Chapter 5. Porphyrin-encapsulating Metal–Organic Materials as Solid-state Mimics of Heme Enzymes

2021 ◽  
pp. 166-187
Author(s):  
Randy W. Larsen
2011 ◽  
Vol 133 (27) ◽  
pp. 10356-10359 ◽  
Author(s):  
Randy W. Larsen ◽  
Lukasz Wojtas ◽  
Jason Perman ◽  
Ronald L. Musselman ◽  
Michael J. Zaworotko ◽  
...  

2016 ◽  
Vol 7 (1) ◽  
pp. 707-712 ◽  
Author(s):  
Martin Glavinović ◽  
Feng Qi ◽  
Athanassios D. Katsenis ◽  
Tomislav Friščić ◽  
Jean-Philip Lumb

We develop an associative synthesis of metal–organic materials that combines solid-state metal oxidation and coordination-driven self-assembly into a one-step, waste-free transformation.


2009 ◽  
Vol 9 (12) ◽  
pp. 5021-5023 ◽  
Author(s):  
Jason A. Perman ◽  
Kevin Dubois ◽  
Farid Nouar ◽  
Sandra Zoccali ◽  
Łukasz Wojtas ◽  
...  

Materials ◽  
2019 ◽  
Vol 12 (24) ◽  
pp. 4088
Author(s):  
Javier Martí-Rujas

Thermal treatment is important in the solid-state chemistry of metal organic materials (MOMs) because it can create unexpected new structures with unique properties and applications that otherwise in the solution state are very difficult or impossible to achieve. Additionally, high-temperature solid-state reactivity provide insights to better understand chemical processes taking place in the solid-state. This review article describes relevant thermally induced solid-state reactions in metal organic materials, which include metal organic frameworks (MOFs)/coordination polymers (CPs), and second coordination sphere adducts (SSCs). High temperature solid-state reactivity can occur in a single-crystal-to-single crystal manner (SCSC) usually for cases where there is small atomic motion, allowing full structural characterization by single crystal X-ray diffraction (SC-XRD) analysis. However, for the cases in which the structural transformations are severe, often the crystallinity of the metal-organic material is damaged, and this happens in a crystal-to-polycrystalline manner. For such cases, in the absence of suitable single crystals, structural characterization has to be carried out using ab initio powder X-ray diffraction analysis or pair distribution function (PDF) analysis when the product is amorphous. In this article, relevant thermally induced SCSC reactions and crystal-to-polycrystalline reactions in MOMs that involve significant structural transformations as a result of the molecular/atomic motion are described. Thermal reactivity focusing on cleavage and formation of coordination and covalent bonds, crystalline-to-amorphous-to-crystalline transformations, host–guest behavior and dehydrochlorination reactions in MOFs and SSCs will be discussed.


2013 ◽  
Vol 2013 ◽  
pp. 1-11 ◽  
Author(s):  
Xiao-Lan Tong ◽  
Hai-Lu Lin ◽  
Jian-Hua Xin ◽  
Fen Liu ◽  
Min Li ◽  
...  

Metal-organic frameworks (MOFs), also known as hybrid inorganic-organic materials, represent an emerging class of materials that have attracted the imagination of solid-state chemists because MOFs combine unprecedented levels of porosity with a range of other functional properties that occur through the metal moiety and/or the organic ligand. The purpose of this critical review is to give a representative and comprehensive overview of the arising developments in the field of functional metal-organic frameworks, including luminescence, magnetism, and porosity through presenting examples. This review will be of interest to researchers and synthetic chemists attempting to design multifunctional MOFs.


CrystEngComm ◽  
2018 ◽  
Vol 20 (42) ◽  
pp. 6721-6726 ◽  
Author(s):  
Fang Guo ◽  
Hao-Cheng Wang ◽  
Antonino Famulari ◽  
Hai-Dong Lu ◽  
Javier Martí-Rujas

Nonporous hybrid metal organic materials have been studied in the solid-state by mechanochemical reactions, chemisorption and release of HCl by heating. The dynamic behavior of the hybrid materials allows the breaking and formation of chemical bonds.


2016 ◽  
Vol 45 (35) ◽  
pp. 13648-13662 ◽  
Author(s):  
Fang Guo ◽  
Javier Martí-Rujas

An overview of early work and current developments focussing on the solid-state chemistry of hybrid metal–organic complexes assembled by outer sphere coordination involving is presented.


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