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含脒基配体以及η2-吡唑基、η(2)-1,2,4-三唑基或η1-四唑基配体的铬(III)配合物的合成、结构表征及性质

Synthesis, structural characterization, and properties of chromium(III) complexes containing amidinato ligands and eta2-pyrazolato, eta(2)-1,2,4-triazolato, or eta1-tetrazolato ligands.

作者信息

El-Kadri Oussama M, Heeg Mary Jane, Winter Charles H

机构信息

Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, Michigan 48202, USA.

出版信息

Dalton Trans. 2006 Oct 7(37):4506-13. doi: 10.1039/b607903b. Epub 2006 Jul 31.

Abstract

Treatment of anhydrous chromium(III) chloride with 2 or 3 equivalents of 1,3-di-tert-butylacetamidinatolithium or 1,3-diisopropylacetamidinatolithium in tetrahydrofuran at ambient temperature afforded Cr(tBuNC(CH3)NtBu)2(Cl)(THF) and Cr(iPrNC(CH3)NiPr)3 in 78% and 65% yields, respectively. Treatment of Cr(tBuNC(CH3)NtBu)2(Cl)(THF) with the potassium salts derived from pyrazoles and 1,2,4-triazoles afforded Cr(tBuNC(CH3)NtBu)2(X), where X=3,5-disubstituted pyrazolato or 3,5-disubstituted 1,2,4-triazolato ligands, in 65-70% yields. X-Ray crystal structure analyses of Cr(tBuNC(CH3)NtBu)2(Me2pz) (Me2pz=3,5-dimethylpyrazolato) and Cr(tBuNC(CH3)NtBu)2(Me2trz) (Me2trz=3,5-dimethyl-1,2,4-triazolato) revealed eta2-coordination of the Me2pz and Me2trz ligands. Treatment of Cr(tBuNC(CH3)NtBu)2(Cl)(THF) with trifluoromethyltetrazolatosodium (NaCF3tetz) in the presence of 4-tert-butylpyridine afforded Cr(tBuNC(CH3)NtBu)2(CF3tetz)(4-tBupy) in 30% yield. An X-ray crystal structure determination showed eta1-coordination of the tetrazolato ligand through the 2-nitrogen atom. The complexes Cr(iPrNC(CH3)NiPr)3 and Cr(tBuNC(CH3)NtBu)2(X) are volatile and sublime with <1% residue between 120 and 165 degrees C at 0.05 Torr. In addition, these complexes are thermally stable at >300 degrees C under an inert atmosphere such as nitrogen or argon. Due to the good volatility and high thermal stability, these new compounds are promising precursors for the growth of chromium-containing thin films using atomic layer deposition.

摘要

在室温下,于四氢呋喃中用2或3当量的1,3 - 二叔丁基乙酰脒基锂或1,3 - 二异丙基乙酰脒基锂处理无水三氯化铬,分别以78%和65%的产率得到Cr(tBuNC(CH3)NtBu)2(Cl)(THF)和Cr(iPrNC(CH3)NiPr)3。用吡唑和1,2,4 - 三唑衍生的钾盐处理Cr(tBuNC(CH3)NtBu)2(Cl)(THF),得到产率为65 - 70%的Cr(tBuNC(CH3)NtBu)2(X),其中X = 3,5 - 二取代吡唑基或3,5 - 二取代1,2,4 - 三唑基配体。Cr(tBuNC(CH3)NtBu)2(Me2pz)(Me2pz = 3,5 - 二甲基吡唑基)和Cr(tBuNC(CH3)NtBu)2(Me2trz)(Me2trz = 3,5 - 二甲基 - 1,2,4 - 三唑基)的X射线晶体结构分析表明Me2pz和Me2trz配体为η2配位。在4 - 叔丁基吡啶存在下,用三氟甲基四唑钠(NaCF3tetz)处理Cr(tBuNC(CH3)NtBu)2(Cl)(THF),以30%的产率得到Cr(tBuNC(CH3)NtBu)2(CF3tetz)(4 - tBupy)。X射线晶体结构测定表明四唑基配体通过2 - 氮原子为η1配位。配合物Cr(iPrNC(CH3)NiPr)3和Cr(tBuNC(CH3)NtBu)2(X)具有挥发性,在0.05托的压力下于120至165摄氏度之间升华,残留量小于1%。此外,这些配合物在氮气或氩气等惰性气氛下于300摄氏度以上热稳定。由于良好的挥发性和高热稳定性,这些新化合物有望成为使用原子层沉积法生长含铬薄膜的前驱体。

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