Catalytic Dehydrogenation of Amine-Boranes using Geminal Phosphino-Boranes

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http://hdl.handle.net/10138/318384

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Boom , D H A , de Boed , E J J , Nicolas , E , Nieger , M , Ehlers , A W , Jupp , A R & Slootweg , J C 2020 , ' Catalytic Dehydrogenation of Amine-Boranes using Geminal Phosphino-Boranes ' , Zeitschrift für anorganische und allgemeine Chemie , vol. 646 , no. 13 , pp. 586-592 . https://doi.org/10.1002/zaac.201900313

Title: Catalytic Dehydrogenation of Amine-Boranes using Geminal Phosphino-Boranes
Author: Boom, Devin H. A.; de Boed, Ewoud J. J.; Nicolas, Emmanuel; Nieger, Martin; Ehlers, Andreas W.; Jupp, Andrew R.; Slootweg, J. Chris
Contributor organization: Department of Chemistry
Date: 2020-07-15
Language: eng
Number of pages: 7
Belongs to series: Zeitschrift für anorganische und allgemeine Chemie
ISSN: 0044-2313
DOI: https://doi.org/10.1002/zaac.201900313
URI: http://hdl.handle.net/10138/318384
Abstract: The reaction of the intramolecular frustrated Lewis pair (FLP) tBu2PCH2BPh2 with the amine-boranes NH3·BH3 and Me2NH·BH3 leads to the formation of the corresponding FLP-H2 adducts as well as novel five-membered heterocycles that result from capturing the in situ formed amino-borane by a second equivalent of FLP. The sterically more demanding tBu2PCH2BMes2 does not form such a five-membered heterocycle when reacted with Me2NH·BH3 and its H2 adduct liberates dihydrogen at elevated temperatures, promoting the metal-free catalytic dehydrogenation of amine-boranes.
Subject: 3RD-ROW ATOMS
AMMONIA-BORANE
Amine-boranes
BASIS-SETS
DIMESITYLBORYL COMPOUNDS
Dehydrogenation
Density functional calculations
FREE HYDROGEN-TRANSFER
FRUSTRATED LEWIS PAIR
Frustrated Lewis pairs
GAUSSIAN-TYPE BASIS
MOLECULAR-ORBITAL METHODS
Main-group catalysis
REACTIVITY
116 Chemical sciences
Peer reviewed: Yes
Rights: cc_by_nc_nd
Usage restriction: openAccess
Self-archived version: publishedVersion


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