Computer‐Aided Living Polymerization Conducted under Continuous‐Flow Conditions

Author(s):  
Zeyu Wang ◽  
Yang Zhou ◽  
Mao Chen
2021 ◽  
Vol 50 (7) ◽  
pp. 2493-2500
Author(s):  
Sara Rojas ◽  
Jorge A. R. Navarro ◽  
Patricia Horcajada

A defective Metal-Organic Frameworks as an improved material for the construction of a fixed-bed system working under continuous flow conditions for the removal of the emerging contaminant atenolol.


Tetrahedron ◽  
2021 ◽  
pp. 132305
Author(s):  
Harry R. Smallman ◽  
Jamie A. Leitch ◽  
Tom McBride ◽  
Steven V. Ley ◽  
Duncan L. Browne

Author(s):  
Paolo Zardi ◽  
Michele Maggini ◽  
Tommaso Carofiglio

AbstractThe post-functionalization of porphyrins through the bromination in β position of the pyrrolic rings is a relevant transformation because the resulting bromoderivatives are useful synthons to covalently link a variety of chemical architectures to a porphyrin ring. However, single bromination of porphyrins is a challenging reaction for the abundancy of reactive β-pyrrolic positions in the aromatic macrocycle. We herein report a synthetic procedure for the efficient preparation of 2-bromo-5,10,15,20-tetraphenylporphyrin (1) under continuous flow conditions. The use of flow technology allows to reach an accurate control over critical reaction parameters such as temperature and reaction time. Furthermore, by performing the optimization process through a statistical DoE (Design of Experiment) approach, these parameters could be properly adjusted with a limited number of experiments. This process led us to a better understanding of the relevant factors that govern porphyrins monobromination and to obtain compound 1 with an unprecedent 80% yield.


RSC Advances ◽  
2014 ◽  
Vol 4 (26) ◽  
pp. 13620-13625 ◽  
Author(s):  
Amanda S. de Miranda ◽  
Rodrigo O. M. A. de Souza ◽  
Leandro S. M. Miranda

The chemoenzymatic dynamic kinetic resolution of (+/−)-α-methylbenzylamine under continuous flow conditions in the presence of Pd/BaSO4as racemization catalyst and ammonium formate as reductant is described.


2008 ◽  
Vol 18 (6) ◽  
pp. 922-927 ◽  
Author(s):  
Suk Fun Chin ◽  
K. Swaminathan Iyer ◽  
Colin L. Raston ◽  
Martin Saunders

1995 ◽  
Vol 32 (8) ◽  
pp. 205-212 ◽  
Author(s):  
A. Wobus ◽  
S. Ulrich ◽  
I. Röske

Two identical fixed bed reactors containing gas-permeable tubings as carrier material were compared for the elimination of chlorophenols. Under plug flow conditions, the continuous flow operation resulted in a stratification of biomass due to concentration gradients. To achieve a homogeneous colonization, the sequencing batch mode has been applicated to one biofilm reactor (Sequencing Batch Biofilm Reactor - SBBR). Concentration gradients after filling, probably due to sorption phenomena, caused an uneven distribution of biomass in the SBBR. However, the colonization of the SBBR was more homogeneous as compared to the continuously operated reactor (CFBR). As to the elimination of a trichlorophenol (2,4,5-trichlorophenol - TCP), no significant differences between the SBBR and the CFBR were observed with regard to its sensitivity against load surges. It is to be supposed that sorption to the biofilm was included in the elimination of chlorophenols. A higher diversity of protozoan community and meiofauna is obviously to be attributed to continuous flow.


2011 ◽  
Vol 7 ◽  
pp. 1164-1172 ◽  
Author(s):  
Sukhdeep Singh ◽  
J Michael Köhler ◽  
Andreas Schober ◽  
G Alexander Groß

The Eschenmoser coupling is a useful carbon–carbon bond forming reaction which has been used in various different synthesis strategies. The reaction proceeds smoothly if S-alkylated ternary thioamides or thiolactames are used. In the case of S-alkylated secondary thioamides or thiolactames, the Eschenmoser coupling needs prolonged reaction times and elevated temperatures to deliver valuable yields. We have used a flow chemistry system to promote the Eschenmoser coupling under enhanced reaction conditions in order to convert the demanding precursors such as S-alkylated secondary thioamides and thiolactames in an efficient way. Under pressurized reaction conditions at about 220 °C, the desired Eschenmoser coupling products were obtained within 70 s residence time. The reaction kinetics was investigated and 15 examples of different building block combinations are given.


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