Solid state reactivity of organic compounds with inorganic compounds II.

1988 ◽  
Vol 34 (3) ◽  
pp. 723-732
Author(s):  
P. S. Bassi ◽  
G. S. Chopra ◽  
R. Prasher
Keyword(s):  
Solid State ◽  
Organic Compounds ◽  
Inorganic Compounds

scholarly journals Guidelines for measurement of luminescence spectra and quantum yields of inorganic and organometallic compounds in solution and solid state (IUPAC Technical Report)

2016 ◽  
Vol 88 (7) ◽  
pp. 701-711 ◽  
Author(s):  
Hitoshi Ishida ◽  
Jean-Claude Bünzli ◽  
Andrew Beeby
Keyword(s):  
Solid State ◽  
Organic Compounds ◽  
Room Temperature ◽  
Inorganic Compounds ◽  
Organometallic Compounds ◽  
Quantum Yields ◽  
Luminescence Spectra ◽  
Room Temperature Phosphorescence ◽  
Emission Data ◽  
Technical Report

AbstractGuidelines for measuring the luminescence of inorganic compounds, metal complexes, and organometallic compounds are described. Common textbooks and manuals describing luminescence measurements are usually targeted for organic compounds, and are not always suitable for inorganic and organometallic compounds, which emit room-temperature phosphorescence. The report describes problems that researchers may confront while recording emission data and elaborates clear procedures to avoid these problems and provide adequate standardized protocols.

Solid state chemical ionization for characterization of organic compounds by laser mass spectrometry

Talanta ◽  
1989 ◽  
Vol 36 (1-2) ◽  
pp. 117-124 ◽  
Author(s):  
Kesagapillai Balasanmugam ◽  
Somayajula Kasi Viswanadham ◽  
David M. Hercules
Keyword(s):  
Mass Spectrometry ◽  
Solid State ◽  
Organic Compounds ◽  
Chemical Ionization ◽  
Laser Mass Spectrometry ◽  
State Chemical

A double-frequency solid-state laser on organic compounds

2009 ◽  
Vol 52 (7) ◽  
pp. 655-660 ◽  
Author(s):  
T. N. Kopylova ◽  
G. V. Maier ◽  
E. N. Telminov ◽  
V. A. Svetlichnyi ◽  
K. M. Degtyarenko
Keyword(s):  
Solid State ◽  
Organic Compounds ◽  
Solid State Laser ◽  
State Laser ◽  
Double Frequency

The Mode of Action of Disulfide Accelerators of Vulcanization

1937 ◽  
Vol 10 (1) ◽  
pp. 158-163
Author(s):  
W. Langenbeck ◽  
H. C. Rhiem
Keyword(s):  
Organic Compounds ◽  
Mode Of Action ◽  
Common Knowledge ◽  
Inorganic Compounds ◽  
Technical Problem ◽  
The Other ◽  
Rubber Industry ◽  
Organic Catalysis ◽  
Catalytic Power ◽  
Organic Catalysts

Abstract The catalytic power of organic compounds in general has up to the present time been studied much less extensively than that of inorganic compounds. For about the last ten years, however, the first author has, in collaboration with a number of his students, attempted to fill this gap, though so far efforts have been confined to explaining the mode of action of natural enzymes by means of comparative experiments with organic catalysts. As a result of this work, a theory based on experimental facts has been developed to explain in a satisfactory way the action of enzymes. The other phase of organic catalysis is, strictly speaking, a technical problem. Why for instance should it not be practicable to utilize organic catalysts more extensively than heretofore in industry? If this problem is to be attacked, it seems reasonable to start with the particular industry which already uses organic catalysts to the greatest extent. This is, of course, the rubber industry. The important accomplishments of the chemical industry with respect to the development of vulcanization accelerators is already common knowledge, and the important task at present is not simply to increase the great number of accelerators already known. A problem of more practical value would seem to be to study the mechanism of the acceleration of vulcanization, about which relatively little has been known heretofore.

Soft Chemical Routes to Heterostructured High-Tc Superconducting Materials

MRS Bulletin ◽  
2000 ◽  
Vol 25 (9) ◽  
pp. 32-39 ◽  
Author(s):  
Jin-Ho Choy ◽  
Soon-Jae Kwon ◽  
Seong-Ju Hwang ◽  
Eue-Soon Jang
Keyword(s):  
Solid State ◽  
High Performance ◽  
Inorganic Compounds ◽  
Rechargeable Batteries ◽  
Host Lattice ◽  
Inorganic Materials ◽  
Solid State Reactions ◽  
Metal Chalcogenides ◽  
Structural Anisotropy ◽  
Intercalation Reaction

Recently, inorganic/inorganic and organic/inorganic heterostructured materials have attracted considerable research interest, due to their unusual physicochemical properties, which cannot be achieved by conventional solid-state reactions. In order to develop new hybrid materials, various synthetic approaches, such as vacuum deposition, Langmuir–Blodgett films, selfassembly, and intercalation techniques, have been explored. Among them, the intercalation reaction technique—that is, the reversible insertion of guest species into the two-dimensional host lattice—is expected to be one of the most effective tools for preparing new layered heterostructures because this process can provide a soft chemical way of hybridizing inorganic/inorganic, organic/inorganic, or biological/inorganic compounds. In fact, the intercalation/deintercalation process allows us to design high-performance materials in a solution at ambient temperature and pressure, just as “soft solution processing” provides a simple and economical route for advanced inorganic materials by means of an environmentally benign, lowenergy method. These unique advantages of the intercalation technique have led to its wide application to diverse fields of the solid-state sciences, namely, secondary (rechargeable) batteries, electrochromic systems, oxidation–reduction catalysts, separating agents, sorbents, and so on. Through these extensive studies, many kinds of low-dimensional compounds have been developed as host materials for the intercalation reaction, including graphite, transition-metal chalcogenides, transitionmetal oxides, aluminosilicates, metal phosphates, metal chalcogenohalides, and so on. Recently, the area of intercalation chemistry has been extended to high-Tc superconducting copper oxides, resulting in remarkable structural anisotropy.

scholarly journals Molecular-level electrochemical doping for fine discrimination of volatile organic compounds in organic chemiresistors

2020 ◽  
Vol 8 (33) ◽  
pp. 16884-16891 ◽  
Author(s):  
Sooncheol Kwon ◽  
Yusin Pak ◽  
Bongseong Kim ◽  
Byoungwook Park ◽  
Jehan Kim ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Solid State ◽  
Organic Compounds ◽  
Room Temperature ◽  
Molecular Level ◽  
Interfacial Area ◽  
Volatile Organic ◽  
Molecular Scale ◽  
Ppm Level ◽  
State Ionic

A blend of π-CPs and a solid-state ionic liquid provides an enlarged interfacial area at the molecular scale, thereby enabling two-terminal organic chemiresistors (TOCs) with fine discriminatory abilities for sub-ppm-level VOCs at room temperature.

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