (parallel and perpendicular arrangement). Using variable-temperature ¹³C CP/MAS NMR and quadrupolar echo solid-state ²H NMR spectroscopies, before photoirradiation, the activation energies for the rotation of the parallel and perpendicular Cp* ligands in 1 were determined to be 33 ± 3 and 7.8 ± 1 kJ/mol, respectively, and after photoirradiation, in 2, they were much lower than those in 1 (21 ± 2 and 4.7 ± 0.5 kJ/mol, respectively). The large decrease in the activation energy for the parallel Cp* in 2 is attributed to the relaxation of molecular stress via a stereospecific oxygen-atom rearrangement, which suggests that the rotational motion of the Cp* ligands is coupled to the photochromism.