Room Temperature Solvent-Free Synthesis of Monodisperse Magnetite Nanocrystals

2006 ◽  
Vol 6 (3) ◽  
pp. 852-856 ◽  
Author(s):  
X. R. Ye ◽  
C. Daraio ◽  
C. Wang ◽  
J. B. Talbot ◽  
S. Jin

We have successfully demonstrated a facile, solvent-free synthesis of highly crystalline and monodisperse Fe3O4 nanocrystallites at ambient temperature avoiding any heating. Solid state reaction of inorganic Fe(II) and Fe(III) salts with NaOH was found to produce highly crystalline Fe3O4 nanoparticles. The reaction, if carried out in the presence of surfactant such as oleic acid–oleylamine adduct, generated monodisperse Fe3O4 nanocrystals extractable directly from the reaction mixture. The extracted nanoparticles were capable of forming self-assembled, two-dimensional and uniform periodic array. The new process utilizes inexpensive and nontoxic starting materials, and does not require a use of high boiling point and toxic solvents, thus is amenable to an environmentally desirable, large-scale synthesis of nanocrystals.

2011 ◽  
Vol 76 (10) ◽  
pp. 1339-1346 ◽  
Author(s):  
Anshu Dandia ◽  
Ruby Singh ◽  
Ashok Laxkar

An efficient and mild method for the synthesis of spiro [1,3- oxathiolan/oxathianes] in the solid state reaction at room temperature has been described. This method is a good option to obtain the title compounds in quantitative yields in a simple and inexpensive way. Applying this methodology, different thia heterocycles were synthesized.


2015 ◽  
Vol 17 (2) ◽  
pp. 1088-1099 ◽  
Author(s):  
Hyejin Cho ◽  
Richard Madden ◽  
Bilal Nisanci ◽  
Béla Török

A catalyst and solvent-free room temperature synthesis of pyrroles is described.


ACS Sensors ◽  
2018 ◽  
Vol 3 (5) ◽  
pp. 1032-1039 ◽  
Author(s):  
Nagendra Bala Murali Athreya ◽  
Aditya Sarathy ◽  
Jean-Pierre Leburton

Synlett ◽  
2019 ◽  
Vol 30 (19) ◽  
pp. 2143-2147
Author(s):  
Zhongyou Yin ◽  
Changkun Xiong ◽  
Jianxin Guo ◽  
Xiaoyun Hu ◽  
Zixing Shan ◽  
...  

Several 1,3,5-triaryl-1,5-diketones have been chemoselectively synthesized under solvent-free conditions. It was found that intramolecular weak bifurcated H-bonds interaction of aliphatic C–H group plays a decisive role in the structural arrangement of 3-(2,6-dichlorophenyl)-1,5-diphenylpentane-1,5-dione in a solid state resulting in significant impact on the corresponding bond lengths and dihedral angles.


2014 ◽  
Vol 170 ◽  
pp. 137-153 ◽  
Author(s):  
Ihor Z. Hlova ◽  
Shalabh Gupta ◽  
Jennifer F. Goldston ◽  
Takeshi Kobayashi ◽  
Marek Pruski ◽  
...  

A mechanochemical process for the synthesis of alane (AlH3) starting from lithium hydride (LiH) and aluminium chloride (AlCl3) at room temperature and the underlying reaction pathway have been studied. In contrast to a conventional process using the same two reactants dissolved in diethyl ether, our approach enables a solvent-free synthesis, thereby directly leading to adduct-free alane. The method described here is quick and efficient, resulting in the quantitative conversion of all aluminium in the starting mixture to alane. Both the intermediate compounds formed during the reaction and the final products have been characterized by powder X-ray diffraction, solid-state27Al NMR spectroscopy, and temperature programmed desorption analysis of the as-milled mixtures. We show that excess LiH in the starting mixture (with an optimal ratio of 9LiH : 1AlCl3) is essential for the formation and stability of Al–H bonds, initially in the form of alanates and, eventually, as alane. Further processing of this mixture, gradually adding AlCl3to reach the ideal 3LiH : 1AlCl3stoichiometry, appears to restrict the local accumulation of AlCl3during the ball-milling process, thereby preventing the formation of unstable intermediates that decompose to metallic Al and molecular hydrogen. We also demonstrate that under the milling conditions used, a moderate hydrogen pressure ofca.300 bar is required to suppress competing reactions that lead to the formation of metallic Al at room temperature. The identification of the reaction intermediates at each stage of the synthesis provides significant insight into the mechanism of this solid-state reaction, which may potentially afford a more rational approach toward the production of AlH3in a simple solvent-free process.


2021 ◽  
Vol 17 ◽  
pp. 2642-2649
Author(s):  
Akhil K Dubey ◽  
Raghunath Chowdhury

An enantioselective 1,4-conjugate addition of nitromethane to β-silyl α,β-unsaturated carbonyl compounds catalyzed by bifunctional squaramide catalysts has been developed. This methodology offers both enantiomers of β-silyl nitroalkanes in good to excellent yields (up to 92%) and enantioselectivities (up to 97.5% ee) under solvent-free conditions at room temperature. Control experiments reveal that the presence of a β-silyl group in the enones is crucial for high reactivity under the optimized reaction conditions.


2012 ◽  
Vol 340 ◽  
pp. 012111
Author(s):  
A Remhof ◽  
Y Yan ◽  
O Friedrichs ◽  
J W Kim ◽  
Ph Mauron ◽  
...  

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