TY  - JOUR
A1  - Schlappa, Stephanie
A1  - Brenker, Lee Josephine
A1  - Bressel, Lena
A1  - Hass, Roland
A1  - Münzberg, Marvin
T1  - Process characterization of polyvinyl acetate emulsions applying inline photon density wave spectroscopy at high solid contents
JF  - Polymers / Molecular Diversity Preservation International
N2  - The high solids semicontinuous emulsion polymerization of polyvinyl acetate using poly (vinyl alcohol-co-vinyl acetate) as protective colloid is investigated by optical spectroscopy. The suitability of Photon Density Wave (PDW) spectroscopy as inline Process Analytical Technology (PAT) for emulsion polymerization processes at high solid contents (>40% (w/w)) is studied and evaluated. Inline data on absorption and scattering in the dispersion is obtained in real-time. The radical polymerization of vinyl acetate to polyvinyl acetate using ascorbic acid and sodium persulfate as redox initiator system and poly (vinyl alcohol-co-vinyl acetate) as protective colloid is investigated. Starved-feed radical emulsion polymerization yielded particle sizes in the nanometer size regime. PDW spectroscopy is used to monitor the progress of polymerization by studying the absorption and scattering properties during the synthesis of dispersions with increasing monomer amount and correspondingly decreasing feed rate of protective colloid. Results are compared to particle sizes determined with offline dynamic light scattering (DLS) and static light scattering (SLS) during the synthesis.
KW  - photon density wave spectroscopy
KW  - multiple light scattering
KW  - emulsion
KW  - polymerization
KW  - process analytical technology
KW  - polyvinyl acetate
Y1  - 2021
U6  - https://doi.org/10.3390/polym13040669
SN  - 2073-4360
VL  - 13
IS  - 4
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Koc, Julian
A1  - Schardt, Lisa
A1  - Nolte, Kim
A1  - Beyer, Cindy
A1  - Eckhard, Till
A1  - Schwiderowski, Philipp
A1  - Clarke, Jessica L.
A1  - Finlay, John A.
A1  - Clare, Anthony S.
A1  - Muhler, Martin
A1  - Laschewsky, André
A1  - Rosenhahn, Axel
T1  - Effect of dipole orientation in mixed, charge-equilibrated self-assembled monolayers on protein adsorption and marine biofouling
JF  - ACS applied materials & interfaces
N2  - While zwitterionic interfaces are known for their excellent low-fouling properties, the underlying molecular principles are still under debate. In particular, the role of the zwitterion orientation at the interface has been discussed recently. For elucidation of the effect of this parameter, self-assembled monolayers (SAMs) on gold were prepared from stoichiometric mixtures of oppositely charged alkyl thiols bearing either a quaternary ammonium or a carboxylate moiety. The alkyl chain length of the cationic component (11-mercaptoundecyl)-N,N,N-trimethylammonium, which controls the distance of the positively charged end group from the substrate's surface, was kept constant. In contrast, the anionic component and, correspondingly, the distance of the negatively charged carboxylate groups from the surface was varied by changing the alkyl chain length in the thiol molecules from 7 (8-mercaptooctanoic acid) to 11 (12-mercaptododecanoic acid) to 15 (16-mercaptohexadecanoic acid). In this way, the charge neutrality of the coating was maintained, but the charged groups exposed at the interface to water were varied, and thus, the orientation of the dipoles in the SAMs was altered. In model biofouling studies, protein adsorption, diatom accumulation, and the settlement of zoospores were all affected by the altered charge distribution. This demonstrates the importance of the dipole orientation in mixed-charged SAMs for their inertness to nonspecific protein adsorption and the accumulation of marine organisms. Overall, biofouling was lowest when both the anionic and the cationic groups were placed at the same distance from the substrate's surface.
