Magnetic Property Mr Sonaji V Gayakwad Asst professor

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Magnetic Property Mr. Sonaji V. Gayakwad Asst. professor Dept of chemistry Mrs. K. S.

Magnetic Property Mr. Sonaji V. Gayakwad Asst. professor Dept of chemistry Mrs. K. S. K. College, Beed

◦ Why are we doing this experiment? �Magnetic Properties reveal numbers of unpaired electrons

◦ Why are we doing this experiment? �Magnetic Properties reveal numbers of unpaired electrons �The number of unpaired electrons tell us about oxidation state, geometry, ligand field strength, etc… ◦ How are we doing this experiment? �We are using a Johnson-Matthey MSB-Auto Magnetic Susceptibility Balance �It uses the Evan’s detector which is a modified Gouy Magnetic Susceptibility

C. How do we work up the data? 1. The MSB-Auto output data is

C. How do we work up the data? 1. The MSB-Auto output data is Volume Susceptibility = c. V Example: [Mn(B 13 N 4)Cl 2]PF 6 c. V = 3. 80 x 10 -6 (unitless) average value 2. We will need the volume of our sample: V = pr 2 l = (3. 1416)(0. 162 cm)2(3. 01 cm) = 0. 248 cm 3 observed paramag 3. We will need the density of our sample: d = m/V = (0. 1549 g)(0. 248 cm 3) = 0. 624 g/cm 3 diamag. 4. We can calculate Mass Susceptibility = cg cg = c. V/d = (3. 80 x 10 -6)/(0. 624 g/cm 3) = 6. 09 x 10 -6 cm 3/g 5. Next we need to calculate Molar Susceptibility = c. M = (cg)(Mol. Wt) = (5. 61 x 10 -6 cm 3/g)(511. 200 g/mol) = 3. 11 x 10 -3 cm 3/mol 6. We now need to correct for diamagnetic influences of the ligands a. We are wanting the metal only, but the ligand is interfering b. Ligand atoms (and even the metal core electrons) are diamagnetic c. We need to add back in the sum of the ligand diamagnetism

8. Use the table in your notebook for diamagnetic corrections Mn. C 13 H

8. Use the table in your notebook for diamagnetic corrections Mn. C 13 H 28 N 4 Cl 2 PF 6 (13)+(6)(13)+(28)(2. 93)+(4 )(4. 61)+(2)(23. 4) +(26. 3)+(6)(9. 1) = -319 x 10 -6 cm 3/mol meff 9. Calculate the corrected c. M’ = c. M - (diamag. Correc) c. M’ = (3. 11 x 10 -3 cm 3/mol) – (-319 x 106 cm 3/mol) = 3. 43 x 10 -3 cm 3/mol 10. Calculate the magnetic moment = meff = 2. 83[(c. M’)(T)]½ = 2. 83[(3. 43 x 10 -3 cm 3/mol)(298 K)]½ = 2. 86 J/T = 2. 86 Bohr Magnetons 11. Calculate the number of unpaired e- = n meff = [n(n+2)]½ (meff)2 = n(n+2) = (2. 86)2 = 8. 19 n ≈ 2

D. How do we interpret the results? 1. We can compare the magnetic moment

D. How do we interpret the results? 1. We can compare the magnetic moment with literature values for that ion 2. We can decide if the expected oxidation state of the metal matches 3. We can decide what the geometry of the complex is 4. We can decide if the complex is high spin or low spin 5. We can decide if the ligand(s) is/are weak or strong field

E. Conclusions 1. Our magnetic moment (ueff = 2. 86) is a bit low

E. Conclusions 1. Our magnetic moment (ueff = 2. 86) is a bit low compared to the table for low spin Mn 3+ (3. 18). Measurement error due to our inexperience could account for this. However, magnetic moments are variable, and this could be normal. A standard deviation of our 3 measurements might tell us how reproducible they were. 2. The magnetic moment we found and the n = 2 calculated from it, are consistent with low spin Mn 3+, which is the ion we were trying to make. 3. Six coordinate Mn 3+ is most likely octahedral, due to the usual preference for this ion. In a low spin configuration, n = 2 is consistent with this geometry. 4. Since the complex appears to be low spin, the combination of the B 13 N 4 ligand the two chloride ligands must be strong field enough that Do is large enough to cause the low spin configuration.