@article{DrexlerGrotjahnKleinpeteretal.1999,
  author    = {Drexler, Hans-Joachim and Grotjahn, Manuela and Kleinpeter, Erich and Holdt, Hans-J{\"u}rgen},
  title     = {A novel polymeric disilver(I) complex containing both macrocyclic- and linear-coordinate silver(I) centres : [Ag-2(mn-15S(2)O(3))](infinity)(ClO4)(2 infinity) (mn-15S(2)O(3) = maleonitrile-dithia[15]crown-5)},
  year      = {1999},
  language  = {en}
}
@article{KleinpeterGrotjahnKlinkaetal.2001,
  author    = {Kleinpeter, Erich and Grotjahn, Manuela and Klinka, Karel D. and Drexler, Hans-Joachim and Holdt, Hans-J{\"u}rgen},
  title     = {Conformational and complexational study of some maleonitrile mixed oxadithia crown ethers by NMR spectroscopy and molecular modelling},
  year      = {2001},
  abstract  = {The macrocyclic ring interconversion of four maleonitrile mixed oxadithia crown ethers of variable ring size, mn-12-S2O2, mn-15-S2O3, mn-18-S2O4 and fn-12-S2O2, were studied by 1H and 13C NMR spectroscopy and by molecular modelling. The barriers to ring interconversion were estimated using variable temperature NMR spectroscopy and from the calculated activation energies, together with the spin-lattice relaxation times of the CH2 carbon atoms, conclusions were drawn regarding the intramolecular flexibility of the crown ethers in both the free state as well as the complexed state incorporating either AgI, BiIII, SbIII, PdII or PtII metal cations. Furthermore, both the stoichiometry of the complexes and the coordination sites of the crown ethers to the various cations were also clearly implicated. Molecular modelling was also utilised to ascertain the preferred conformers of the four compounds and their corresponding complexes, the results of which corroborated the experimental NMR results to a high degree.},
  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{HoldtMuellerKellingetal.2006,
  author    = {Holdt, Hans-J{\"u}rgen and M{\"u}ller, Holger and Kelling, Alexandra and Drexler, Hans-Joachim and M{\"u}ller, Thomas and Schwarze, Thomas and Schilde, Uwe and Starke, Ines},
  title     = {Mercury(II) chloride and iodide complexes of dithia- and tetrathiacrown ethers},
  issn      = {0044-2313},
  doi       = {10.1002/zaac.200500281},
  year      = {2006},
  abstract  = {The complexes [(HgCl2)(2)((ch)(2)30S(4)O(6))] (1), [HgCl,(mn21S(2)O(5))] (2), [HgCl2(ch18S(2)O(4))] (3) and [HgI(meb12S(2)O(2))](2)[Hg2I6] (4) have been synthesized, characterized and their crystal structures were determined. In [(HgCl2)(2)((ch)(2)3OS(4)O(6))] two HgCl2 units are discretely bonded within the ligand cavity of the 30-membered dichinoxaline-tetrathia-30-crown-10 ((ch)(2)30S(4)O(6)) forming a binuclear complex. HgCl2 forms I : I "in-cavity" complexes with the 21-membered maleonitrile-dithia-21-crown-7(mn21S(2)O(5)) ligand and the 18-membered chinoxaline- dithia-18-crown-6 (ch18S(2)O(4)) ligand, respectively. The 12-membered 4-methyl-benzo-dithia-12-crown-4 (meb12S(2)O(2)) ligand gave with two equivalents HgI2 the compound [HgI(meb12S(2)O(2))](2)[Hg2I6]. In the cation [HgI(meb12S(2)O(2))](+) meb12S(2)O(2) forms with the cation HgI+ a half-sandwich complex},
  language  = {en}
}
@article{GrotjahnDrexlerJaegeretal.1997,
  author    = {Grotjahn, Manuela and Drexler, Hans-Joachim and J{\"a}ger, Norbert and Kleinpeter, Erich and Holdt, Hans-J{\"u}rgen},
  title     = {Molecular dynamic and conformational study of an unsaturated 12-crown-S202 ether and its AgI complexes},
  year      = {1997},
  language  = {en}
}
@article{GrotjahnJaegerDrexleretal.1999,
  author    = {Grotjahn, Manuela and J{\"a}ger, Norbert and Drexler, Hans-Joachim and Holdt, Hans-J{\"u}rgen and Kleinpeter, Erich},
  title     = {Molecular modeling study of the PtCl2 complexes of unsaturated S2On+1- coronands: dynamic simulations and investigation of the ring interconversion},
  year      = {1999},
  language  = {en}
}
@article{DrexlerStarkeGrojahnetal.1999,
  author    = {Drexler, Hans-Joachim and Starke, Ines and Grojahn, Manuela and Reinke, H. and Kleinpeter, Erich and Holdt, Hans-J{\"u}rgen},
  title     = {SbCl3, BiCl3 and Na+ Complexes of maleonitrile-dithiacrown ethers: synthesis, crystal structures and DEP-MS experiments},
  year      = {1999},
  language  = {en}
}
@article{RudershausenDrexlerBansseetal.2007,
  author    = {Rudershausen, S. and Drexler, Hans-Joachim and Banße, Wolfgang and Kelling, Alexandra and Schilde, Uwe and Holdt, Hans-Joachim},
  title     = {Three polymorphs of bis(5-methylthio-1,2-dithiole-3-thione)-disulfide},
  doi       = {10.1002/crat.200610776},
  year      = {2007},
  abstract  = {The title compound, bis(5-methylthio-1,2-dithiole-3-thione)-disulfide, was yielded for the first time as by- product of the reaction of nickel(II) and cobalt(II) ions with 5-methylthio-1,2-dithiole-3-thione-4-thiolate. The compound can be obtained directly by oxidation of the ammonium salt of the ligand. C8H6S10 forms three polymorphs: (I), which crystallizes in the orthorhombic space group P212121, (II) and (III), which crystallize in the monoclinic space groups P21/c and P21/n, respectively. The crystal and molecular structures are presented here. The determination of the absolute configuration of (I) indicated the P-helical enantiomer. In contrast to this, the crystals of (II) und (III) are racemic, containing P- and M-helical enantiomers. The polymorphs differ in the kind of skewing around the disulfide bond and of the positions of the both dithiole rings to the S-S-moiety},
  language  = {en}
}