TY  - JOUR
A1  - Steeples, Elliot
A1  - Kelling, Alexandra
A1  - Schilde, Uwe
A1  - Esposito, Davide
T1  - Amino acid-derived N-heterocyclic carbene palladium complexes for aqueous phase Suzuki-Miyaura couplings
JF  - New journal of chemistry
N2  - In this work, three ligands produced from amino acids were synthesized and used to produce five bis- and PEPPSI-type palladium-NHC complexes using a novel synthesis route from sustainable starting materials. Three of these complexes were used as precatalysts in the aqueous-phase Suzuki-Miyaura coupling of various substrates displaying high activity. TEM and mercury poisoning experiments provide evidence for Pd-nanoparticle formation stabilized in water.
Y1  - 2016
U6  - https://doi.org/10.1039/c5nj03337c
SN  - 1144-0546
SN  - 1369-9261
VL  - 40
SP  - 4922
EP  - 4930
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - GEN
A1  - Steeples, Elliot
A1  - Kelling, Alexandra
A1  - Schilde, Uwe
A1  - Esposito, Davide
T1  - Amino acid-derived N-heterocyclic carbene palladium complexes for aqueous phase Suzuki–Miyaura couplings
N2  - In this work, three ligands produced from amino acids were synthesized and used to produce five bis- and PEPPSI-type palladium–NHC complexes using a novel synthesis route from sustainable starting materials. Three of these complexes were used as precatalysts in the aqueous-phase Suzuki–Miyaura coupling of various substrates displaying high activity. TEM and mercury poisoning experiments provide evidence for Pd-nanoparticle formation stabilized in water.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 319 
KW  - transition-metal-complexes
KW  - imidazolium salts
KW  - green chemistry
KW  - water
KW  - catalysts
KW  - nhc
KW  - hydrogenation
KW  - isomerization
KW  - nanoparticles
KW  - precatalysts
Y1  - 2016
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-394488
SP  - 4922
EP  - 4930
ER  - 
TY  - JOUR
A1  - Kirchhecker, Sarah
A1  - Tröger-Müller, Steffen
A1  - Bake, Sebastian
A1  - Antonietti, Markus
A1  - Taubert, Andreas
A1  - Esposito, Davide
T1  - Renewable pyridinium ionic liquids from the continuous hydrothermal decarboxylation of furfural-amino acid derived pyridinium zwitterions
JF  - Green chemistry : an international journal and green chemistry resource
N2  - Fully renewable pyridinium ionic liquids were synthesised via the hydrothermal decarboxylation of pyridinium zwitterions derived from furfural and amino acids in flow. The functionality of the resulting ionic liquid (IL) can be tuned by choice of different amino acids as well as different natural carboxylic acids as the counter-ions. A representative member of this new class of ionic liquids was successfully used for the synthesis of ionogels and as a solvent for the Heck coupling.
Y1  - 2015
U6  - https://doi.org/10.1039/c5gc00913h
SN  - 1463-9262
SN  - 1463-9270
VL  - 17
IS  - 8
SP  - 4151
EP  - 4156
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  -