Karsten Busse

ORCID: 0000-0003-4168-0957
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Research Areas
  • Advanced Polymer Synthesis and Characterization
  • biodegradable polymer synthesis and properties
  • Polymer crystallization and properties
  • Surfactants and Colloidal Systems
  • Polymer Surface Interaction Studies
  • Polymer Nanocomposites and Properties
  • Block Copolymer Self-Assembly
  • Silicone and Siloxane Chemistry
  • Fuel Cells and Related Materials
  • Electrospun Nanofibers in Biomedical Applications
  • Surface Modification and Superhydrophobicity
  • Material Dynamics and Properties
  • Advanced Sensor and Energy Harvesting Materials
  • Microplastics and Plastic Pollution
  • Conducting polymers and applications
  • Synthesis and properties of polymers
  • Synthesis and characterization of novel inorganic/organometallic compounds
  • Lipid Membrane Structure and Behavior
  • Hydrogels: synthesis, properties, applications
  • Mesoporous Materials and Catalysis
  • Ionic liquids properties and applications
  • X-ray Diffraction in Crystallography
  • N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
  • Molecular Junctions and Nanostructures
  • Organoboron and organosilicon chemistry

Martin Luther University Halle-Wittenberg
2016-2025

Luther University
2016-2025

John Wiley & Sons (United States)
2020

University of Alabama in Huntsville
2012

Saarland University
2009

University of Rostock
1997-2005

University of Applied Sciences Potsdam
1971

Poly(ethylene) (PE) is a commonly used semi-crystalline polymer which, due to the lack of polar groups in repeating unit, not able form Langmuir or Langmuir–Blodgett (LB) films. This problem can be solved using PEs with hydrophilic arranged at regular distances within backbone. With acyclic diene metathesis (ADMET) polymerization, tool for precise addition after certain interval methylene sequence available. In this study, we demonstrate formation Langmuir/LB films from two different...

10.3390/polym12102408 article EN Polymers 2020-10-19

Poly(ethylene oxide) (PEO) is a polymer of great interest due to its prevalence in biomedical, pharmaceutical, and ion conductive systems. In this study, the crystallization behaviors PEO with 22 monomer units (PEO22) having same degree polymerization but an additional 1,4-disubstituted 1,2,3-triazole ring central position chain (PEO11-TR-PEO11) are investigated. PEO11-TR-PEO11 shows one type lamella crystal after cooling T = 0 °C, structural changes during heating below their final melting...

10.1021/acs.macromol.6b01107 article EN Macromolecules 2016-08-15

An isotactic polypropene (i-PP) prepared with a metallocene catalyst system and two random copolymers of propene ethene 2.8 5.7 wt % ethene, respectively (PP-co-E-2.8, PP-co-E-5.7), were isothermally crystallized during simultaneous small- wide-angle X-ray scattering (SAXS, WAXS) in synchrotron measurements. Identical measurements carried out after adding 0.3 N,N'-dicyclohexyl-2,6-naphthalene dicarboxamide, β nucleating agent (β-NA). All samples form the γ-modification to certain extent....

10.1021/ma000719r article EN Macromolecules 2000-10-21

A series of amphiphilic diblock copolymers and triphilic triblock copolymer analogues the architectures BA, CAB, CBA have been synthesized characterized with respect to their aggregation behavior in water. The A, B, C components block are formed by hydrophilic poly(glycerol monomethacrylate) (PGMA), lipophilic poly(propylene oxide) (PPO), a fluorophilic perfluoroalkyl segment, respectively. Their critical micelle concentrations water determined from surface tension measurements. copolymers,...

10.1021/ma102232z article EN Macromolecules 2011-01-10

This work focuses on the reaction mechanism of poly(sulfur nitride) ((SN)x, (S15N)x), with ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate [EMIm][OAc]. We compare this IL S4N4 or its 15N labeled form S415N4, a precursor for synthesis (SN)x and (S15N)x. After purification S4N4-IL- S415N4-system via column chromatography, we characterize products 1H, 13C nuclear magnetic resonance (NMR) spectroscopy electron spray ionization time-of-flight mass spectrometry (ESI-ToF-MS). Furthermore,...

