@book{BechmannSchmidtElschenbroichetal.2001,
  author    = {Bechmann, Wolfgang and Schmidt, Joachim and Elschenbroich, Christoph and Hensel, Friedrich and Hopf, Henning},
  title     = {Einstieg in die Physikalische Chemie f{\"u}r Nebenf{\"a}chler},
  series = {Teubner Studienb{\"u}cher Chemie},
  journal   = {Teubner Studienb{\"u}cher Chemie},
  publisher = {Vieweg+Teubner Verlag},
  address   = {Wiesbaden},
  isbn      = {3-519-00352-X},
  doi       = {10.1007/978-3-322-94876-2},
  pages     = {303 S.},
  year      = {2001},
  abstract  = {Mit einer ausgewogenen Stoffauswahl wird der Leser an das Studium der Physikalischen Chemie herangef{\"u}hrt. Das Verst{\"a}ndnis der Theorie wird durch zahlreiche Aufgabenstellungen und die Angabe ihrer L{\"o}sungswege erleichtert. Das vorliegende Buch gibt dem Studenten dar{\"u}ber hinaus Anregungen f{\"u}r ausgew{\"a}hlte Experimente zu den behandelten Teilgebieten. In der Durchf{\"u}hrung und Auswertung der Experimente kann der Student erneut {\"u}berpr{\"u}fen, wie gut es ihm gelungen ist, ein Grundverst{\"a}ndnis f{\"u}r physikalisch-chemische Zusammenh{\"a}nge zu entwickeln.},
  language  = {de}
}
@article{BeitzKoetzWolfetal.2001,
  author    = {Beitz, Toralf and Koetz, Joachim and Wolf, Gunter and Kleinpeter, Erich and Friberg, Stig E.},
  title     = {Poly(N-vinyl-2-pyrrolidone) and 1-octyl-2-pyrrolidinone modified ionic microemulsions},
  year      = {2001},
  language  = {en}
}
@phdthesis{Drechsler2001,
  author    = {Drechsler, Ulrich},
  title     = {Statische Lichtstreuung an Cellulose in L{\"o}sungsmittelsystemen mit N-Methylmorpholin-N-oxid},
  pages     = {94 S.},
  year      = {2001},
  language  = {de}
}
@article{GrotjahnLehmannAurichetal.2001,
  author    = {Grotjahn, Manuela and Lehmann, S. and Aurich, Ines and Holdt, Hans-Joachim and Kleinpeter, Erich},
  title     = {NMR spectroscopic and molecular modelling studies of the solution structure and complexational behaviour of some bis(benzocrown ether)s},
  year      = {2001},
  abstract  = {Structural information about the bis(benzo crown ether)s I-VI and their complexes with alkali metal cations was deduced from the 13C NMR chemical shifts, the salt-induced 1H and 13C chemical shifts and the vicinal 1H,1H coupling constants. Especially the isomerism with respect to the amide O=C - NH bonds and imine fragments were assigned by various useful NMR parameters ( C=O, 1JN,H, 1JC,H) and proved to be E,E-anti,anti. Furthermore, stereochemical information about preferred conformations about flexible bonds was obtained from 2D ROESY NMR experiments. The complex formation (2:1 complexes and sandwich-like 1:1 complexes, respectively) were determined also by 23Na NMR spectroscopy. The conformational study of the crown ethers was accompanied and corroborated by molecular dynamics and quantum chemical calculations.},
  language  = {en}
}
@article{HeinzeHeinzeGrotheetal.2001,
  author    = {Heinze, Thomas and Heinze, Ute and Grothe, Carsten and Koetz, Joachim and Lazik, Waldemar},
  title     = {Starch derivatives of high degree of functionalization : 4. Homogeneous tritylation of starch an subsequent carboxymethylation},
  year      = {2001},
  language  = {en}
}
@article{HoldtDrexlerStarkeetal.2001,
  author    = {Holdt, Hans-J{\"u}rgen and Drexler, Hans-Joachim and Starke, Ines and Grotjahn, Manuela and Kleinpeter, Erich},
  title     = {Homologous series of the PdCl2 and PtCl2 complexes of maleonitrile-dithiacrown ethers : synthesis, crystal structures, NMR spectroscopy and mass spectrometry},
  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{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}
}
@article{KalliesMeier2001,
  author    = {Kallies, Bernd and Meier, R.},
  title     = {The electronic structure od 3 [M(H20)6)3+ions from Sc(III)till Fe (III) : a quantum mechanical study based on DFT computations and natural bond orbital analyses},
  year      = {2001},
  language  = {en}
}
@article{KamlageSefkowPeter2001,
  author    = {Kamlage, Stefan and Sefkow, Michael and Peter, Martin G.},
  title     = {A short synthesis of biologically active lignan analogues},
  year      = {2001},
  abstract  = {beta-Benzyl-gamma-butyrolactones were synthesized in four transition metal catalysed reactions from butynediol, and alkylated to afford new, biologically active lignan analogues.},
  language  = {en}
}