scholarly journals Facile Synthesis of Ambient Stable Pyreno[4,5-b]pyrrole Monoanion and Pyreno[4,5-b:9,10-b’]dipyrrole Dianion: From Serendipity to Design

2022 ◽  
Author(s):  
sharvan Kumar ◽  
Kohshi Yoshida ◽  
Yusuke Hattori ◽  
Tomohiro Higashino ◽  
Hiroshi Imahori ◽  
...  
Keyword(s):  
Organic Compounds ◽  
Facile Synthesis ◽  
Electronic Delocalization ◽  
The Stability

The stability of single or multiple negatively charged π-conjugated organic compounds is greatly influenced by its electronic delocalization. Herein, we report a strategic methodology for isolation of a mysterious compound....

Theoretical Study on Thermal Hazardous Properties of C18H10O11 and C18H18O7 Organic Peroxides

2013 ◽  
Vol 787 ◽  
pp. 301-305
Author(s):  
Yun Bo He ◽  
Wei Wang ◽  
Shi Xiong Wang ◽  
Xiang Jun Yang ◽  
Hong Guo
Keyword(s):  
Molecular Structure ◽  
Thermal Decomposition ◽  
Quantum Chemistry ◽  
Organic Compounds ◽  
Theoretical Study ◽  
Organic Peroxides ◽  
Quantum Chemistry Calculation ◽  
The Past ◽  
Chemistry Calculation ◽  
The Stability

The thermal decomposition of organic peroxides are widely used as coagulant for organic compounds, however, its thermal hazardous characteristics have already caused serious accidents in chemical industries, which limited its application in much more strict conditions. Organic peroxides of C18H10O11 and C18H18O7 are two new candidates fitted for industrial explosive. However, as we best known there is little reports available on the geometry structure in the past decades. In this work, by means of quantum chemistry calculation, the relation of safety with molecular structure of C18H10O11 and C18H18O7 are discussed. The molecules with more activity O and the activity part more dispersedly exhibit higher stable, and the configuration has good safety. All the energy of molecule b is higher than that of molecule a. The stability of different configurations are 6a>7a>8a>9a>5a>1a>4a>3a=2a and 1b>7b>5b>6b>4b>2b>3b>8b, respectively, suggesting the structures of 6a,3a,2a,1b,8b exhibit high safety.

scholarly journals Advances in the Stability of Halide Perovskite Nanocrystals

Materials ◽  
2019 ◽  
Vol 12 (22) ◽  
pp. 3733 ◽  
Author(s):  
Maning Liu ◽  
Anastasia Matuhina ◽  
Haichang Zhang ◽  
Paola Vivo
Keyword(s):  
Special Focus ◽  
Next Generation ◽  
Facile Synthesis ◽  
Research Directions ◽  
Rapid Degradation ◽  
Perovskite Nanocrystals ◽  
Final Goal ◽  
Tunable Properties ◽  
Halide Perovskite ◽  
The Stability

Colloidal halide perovskite nanocrystals are promising candidates for next-generation optoelectronics because of their facile synthesis and their outstanding and size-tunable properties. However, these materials suffer from rapid degradation, similarly to their bulk perovskite counterparts. Here, we survey the most recent strategies to boost perovskite nanocrystals stability, with a special focus on the intrinsic chemical- and compositional-factors at synthetic and post-synthetic stage. Finally, we review the most promising approaches to address the environmental extrinsic stability of perovskite nanocrystals (PNCs). Our final goal is to outline the most promising research directions to enhance PNCs’ lifetime, bringing them a step closer to their commercialization.

FORMIC ACID AS A SOLVENT FOR OZONIZATION INVESTIGATIONS

1940 ◽  
Vol 18b (1) ◽  
pp. 30-34 ◽  
Author(s):  
Rodger M. Dorland ◽  
Harold Hibbert
Keyword(s):  
Formic Acid ◽  
Ethyl Acetate ◽  
Organic Compounds ◽  
Aromatic Nucleus ◽  
Carboxyl Group ◽  
The Stability

The use of formic acid as a solvent in ozonization investigations has been developed and its suitability demonstrated by experiments on organic compounds of known structure. This solvent shows a remarkable tendency to protect the aldehyde from oxidation to the carboxyl group. The stability of the aromatic nucleus to ozone is apparently somewhat greater in this solvent than in ethyl acetate.

Facile Synthesis of Thiols and Sulfides

1975 ◽  
Vol 53 (10) ◽  
pp. 1480-1483 ◽  
Author(s):  
Jean-Rock Brindle ◽  
Jean-Louis Liard
Keyword(s):  
Aromatic Ring ◽  
Sodium Borohydride ◽  
Facile Synthesis ◽  
Experimental Conditions ◽  
The Stability ◽  
High Yields

Sulfurated sodium borohydride reacts with benzylic halides to give high yields of α-toluenethiol or benzylic polysulfldes depending upon the experimental conditions and the mode of hydrolysis.Aliphatic halides and dibenzylic halides react in the same manner as benzylic halides for a given experimental condition whereas benzylic halides substituted with other groups can be totally or partially reduced depending on the stability of the substituent towards NaBH2S3.Halogens directly attached on the aromatic ring do not react with NaBH2S3.

Mineral Redox Buffers and The Stability of Organic Compounds Under Hydrothermal Conditions

1996 ◽  
Vol 432 ◽  
Author(s):  
J. S. Seewald
Keyword(s):  
Organic Compounds ◽  
Active Species ◽  
Hydrothermal Systems ◽  
Hydrothermal Conditions ◽  
Sulfur Species ◽  
Sedimentary Environments ◽  
Mineral Assemblages ◽  
Catalytically Active ◽  
Chemical Conditions ◽  
The Stability

AbstractOrganic compounds play an integral role in numerous geochemical process in subsurface environments. To evaluate factors that regulate the stability of ethane, ethene, propane, and propene in hydrothermal systems a series of experiments were conducted at 300 to 325°C and 350 bars. The experiments contained the mineral assemblages pyrite-pyrrhotite-magnetite, hematite-magnetite-pyrite, and hematite-magnetite to buffer fO2, aH2(aq) and aH2S(aq) at geologically reasonable values.Results of the experiments suggest that under appropriate physical and chemical conditions, metastable redox dependent thermodynamic equilibrium involving liquid water and inorganic iron-bearing mineral assemblages may regulate the relative abundance of short chain alkanes and their corresponding alkenes. In addition, alkenes represent an important intermediary in the conversion of n-alkanes to methane and oxidized species such as carbon dioxide, ketones alcohols, and organic acids.The rates of redox dependent organic reactions during the experiments were strongly influenced by the presence of sulfur. Under relatively oxidizing conditions greater catalytic activity due to the presence of dissolved sulfur species was observed. Fluid speciation calculations suggest that oxidized aquous sulfur compounds represent the catalytically active species.These results suggest that redox conditions and the presence or absence of dissolved sulfur species in natural sedimentary environments may strongly influence the stability of hydrocarbons. Accordingly, models used to predict the stability of oil and the formations of natural gas need to account for chemical processes that involve both organic and inorganic sedimentary components.

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