KW  - SAM
KW  - antifouling coatings
KW  - zwitterionic
KW  - XPS
KW  - Navicula perminuta
KW  - Ulva linza
KW  - SPR
Y1  - 2020
U6  - https://doi.org/10.1021/acsami.0c11580
SN  - 1944-8244
SN  - 1944-8252
VL  - 12
IS  - 45
SP  - 50953
EP  - 50961
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Machatschek, Rainhard Gabriel
A1  - Lendlein, Andreas
T1  - Fundamental insights in PLGA degradation from thin film studies
JF  - Journal of controlled release : official journal of the Controlled Release Society and of the Japanese Society of Drug Delivery Systems
N2  - Poly(lactide-co-glycolide)s are commercially available degradable implant materials, which are typically selected based on specifications given by the manufacturer, one of which is their molecular weight. Here, we address the question whether variations in the chain length and their distribution affect the degradation behavior of Poly[(rac-lactide)-co-glycolide]s (PDLLGA). The hydrolysis was studied in ultrathin films at the air-water interface in order to rule out any morphological effects. We found that both for purely hydrolytic degradation as well as under enzymatic catalysis, the molecular weight has very little effect on the overall degradation kinetics of PDLLGAs. The quantitative analysis suggested a random scission mechanism. The monolayer experiments showed that an acidic micro-pH does not accelerate the degradation of PDLLGAs, in contrast to alkaline conditions. The degradation experiments were combined with interfacial rheology measurements, which showed a drastic decrease of the viscosity at little mass loss. The extrapolated molecular weight behaved similar to the viscosity, dropping to a value near to the solubility limit of PDLLGA oligomers before mass loss set in. This observation suggests a solubility controlled degradation of PDLLGA. Conclusively, the molecular weight affects the degradation of PDLLGA devices mostly in indirect ways, e.g. by determining their morphology and porosity during fabrication. Our study demonstrates the relevance of the presented Langmuir degradation method for the design of controlled release systems.
KW  - PDLLGA
KW  - Degradation
KW  - Langmuir monolayer
Y1  - 2019
U6  - https://doi.org/10.1016/j.jconrel.2019.12.044
SN  - 0168-3659
SN  - 1873-4995
VL  - 319
SP  - 276
EP  - 284
PB  - Elsevier
CY  - New York
ER  - 
TY  - JOUR
A1  - Schürmann, Robin
A1  - Titov, Evgenii
A1  - Ebel, Kenny
A1  - Kogikoski Junior, Sergio
A1  - Mostafa, Amr
A1  - Saalfrank, Peter
A1  - Milosavljević, Aleksandar R.
A1  - Bald, Ilko
T1  - The electronic structure of the metal-organic interface of isolated ligand coated gold nanoparticles
JF  - Nanoscale Advances
N2  - Light induced electron transfer reactions of molecules on the surface of noble metal nanoparticles (NPs) depend significantly on the electronic properties of the metal-organic interface. Hybridized metal-molecule states and dipoles at the interface alter the work function and facilitate or hinder electron transfer between the NPs and ligand. X-ray photoelectron spectroscopy (XPS) measurements of isolated AuNPs coated with thiolated ligands in a vacuum have been performed as a function of photon energy, and the depth dependent information of the metal-organic interface has been obtained. The role of surface dipoles in the XPS measurements of isolated ligand coated NPs is discussed and the binding energy of the Au 4f states is shifted by around 0.8 eV in the outer atomic layers of 4-nitrothiophenol coated AuNPs, facilitating electron transport towards the molecules. Moreover, the influence of the interface dipole depends significantly on the adsorbed ligand molecules. The present study paves the way towards the engineering of the electronic properties of the nanoparticle surface, which is of utmost importance for the application of plasmonic nanoparticles in the fields of heterogeneous catalysis and solar energy conversion.
Y1  - 2022
U6  - https://doi.org/10.1039/d1na00737h
SN  - 2516-0230
VL  - 4
IS  - 6
SP  - 1599
EP  - 1607
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Harmanli, İpek
A1  - Tarakina, Nadezda
A1  - Antonietti, Markus
A1  - Oschatz, Martin
T1  - "Giant" nitrogen uptake in ionic liquids confined in carbon pores
JF  - Journal of the American Chemical Society
N2  - Ionic liquids are well known for their high gas absorption capacity. It is shown that this is not a solvent constant, but can be enhanced by another factor of 10 by pore confinement, here of the ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate (EmimOAc) in the pores of carbon materials. A matrix of four different carbon compounds with micro- and mesopores as well as with and without nitrogen doping is utilized to investigate the influence of the carbons structure on the nitrogen uptake in the pore-confined EmimOAc. In general, the absorption is most improved for IL in micropores and in nitrogen-doped carbon. This effect is so large that it is already seen in TGA and DSC experiments. Due to the low vapor pressure of the IL, standard volumetric sorption experiments can be used to quantify details of this effect. It is reasoned that it is the change of the molecular arrangement of the ions in the restricted space of the pores that creates additional free volume to host molecular nitrogen.
