Macpherson Brendan P, Alzoubi Basam M, Bernhardt Paul V, Martínez Manuel, Tregloan Peter A, van Eldik Rudi
Department of Chemistry, University of Queensland, Brisbane, 4072, Australia.
Dalton Trans. 2005 Apr 21(8):1459-67. doi: 10.1039/b418054b. Epub 2005 Mar 17.
The effects of pressure and temperature on the energy (Eop) of the metal-to-metal charge transfer (MMCT, FeII-->CoIII) transition of the cyano-bridged complexes trans-[L14CoNCFe(CN)5]- and cis-[L14CoNCFe(CN)5]- (where L14=6-methyl-1,4,8,11-tetraazacyclotetradecan-6-amine) were examined. The changes in the redox potentials of the cobalt and iron metal centres with pressure and temperature were also examined and the results interpreted with Marcus-Hush theory. The observed redox reaction volumes can mainly be accounted for in terms of localised electrostriction effects. The shifts in Eop due to both pressure and temperature were found to be less than the shifts in the energy difference (DeltaE degrees]) between the CoIII-FeII and CoII-FeIII redox isomers. The pressure and temperature dependence of the reorganisational energy, as well as contributions arising from the different spin states of CoII, are discussed in order to account for this trend. To study the effect of pressure on CoIII electronic absorption bands, a new cyano-bridged complex, trans-[L14CoNCCo(CN)5], was prepared and characterised spectroscopically and structurally. X-Ray crystallography revealed this complex to be isostructural with trans-[L14CoNCFe(CN)5].5H2O.
研究了压力和温度对氰基桥联配合物反式-[L14CoNCFe(CN)5]-和顺式-[L14CoNCFe(CN)5]-(其中L14 = 6-甲基-1,4,8,11-四氮杂环十四烷-6-胺)的金属-金属电荷转移(MMCT,FeII→CoIII)跃迁能量(Eop)的影响。还研究了钴和铁金属中心的氧化还原电位随压力和温度的变化,并根据Marcus-Hush理论对结果进行了解释。观察到的氧化还原反应体积主要可以用局部电致伸缩效应来解释。发现由于压力和温度导致的Eop位移小于CoIII-FeII和CoII-FeIII氧化还原异构体之间的能量差(ΔE°)的位移。为了解释这一趋势,讨论了重组能的压力和温度依赖性以及CoII不同自旋态产生的贡献。为了研究压力对CoIII电子吸收带的影响,制备了一种新的氰基桥联配合物反式-[L14CoNCCo(CN)5],并通过光谱和结构表征。X射线晶体学表明该配合物与反式-[L14CoNCFe(CN)5]·5H2O同构。