Structures and photoactivation of the charge-transfer complexes of bis(arene)iron(II) dications with ferrocene and arene donors
Structures and photoactivation of the charge-transfer complexes of bis(arene)iron(II) dications with ferrocene and arene donors
复制标题
双(芳烃)铁(II)阳离子与二茂铁和芳烃供体的电荷转移配合物的结构和光活化
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发表时间：
1991
期刊：
影响因子：
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通讯作者：
J. Kochi
中科院分区：
文献类型：
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作者：
R. Lehmann;J. Kochi
Ferrocene forms a series of unusual charge-transfer crystals with the isoelectronic bis(arene)iron(II) dication, in which X-ray crystallography establishes the alternate (heterosoric) stacking of sandwich structures comprising the donor-acceptor pairs. In acetonitrile, the 1:1 complex (Cp{sub 2}Fe, Ar{sub 2}Fe{sup 2+}) shows a broad absorption band centered at {lambda}{sub max} {approximately} 630 nm. Bis(arene)iron(II) acceptors also form highly colored crystals with various arene donors, in which the charge-transfer absorption (hv{sub CT}) derives from the same heterosoric stacking of donor-acceptor pairs-despite the structurally divergent nature of the arene (planar) and ferrocene (sandwich) donors. These absorptions undergo a predictable red-shift with increasing acceptor strength in the order (BZ){sub 2}Fe{sup 2+} > (MES){sub 2}Fe{sup 2+} > (DUR){sub 2}Fe{sup 2+} > (HMB){sub 2}Fe{sup 2+}, as judged by the reduction potentials E {sub red} of the benzene, mesitylene, durene, and hexamethylbenzene derivatives, respectively.
Ferrocene forms a series of unusual charge-transfer crystals with the isoelectronic bis(arene)iron(II) dication, in which X-ray crystallography establishes the alternate (heterosoric) stacking of sandwich structures comprising the donor-acceptor pairs. In acetonitrile, the 1:1 complex (Cp{sub 2}Fe, Ar{sub 2}Fe{sup 2+}) shows a broad absorption band centered at {lambda}{sub max} {approximately} 630 nm. Bis(arene)iron(II) acceptors also form highly colored crystals with various arene donors, in which the charge-transfer absorption (hv{sub CT}) derives from the same heterosoric stacking of donor-acceptor pairs-despite the structurally divergent nature of the arene (planar) and ferrocene (sandwich) donors. These absorptions undergo a predictable red-shift with increasing acceptor strength in the order (BZ){sub 2}Fe{sup 2+} > (MES){sub 2}Fe{sup 2+} > (DUR){sub 2}Fe{sup 2+} > (HMB){sub 2}Fe{sup 2+}, as judged by the reduction potentials E {sub red} of the benzene, mesitylene, durene, and hexamethylbenzene derivatives, respectively.