@article{ZieglerFischerMenzeletal.1998, author = {Ziegler, A. and Fischer, Thomas M. and Menzel, Henning and Stumpe, Joachim}, title = {Photo-Induced modification and photo-orientation in LB-multilayers of thermotropic polymers containing azobenzene side groups}, year = {1998}, language = {en} } @article{VixSapichStumpeetal.1998, author = {Vix, A. and Sapich, B. and Stumpe, Joachim and Stocker, W. and Rabe, J. P.}, title = {Interfacial ordering and photo-orientation of a liquid crystalline main polymer}, year = {1998}, language = {en} } @article{TomczykSobolewskaNagyetal.2013, author = {Tomczyk, Jaroslaw and Sobolewska, Anna and Nagy, Zsuzsanna T. and Guillon, Daniel and Donnio, Bertrand and Stumpe, Joachim}, title = {Photo- and thermal-processing of azobenzene-containing star-shaped liquid crystals}, series = {Journal of materials chemistry : C, Materials for optical and electronic devices}, volume = {1}, journal = {Journal of materials chemistry : C, Materials for optical and electronic devices}, number = {5}, publisher = {Royal Society of Chemistry}, address = {Cambridge}, issn = {2050-7526}, doi = {10.1039/c2tc00627h}, pages = {924 -- 932}, year = {2013}, abstract = {A new class of star-shaped, liquid crystalline, low-molecular weight compounds functionalized with photochromic azobenzene and mesogenic groups was investigated in terms of light-induced anisotropy. The behaviour of the materials under the action of light with simultaneous or subsequent thermal treatment was examined with respect to the induction of anisotropy. The unconventional UV light treatment prior to the irradiation with linearly polarized light allowed induction of very high values of anisotropy (D = 0.77) at room temperature. Moreover, the simultaneous action of light and temperature led to the induction of higher values of dichroism in comparison with anisotropy generated by the standard procedure. Subsequent thermal treatment led to dewetting and the formation of 3D macroscopic stripe- and dome-like structures for one of the investigated compounds. Despite photoinduction of anisotropy by a single beam, the formation of polarization and surface relief gratings by two-beam interference pattern was also investigated.}, language = {en} } @article{TejedorOriolPinoletal.2005, author = {Tejedor, R. M. and Oriol, L. and Pinol, M. and Serrano, J. L. and Strehmel, Veronika and Stiller, Burkhard and Stumpe, Joachim}, title = {Photoreactive main-chain liquid-crystalline polyesters : Synthesis, characterization, and photochemistry}, issn = {0887-624X}, year = {2005}, abstract = {Three series of semiflexible and rigid main-chain polyesters containing photoreactive mesogenic units derived from p-phenylenediacrylic acid (PDA) and cinnamic acid have been synthesized by high-temperature polycondensation. The thermal and mesomorphic properties of the polymers have been determined. The photochemical behavior of polymer P-[1]-T, which contains a PDA unit, has been studied both in solution and in films. In solution, [2+2] photocycloaddition, E/Z photoisomerization, and photo-Fries rearrangement can take place. In contrast, the dominant process in spin-coated films is the [2+2] photocycloaddition reaction, which causes crosslinking of the polymer. In films, the photochemistry and induction of anisotropy are strongly influenced by the aggregation of the PDA phenylester unit. A dichroism of about 0.2 has been induced in films by irradiation with linearly polarized UV light, and thus the capability of these films to induce optical anisotropy and align liquid crystals has been demonstrated. Liquid-crystalline cells have been made with polarized irradiated films of P[1]-T as aligning layers. A commercial liquid-crystalline mixture has been used for this study, and a similar liquid-crystalline order determined by polarized Fourier transform infrared to a commercial cell with rubbed polyimide as an aligning layer has been detected. Because of crosslinking of the irradiated P[1]-T photoaligning layer, the photoinduced anisotropy is stable at high temperatures, and the liquid-crystalline molecules are insoluble in the irradiated polymer. (c) 2005 Wiley Periodicals, Inc}, language = {en} } @article{StumpeSakhnoGritsaietal.2014, author = {Stumpe, Joachim and Sakhno, O. and Gritsai, Y. and Rosenhauer, R. and Fischer, Th. and Rutloh, Michael and Schaal, F. and Weidenfeld, S. and Jetter, M. and Michler, P. and Pruss, C. and Osten, W.}, title = {Active and passive LC based polarization elements}, series = {Molecular crystals and liquid crystals}, volume = {594}, journal = {Molecular crystals and liquid crystals}, number = {1}, publisher = {Routledge, Taylor \& Francis Group}, address = {Abingdon}, issn = {1542-1406}, doi = {10.1080/15421406.2014.917503}, pages = {140 -- 149}, year = {2014}, abstract = {Passive and active polarization elements were created by surface and bulk photo-alignment of LCs, reactive LCs, photo-sensitive LCP and photo-curable monomer/LC composites. The use of different photo-sensitive liquid crystalline materials for the development of highly anisotropic elements with high spatial resolution and stability or, alternatively, fast switch ability will be discussed. Photo-active and voltage tunable polarization and diffraction elements are presented. For active micro-optic application a photo-addressed patterned retarder was created. Electrically switchable diffraction gratings were generated by interference exposure of photo-curable LC composites at room temperature characterized by droplet free morphology. These polarization sensitive diffraction elements are characterized be excellent optical properties and low switching times.