@article{MeshcheryakovMoskalikKellingetal.2008,
  author    = {Meshcheryakov, Vladimir I. and Moskalik, Mikail Yu. and Kelling, Alexandra and Schilde, Uwe and Ushakov, Igor A. and Shainyan, Bagrat A.},
  title     = {Oxymethylation of trifluoromethanesulfonamide with paraformaldehyde in ethyl acetate},
  issn      = {1070-4280},
  doi       = {10.1134/S1070428008020206},
  year      = {2008},
  abstract  = {Acid-catalyzed reaction of trifluoromethanesulfonamide with paraformaldehyde in ethyl acetate led to the formation of oxymethylated products that did not form in the reaction carried out in sulfuric acid. Following products were obtained: 5-trifluoromethylsulfonyl-1,3-dioxazinane, 3,7-bis-(trifluoromethylsulfonyl)-1,5,3,7-dioxadiazocane, and a complex of trifluoromethanesulfonamide with 2,4,8,10-tetraoxospiro[5,5]undecene, 1:1. The spiroring resulted from the cyclization of pentaerythritol under the action of formaldehyde. The pentaerythritol formed in its turn by oxymethylation of the methyl group of ethyl acetate with paraformaldehyde followed by the reduction of the COOEt group into CH2 OH by the formaldehyde.},
  language  = {en}
}
@article{SengeHatscherWieheetal.2004,
  author    = {Senge, Mathias O. and Hatscher, S. S. and Wiehe, A. and Dahms, Katja and Kelling, Alexandra},
  title     = {The dithianyl group as a synthon in porphyrin chemistry : condensation reactions and preparation of formylporphyrins under basic conditions},
  issn      = {0002-7863},
  year      = {2004},
  language  = {en}
}
@article{ShainyanMeshcheryakovSterkhovaetal.2008,
  author    = {Shainyan, Bagrat A. and Meshcheryakov, Vladimir I. and Sterkhova, I. V. and Kelling, Alexandra and Schilde, Uwe},
  title     = {Structure of the molecule of 1,2-bis(1-ethyl-1 H -1,2,3-triazol-4-yl)diazene 1-oxide in the crystal and in solutions},
  issn      = {1070-4280},
  year      = {2008},
  abstract  = {Reduction of 4-nitro-1-ethyl-1H-1,2,3-triazole with aluminum in alkaline medium resulted in a syn-isomer of 1,2- bis(1-ethyl-1H-1,2,3-triazol-4-yl)diazene 1-oxide. The latter according to the data of X-ray diffraction analysis existed in the crystal as the most stable s-cis,s-trans-conformer, and in solution, as showed NMR data, as a mixture of s-cis,s-trans- and s-trans,s-trans-conformers. The data of quantum-chemical calculations are in agreement with the results of the structural studies.},
  language  = {en}
}
@article{DudekCleggGlassonetal.2011,
  author    = {Dudek, Melanie and Clegg, Jack K. and Glasson, Christopher R. K. and Kelly, Norman and Gloe, Kerstin and Gloe, Karsten and Kelling, Alexandra and Buschmann, Hans-J{\"u}rgen and Jolliffe, Katrina A. and Lindoy, Leonard F. and Meehan, George V.},
  title     = {Interaction of Copper(II) with Ditopic Pyridyl-beta-diketone Ligands dimeric, framework, and metallogel structures},
  series = {Crystal growth \& design : integrating the fields of crystal engineering and crystal growth for the synthesis and applications of new materials},
  volume    = {11},
  journal   = {Crystal growth \& design : integrating the fields of crystal engineering and crystal growth for the synthesis and applications of new materials},
  number    = {5},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1528-7483},
  doi       = {10.1021/cg101629w},
  pages     = {1697 -- 1704},
  year      = {2011},
