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Now showing 1 - 8 of 8
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    Methods for Exerting and Sensing Force in Polymer Materials Using Mechanophores
    (Weinheim : Wiley-VCH, 2020) Stratigaki, Maria; Göstl, Robert
    In recent years, polymer mechanochemistry has evolved as a methodology to provide insights into the action-reaction relationships of polymers and polymer-based materials and composites in terms of macroscopic force application (stress) and subsequent deformation (strain) through a mechanophore-assisted coupling of mechanical and chemical phenomena. The perplexity of the process, however, from the viewpoint of mechanophore activation via a molecular-scaled disruption of the structure that yields a macroscopically detectable optical signal, renders this otherwise rapidly evolving field challenging. Motivated by this, we highlight here recent advancements of polymer mechanochemistry with particular focus on the establishment of methodologies for the efficient activation and quantification of mechanophores and anticipate to aptly pinpoint unresolved matters and limitations of the respective approaches, thus highlighting possible developments. © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
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    Singlet-Oxygen Generation by Peroxidases and Peroxygenases for Chemoenzymatic Synthesis
    (Weinheim : Wiley-VCH, 2020) Ingenbosch, Kim N.; Quint, Stephan; Dyllick-Brenzinger, Melanie; Wunschik, Dennis S.; Kiebist, Jan; Süss, Philipp; Liebelt, Ute; Zuhse, Ralf; Menyes, Ulf; Scheibner, Katrin; Mayer, Christian; Opwis, Klaus; Gutmann, Jochen S.; Hoffmann-Jacobsen, Kerstin
    Singlet oxygen is a reactive oxygen species undesired in living cells but a rare and valuable reagent in chemical synthesis. We present a fluorescence spectroscopic analysis of the singlet-oxygen formation activity of commercial peroxidases and novel peroxygenases. Singlet-oxygen sensor green (SOSG) is used as fluorogenic singlet oxygen trap. Establishing a kinetic model for the reaction cascade to the fluorescent SOSG endoperoxide permits a kinetic analysis of enzymatic singlet-oxygen formation. All peroxidases and peroxygenases show singlet-oxygen formation. No singlet oxygen activity could be found for any catalase under investigation. Substrate inhibition is observed for all reactive enzymes. The commercial dye-decolorizing peroxidase industrially used for dairy bleaching shows the highest singlet-oxygen activity and the lowest inhibition. This enzyme was immobilized on a textile carrier and successfully applied for a chemical synthesis. Here, ascaridole was synthesized via enzymatically produced singlet oxygen. © 2020 Wiley-VCH GmbH
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    Curcuminoid–BF2 complexes: Synthesis, fluorescence and optimization of BF2 group cleavage
    (Frankfurt a.M. : Beilstein-Institut, 2017) Weiß, Henning; Reichel, Jeannine; Görls, Helmar; Schneider, Kilian R.A.; Micheel, Mathias; Pröhl, Michael; Gottschaldt, Michael; Dietzek, Benjamin; Weigand, Wolfgang
    Eight difluoroboron complexes of curcumin derivatives carrying alkyne groups containing substituents have been synthesized following an optimised reaction pathway. The complexes were received in yields up to 98% and high purities. Their properties as fluorescent dyes have been investigated. Furthermore, a strategy for the hydrolysis of the BF2 group has been established using aqueous methanol and sodium hydroxide or triethylamine.
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    A thiazolo[5,4-: D] thiazole-bridged porphyrin organic framework as a promising nonlinear optical material
    (London : Royal Society of Chemistry (RSC), 2019) Samal, Mahalaxmi; Valligatla, Sreeramulu; Saad, Nabil A.; Rao, M. Veeramohan; Rao, D. Narayana; Sahu, Rojalin; Biswal, Bishnu P.
    Porphyrin-based porous organic frameworks are an important group of materials gaining interest due to their structural diversity and distinct opto-electronic properties. However, these materials are seldom explored for nonlinear optical (NLO) applications. In this work, we investigate a thiazolo[5,4-d]thiazole-bridged porous, porphyrin framework (Por-TzTz-POF) with promising NLO properties. The planar TzTz moiety coupled with integrated porphyrin units enables efficient π-conjugation and charge distribution in the Por-TzTz-POF resulting in a high nonlinear absorption coefficient (β = 1100 cm GW-1) with figure of merit (FoM) σ1/σ0 = 5571, in contrast to analogous molecules and material counterparts e.g. metal-organic frameworks (MOFs; β = ∼0.3-0.5 cm GW-1), molecular porphyrins (β = ∼100-400 cm GW-1), graphene (β = 900 cm GW-1), and covalent organic frameworks (Por-COF-HH; β = 1040 cm GW-1 and FoM = 3534). This journal is © The Royal Society of Chemistry.
