TY  - JOUR
A1  - Peng, Xingzhou
A1  - Behl, Marc
A1  - Zhang, Pengfei
A1  - Mazurek-Budzyńska, Magdalena
A1  - Feng, Yakai
A1  - Lendlein, Andreas
T1  - Synthesis and characterization of multiblock poly(ester-amide-urethane)s
JF  - MRS advances : a journal of the Materials Research Society (MRS)
N2  - In this study, a multiblock copolymer containing oligo(3-methyl-morpholine-2, 5-dione) (oMMD) and oligo(3-sec-butyl-morpholine-2, 5-dione) (oBMD) building blocks obtained by ring-opening polymerization (ROP) of the corresponding monomers, was synthesized in a polyaddition reaction using an aliphatic diisocyanate. The multiblock copolymer (pBMD-MMD) provided a molecular weight of 40, 000 g·mol−1, determined by gel permeation chromatography (GPC). Incorporation of both oligodepsipeptide segments in multiblock copolymers was confirmed by 1H NMR and Matrix Assisted Laser Desorption/Ionization Time Of Flight Mass Spectroscopy (MALDI-TOF MS) analysis. pBMD-MMD showed two separated glass transition temperatures (61 °C and 74 °C) indicating a microphase separation. Furthermore, a broad glass transition was observed by DMTA, which can be attributed to strong physical interaction i.e. by H-bonds formed between amide, ester, and urethane groups of the investigated copolymers. The obtained multiblock copolymer is supposed to own the capability to exhibit strong physical interactions.
Y1  - 2017
U6  - https://doi.org/10.1557/adv.2017.486
SN  - 2059-8521
VL  - 2
SP  - 2551
EP  - 2559
PB  - Cambridge University Press
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Peng, Xingzhou
A1  - Behl, Marc
A1  - Zhang, Pengfei
A1  - Mazurek-Budzynska, Magdalena
A1  - Feng, Yakai
A1  - Lendlein, Andreas
T1  - Synthesis of Well-Defined Dihydroxy Telechelics by (Co)polymerization of Morpholine-2,5-Diones Catalyzed by Sn(IV) Alkoxide
JF  - Macromolecular bioscience
N2  - Well-defined dihydroxy telechelic oligodepsipeptides (oDPs), which have a high application potential as building blocks for scaffold materials for tissue engineering applications or particulate carrier systems for drug delivery applications are synthesized by ring-opening polymerization (ROP) of morpholine-2,5-diones (MDs) catalyzed by 1,1,6,6-tetra-n-butyl-1,6-distanna-2,5,7,10-tetraoxacyclodecane (Sn(IV) alkoxide). In contrast to ROP catalyzed by Sn(Oct)(2), the usage of Sn(IV) alkoxide leads to oDPs, with less side products and well-defined end groups, which is crucial for potential pharmaceutical applications. A slightly faster reaction of the ROP catalyzed by Sn(IV) alkoxide compared to the ROP initiated by Sn(Oct)(2)/EG is found. Copolymerization of different MDs resulted in amorphous copolymers with T(g)s between 44 and 54 degrees C depending on the molar comonomer ratios in the range from 25% to 75%. Based on the well-defined telechelic character of the Sn(IV) alkoxide synthesized oDPs as determined by matrix-assisted laser desorption/ionization time of flight measurements, they resemble interesting building blocks for subsequent postfunctionalization or multifunctional materials based on multiblock copolymer systems whereas the amorphous oDP-based copolymers are interesting building blocks for matrices of drug delivery systems.
KW  - oligodepsipeptides
KW  - ring-opening polymerization
KW  - Sn(IV) alkoxide
KW  - telechelics
KW  - tin(II) 2-ethylhexanoate
Y1  - 2018
U6  - https://doi.org/10.1002/mabi.201800257
SN  - 1616-5187
SN  - 1616-5195
VL  - 18
IS  - 12
PB  - Wiley-VCH
CY  - Weinheim
ER  -