首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and characterisation of new titanium amino-alkoxides: precursors for the formation of TiO2 materials
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Synthesis and characterisation of new titanium amino-alkoxides: precursors for the formation of TiO2 materials

机译:新型钛氨基醇盐的合成与表征:TiO2材料形成的前体

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摘要

Reaction of the amino-alkoxides HOCH(CH_2NMe_2)(2) (Hbdmap) and HOC(CH_2NMe_2)_3 (Htdmap) with [Ti(OR)_4] yields a series of heteroleptic titanium alkoxides [Ti(OR)_(4-n)(L)_n)] (L = bdmap, tdmap). Substitution of the monodentate alkoxide with the chelating alkoxides becomes progressively more difficult, with homogeneous products being obtained only for n = 1, 2. The structure of [Ti(ORrEt)_3(bdmap)](_2), a mu-OEt bridged dimer, has been determined. Hydrolysis of [Ti(OR)(_2)(L)(_2)], by adventitious moisture affords the dimeric oxo-alkoxides [Ti(O)(L)(2)](2), both of which have been characterised crystallographically. These two compounds have also been prepared by reaction of [Ti(NMe2)(_2)(L)(2)] with the hydrated metal salts [Zn(acac)(2)center dot 2H(2)O] and [Zn(OAc)(2)center dot 2H(2)O] using the intrinsic water molecules in these salts to react with the labile amido groups, though the former also produces Me(Me2N)C=C(H)C(O)Me from reaction of liberated HNMe2 with the coordinated acac ligand, while the latter also affords the ligand exchange product [Zn(OAc)(bdmap)]. In neither case does the free dimethylamino group of [Ti(O)(L)2]2 coordinate a second metal. The dimeric structure of [Zn(OAc)(bdmap)](2) has been established, and the structure of the tetrameric oxo-alkoxide [Ti(O)(OPri)(OCH2CH2NMe2)](4) is reported for comparison with others in this study. [Ti(OEt),(bdmap)]2 has been used as a precursor in AACVD (Aerosol-Assisted Chemical Vapour Deposition) to generate amorphous TiO2 films on glass at 440 degrees C, and TiO2@C nanoparticles of approximate diameter 350 nm with a carbon coating of width ca. 75 nm on heating in a sealed container at 700 degrees C.
机译:氨基醇盐HOCH(CH_2NMe_2)(2)(Hbdmap)和HOC(CH_2NMe_2)_3(Htdmap)与[Ti(OR)_4]的反应产生了一系列杂配钛醇盐[Ti(OR)_(4-n )(L)_n)](L = bdmap,tdmap)。用螯合的醇盐取代单齿的醇盐变得越来越困难,仅在n = 1、2时才能获得均质产物。[Ti(ORrEt)_3(bdmap)](_ 2)的结构是mu-OEt桥接的二聚体,已确定。不定水分将[Ti(OR)(_ 2)(L)(_ 2)]水解,得到二聚氧代醇盐[Ti(O)(L)(2)](2),这两种晶体均已通过结晶学表征。还可以通过[Ti(NMe2)(_ 2)(L)(2)]与水合金属盐[Zn(acac)(2)中心点2H(2)O]和[Zn( OAc)(2)中心点2H(2)O]使用这些盐中的固有水分子与不稳定的酰胺基反应,尽管前者还会从中产生Me(Me2N)C = C(H)C(O)Me释放的HNMe2与配位的acac配体反应,后者也提供了配体交换产物[Zn(OAc)(bdmap)]。在任何情况下,[Ti(O)(L)2] 2的游离二甲基氨基都不与第二种金属配位。已建立[Zn(OAc)(bdmap)](2)的二聚结构,并报道了四聚氧代醇盐[Ti(O)(OPri)(OCH2CH2NMe2)](4)的结构,以便与他人进行比较在这个研究中。 [Ti(OEt),(bdmap)] 2已被用作AACVD(气溶胶辅助化学气相沉积)的前驱物,以在440摄氏度的玻璃上生成非晶TiO2薄膜,以及直径约为350 nm的TiO2 @ C纳米粒子宽度约为a的碳涂层。在700摄氏度的密闭容器中加热75纳米。

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