{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["66(Pt 5)"],"submitter":["Hernandez Linares MG"],"pubmed_abstract":["In the crystal structure of the title salt, C(8)H(12)N(+)·C(2)F(3)O(2) (-), all of the ammonium H atoms serve as donors for hydrogen bonds to carboxyl-ate O atoms, forming an R(4) (3)(10) ring motif based on two cations and two anions. Since both cations and anions act as inter-ion bridging groups, R(10) rings aggregate in a one-dimensional supra-molecular network by sharing the strongest N-H⋯O bond. Edge-sharing motifs lie on the twofold screw axis parallel to [010], and anti-parallel packing of these 2(1)-column structural units results in the crystal structure. This arrangement is one of the most commonly occurring in conglomerates of chiral 1-phenyl-ethyl-amine with achiral monocarboxylic acids, confirming that these ionic salts are particularly robust supra-molecular heterosynthons us"],"journal":["Acta crystallographica. Section E, Structure reports online"],"pagination":["o1118"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2979250"],"repository":["biostudies-literature"],"pubmed_title":["(R)-1-Phenyl-ethyl-ammonium trifluoro-acetate."],"pmcid":["PMC2979250"],"pubmed_authors":["Guerrero Luna G","Bernes S","Hernandez Linares MG"],"additional_accession":[]},"is_claimable":false,"name":"(R)-1-Phenyl-ethyl-ammonium trifluoro-acetate.","description":"In the crystal structure of the title salt, C(8)H(12)N(+)·C(2)F(3)O(2) (-), all of the ammonium H atoms serve as donors for hydrogen bonds to carboxyl-ate O atoms, forming an R(4) (3)(10) ring motif based on two cations and two anions. Since both cations and anions act as inter-ion bridging groups, R(10) rings aggregate in a one-dimensional supra-molecular network by sharing the strongest N-H⋯O bond. Edge-sharing motifs lie on the twofold screw axis parallel to [010], and anti-parallel packing of these 2(1)-column structural units results in the crystal structure. This arrangement is one of the most commonly occurring in conglomerates of chiral 1-phenyl-ethyl-amine with achiral monocarboxylic acids, confirming that these ionic salts are particularly robust supra-molecular heterosynthons us","dates":{"release":"2010-01-01T00:00:00Z","publication":"2010 Apr","modification":"2025-04-04T14:42:45.156Z","creation":"2019-03-27T00:00:23Z"},"accession":"S-EPMC2979250","cross_references":{"pubmed":["21579169"],"doi":["10.1107/S1600536810013565"]}}