Journal
ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS
Volume 73, Issue -, Pages 569-+Publisher
INT UNION CRYSTALLOGRAPHY
DOI: 10.1107/S205698901700425X
Keywords
crystal structure; formamidinium iodide; phase transitions; powder diffraction; synchrotron radiation
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Funding
- Ministry of Education and Science of the Russian Federation [02.a03.21.0008]
- Russian Foundation for Basic Research [16-29-03291]
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At a temperature of 100 K, CH5N2+center dot I- (I), crystallizes in the monoclinic space group P2(1)/ c. The formamidinium cation adopts a planar symmetrical structure [the r. m. s. deviation is 0.002 angstrom, and the C-N bond lengths are 1.301 (7) and 1.309 (8) angstrom]. The iodide anion does not lie within the cation plane, but deviates from it by 0.643 (10) angstrom. The cation and anion of I form a tight ionic pair by a strong N-H center dot center dot center dot I hydrogen bond. In the crystal of I, the tight ionic pairs form hydrogen-bonded zigzag-like chains propagating toward [20 (1) over bar] via strong N-H center dot center dot center dot I hydrogen bonds. The hydrogen-bonded chains are further packed in stacks along [100]. The thermal behaviour of I was studied by different physicochemical methods (thermogravimetry, differential scanning calorimetry and powder diffraction). Differential scanning calorimetry revealed three narrow endothermic peaks at 346, 387 and 525 K, and one broad endothermic peak at similar to 605 K. The first and second peaks are related to solid-solid phase transitions, while the third and fourth peaks are attributed to the melting and decomposition of I. The enthalpies of the phase transitions at 346 and 387 K are estimated as 2.60 and 2.75 kJ mol(-1), respectively. The X-ray powder diffraction data collected at different temperatures indicate the existence of I as the monoclinic (100-346 K), orthorhombic (346-387 K) and cubic (387-525 K) polymorphic modifications.
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