<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Betz R</submitter><funding>NHGRI NIH HHS</funding><pagination>o2587-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3201484</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>67(Pt 10)</volume><pubmed_abstract>The title compound {systematic name: 4-[bis(4-fluorophenyl)methyl]piperazin-1-ium 2,4,6-tri-nitro-phenolate}, C(17)H(19)F(2)N(2) (+)·C(6)H(2)N(3)O(7) (-), is the picrate salt of a piperazine-supported amine bearing a benzhydryl substituent on one of its N atoms. During co-crystallisation, protonation took place on the N atom of the secondary amine functionality. The non-aromatic six-membered heterocycle adopts a chair conformation. In the crystal, N-H⋯O hydrogen bonds as well as C-H⋯O contacts connect the components into a three-dimensional network.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pubmed_title>4-[Bis(4-fluorophenyl)methyl]piperazin-1-ium picrate.</pubmed_title><pmcid>PMC3201484</pmcid><funding_grant_id>R21 HG005090</funding_grant_id><pubmed_authors>Hosten E</pubmed_authors><pubmed_authors>Yathirajan HS</pubmed_authors><pubmed_authors>Dayananda AS</pubmed_authors><pubmed_authors>Gerber T</pubmed_authors><pubmed_authors>Narayana B</pubmed_authors><pubmed_authors>Betz R</pubmed_authors></additional><is_claimable>false</is_claimable><name>4-[Bis(4-fluorophenyl)methyl]piperazin-1-ium picrate.</name><description>The title compound {systematic name: 4-[bis(4-fluorophenyl)methyl]piperazin-1-ium 2,4,6-tri-nitro-phenolate}, C(17)H(19)F(2)N(2) (+)·C(6)H(2)N(3)O(7) (-), is the picrate salt of a piperazine-supported amine bearing a benzhydryl substituent on one of its N atoms. During co-crystallisation, protonation took place on the N atom of the secondary amine functionality. The non-aromatic six-membered heterocycle adopts a chair conformation. In the crystal, N-H⋯O hydrogen bonds as well as C-H⋯O contacts connect the components into a three-dimensional network.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Oct</publication><modification>2025-04-04T08:06:19.311Z</modification><creation>2019-03-27T00:01:08Z</creation></dates><accession>S-EPMC3201484</accession><cross_references><pubmed>22064439</pubmed><doi>10.1107/S160053681103580X</doi></cross_references></HashMap>