}, language = {en} } @article{StumpeGeueFischeretal.1995, author = {Stumpe, Joachim and Geue, Thomas and Fischer, Thomas M. and Menzel, Henning}, title = {Photochemically induced changes of structures in LB-multilayers of amphotropic polymers}, year = {1995}, language = {en} } @article{StumpeFischerRutlohetal.1998, author = {Stumpe, Joachim and Fischer, Thomas M. and Rutloh, M. and Meier, Johann Georg}, title = {Photo-Induced orientation effects parallel and perpendicular to the polarization vector of the incident light observed in the same Azobenzene containing LC polymer.}, year = {1998}, language = {en} } @article{SchabBalcerzakFlakusJarczykJedrykaetal.2015, author = {Schab-Balcerzak, Ewa and Flakus, Henryk and Jarczyk-Jedryka, Anna and Konieczkowska, Jolanta and Siwy, Mariola and Bijak, Katarzyna and Sobolewska, Anna and Stumpe, Joachim}, title = {Photochromic supramolecular azopolyimides based on hydrogen bonds}, series = {Optical materials : an international journal on the physics and chemistry of optical materials and their applications, including devices}, volume = {47}, journal = {Optical materials : an international journal on the physics and chemistry of optical materials and their applications, including devices}, publisher = {Elsevier}, address = {Amsterdam}, issn = {0925-3467}, doi = {10.1016/j.optmat.2015.06.029}, pages = {501 -- 511}, year = {2015}, abstract = {The approach of deriving new photoresponsive active supramolecular azopolymers based on the hydrogen bonds is described. Polymers with imide rings, i.e., poly(esterimide)s and poly(etherimide)s, with phenolic hydroxyl or carboxylic groups were applied as matrixes for the polymer dye supramolecular systems. Supramolecular films were built on the basis of the hydrogen bonds between the functional groups of the polymers and various azochromophores, that is, 4-phenylazophenol, 4-[4-(6-hydroxyhexy loxy)phenylazo]benzene, 4[4-(6-hexadecaneoxy)phenylazo]pyridine and 4-(4-hydroxyphenylazo)-pyridine. The hydrogen bonding interaction in azo-systems were studied by Fourier transform infrared spectroscopy and for selected assembles by H-1 NMR technique. The obtained polyimide azo-assembles were characterized by X-ray diffraction and DSC measurements. H-bonds allow attaching a chromophore to each repeating unit of the polymer, thereby suppressing the macroscopic phase separation except for the systems based on 4-[4-(6-hydroxyhexyloxy)phenylazo]benzene. H-bonds systems were amorphous and revealed glass transition temperatures lower than for the polyimide matrixes (170-260 degrees C). The photoresponsive behavior of the azo-assemblies was tasted in holographic recording experiment. (C) 2015 Elsevier B.V. All rights reserved.}, language = {en} } @article{SchaalRutlohWeidenfeldetal.2018, author = {Schaal, Frederik and Rutloh, Michael and Weidenfeld, Susanne and Stumpe, Joachim and Michler, Peter and Pruss, Christof and Osten, Wolfgang}, title = {Optically addressed modulator for tunable spatial polarization control}, series = {Optics express : the international electronic journal of optics}, volume = {26}, journal = {Optics express : the international electronic journal of optics}, number = {21}, publisher = {Optical Society of America}, address = {Washington}, issn = {1094-4087}, doi = {10.1364/OE.26.028119}, pages = {28119 -- 28130}, year = {2018}, abstract = {We present an optically addressed non-pixelated spatial light modulator. The system is based on reversible photoalignment of a LC cell using a red light sensitive novel azobenzene photoalignment layer. It is an electrode-free device that manipulates the liquid crystal orientation and consequently the polarization via light without artifacts caused by electrodes. The capability to miniaturize the spatial light modulator allows the integration into a microscope objective. This includes a miniaturized 200 channel optical addressing system based on a VCSEL array and hybrid refractive-diffractive beam shapers. As an application example, the utilization as a microscope objective integrated analog phase contrast modulator is shown. (C) 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement}, language = {en} } @article{SapichKrawinkelKricheldorfetal.1998, author = {Sapich, B. and Krawinkel, Th. and Kricheldorf, H. R. and Stumpe, Joachim}, title = {New polymer syntheses 95. Photosetting cholesteric polyesters derived from 4-hydroxycinnamic acid and isosorbide.}, year = {1998}, language = {en} }