Close Amide NH•••F Hydrogen Bonding Interactions in 1,8-Disubstituted Naphthalenes

In this note, we present a series of N-(8-fluoronaphthalen-1-yl)benzamide derivatives designed to maximize amide-NH center dot center dot center dot F hydrogen bond interactions therein. A combination of IR and NMR spectroscopy indicates a linear correlation between the high energy shift in NH stretching frequency and the electron withdrawing nature of the substituent, consistent with the trend predicted by DFT calculations. Additionally, a limiting case of hydrogen bonding is observed when the benzamide derivatives are replaced with trifluoroacetamide, causing an additional red shift of 44 cm(-1) in the NH stretching frequency. Most importantly, H-1-F-19 coupling constants in this series are among the largest measured for amide-NH-F interactions. X-ray crystallography reveals face-to-face alignment of naphthalene rings in these derivatives resulting in part from the NH center dot center dot center dot F hydrogen bonds. This motif also dictates the formation of sheets composed of stacked naphthalene rings in the crystal structure as opposed to unfluorinated analogues wherein NH center dot center dot center dot OC hydrogen-bonding interactions force benzamide and naphthalene rings to engage in T-shaped pi-pi interactions instead. Additionally, the NH proton in the trifluoroacetamide derivative engages in extended H-bond interactions in its crystal structure.