You are signed out
Join Innoget to connect with Henrik Sunden and thousands
of innovation-driven professionals and organizations
Faculty Member at Chalmers University of Technology
Organic synthetic with interest in greener synthesis and modular synthesis of low molecular weight gels for smart materials applications.
Goethe University
September 2007 - December 2008
Frankfurt am Main
Gothenburg University
February 2009 - December 2012
Gothenburg
Chalmers University of Technology
February 2013 - Present
Gothenburg
Stockholm University
January 2004 - January 2007
Organic chemistry
Thesis title: Organocatlytic domino reactions
Linda Ta Anton Axelsson Joachim Bijl Prof. Matti Haukka Dr. Henrik Sundén
Imidazolium‐based ionic liquids (ILs) serve both as recyclable reaction media and as precatalysts for the N‐heterocyclic carbene‐catalyzed conjugate addition of α,β‐unsaturated aldehydes to chalcones. The reaction produces a broad scope of 1,6‐ketoesters incorporating an anti‐diphenyl moiety in high yields and with high stereoselectivity. In recycling experiments, the IL can be reused up to five times with retained reactivity and selectivity. Moreover, the 1,6‐ketoesters form self‐assembled organogels in aliphatic hydrocarbons. The reaction protocol is robust, easily operated, scalable and highly functionalized compounds can be obtained from inexpensive and readily accessible starting materials.
Dr. Claire Sauvée Dr. Anna Ström Dr. Matti Haukka Dr. Henrik Sundén
Herein we report a multi‐component reaction approach for the development of a new class of hydrogelators based on the OxoTriphenylHexanOate (OTHO) backbone. A focused library of OTHOs has been synthesized and their hydrogelation features evaluated. The two most potent hydrogelators were studied by rheology revealing different stiffness, appearances and thixotropic behavior of the gels. The new gelators showcase the versatility of the OTHO backbone as a platform for the design of functionalized hydrogels with tunable gel properties.
Chien-Wei Hsu, Claire Sauvée, Henrik Sundén and Joakim Andréasson
A facile cocktail approach implying the mixing of diarylethene (DAE) photoswitches and low molecular weight gelators (LMWG) is presented. The photoresponsive gels exhibit multicolored emission that can be precisely controlled by different light exposure schemes (wavelength and dose), applicable for fluorescence patterning/writing. Including also a blue-emitting fluorophore allows for tri-chromatic color tuning of the emission via multistep energy transfer reactions, which in turn yields a non-linear response between the emission spectra and the light dose. This feature is highly desired in data security and anti-counterfeiting contexts. The information written in the gels can be conveniently erased by light, mass diffusion, or shaking; the latter being due to the thixotropic properties of the gels.