@misc{KortPeterKoopmanschap1983,
  author    = {Kort, C. A. D. de and Peter, Martin G. and Koopmanschap, A. B.},
  title     = {Binding and degradation of juvenile hormone III by haemolymph proteins of the Colorado potato beetle: a re-examination},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16777},
  year      = {1983},
  abstract  = {The haemolymph of the adult Colorado potato beetle, Lepinotarsa decemlineata Say, contains a high molecular weight (MW > 200,000) JH-III specific binding protein. The Kd value of the protein for racemic JH-III is 1.3 ± 0.2 × 10-7 M. It has a lower affinity for racemic JH-I and it does not bind JH-III-diol or JH-III-acid. The binding protein does discriminate between the enantiomers of synthetic, racemic JH-III as was determined by stereochemical anaysis of the bound and the free JH-III. Incubation of racemic JH-III with crude haemolymph results in preferential formation of (10S)-JH-III-acid, the unnatural configuration. The JH-esterase present in L. decemlineata haemolymph is not enantioselective. It is concluded that the most important function of the binding protein is that of a specific carrier, protecting the natural hormone against degradation by esterases. The carrier does not protect JH-I as efficiently as the lower homologue.},
  language  = {en}
}
@misc{ErdelenLaschewskyRingsdorfetal.1989,
  author    = {Erdelen, C. and Laschewsky, Andr{\´e} and Ringsdorf, H. and Schneider, J. and Schuster, A.},
  title     = {Thermal behaviour of polymeric Langmuir-Blodgett multilayers},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17378},
  year      = {1989},
  abstract  = {Langmuir-Blodgett multilayers of hydrocarbon and fluorocarbon polymers with hydrophilic spacer, lipid-polyelectrolyte complexes and mesogenic polymers have been prepared. The thermal behaviour of the multilayers was studied by small angle X-ray scattering, IR and UV—visible spectroscopy. Good thermal stabilities were found for the various classes of polymers. In addition, for both complexed multilayers and mesogenic polymer films, reorientation processes were observed.},
  language  = {en}
}
@misc{PeterBoldtNiedersteinetal.1990,
  author    = {Peter, Martin G. and Boldt, Peter C. and Niederstein, Yvonne and Peter-Katalinić, Jasna},
  title     = {Synthesen von Galactose-Cluster-haltigen Steroid-Derivaten},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16783},
  year      = {1990},
  abstract  = {The synthesis of galactose clusters that are linked to a steroid moiety by a peptide-like spacer unit is described. The galactose cluster is obtained by Koenigs-Knorr glycosylation of TRIS-Gly-Fmoc (2b) under Helferich conditions. Peptide and ester bonds are formed after activation of carboxylic acids as diphenylthiophene dioxide (TDO) esters. 6a is synthesized in a convergent way by coupling of (Ac4Gal)3-TRIS-Gly (3e) with cholesteryl TDO succinate (5b). Coupling of (Ac4Gal)3-TRIS-Gly hydrogen succinate (3f) with Gly-O-Chol (5d) by means of EEDQ yields 6d. Reaction of (Ac4Gal)3-TRIS-Gly-SUCC-O-TDO (3g) with 25-hydroxycholesterol leads in a linear sequence to the oxysterol derivative 6f. Selective cleavage of the acetyl groups from galactose units yields the known compound 6b and the new derivatives 6e and 6g.},
  language  = {de}
}
@article{GrielStroehlJeschkeitetal.1992,
  author    = {Griel, C. and Str{\"o}hl, D. and Jeschkeit, H. and Kleinpeter, Erich},
  title     = {Synthetische und NMR-spektroskopische Untersuchungen der Benzzyl-aminaddition an N-Maleyl- aminos{\"a}urederivaten},
  year      = {1992},
  language  = {de}
}
@article{JaniakScharmannGreenetal.1996,
  author    = {Janiak, Chr. and Scharmann, T. G. and Green, J. C. and Parkin, R. P. G. and Kolm, M. J. and Riedel, E. and Mickler, Wulfhard and Elguero, J. and Claramunt, R. M. and Sanz, D.},
  title     = {Effects of nitrogen substitution in Poly(pyrazolyl)borato Ligands : from orbital energy levels to C-H...O Hydrogen Bonding},
  year      = {1996},
  language  = {en}
}
@article{KleinpeterKochFischeretal.1997,
  author    = {Kleinpeter, Erich and Koch, Andreas and Fischer, G. and Askolin, C.-P.},
  title     = {13 C NMR, 15 N NMR and quantum-chemical study of the tautomerism of 2-substituted 5-ME-7-OH-1,2,4-triazolo[1,5- a]pyrimidines},
  year      = {1997},
  language  = {en}
}
@article{LetzelSynstadEijsinketal.1999,
  author    = {Letzel, Matthias C. and Synstad, Bjoenar and Eijsink, Vincent G. H. and Peter-Katalinic, Jasna and Peter, Martin G.},
