<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ashfaq M</submitter><funding>King Khalid University</funding><pagination>22357-22366</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8412916</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(34)</volume><pubmed_abstract>A novel Schiff base compound named as phenylmethanaminium (&lt;i>E&lt;/i>)-4-((benzylimino)methyl)benzoate C&lt;sub>7&lt;/sub>H&lt;sub>10&lt;/sub>N&lt;sup>+&lt;/sup>. C&lt;sub>15&lt;/sub>H&lt;sub>12&lt;/sub>NO&lt;sub>2&lt;/sub> &lt;sup>-&lt;/sup> (&lt;b>A&lt;/b>) is synthesized by the chemical reaction of benzylamine and 4-carboxybenzaldehyde in ethanol, and the structure of the titled compound is verified using the single-crystal X-ray diffraction technique. Structural investigation inferred that the crystal packing is mainly stabilized by N-H···O and comparatively weak C-H···O bonding between the cation and anion and further stabilized by weak C-H···π and C-O···π interactions. Hirshfeld surface analysis is employed to explore the noncovalent interactions that are responsible for crystal packing quantitatively. Furthermore, we have used stat</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Synthesis, Crystal Structure, Hirshfeld Surface Analysis, and Computational Study of a Novel Organic Salt Obtained from Benzylamine and an Acidic Component.</pubmed_title><pmcid>PMC8412916</pmcid><funding_grant_id>R.G.P.2/128/42</funding_grant_id><pubmed_authors>Arshad MU</pubmed_authors><pubmed_authors>Ashfaq M</pubmed_authors><pubmed_authors>Yaman M</pubmed_authors><pubmed_authors>Alarfaji SS</pubmed_authors><pubmed_authors>Kargar H</pubmed_authors><pubmed_authors>Dege N</pubmed_authors><pubmed_authors>Muhammad S</pubmed_authors><pubmed_authors>Munawar KS</pubmed_authors><pubmed_authors>Tahir MN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, Crystal Structure, Hirshfeld Surface Analysis, and Computational Study of a Novel Organic Salt Obtained from Benzylamine and an Acidic Component.</name><description>A novel Schiff base compound named as phenylmethanaminium (&lt;i>E&lt;/i>)-4-((benzylimino)methyl)benzoate C&lt;sub>7&lt;/sub>H&lt;sub>10&lt;/sub>N&lt;sup>+&lt;/sup>. C&lt;sub>15&lt;/sub>H&lt;sub>12&lt;/sub>NO&lt;sub>2&lt;/sub> &lt;sup>-&lt;/sup> (&lt;b>A&lt;/b>) is synthesized by the chemical reaction of benzylamine and 4-carboxybenzaldehyde in ethanol, and the structure of the titled compound is verified using the single-crystal X-ray diffraction technique. Structural investigation inferred that the crystal packing is mainly stabilized by N-H···O and comparatively weak C-H···O bonding between the cation and anion and further stabilized by weak C-H···π and C-O···π interactions. Hirshfeld surface analysis is employed to explore the noncovalent interactions that are responsible for crystal packing quantitatively. Furthermore, we have used stat</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2026-05-09T11:35:31.682Z</modification><creation>2022-02-11T10:46:53.887Z</creation></dates><accession>S-EPMC8412916</accession><cross_references><pubmed>34497924</pubmed><doi>10.1021/acsomega.1c03078</doi></cross_references></HashMap>