scholarly journals High-yield, fluoride-free and large-scale synthesis of MIL-101(Cr)

2015 ◽  
Vol 44 (38) ◽  
pp. 16791-16801 ◽  
Author(s):  
Tian Zhao ◽  
Felix Jeremias ◽  
Ishtvan Boldog ◽  
Binh Nguyen ◽  
Stefan K. Henninger ◽  
...  

MIL-101(Cr), one of the most important prototypical MOFs, is well investigated and widely used in many scientific fields.

2006 ◽  
Vol 510-511 ◽  
pp. 66-69 ◽  
Author(s):  
Yan Fang Chen ◽  
Yun Soo Lim

Carbon nanotubes (CNTs) in a high yield were synthesized by the decomposition of the methane gas with CCVD, in which two different reaction routes of sol-gel method prepared Fe-Mo- Mg-O catalyst. The two different routs influenced the wall number and defects of CNTs and the formation of CNTs. The concentration of Mo in the catalyst played a very important role in the yield of CNTs.


2016 ◽  
Vol 40 (2) ◽  
pp. 1571-1579 ◽  
Author(s):  
Kumud Malika Tripathi ◽  
Amit Kumar Sonker ◽  
Anshu Bhati ◽  
Jagannath Bhuyan ◽  
Anupriya Singh ◽  
...  

A high-yield synthesis of water-soluble photoluminescent carbon nanorods is described. The wsCNRs were used for the selective determination of DNA molecules via a fluorescent turn-off/turn-on mechanism.


RSC Advances ◽  
2015 ◽  
Vol 5 (112) ◽  
pp. 92144-92150 ◽  
Author(s):  
Jens Helmlinger ◽  
Martin Heise ◽  
Marc Heggen ◽  
Michael Ruck ◽  
Matthias Epple

Silver nanoparticles, often applied in medical devices and consumer products, can be conveniently prepared by microwave-based synthesis.


2009 ◽  
Vol 131 (46) ◽  
pp. 16672-16674 ◽  
Author(s):  
Zhikun Wu ◽  
Eric Lanni ◽  
Wenqian Chen ◽  
Mark E. Bier ◽  
Danith Ly ◽  
...  

2019 ◽  
Author(s):  
Yongzheng Ding ◽  
Shuai Fan ◽  
Xiaoxi Chen ◽  
yuzhen gao ◽  
Gang Li

A Pdᴵᴵ-catalyzed, ligand-enabled gamma-C(sp3)–H arylation of free primary aliphatic amines and amino esters without using an exogenous directing group is reported. This reaction is compatible with unhindered free aliphatic amines, and it is also be applicable to the rapid synthesis of biologically and synthetically valuable unnatural α-amino acids. Large scale synthesis is also feasible using this method.<br>


2019 ◽  
Author(s):  
Alyssa Garreau ◽  
Hanyang Zhou ◽  
Michael Young

<div>Methods to catalytically introduce deuterium in synthetically useful yields ortho to a carboxylic acid directing group on arenes typically requires D2 or CD3CO2D, which makes using these approaches cost prohibitive for large scale synthesis (equipment and reagent costs respectively). Herein we present a simplified approach using catalytic RhIII and D2O as deuterium source, and show its application to H/D exchange on various acidic substrates.</div>


2019 ◽  
Author(s):  
Alyssa Garreau ◽  
Hanyang Zhou ◽  
Michael Young

<div>Methods to catalytically introduce deuterium in synthetically useful yields ortho to a carboxylic acid directing group on arenes typically requires D2 or CD3CO2D, which makes using these approaches cost prohibitive for large scale synthesis (equipment and reagent costs respectively). Herein we present a simplified approach using catalytic RhIII and D2O as deuterium source, and show its application to H/D exchange on various acidic substrates.</div>


2020 ◽  
Vol 17 (8) ◽  
pp. 628-630
Author(s):  
Vu Binh Duong ◽  
Pham Van Hien ◽  
Tran Thai Ngoc ◽  
Phan Dinh Chau ◽  
Tran Khac Vu

A simple and practical method for the synthesis on a large scale of altretamine (1), a wellknown antitumor drug, has been successfully developed. The synthesis method involves the conversion of cyanuric chloride (2) into altretamine (1) by dimethylamination of 2 with an aqueous solution of 40% dimethylamine and potassium hydroxide in 1, -dioxan 4in one step to give altretamine (1) in high yield.


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