  title     = {Libraries of chito-oligosaccharides of mixed acetylation patterns and their interactions with chitinases},
  isbn      = {3-9806494-5-8},
  year      = {1999},
  language  = {en}
}
@article{SchwarzAndraeArnoldetal.1999,
  author    = {Schwarz, W. H. Eugen and Andrae, Dirk and Arnold, S. R. and Heidberg, Joachim and Hellmann jr., H. and Hinze, J. and Karachalios, A. and Kovner, M. A. and Schmidt, P. C. and Z{\"u}licke, Lutz},
  title     = {Hans G. Hellmann (1903 - 1938) : ein deutscher Pionier der Quantenchemie in Moskau},
  year      = {1999},
  language  = {de}
}
@article{SchwarzAndraeArnoldetal.1999,
  author    = {Schwarz, W. H. Eugen and Andrae, Dirk and Arnold, S. R. and Heidberg, Joachim and Hellmann jr., H. and Hinze, J. and Karachalios, A. and Kovner, M. A. and Schmidt, P. C. and Z{\"u}licke, Lutz},
  title     = {Hans G. Hellmann (1903 - 1938) : ein Pionier der Quantenchemie},
  year      = {1999},
  language  = {de}
}
@article{KumkeSpechtFrimmel2000,
  author    = {Kumke, Michael Uwe and Specht, C. H. and Frimmel, Fritz Hartmann},
  title     = {Characterization of NOM adsorption to clay minerals by sizs exclusion chromatography},
  year      = {2000},
  language  = {en}
}
@article{BenassiBertariniKleinpeteretal.2000,
  author    = {Benassi, Rois and Bertarini, C. and Kleinpeter, Erich and Taddei, F. and Thomas, Steffen},
  title     = {Exocyclic push-pull conjugated compounds : Part 1 ; theoretical study of the effect of ring size on the structure, electronic properties and rotational barriers of cyclic analogoues of 1,1-diamino-2.2-dicyanoethylene},
  year      = {2000},
  language  = {en}
}
@article{BenassiBertariniKleinpeteretal.2000,
  author    = {Benassi, Rois and Bertarini, C. and Kleinpeter, Erich and Taddei, F.},
  title     = {Exocyclic push-pull conjugated compounds, Part 2 : the effect of donor and acceptor substituents on the rotational barrier of push-pull ethylenes},
  year      = {2000},
  language  = {en}
}
@article{BenassiBertariniHilfertetal.2000,
  author    = {Benassi, Rois and Bertarini, C. and Hilfert, Liane and Kempter, Gerhard and Kleinpeter, Erich and Spindler, J{\"u}rgen and Taddei, F. and Thomas, Steffen},
  title     = {Exocyclic push-pull conjugated compounds : Part 3},
  year      = {2000},
  language  = {en}
}
@article{LetzelPeterKatalinicPeter2001,
  author    = {Letzel, Matthias C. and Peter-Katalinic, Jasna and Peter, Martin G.},
  title     = {Mass spectrometry of chitin and chitosan oligosaccharides},
  year      = {2001},
  language  = {en}
}
@article{Illenseer2001,
  author    = {Illenseer, C.},
  title     = {Investigation of ion-molecule collisions with laser-based ion mobility spectrometry},
  year      = {2001},
  language  = {en}
}
@article{StrehmelHenbestSarkeretal.2001,
  author    = {Strehmel, Bernd and Henbest, K. B. and Sarker, A. M. and Malpert, J. H. and Chen, D. Y. and Rodgers, M. A. J. and Neckers, D. C.},
  title     = {Ion induced man ipulation of photochemical pathways in crown ether compounends based on fluorinated oligophenylenevinylenes},
  publisher = {Journal of nanoscience and nanotechnology. - 1 (2001), 1, S. 107 - 124},
  year      = {2001},
  language  = {en}
}
@article{JansenBuschmannWegoetal.2001,
  author    = {Jansen, K. and Buschmann, Hans-J{\"u}rgen and Wego, A. and Dopp, D. and Mayer, C. and Holdt, Hans-Joachim and Schollmeyer, E.},
  title     = {Curcubit[5]uril, decamethylcururbit[5]uril and curcurbit[6]uril : synthesis, solubility and amin complex formation},
  year      = {2001},
  abstract  = {A simple way to prepare cucurbit[5]uril is described. The macrocycles of the cucurbituril type are nearly insoluble in water. The solubilities of cucurbit[5]uril, decamethylcucurbit[5]uril and cucurbit[6]uril in hydrochloric acid, formic acid and acetic acid of different concentrations have been investigated. Due to the formation of complexes between cucurbit[n]urils and protons the solubility increases in aqueous acids. The macrocyclic ligands are able to form complexes with several organic compounds. Thus, the complex formation of the cucurbituril macrocycles with different amines has beenstudied by means of calorimetric titrations. The reaction enthalpy gives noevidence of the formation of inclusion or exclusion complexes. 1H-NMR measurements show that in the case of cucurbit[5]uril and cucurbit[6]uril the organic guest compound is included within the hydrophobic cavity. Decamethylcucurbit[5]uril forms only exclusion complexes with organicamines. This was confirmed by the crystal structure of the decamethylcucurbit[5]uril-1,6- diaminohexane complex. complex formation - cucurbit[5]uril - cucurbit[6]uril - decamethylcucurbit[5]uril - solubility - synthesis},
