Publikationen

Our research

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T. Haj Hassani Sohi, F. Maass, C. Czekelius, V. Vasylyeva*, A Comparison Study of Roseolumiflavin Solvates: Structural and Energetic Perspective on Their Stability, Crystals 2023, 13(10), 1512. doi: 10.3390/cryst13101512.
D. Komisarek, F. Demirbas, T. Haj Hassani Sohi, K. Merz, C. Schauerte, V. Vasylyeva*, Special Issue Controlled Crystallization of Active Pharmaceutical Ingredients, 2nd Edition, Polymorphism and Multi-Component Crystal Formation of GABA and Gabapentin, Pharmaceutics 2023, 15(9), 2299. doi 10.3390/pharmaceutics15092299
T. Heinen, S. Merzenich, A. Kwill, V. Vasylyeva*, Special Issue Covalent and Noncovalent Interactions in Crystal Chemistry II, Halogen Bonding in Sulphonamide Co-Crystals: X···π Preferred over X···O/N? Molecules 2023, 28, 5910. doi: 10.3390/molecules28155910
D. Komisarek, E. Taskiran, V. Vasylyeva*, Special Issue Advances in Crystal Material: Design, Characterization, and Applications, Maleic Acid as a Co-Former for Pharmaceutically Active GABA Derivatives: Mechanochemistry or Solvent Crystallization? Materials 2023, 16, 2242. doi: 10.3390/ma16062242
D. Komisarek, T. Haj Hassani Sohi, V. Vasylyeva*, Back Cover, "Co-Crystals of Zwitterionic GABA API's Pregabalin and Phenibut: Properties and Application", CrystEngComm, 2022, 24, 8390-8398, DOI: 10.1039/D2CE01416E
M. Herbst, D. Komisarek, T. Strothmann, V. Vasylyeva*, Special issue: Advances in Pharmaceutical Crystals: Control over Nucleation and Polymorphism, "A Lection in Humbleness: Crystallization of Chiral and Zwitterionic APIs Baclofen and Phenibut", Crystals, 2022, 12(10), 1393. https://www.mdpi.com/2073-4352/12/10/1393
T. Haj Hassani Sohi, F. Maaß, C. Czekelius, M. Suta, V. Vasylyeva*, Special issue: New Talent 2022, "Co-crystallization of organic chromophore roseolumiflavin and effect on its optical characteristics", CrystEngComm, 2022, 24, 7315-7325. DOI: 10.1039/D2CE00589A, https://pubs.rsc.org/en/content/articlelanding/2022/ce/d2ce00589a
T. Heinen, S. Hölscher, V. Vasylyeva*, Special Issue: Spotlight on Germany’s Young Crystallographers, " Structural study of anhydrous and hydrated 5-fluorouracil co-crystals with nicotinamide and isonicotinamide", Z. Kristallogr., 2021, 237(4–5), 109–116. https://www.degruyter.com/document/doi/10.1515/zkri-2021-2052/html
D. Komisarek, M. Pallaske, V. Vasyleva*, "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, 647, 984–991, 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.

Service

E. Nieland, D. Komisarek, S. Hohloch, K. Wurst, V. Vasylyeva, O. Weingart, B. M. Schmidt, Chem. Commun., 2022, 58, 5233. DOI: 10.1039/d2cc00799a
A. Karagianni, J. Quodbach, O. Weingart, A. Tsiaxerli, V. Katsanou, V. Vasylyeva, C. Janiak, K. Kachrimanis, Solids 2022, 3, 66–92. https://doi.org/10.3390/solids3010006
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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