Reactivity of vanadium oxytrichloride with β-diketones and diesters as precursors for vanadium nitride and carbide

被引:13
作者
Blackburn, Ben J. [1 ]
Crane, Jared H. [1 ]
Knapp, Caroline E. [1 ]
Powell, Michael J. [1 ]
Marchand, Peter [1 ]
Pugh, David [2 ]
Bear, Joseph C. [1 ]
Parkin, Ivan P. [1 ]
Carmalt, Claire J. [1 ]
机构
[1] UCL, Dept Chem, Mat Chem Ctr, 20 Gordon St, London WC1H 0AJ, England
[2] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
基金
英国工程与自然科学研究理事会;
关键词
Vanadium oxychloride; Precursors; Ester adducts; Vanadium carbide; Vanadium nitride; Hard materials; CHEMICAL-VAPOR-DEPOSITION; TRANSITION-METAL CARBIDES; SOLID-STATE SYNTHESIS; CRYSTAL-STRUCTURES; LOW-TEMPERATURE; MECHANICAL-PROPERTIES; COORDINATION POLYMER; VN; COMPLEXES; TITANIUM;
D O I
10.1016/j.matdes.2016.06.029
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Vanadium(V) oxytrichloride was reacted with 2,4-pentanedione, diethyl malonate, and diethyl succinate under inert conditions, forming compounds: dichloro(oxo)(2,4-pentanedione) vanadium(V) [1], dichloro(oxo)(diethyl malonate) vanadium(IV) [2] and dichloro(oxo)(diethyl succinate) vanadium(IV) [3]. Compounds 1-3 are coordinated to the vanadium centre through the two carbonyl oxygen atoms of the bidentate ligand. It was determined by X-ray crystallography that the structures of the resulting complexes were significantly different, resulting in a monomeric complex (1), a tetrameric ring (2) and a 1D coordination polymer (3). Following the synthesis and isolation of 1-3, they were tested as precursors for vanadium nitride and vanadium carbide by annealing under nitrogen and argon respectively at 1200 degrees C for 24 h. The resulting materials were characterised by: XRD, EDS, XPS and TEM. (C) 2016 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:780 / 790
页数:11
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