Matches in SemOpenAlex for { <https://semopenalex.org/work/W2078647562> ?p ?o ?g. }
- W2078647562 endingPage "2789" @default.
- W2078647562 startingPage "2775" @default.
- W2078647562 abstract "Arylpalladium aryloxide complexes containing sterically and electronically varied phosphine ligands were prepared, and the rates for reductive elimination of diaryl ethers from these complexes were studied to determine the ligand properties that most strongly accelerate this unusual reaction. Electronic and steric effects were probed by preparing monomeric palladium complexes of the type (L)Pd(Ar)(OAr‘), in which L = DPPF (1,1‘-bis-diphenylphosphinoferrocene), CF3-DPPF (1,1‘-bis[di(4-(trifluoromethyl)phenyl)phosphino]ferrocene), and D-t-BPF (1,1‘-bis(di-tert-butylphosphino)ferrocene) and Ar = electron-deficient and electron-neutral aryl groups. Direct C−O bond-forming reductive elimination to form diaryl ethers in high yield was observed after warming the complexes that contained an electron-deficient aryl group bound to palladium. The rate constant for C−O bond-forming reductive elimination from the CF3-DPPF-ligated palladium complex was twice that obtained for the analogous DPPF-ligated complex. Reductive elimination of diaryl ether from the more bulky D-t-BPF complex occurred roughly 100 times faster than from the DPPF complex. Thermolysis of DPPF and CF3-DPPF complexes containing an electron-neutral aryl group did not form diaryl ether. Thermolysis of (D-t-BPF)Pd(Ph)(OC6H4-4-OMe) also did not form diaryl ether and generated the two monophosphines PhP(t-Bu)2 and FcP(t-Bu)2 (di-tert-butylphosphinoferrocene). However, heating of a FcP(t-Bu)2-ligated aryloxide complex containing an electron-neutral, palladium-bound aryl group generated diaryl ether in 10−25% yield. Moreover, heating of this complex in the presence of an excess of P(t-Bu)3 or Ph5FcP(t-Bu)2 or 1 equiv of 2-di-tert-butylphosphino-1,1‘-binaphthyl generated diaryl ether in higher, 58−95%, yields. The effect of ligand concentrations on reaction yields implied that exchange of the bulkier ligands with FcP(t-Bu)2 induced the reductive elimination of diaryl ether." @default.
- W2078647562 created "2016-06-24" @default.
- W2078647562 creator A5024802794 @default.
- W2078647562 creator A5063148731 @default.
- W2078647562 creator A5072074183 @default.
- W2078647562 creator A5088865204 @default.
- W2078647562 date "2003-05-29" @default.
- W2078647562 modified "2023-10-16" @default.
- W2078647562 title "Electronic and Steric Effects on the Reductive Elimination of Diaryl Ethers from Palladium(II)" @default.
- W2078647562 cites W1969224698 @default.
- W2078647562 cites W1970213934 @default.
- W2078647562 cites W1973723982 @default.
- W2078647562 cites W1977837380 @default.
- W2078647562 cites W1988576102 @default.
- W2078647562 cites W1993456302 @default.
- W2078647562 cites W1998122690 @default.
- W2078647562 cites W1998722626 @default.
- W2078647562 cites W1999725493 @default.
- W2078647562 cites W2001109176 @default.
- W2078647562 cites W2001599272 @default.
- W2078647562 cites W2006147901 @default.
- W2078647562 cites W2008463722 @default.
- W2078647562 cites W2012446399 @default.
- W2078647562 cites W2016086894 @default.
- W2078647562 cites W2017806859 @default.
- W2078647562 cites W2020516502 @default.
- W2078647562 cites W2023100599 @default.
- W2078647562 cites W2027456242 @default.
- W2078647562 cites W2029405156 @default.
- W2078647562 cites W2030628791 @default.
- W2078647562 cites W2032956361 @default.
- W2078647562 cites W2035547337 @default.
- W2078647562 cites W2036452553 @default.
- W2078647562 cites W2039404986 @default.
- W2078647562 cites W2042653815 @default.
- W2078647562 cites W2049619194 @default.
- W2078647562 cites W2058539240 @default.
- W2078647562 cites W2060469597 @default.
- W2078647562 cites W2061879106 @default.
- W2078647562 cites W2062650417 @default.
- W2078647562 cites W2067974165 @default.
- W2078647562 cites W2068755552 @default.
- W2078647562 cites W2080925478 @default.
- W2078647562 cites W2081623733 @default.
- W2078647562 cites W2083072239 @default.
- W2078647562 cites W2085639524 @default.
- W2078647562 cites W2088346506 @default.
- W2078647562 cites W2091702998 @default.
- W2078647562 cites W2092623245 @default.
- W2078647562 cites W2093317023 @default.
- W2078647562 cites W2095375312 @default.
- W2078647562 cites W2115135211 @default.
- W2078647562 cites W2122751252 @default.
- W2078647562 cites W2123644937 @default.
- W2078647562 cites W2160889905 @default.
- W2078647562 cites W2409340896 @default.
- W2078647562 cites W2950185929 @default.
- W2078647562 cites W2951043764 @default.
- W2078647562 cites W2952551975 @default.
- W2078647562 cites W2952769981 @default.
- W2078647562 cites W2953222240 @default.
- W2078647562 doi "https://doi.org/10.1021/om030230x" @default.
- W2078647562 hasPublicationYear "2003" @default.
- W2078647562 type Work @default.
- W2078647562 sameAs 2078647562 @default.
- W2078647562 citedByCount "179" @default.
- W2078647562 countsByYear W20786475622012 @default.
- W2078647562 countsByYear W20786475622013 @default.
- W2078647562 countsByYear W20786475622014 @default.
- W2078647562 countsByYear W20786475622015 @default.
- W2078647562 countsByYear W20786475622016 @default.
- W2078647562 countsByYear W20786475622017 @default.
- W2078647562 countsByYear W20786475622018 @default.
- W2078647562 countsByYear W20786475622019 @default.
- W2078647562 countsByYear W20786475622020 @default.
- W2078647562 countsByYear W20786475622021 @default.
- W2078647562 countsByYear W20786475622022 @default.
- W2078647562 countsByYear W20786475622023 @default.
- W2078647562 crossrefType "journal-article" @default.
- W2078647562 hasAuthorship W2078647562A5024802794 @default.
- W2078647562 hasAuthorship W2078647562A5063148731 @default.
- W2078647562 hasAuthorship W2078647562A5072074183 @default.
- W2078647562 hasAuthorship W2078647562A5088865204 @default.
- W2078647562 hasConcept C116569031 @default.
- W2078647562 hasConcept C147789679 @default.
- W2078647562 hasConcept C155647269 @default.
- W2078647562 hasConcept C160434732 @default.
- W2078647562 hasConcept C161790260 @default.
- W2078647562 hasConcept C170493617 @default.
- W2078647562 hasConcept C17525397 @default.
- W2078647562 hasConcept C178790620 @default.
- W2078647562 hasConcept C185592680 @default.
- W2078647562 hasConcept C201194858 @default.
- W2078647562 hasConcept C2776442012 @default.
- W2078647562 hasConcept C2777237805 @default.
- W2078647562 hasConcept C2777716191 @default.
- W2078647562 hasConcept C2778815869 @default.
- W2078647562 hasConcept C2780263894 @default.