Y1  - 2021
U6  - https://doi.org/10.1021/jacs.1c00783
SN  - 0002-7863
SN  - 1520-5126
VL  - 143
IS  - 25
SP  - 9377
EP  - 9384
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Frieß, Fabian
A1  - Lendlein, Andreas
A1  - Wischke, Christian
T1  - Switching microobjects from low to high aspect ratios using a shape-memory effect
JF  - Soft matter
N2  - Spherical particles from shape-memory polymers (SMP) can be stretched to ellipsoids with high aspect ratio (AR) and temporarily stabilized. They can switch back to low AR upon thermal stimulation. Here, the creation of an alternative shape-switching capability of particles from low to high AR is introduced, where a SMP matrix from polyvinyl alcohol (PVA) is used to create crosslinked high AR particles and to program the embedded micrometer-sized particles from a second SMP (oligo(epsilon-caprolactone) micronetworks, MN) with a low switching temperature T-sw. This programming proceeds through shape-recovery of the PVA matrix, from which the MN are harvested by PVA matrix dissolution. The use of a dissolvable SMP matrix may be a general strategy to efficiently create systems with complex moving capabilities.
Y1  - 2021
U6  - https://doi.org/10.1039/d1sm00947h
SN  - 1744-6848
VL  - 17
IS  - 41
SP  - 9326
EP  - 9331
PB  - Royal Society of Chemistry
CY  - London
ER  - 
TY  - JOUR
A1  - Lau, Skadi
A1  - Gossen, Manfred
A1  - Lendlein, Andreas
T1  - Designing cardiovascular implants taking in view the endothelial basement membrane
JF  - International journal of molecular sciences
N2  - Insufficient endothelialization of cardiovascular grafts is a major hurdle in vascular surgery and regenerative medicine, bearing a risk for early graft thrombosis. Neither of the numerous strategies pursued to solve these problems were conclusive. Endothelialization is regulated by the endothelial basement membrane (EBM), a highly specialized part of the vascular extracellular matrix. Thus, a detailed understanding of the structure-function interrelations of the EBM components is fundamental for designing biomimetic materials aiming to mimic EBM functions. In this review, a detailed description of the structure and functions of the EBM are provided, including the luminal and abluminal interactions with adjacent cell types, such as vascular smooth muscle cells. Moreover, in vivo as well as in vitro strategies to build or renew EBM are summarized and critically discussed. The spectrum of methods includes vessel decellularization and implant biofunctionalization strategies as well as tissue engineering-based approaches and bioprinting. Finally, the limitations of these methods are highlighted, and future directions are suggested to help improve future design strategies for EBM-inspired materials in the cardiovascular field.
KW  - endothelial cells
KW  - bioinstructive implants
KW  - vascular grafts
KW  - tissue
KW  - engineering
KW  - bioprinting
KW  - bioinspired materials
KW  - biological membrane
KW  - endothelial basement membrane
KW  - biomaterial
Y1  - 2021
U6  - https://doi.org/10.3390/ijms222313120
SN  - 1422-0067
VL  - 22
IS  - 23
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Li, Zhen
A1  - Spangenberg, Erik
A1  - Schicks, Judith Maria
A1  - Kempka, Thomas
T1  - Numerical simulation of hydrate formation in the LArge-Scale Reservoir Simulator (LARS)
JF  - Energies : open-access journal of related scientific research, technology development and studies in policy and management
N2  - The LArge-scale Reservoir Simulator (LARS) has been previously developed to study hydrate dissociation in hydrate-bearing systems under in-situ conditions. In the present study, a numerical framework of equations of state describing hydrate formation at equilibrium conditions has been elaborated and integrated with a numerical flow and transport simulator to investigate a multi-stage hydrate formation experiment undertaken in LARS. A verification of the implemented modeling framework has been carried out by benchmarking it against another established numerical code. Three-dimensional (3D) model calibration has been performed based on laboratory data available from temperature sensors, fluid sampling, and electrical resistivity tomography. The simulation results demonstrate that temperature profiles, spatial hydrate distribution, and bulk hydrate saturation are consistent with the observations. Furthermore, our numerical framework can be applied to calibrate geophysical measurements, optimize post-processing workflows for monitoring data, improve the design of hydrate formation experiments, and investigate the temporal evolution of sub-permafrost methane hydrate reservoirs.
