Publications

Published:

• 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.

An extremely electron poor cationic triazoliumylidene NHC: experimental and computanional studies" T. Hölzel, M. Otto, H. Buhl, C. Ganter, Organometallics 2017, 36, 4443-4450. available online

"An N-Heterocyclic carbene with a sulfonamide group embedded within the heterocyclic backbone" M. Jonek, A. Makhloufi, C. Ganter, J. Organomet. Chem. 2017, 838, 37-41. available online

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