This research is supported by a Marie Curie Action

This research is supported by a Marie Curie Action
This research has received funding from the People Programme (Marie Curie Actions) of the EU (FP7/2007-2013) under REA grant agreement nº PIEF-GA-2013-622413

Saturday, 12 December 2015

How to dry molecular sieves?

In this post, I will move from the topic of asymmetric catalysis and I will explain a basic operation in organic chemistry lab.
Laboratories involved with organic synthesis require efficient methods with which to dry (i.e. removal of water) organic solvents. In some cases, water present in organic solvents can be deleterious for the chemical reaction since reactants and/or reagents can react faster with water being deactivated with the consequent loss of performance of the reaction.
Among the different methods available for drying solvents, the use of molecular sieves is one of the most efficient ones. A molecular sieve is a material with pores (very small holes) of uniform size. These pore diameters are of the dimensions of small molecules, thus large molecules cannot be absorbed, while smaller molecules can.

Molecular sieves
From the chemistry point of view, molecular sieves are crystalline metal aluminosilicates having a three dimensional interconnecting network of silica and alumina tetrahedra. Natural water of hydration is removed from this network by heating to produce uniform cavities which selectively adsorb molecules of a specific size.
Commercially available molecular sieves contain water, therefore it is needed to remove this water content before use as dessicant in organic solvents. This process is called "activation" of molecular sieves.
In the following video created by my lab mate Rasmus Mose you will find a short description on how to activate molecular sieves and store solvents in a schlenk flask.
Very useful in case you work in an organic chemistry lab!

Saturday, 5 December 2015

Publication in Angewandte Chemie International Edition (this post is for specialists only)

Recently, it has been published in Angewandte Chemie International Edition research I have been involved with my lab mates Yang, Rune, and Hao.
For those who are familiar with organic chemistry, you will find the link to the original article below. Hope you enjoy reading it!

Li, Y., Tur, F., Nielsen, R. P., Jiang, H., Jensen, F. and Jørgensen, K. A. (2015), Enantioselective Formal [4+2] Cycloadditions to 3-Nitroindoles by Trienamine Catalysis: Synthesis of Chiral Dihydrocarbazoles. Angew. Chem. Int. Ed. 2015, 54, 1020-1024 doi:10.1002/anie.201509693

Aarhus University

Aarhus University
Aarhus University website

Center for Catalysis, AU

Center for Catalysis, AU
Center for Catalysis, AU website

Marie Curie Actions

Marie Curie Actions
Marie Curie Actions website