<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>66(Pt 2)</volume><submitter>Journot G</submitter><pubmed_abstract>The title compound, C(11)H(14)N(2), crystallized with two independent mol-ecules (A and B) in the asymmetric unit. The two mol-ecules differ only slightly, with the pyrrole rings being inclined to one another at a dihedral angle of 87.67 (8)° in mol-ecule A and 88.09 (7)° in mol-ecule B. In the crystal, there are no classical hydrogen bonds, but the two pyrrole NH groups of one mol-ecule are involved in N-H⋯π inter-actions with the pyrrole rings of the other mol-ecule. In this manner, a compact box-like arrangement of the two independent mol-ecules is formed.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o392</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2979882</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>2,2'-(Propane-2,2-di-yl)bis-(1H-pyrrole).</pubmed_title><pmcid>PMC2979882</pmcid><pubmed_authors>Journot G</pubmed_authors><pubmed_authors>Neier R</pubmed_authors><pubmed_authors>Stoeckli-Evans H</pubmed_authors></additional><is_claimable>false</is_claimable><name>2,2'-(Propane-2,2-di-yl)bis-(1H-pyrrole).</name><description>The title compound, C(11)H(14)N(2), crystallized with two independent mol-ecules (A and B) in the asymmetric unit. The two mol-ecules differ only slightly, with the pyrrole rings being inclined to one another at a dihedral angle of 87.67 (8)° in mol-ecule A and 88.09 (7)° in mol-ecule B. In the crystal, there are no classical hydrogen bonds, but the two pyrrole NH groups of one mol-ecule are involved in N-H⋯π inter-actions with the pyrrole rings of the other mol-ecule. In this manner, a compact box-like arrangement of the two independent mol-ecules is formed.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jan</publication><modification>2025-04-26T05:06:50.058Z</modification><creation>2019-03-27T00:00:56Z</creation></dates><accession>S-EPMC2979882</accession><cross_references><pubmed>21579813</pubmed><doi>10.1107/S1600536809054701</doi></cross_references></HashMap>