KW  - methane hydrate
KW  - temperature sensor
KW  - electrical resistivity tomography
KW  - hydrate formation
KW  - numerical simulation
Y1  - 2022
U6  - https://doi.org/10.3390/en15061974
SN  - 1996-1073
VL  - 15
IS  - 6
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Kogikoski Junior, Sergio
A1  - Dutta, Anushree
A1  - Bald, Ilko
T1  - Spatial separation of plasmonic hot-electron generation and a hydrodehalogenation reaction center using a DNA wire
JF  - ACS nano
N2  - Using hot charge carriers far from a plasmonic nanoparticle surface is very attractive for many applications in catalysis and nanomedicine and will lead to a better understanding of plasmon-induced processes, such as hot-charge-carrier- or heat-driven chemical reactions. Herein we show that DNA is able to transfer hot electrons generated by a silver nanoparticle over several nanometers to drive a chemical reaction in a molecule nonadsorbed on the surface. For this we use 8-bromo-adenosine introduced in different positions within a double-stranded DNA oligonucleotide. The DNA is also used to assemble the nanoparticles into nanoparticles ensembles enabling the use of surface-enhanced Raman scattering to track the decomposition reaction. To prove the DNA-mediated transfer, the probe molecule was insulated from the source of charge carriers, which hindered the reaction. The results indicate that DNA can be used to study the transfer of hot electrons and the mechanisms of advanced plasmonic catalysts.
KW  - plasmonics
KW  - DNA nanotechnology
KW  - hot electrons
KW  - charge transfer
KW  - SERS
KW  - superlattices
Y1  - 2021
U6  - https://doi.org/10.1021/acsnano.1c09176
SN  - 1936-0851
SN  - 1936-086X
VL  - 15
IS  - 12
SP  - 20562
EP  - 20573
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Fudickar, Werner
A1  - Bauch, Marcel
A1  - Ihmels, Heiko
A1  - Linker, Torsten
T1  - DNA-triggered enhancement of singlet oxygen production by pyridinium alkynylanthracenes
JF  - Chemistry - a European journal
N2  - There is an ongoing interest in O-1(2) sensitizers, whose activity is selectively controlled by their interaction with DNA. To this end, we synthesized three isomeric pyridinium alkynylanthracenes 2 o-p and a water-soluble trapping reagent for O-1(2). In water and in the absence of DNA, these dyes show a poor efficiency to sensitize the photooxygenation of the trapping reagent as they decompose due to electron transfer processes. In contrast, in the presence of DNA O-1(2) is generated from the excited DNA-bound ligand. The interactions of 2 o-p with DNA were investigated by thermal DNA melting studies, UV/vis and fluorescence spectroscopy, and linear and circular dichroism spectroscopy. Our studies revealed an intercalative binding with an orientation of the long pyridyl-alkynyl axis parallel to the main axis of the DNA base pairs. In the presence of poly(dA : dT), all three isomers show an enhanced formation of singlet oxygen, as indicated by the reaction of the latter with the trapping reagent. With green light irradiation of isomer 2 o in poly(dA : dT), the conversion rate of the trapping reagent is enhanced by a factor >10. The formation of O-1(2) was confirmed by control experiments under anaerobic conditions, in deuterated solvents, or by addition of O-1(2) quenchers. When bound to poly(dG : dC), the opposite effect was observed only for isomers 2 o and 2 m, namely the trapping reagent reacted significantly slower. Overall, we showed that pyridinium alkynylanthracenes are very useful intercalators, that exhibit an enhanced photochemical O-1(2) generation in the DNA-bound state.
