Tetraamine Me6TREN induced monomerization of alkali metal borohydrides and aluminohydrides

被引:14
|
作者
Kennedy, Alan R. [1 ]
McLellan, Ross [1 ]
McNeil, Greg J. [1 ]
Mulvey, Robert E. [1 ]
Robertson, Stuart D. [1 ]
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
Alkali-metal; Borohydride; Aluminohydride; Structure elucidation; NMR spectroscopy; LITHIUM-MEDIATED ALUMINATION; CRYSTAL-STRUCTURES; HYDROGEN; COMPLEXES; HYDRIDES; LIGANDS; LIALH4; LIBH4; DONOR;
D O I
10.1016/j.poly.2015.08.046
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Monomeric 1:1 complexes of MEH4 (M, E = Li, B, 1; Na, B, 2; Li, Al, 3; Na, Al, 4) and the tripodal tetradentate ligand (Me2NCH2CH2)(3)N (Me6TREN) have been prepared in good yields by refluxing in THF and allowing the solutions to cool slowly. X-ray diffraction studies show that the BH4 group binds to either Li or Na via three hydride bridges while the AlH4 group connects to Li via a single hydride bridge. Surprisingly, Me6TREN center dot LiAlH4 represents the first monomeric contacted ion pair LiAlH4 derivative to be structurally characterized. In every case the tetraamine coordinates via all four of its Lewis basic nitrogen atoms. A similar protocol using the alkyl-rich borohydride MBEt3H also gives monomeric species (M = Li, 5; Na, 6). All complexes have been characterized in solution by multinuclear (H-1, Li-7, B-11, C-13 and Al-27, where appropriate) NMR spectroscopy which reveals excellent textbook examples of (1)J coupling between B/Al and H in the cases of complexes 1-4 and between B and C in the cases of complexes 5 and 6. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:94 / 99
页数:6
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