z-logo
open-access-imgOpen Access
Sodium 1‐carboxycyclopropane‐1‐carboxylate cyclopropane‐1,1‐dicarboxylic acid monohydrate
Author(s) -
Muir Kenneth W.,
MacDonald Alistair,
MacDonald Alan
Publication year - 2004
Publication title -
acta crystallographica section c
Language(s) - English
Resource type - Journals
eISSN - 1600-5759
pISSN - 0108-2701
DOI - 10.1107/s0108270104027052
Subject(s) - octahedron , cyclopropane , hydrogen bond , chemistry , molecule , carboxylate , crystallography , hydrate , salt (chemistry) , sodium , medicinal chemistry , stereochemistry , ring (chemistry) , crystal structure , organic chemistry
In the title type B 2 acid salt, Na( L H)( L H 2 )·H 2 O [ L H 2 = C 2 H 4 C(CO 2 H) 2 ] or Na + ·C 5 H 5 O 4 − ·C 5 H 6 O 4 ·H 2 O, the vertices of a distorted octahedron centred on each Na + cation are defined by six O atoms, one from a water molecule, one from an internally hydrogen‐bonded L H − anion and four from three neutral L H 2 acid molecules. Chains of edge‐sharing O 6 octahedra are stabilized by hydrogen bonds, which interconnect the donor H 2 O and L H 2 molecules and L H − anions. In particular, the L H 2 molecule donates H atoms to L H − and H 2 O and forgoes the internal hydrogen bond which stabilizes the free acid and all of its characterized salts.

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