The Structure of Boron Monoxide

被引:9
作者
Perras, Frederic A. [1 ,2 ]
Thomas, Henry [1 ]
Heintz, Patrick [1 ]
Behera, Ranjan [1 ]
Yu, Jiaqi [1 ]
Viswanathan, Gayatri [1 ,2 ]
Jing, Dapeng [3 ]
Southern, Scott A. [2 ]
Kovnir, Kirill [1 ,2 ]
Stanley, Levi [1 ]
Huang, Wenyu [1 ,2 ]
机构
[1] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
[2] Ames Natl Lab, Chem & Biol Sci Div, Ames, IA 50011 USA
[3] Iowa State Univ, Mat Anal & Res Lab, Ames, IA 50011 USA
关键词
SOLID-STATE NMR; NUCLEAR-MAGNETIC-RESONANCE; INTEGER QUADRUPOLAR NUCLEI; DOUBLE-QUANTUM NMR; CHEMICAL-SHIFT; OXIDATIVE DEHYDROGENATION; SINGLE-CRYSTAL; TENSOR CORRELATION; TORSION ANGLES; NITRIDE;
D O I
10.1021/jacs.3c02070
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Boron monoxide (BO), prepared by the thermal condensationof tetrahydroxydiboron,was first reported in 1955; however, its structure could not be determined.With the recent attention on boron-based two-dimensional materials,such as borophene and hexagonal boron nitride, there is renewed interestin BO. A large number of stable BO structures have been computationallyidentified, but none are supported by experiments. The consensus isthat the material likely forms a boroxine-based two-dimensional material.Herein, we apply advanced B-11 NMR experiments to determinethe relative orientations of B(B)O-2 centers in BO. We findthat the material is composed of D (2h )-symmetric O2B-BO2 units thatorganize to form larger B4O2 rings. Further,powder diffraction experiments additionally reveal that these unitsorganize to form two-dimensional layers with a random stacking pattern.This observation is in agreement with earlier density functional theory(DFT) studies that showed B4O2-based structuresto be the most stable.
引用
收藏
页码:14660 / 14669
页数:10
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