Ammonia-Borane Derived BN Fragments Trapped on Bi- and Trimetallic Titanium(III) Systems
Authors
Horno Martín, Estefanía delIdentifiers
Permanent link (URI): http://hdl.handle.net/10017/38447DOI: 10.1002/chem.201900083
ISSN: 0947-6539
Date
2019-05-23Embargo end date
2020-03-13Academic Departments
Universidad de Alcalá. Departamento de Química Orgánica y Química Inorgánica
Teaching unit
Unidad docente Química Inorgánica
Funders
Ministerio de Economía y Competitividad
Universidad de Alcalá
Agencia Estatal de Investigación
Bibliographic citation
Chemistry - A European Journal, 2019, v. 25, n. 29, p. 7096-7100
Keywords
Ammonia-borane
Boranes
dehydrogenation
density functional calculations
titanium
Project
info:eu-repo/grantAgreement/UAH//CCG2017-EXP%2F021/ES
info.eu-repo/grantAgreement/AEI//CTQ2013-33625-R/ES
info:eu-repo/grantAgreement/AEI//CTQ2015-64579-C3-1-P/ES/Estructura electrónica y propiedades de moléculas y sólidos
Document type
info:eu-repo/semantics/article
Version
info:eu-repo/semantics/publishedVersion
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
© Wiley-VCH Verlag GmbH & Co. KGaA, 2019
Access rights
info:eu-repo/semantics/openAccess
Abstract
Titanium(III) complexes containing unprecedented (NH2BH2NHBH3)2‒ and {N(BH3)3}3‒ ligands have been isolated and their structures elucidated by a combination of experimental and theoretical methods. The treatment of the trimethyl derivative [TiCp*Me3] (Cp* = η5-C5Me5) with NH3BH3 (3 equiv) at room temperature gives the paramagnetic dinuclear complex [{TiCp*(NH2BH3)}2(μ-NH2BH2NHBH3)], which at 80 ºC leads to the trinuclear hydride derivative [{TiCp*(μ-H)}3{μ3-N(BH3)3}]. The bonding modes of the anionic BN fragments in those complexes as well as the dimethylaminoborane group trapped on the analogous trinuclear [{TiCp*(μ-H)}3(μ3-H)(μ3-NMe2BH2)] have been studied by X-ray crystallography and density functional theory (DFT) calculations.
Files in this item
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| Ammonia_Mena_ChemEurJ_2019.pdf | 799.9Kb |
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