1,1′-Dimethoxy-3,3′-dimethyl-3,3′-(hexane-1,6-diyl)bis(triazen-2-ium-2-olate): a nitric oxide donor

Abstract

The title compound, C10H24N6O4, is the most stable type of nitric oxide (NO) donor among the broad category of discrete N‐diazeniumdiolates (NO adducts of nucleophilic small molecule amines). Sitting astride a crystallographic inversion center, the molecule contains a symmetric dimethylhexane‐1,6‐diamine structure bearing two planar O2‐methylated N‐diazeniumdiolate functional groups [N(O)=NOMe]. These two groups are parallel to each other and have the potential to release four molecules of NO. The methylated diazeniumdiolate substituent removes the negative charge from the typical N(O)=NO− group, thereby increasing the stability of the diazeniumdiolate structure. The crystal was nonmerohedrally twinned by a 180° rotation about the real [101] axis. This is the first N‐based bis‐diazeniumdiolate compound with a flexible aliphatic main unit to have its structure analyzed and this work demonstrates the utility of stabilizing the N‐diazeniumdiolate functional group by methylation.