<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Alvarez MA</submitter><funding>Ministerio de Ciencia, Innovaci?n y Universidades</funding><funding>Gobierno del Principado de Asturias</funding><funding>Universidad de Oviedo</funding><funding>Agencia Estatal de Investigaci?n</funding><funding>European Regional Development Fund</funding><pagination>18486-18495</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9682477</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(46)</volume><pubmed_abstract>Reactions of the heterometallic MoRe complex [MoReCp(μ-PR*)(CO)&lt;sub>6&lt;/sub>] and its MoMn analogue with some small molecules having N-N multiple bonds, such as diazoalkanes and organic azides, were investigated (R* = 2,4,6-C&lt;sub>6&lt;/sub>H&lt;sub>2&lt;/sub>&lt;sup>&lt;i>t&lt;/i>&lt;/sup>Bu&lt;sub>3&lt;/sub>). Reactions with excess ethyl diazoacetate proceeded slowly and with concomitant denitrogenation to give complexes [MoMCp(μ-η&lt;sup>2&lt;/sup>&lt;sub>P,C&lt;/sub>:κ&lt;sup>2&lt;/sup>&lt;sub>P,O&lt;/sub>-PR*CHCO&lt;sub>2&lt;/sub>Et)(CO)&lt;sub>5&lt;/sub>], which display a bridging phosphaalkene ligand in a novel μ-η&lt;sup>2&lt;/sup>:κ&lt;sup>2&lt;/sup> coordination mode, while reactions with other diazoalkanes resulted only in the decomposition of the organic reagent. The MoRe complex reacted with benzyl- or &lt;i>p&lt;/i>-tolyl azide at room temperature to give t</pubmed_abstract><journal>Inorganic chemistry</journal><pubmed_title>P-C, P-N, and M-N Bond Formation Processes in Reactions of Heterometallic Phosphinidene-Bridged MoMn and MoRe Complexes with Diazoalkanes and Organic Azides to Build Three- to Five-Membered Phosphametallacycles.</pubmed_title><pmcid>PMC9682477</pmcid><funding_grant_id>PGC2018-097366-B-I00</funding_grant_id><pubmed_authors>Garcia ME</pubmed_authors><pubmed_authors>Ruiz MA</pubmed_authors><pubmed_authors>Cuervo PM</pubmed_authors><pubmed_authors>Alvarez MA</pubmed_authors><pubmed_authors>Vega P</pubmed_authors></additional><is_claimable>false</is_claimable><name>P-C, P-N, and M-N Bond Formation Processes in Reactions of Heterometallic Phosphinidene-Bridged MoMn and MoRe Complexes with Diazoalkanes and Organic Azides to Build Three- to Five-Membered Phosphametallacycles.</name><description>Reactions of the heterometallic MoRe complex [MoReCp(μ-PR*)(CO)&lt;sub>6&lt;/sub>] and its MoMn analogue with some small molecules having N-N multiple bonds, such as diazoalkanes and organic azides, were investigated (R* = 2,4,6-C&lt;sub>6&lt;/sub>H&lt;sub>2&lt;/sub>&lt;sup>&lt;i>t&lt;/i>&lt;/sup>Bu&lt;sub>3&lt;/sub>). Reactions with excess ethyl diazoacetate proceeded slowly and with concomitant denitrogenation to give complexes [MoMCp(μ-η&lt;sup>2&lt;/sup>&lt;sub>P,C&lt;/sub>:κ&lt;sup>2&lt;/sup>&lt;sub>P,O&lt;/sub>-PR*CHCO&lt;sub>2&lt;/sub>Et)(CO)&lt;sub>5&lt;/sub>], which display a bridging phosphaalkene ligand in a novel μ-η&lt;sup>2&lt;/sup>:κ&lt;sup>2&lt;/sup> coordination mode, while reactions with other diazoalkanes resulted only in the decomposition of the organic reagent. The MoRe complex reacted with benzyl- or &lt;i>p&lt;/i>-tolyl azide at room temperature to give t</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-19T16:09:33.579Z</modification><creation>2025-04-19T16:09:33.579Z</creation></dates><accession>S-EPMC9682477</accession><cross_references><pubmed>36350690</pubmed><doi>10.1021/acs.inorgchem.2c02720</doi></cross_references></HashMap>