  language  = {en}
}
@misc{DoscheLoehmannsroebenBieseretal.2002,
  author    = {Dosche, Carsten and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Bieser, A. and Dosa, P. I. and Han, S. and Iwamoto, M. and Schleifenbaum, A. and Vollhardt, K. Peter C.},
  title     = {Photophysical properties of [N]phenylenes},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-11936},
  year      = {2002},
  abstract  = {In the present study, photophysical properties of [N]phenylenes were studied by means of stationary and time-resolved absorption and fluorescence spectroscopy (in THF at room temperature). For biphenylene (1) and linear [3]phenylene (2a), internal conversion (IC) with quantum yields ΦIC > 0.99 is by far the dominant mechanism of S1 state deactivation. Angular [3]phenylene (3a), the zig-zag [4]- and [5]phenylenes (3b), (3c), and the triangular [4]phenylene (4) show fluorescence emission with fluorescence quantum yieds and lifetimes between ΦF = 0.07 for (3a) and 0.21 for (3c) and τF = 20 ns for (3a) and 81 ns for (4). Also, compounds (3) and (4) exhibit triplet formation upon photoexcitation with quantum yields as high as ΦISC = 0.45 for (3c). The strong differences in the fluorescence properties and in the triplet fromation efficiencies between (1) and (2a) on one hand and (3) and (4) on the other are related to the remarkable variation of the internal conversion (IC) rate constants kIC. A tentative classification of (1) and (2a) as "fast IC compounds", with kIC > 109 s-1, and of (3) and (4) as "slow IC compounds", with kIC ≈ 107 s-1, is suggested. This classification cannot simply be related to H{\"u}ckel's rule-type concepts of aromaticity, because the group of "fast IC compounds" consists of "antiaromatic" (1) and "aromatic" (2a), and the group of "slow IC compounds" consists of "antiaromatic" (3b), (4) and "aromatic" (3a), (3c). The IC in the [N]phenylenes is discussed within the framework of the so-called energy gap law established for non-radiative processes in benzenoid hydrocarbons.},
  language  = {en}
}
@misc{KaafaraniWexStrehmeletal.2002,
  author    = {Kaafarani, Bilal R. and Wex, Brigitte and Strehmel, Bernd and Neckers, Douglas C.},
  title     = {Structural concept for fluorinated Y-enynes with solvatochromic properties},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-13168},
  year      = {2002},
  abstract  = {An approach to the development of fluorescent probes to follow polymerizations in situ using fluorinated cross-conjugated enediynes (Y-enynes) is reported. Different substitution patterns in the Y-enynes result in distinct solvatochromic behavior. β,β-Bis(phenylethynyl)pentafluorostyrene 7, which bears no donor substituents and only fluorine at the styrene moiety, shows no solvatochromism. Donor substituted β,β-bis(3,4,5-trimethoxyphenylethynyl) pentafluorostyrene 8 and β,β-bis(4-butyl-2,3,5,6-tetrafluorophenylethynyl)-3,4,5-trimethoxystyrene 9 exhibit solvatochromism upon change of solvent polarity. Y-enyne 8 showed the largest solvatochromic shift (94 nm bathochromic shift) upon changing solvent from cyclohexane to acetonitrile. A smaller solvatochromic response (44 nm bathochromic shift) was observed for 9. Lippert-Mataga treatment of 8 and 9 yields slopes of -10,800 and -6,400 cm -1, respectively. This corresponds to a change in dipole moment of 9.6 and 6.9 D, respectively. The solvatochromic behavior in 8 and 9 supports the formation of an intramolecular charge transfer (ICT) state. The low fluorescence quantum yields are caused by competitive double bond rotation. The fluorescence decay time of 9 decreases in methyltetrahydrofuran from 2.1 ns at 77 K to 0.11 ns at 200 K. Efficient single bond rotation in 9 was frozen at -50 °C in a configuration in which the trimethoxyphenyl ring is perpendicular to the fluorinated rings. 7-9 are photostable compounds. The X-ray structure of 7 shows it is not planar and that its conjugation is distorted. Y-enyne 7 stacks in the solid state showing coulombic, actetylene-arene, and fluorine-π interactions.},
  language  = {en}
}
@article{DoscheLoehmannsroebenBieseretal.2002,
  author    = {Dosche, Carsten and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Bieser, A. and Dosa, P. I. and Han, S. and Iwamoto, M. and Schleifenbaum, A. and Vollhardt, K. Peter C.},
  title     = {Photophysical properties of [N]phenylenes},
  year      = {2002},
  language  = {en}
}