<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Franz R</submitter><funding>János Bolyai Research Scholarship and Project</funding><funding>German Science Fund</funding><pagination>e2306805</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10953586</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(11)</volume><pubmed_abstract>Coordination of a stereochemically defined P&lt;sub>3&lt;/sub> -chain to a series of transition metal carbonyls [M(CO)&lt;sub>x&lt;/sub> ]&lt;sup>z-&lt;/sup> (M = Mn (x = 5, z = 1), Fe (x = 4, z = 2) or Co (x = 4, z = 1)) is explored using a [3]ferrocenophane scaffold. A gradual transition from η&lt;sup>1&lt;/sup> -, η&lt;sup>2&lt;/sup> - to η&lt;sup>3&lt;/sup> -coordination is observed where in the η&lt;sup>2&lt;/sup> -mode the terminal positions of the phosphorus chain are bridged. With an excess of cobalt carbonyl successive P-P bond activation and gradual separation of the central phosphorus atoms from the phosphorus chain has been observed. This process is reversible and with suitable reagents such as methyl lithium, the P&lt;sub>3&lt;/sub> -unit is regenerated in stereospecific manner. The bonding situation and steps of the gradua</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Gradual Coordination and Reversible P-P Bond Activation of a P&lt;sub>3&lt;/sub> -Unit with Transition Metal Carbonyls.</pubmed_title><pmcid>PMC10953586</pmcid><funding_grant_id>UNKP-22-5-BME-298</funding_grant_id><funding_grant_id>CRC 1319</funding_grant_id><pubmed_authors>Gal D</pubmed_authors><pubmed_authors>Kelemen Z</pubmed_authors><pubmed_authors>Franz R</pubmed_authors><pubmed_authors>Pietschnig R</pubmed_authors><pubmed_authors>Bruhn C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gradual Coordination and Reversible P-P Bond Activation of a P&lt;sub>3&lt;/sub> -Unit with Transition Metal Carbonyls.</name><description>Coordination of a stereochemically defined P&lt;sub>3&lt;/sub> -chain to a series of transition metal carbonyls [M(CO)&lt;sub>x&lt;/sub> ]&lt;sup>z-&lt;/sup> (M = Mn (x = 5, z = 1), Fe (x = 4, z = 2) or Co (x = 4, z = 1)) is explored using a [3]ferrocenophane scaffold. A gradual transition from η&lt;sup>1&lt;/sup> -, η&lt;sup>2&lt;/sup> - to η&lt;sup>3&lt;/sup> -coordination is observed where in the η&lt;sup>2&lt;/sup> -mode the terminal positions of the phosphorus chain are bridged. With an excess of cobalt carbonyl successive P-P bond activation and gradual separation of the central phosphorus atoms from the phosphorus chain has been observed. This process is reversible and with suitable reagents such as methyl lithium, the P&lt;sub>3&lt;/sub> -unit is regenerated in stereospecific manner. The bonding situation and steps of the gradua</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-01T18:55:17.335Z</modification><creation>2024-11-20T19:05:37.016Z</creation></dates><accession>S-EPMC10953586</accession><cross_references><pubmed>38161225</pubmed><doi>10.1002/advs.202306805</doi></cross_references></HashMap>