Abstract
We report the preparation and electronic structure determination of chelate-reduced Mn(I) compounds that are relevant to electrocatalytic proton reduction mediated by [(Ph2PPrPDI)Mn(CO)][Br]. Reducing [(Ph2PPrPDI)Mn(CO)][Br] with excess Na-Hg afforded a neutral paramagnetic complex, (Ph2PPrPDI)Mn(CO). This compound was found to feature a low spin Mn(I) center and a PDI radical anion as determined by magnetic susceptibility measurement (1.97 μB), EPR spectroscopy (S = 1/2), and density functional theory calculations. When [(Ph2PPrPDI)Mn(CO)][Br] was reduced with K-Hg, Mn(I) complexes with highly activated CO ligands were obtained. Recrystallization of the reduced product from diethyl ether solution allowed for the isolation of dimeric [(κ4-Ph2PPrPDI)Mn(μ-n1, n 1, n 2-CO)K(Et2O)]2 (ν CO = 1710 cm-1, 1656 cm-1), while methyl tert-butyl ether treatment afforded dimeric [(κ4-Ph2PPrPDI)Mn(μ- n 1, n 1-CO)K(MTBE)2]2 (ν CO = 1695 cm-1, MTBE = methyl tert-butyl ether). Addition of 18-crown-6 to these products, or conducting the K-Hg reduction of [(Ph2PPrPDI)Mn(CO)][Br] in the presence of 18-crown-6, allowed for the isolation of a monomeric example, (κ4-Ph2PPrPDI)Mn(μ- n 1, n 2-CO)K(18-crown-6) (ν CO = 1697 cm-1). All three complexes were found to be diamagnetic and were characterized thoroughly by multinuclear 1D and 2D NMR spectroscopy and single crystal X-ray diffraction. Detailed analysis of the metrical parameters and spectroscopic properties suggest that all three compounds possess a Mn(I) center that is supported by a PDI dianion. Importantly, (κ4-Ph2PPrPDI)Mn(μ- n 1, n 2-CO)K(18-crown-6) was found to react instantaneously with either HBF4·OEt2 or HOTf to evolve H2 and generate the corresponding Mn(I) complex, [(Ph2PPrPDI)Mn(CO)][BF4] or [(Ph2PPrPDI)Mn(CO)][OTf], respectively. These products are spectroscopically and electrochemically similar to previously reported [(Ph2PPrPDI)Mn(CO)][Br]. It is believed that the mechanism of [(Ph2PPrPDI)Mn(CO)][Br]-mediated proton reduction involves intermediates that are related to the compounds described herein and that their ambient temperature isolation is aided by the redox active nature of Ph2PPrPDI.
| Original language | English |
|---|---|
| Pages (from-to) | 6065-6075 |
| Number of pages | 11 |
| Journal | Inorganic Chemistry |
| Volume | 57 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - May 21 2018 |
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ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry
Cite this
Isolation of Mn(I) Compounds Featuring a Reduced Bis(imino)pyridine Chelate and Their Relevance to Electrocatalytic Hydrogen Production. / Mukhopadhyay, Tufan K.; Maclean, Nicholas L.; Flores, Marco; Groy, Thomas L.; Trovitch, Ryan.
In: Inorganic Chemistry, Vol. 57, No. 10, 21.05.2018, p. 6065-6075.Research output: Contribution to journal › Article
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TY - JOUR
T1 - Isolation of Mn(I) Compounds Featuring a Reduced Bis(imino)pyridine Chelate and Their Relevance to Electrocatalytic Hydrogen Production
AU - Mukhopadhyay, Tufan K.
AU - Maclean, Nicholas L.
AU - Flores, Marco
AU - Groy, Thomas L.