KW  - Anthracene
KW  - DNA
KW  - intercalations
KW  - photochemistry
KW  - singlet oxygen
Y1  - 2021
U6  - https://doi.org/10.1002/chem.202101918
SN  - 1521-3765
VL  - 27
IS  - 54
SP  - 13591
EP  - 13604
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Goswami, Koushik
T1  - Inertial particle under active fluctuations
BT  - diffusion and work distributions
JF  - Physical review E, Statistical, nonlinear, and soft matter physics
N2  - We study the underdamped motion of a passive particle in an active environment. Using the phase space path integral method we find the probability distribution function of position and velocity for a free and a harmonically bound particle. The environment is characterized by an active noise which is described as the Ornstein-Uhlenbeck process (OUP). Taking two similar, yet slightly different OUP models, it is shown how inertia along with other relevant parameters affect the dynamics of the particle. Further we investigate the work fluctuations of a harmonically trapped particle by considering the trap center being pulled at a constant speed. Finally, the fluctuation theorem of work is validated with an effective temperature in the steady-state limit.
Y1  - 2022
U6  - https://doi.org/10.1103/PhysRevE.105.044123
SN  - 2470-0045
SN  - 2470-0053
VL  - 105
IS  - 4
PB  - American Physical Society
CY  - College Park
ER  - 
TY  - JOUR
A1  - Xie, Dongjiu
A1  - Jouini, Oumeima
A1  - Mei, Shilin
A1  - Quan, Ting
A1  - Xu, Yaolin
A1  - Kochovski, Zdravko
A1  - Lu, Yan
T1  - Spherical polyelectrolyte brushes templated hollow C@MnO nanospheres as sulfur host materials for Li-S batteries
JF  - ChemNanoMat : Chemistry of Nanomaterials for Energy, Biology and More
N2  - Li-S battery has been considered as the next-generation energy storage device, which still suffers from the shuttle effect of lithium polysulfides (LiPSs). In this work, mesoporous hollow carbon-coated MnO nanospheres (C@MnO) have been designed and synthesized using spherical polyelectrolyte brushes (SPB) as template, KMnO4 as MnO precursor, and polydopamine as carbon source to improve the electrochemical performance of Li-S battery. The hollow C@MnO nanospheres enable the combination of physical confinement and chemical adsorption of the LiPSs. The thin carbon coating layer can provide good electrical conductivity and additional physical confinement to polysulfides. Moreover, the encapsulated MnO inside the carbon shell exhibits strong chemical adsorption to polysulfides. The constructed C@MnO/S cathode shows the discharge capacity of 1026 mAh g(-1) at 0.1 C with 79% capacity retention after 80 cycles. The synthesized hollow C@MnO nanoparticles can work as highly efficient sulfur host materials, providing an effective solution to suppress the shuttle effect in Li-S battery.
KW  - hollow nanospheres
KW  - lithium-sulfur battery
KW  - manganese monoxide
KW  - sperical
KW  - polyelectrolyte brushes
Y1  - 2022
U6  - https://doi.org/10.1002/cnma.202100455
SN  - 2199-692X
VL  - 8
IS  - 4
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Fischer, Eric Wolfgang
A1  - Werther, Michael
A1  - Bouakline, Foudhil
A1  - Grossmann, Frank
A1  - Saalfrank, Peter
T1  - Non-Markovian vibrational relaxation dynamics at surfaces
JF  - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr
N2  - Vibrational dynamics of adsorbates near surfaces plays both an important role for applied surface science and as a model lab for studying fundamental problems of open quantum systems. We employ a previously developed model for the relaxation of a D-Si-Si bending mode at a D:Si(100)-(2 x 1) surface, induced by a "bath " of more than 2000 phonon modes [Lorenz and P. Saalfrank, Chem. Phys. 482, 69 (2017)], to extend previous work along various directions. First, we use a Hierarchical Effective Mode (HEM) model [Fischer et al., J. Chem. Phys. 153, 064704 (2020)] to study relaxation of higher excited vibrational states than hitherto done by solving a high-dimensional system-bath time-dependent Schrodinger equation (TDSE). In the HEM approach, (many) real bath modes are replaced by (much less) effective bath modes. Accordingly, we are able to examine scaling laws for vibrational relaxation lifetimes for a realistic surface science problem. Second, we compare the performance of the multilayer multiconfigurational time-dependent Hartree (ML-MCTDH) approach with that of the recently developed coherent-state-based multi-Davydov-D2 Ansatz [Zhou et al., J. Chem. Phys. 143, 014113 (2015)]. Both approaches work well, with some computational advantages for the latter in the presented context. Third, we apply open-system density matrix theory in comparison with basically "exact " solutions of the multi-mode TDSEs. Specifically, we use an open-system Liouville-von Neumann (LvN) equation treating vibration-phonon coupling as Markovian dissipation in Lindblad form to quantify effects beyond the Born-Markov approximation. Published under an exclusive license by AIP Publishing.
