Abstract:This chapter attempts to briefly summarise the research carried out on the design, synthesis and practical, mostly catalytic, applications of phosphinoferrocene donors. Presented are selected basic concepts that illustrate milestones and major routes in the development of ferrocene‐based phosphines since the discovery of ferrocene, as well as recent trends demonstrating the vast applications of these compounds as ligands in coordination chemistry and, mainly, in numerous conventional and asymmetric transition‐… Show more
“…The elaborate synthetic methodology and facile preparation of stable chiral derivatives make ferrocene particularly attractive as a scaffold for ligand design, which is indeed reflected in the vast number of ferrocene-based ligands, mostly phosphines, and their numerous applications in coordination chemistry, transition-metal catalysis and organocatalysis. 1,61…”
Section: Applications Of Ferrocene and Ferrocene Derivativesmentioning
The discovery of ferrocene, [Fe(η5-C5H5)2], seventy years ago has significantly influenced chemical research and provided a key impetus for establishing and rapidly expanding organometallic chemistry, which has continued at a...
“…The elaborate synthetic methodology and facile preparation of stable chiral derivatives make ferrocene particularly attractive as a scaffold for ligand design, which is indeed reflected in the vast number of ferrocene-based ligands, mostly phosphines, and their numerous applications in coordination chemistry, transition-metal catalysis and organocatalysis. 1,61…”
Section: Applications Of Ferrocene and Ferrocene Derivativesmentioning
The discovery of ferrocene, [Fe(η5-C5H5)2], seventy years ago has significantly influenced chemical research and provided a key impetus for establishing and rapidly expanding organometallic chemistry, which has continued at a...
Stimuli‐responsive ancillary ligands are valuable tools to control the activity and selectivity of transition‐metal catalysts. The synthesis and characterization of a series of metal complexes containing phosphines with proton‐responsive imidazolin‐2‐ylidenamino substituents are reported. Determination of the ligand‐donor properties revealed that protonation of each substituent increases the Tolman electronic parameter (TEP) of the phosphine by 22 cm−1, hence allowing for switching of the electron‐donor power of phosphine 2 within an unprecedented range (ΔTEP=43.4 cm−1).
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