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Incorporation of 4d and 5d transition metal cyanometallates into magnetic clusters and materials.

机译:将4d和5d过渡金属氰基金属盐掺入磁性簇和材料中。

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摘要

The work presented herein describes efforts to synthesize and characterize new types of cyanide-bridged molecular materials encompassing both discrete clusters and extended solids. This investigation focused on the incorporation of anisotropic 4d and 5d transition metal ion building blocks into such materials. In this vein, systematic studies on the magnetic properties of families of these cyano-bridges species were conducted and these new materials represent a new addition to the field of cyanide chemistry incorporating for the first time the hexacyanometallates of [Ru(CN)6]3- and [Os(CN)6]3- into discrete molecules and extended networks. These compounds will serve as models for new theoretical studies in understanding the role of magnetic exchange interactions, both isotropic and anisotropic, in the study of nanomagnetic materials.;Results were obtained from using the well known octacyanometallates of MoV and WV as building blocks for the synthesis and the magnetic investigation of both trigonal bipyramidal and pentadecanuclear clusters including the discovery of a new SMM. By expanding the research to previously unused hexacyanometallates, the synthesis and characterization of the first known examples of clusters based on hexacyanoosmate(III) and hexacyanoruthenate(III) building blocks and their use in preparing new theoretical models of magnetic species. A novel pair of clusters is further detailed in the study of the trigonal bipyramidal clusters of [Fe(tmphen)2] 3[Os(CN)6]2 and [Fe(tmphen)2] 3[Ru(CN)6]2 and an in depth study of the CTIST behavior of these clusters using Mossbauer spectroscopy, variable temperature crystallography, epr, and variable temperature IR measurements. Finally, this work discusses new magnetic Prussian Blue analogs prepared from the hexacyanoosmate(III) and hexacyanoruthenate(III) anions with a comparison to the trigonal bipyramidal clusters presented based on these hexacyanoosmate(III) and hexacyanoruthenate(III) building blocks.
机译:本文介绍的工作描述了合成和表征新型氰化物桥接分子材料的工作,这些材料涵盖了离散的簇和扩展的固体。这项研究的重点是将各向异性的4d和5d过渡金属离子构建基结合到此类材料中。在这种情况下,对这些氰基桥物种的族的磁性进行了系统的研究,这些新材料代表了氰化物化学领域的新成员,该领域首次包含了[Ru(CN)6] 3的六氰基金属盐。 -和[Os(CN)6] 3-转化为离散分子和扩展网络。这些化合物将作为新的理论研究的模型,以了解各向同性和各向异性的磁交换相互作用在纳米磁性材料研究中的作用。;通过使用众所周知的MoV和WV八氰基金属酸盐作为分子结构的基础而获得了结果。三角锥体和五核簇的合成和磁学研究,包括发现新的SMM。通过将研究扩展到以前未使用的六氰基金属盐,合成和表征了基于六氰基甲酸酯(III)和六氰基甲酸酯(III)构建基团的第一个已知实例,并将其用于制备磁性物种的新理论模型。在[Fe(tmphen)2] 3 [Os(CN)6] 2和[Fe(tmphen)2] 3 [Ru(CN)6] 2的三角双锥体簇的研究中,将进一步详细描述一对新的簇。并使用Mossbauer光谱,可变温度晶体学,epr和可变温度IR测量对这些簇的CTIST行为进行了深入研究。最后,这项工作讨论了由六氰氨基甲酸酯(III)和六氰基尿酸酯(III)阴离子制备的新型磁性普鲁士蓝类似物,并与基于这些六氰基氨基甲酸酯(III)和六氰基甲酸酯(III)构建基团的三角双锥体团簇进行了比较。

著录项

  • 作者

    Hilfiger, Matthew Gary.;

  • 作者单位

    Texas A&M University.;

  • 授予单位 Texas A&M University.;
  • 学科 Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 234 p.
  • 总页数 234
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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