AU - Trovitch, Ryan
PY - 2018/5/21
Y1 - 2018/5/21
N2 - We report the preparation and electronic structure determination of chelate-reduced Mn(I) compounds that are relevant to electrocatalytic proton reduction mediated by [(Ph2PPrPDI)Mn(CO)][Br]. Reducing [(Ph2PPrPDI)Mn(CO)][Br] with excess Na-Hg afforded a neutral paramagnetic complex, (Ph2PPrPDI)Mn(CO). This compound was found to feature a low spin Mn(I) center and a PDI radical anion as determined by magnetic susceptibility measurement (1.97 μB), EPR spectroscopy (S = 1/2), and density functional theory calculations. When [(Ph2PPrPDI)Mn(CO)][Br] was reduced with K-Hg, Mn(I) complexes with highly activated CO ligands were obtained. Recrystallization of the reduced product from diethyl ether solution allowed for the isolation of dimeric [(κ4-Ph2PPrPDI)Mn(μ-n1, n 1, n 2-CO)K(Et2O)]2 (ν CO = 1710 cm-1, 1656 cm-1), while methyl tert-butyl ether treatment afforded dimeric [(κ4-Ph2PPrPDI)Mn(μ- n 1, n 1-CO)K(MTBE)2]2 (ν CO = 1695 cm-1, MTBE = methyl tert-butyl ether). Addition of 18-crown-6 to these products, or conducting the K-Hg reduction of [(Ph2PPrPDI)Mn(CO)][Br] in the presence of 18-crown-6, allowed for the isolation of a monomeric example, (κ4-Ph2PPrPDI)Mn(μ- n 1, n 2-CO)K(18-crown-6) (ν CO = 1697 cm-1). All three complexes were found to be diamagnetic and were characterized thoroughly by multinuclear 1D and 2D NMR spectroscopy and single crystal X-ray diffraction. Detailed analysis of the metrical parameters and spectroscopic properties suggest that all three compounds possess a Mn(I) center that is supported by a PDI dianion. Importantly, (κ4-Ph2PPrPDI)Mn(μ- n 1, n 2-CO)K(18-crown-6) was found to react instantaneously with either HBF4·OEt2 or HOTf to evolve H2 and generate the corresponding Mn(I) complex, [(Ph2PPrPDI)Mn(CO)][BF4] or [(Ph2PPrPDI)Mn(CO)][OTf], respectively. These products are spectroscopically and electrochemically similar to previously reported [(Ph2PPrPDI)Mn(CO)][Br]. It is believed that the mechanism of [(Ph2PPrPDI)Mn(CO)][Br]-mediated proton reduction involves intermediates that are related to the compounds described herein and that their ambient temperature isolation is aided by the redox active nature of Ph2PPrPDI.
AB - We report the preparation and electronic structure determination of chelate-reduced Mn(I) compounds that are relevant to electrocatalytic proton reduction mediated by [(Ph2PPrPDI)Mn(CO)][Br]. Reducing [(Ph2PPrPDI)Mn(CO)][Br] with excess Na-Hg afforded a neutral paramagnetic complex, (Ph2PPrPDI)Mn(CO). This compound was found to feature a low spin Mn(I) center and a PDI radical anion as determined by magnetic susceptibility measurement (1.97 μB), EPR spectroscopy (S = 1/2), and density functional theory calculations. When [(Ph2PPrPDI)Mn(CO)][Br] was reduced with K-Hg, Mn(I) complexes with highly activated CO ligands were obtained. Recrystallization of the reduced product from diethyl ether solution allowed for the isolation of dimeric [(κ4-Ph2PPrPDI)Mn(μ-n1, n 1, n 2-CO)K(Et2O)]2 (ν CO = 1710 cm-1, 1656 cm-1), while methyl tert-butyl ether treatment afforded dimeric [(κ4-Ph2PPrPDI)Mn(μ- n 1, n 1-CO)K(MTBE)2]2 (ν CO = 1695 cm-1, MTBE = methyl tert-butyl ether). Addition of 18-crown-6 to these products, or conducting the K-Hg reduction of [(Ph2PPrPDI)Mn(CO)][Br] in the presence of 18-crown-6, allowed for the isolation of a monomeric example, (κ4-Ph2PPrPDI)Mn(μ- n 1, n 2-CO)K(18-crown-6) (ν CO = 1697 cm-1). All three complexes were found to be diamagnetic and were characterized thoroughly by multinuclear 1D and 2D NMR spectroscopy and single crystal X-ray diffraction. Detailed analysis of the metrical parameters and spectroscopic properties suggest that all three compounds possess a Mn(I) center that is supported by a PDI dianion. Importantly, (κ4-Ph2PPrPDI)Mn(μ- n 1, n 2-CO)K(18-crown-6) was found to react instantaneously with either HBF4·OEt2 or HOTf to evolve H2 and generate the corresponding Mn(I) complex, [(Ph2PPrPDI)Mn(CO)][BF4] or [(Ph2PPrPDI)Mn(CO)][OTf], respectively. These products are spectroscopically and electrochemically similar to previously reported [(Ph2PPrPDI)Mn(CO)][Br]. It is believed that the mechanism of [(Ph2PPrPDI)Mn(CO)][Br]-mediated proton reduction involves intermediates that are related to the compounds described herein and that their ambient temperature isolation is aided by the redox active nature of Ph2PPrPDI.
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U2 - 10.1021/acs.inorgchem.8b00588
DO - 10.1021/acs.inorgchem.8b00588
M3 - Article
VL - 57
SP - 6065
EP - 6075
JO - Inorganic Chemistry
JF - Inorganic Chemistry
SN - 0020-1669
IS - 10
ER -