Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/17527
Title: Anion-/cation-directed reaction routes to polymorphic forms of a pyrazole-type ligand and its coordination compounds with zinc. Key structural differences between polymorphs’
Authors: Holló Berta 
Mesaroš-Sečenji (Mészáros Szécsényi) Katalin 
Mária Deli
Kiss Lóránd
Kállay-Menyhárd Alfréd
Živković Radovanović Vukosava
Tomić Zoran D.
Issue Date: 2016
Journal: Structural Chemistry
Abstract: © 2016, Springer Science+Business Media New York. Synthetic paths toward the two polymorphs of a monohydrate, one anhydrous polymorph of 1-carboxamidino-5-hydroxy-3-methylpyrazole (hcmp) and two polymorphs of zinc complexes containing hcmp ligand are presented. By choosing ions which are not part of the final product, it is possible to direct the synthesis toward the particular polymorph. In all three modifications of hcmp, the same hydrogen bonding motif appears, leading to formation of similar molecular chains. Differences arise due to different modes of chain aggregation and the presence of solvent water. Analysis of the crystal packing and the energetic features of hcmp polymorphs is made using the PIXEL model. The thermal decomposition processes are examined using differential scanning calorimetry and thermogravimetry. Analysis of crystal packing in the two polymorphs of zinc complex suggests the key role of the hydrogen bonding capacity of the aqua ligand for the appearance of the two polymorphic forms. In both polymorphs of zinc complex, stacking interactions have an important role. However, the enhanced hydrogen bonding capacity of the aqua ligand influences the formation of multistacking arrangement.
URI: https://open.uns.ac.rs/handle/123456789/17527
ISSN: 1040-0400
1572-9001
DOI: 10.1007/s11224-015-0734-1
Appears in Collections:PMF Publikacije/Publications

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