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Lecture 20 Dinuclear metal complexes with multiple M-M bonds 1) Transition metal-metal bonding: MO diagram. Compared to main group elements, transition metals (TM’s) have more options for bonding with one another.
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Lecture 20 Dinuclear metal complexes with multiple M-M bonds 1) Transition metal-metal bonding: MO diagram • Compared to main group elements, transition metals (TM’s) have more options for bonding with one another. • In addition to one s- and up to two p-bonds common for organic compounds (acetylenes, cumulenes) and some other main group elements two more bonds of d-symmetry are possible for TM’s (five bonds in total). • If the metal dx2-y2 orbitals are involved in s-bonding with ligands, four metal atomic orbitals remain only available to form M-M bonds. • Species with TM-TM bond orders 1-4 are well known. • Multiple M-M bonds are most typical for such metals as V-Ta, Cr-W, Re, Ru, Os, Rh.
2) Evidences for M-M double, triple and quadruple bonding • One of the arguments in favor of multiple bonds is M-M bond length (Å): • Look now at the solid state structures of salts derived from [Re2Me8]2- anion which shows the eclipsed conformation of the methyl groups. • This unfavorable conformation is possible if stabilized by dxy-dxyd-bonding between two rhenium atoms (l(ReRe)=2.18 Å). • The dxy-dxy orbital overlap is impossible in the staggered conformation. • The barrier of rotation about M-M quadruple bond was estimated in a dinuclear MoII porphyrin complex to be of 10 kcal/mol.
3) More ways to form multiple M-M bonds • The M/M bond order is a function of transition metal electron configuration. The Table below is valid for the case when metal dx2-y2 orbital is used for s-bonding with ligands. • Some examples are given on the previous page and on the right. A very week quadruple Cr/Cr bond is believed to exist in Cr2(OAc)4(OH2)2 paddlewheel complex above. • Another way to form M-M’ multiple bonds is through donor-acceptor mechanism. • Ti center is roughly tetrahedral (Rh-Ti-O = 109o; sp3 hybridization) while RhP3 fragment is almost planar (d2s hybridization). Rh atom has two filled dxz and dyz orbitals suitable for formation of two p-bonds with Ti atom. The latter uses the empty dxz and dyz orbitals.