Catalysis and destabilization strategies for the hydrogenation and dehydrogenation of boron/nitrogen systems
Lead Research Organisation:
University of Oxford
Department Name: Oxford Chemistry
Abstract
The primary objective of this proposal is the development of novel chemistry/catalysis to optimize the kinetics and extent of dihydrogen evolution from ammonia borane (AB). AB represents a very promising hydrogen storage material (19.6 wt % hydrogen), the exploitation of which will be significantly advanced by the application of two complementary approaches, based around either stoichiometric or catalytic exploitation of metal reagents: (i) chemical modification designed to disrupt the framework of dihydrogen bonding in the solid state and thereby facilitate more facile and complete evolution of H2; and (ii) transition metal catalysis of AB dehydrogenation, focussing in particular on the elucidation of mechanistic information, thereby allowing for the rational design of more efficient catalyst systems.
Organisations
Publications
Tang CY
(2010)
Dehydrogenation of saturated CC and BN bonds at cationic N-heterocyclic carbene stabilized M(III) centers (M = Rh, Ir).
in Journal of the American Chemical Society
Diyabalanage HV
(2010)
Potassium(I) amidotrihydroborate: structure and hydrogen release.
in Journal of the American Chemical Society
Wu C
(2010)
Stepwise Phase Transition in the Formation of Lithium Amidoborane
in Inorganic Chemistry
Tang CY
(2010)
Rhodium and iridium aminoborane complexes: coordination chemistry of BN alkene analogues.
in Angewandte Chemie (International ed. in English)
Tang CY
(2011)
Responses to unsaturation in iridium mono(N-heterocyclic carbene) complexes: synthesis and oligomerization of [LIr(H)2Cl] and [LIr(H)2]+.
in Chemical communications (Cambridge, England)
Tang CY
(2011)
Iridium-mediated borylation of benzylic C-H bonds by borohydride.
in Angewandte Chemie (International ed. in English)
Mansaray H
(2012)
Interaction of In(I) and Tl(I) Cations with 2,6-Diaryl Pyridine Ligands: Cation Encapsulation within a Very Weakly Interacting N/Arene Host Environment
in Inorganic Chemistry
| Description | Reactions of saturated and unsaturated organic molecules with boron-containing reagents represent a very powerful and versatile range of methodologies for the introduction of functionality into organic substrates, which have been widely exploited, e.g. in the syntheses of pharmaceuticals, natural products and functional materials. this research has developed new methodologies for carrying out the synthesis of these key intermediates |
| Exploitation Route | Initially through academic dissemination and use of methodologies by others in synthesis; in the medium term - within fine chemical synthesis |
| Sectors | Chemicals |
| Description | The findings from this work have been utilised in developing new methods for the synthesis of key types of intermediate relevant to chemical manufacture |
| First Year Of Impact | 2009 |
| Sector | Chemicals |
| Impact Types | Economic |