Phosphines :PR 3 - very important ligands -  -donors -  -acceptors  For years, it was assumed that  -backdonation occurred from the metal into empty.

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Presentation transcript:

Phosphines :PR 3 - very important ligands -  -donors -  -acceptors  For years, it was assumed that  -backdonation occurred from the metal into empty d ‑ orbitals on phosphorus.  Actually:  -backdonation occurs into MOs formed by combination of two d ‑ orbitals on phosphorus and the  * orbitals involved in P-R bonding.  Each acceptor MO has 2 lobes (similar to a d-orbital) but is antibonding with respect to the P-R bond  As the amount of  -backdonation increases, the length of P-R increases. This can be observed in the crystal structures of phosphine complexes Average Co-P pm pm Average P-C pm pm  A huge variety of phosphines have been prepared, many of which are commercially available. One can just choose a phosphine with the desired steric (size) and electronic properties (  ‑ donation/  ‑ acceptance).

 The size of ligands (not just phosphines) can be measured using the concept of a cone angle (Chadwick A. Tolman, Chem. Rev., 1977, 313). -TM-P distance fixed at 228 pm to standardize the cone angle (  ). -The cone encompases the van der Waals radii of the outermost atoms of the ligand. Cone angles measured by crystallography (although TM-P bond distance fixed at 228 pm)  Electronic properties measured by IR and electrochemistry – (CO) and E 1/2 for oxidation or reduction measured for a large series of carbonyl phosphine complexes with different PR 3 (e.g. [Ni(CO) 3 (PR 3 )] or [CpFeMe(CO)(PR 3 )]) [  = old fashioned abbreviation for phenyl] x-axis = cone angle (  ) y-axis = (CO) for [Ni(CO) 3 L]

Typical Ligands – 2 (Phosphines) - Bite angles for bidentate ligands Bite angle can have a profound effect on the rate and selectivity of metal catalyzed reactions Reviews: (1) P. C. J. Kamer, P. W. N. M. van Leeuwen, Wide Bite Angle Diphosphines: Xantphos Ligands in Transition Metal Complexes and Catalysis, Acc. Chem. Res., 2001, ; (2) Z. Freixa, P. W. N. M. van Leeuwen, Bite angle effects in diphosphine metal catalysis: steric or electronic?, Dalton Trans., 2003, ; (3) P. W. N. M. van Leeuwen, Ligand Bite Angle Effects in Metal-catalyzed C-C bond formation, Chem. Rev., 2000,

Phosphines/Arsines in early TM and lanthanide chemistry PR 3 excellent ligands for soft late transition metals PR 3 typically NOT v. suitable to form complexes with hard early TMs (PR 3 > PAr 3 ) AsR 3 even worse, and early TM SbR 3 or BiR 3 complexes unknown NPh 3 useless as a ligand for early or late TMs (terrible donor), NMe 3 OK for early TMs R. G. Cavell (U of A), OM, 1991, 539 Route to early/late heterobimetallics M. D. Fryzuk (UBC), OM, 2005, xs TMS-Cl Hard/Soft donor combination G. Reid (U Southampton), DT, 2004, 3005 & EJIC, 2001, 2927 Rare early TM (Ti, Zr, Hf) arsine complexes