Matches in SemOpenAlex for { <https://semopenalex.org/work/W2329092746> ?p ?o ?g. }
- W2329092746 endingPage "7052" @default.
- W2329092746 startingPage "7043" @default.
- W2329092746 abstract "Highly efficient alkene hydrogenations were developed using NO-functionalized hydrido dinitrosyl rhenium catalysts of the type [ReH(PR3)2(NO)(NO(LA))][Z] (2, LA = B(C6F5)3; 3, LA = [Et]+, Z = [B(C6F5)4]−; 4, LA = [SiEt3]+, Z = [HB(C6F5)3]−; R = iPr a, Cy b). Lewis acid attachment to the NO ligand was found to facilitate bending at the NOLA atom and concomitantly to open up a vacant site at the rhenium center. According to DFT calculations, the ability to bend follows the order 4 > 3 > 2, which did not match with the order of increasing hydrogenation activities: 3 > 4 > 2. The main factor spoiling catalytic performance was catalyst deactivation by detachment of the LA group occurring during the catalytic reaction course, which was found to go along with the decrease in order of DFT-calculated strengths of the ONO–LA bonds. LA detachment from the ONO atom could at least partly be prevented by LA addition as cocatalysts, which led to an extraordinary boost of the hydrogenation activities. For instance the “1/hydrosilane/B(C6F5)3” (1:5:5) system exhibited the highest performance, with TOFs up to 1.2 × 105 h–1 (1-hexene, 1-octene, cyclooctene, cyclohexene). The cocatalyst [Et3O][B(C6F5)4] showed the smallest effect, presumably due to the strong Lewis acidic character of the reagent causing side-reactions before reacting with 1a,b. The catalytic reaction course crucially involves not only reversible bending at the NOLA atom but also loss of a PR3 ligand, forming 16e or 14e monohydride reactive intermediates, which drive an Osborn-type hydrogenation cycle with olefin before H2 addition." @default.
- W2329092746 created "2016-06-24" @default.
- W2329092746 creator A5001794559 @default.
- W2329092746 creator A5001975504 @default.
- W2329092746 creator A5011276051 @default.
- W2329092746 creator A5041097915 @default.
- W2329092746 creator A5048074828 @default.
- W2329092746 creator A5062932399 @default.
- W2329092746 date "2013-11-04" @default.
- W2329092746 modified "2023-09-25" @default.
- W2329092746 title "Efficient Lewis Acid Promoted Alkene Hydrogenations Using Dinitrosyl Rhenium(−I) Hydride Catalysts" @default.
- W2329092746 cites W1554073732 @default.
- W2329092746 cites W1971030478 @default.
- W2329092746 cites W1974439305 @default.
- W2329092746 cites W1976651404 @default.
- W2329092746 cites W1979640190 @default.
- W2329092746 cites W1982912042 @default.
- W2329092746 cites W1984614201 @default.
- W2329092746 cites W1987120254 @default.
- W2329092746 cites W1987753766 @default.
- W2329092746 cites W1987898154 @default.
- W2329092746 cites W1988636692 @default.
- W2329092746 cites W1988841674 @default.
- W2329092746 cites W1992677164 @default.
- W2329092746 cites W1994412962 @default.
- W2329092746 cites W1999381364 @default.
- W2329092746 cites W2001248785 @default.
- W2329092746 cites W2010797442 @default.
- W2329092746 cites W2013160605 @default.
- W2329092746 cites W2015784886 @default.
- W2329092746 cites W2017678943 @default.
- W2329092746 cites W2022435979 @default.
- W2329092746 cites W2023271753 @default.
- W2329092746 cites W2023971266 @default.
- W2329092746 cites W2027056314 @default.
- W2329092746 cites W2028257896 @default.
- W2329092746 cites W2029734167 @default.
- W2329092746 cites W2030054392 @default.
- W2329092746 cites W2030794481 @default.
- W2329092746 cites W2031158103 @default.
- W2329092746 cites W2033288172 @default.
- W2329092746 cites W2035252589 @default.
- W2329092746 cites W2044520616 @default.
- W2329092746 cites W2045396842 @default.
- W2329092746 cites W2045411127 @default.
- W2329092746 cites W2045546544 @default.
- W2329092746 cites W2048997372 @default.
- W2329092746 cites W2053470083 @default.
- W2329092746 cites W2057390396 @default.
- W2329092746 cites W2058363175 @default.
- W2329092746 cites W2059557791 @default.
- W2329092746 cites W2060572918 @default.
- W2329092746 cites W2061186232 @default.
- W2329092746 cites W2067181001 @default.
- W2329092746 cites W2071459784 @default.
- W2329092746 cites W2072590939 @default.
- W2329092746 cites W2074725436 @default.
- W2329092746 cites W2078583965 @default.
- W2329092746 cites W2081496003 @default.
- W2329092746 cites W2081890623 @default.
- W2329092746 cites W2082339081 @default.
- W2329092746 cites W2087300119 @default.
- W2329092746 cites W2090130090 @default.
- W2329092746 cites W2091697703 @default.
- W2329092746 cites W2092816490 @default.
- W2329092746 cites W2093789466 @default.
- W2329092746 cites W2101826827 @default.
- W2329092746 cites W2105189720 @default.
- W2329092746 cites W2105249240 @default.
- W2329092746 cites W2107055594 @default.
- W2329092746 cites W2121815753 @default.
- W2329092746 cites W2124845977 @default.
- W2329092746 cites W2125454909 @default.
- W2329092746 cites W2131350133 @default.
- W2329092746 cites W2143981217 @default.
- W2329092746 cites W2146743772 @default.
- W2329092746 cites W2152471164 @default.
- W2329092746 cites W2159458318 @default.
- W2329092746 cites W2163508329 @default.
- W2329092746 cites W2313757320 @default.
- W2329092746 cites W2314191910 @default.
- W2329092746 cites W2315752527 @default.
- W2329092746 cites W2317639033 @default.
- W2329092746 cites W2317908686 @default.
- W2329092746 cites W2318592849 @default.
- W2329092746 cites W2324969175 @default.
- W2329092746 cites W2335775041 @default.
- W2329092746 cites W2493803916 @default.
- W2329092746 cites W2951913084 @default.
- W2329092746 cites W2952008384 @default.
- W2329092746 cites W2953038145 @default.
- W2329092746 cites W3004773220 @default.
- W2329092746 cites W3005517822 @default.
- W2329092746 cites W4230458395 @default.
- W2329092746 cites W4239548194 @default.
- W2329092746 cites W4242347576 @default.
- W2329092746 cites W4247679722 @default.
- W2329092746 doi "https://doi.org/10.1021/om400733u" @default.