Investigation of LiAlH4–THF formation by direct hydrogenation of catalyzed Al and LiH

Abstract

The formation of LiAlH₄–THF by direct hydrogenation of Al and LiH in tetrahydrofuran (THF) was investigated using spectroscopic and computational methods. The molecular structures and free energies of the various possible adducts (THF–AlH₃, THF–LiH and THF–LiAlH₄) present in a LiAlH₄/THF solution were calculated and the dominant species were determined to be contact ion pairs where three THF molecules coordinate the lithium. Raman and X-ray absorption spectroscopy were used to investigate the effect of different Ti precursors on the formation of Al–H species and LiAlH₄–THF and determine the optimal reaction conditions. A unique sample stage was developed from a microfluidic cell to evaluate the catalysts in situ. The effectiveness of two types of catalysts, titanium chloride (TiCl₃) and titanium butoxide (Ti(C₄H₉O)₄), and the catalyst concentration were evaluated under similar reaction conditions. Both catalysts were effective at facilitating hydrogenation, although TiCl₃ was more effective over the first few cycles with the greatest kinetic enhancement achieved with a low concentration of around 0.15 mol%. These results were qualitatively supported by infrared spectroscopy, which indicated that although a small amount of Ti is necessary for disassociating H₂, excess surface Ti (>0.1 ML) hinders the formation of Al–H species.