@article{JanietzHofmannReiche1994,
  author    = {Janietz, Dietmar and Hofmann, Dieter and Reiche, J{\"u}rgen},
  title     = {Molecular organization of amphiphilic disc-shaped penta-alkynes in LB-mono- and multilayers},
  year      = {1994},
  abstract  = {Amphiphilic disc-shaped penta-alkynes were studied with regard to their molecular organization in Langmuir-Blod- gett (LB) mono- and multilayers. It was found that each compound investigated forms edge-on arranged stable monolayers at the air-water interface. LB-multilayers derived from fivefold pentyl-substituted pentaynes are characterized by an edge-on ordering of the molecules within Y-type bilayers. One of these compounds, containing a hydoxy substituent as hydrophilic head group, is exemplified and two possible rectangular molecular assemblies perpendicular to the substrate, each with a columnar in-plane packing, will be discussed as a result of molecular modelling. Based on the experimental results, hexagonal layer packing in the LB-film of a disc-shaped penta-alkynyl carboxylic acid without lateral substituents proved to be possible, which, furthermore, could be confirmed by molecular mechanics simulation.},
  language  = {en}
}
@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{ReicheJanietzBarberkaetal.1995,
  author    = {Reiche, J{\"u}rgen and Janietz, Dietmar and Barberka, Thomas Andreas and Hofmann, Dieter and Brehmer, Ludwig},
  title     = {Comprehensive structure investigation of Langmuir-Blodgett films of disc-shaped molecules},
  year      = {1995},
  abstract  = {The structure of mono- and multilayers of amphiphilic disc-shaped pentaynes wa inbestigated by Brewsterangle microscopy, X-ray specular reflection and grazing incidence diffraction (GID). X-ray specular reflection experiments confirm the "edge on" arrangement of the molecular discs. The molecular modelling of the Langmuir-Blodgett (LB)- multilayers predicts a columnar in-plane packing of the molecules. A GID experiment with monochromatic synchrotron radiation was used to verify the predicted multilayer structure on molecular level, while the Brewsterangle microscopy gave a deeper insight in the monolayer in-plane structure on micron scale.},
  language  = {en}
}
@article{JanietzHofmannReiche1995,
  author    = {Janietz, Dietmar and Hofmann, Dieter and Reiche, J{\"u}rgen},
  title     = {Reply to comment on "Molecular organization of amphiphilic disc-shaped penta-alkynes in LB mono- and multilayers"},
  year      = {1995},
  abstract  = {The model for the Langmuir-Blodgett (LB) film structure of amphiphilic disc-shaped penta-alkynes is refined. It is shown that LB experiments reported in a comment on one of our papers do not contradict the molecular organization within the LB films of the penta-alkynes we proposed.},
  language  = {en}
}
@misc{ReicheKratzHofmannetal.2011,
  author    = {Reiche, J{\"u}rgen and Kratz, Karl and Hofmann, Dieter and Lendlein, Andreas},
  title     = {Current status of Langmuir monolayer degradation of polymeric biomaterials},
  series = {The international journal of artificial organs},
  volume    = {34},
  journal   = {The international journal of artificial organs},
  number    = {2},
  publisher = {Wichtig},
  address   = {Milano},
  issn      = {0391-3988},
  doi       = {10.5301/IJAO.2011.6401},
  pages     = {123 -- 128},
  year      = {2011},
  abstract  = {Langmuir monolayer degradation (LMD) experiments with polymers possessing outstanding biomedical application potential yield information regarding the kinetics of their hydrolytic or enzymatic chain scission under well-defined and adjustable degradation conditions. A brief review is given of LMD investigations, including the author's own work on 2-dimensional (2D) polymer systems, providing chain scission data, which are not disturbed by simultaneously occurring transport phenomena, such as water penetration into the sample or transport of scission fragments out of the sample. A knowledge-based approach for the description and simulation of polymer hydrolytic and enzymatic degradation based on a combination of fast LMD experiments and computer simulation of the water penetration is briefly introduced. Finally, the advantages and disadvantages of this approach are discussed.},
  language  = {en}
}
@article{ZaupaNeffePierceetal.2011,
  author    = {Zaupa, Alessandro and Neffe, Axel T. and Pierce, Benjamin F. and Lendlein, Andreas and Hofmann, Dieter},
  title     = {A molecular dynamic analysis of gelatin as an amorphous material Prediction of mechanical properties of gelatin systems},
  series = {The international journal of artificial organs},
  volume    = {34},
  journal   = {The international journal of artificial organs},
  number    = {2},
  publisher = {Wichtig},
  address   = {Milano},
  issn      = {0391-3988},
  doi       = {10.5301/IJAO.2010.6083},
  pages     = {139 -- 151},
  year      = {2011},
  abstract  = {Biomaterials are used in regenerative medicine for induced autoregeneration and tissue engineering. This is often challenging, however, due to difficulties in tailoring and controlling the respective material properties. Since functionalization is expected to offer better control, in this study gelatin chains were modified with physically interacting groups based on tyrosine with the aim of causing the formation of physical crosslinks. This method permits application-specific properties like swelling and better tailoring of mechanical properties. The design of the crosslink strategy was supported by molecular dynamic (MD) simulations of amorphous bulk models for gelatin and functionalized gelatins at different water contents (0.8 and 25 wt.-\%). The results permitted predictions to be formulated about the expected crosslink density and its influence on equilibrium swelling behavior and on elastic material properties. The models of pure gelatin were used to validate the strategy by comparison between simulated and experimental data such as density, backbone conformation angle distribution, and X-ray scattering spectra. A key result of the simulations was the prediction that increasing the number of aromatic functions attached to the gelatin chain leads to an increase in the number of physical netpoints observed in the simulated bulk packing models. By comparison with the Flory-Rehner model, this suggested reduced equilibrium swelling of the functionalized materials in water, a prediction that was subsequently confirmed by our experimental work. The reduction and control of the equilibrium degree of swelling in water is a key criterion for the applicability of functionalized gelatins when used, for example, as matrices for induced autoregeneration of tissues.},
  language  = {en}
}