  abstract  = {The interaction of Cu(II) with three beta-diketone ligands of type R(1)C(O)CH(2)C(O)R(2) (where R(1) = 2-, 3-, or 4-pyridyl and R(2) = C(6)H(5), respectively), HL(1)-HL(3), along with the X-ray structures and the pK(a) values of each ligand, are reported. HL(1) yields a dimeric complex of type [Cu(L(1))(2)](2). In this structure, two deprotonated HL(1) ligands coordinate in a trans planar fashion around each Cu(II) center, one oxygen from each CuL(2) unit bridges to an axial site of the second complex unit such that both Cu(II) centers attain equivalent five-coordinate square pyramidal geometries. The two-substituted pyridyl groups in this complex do not coordinate, perhaps reflecting steric factors associated with the closeness of the pyridyl nitrogen to the attached (conjugated) beta-diketonato backbone of each ligand. The remaining two Cu(II) species, derived from HL(2) and HL(3), are both coordination polymers of type [Cu(L)(2)](n) in which the terminal pyridine group of each ligand is intermolecularly linked to an adjacent copper center to generate the respective infinite structures. HL(2) was also demonstrated to form a fibrous metallogel when reacted with CuCl(2) in an acetonitrile/water mixture under defined conditions.},
  language  = {en}
}
@article{TraegerKellingSchildeetal.2012,
  author    = {Tr{\"a}ger, J. and Kelling, A. and Schilde, Uwe and Holdt, H. -J.},
  title     = {rac-1-[(2-Methoxyethyl)sulfanyl]-2-[(2-methoxyethyl)sulfinyl]benzene and its PdCl2 complex},
  series = {Acta crystallographica : Section C, Crystal structure communications},
  volume    = {68},
  journal   = {Acta crystallographica : Section C, Crystal structure communications},
  number    = {9},
  publisher = {Wiley-Blackwell},
  address   = {Hoboken},
  issn      = {0108-2701},
  doi       = {10.1107/S0108270112032192},
  pages     = {M238 -- +},
  year      = {2012},
  abstract  = {As an extension of recent findings on the recovery of palladium with dithioether extractants, single crystals of the chelating vicinal thioether sulfoxide ligand rac-1-[(2-methoxyethyl)sulfanyl]-2-[(2-methoxyethyl)sulfinyl]benzene, C12H18O3S2, (I), and its square-planar dichloridopalladium complex, rac-dichlorido{1-[(2-methoxyethyl)sulfanyl]-2-[(2-methoxyethyl)sulfinyl]benzene-?2S,S'}palladium(II), [PdCl2(C12H18O3S2)], (II), have been synthesized and their structures analysed. The molecular structure of (II) is the first ever characterized involving a dihalogenidePdII complex in which the palladium is bonded to both a thioether and a sulfoxide functional group. The structural and stereochemical characteristics of the ligand are compared with those of the analogous dithioether compound [Traeger et al. (2012). Eur. J. Inorg. Chem. pp. 23412352]. The sulfinyl O atom suppresses the electron-pushing and mesomeric effect of the SC...;CS unit in ligand (I), resulting in bond lengths significantly different than in the dithioether reference compound. In contrast, in complex (II), those bond lengths are nearly the same as in the analogous dithioether complex. As observed previously, there is an interaction between the central PdII atom and the O atom that is situated above the plane.},
  language  = {en}
}
@misc{MondalDeyBaburinetal.2013,
  author    = {Mondal, Suvendu Sekhar and Dey, Subarna and Baburin, Igor A. and Kelling, Alexandra and Schilde, Uwe and Seifert, Gotthard and Janiak, Christoph and Holdt, Hans-J{\"u}rgen},
  title     = {Syntheses of two imidazolate-4-amide-5-imidate linker-based hexagonal metal-organic frameworks with flexible ethoxy substituent},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-94360},
  pages     = {9394 -- 9399},
  year      = {2013},
  abstract  = {A rare example of in situ linker generation with the formation of soft porous Zn- and Co-MOFs (IFP-9 and -10, respectively) is reported. The flexible ethoxy groups of IFP-9 and -10 protrude into the 1D hexagonal channels. The gas-sorption behavior of both materials for H2, CO2 and CH4 showed wide hysteretic isotherms, typical for MOFs having a flexible substituent which can give rise to a gate effect.},
