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Medium and pressure effects on the reactivity and spectra of iron(ii)-diimine complexes.

机译:介质和压力对铁(ii)-二亚胺配合物的反应性和光谱的影响。

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摘要

Solvation trends of ternary iron(II)-cyanide-diimine complexes in binary aqueous media are examined using spectroscopic and thermodynamic techniques. The observed trends are discussed in terms of the solvent-solute interactions present, and how the relative importance of these interactions varies with the technique and the complex. Crystallographic data for two of these structures are reported and show the effect of the solvate molecules on the structure. Pressure effects on MLCT frequencies are investigated, and the correlation between piezochromic and solvatochromic effects for mono- and binuclear iron(II) and iron(III)-diimine complexes is shown. Pressure and solvent modification of the rate of oxidation of a series of iron(II)-diimine complexes are interpreted and discussed in terms of the solvation changes that occur upon transition state formation. Complementary partial molar volume data for these complexes are also reported, and combined to form a volume profile for one reactant pair. The structure of a binuclear iron(II)-diimine complex is examined in the solid state and in solution. Solvation trends in binary aqueous media are reported for this binuclear cation, and comparisons are made with mononuclear iron(II) and cobalt(III), and with binuclear cobalt(III) complexes. Kinetics of base hydrolysis of several binuclear iron(II)-diimine complexes are discussed in terms of the structural differences between these complexes. The effects of added organic cosolvents on the rate constants for one of these binuclear complexes is also reported. Spectroscopic evidence for a ligand substituted intermediate is found. The structure of such intermediates is discussed with respect to existing data for mononuclear iron(II)-diimine complexes. Finally, a preliminary chemical and electrochemical redox investigation is made on the most suitable binuclear iron(II)-diimine complex in light of the base hydrolysis reactivity patterns established.
机译:使用光谱学和热力学技术研究了二元水性介质中三价铁(II)-氰化物-二亚胺配合物的溶剂化趋势。根据存在的溶剂-溶质相互作用以及这些相互作用的相对重要性如何随技术和复合物变化而讨论了观察到的趋势。报告了其中两个结构的晶体学数据,并显示了溶剂化物分子对该结构的影响。研究了压力对MLCT频率的影响,并显示了单核和双核铁(II)和铁(III)-二亚胺络合物的变色和变色效应之间的相关性。根据过渡态形成时发生的溶剂化变化来解释和讨论一系列铁(II)-二亚胺配合物的氧化速率的压力和溶剂改性。还报告了这些配合物的补充部分摩尔体积数据,并将其合并以形成一对反应物的体积分布。在固态和溶液中检查双核铁(II)-二亚胺配合物的结构。已报道了该双核阳离子在二元水性介质中的溶剂化趋势,并与单核铁(II)和钴(III)以及双核钴(III)配合物进行了比较。根据这些配合物之间的结构差异,讨论了几种双核铁(II)-二亚胺配合物的碱水解动力学。还报道了添加的有机助溶剂对这些双核络合物之一的速率常数的影响。发现了配体取代的中间体的光谱证据。关于单核铁(II)-二亚胺配合物的现有数据,讨论了这类中间体的结构。最后,根据建立的碱水解反应模式,对最合适的双核铁(II)-二亚胺配合物进行了初步的化学和电化学氧化还原研究。

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  • 作者

    Blundell, Nicholas J.;

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  • 年度 1991
  • 总页数
  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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