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Publikationen

Aus eigener Forschung

 

Die aktuellsten Publikationen aus unserer Forschung sind bereits in Vorbereitung:

  • J. Rödder, V. Vasylyeva*, in prep.
  • K. Caner, V. Vasylyeva*, in prep.
  • V. Kohlbach, V. Vasylyeva*, in prep.
  • M. Marin, V. Vasylyeva*, in prep.
  • T. Stollenwerk, H. Thiemeier, M. Kamper, G. Roth, V. Vasylyeva*, in prep.

Veröffentlicht:

  • D. Komisarek, M. Pallaske, V. Vasyleva*, Special issue "Crystal Structure and Thermal Properties of Phenibut, Phenibut∙H2O and Phenibut∙HCl: a case for phase stability based on structural considerations", Z. Anorg. Allg. Chem., 2021, just accepted, https://doi.org/10.1002/zaac.202100012
     
  • V. Vasylyeva*, M. Amini, Special issue "In celebration of the 60th birthday of Christoph Janiak", Z. Anorg. Allg. Chem., 2021, 647, 414– 414, https://doi.org/10.1002/zaac.202100067
     
  • O. V. Shishkin, K. Merz, V. Vasylyeva, R. I Zubatyuk, “Isotypic Transformation Principle in Molecular Crystals. Analysis of Supramolecular Architecture of Fluorinated Benzenes and Pyridines”, Cryst. Growth Des., 2018, 18, 8, 4445-4448.
     
  • V. Vasylyeva, L. Catalano, C. Nervi, R. Gobetto, P. Metrangolo, G. Resnati, Issue cover: ”Characteristic redshift and intensity enhancement as far-IR fingerprints of the halogen bond involving aromatic donors”, CrystEngComm, 2016, 18, 2247.
  • P. Cerreia Vioglio, L. Catalano, V. Vasylyeva, C. Nervi, M. R. Chierotti, G. Resnati, R. Gobetto, P. Metrangolo, Hot Paper: “Natural Abundance 15N and 13C Solid-State NMR Chemical Shifts:High Sensitivity Probes of the Halogen Bond Geometry”, Chem. Eur. J., 2016, 22, 1.
  • V. Vasylyeva, D.W.M. Hofmann, K. Merz, “Crystal structures of 2-chloropyridine and 2-fluoropyridine: Isostructural crystal packing or not?”, Structural Chem., 2016, 27 (1), 331.
  • V. Vasylyeva, S. K. Nayak, G. Terraneo, G. Cavallo, P. Metrangolo, G. Resnati, Hot Article: “Orthogonal halogen and hydrogen bonds involving a peptide bond model”, CrystEngComm, 2014, 16, 8102.
  • V. Vasylyeva, K. Merz, Special issue on cryo-crystallography, issue cover: “Crystal architecture of the low melting nitrogen heterocycles tetrafluoropyrimidine and trifluorotriazine”, Z. Kristallogr.- Cryst. Mat., 2014, 229 (9), 603.
  • O. V. Shishkin, S. V. Shishkina, A. V. Maleev, R. I Zubatyuk, V. Vasylyeva, K. Merz, “Influence of deuteration and fluorination on the supramolecular architecture of pyridine-N-oxide crystals”, ChemPhysChem, 2013, 14(4), 847.
  • V. Vasylyeva, O. V. Shishkin, A. Maleev, K. Merz, “Crystal structures of fluorinated pyridines from geometrical and energetic perspectives” Cryst. Growth Des., 2012, 12, 1032.
  • A. Kupka, V. Vasylyeva, K. Yusenko. D. W. M. Hofmann, K. Merz, „Solvent and isotopic effects on acridine and deuterated acridine polymorphism“, Cryst. Growth Des, 2012, 12, 5966.
  • K. Merz, V. Vasylyeva, Highlight Article, a Review “Development and boundaries in the field of supramolecular synthons”, CrystEngComm, 2010, 12, 3989.
  • V. Vasylyeva, K. Merz, “Aggregation of fluorine-substituted pyridines”, J. Fluorine Chem., 2010, 131, 446.
  • V. Vasylyeva, T. Kedziorski, N. Metzler-Nolte, C. Schauerte, K. Merz, „Polymorphism of pyridine-N-oxide and its deuterated analogues“, Cryst. Growth Des., 2010, 10, 4224.
  • V. Vasylyeva, K. Merz, “Fluorobenzonitriles: influence of the substitution pattern on melting and crystallization properties”, Cryst. Growth Des., 2010, 10, 4250.

