Photoactive Molecules within MOFs
Photochromic molecules have been considered to be applied in responsive functional materials. Recently, the combination of a porous host matrix and these photoactive species has become an emerging field of research. Especially the use of crystalline nanop
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Photoactive Molecules within MOFs Heidi Annemarie Schwartz and Uwe Ruschewitz
Contents 1 General Introduction 1.1 Photochromism 1.2 Solvatochromism 1.3 Metal-Organic Frameworks 1.4 Implementing Photoswitches into MOFs 2 Switch@MOF Systems 2.1 Stilbenes in MOFs 2.2 Azobenzene and Its Derivatives in MOFs 2.3 Diarylethenes in MOFs 2.4 Spiropyrans in MOFs 2.5 Spirooxazines in MOFs 3 Conclusion and Future Perspectives Appendix References
Abstract Photochromic molecules have been considered to be applied in responsive functional materials. Recently, the combination of a porous host matrix and these photoactive species has become an emerging field of research. Especially the use of crystalline nanoporous metal-organic frameworks (MOFs) as host materials has proven to be very promising. The combination of crystallinity and the ability to be systematically functionalized is one of the main advantages of these porous host materials. The resulting switch@MOF hybrid systems exhibit fascinating and even surprising properties ranging from the “simple” possibility of solid-state switching to remote control gas uptake and conductance photoswitching. After a short
H. A. Schwartz Institute of General, Inorganic and Theoretical Chemistry, University of Innsbruck, Innsbruck, Austria e-mail: [email protected] U. Ruschewitz (*) Department of Chemistry, University of Cologne, Cologne, Germany e-mail: [email protected]
H. A. Schwartz and U. Ruschewitz
introduction to photochromism, solvatochromism, and MOFs, this chapter discusses the formation and the developments of these switch@MOF materials and the recent advances in exploitation of the light-induced structural changes. Keywords 2-Phenylazopyridine · Azobenzenes · Diarylethenes · Hybrid materials · Metal-organic frameworks (MOFs) · Photochromism · Porous coordination polymers · Solid-state switching · Solvatochromism · Spirooxazines · Spiropyrans · Stilbenes · Thin MOF films
Abbreviations AZB BET BSP c COF CT d DAE DC DFT DMF DSC DTE EDS/EDX EDTM EtOH ext h HKUST IR IR-MOF IRRA irrad JUC LED LPE max MC MeOH MIL min MOF nm
Azobenzene Brunauer-Emmett-Teller 1-(2-hydroxy-ethyl)-3,3-dimethyl-indolino-60 -nitrobenzospiropyran Closed Covalent-organic framework Charge-transfer Day(s) Diarylethenes Direct current Density functional theory N,N0 -dimethylformamide Difference scanning calorimetry Dithienylethenes Energy dispersive X-ray spectroscopy Electric dipole transition moment Ethanol Extinction Hour(s) Hong Kong University of Science and Technology Infrared Isoreticular MOF Infrared reflection-absorption Irradiated Jilin University China Light-emitting diode Liquid phase epitaxial growth Maximum Merocyanine Methanol Matériaux de l’Institut Lavoisier Minute or minimal Metal-organic framework Nanometer
Photoactive Molecules within MOFs
NMR o oF PAP PCN PCP PDF PEG pF PIZOF PM PSS QCM SBU SEM SP SP-Nitro SP-O SURMOF tF TGA ToF-SIMS UHPLC UiO UV vis XPS XR(P)D ε0 λ
Nuclear magnetic resonance Open 4H, 4H’-octafluoro 2-phenylazopyridine Porous coordination network Poro
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