@article{ReicheBarberkaJanietzetal.1994, author = {Reiche, J{\"u}rgen and Barberka, Thomas Andreas and Janietz, Dietmar and Hofmann, Dieter and Pietsch, Ullrich and Brehmer, Ludwig}, title = {X-ray structure investigation and computer modelling of Langmuir-Blodgett films formed from disc-shaped pentaalkines}, year = {1994}, language = {en} } @article{ReicheFreydankHelmsetal.1999, author = {Reiche, J{\"u}rgen and Freydank, Anke-Christine and Helms, Andreas and Geue, Thomas and Schulz, Burkhard and Brehmer, Ludwig and Stiller, Burkhard and Knochenhauer, Gerald}, title = {Vacuum deposition films of oxadiazole compounds : formation and structure investigation}, year = {1999}, abstract = {The search for alternative routes of organic thin film formation is stimulated by the outstanding properties of these films in such fields as nonlinear optics, photonic data processing and molecular electronics. The formation of highly ordered multilayer structures by thermal vacuum deposition (VD) of organic compounds is an essential step toward the application of supramolecular organic architectures in technical systems. The VD of an amphiphilic substituted 2,5- diphenylene-1,3,4-oxadiazole 1 onto silicon substrates at defined temperature was used for the formation of ultrathin films. The structural data obtained for the VD-films of oxadiazole 1 by means of X-ray reflectivity, X-ray grazing incidence diffraction and atomic force microscopy (AFM) investigations indicate the formation of well ordered oxadiazole multilayers. The structure of the VD-multilayers is compared with that of Langmuir-Blodgett (LB) films and thermally treated LB-multilayers prepared from the same compound.}, language = {en} } @article{AkpoWeberReiche2006, author = {Akpo, Claudia and Weber, Edwin and Reiche, J{\"u}rgen}, title = {Synthesis, Langmuir and Langmuir-Blodgett film behaviour of new dendritic amphiphiles}, series = {New journal of chemistry}, volume = {30}, journal = {New journal of chemistry}, publisher = {RSC}, address = {Cambridge}, issn = {1144-0546}, doi = {10.1039/b609645j}, pages = {1820 -- 1833}, year = {2006}, abstract = {New amphiphilic compounds 1-9 that feature a construction with dendronized hydrophilic and hydrophobic segment groups connected to a specific aromatic or aliphatic spacer unit have been synthesized, following a modular building block strategy. The hydrophilic dendrons are typically branched elements with peripheral carboxylic groups, unlike the hydrophobic dendrons that contain peripheral alkyl chains as part of respective amide functions. The hydrophilic dendrons are in different generations of branching, while the hydrophobic dendrons are all in the first generation of branching (three terminal branching), but differ in the length of the alkyl chains, thus giving rise to designed structure and amphiphilic properties in the new compounds. The resulting surfactants are capable of forming well-defined Langmuir films of remarkable stability when spread from a solution onto an aqueous subphase. Nevertheless, specific packing behaviour and orientation of the amphiphilic molecules were found, depending on the molecular structure, as determined using analysis of the surface pressure-area (pi-A) isotherms. Langmuir-Blodgett transfer of the first monolayer from a pure water subphase to a clean silicon wafer proved possible for the amphiphiles of peripheral alkyl chain length C-12, while the amphiphiles with the longer alkyl chains failed, possibly due to the more rigid monolayers they form, impeding the transfer.}, language = {en} } @article{WuestneckReicheFoerster1997, author = {W{\"u}stneck, Rainer and Reiche, J{\"u}rgen and F{\"o}rster, Stephan}, title = {Surface dilational behavior of docosanic acid monolayers spread on the surface of drops of polymer solutions}, year = {1997}, abstract = {The pendant drop technique was used to determine p/A isotherms of docosanic acid spread on the drop surface of an aqueous polymer solution. Two water soluble polymers were used, poly(dimethyl-diallyl-ammoniumchloride) and sodium poly(styrene sulfonate-b-ethylethylene). By fast changes of the drop volume, the monolayers were compressed and dilated. The stress relaxation was monitored and surface rheological dilation parameters were obtained. It is shown that the fatty acid monolayer can be mechanically stabilized by both interacting anionic and cationic polymers. In the case of the anionic polymer, the interaction becomes more pronounced in the presence of salts in the subphase (counterions). Brewster angle microscopy shows that the typical tilt-orientation of crystalline domains of the fatty acid monolayers transforms into a more uniform and fluid-like structure caused by the polymer/monolayer interaction. The surface rheological behavior is dramatically influenced by the polymer binding. The interaction results in surface dilational viscoelastic properties and show that there is a strong resistance against expansion of the complex fatty acid/polymer layer.