scholarly journals Novel Problems in the Solid State Cathodoluminescence of Organic Materials

10.5772/33546 ◽  
2012 ◽  
Author(s):  
Zheng Xu ◽  
Suling Zhao
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.


2004 ◽  
Vol 53 (12) ◽  
pp. 4387
Author(s):  
Qu Chong ◽  
Xu Zheng ◽  
Teng Feng ◽  
Qian Lei ◽  
Yu Wen-Ge ◽  
...  

1999 ◽  
Vol 102 (1-3) ◽  
pp. 1443-1446 ◽  
Author(s):  
Paul F. van Hutten ◽  
Hendrik-Jan Brouwer ◽  
Victor V. Krasnikov ◽  
Lahoussine Ouali ◽  
Ulf Stalmach ◽  
...  

2018 ◽  
Vol 6 (17) ◽  
pp. 4603-4626 ◽  
Author(s):  
Alessandra Forni ◽  
Elena Lucenti ◽  
Chiara Botta ◽  
Elena Cariati

Purely organic materials showing solid state room temperature phosphorescence (RTP) are receiving an ever growing interest due to their low toxicity, cost and environmental load compared to their organometallic counterparts.


2007 ◽  
Vol 16 (5) ◽  
pp. 1464-1466 ◽  
Author(s):  
Zhang Fu-Jun ◽  
Zhao Su-Ling ◽  
Xu Zheng ◽  
Huang Jin-Zhao ◽  
Xu Xu-Rong

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.


Soil Research ◽  
1997 ◽  
Vol 35 (5) ◽  
pp. 1061 ◽  
Author(s):  
J. A. Baldock ◽  
J. M. Oades ◽  
P. N. Nelson ◽  
T. M. Skene ◽  
A. Golchin ◽  
...  

Solid-state 13C nuclear magnetic resonance (NMR) spectroscopy has become an important tool for examining the chemical structure of natural organic materials and the chemical changes associated with decomposition. In this paper, solid-state 13C NMR data pertaining to changes in the chemical composition of a diverse range of natural organic materials, including wood, peat, composts, forest litter layers, and organic materials in surface layers of mineral soils, were reviewed with the objective of deriving an index of the extent of decomposition of such organic materials based on changes in chemical composition. Chemical changes associated with the decomposition of wood varied considerably and were dependent on a strong interaction between the species of wood examined and the species composition of the microbial decomposer community, making the derivation of a single general index applicable to wood decomposition unlikely. For the remaining forms of natural organic residues, decomposition was almost always associated with an increased content of alkyl C and a decreased content of O-alkyl C. The concomitant increase and decrease in alkyl and O-alkyl C contents, respectively, suggested that the ratio of alkyl to O-alkyl carbon (A/O-A ratio) may provide a sensitive index of the extent of decomposition. Contrary to the traditional view that humic substances with an aromatic core accumulate as decomposition proceeds, changes in the aromatic region were variable and suggested a relationship with the activity of lignin-degrading fungi. The A/O-A ratio did appear to provide a sensitive index of extent of decomposition provided that its use was restricted to situations where the organic materials were derived from a common starting material. In addition, the potential for adsorption of highly decomposable materials on mineral soil surfaces and the impacts which such an adsorption may have on bioavailability required consideration when the A/O-A ratio was used to assess the extent of decomposition of organic materials found in mineral soils.


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