10.26434/chemrxiv-2025-3bx69 preprint EN cc-by-nc 2025-02-06

This work focuses on the reaction mechanism of poly(sulfur nitride) ((SN)x, (S15N)x), with ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate [EMIm][OAc]. We compare this IL S4N4 or its 15N-labeled form S415N4, a precursor for synthesis (SN)x and (S15N)x. After purification S4N4-IL- S415N4-IL systems via column chromatography, we characterized products 1H, 13C, 15N nuclear magnetic resonance spectroscopy electron spray ionization time-of-flight mass spectrometry. Furthermore,...

10.1021/acs.jpcb.5c00294 article EN cc-by The Journal of Physical Chemistry B 2025-04-10

Abstract Amphiphilic di‐ and triblock copolymers containing poly(ethylene oxide) (PEO) as the hydrophilic block poly(perfluorohexylethyl methacrylate) (PFMA) hydrophobic were synthesized by atom‐transfer radical polymerization using hydroxy‐terminated PEO macroinitiator. The characterized size exclusion chromatography 1 H NMR spectroscopy. Self‐association in aqueous solution has been investigated surface tension measurements, dynamic light scattering (DLS), transmission electron microscopy...

10.1002/macp.200390070 article EN Macromolecular Chemistry and Physics 2003-04-29

Aliphatic polyesters having pendant azide groups were prepared by enzymatic polycondensation in the presence of lipase from Candida antarctica type B (CAL-B). The grafting reaction to N3-functional polyester was carried out quantitatively at room temperature using copper-catalyzed azide−alkyne cycloaddition (CuAAC, "click" reaction) with monoalkyne-functional poly(ethylene oxide) (alkyne-PEO, Mn = 750 g/mol). Furthermore, both and successfully sequential one-pot reaction. graft copolymer...

10.1021/bm1011085 article EN Biomacromolecules 2010-11-18

Blends of poly(ethylene oxide) (PEO) and poly(methyl acrylate) (PMA) as well the respective diblock copolymers PEO-b-PMA form a homogeneous melt undergo crystallization PEO upon cooling. Although an identical (Mn = 5000 g/mol) is used in blends copolymers, melting behavior at comparable PMA contents differs strongly revealed by temperature-resolved small-angle X-ray scattering (TR-SAXS) differential scanning calorimetry (DSC) measurements. After isothermal crystallization, lamellae thicken...

10.1021/ma102867d article EN Macromolecules 2011-03-16

The contributions of proton hopping and vehicle mechanism to the intrinsic conductivity was investigated in crystalline liquid 1,2,3-triazole.

10.1039/c5cp07603j article EN Physical Chemistry Chemical Physics 2016-01-01

A new series of poly(perfluorohexylethyl methacrylate)-block-poly(ethylene oxide)-block-poly(perfluorohexylethyl methacrylate), PFMA-b-PEO-b-PFMA triblock copolymers has been synthesized by atom transfer radical polymerization using bifunctional PEO macroinitiators. The molecular structure the block was confirmed 1H NMR spectroscopy and SEC. X-ray scattering studies have carried out to investigate their bulk properties. SAXS shown cubic arrangement spheres (bcc), hexagonally packed cylinders...

10.1002/1521-3935(200210)203:14<2103::aid-macp2103>3.0.co;2-x article EN Macromolecular Chemistry and Physics 2002-10-01

Langmuir monolayers and Langmuir−Blodgett (LB) film morphologies of block copolymers hydrophobically modified iron oxide nanoparticles were studied by surface pressure−mean molecular area (π−mmA) measurements tapping mode atomic force microscopy (AFM). The amphiphilic diblock consisted a hydrophilic poly(ethylene oxide) (PEO) hydrophobic poly(isobutylene) (PIB) block. π−mmA isotherm PEO97-b-PIB37 (the subscripts refer to the respective degrees polymerization) at air/water interface had an...

10.1021/la900549h article EN Langmuir 2009-05-14

Di- and triblock copolymers of tert-butyl methacrylate (tBMA) 2-(N-methylperfluorobutanesulfonamido)ethyl (FMA) were synthesized by sequential anionic polymerization. These polymers characterized size-exclusion chromatography 1H 19F NMR spectroscopy. The microphase separation bulk samples was studied atomic force microscopy small-angle X-ray scattering. Thermal annealing the block at 200 °C yielded inter- intramolecular anhydrides due to splitting ester having groups connected with isobutene...