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    Between Aromatic and Quinoid Structure: A Symmetrical UV to Vis/NIR Benzothiadiazole Redox Switch
    (Weinheim : Wiley-VCH, 2020) Rietsch, Philipp; Sobottka, Sebastian; Hoffmann, Katrin; Popov, Alexey A.; Hildebrandt, Pascal; Sarkar, Biprajit; Resch-Genger, Ute; Eigler, Siegfried
    Reversibly switching the light absorption of organic molecules by redox processes is of interest for applications in sensors, light harvesting, smart materials, and medical diagnostics. This work presents a symmetrical benzothiadiazole (BTD) derivative with a high fluorescence quantum yield in solution and in the crystalline state and shows by spectroelectrochemical analysis that reversible switching of UV absorption in the neutral state, to broadband Vis/NIR absorption in the 1st oxidized state, to sharp band Vis absorption in the 2nd oxidized state, is possible. For the one-electron oxidized species, formation of a delocalized radical is confirmed by electron paramagnetic resonance spectroelectrochemistry. Furthermore, our results reveal an increasing quinoidal distortion upon the 1st and 2nd oxidation, which can be used as the leitmotif for the development of BTD based redox switches. © 2020 The Authors. Published by Wiley-VCH GmbH
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    Light emission intensities of luminescent Y2O3:Eu and Gd2O3:Eu particles of various sizes
    (Basel : MDPI, 2017) Adam, Jens; Metzger, Wilhelm; Koch, Marcus; Rogin, Peter; Coenen, Toon; Atchison, Jennifer S.; König, Peter
    There is great technological interest in elucidating the effect of particle size on the luminescence efficiency of doped rare earth oxides. This study demonstrates unambiguously that there is a size effect and that it is not dependent on the calcination temperature. The Y2O3:Eu and Gd2O3:Eu particles used in this study were synthesized using wet chemistry to produce particles ranging in size between 7 nm and 326 nm and a commercially available phosphor. These particles were characterized using three excitation methods: UV light at 250 nm wavelength, electron beam at 10 kV, and X-rays generated at 100 kV. Regardless of the excitation source, it was found that with increasing particle diameter there is an increase in emitted light. Furthermore, dense particles emit more light than porous particles. These results can be explained by considering the larger surface area to volume ratio of the smallest particles and increased internal surface area of the pores found in the large particles. For the small particles, the additional surface area hosts adsorbates that lead to non-radiative recombination, and in the porous particles, the pore walls can quench fluorescence. This trend is valid across calcination temperatures and is evident when comparing particles from the same calcination temperature.
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    Conjugated Polymer Nanoparticles toward In Vivo Theranostics – Focus on Targeting, Imaging, Therapy, and the Importance of Clearance
    (Weinheim : Wiley-VCH, 2017) Kuehne, Alexander J.C.
    Conjugated polymer nanoparticles are highly fluorescent colloids with tunable emission colors ranging from the visible deep into the near infrared spectrum. Conjugated polymer nanoparticles are easy to prepare, tunable in their size, and virtually nonbleachable. Conjugated polymer particles can also be designed to give off heat upon irradiation. All these properties make conjugated polymer particles ideal materials for biomedical fluorescence and photoacoustic imaging as well as for theranostic applications. Here, different examples of surface functionalization to attach pathological homing devices, imaging modalities, as well as the emerging possibilities for therapeutic measures are discussed. Furthermore, clearance of the particles is considered, which is important to ultimately apply the materials for in vivo theranostics. Due to the conjugated backbone of the conjugated polymers, established degradation strategies, as known from hydrophilic nonconjugated polymer carriers, cannot be applied. Bioinspired strategies and potential pathways for degradation and clearance via structural changes upon triggers such as pH, oxidation, and temperature are also discussed in this progress report. © 2017 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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    In vivo detection of changes in cutaneous carotenoids after chemotherapy using shifted excitation resonance Raman difference and fluorescence spectroscopy
    (Oxford [u.a.] : Wiley-Blackwell, 2020) Jung, Sora; Darvin, Maxim E.; Schleusener, Johannes; Thiede, Gisela; Lademann, Juergen; Braune, Marcel; Elban, Felia; Fuss, Harald
    Background: Various cutaneous toxicities under chemotherapy indicate a local effect of chemotherapy by secretion after systemic application. Here, changes in the fluorescence and Raman spectral properties of the stratum corneum subsequent to intravenous chemotherapy were assessed. Methods: Twenty healthy subjects and 20 cancer patients undergoing chemotherapy were included. Measurement time points in cancer patients were before the first cycle of chemotherapy (Tbase) and immediately after intravenous application of the chemotherapy (T1). Healthy subjects were measured once without any further intervention. Measurements were conducted using an individually manufactured system consisting of a handheld probe and a wavelength-tunable diode laser-based 488 nm SHG light source. Hereby, changes in both skin fluorescence and shifted excitation resonance Raman difference spectroscopy (SERRDS) carotenoid signals were assessed. Results: Healthy subjects showed significantly (P <.001) higher mean concentrations of carotenoids compared to cancer subjects at Tbase. An increase in fluorescence intensity was detected in almost all patients after chemotherapy, especially after doxorubicin infusion. Furthermore, a decrease in the carotenoid concentration in the skin after chemotherapy was found. Conclusion: The SERRDS based noninvasive detection can be used as an indirect quantitative assessment of fluorescent chemotherapeutics. The lower carotenoid SERRDS intensities at Tbase might be due to cancerous diseases and co-medication. © 2020 The Authors. Skin Research and Technology Published by John Wiley & Sons Ltd.