TY - JOUR A1 - von Klitzing, Regine A1 - Stehl, Dimitrij A1 - Pogrzeba, Tobias A1 - Schomaäcker, Reinhard A1 - Minullina, Renata A1 - Panchal, Abhishek A1 - Konnova, Svetlana A1 - Fakhrullin, Rawil A1 - Koetz, Joachim A1 - Moehwald, Helmuth A1 - Lvov, Yuri T1 - Halloysites Stabilized Emulsions for Hydroformylation of Long Chain Olefins JF - Advanced materials interfaces N2 - Halloysites as tubular alumosilicates are introduced as inexpensive natural nanoparticles to form and stabilize oil-water emulsions. This stabilized emulsion is shown to enable efficient interfacial catalytic reactions. Yield, selectivity, and product separation can be tremendously enhanced, e.g., for the hydroformylation reaction of dodecene to tridecanal. In perspective, this type of formulation may be used for oil spill dispersions. The key elements of the described formulations are clay nanotubes (halloysites) which are highly anisometric, can be filled by helper molecules, and are abundantly available in thousands of tons, making this technology scalable for industrial applications. Y1 - 2016 U6 - https://doi.org/10.1002/admi.201600435 SN - 2196-7350 VL - 4 IS - 1 PB - Wiley CY - Hoboken ER - TY - JOUR A1 - Schimka, Selina A1 - Lomadze, Nino A1 - Rabe, Maren A1 - Kopyshev, Alexey A1 - Lehmann, Maren A1 - von Klitzing, Regine A1 - Rumyantsev, Artem M. A1 - Kramarenko, Elena Yu. A1 - Santer, Svetlana T1 - Photosensitive microgels containing azobenzene surfactants of different charges JF - Physical chemistry, chemical physics : a journal of European Chemical Societies N2 - We report on light sensitive microgel particles that can change their volume reversibly in response to illumination with light of different wavelengths. To make the anionic microgels photosensitive we add surfactants with a positively charged polyamine head group and an azobenzene containing tail. Upon illumination, azobenzene undergoes a reversible photo-isomerization reaction from a trans- to a cis-state accompanied by a change in the hydrophobicity of the surfactant. Depending on the isomerization state, the surfactant molecules are either accommodated within the microgel (trans- state) resulting in its shrinkage or desorbed back into water (cis-isomer) letting the microgel swell. We have studied three surfactants differing in the number of amino groups, so that the number of charges of the surfactant head varies between 1 and 3. We have found experimentally and theoretically that the surfactant concentration needed for microgel compaction increases with decreasing number of charges of the head group. Utilization of polyamine azobenzene containing surfactants for the light triggered remote control of the microgel size opens up a possibility for applications of light responsive microgels as drug carriers in biology and medicine. Y1 - 2016 U6 - https://doi.org/10.1039/c6cp04555c SN - 1463-9076 SN - 1463-9084 VL - 19 SP - 108 EP - 117 PB - Royal Society of Chemistry CY - Cambridge ER - TY - JOUR A1 - Schimka, Selina A1 - Gordievskaya, Yulia D. A1 - Lomadze, Nino A1 - Lehmann, Maren A1 - von Klitzing, Regine A1 - Rumyantsev, Artem M. A1 - Kramarenko, Elena Yu. A1 - Santer, Svetlana T1 - Communication: Light driven remote control of microgels’ size in the presence of photosensitive surfactant: Complete phase diagram JF - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr N2 - Here we report on a light triggered remote control of microgel size in the presence of photosensitive surfactant. The hydrophobic tail of the cationic surfactant contains azobenzene group that undergoes a reversible photo-isomerization reaction from a trans-to a cis-state accompanied by a change in the hydrophobicity of the surfactant. We have investigated light assisted behaviour and the complex formation of the microgels with azobenzene containing surfactant over the broad concentrational range starting far below and exceeding several times of the critical micelle concentration (CMC). At small surfactant concentration in solution (far below CMC), the surfactant in the trans-state accommodates within the microgel causing its compaction, while the cis-isomer desorbs out of microgel resulting in its swelling. The process of the microgel size change can be described as swelling on UV irradiation (trans-cis isomerization) and shrinking on irradiation with blue light (cis-trans isomerization). However, at the surfactant concentrations larger than CMC, the opposite behaviour is observed: the microgel swells on blue irradiation and shrinks during exposure to UV light. We explain this behaviour theoretically taking into account isomer dependent micellization of surfactant within the microgels. Published by AIP Publishing. Y1 - 2017 U6 - https://doi.org/10.1063/1.4986143 SN - 0021-9606 SN - 1089-7690 VL - 147 PB - American Institute of Physics CY - Melville ER -