<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mai J</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>e202212463</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10107259</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(3)</volume><pubmed_abstract>Complex [(&lt;sup>DIPeP&lt;/sup> BDI)Ca]&lt;sub>2&lt;/sub> (C&lt;sub>6&lt;/sub> H&lt;sub>6&lt;/sub> ), with a C&lt;sub>6&lt;/sub> H&lt;sub>6&lt;/sub> &lt;sup>2-&lt;/sup> dianion bridging two Ca&lt;sup>2+&lt;/sup> ions, reacts with benzene to yield [(&lt;sup>DIPeP&lt;/sup> BDI)Ca]&lt;sub>2&lt;/sub> (biphenyl) with a bridging biphenyl&lt;sup>2-&lt;/sup> dianion (&lt;sup>DIPeP&lt;/sup> BDI=HC[C(Me)N-DIPeP]&lt;sub>2&lt;/sub> ; DIPeP=2,6-CH(Et)&lt;sub>2&lt;/sub> -phenyl). The biphenyl complex was also prepared by reacting [(&lt;sup>DIPeP&lt;/sup> BDI)Ca]&lt;sub>2&lt;/sub> (C&lt;sub>6&lt;/sub> H&lt;sub>6&lt;/sub> ) with biphenyl or by reduction of [(&lt;sup>DIPeP&lt;/sup> BDI)CaI]&lt;sub>2&lt;/sub> with KC&lt;sub>8&lt;/sub> in presence of biphenyl. Benzene-benzene coupling was also observed when the deep purple product of ball-milling [(&lt;sup>DIPP&lt;/sup> BDI)CaI(THF)]&lt;sub>2&lt;/sub> with K/KI was extracted with benzene (DIP</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>Alkaline-Earth Metal Mediated Benzene-to-Biphenyl Coupling.</pubmed_title><pmcid>PMC10107259</pmcid><funding_grant_id>HA 3218/11-1</funding_grant_id><pubmed_authors>Langer J</pubmed_authors><pubmed_authors>Rosch B</pubmed_authors><pubmed_authors>Harder S</pubmed_authors><pubmed_authors>Morasch M</pubmed_authors><pubmed_authors>Mai J</pubmed_authors><pubmed_authors>Jedrzkiewicz D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Alkaline-Earth Metal Mediated Benzene-to-Biphenyl Coupling.</name><description>Complex [(&lt;sup>DIPeP&lt;/sup> BDI)Ca]&lt;sub>2&lt;/sub> (C&lt;sub>6&lt;/sub> H&lt;sub>6&lt;/sub> ), with a C&lt;sub>6&lt;/sub> H&lt;sub>6&lt;/sub> &lt;sup>2-&lt;/sup> dianion bridging two Ca&lt;sup>2+&lt;/sup> ions, reacts with benzene to yield [(&lt;sup>DIPeP&lt;/sup> BDI)Ca]&lt;sub>2&lt;/sub> (biphenyl) with a bridging biphenyl&lt;sup>2-&lt;/sup> dianion (&lt;sup>DIPeP&lt;/sup> BDI=HC[C(Me)N-DIPeP]&lt;sub>2&lt;/sub> ; DIPeP=2,6-CH(Et)&lt;sub>2&lt;/sub> -phenyl). The biphenyl complex was also prepared by reacting [(&lt;sup>DIPeP&lt;/sup> BDI)Ca]&lt;sub>2&lt;/sub> (C&lt;sub>6&lt;/sub> H&lt;sub>6&lt;/sub> ) with biphenyl or by reduction of [(&lt;sup>DIPeP&lt;/sup> BDI)CaI]&lt;sub>2&lt;/sub> with KC&lt;sub>8&lt;/sub> in presence of biphenyl. Benzene-benzene coupling was also observed when the deep purple product of ball-milling [(&lt;sup>DIPP&lt;/sup> BDI)CaI(THF)]&lt;sub>2&lt;/sub> with K/KI was extracted with benzene (DIP</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-18T14:25:47.05Z</modification><creation>2025-04-07T00:35:03.079Z</creation></dates><accession>S-EPMC10107259</accession><cross_references><pubmed>36426597</pubmed><doi>10.1002/anie.202212463</doi></cross_references></HashMap>