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Cyanide bridged multimetallics derived from extended arrays of alkaline earth, rare earth, and transition metals: A study from complexes to catalysts.

机译:氰化物桥接的多金属化合物,其衍生自碱土,稀土和过渡金属的扩展阵列:从络合物到催化剂的研究。

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摘要

Several new cyanide bridged bimetallic compounds were synthesized for use as novel heterogeneous catalysts. With this in mind specific metal -- metal combinations were chosen. In the search for bimetallic catalyst precursors containing either cobalt or iron, two new alkaline earth(II) hexacyanometalate(III) complexes, (DMF)14Sr3[M(CN)6]2 (DMF = N,N-dimethylformamide; M = Co or Fe), were synthesized using a novel preparation utilizing both DMF and H2O as solvents. Several new alkaline earth(II) tetracyanometalate(II) (DMF)nAeM(CN) 4 (Ae = Sr, Ba, and Ca; M = Pd and Pt) were synthesized as well. The strontium palladium containing complexes were converted to bimetallic heterogeneous catalysts and served as excellent hydrodechlorination catalysts.;In view of their use as catalytic precursors, several experiments were devised to study rare earth(III) tetracyanometalate(II) [(DMF)5Ln] 2[M(CN)4]3 (M = Ni, Pd, and Pt) combinations. A new synthesis, again utilizing H2O, was devised to reduce synthesis time from two weeks to a few days. Several new complexes containing interstitial K2M(CN)4 units were synthesized. The rare earth to catalytic metal ratio (2:3 in the previously studied complexes) was changed to one to one by varying reaction conditions and new (DMF)5LnXM(CN) 4 (X = Cl- or NO3-) complexes were synthesized. All complexes were characterized by IR, elemental analysis, and single crystal X-ray diffraction.;Supported bimetallic catalysts were prepared using a novel reduction method. A solution of ammonia borane in tetrahydrofuran replaced hydrogen as the reducing agent in the conversion of the precursors into SiO2 supported catalysts. XPS studies of these catalysts confirm that both metals from the precursor material are reduced by ammonia borane. A model Suzuki coupling reaction was used to test these new catalysts. These studies confirm that YbPd/SiO2 reduced with ammonia borane from the precursor [(DMF) 5Yb]2[Pd(CN)4]3 is an active catalysts in the Suzuki coupling of phenylboronic acid with 4'-iodoacetophenone.
机译:合成了几种新的氰化物桥联的双金属化合物用作新型多相催化剂。考虑到这一点,选择了特定的金属-金属组合。在寻找含有钴或铁的双金属催化剂前体时,需要使用两种新的碱土金属(II)六氰基金属酸盐(III)配合物(DMF)14Sr3 [M(CN)6] 2(DMF = N,N-二甲基甲酰胺; M = Co使用DMF和H2O作为溶剂的新型制备方法合成。还合成了几种新的碱土金属(II)四氰基金属盐(II)(DMF)nAeM(CN)4(Ae = Sr,Ba和Ca; M = Pd和Pt)。含锶钯配合物被转化为双金属多相催化剂,并作为优异的加氢脱氯催化剂。鉴于其作为催化前体的用途,设计了一些实验来研究稀土金属氰化物(III)四氰基金属酸盐(II)[(DMF)5Ln] 2 [M(CN)4] 3(M = Ni,Pd和Pt)组合。设计了再次利用H 2 O的新合成方法,以将合成时间从两周减少至几天。几个新的复合物,包含间隙K2M(CN)4单位。通过改变反应条件,稀土金属与催化金属的比例(在先前研究的配合物中为2:3)变为一对一,并合成了新的(DMF)5LnXM(CN)4(X = Cl-或NO3-)配合物。通过IR,元素分析和单晶X射线衍射对所有配合物进行表征。采用新型还原方法制备了负载型双金属催化剂。在将前体转化为SiO2负载的催化剂时,氨硼烷在四氢呋喃中的溶液代替氢气作为还原剂。对这些催化剂的XPS研究证实,氨硼烷可以还原前体材料中的两种金属。使用铃木偶合反应模型测试了这些新催化剂。这些研究证实,从前体[(DMF)5Yb] 2 [Pd(CN)4] 3用氨硼烷还原的YbPd / SiO2是苯硼酸与4'-碘苯乙酮的铃木偶联反应中的活性催化剂。

著录项

  • 作者

    Sturgeon, Matthew Robert.;

  • 作者单位

    The Ohio State University.;

  • 授予单位 The Ohio State University.;
  • 学科 Chemistry General.;Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 190 p.
  • 总页数 190
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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