 

Aus den Servicemessungen

  • M. Enamullah, V. Vasylyeva, M. A. Quddus, M. K. Islam, S.-P. Höfert, C. Janiak, Issue cover, CrystEngComm, 2018, 20, 4724.
  • V. Krieger, E. Ciglia, R. Thoma, V. Vasylyeva, B. Frieg, N. de Sousa Amadeu, T. Kurz, C. Janiak, H. Gohlke, F. K. Hansen, Chem. Eur. J., 2017, 23, 3699.
  • M. Enamullah, M. A. Quddus, M. R. Hasan, G. Pescitelli, R. Berardozzi, G. Makhloufi, V. Vasylyeva, C. Janiak, Dalton Trans, 2016, 45, 667.
  • M. Enamullah, M. A. Quddus, M. A. Halim, M. K. Islam, V. Vasylyeva, C. Janiak, Inorg. Chim. Acta, 2015, 427, 103.
  • R. Bikas, F. Hosseini-Monfared, V. Vasylyeva, J. Sanchiz, J. Alonso, J. M. Barandiaran, C. Janiak, Dalton Trans, 2014, 43, 11925.
  • M. Enamullah, A. KM R. Uddin, G. Pescitelli, R. Berardozzi, G. Makhloufi, V. Vasylyeva, A.-C. Chamayou, C. Janiak, Dalton Trans, 2014, 43, 3313.
  • C. Heering, I. Boldog, V. Vasylyeva, J. Sanchiz, C. Janiak, CrystEngComm, 2013, 15 (45), 9757.
  • G. S. Yellol, A. Donaire, J. G. Yellol, V. Vasylyeva, C. Janiak, J. Ruiz, Chem. Comm., 2013, 49, 11533.
  • M. Enamullah, V. Vasylyeva, C. Janiak, Inorg. Chim. Acta, 2013, 408, 109.
  • A. Bhunia, V. Vasylyeva, C. Janiak, Chem. Comm, 2013, 49 (38), 3961.
  • D. Rönsberg, A. Debbab, A. Mándi, V. Vasylyeva, P. Böhler, B. Stork, L. Engelke, A. Hamacher, R. Sawadogo, M. Diederich, V. Wray, W. Lin, M. Kassack, C. Janiak, S. Scheu, S. Wesselborg, T. Kurtán, A. H. Aly, P. Proksch, J. Org. Chem., 2013, 78, 12409.
  • T. Backer, O. Breunig, M. Valldor, K. Merz, V. Vasylyeva, A.-V. Mudring, Cryst. Growth Des., 2011, 11, 2564.
  • M. R. Malik, V. Vasylyeva, K. Merz, N. Metzler-Nolte, M. Saleem, S. Ali, A. A. Isab, K. S. Munawar, S. Ahmad, Inorg. Chimica Acta, 2011, 376, 207.
  • S. Nawaz, A. A. Isab, K. Merz, V. Vasylyeva, N. Metzler-Nolte, M. Saleem, S. Ahmad, Polyhedron, 2011, 30, 1502.
  • K. Splith, I. Neundorf, W. Hu, H. W. P. N'Dongo, V. Vasylyeva, K. Merz, U. Schatzschneider, Dalton Transactions, 2010, 39, 2536.
  • J. Lemke, A. Pinto, P. Niehoff, V. Vasylyeva, N. Metzler-Nolte, Dalton Trans., 2009, 35, 7063.
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