10.1021/ma0116809 article EN Macromolecules 2001-12-04

The tremendous influence of hydrophilic block length tuning on the aggregation behavior novel water-soluble triphilic (i.e., hydrophilic, lipophilic, and fluorophilic) α,ω-perfluoroalkyl end-capped symmetric ABA triblock copolymers is demonstrated. A lipophilic B blocks are comprised poly(glycerol monomethacrylate) (PGMA) poly(propylene oxide) (PPO), respectively. fluorophilic component consists two "clicked" perfluoroalkyl segments (C9F19) at ends copolymers. Two different synthesized,...

10.1021/ma902753y article EN Macromolecules 2010-02-04

This study investigated and correlated physical properties cell interactions of copolymers obtained by a poly(ethylene glycol) (PEG)-modulated fermentation Azotobacter vinelandii UWD. PEGs with molecular weights 400 3400 Da di(ethylene (DEG) were used to modulate the bacterial synthesis poly(beta-hydroxybutyrate) (PHB). The PHB crystallinity was determined wide-angle X-ray scattering (WAXS). Small-angle (SAXS) showed that lamellar distances decreased between modulated PEG or DEG....

10.1021/bp050044h article EN Biotechnology Progress 2005-06-03

Langmuir films of multifunctional, hydrophilic polyethers containing a hydrophobic cholesterol group (Ch) were studied by surface pressure-mean molecular area (π-mmA) measurements and Brewster angle microscopy (BAM). The either homopolymers or diblock copolymers linear poly(glycerol) (lPG), poly(glyceryl glycidyl ether) (lPGG), poly(ethylene glycol) (lPEG), hyperbranched (hbPG). Surface pressure revealed that the lPG hbPG did not stay at water after spreading solvent evaporation, in contrast...

10.1021/la104274d article EN Langmuir 2010-12-22

ABSTRACT The crystallization and melting behavior of a series poly(glycerol adipate) (PGA) based graft copolymers with either poly(ε‐caprolactone) (PCL), poly(ethylene oxide) (PEO), or PCL‐ b ‐PEO diblock copolymer side chains (i.e., PGA‐ g ‐PCL, ‐PEO, ‐(PCL‐ ‐PEO)) was studied using polarized light optical microscopy (POM), differential scanning calorimetry (DSC), small‐angle X‐ray scattering (SAXS), wide‐angle diffraction (WAXD). These results were compared the corresponding linear analogs...

10.1002/polb.23373 article EN Journal of Polymer Science Part B Polymer Physics 2013-09-11

We investigate the reactive dissolution process of poly(sulfur nitride) (SN)x in ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate [EMIm][OAc] comparison to elemental sulfur same IL. It has been known from literature that during reaction S8 with [EMIm][OAc], respective thione is formed via a radical mechanism. Here, we present new results on kinetics formation imidazole (EMImS) hexasulfur dianion [S6]2– and trisulfur anion [S3]•–. can show first, which dissociates then Also, long-term...

10.1021/acs.jpcb.4c01536 article EN cc-by The Journal of Physical Chemistry B 2024-06-01

Abstract A simple approach using comb‐like polymers that undergo nanophase separation between the polyester backbone and stearoyl side chains is proposed for preparation of structured non‐spherical nanoparticles from a nanoemulsion. Depending on degree esterification OH groups poly(glycerol adipate) differently ordered nanostructures obtained. perfect lamellar arrangement obtained with high leads to spherical an internal onion‐like structure. However, when only 20 mol%, polygonal...

10.1002/marc.201100565 article EN Macromolecular Rapid Communications 2011-11-22

Monolayers of ABA amphiphilic triblock block copolymers are studied using surface pressure−area and X-ray reflectivity (XR) measurements. The composed long poly(ethylene oxide) (PEO) middle blocks with poly((perfluorohexyl)ethyl methacrylate) (PFMA) end blocks. isotherms water-insoluble species show two pseudoplateaus. plateau at low pressure is consistent the pseudoplateau observed for PEO in literature. brush region can be assigned to horizontal vertical rearrangement whole PFMA chains...

10.1021/la0637059 article EN Langmuir 2007-05-16
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