TY  - JOUR
A1  - Biermann, Ursula
A1  - Meier, Michael A. R.
A1  - Butte, Werner
A1  - Metzger, Jürgen O.
T1  - Cross-metathesis of unsaturated triglycerides with methyl acrylate  synthesis of a dimeric metathesis product
JF  - European journal of lipid science and technology
N2  - Highly functionalized dimeric triglycerides, such as compound 2, are obtained as minor products besides branched macromolecules from the acyclic triene metathesis (ATMET) polymerization of unsaturated triglycerides such as glyceryl triundec-10-enoate 1 and methyl acrylate (MA) in the presence of the second generation Hoveyda-Grubbs catalyst. The formed amount of interesting products of lower molecular weight during the ATMET reaction depends on the ratio of MA and triglyceride, reaction time, and temperature. We isolated the dimeric metathesis product 2 and synthesized the respective partially hydrogenated dimer 3 regioselectivly in a seven step reaction sequence starting from 10-undecenoic acid 7 and glycerol. Product 3 was unambiguously characterized by (13)C and (1)H NMR and MS as well as the further intermediate products of the seven step reaction including 10,11 bromo-undecanoic acid 8, the respective brominated 1,3-diglyceride 9, the brominated 1,3-triglyceride 6, and the self-metathesis products 4 and 5 which were isolated and purified.
KW  - Highly functionalized dimeric triglycerides
KW  - Olefin self- and cross-metathesis
KW  - Renewable resources
Y1  - 2011
U6  - https://doi.org/10.1002/ejlt.201000109
SN  - 1438-7697
VL  - 113
IS  - 1
SP  - 39
EP  - 45
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Träger, Juliane
A1  - Klamroth, Tillmann
A1  - Kelling, Alexandra
A1  - Lubahn, Susanne
A1  - Cleve, Ernst
A1  - Mickler, Wulfhard
A1  - Heydenreich, Matthias
A1  - Müller, Holger
A1  - Holdt, Hans-Jürgen
T1  - Complexation of Palladium(II) with unsaturated Dithioethers a systematic development of highly selective ligands for solvent extraction
JF  - European journal of inorganic chemistry : a journal of ChemPubSoc Europe
N2  - There is a demand for new and robust PdII extractants due to growing recycling rates. Chelating dithioethers are promising substances for solvent extraction as they form stable square-planar complexes with PdII. We have modified unsaturated dithioethers, which are known to coordinate PdII, and adapted them to the requirements of industrial practice. The ligands are analogues of 1,2-dithioethene with varying electron-withdrawing backbones and polar end-groups. The crystal structures of several ligands and their palladium complexes were determined as well as their electro- and photochemical properties, complex stability and behaviour in solution. Solvent extraction experiments showed the superiority of some of our ligands over conventionally used extractants in terms of their very fast reaction rates. With highly selective 1,2-bis(2-methoxyethylthio)benzene (4) it is possible to extract PdII from a highly acidic medium in the presence of other base and palladium-group metals.
KW  - Renewable resources
KW  - Palladium
KW  - Chelates
KW  - Ligand design
KW  - S li-gands
Y1  - 2012
U6  - https://doi.org/10.1002/ejic.201101406
SN  - 1434-1948
IS  - 14
SP  - 2341
EP  - 2352
PB  - Wiley-VCH
CY  - Weinheim
ER  -