Coordination Chemistry II

1. Coordination Chemistry II Bonding, including crystal field theory and ligand field theory

2. Basis for Bonding Theories Models for the bonding in transition metal complexes must be consistent with observed behavior. Specific data used include stability (or formation) constants, magnetic susceptibility, and the electronic (UV/Vis) spectra of the complexes.

3. Bonding Approaches Valence Bond theory provides the hybridization for octahedral complexes. For the first row transition metals, the hybridization can be: d2sp3 (using the 3d, 4s and 4p orbitals), or sp3d2 (using the 4s, 4p and 4d orbitals). The valence bond approach isn’t used because it fails to explain the electronic spectra and magnetic moments of most complexes.

5. Crystal Field Theory In crystal field theory, the electron pairs on the ligands are viewed as point negative charges that interact with the d orbitals on the central metal. The nature of the ligand and the tendency toward covalent bonding is ignored.

6. d Orbitals

7. Crystal Field Theory Ligands, viewed as point charges, at the corners of an octahedron affect the various d orbitals differently.

8. Crystal Field Theory

9. Crystal Field Theory The repulsion between ligand lone pairs and the d orbitals on the metal results in a splitting of the energy of the d orbitals.

10. d Orbital Splitting __ __ dz2 dx2-y2 eg 0.6∆o ∆o __ __ __ __ __ Spherical field 0.4∆o __ __ __ dxydxz dyz t2g Octahedral field

11. d Orbital Splitting In some texts and articles, the gap in the d orbitals is assigned a value of 10Dq. The upper (eg) set goes up by 6Dq, and the lower set (t2g) goes down by 4Dq. The actual size of the gap varies with the metal and the ligands.

12. d Orbital Splitting The colors exhibited by most transition metal complexes arises from the splitting of the d orbitals. As electrons transition from the lower t2g set to the eg set, light in the visible range is absorbed.

13. d Orbital Splitting The splitting due to the nature of the ligand can be observed and measured using a spectrophotometer. Smaller values of ∆o result in colors in the green range. Larger gaps shift the color to yellow.

14. The Spectrochemical Series Based on measurements for a given metal ion, the following series has been developed: I-<Br-<S2-<Cl-<NO3-<N3-<F-<OH-<C2O42-<H2O <NCS-<CH3CN<pyridine<NH3<en<bipy<phen <NO2-<PPh3<CN-<CO

15. The Spectrochemical Series The complexes of cobalt (III) show the shift in color due to the ligand. (a) CN–, (b) NO2–, (c) phen, (d) en, (e) NH3, (f) gly, (g) H2O, (h) ox2–, (i) CO3 2–.

16. Ligand Field Strength Observations 1. ∆o increases with increasing oxidation number on the metal. Mn+2<Ni+2<Co+2<Fe+2<V+2<Fe+3<Co+3 <Mn+4<Mo+3<Rh+3<Ru+3<Pd+4<Ir+3<Pt+4 2. ∆o increases with increases going down a group of metals.

17. Ligand Field Theory Crystal Field Theory completely ignores the nature of the ligand. As a result, it cannot explain the spectrochemical series. Ligand Field Theory uses a molecular orbital approach. Initially, the ligands can be viewed as having a hybrid orbital or a p orbital pointing toward the metal to make σ bonds.

19. Octahedral Symmetry http://www.iumsc.indiana.edu/morphology/symmetry/octahedral.html

20. Ligand Field Theory Consider the sigma bonds to all six ligands in octahedral geometry. This reduces to A1g + Eg + T1u

21. Ligand Field Theory The A1g group orbitals have the same symmetry as an s orbital on the central metal.

22. Ligand Field Theory The T1u group orbitals have the same symmetry as the p orbitals on the central metal. (T representations are triply degenerate.)

23. Ligand Field Theory The Eg group orbitals have the same symmetry as the dz2 and dx2-y2 orbitals on the central metal. (E representations are doubly degenerate.)

24. Ligand Field Theory Since the ligands don’t have a combination with t2g symmetry, the dxy, dyz and dxy orbitals on the metal will be non-bonding when considering σ bonding.

25. Ligand Field Theory The molecular orbital diagram is consistent with the crystal field approach. Note that the t2g set of orbitals is non-bonding, and the eg set of orbitals is antibonding.

26. Ligand Field Theory The electrons from the ligands (12 electrons from 6 ligands in octahedral complexes) will fill the lower bonding orbitals. {

27. Ligand Field Theory The electrons from the 4s and 3d orbitals of the metal (in the first transition row) will occupy the middle portion of the diagram. {

28. Experimental Evidence for Splitting Several tools are used to confirm the splitting of the t2g and eg molecular orbitals. The broad range in colors of transition metal complexes arises from electronic transitions as seen in the UV/visible spectra of complexes. Additional information is gained from measuring the magnetic moments of the complexes.