}, language = {en} } @article{ReicheSchulzKnochenhaueretal.1997, author = {Reiche, J{\"u}rgen and Schulz, Burkhard and Knochenhauer, Gerald and Dietzel, Birgit and Freydank, Anke-Christine and Zetzsche, Thomas and Brehmer, Ludwig}, title = {Supramolecular structures formed from heterocyclic aromatic molecules}, year = {1997}, abstract = {This paper describes the formation and structure investigation of Langmuir monolayers and Langmuir-Blodgett multilayers formed from amphiphilic derivatives of 2,5-diphenyl-1,3,4-oxadiazole. The 2,5-diphenyl-1,3,4-oxadiazole group as a functional unit with interesting physical and chemical properties is maintained, while the head group, the length of the alkyl chain and the structure of the coupling unit between aromatic and aliphatic part of these linear short-chain amphiphiles is systematically varied in order to explore the influence of this change on the film forming properties and the stability of Langmuir and Langmuir-Blodgett films. Molecular mechanics simulations are shown by these systematic variations to be suitable for the prediction of optimal chemical structures allowing for a stable stratified molecular packing. The combination of a detailed structure investigation of the multilayers based on scanning force microscopy and X-ray data with molecular mechanics simulations yields an insight into the packing of the molecules and the intermolecular interactions.}, language = {en} } @article{JanietzMoebiusFestagetal.1994, author = {Janietz, Dietmar and M{\"o}bius, Dietmar and Festag, R. and Wendorff, Joachim Heinz and Ahuja, Rajeev C. and Reiche, J{\"u}rgen}, title = {Supramolecular organization of amphiphilic discotic mesogens}, year = {1994}, language = {en} } @article{ReicheKamusewitzKelleretal.1995, author = {Reiche, J{\"u}rgen and Kamusewitz, Helmut and Keller, Manuela and Brehmer, Ludwig and Pe{\~n}acorada, Florencio}, title = {Study of gas transport through composite membranes with a stabilised Langmuir-Blodgett skin layer}, year = {1995}, abstract = {The Langmuir-Blodgett (LB-) technique is used to deposit molecular reinforced separation layers on porous polymer substrates resulting in composite membranes for gas separation. The adsorption of a polycation to the arachidic acid Langmuir layer and the subsequent transfer of the highly ordered and stabilised monolayer onto a polypropylene membrane (Cellgard 2400) yields a laminated separation layer combining the advantageous high degree of order of fatty acid films and the stability of thin polymeric films. X-ray reflectivity data of these films confirm the transfer of the assembled polymer layer together with the fatty acid monolayer and the formation of ordered Y-type LB-films. SFM pictures show a dense film without pinholes completely covering the porous support. Gas permeation measurements are used to study the transport process of different gases through the composite membrane.}, language = {en} } @article{PenacoradaDietelReicheetal.1995, author = {Penacorada, Florencio and Dietel, Reinhard and Reiche, J{\"u}rgen and Zetzsche, Thomas and Knobloch, Harald and Katholy, Stefan and Brehmer, Ludwig}, title = {Studium des Einflusses von Uranyl-Gegenionen auf die Struktur von Langmuir- und Langmuir-Blodgett Filmen der Arachins{\"a}ure}, year = {1995}, language = {de} } @article{KatholyReicheBrehmer1995, author = {Katholy, Stefan and Reiche, J{\"u}rgen and Brehmer, Ludwig}, title = {Strukturuntersuchungen an Langmuir-Monoschichten organischer Amphiphile mittels Brewsterwinkelmikroskopie}, year = {1995}, language = {de} } @article{ReicheKnochenhauerDieteletal.1997, author = {Reiche, J{\"u}rgen and Knochenhauer, Gerald and Dietel, Reinhard and Freydank, Anke-Christine and Zetzsche, Thomas and Pietsch, Ullrich and Brehmer, Ludwig and Barberka, Thomas Andreas and Geue, Thomas}, title = {Structure of thermally treated oxadiazoleamide Langmuir-Blodgett films}, year = {1997}, abstract = {The thermal treatment of Y-type Langmuir-Blodgett (LB) films formed from the amphiphilic derivative of 2,5- diphenyl-1,3,4-oxadiazole 1 results in changes of the molecular packing. These changes have been analysed by a combination of X-ray specular reflectivity data, X-ray grazing incidence diffraction data and scanning force microscopy images, On the basis of these experimental data we have simulated possible supramolecular structures, These simulations provide insight into the intermolecular interactions giving rise to the observed structural transitions. The crystalline structure induced by thermal treatment of the LB films is characterized by a uniaxial texture, which is correlated with the dipping direction during deposition of the LB film.}, language = {en} }