N,N'-dihydroxy-1,4,5,8-naphthalenetetracarboxdiimide (NDI-(OH)2 ) has attracted much attention in recent years, because its doubly deprotonated state, (O-NDI-O)2- , has metal-coordination ability and characteristic electronic transition useful for designing electronic and optical functions. In contrast, a molecular crystal with the mono-deprotonated (HO-NDI-O)- ion remains unknown. We herein report an organic crystal containing non-disproportionated (HO-NDI-O)- ions, which are connected by very strong O-H-O hydrogen bonds. Its lowest energy absorption band (450 to 650 nm) is observed in between that of NDI-(OH)2 (380 nm) and isolated (O-NDI-O)2- (500 to 850 nm) species, consistent with the molecular orbital calculations. This absorption originates from the electronic transition from deprotonated imide-based orbitals to NDI-core orbitals, which can be influenced by the hydrogen bonds around imide group. Consequently, the optical properties of NDI-(OH)2 can be modulated by the stepwise deprotonation and hydrogen-bonding interactions.
Keywords: chromophores; crystal engineering; deprotonation; hydrogen bonds; naphthalenediimide.
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