Towards the design of novel boron- and nitrogen-substituted ammonia-borane and bifunctional arene ruthenium catalysts for hydrogen storage
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|Title:||Towards the design of novel boron- and nitrogen-substituted ammonia-borane and bifunctional arene ruthenium catalysts for hydrogen storage||Authors:||Bandaru, Sateesh
English, Niall J.
Phillips, Andrew D.
MacElroy, J. M. Don
|Permanent link:||http://hdl.handle.net/10197/5381||Date:||5-Feb-2014||Abstract:||Electronic-structure density functional theory calculations have been performed to construct the potential energy surface for H2 release from ammonia-borane, with a novel bifunctional cationic ruthenium catalyst based on the sterically bulky β-diketiminato ligand (Schreiber et al., ACS Catal. 2012, 2, 2505). The focus is on identifying both a suitable substitution pattern for ammonia-borane optimized for chemical hydrogen storage and allowing for low-energy dehydrogenation. The interaction of ammonia-borane, and related substituted ammonia-boranes, with a bifunctional η6-arene ruthenium catalyst and associated variants is investigated for dehydrogenation. Interestingly, in a number of cases, hydride-proton transfer from the substituted ammonia-borane to the catalyst undergoes a barrier-less process in the gas phase, with rapid formation of hydrogenated catalyst in the gas phase. Amongst the catalysts considered, N,N-difluoro ammonia-borane and N-phenyl ammonia-borane systems resulted in negative activation energy barriers. However, these types of ammonia-boranes are inherently thermodynamically unstable and undergo barrierless decay in the gas phase. Apart from N,N-difluoro ammonia-borane, the interaction between different types of catalyst and ammonia borane was modeled in the solvent phase, revealing free-energy barriers slightly higher than those in the gas phase. Amongst the various potential candidate Ru-complexes screened, few are found to differ in terms of efficiency for the dehydrogenation (rate-limiting) step. To model dehydrogenation more accurately, a selection of explicit protic solvent molecules was considered, with the goal of lowering energy barriers for H-H recombination. It was found that primary (1°), 2°, and 3° alcohols are the most suitable to enhance reaction rate. © 2014 Wiley Periodicals, Inc.||Funding Details:||Science Foundation Ireland||Type of material:||Journal Article||Publisher:||Wiley||Copyright (published version):||2014 Wiley Periodicals, Inc.||Keywords:||Ammonia-borane; Density functional theory; Dehydrogenation; Ruthenium; Bifunctional; Catalysis||DOI:||10.1002/jcc.23534||Language:||en||Status of Item:||Peer reviewed|
|Appears in Collections:||Chemical and Bioprocess Engineering Research Collection|
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