BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20250817T124117EDT-93040XUVVc@132.216.98.100 DTSTAMP:20250817T164117Z DESCRIPTION:The use of hydrogen as an energy carrier offers a clean\naltern ative to current combustion of fossil fuels that produces\nharmful carbon particulates\, oxides of nitrogen and sulfur\, and\nvoluminous quantities of carbon dioxide. As others work on\nefficient production of hydrogen fro m water and sunlight\, we are\ninvestigating options for on-board hydrogen storage to enable\nlong-haul transportation that is key to moving goods a cross North\nAmerica. While metal hydrides and metal organic framework sor bents\nprovide reversible storage options\, they are currently unable to\n meet the storage capacity requirements for long-haul\ntransportation. So-c alled “chemical hydrides” such as\nazacycloalkanes can also serve as rever sible hydrogen storage\nmedia\, but activation barriers are high and dehyd rogenation rates\nremain slow with the best catalysts.\nWith both protic N -H and hydridic B-H bonds as well as three\nhydrogen atoms per main group element\, ammonia-borane (AB\, H3NBH3)\nis a promising material for high c apacity hydrogen storage\napplications.1 Detailed studies of the dehydro-o ligomerization of\nAB has revealed a wealth of reaction products and react ion pathways\ndepending on reaction media and conditions\, additives and\n catalysts. Through detailed in situ NMR studies of AB\ndehydrogenation usi ng a variety of catalyst precursors we have\nidentified a key reaction int ermediate proposed to arise by\ntrapping of reactive aminoborane monomer\, H2NBH2\, by AB.2 A new\nfamily of chelating diamine bis(phosphine) iron c atalysts is\nproposed to dehydrogenate amine-boranes via a Noyori-type\nhe terolytic activation mechanism.3 Finally\, remaining technical\nbarriers t o commercialization of amine-borane fuels will be\ndescribed.\n1 Stephens\ , F. H.\; Pons\, V.\; Baker\, R. T. Dalton Trans.\n2007\, 2613\; Marder\, T. B. Angew. Chem. Int.\nEd. 2007\, 46\, 8116\; Hamilton\, C. H.\;\nBaker\ , R. T.\; Staubitz\, A.\; Manners\, I. Chem. Soc. Rev.\n2009\, 38\, 279.\n 2 Pons\, V.\; Baker\, R. T.\; Szymczak\, N. K.\; Heldebrant\, D. J.\;\nLin ehan\, J. C.\; Matus\, M. H.\; Grant\, D. J.\; Dixon\, D. A. Chem.\nCommun . 2008\, 6597.\n3 Blaquiere\, N.\; Diallo-Garcia\, S.\; Gorelsky\, S. I.\; Black\, D.\nA.\; Fagnou\, K. J. Am. Chem. Soc.\n2008\, 130\, 14034\; Kass \, M.\;\nFriedrich\, A.\; Drees\, M.\; Schneider\, S. Angew. Chem. Int.\nE d. 2009\, 48\, 905.\n DTSTART:20091026T220000Z DTEND:20091026T233000Z LOCATION:Maass Chemistry Building\, CA\, QC\, Montreal\, H3A 0B8\, 801 rue Sherbrooke Ouest SUMMARY:Sigma Xi Lecture URL:/channels/event/sigma-xi-lecture-111402 END:VEVENT END:VCALENDAR