@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}
}
@article{PaschkeGeueBarberkaetal.1997,
  author    = {Paschke, K. and Geue, Thomas and Barberka, Thomas Andreas and Bolm, A. and Pietsch, Ullrich and R{\"o}sch, M. and Batke, Edwin and Faller, F. and Kerkel, K. and Oshiniwo, J. and Forchel, Alfred},
  title     = {Characterization of lateral semiconductor nano structures by means of x-ray grazing-incidence diffraction},
  year      = {1997},
  language  = {en}
}
@article{ReicheKnochenhauerBarberkaetal.1995,
  author    = {Reiche, J{\"u}rgen and Knochenhauer, Gerald and Barberka, Thomas Andreas and Geue, Thomas and Pietsch, Ullrich and Brehmer, Ludwig and Hodge, P. and Tredgold, Richard H.},
  title     = {In-plane structure of perfluorotetra decanoic acid Langmuir-Blodgett films and films formed by vacuum deposition},
  year      = {1995},
  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{PietschBarberkaGeueetal.1997,
  author    = {Pietsch, Ullrich and Barberka, Thomas Andreas and Geue, Thomas and St{\"o}mmer, Ralph},
  title     = {X-ray scattering from thin organic films and multilayers},
  year      = {1997},
  language  = {en}
}
@article{EichhornBruceGuillonetal.2001,
  author    = {Eichhorn, Holger and Bruce, Duncan W. and Guillon, D. and Gallani, Jean Louis and Fischer, Thomas and Stumpe, Joachim and Geue, Thomas},
  title     = {Metal ion mediated mesomorphism and thin film behaviour of amphitropic tetraazaporphyrin complexes},
  year      = {2001},
  language  = {en}
}
@article{SchwarzSieversBodenthinetal.2010,
  author    = {Schwarz, Guntram and Sievers, Torsten K. and Bodenthin, Yves and Hasslauer, Ires and Geue, Thomas and Koetz, Joachim and Kurth, Dirk G.},
  title     = {The structure of metallo-supramolecular polyelectrolytes in solution and on surfaces},
  issn      = {0959-9428},
  doi       = {10.1039/B926783b},
  year      = {2010},
  abstract  = {Metal ion induced self-assembly of the rigid ligand 1,4-bis(2,2':6',2 ''-terpyridine- 4'-yl) benzene (1) with Fe(II), Co(II), Ni(II) and Zn(II) acetate in aqueous solution results in extended, rigid- rod like metallosupramolecular coordination polyelectrolytes (MEPE-1). Under the current experimental conditions the molar masses range from 1000 g mol(-1) up to 500 000 g mol(-1). The molar mass depends on concentration, stoichiometry, metal-ion and time. In addition, we present viscosity measurements, small angle neutron scattering and AFM data. We introduce a protocol to precisely control the stoichiometry during self-assembly using conductometry. The protocol can be used with different terpyridine ligands and the above-mentioned metal ions and is of paramount importance to obtain meaningful and reproducible results. As a control experiment we studied the mononuclear 4'- (phenyl)2,2':6',2 ''-terpyridine (3) complex with Ni(II) and Zn(II) and the flexible ligand 1,3- bis[4'-oxa(2,2': 6',2 ''-terpyridinyl)] propane (2) with Ni(II) acetate (Ni-MEPE-2). This ligand does not form extended macroassemblies but likely ring-like structures with 3 to 4 repeat units. Through spin- coating of Ni-MEPE-1 on a solid surface we can image the MEPEs in real space by AFM. SANS measurements of Fe-MEPE-1 verify the extended rigid-rod type structure of the MEPEs in aqueous solution.},
  language  = {en}
}
@article{SchwarzBodenthinGeueetal.2010,
  author    = {Schwarz, Guntram and Bodenthin, Yves and Geue, Thomas and Koetz, Joachim and Kurth, Dirk G.},
  title     = {Structure and properties of dynamic rigid rod-like metallo-supramolecular polyelectrolytes in solution},
  issn      = {0024-9297},
  doi       = {10.1021/Ma902057f},
  year      = {2010},
  abstract  = {Metal-ion-induced self-assembly in aqueous solution of the rigid ligand 1,4-bis(2,2':6',2 ''-terpyridine-4'-yl)benzene (1) with Fe(OAc)(2) and Ni(OAc)(2) is investigated with viscosimetry, SANS, and AFM. Ligand 1 forms extended, rigid-rod like metallo-supramolecular coordination polyeectrolytes (MEPEs) with a molar mass of up to 200 000 g mol(-1) under the Current experimental conditions. The molar mass depends oil concentration, stoichiometry, and time. By spin-coating MEPEs oil a solid surface, we call image the MEPEs in real space by AFM. Both AFM and SANS confirm the extended rigid-rod-type structure of the MEPEs. As a control experiment, we also studied the flexible ligand 1,3-bis[4'-oxa(2,2':6',2 ''-terpyridinyl)]propane (2). Ligand 2 does not form extended macro-assemblies but likely ringlike structures with three 10 four repeat units. Finally, we present it protocol to control the stoichiometry during self-assembly using conductometry, which is of paramount importance to obtain meaningful and reproducible results.},
  language  = {en}
}
@article{PietschBodenthinGrenzeretal.2005,
  author    = {Pietsch, Ullrich and Bodenthin, Yves and Grenzer, J{\"o}rg and Geue, Thomas and M{\"o}hwald, Helmuth and Kurth, Dirk G.},
  title     = {Structure and temperature behavior of metallo-supramolecular assemblies},
  year      = {2005},
  abstract  = {A detailed structural analysis of a Langmuir-Blodgett (LB) multilayer composed of a polyelectrolyte-amphiphile complex (PAC) is presented. The PAC is self-assembled from metal ions, ditopic bis-terpyridines, and amphiphiles. The vertical structure of the LB multilayer is investigated by X-ray reflectometry. The multilayer has a periodicity of 57 A, which corresponds to an architecture of flat lying metallo-supramolecular coordination polyelectrolyte (MEPE) rods and upright-standing amphiphiles (dihexadecyl phosphate, DHP). In-plane diffraction reveals hexagonal packing of the DHP molecules. Using extended X-ray absorption fine structure (EXAFS) experiments, we prove that the central metal ion is coordinated to the terpyridine moieties in a pseudo-octahedral coordination environment. The Fe-N bond distances are 1.82 and 2.0 angstrom, respectively. Temperature resolved measurements indicate a reversible phase transition in a temperature range up to 55 degrees C. EXAFS measurements indicate a lengthening of the average Fe-N bond distance from 1.91 to 1.95 angstrom. The widening of the coordination cage upon heating is expected to lower the ligand field stabilization, thus giving rise to spin transitions in these composite materials},
  language  = {en}
}
@article{PietschBhattacharyaSanyaletal.2005,
  author    = {Pietsch, Ullrich and Bhattacharya, M. K. and Sanyal, M. K. and Geue, Thomas},
  title     = {Glass transition in Ultrathin Polymer Films : a Thermal Expansion Study},
  year      = {2005},
  abstract  = {The glass transition process gets affected in ultrathin films having thickness comparable to the size of the molecules. We observe systematic broadening of the glass transition temperature (T-g) as the thickness of an ultrathin polymer film reduces below the radius of gyration but the change in the average T-g was found to be very small. The existence of reversible negative and positive thermal expansion below and above T-g increased the sensitivity of our thickness measurements performed using energy-dispersive x-ray reflectivity. A simple model of the T-g variation as a function of depth expected from sliding motion could explain the results},
  language  = {en}
}