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铌的混合酰胺基/亚氨基/胍基配合物:氮化铌薄膜MOCVD的潜在前驱体。

Mixed amido/imido/guanidinato complexes of niobium: potential precursors for MOCVD of niobium nitride thin films.

作者信息

Baunemann Arne, Bekermann Daniela, Thiede Tobias B, Parala Harish, Winter Manuela, Gemel Christian, Fischer Roland A

机构信息

Lehrstuhl für Anorganische Chemie II, Organometallics and Materials, Ruhr-Universtät Bochum Universitätsstr. 150, D-44780, Bochum, Germany.

出版信息

Dalton Trans. 2008 Jul 28(28):3715-22. doi: 10.1039/b719688a. Epub 2008 Jun 2.

DOI:10.1039/b719688a
PMID:18615218
Abstract

Novel mixed amido/imido/guanidinato complexes of niobium are reported. The complexes were synthesized by insertion of two equivalents of di-isopropylcarbodiimide (i-Pr-cdi) or bis-cyclohexylcarbodiimide (Cy-cdi) respectively, into the niobium-amido bonds of [Nb(NR(2))(3)(N-t-Bu)] (, R = Me; , R = Et) starting out from [NbCl(3)(N-t-Bu)(py)(2)] and the respective LiNR(2) reagent (py = pyridine). Four representative examples of these mixed ligand amido/imido/guanidinato compounds were synthesized and were characterized by (1)H-NMR, (13)C-NMR, (15)N-NMR, CHN-analysis, mass spectrometry and infra-red spectroscopy. The molecular structures of [Nb(NR(2)){eta(2)-(i-Pr-N)(2)C(NR(2))}(2)(N-t-Bu)] (, R = Me; , R = Et) in the solid state were determined by single-crystal X-ray diffraction studies and are discussed together with the molecular structure of the starting compound [Nb(NMe(2))(3)(N-t-Bu)] (). The thermal properties of the new compounds depend on the substitution at the guanidinato ligand. Complexes of i-Pr-cdi are significantly more volatile than complexes of Cy-cdi as revealed by thermogravimetric analysis. Preliminary experiments using as a single-molecule source for metal-organic chemical vapour deposition (MOCVD) in the absence of ammonia indicate the formation of the stoichiometric, and surprisingly carbon-free, cubic niobium nitride phase.

摘要

报道了新型铌的混合酰胺/亚胺/胍基配合物。这些配合物分别通过将两当量的二异丙基碳二亚胺(i-Pr-cdi)或双环己基碳二亚胺(Cy-cdi)插入到[Nb(NR(2))(3)(N-t-Bu)](R = Me;R = Et)的铌-酰胺键中合成,起始原料为[NbCl(3)(N-t-Bu)(py)(2)]和相应的LiNR(2)试剂(py = 吡啶)。合成了这些混合配体酰胺/亚胺/胍基化合物的四个代表性实例,并通过(1)H-NMR、(13)C-NMR、(15)N-NMR、CHN分析、质谱和红外光谱进行了表征。通过单晶X射线衍射研究确定了固态下[Nb(NR(2)){η(2)-(i-Pr-N)(2)C(NR(2))}(2)(N-t-Bu)](R = Me;R = Et)的分子结构,并与起始化合物[Nb(NMe(2))(3)(N-t-Bu)]的分子结构一起进行了讨论。新化合物的热性质取决于胍基配体上的取代情况。热重分析表明,i-Pr-cdi的配合物比Cy-cdi的配合物挥发性明显更高。在没有氨的情况下,使用作为金属有机化学气相沉积(MOCVD)的单分子源的初步实验表明形成了化学计量比的、令人惊讶的无碳立方氮化铌相。

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