KW  - phonons
KW  - Vibrational states
KW  - Chemical dynamics
KW  - Adsorption
KW  - Surface science
KW  - Open quantum systems
KW  - Density-matrix
KW  - Coherent states
KW  - Markov processes
Y1  - 2022
U6  - https://doi.org/10.1063/5.0092836
SN  - 0021-9606
SN  - 1089-7690
SN  - 1520-9032
VL  - 156
IS  - 21
PB  - AIP Publishing
CY  - Melville
ER  - 
TY  - JOUR
A1  - Chea, Sany
A1  - Nguyen, Khac Toan
A1  - Rosencrantz, Ruben R.
T1  - Microwave-Assisted Synthesis of 5 '-O-methacryloylcytidine Using the Immobilized Lipase Novozym 435
JF  - Molecules
N2  - Nucleobase building blocks have been demonstrated to be strong candidates when it comes to DNA/RNA-like materials by benefiting from hydrogen bond interactions as physical properties. Modifying at the 5 ' position is the simplest way to develop nucleobase-based structures by transesterification using the lipase Novozym 435. Herein, we describe the optimization of the lipase-catalyzed synthesis of the monomer 5 '-O-methacryloylcytidine with the assistance of microwave irradiation. Variable reaction parameters, such as enzyme concentration, molar ratio of the substrate, reaction temperature and reaction time, were investigated to find the optimum reaction condition in terms of obtaining the highest yield.
KW  - microwave irradiation
KW  - Novozym 435
KW  - cytidine
KW  - monomer
KW  - smart materials
Y1  - 2022
U6  - https://doi.org/10.3390/molecules27134112
SN  - 1420-3049
VL  - 27
IS  - 13
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Balk, Maria
A1  - Behl, Marc
A1  - Nöchel, Ulrich
A1  - Lendlein, Andreas
T1  - Enzymatically triggered Jack-in-the-box-like hydrogels
JF  - ACS applied materials & interfaces / American Chemical Society
N2  - Enzymes can support the synthesis or degradation of biomacromolecules in natural processes. Here, we demonstrate that enzymes can induce a macroscopic-directed movement of microstructured hydrogels following a mechanism that we call a "Jack-in-the-box" effect. The material's design is based on the formation of internal stresses induced by a deformation load on an architectured microscale, which are kinetically frozen by the generation of polyester locking domains, similar to a Jack-in-thebox toy (i.e., a compressed spring stabilized by a closed box lid). To induce the controlled macroscopic movement, the locking domains are equipped with enzyme-specific cleavable bonds (i.e., a box with a lock and key system). As a result of enzymatic reaction, a transformed shape is achieved by the release of internal stresses. There is an increase in entropy in combination with a swelling-supported stretching of polymer chains within the microarchitectured hydrogel (i.e., the encased clown pops-up with a pre-stressed movement when the box is unlocked). This utilization of an enzyme as a physiological stimulus may offer new approaches to create interactive and enzyme-specific materials for different applications such as an optical indicator of the enzyme's presence or actuators and sensors in biotechnology and in fermentation processes.
KW  - enzyme
KW  - hydrogels
KW  - stimuli-sensitive materials
KW  - shape change
KW  - poly(e-caprolactone)
KW  - switch
KW  - microporous
Y1  - 2021
U6  - https://doi.org/10.1021/acsami.1c00466
SN  - 1944-8244
SN  - 1944-8252
VL  - 13
IS  - 7
SP  - 8095
EP  - 8101
PB  - American Chemical Society
CY  - Washington, DC
ER  - 
TY  - JOUR
A1  - Löwenberg, Candy
A1  - Tripodo, Giuseppe
A1  - Julich-Gruner, Konstanze K.
