TY  - GEN
A1  - Al-Naji, Majd
A1  - Schlaad, Helmut
A1  - Antonietti, Markus
T1  - New (and old) monomers from biorefineries to make polymer chemistry more sustainable
T2  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
N2  - This opinion article describes recent approaches to use the "biorefinery" concept to lower the carbon footprint of typical mass polymers, by replacing parts of the fossil monomers with similar or even the same monomer made from regrowing dendritic biomass. Herein, the new and green catalytic synthetic routes are for lactic acid (LA), isosorbide (IS), 2,5-furandicarboxylic acid (FDCA), and p-xylene (pXL). Furthermore, the synthesis of two unconventional lignocellulosic biomass derivable monomers, i.e., alpha-methylene-gamma-valerolactone (MeGVL) and levoglucosenol (LG), are presented. All those have the potential to enter in a cost-effective way, also the mass market and thereby recover lost areas for polymer materials. The differences of catalytic unit operations of the biorefinery are also discussed and the challenges that must be addressed along the synthesis path of each monomers.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1385 
KW  - biodegradable polymers
KW  - biorefineries
KW  - carbohydrate‐ based
KW  - monomers
KW  - green polymers
KW  - lignocellulosic biomass
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-570614
SN  - 1866-8372
IS  - 3
ER  - 
TY  - JOUR
A1  - Al-Naji, Majd
A1  - Schlaad, Helmut
A1  - Antonietti, Markus
T1  - New (and old) monomers from biorefineries to make polymer chemistry more sustainable
JF  - Macromolecular rapid communications
N2  - This opinion article describes recent approaches to use the "biorefinery" concept to lower the carbon footprint of typical mass polymers, by replacing parts of the fossil monomers with similar or even the same monomer made from regrowing dendritic biomass. Herein, the new and green catalytic synthetic routes are for lactic acid (LA), isosorbide (IS), 2,5-furandicarboxylic acid (FDCA), and p-xylene (pXL). Furthermore, the synthesis of two unconventional lignocellulosic biomass derivable monomers, i.e., alpha-methylene-gamma-valerolactone (MeGVL) and levoglucosenol (LG), are presented. All those have the potential to enter in a cost-effective way, also the mass market and thereby recover lost areas for polymer materials. The differences of catalytic unit operations of the biorefinery are also discussed and the challenges that must be addressed along the synthesis path of each monomers.
KW  - biodegradable polymers
KW  - biorefineries
KW  - carbohydrate‐ based
KW  - monomers
KW  - green polymers
KW  - lignocellulosic biomass
Y1  - 2020
U6  - https://doi.org/10.1002/marc.202000485
SN  - 1022-1336
SN  - 1521-3927
VL  - 42
IS  - 3
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Herfurth, Christoph
A1  - Voll, Dominik
A1  - Buller, Jens
A1  - Weiss, Jan
A1  - Barner-Kowollik, Christopher
A1  - Laschewsky, André
T1  - Radical addition fragmentation chain transfer (RAFT) polymerization of ferrocenyl (meth)acrylates
JF  - Journal of polymer science : A, Polymer chemistry
N2  - We report on the controlled free radical homopolymerization of 1-ferrocenylethyl acrylate as well as of three new ferrocene bearing monomers, namely 4-ferrocenylbutyl acrylate, 2-ferrocenylamido-2-methylpropyl acrylate, and 4-ferrocenylbutyl methacrylate, by the RAFT technique. For comparison, the latter monomer was polymerized using ATRP, too. The ferrocene containing monomers were found to be less reactive than their analogues free of ferrocene. The reasons for the low polymerizability are not entirely clear. As the addition of free ferrocene to the reaction mixture did not notably affect the polymerizations, sterical hindrance by the bulky ferrocene moiety fixed on the monomers seems to be the most probable explanation. Molar masses found for 1-ferrocenylethyl acrylate did not exceed 10,000 g mol(-1), while for 4-ferrocenylbutyl (meth) acrylate molar masses of 15,000 g mol(-1) could be obtained. With PDIs as low as 1.3 in RAFT polymerization of the monomers, good control over the polymerization was achieved.
KW  - ferrocene
KW  - living radical polymerization (LRP)
KW  - monomers
KW  - radical addition fragmentation chain transfer (RAFT)
KW  - radical polymerization
KW  - redox polymers
KW  - synthesis
Y1  - 2012
U6  - https://doi.org/10.1002/pola.24994
SN  - 0887-624X
VL  - 50
IS  - 1
SP  - 108
EP  - 118
PB  - Wiley-Blackwell
CY  - Malden
ER  -