135907 20260217205524.0 doi 10.1021/acscatal.4c00264 sideral 138905 ART-2024-138905 eng Heras, Laura A. de las (orcid)0000-0001-9491-7167 Homo- and Cross-Coupling of Phenylacetylenes and a-Hydroxyacetylenes Catalyzed by a Square-Planar Rhodium Monohydride 2024 Access copy available to the general public Unrestricted The C–C triple bond of phenylacetylene undergoes the anti-Markovnikov addition of the Rh–H bond of RhH{κ3-P,O,P-[xant(PiPr2)2]} (1; xant(PiPr2)2 = 9,9-dimethyl-4,5-bis(diisopropylphosphino)xanthene) to give Rh{(E)–CH═CHPh}{κ3-P,O,P-[xant(PiPr2)2]} (2), which reacts with a second alkyne molecule to produce Rh(C≡CPh){κ3-P,O,P-[xant(PiPr2)2]} (3) and styrene before the transformation from 1 to 2 is complete. The metal center of 3 undergoes the oxidative addition of the C(sp)–H bond of another alkyne molecule to produce RhH(C≡CPh)2{κ3-P,O,P-[xant(PiPr2)2]} (4), which also reacts with more phenylacetylene before completing the transformation from 3 to 4. The reaction leads to Rh{(E)–CH═CHPh}(C≡CPh)2{κ3-P,O,P-[xant(PiPr2)2]} (5), which reductively eliminates (E)-1,4-diphenyl-1-buten-3-yne to regenerate 3. Complexes 3, 4, and 5 constitute a cycle for head-to-head dimerization of phenylacetylene. Consequently, complex 1 promotes the catalytic homocoupling of terminal alkynes to (E)-enynes, including the dimerization of α-hydroxyacetylenes to (E)-enyne-diols. The rate-determining step of the couplings depends on the nature of the alkyne, being the insertion of the C–C triple bond into the Rh–H bond of a bis(acetylide)-rhodium(III)-hydride intermediate for phenylacetylenes and the reductive elimination of the product (E)-enyne-diol for α-hydroxyacetylenes. In support of the latter, complex Rh{(E)–CH═CHC(OH)Ph2}{C≡CC(OH)Ph2}2{κ3-P,O,P-[xant(PiPr2)2]} (6) has been isolated and characterized by X-ray diffraction analysis. Complex 1 also effectively promotes the formation of compounds of the type (E)-5-phenyl-2-penten-4-yn-1-ol, by cross-coupling between phenylacetylenes and α-hydroxyacetylenes. These reactions take place through two cycles similar to the cycle that produces the homocouplings, the rate-determining step being the reductive elimination of (E)-enyn-ol for both. The catalytic performance of 1 provides good efficiency in homocoupling and cross-coupling reactions involving progestin-type compounds such as ethisterone. info:eu-repo/grantAgreement/ES/DGA/E06-23R fo:eu-repo/grantAgreement/ES/DGA-FSE/LMP23-21 info:eu-repo/grantAgreement/ES/MCIN/AEI/10.13039/501100011033 info:eu-repo/grantAgreement/ES/MICINN/PID2020-115286GB-I00/AEI/10.13039/501100011033 info:eu-repo/grantAgreement/ES/MICINN/RED2022-134287-T info:eu-repo/semantics/openAccess by https://creativecommons.org/licenses/by/4.0/deed.es 13.1 2024 CHEMISTRY, PHYSICAL 21 / 185 = 0.114 2024 Q1 T1 3.782 2024 Chemistry (miscellaneous) 2024 Q1 Catalysis 2024 Q1 19.5 2024 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Esteruelas, Miguel A. (orcid)0000-0002-4829-7590 Oliván, Montserrat (orcid)0000-0003-0381-0917 Oñate, Enrique (orcid)0000-0003-2094-719X 14, 11 (2024), 8389-8404 ACS catal. ACS CATALYSIS 2155-5435 3311941 http://zaguan.unizar.es/record/135907/files/texto_completo.pdf Versión publicada 2817401 http://zaguan.unizar.es/record/135907/files/texto_completo.jpg?subformat=icon icon Versión publicada oai:zaguan.unizar.es:135907 articulos driver 2026-02-17-20:29:44 ARTICLE