A1  - Neffe, Axel T.
A1  - Lendlein, Andreas
T1  - Supramolecular gelatin networks based on inclusion complexes
JF  - Macromolecular bioscience
N2  - Hydrogel forming physical networks based on gelatin are an attractive approach toward multifunctional biomaterials with the option of reshaping, self-healing, and stimuli-sensitivity. However, it is challenging to design such gelatin-based hydrogels to be stable at body temperature. Here, gelatin functionalized with desaminotyrosine (DAT) or desaminotyrosyl tyrosine (DATT) side chains is crosslinked with cyclodextrin (CD) dimers under formation of inclusions complexes. The supramolecular networks displayed at room temperature decreased water uptake (200-600 wt% for DAT-based systems, 200 wt% for DATT based systems), and increased storage moduli up to 25.6 kPa determined by rheology compared to DAT(T) gelatin. The gel-sol transition temperature increased from 33 up to 42 degrees C. The presented system that is completely based on natural building blocks may form the basis for materials that may potentially respond by dissolution or changes of properties to changes in environmental conditions or to the presence of CD guest molecules.
KW  - cyclodextrin
KW  - gelatin
KW  - inclusion complex
KW  - supramolecular polymer network
Y1  - 2020
U6  - https://doi.org/10.1002/mabi.202000221
SN  - 1616-5187
SN  - 1616-5195
VL  - 20
IS  - 10
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Balischewski, Christian
A1  - Bhattacharyya, Biswajit
A1  - Sperlich, Eric
A1  - Günter, Christina
A1  - Beqiraj, Alkit
A1  - Klamroth, Tillmann
A1  - Behrens, Karsten
A1  - Mies, Stefan
A1  - Kelling, Alexandra
A1  - Lubahn, Susanne
A1  - Holtzheimer, Lea
A1  - Nitschke, Anne
A1  - Taubert, Andreas
T1  - Tetrahalidometallate(II) ionic liquids with more than one metal
BT  - the effect of bromide versus chloride
JF  - Chemistry - a European journal
N2  - Fifteen N-butylpyridinium salts - five monometallic [C4Py](2)[MBr4] and ten bimetallic [C4Py](2)[(M0.5M0.5Br4)-M-a-Br-b] (M=Co, Cu, Mn, Ni, Zn) - were synthesized, and their structures and thermal and electrochemical properties were studied. All the compounds are ionic liquids (ILs) with melting points between 64 and 101 degrees C. Powder and single-crystal X-ray diffraction show that all ILs are isostructural. The electrochemical stability windows of the ILs are between 2 and 3 V. The conductivities at room temperature are between 10(-5) and 10(-6) S cm(-1). At elevated temperatures, the conductivities reach up to 10(-4) S cm(-1) at 70 degrees C. The structures and properties of the current bromide-based ILs were also compared with those of previous examples using chloride ligands, which illustrated differences and similarities between the two groups of ILs.
KW  - electrochemistry
KW  - ionic liquids
KW  - metal-containing ionic liquids;
KW  - N-butylpyridinium bromide
KW  - tetrahalidometallates
Y1  - 2022
U6  - https://doi.org/10.1002/chem.202201068
SN  - 1521-3765
VL  - 28
IS  - 64
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - JOUR
A1  - Piekarczyk, Andreas
A1  - Heitmann, Ulrike
A1  - Weiß, Karl-Anders
A1  - Köhl, Michael
A1  - Bald, Ilko
T1  - Development of a simple setup for temperature dependent mass spectrometric measurements for the investigation of outgassing effects in polymeric materials for solar application
JF  - Polymer testing
N2  - A simple experimental setup for temperature dependent mass spectrometric measurements has been constructed. It consists of a heated sample chamber and a mass spectrometer and allows for measurements under inert gas and ambient air. Based on initial measurements on two extruded polystyrene (XPS) samples a methodology for the data analysis has been developed. With this methodology the outgassing temperature of volatile compounds, which were used as blowing agents, has been identified. Furthermore, the composition of the blowing agents has been analyzed by temperature dependent mass spectra. The results indicate the use of ambient air in one material and a mixture of the banned blowing agents R142b and R22, both hydrochlorofluorocarbons (HCFC), in the other material. The here described methodology provides an easy to use approach to identify such compounds, for example as part of environmental or quality control.
