Selective synthesis of TiO2 nanocrystals with morphology control with the microwave-solvothermal method

CrystEngComm ◽  
2014 ◽  
Vol 16 (9) ◽  
pp. 1817 ◽  
Author(s):  
Claudia Carlucci ◽  
Hua Xu ◽  
Barbara Federica Scremin ◽  
Cinzia Giannini ◽  
Davide Altamura ◽  
...  
CrystEngComm ◽  
2017 ◽  
Vol 19 (28) ◽  
pp. 3867-3891 ◽  
Author(s):  
Giovanna Canu ◽  
Vincenzo Buscaglia

The hydrothermal/solvothermal method is one of the most versatile synthetic routes for producing a large number of compounds. The thermodynamic aspects, the control of morphology and the crystallisation mechanisms are reviewed and discussed in this highlight, with special emphasis on the synthesis of SrTiO3, as a model system.


Author(s):  
Leiyun Han ◽  
Xilong Liu ◽  
zheng cui ◽  
Yingjie Hua ◽  
Chongtai Wang ◽  
...  

Hierarchical copper cobalt sulfide nanobelt array structures with well-defined morphology control are first reported as high energy density electrode materials for asymmetric supercapacitors using a simple two-step solvothermal method. Through...


Author(s):  
William Finnigan ◽  
Lorna J. Hepworth ◽  
Nicholas J. Turner ◽  
Sabine Flitsch

As the enzyme toolbox for biocatalysis has expanded, so has the potential for the construction of powerful enzymatic cascades for efficient and selective synthesis of target molecules. Additionally, recent advances in computer-aided synthesis planning (CASP) are revolutionizing synthesis design in both synthetic biology and organic chemistry. However, the potential for biocatalysis is not well captured by tools currently available in either field. Here we present RetroBioCat, an intuitive and accessible tool for computer-aided design of biocatalytic cascades, freely available at retrobiocat.com. Our approach uses a set of expertly encoded reaction rules encompassing the enzyme toolbox for biocatalysis, and a system for identifying literature precedent for enzymes with the correct substrate specificity where this is available. Applying these rules for automated biocatalytic retrosynthesis, we show our tool to be capable of identifying promising biocatalytic pathways to target molecules, validated using a test-set of recent cascades described in the literature.


2018 ◽  
Author(s):  
Matthew L. Landry ◽  
Grace McKenna ◽  
Noah Burns

A concise and selective synthesis of the dichlorinated meroterpenoid azamerone is described. The paucity of tactics for the synthesis of chiral organochlorides motivated the development of unique strategies for accessing these motifs in enantioenriched forms. The route features a novel enantioselective chloroetherification reaction, a Pd-catalyzed cross-coupling between a quinone diazide and a boronic hemiester, and a late-stage tetrazine [4+2]-cycloaddition/oxidation cascade.


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