2000
DOI: 10.1039/b002403l
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Half-sandwich complexes of molybdenum-(III), -(IV) and -(V) with P–O and P–N bifunctional ligands Ph2PCH2X (X = 2-oxazolinyl, or C(O)NPh2)

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Cited by 13 publications
(12 citation statements)
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“…Complexes 5a-c were stable in solution for several hours and in the solid state for a few days, in the absence of oxygen. Contrary to the situation reported for the Mo complexes mentioned in the introduction, 20,22,23 there was no observed tendency for chelation for 1 in complexes 5a-c.…”
Section: Formation Of P-monoadductscontrasting
confidence: 97%
“…Complexes 5a-c were stable in solution for several hours and in the solid state for a few days, in the absence of oxygen. Contrary to the situation reported for the Mo complexes mentioned in the introduction, 20,22,23 there was no observed tendency for chelation for 1 in complexes 5a-c.…”
Section: Formation Of P-monoadductscontrasting
confidence: 97%
“…The oxidation process, on the other hand, is completely irreversible up to 5 V s -1 for all derivatives. In this respect, these compounds behave similarly to the previously described diene complexes, CpMoCl 2 (η 4 -diene), [26][27][28]30 while derivatives with more electron donating ligands (phosphines, phosphine-thioethers, phosphine-oxazolines, and phosphineamides) 35,39,40 show a reversible oxidation process at much lower potentials and no reduction process or, at the most, an irreversible reduction before the solvent discharge. A closer comparison of the reduction potentials between the isoelectronic complexes with the 4-electron donors alkyne (σ + π) and diene (2σ) ligands in Table 3 indicates that the alkynes transfer about the same amount of electron density to the metal center.…”
Section: Resultssupporting
confidence: 71%
“…28, and the corresponding antibonding component in orbital no. 40. The alkyne-to-M σ donation is in a deeper energy orbital, while the orbitals no.…”
Section: Resultsmentioning
confidence: 97%
See 1 more Smart Citation
“…Phosphine 1 has proven to be an efficient and versatile bidentate ligand. As seen in this and previous works, it can readily form stable monochelated nickel(II), 4 palladium(II), 9 platinum(II) 6 and molybdenum(III) 25 complexes, bischelated octahedral ruthenium(II) 8 or nickel(II) complexes, such as 3 and 4, and much more rarely, act as a bridging ligand. To the best of our knowledge, this situation has only been encountered in a Fe-Co, 13 Fe-Cu 14 and Co-Co 11 complex and in [{PdCl(1)} + (m-1)(CoCl 3 ) -] (2) which contains in addition a P,N-chelating ligand 1.…”
Section: Discussionsupporting
confidence: 71%