  language  = {en}
}
@misc{MondalBhuniaBaburinetal.2013,
  author    = {Mondal, Suvendu Sekhar and Bhunia, Asamanjoy and Baburin, Igor A. and J{\"a}ger, Christian and Kelling, Alexandra and Schilde, Uwe and Seifert, Gotthard and Janiak, Christoph and Holdt, Hans-J{\"u}rgen},
  title     = {Gate effects in a hexagonal zinc-imidazolate-4-amide-5-imidate framework with flexible methoxy substituents and CO2 selectivity},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-94341},
  pages     = {7599 -- 7601},
  year      = {2013},
  abstract  = {A new imidazolate-4-amide-5-imidate based MOF, IFP-7, is generated, having flexible methoxy groups, which act as molecular gates for guest molecules. This allows highly selective CO2 sorption over N2 and CH4 gases.},
  language  = {en}
}
@article{MondalDeyBaburinetal.2013,
  author    = {Mondal, Suvendu Sekhar and Dey, Subarna and Baburin, Igor A. and Kelling, Alexandra and Schilde, Uwe and Seifert, Gotthard and Janiak, Christoph and Holdt, Hans-J{\"u}rgen},
  title     = {Syntheses of two imidazolate-4-amide-5-imidate linker-based hexagonal metal-organic frameworks with flexible ethoxy substituent},
  series = {CrystEngComm},
  volume    = {15},
  journal   = {CrystEngComm},
  number    = {45},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1466-8033},
  doi       = {10.1039/c3ce41632a},
  pages     = {9394 -- 9399},
  year      = {2013},
  abstract  = {A rare example of in situ linker generation with the formation of soft porous Zn- and Co-MOFs (IFP-9 and -10, respectively) is reported. The flexible ethoxy groups of IFP-9 and -10 protrude into the 1D hexagonal channels. The gas-sorption behavior of both materials for H-2, CO2 and CH4 showed wide hysteretic isotherms, typical for MOFs having a flexible substituent which can give rise to a gate effect.},
  language  = {en}
}
@article{MondalBhuniaBaburinetal.2013,
  author    = {Mondal, Suvendu Sekhar and Bhunia, Asamanjoy and Baburin, Igor A. and J{\"a}ger, Christian and Kelling, Alexandra and Schilde, Uwe and Seifert, Gotthard and Janiak, Christoph and Holdt, Hans-J{\"u}rgen},
  title     = {Gate effects in a hexagonal zinc-imidazolate-4-amide-5-imidate framework with flexible methoxy substituents and CO2 selectivity},
  series = {Chemical communications},
  volume    = {49},
  journal   = {Chemical communications},
  number    = {69},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1359-7345},
  doi       = {10.1039/c3cc42156b},
  pages     = {7599 -- 7601},
  year      = {2013},
  abstract  = {A new imidazolate-4-amide-5-imidate based MOF, IFP-7, is generated, having flexible methoxy groups, which act as molecular gates for guest molecules. This allows highly selective CO2 sorption over N-2 and CH4 gases.},
  language  = {en}
}
@article{MondalDeyBaburinetal.2008,
  author    = {Mondal, Suvendu Sekhar and Dey, Subarna and Baburin, Igor A. and Kelling, Alexandra and Schilde, Uwe and Janiak, Christoph and Holdt, Hans-J{\"u}rgen},
  title     = {Syntheses of two imidazolate-4-amide-5-imidate linker based hexagonal metal-organic frameworks with flexible ethoxy substituent},
  doi       = {10.1039/C3CE41632A},
  year      = {2008},
  abstract  = {A rare example of in situ linker generation with the formation of soft porous Zn- and Co-MOFs (IFP-9 and -10, respectively) is reported. The flexible ethoxy groups of IFP-9 and -10 protrude into the 1D hexagonal channels. The gas- sorption behavior of both materials for H2, CO2 and CH4 showed wide hysteretic isotherms, typical for MOFs having a flexible substituent which can give rise to a gate effect.},
  language  = {en}
}