Ultrafast Aggregation-Induced Tunable Emission Enhancement in a Benzothiadiazole-Based Fluorescent Metal–Organic Framework Linker

2021 ◽  
Author(s):  
Luis Gutiérrez-Arzaluz ◽  
Issatay Nadinov ◽  
George Healing ◽  
Justyna Czaban-Jóźwiak ◽  
Jiangtao Jia ◽  
...  
Keyword(s):  
Metal Organic Framework ◽  
Emission Enhancement ◽  
Metal Organic ◽  
Tunable Emission ◽  
Organic Framework

A new anionic metal–organic framework showing tunable emission by lanthanide(III) doping and highly selective CO2 adsorption properties

RSC Advances ◽  
2015 ◽  
Vol 5 (31) ◽  
pp. 24655-24660 ◽  
Author(s):  
Rong-Ying Chen ◽  
Dan Tian ◽  
Yun-Wu Li ◽  
Ying-Bin Lv ◽  
Hong-Wei Sun ◽  
...  
Keyword(s):  
Co2 Adsorption ◽  
Metal Organic Framework ◽  
Adsorption Properties ◽  
High Adsorption ◽  
Adsorption Selectivity ◽  
Metal Organic ◽  
Tunable Emission ◽  
Organic Framework

A 3D porous anionic MOF (1), decorated with -NH2 and N sites, can serve as a host for the encapsulation of lanthanide(iii) cations for emission tuning. Besides, it also shows high adsorption selectivity for CO2 over CH4 and N2 at 273 K.

A new type of double-chain based 3D lanthanide(iii) metal–organic framework demonstrating proton conduction and tunable emission

2014 ◽  
Vol 50 (15) ◽  
pp. 1912 ◽  
Author(s):  
Min Zhu ◽  
Zhao-Min Hao ◽  
Xue-Zhi Song ◽  
Xing Meng ◽  
Shu-Na Zhao ◽  
...  
Keyword(s):  
Metal Organic Framework ◽  
Proton Conduction ◽  
Double Chain ◽  
Metal Organic ◽  
New Type ◽  
Tunable Emission ◽  
Organic Framework

Tuning the photoluminescence of lanthanide metal–organic framework nanospheres through ligand-induced phase transition towards sensing

2021 ◽  
Author(s):  
Peng Zhang ◽  
Nan Song ◽  
Songbin Liu ◽  
Qiqing Li ◽  
Yu Wang ◽  
...  
Keyword(s):  
Phase Transition ◽  
Metal Organic Framework ◽  
Great Promise ◽  
Metal Organic ◽  
New Type ◽  
Lanthanide Metal ◽  
Water Ligands ◽  
Tunable Emission ◽  
Organic Framework

A new type of ligand-induced lanthanide metal–organic framework nanosphere is reported, which yields tunable emission colors by adding or removing water ligands, showing great promise in MOF sensors and anti-counterfeiting.

Multifunctional metal–organic framework heterostructures for enhanced cancer therapy

2021 ◽  
Author(s):  
Jintong Liu ◽  
Jing Huang ◽  
Lei Zhang ◽  
Jianping Lei
Keyword(s):  
Cancer Therapy ◽  
General Principle ◽  
Biomedical Applications ◽  
Metal Organic Framework ◽  
Metal Organic ◽  
Functional Modulation ◽  
Organic Framework

We review the general principle of the design and functional modulation of nanoscaled MOF heterostructures, and biomedical applications in enhanced therapy.

Magnetic Ordering via Itinerant Ferromagnetism in a Metal-Organic Framework

2020 ◽  
Author(s):  
Jesse Park ◽  
Brianna Collins ◽  
Lucy Darago ◽  
Tomce Runcevski ◽  
Michael Aubrey ◽  
...  
Keyword(s):  
Charge Transport ◽  
Magnetic Order ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Magnetic Ordering ◽  
Double Exchange ◽  
Itinerant Ferromagnetism ◽  
Organic Solids ◽  
Metal Organic ◽  
Organic Framework

<b>Materials that combine magnetic order with other desirable physical attributes offer to revolutionize our energy landscape. Indeed, such materials could find transformative applications in spintronics, quantum sensing, low-density magnets, and gas separations. As a result, efforts to design multifunctional magnetic materials have recently moved beyond traditional solid-state materials to metal–organic solids. Among these, metal–organic frameworks in particular bear structures that offer intrinsic porosity, vast chemical and structural programmability, and tunability of electronic properties. Nevertheless, magnetic order within metal–organic frameworks has generally been limited to low temperatures, owing largely to challenges in creating strong magnetic exchange in extended metal–organic solids. Here, we employ the phenomenon of itinerant ferromagnetism to realize magnetic ordering at <i>T</i><sub>C</sub> = 225 K in a mixed-valence chromium(II/III) triazolate compound, representing the highest ferromagnetic ordering temperature yet observed in a metal–organic framework. The itinerant ferromagnetism is shown to proceed via a double-exchange mechanism, the first such observation in any metal–organic material. Critically, this mechanism results in variable-temperature conductivity with barrierless charge transport below <i>T</i><sub>C</sub> and a large negative magnetoresistance of 23% at 5 K. These observations suggest applications for double-exchange-based coordination solids in the emergent fields of magnetoelectrics and spintronics. Taken together, the insights gleaned from these results are expected to provide a blueprint for the design and synthesis of porous materials with synergistic high-temperature magnetic and charge transport properties. </b>

Solvent-Free Powder Synthesis and MOF-CVD Thin Films of the Mesoporous Metal-Organic Framework MAF-6

2019 ◽  
Author(s):  
Timothée Stassin ◽  
Ivo Stassen ◽  
Joao Marreiros ◽  
Alexander John Cruz ◽  
Rhea Verbeke ◽  
...  
Keyword(s):  
Vapor Phase ◽  
Metal Organic Framework ◽  
Chemical Vapor ◽  
Uptake Capacity ◽  
Powder Synthesis ◽  
Crystalline Films ◽  
Metal Organic ◽  
Mesoporous Metal ◽  
First Time ◽  
Organic Framework

A simple solvent- and catalyst-free method is presented for the synthesis of the mesoporous metal-organic framework (MOF) MAF-6 (RHO-Zn(eIm)2) based on the reaction of ZnO with 2-ethylimidazole vapor at temperatures ≤ 100 °C. By translating this method to a chemical vapor deposition (CVD) protocol, mesoporous crystalline films could be deposited for the first time entirely from the vapor phase. A combination of PALS and Kr physisorption measurements confirmed the porosity of these MOF-CVD films and the size of the MAF-6 supercages (diam. ~2 nm), in close agreement with powder data and calculations. MAF-6 powders and films were further characterized by XRD, TGA, SEM, FTIR, PDF and EXAFS. The exceptional uptake capacity of the mesoporous MAF-6 in comparison to the microporous ZIF-8 is demonstrated by vapor-phase loading of a molecule larger than the ZIF-8 windows.

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