<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(22)</volume><submitter>Kundu G</submitter><pubmed_abstract>Despite recent advancements in the chemistry of multiply bound boron compounds, the laboratory isolation of the parent oxoborane moiety, HBO has long remained an unsolved and well-recognized challenge. The reaction of 6-SIDipp·BH&lt;sub>3&lt;/sub> [6-SIDipp = 1,3-di(2,6-diisopropylphenyl)tetrahydropyrimidine-2-ylidene] with GaCl&lt;sub>3&lt;/sub> afforded an unusual boron-gallium 3c-2e compound (1). The addition of water to 1 resulted in the release of H&lt;sub>2&lt;/sub> and the formation of a rare acid stabilized neutral parent oxoborane, LB(H)[double bond, length as m-dash]O (2). Crystallographic and density functional theory (DFT) analyses support the presence of a terminal B[double bond, length as m-dash]O double bond. Subsequent addition of another equivalent of water molecule led to hydrolysis of the</pubmed_abstract><journal>Chemical science</journal><pagination>5894-5898</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10246693</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Taming the parent oxoborane.</pubmed_title><pmcid>PMC10246693</pmcid><pubmed_authors>Sen SS</pubmed_authors><pubmed_authors>Amrutha PR</pubmed_authors><pubmed_authors>Raj KV</pubmed_authors><pubmed_authors>Vanka K</pubmed_authors><pubmed_authors>Kundu G</pubmed_authors><pubmed_authors>Tothadi S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Taming the parent oxoborane.</name><description>Despite recent advancements in the chemistry of multiply bound boron compounds, the laboratory isolation of the parent oxoborane moiety, HBO has long remained an unsolved and well-recognized challenge. The reaction of 6-SIDipp·BH&lt;sub>3&lt;/sub> [6-SIDipp = 1,3-di(2,6-diisopropylphenyl)tetrahydropyrimidine-2-ylidene] with GaCl&lt;sub>3&lt;/sub> afforded an unusual boron-gallium 3c-2e compound (1). The addition of water to 1 resulted in the release of H&lt;sub>2&lt;/sub> and the formation of a rare acid stabilized neutral parent oxoborane, LB(H)[double bond, length as m-dash]O (2). Crystallographic and density functional theory (DFT) analyses support the presence of a terminal B[double bond, length as m-dash]O double bond. Subsequent addition of another equivalent of water molecule led to hydrolysis of the</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jun</publication><modification>2025-04-27T02:22:42.14Z</modification><creation>2025-04-06T18:31:06.867Z</creation></dates><accession>S-EPMC10246693</accession><cross_references><pubmed>37293651</pubmed><doi>10.1039/d3sc01544k</doi></cross_references></HashMap>