Emergence of Nonlinear Optical Activity by Incorporation of a Linker Carrying the p-Nitroaniline Motif in MIL-53 Frameworks
Karen Markey (Katholieke Universiteit Leuven)
Martin Krüger (Christian-Albrechts-Universität zu Kiel)
Tomasz Seidler (University of Namur, Jagiellonian University)
Helge Reinsch (Christian-Albrechts-Universität zu Kiel)
Thierry Verbiest (Katholieke Universiteit Leuven)
Dirk E. De Vos (Katholieke Universiteit Leuven)
Benoît Champagne (University of Namur)
Norbert Stock (Christian-Albrechts-Universität zu Kiel)
Monique A. Van Der Veen (TU Delft - Applied Sciences)
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Abstract
p-Nitroaniline presents the typical motif of a second-order nonlinear optically (NLO) active molecule. However, because of its crystallization in an antiparallel and hence centrosymmetric structure, the NLO activity is lost. In this contribution, the p-nitroaniline motif was built successfully into the MIL-53 metal-organic framework. More precisely, MIL-53 was synthesized with 2-amino-5-nitroterephthalate as organic linker, with Al3+, Ga3+, or In3+ as inorganic cation. The Al and Ga structures are polar, as confirmed by second-harmonic generation microscopy, yielding stable NLO materials. Indeed, they contain a 22-36% surplus of the dipolar 2-amino-5-nitro-terephthalate oriented in a parallel fashion. The indium compound was shown to be less crystalline and centrosymmetric. Ab initio modeling of the second-order NLO response shows that the Al and Ga materials show a response comparable to typical inorganic commercial NLO materials such as KDP. As a hybrid material, capable of low-temperature synthesis and processing and the ultrafast NLO responses associated with organic materials, this material can potentially provide an interesting venue for applications with respect to traditional inorganic NLO materials.