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Reactions of Hydrazones and Hydrazides with Lewis Acidic Boranes - data

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posted on 2024-09-18, 10:41 authored by Theodore GazisTheodore Gazis, Ayan DasguptaAyan Dasgupta, MS Hill, JM Rawson, Thomas WirthThomas Wirth, Rebecca MelenRebecca Melen

The reaction of (diphenylmethylene)hydrazone or 1,4-bis-hydraQ4 zone-ylidene(phenyl)methyl)benzene with Lewis acidic boranes B(2,4,6-F3C6H2)3 or B(3,4,5-F3C6H2)3 generates the Lewis acid– base adducts. Alternatively, when (9H-fluoren-9-ylidene)hydrazone is employed then several products were isolated including 1,2-di(9H-fluoren-9-ylidene)hydrazone, the 2 : 1 borane adduct of NH2–NH2 and the 1-(diarylboraneyl)-2-(9H-fluoren-9-ylidene) hydrazone in which one ArH group has been eliminated. The benzhydrazide starting material also initially gives an adduct when reacted with Lewis acidic boranes which upon heating eliminates ArH generating a CON2B heterocycle.

Data is provided for the synthesis and characterisation of the compounds generated in this project.

Research results based upon these data are published at http://doi.org/10.1039/C9DT01359H


Funding

From Organic to Inorganic Chemistry: Exploiting the Isolobal Analogy to Develop Main Group Catalysts

Engineering and Physical Sciences Research Council

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History

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Mercury, SHELEX, MNova

Data-collection start date

2018-07-01

Data-collection end date

2019-05-31

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    School of Chemistry

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