29. Experimental Evidence for Splitting Magnetic susceptibility measurements can be used to calculate the number of unpaired electrons in a compound. Paramagnetic substances are attracted to a magnetic field.

30. Magnetic Moments A magnetic balance can be used to determine the magnetic moment of a substance. If a substance has unpaired electrons, it is paramagnetic, and attracted to a magnetic field. For the upper transition metals, the spin-only magnetic moment, μs, can be used to determine the number of unpaired electrons. μs = [n(n+2)]1/2

31. Magnetic Moments The magnetic moment of a substance, in Bohr magnetons, can be related to the number of unpaired electrons in the compound. μs = [n(n+2)]1/2 Where n is the number of unpaired electrons

32. Magnetic Moments Complexes with 4-7 electrons in the d orbitals have two possibilities for the distribution of electrons. The complexes can be low spin, in which the electrons occupy the lower t2g set and pair up, or they can be high spin. In these complexes, the electrons will fill the upper eg set before pairing.

33. High and Low Spin Complexes If the gap between the d orbitals is large, electrons will pair up and fill the lower (t2g) set of orbitals before occupying the eg set of orbitals.The complexes are called low spin.

34. High and Low Spin Complexes In low spin complexes, the size of ∆o is greater than the pairing energy of the electrons.

35. High and Low Spin Complexes If the gap between the d orbitals is small, electrons will occupy the eg set of orbitals before they pair up and fill the lower (t2g) set of orbitals before.The complexes are called high spin.

36. High and Low Spin Complexes In high spin complexes, the size of ∆o is less than the pairing energy of the electrons.

37. Ligand Field Stabilization Energy The first row transition metals in water are all weak field, high spin cases.

38. Experimental Evidence for LFSE The hydration energies of the first row transition metals should increase across the period as the size of the metal ion gets smaller. M2+ + 6 H2O(l)  M(H2O)62+

39. Experimental Evidence for LFSE The heats of hydration show two “humps” consistent with the expected LFSE for the metal ions. The values for d5 and d10 are the same as expected with a LFSE equal to 0.

40. Experimental Evidence of LFSE

41. High Spin vs. Low Spin 3d metals are generally high spin complexes except with very strong ligands. CN- forms low spin complexes, especially with M3+ ions. 4d & 4d metals generally have a larger value of ∆o than for 3d metals. As a result, complexes are typically low spin.

42. Nature of the Ligands Crystal field theory and ligand field theory differ in that LFT considers the nature of the ligands. Thus far, we have only viewed the ligands as electron pairs used for making σ bonds with the metal. Many ligands can also form π bonds with the metal. Group theory greatly simplifies the construction of molecular orbital diagrams.

43. Considering π Bonding To obtain Γred for π bonding, a set of cartesian coordinates is established for each of the ligands. The direction of the σ bonds is arbitrarily set as the y axis (or the py orbitals). The px and pz orbitals are used in π bonding.

44. Considering π Bonding z x z y x y x y y x Consider only the px and pz orbitals on each of the ligands to obtain Γπ. z z y z x y z x

45. Considering π Bonding This reduces to T1g + T2g + T1u + T2u. The T2g set has the same symmetry as the dxy, dyz and dxz orbitals on the metal. The T1u set has the same symmetry as the px, py and pz orbitals on the metal.

46. Considering π Bonding Τπ reduces to: T1g + T2g + T1u + T2u. • The T1g and T2u group orbitals for the ligands don’t match the symmetry of any of the metal orbitals. • The T1u set has the same symmetry as the px, py and pz orbitals on the metal. These orbitals are used primarily to make the σ bonds to the ligands. • The T2g set has the same symmetry as the dxy, dyz and dxz orbitals on the metal.

47. π Bonding The main source of π bonding is between the dxy, dyz and dxz orbitals on the metal and the d, p or π* orbitals on the ligand.

48. π Bonding The ligand may have empty d or π* orbitals and serve as a π acceptor ligand, or full p or d orbitals and serve as a π donor ligand.

49. π Bonding The empty π antibonding orbital on CO can accept electron density from a filled d orbital on the metal. CO is a pi acceptor ligand. empty π* orbital filled d orbital

50. π Donor Ligands (LM) All ligands are σ donors. Ligands with filled p or d orbitals may also serve as pi donor ligands. Examples of π donor ligands are I-, Cl-, and S2-. The filled p or d orbitals on these ions interact with the t2g set of orbitals (dxy, dyz and dxz) on the metal to form bonding and antibonding molecular orbitals.