Y1  - 2019
U6  - https://doi.org/10.1016/j.polymertesting.2019.106164
SN  - 0142-9418
SN  - 1873-2348
VL  - 81
PB  - Elsevier
CY  - Oxford
ER  - 
TY  - JOUR
A1  - Seuffert, Marcel T.
A1  - Wintzheimer, Susanne
A1  - Oppmann, Maximilian
A1  - Granath, Tim
A1  - Prieschl, Johannes
A1  - Alrefai, Anas
A1  - Holdt, Hans-Jürgen
A1  - Müller-Buschbaum, Klaus
A1  - Mandel, Karl
T1  - An all white magnet by combination of electronic properties of a white light emitting MOF with strong magnetic particle systems
JF  - Journal of materials chemistry : C, Materials for optical and electronic devices
N2  - A multi-component particle system was developed that combines the properties of white color, white light emission and strong magnetism on the macroscopic and microscopic scale. The system is constituted by combination of an inorganic white core with either hard or soft magnetic properties and a white light emitting MOF. The key towards this achievement is the supraparticulate character constituted by a magnetic core, of either magnetite or alpha-Fe, surrounded by titania and silica nanoparticles of a certain size in a loose structural shell-arrangement as white components and finally the white light emitting metal-organic framework (MOF) EuTb@IFP-1 as building blocks of a core-shell structure. The supraparticles are created by forced assembly of the inorganic compounds and by combining spray-drying and postsynthetic modification by solvothermal chemistry. Thereby, the gap is bridged that homogenous compounds are either strongly magnetic, white in appearance or white light emitting. The composites presented herein inherit these properties intrinsically as electronic properties. The white characteristics are based on all optical properties that enable white: light reflection, refraction, and light emission. This work shifts the paradigm that strong magnetic materials are always expected to be intrinsically dark.
Y1  - 2020
U6  - https://doi.org/10.1039/d0tc03473h
SN  - 2050-7526
SN  - 2050-7534
VL  - 8
IS  - 45
SP  - 16010
EP  - 16017
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Liebig, Ferenc
A1  - Sarhan, Radwan Mohamed
A1  - Schmitt, Clemens Nikolaus Zeno
A1  - Thünemann, Andreas F.
A1  - Prietzel, Claudia Christina
A1  - Bargheer, Matias
A1  - Koetz, Joachim
T1  - Gold nanotriangles with crumble topping and their influence on catalysis and surface-enhanced raman spectroscopy
JF  - ChemPlusChem
N2  - By adding hyaluronic acid (HA) to dioctyl sodium sulfosuccinate (AOT)-stabilized gold nanotriangles (AuNTs) with an average thickness of 7.5 +/- 1 nm and an edge length of about 175 +/- 17 nm, the AOT bilayer is replaced by a polymeric HA-layer leading to biocompatible nanoplatelets. The subsequent reduction process of tetrachloroauric acid in the HA-shell surrounding the AuNTs leads to the formation of spherical gold nanoparticles on the platelet surface. With increasing tetrachloroauric acid concentration, the decoration with gold nanoparticles can be tuned. SAXS measurements reveal an increase of the platelet thickness up to around 14.5 nm, twice the initial value of bare AuNTs. HRTEM micrographs show welding phenomena between densely packed particles on the platelet surface, leading to a crumble formation while preserving the original crystal structure. Crumbles crystallized on top of the platelets enhance the Raman signal by a factor of around 20, and intensify the plasmon-driven dimerization of 4-nitrothiophenol (4-NTP) to 4,4 '-dimercaptoazobenzene in a yield of up to 50 %. The resulting crumbled nanotriangles, with a biopolymer shell and the absorption maximum in the second window for in vivo imaging, are promising candidates for biomedical sensing.
KW  - gold nanostructures
KW  - HRTEM
KW  - hyaluronic acid
KW  - monolayer formation
KW  - SERS
Y1  - 2020
U6  - https://doi.org/10.1002/cplu.201900745
SN  - 2192-6506
VL  - 85
IS  - 3
SP  - 519
EP  - 526
PB  - Wiley-VCH
CY  - Weinheim
ER  -