z-logo
open-access-imgOpen Access
Bis(ammonium) Zoledronate Dihydrate
Author(s) -
Małgorzata Sikorska,
Jarosław Chojnacki
Publication year - 2013
Publication title -
journal of crystallography
Language(s) - English
Resource type - Journals
eISSN - 2356-7317
pISSN - 2314-5994
DOI - 10.1155/2013/741483
Subject(s) - imidazole , protonation , chemistry , deprotonation , ring (chemistry) , stacking , hydrogen bond , ammonium , medicinal chemistry , crystal structure , zoledronic acid , ion , crystallography , inorganic chemistry , stereochemistry , molecule , organic chemistry , medicine , surgery
Neutralization of 2-(1-imidazole)-1-hydroxyl-1,1′-ethylidenediphosphonic acid (zoledronic acid) by an excess of ammonia yielded bis(ammonium) zoledronate dihydrate, {, 2(H4N+), 2(H2O)}. The product is readily soluble in water and forms monocrystals for which the X-ray structural analysis was carried out. The zoledronic anion is of double negative charge due to deprotonation of three P–OH groups and protonation of the nitrogen in the imidazole ring. The structure is stabilized by extensive network of N–H⋯O and O–H⋯O hydrogen bonds expanding through the crystal in plane (002). The imidazole ring is involved in - stacking interactions with its symmetry equivalents related by inversion centers at (1 0 0) and (1 1/2 0), with distances between centroids (Cg–Cg) of 3.819 (2) and 3.881 (2) Å, respectively

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom