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2,4,6-Tris-(4-fluoro-phen-yl)-2-(1-pyrid-yl)-boroxine.

作者信息

Pearson Wayne H, Lin Shirley, Iovine Peter M

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2007 Dec 12;64(Pt 1):o235. doi: 10.1107/S1600536807064367.

DOI:10.1107/S1600536807064367
PMID:21200802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2915295/
Abstract

Crystals of the title compound, C(23)H(17)B(3)F(3)NO(3), were obtained unintentionally by slow evaporation of a chloro-form solution of the preformed boroxine-pyridine adduct. The mol-ecule contains three fluoro-substituted benzene rings, each bonded to one of the three B atoms of a six-membered boroxine ring. A pyridyl ring is also bound to one of the B atoms through a Lewis acid-base inter-action. The binding of the pyridyl substituent causes the otherwise planar boroxine ring to twist, resulting in a maximum torsion angle within the ring of 17.6 (2)°.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ccc/2915295/0ea0c0e26636/e-64-0o235-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ccc/2915295/f9f35670b0c0/e-64-0o235-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ccc/2915295/0ea0c0e26636/e-64-0o235-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ccc/2915295/f9f35670b0c0/e-64-0o235-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ccc/2915295/0ea0c0e26636/e-64-0o235-fig2.jpg

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本文引用的文献

1
Effect of para-substituents and solvent polarity on the formation of triphenylboroxine.amine adducts.对位取代基和溶剂极性对三苯基硼氧烷-胺加合物形成的影响。
J Phys Chem A. 2006 Jul 6;110(26):8158-66. doi: 10.1021/jp062055e.