low valent, low coordinate complexes using bulky ligandsgbdong.cm.utexas.edu/seminar/old/literature...
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Low Valent, Low Coordinate Complexes Using Bulky
Ligands
01/14/2015
Presented By Michael C. Young
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Topics
•Two and three coordinate low valent complexes of Ni
●Work by the Hillhouse Group
•Bulky m-terphenyl isonitrile ligands for low coordinate transition metal complexes
●Work by the Figueroa Group
•Low coordinate complexes of Fe and Co
●Work by the Betley Group
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Monomeric Terminal Ni(II)-Imido
•Impetus: At the time there was a dearth of examples of nickel complexes with hard imido ligands.
•To prevent dimerization, it was desirable to use both a bulky phosphine ligand as well as a bulky
nitrogen.
Mindiola, D. J.; Hillhouse, G. L. J. Am. Chem. Soc., 2001, 123, 4623.
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Monomeric Ni(II)-Phosphinidene
•Similarly, there was no good example of a phosphinidene complex, and the imido synthesis
suggested the analogous phosphinidene should be easily obtained.
Melenkivitz, R.; Mindiola, D. J.; Hillhouse, G. L. J. Am. Chem. Soc., 2002, 124, 3846.
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Ni(II)-Carbene and Reactions
•Although Ni(II)-diazo complexes were known, it should be possible to extrude nitrogen to give a
carbene.
Mindiola, D. J.; Hillhouse, G. L. J. Am. Chem. Soc., 2002, 124, 9976.
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Ni(II)-Imido Transfer Reactions
•The formed imidos can be used for nitrene transfer reactions.
Mindiola, D. J.; Hillhouse, G. L. Chem. Commun., 2002, 1840.
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Ni(II)=X Group Transfer with C2H4
•All of the Ni(II)=X species thus far discussed can react with olefins
Waterman, R.; Hillhouse, G. L. J. Am. Chem. Soc., 2003, 125, 13350.
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Ni(II)=P Transfer with Alkynes
Waterman, R.; Hillhouse, G. L. Organometallics, 2003, 22, 5182.
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Unsaturated Ni(I) vs Ni(II)-C Species
•Organolithiums can also be added to Ni(I) to give monoalkyls
Kitiachvili, K. D.; Mindiola, D. J.; Hillhouse, G. L. Organometallics, 2004, 126, 10554.
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Ni(0) Coordination of N2 and NO
•N2 binds in a side-on fashion at low temperature
Iluc, V. M.; Miller, A. J. M.; Hillhouse, G. L. Organometallics, 2005, 127, 5091.
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Ni(0) Coordination of N3
•Unsurprisingly, azides can also form stable adducts with this complex.
Waterman, R.; Hillhouse, G. L. J. Am. Chem. Soc., 2008, 130, 23628.
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Dicoordinate Ni(I) and Reactions
Laskowski, C. A.; Hillhouse, G. L. J. Am. Chem. Soc., 2008, 130, 13846.
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Insertion into Ni(II)-Alkyl Bonds
Curley, J. J.; Kitiachvili, K. D.; Waterman, R.; Hillhouse, G. L. Organometallics, 2009, 28, 2568.
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Ni-CarbeneTransfer
Harrold, N. D.; Waterman, R.; Hillhouse, G. L.; Cundari, T. R. J. Am. Chem. Soc., 2009, 131, 12872.
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Catalytic Route to Diimides
Laskowski, C. A.; Hillhouse, G. L. Organometallics, 2009, 28, 6114.
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Catalytic Route to Diimides
Laskowski, C. A.; Hillhouse, G. L. Organometallics, 2009, 28, 6114.
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Towards a Ni(II)-Silylene Complex
Iluc, V. M.; Hillhouse, G. L. J. Am. Chem. Soc., 2010, 132, 11890.
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Reactions of Ni(0) and Ni(I) with CX2
Anderson, J. S.; Iluc, V. M.; Hillhouse, G. L. Inorg. Chem., 2010, 49 10203.
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Ni(I)-XHR to Ni(II)=X Radical Pathway
Iluc, V. M.; Hillhouse, G. L. J. Am. Chem. Soc., 2010, 132, 15148.
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Dicoordinate Ni(II) Complexes
Laskowski, C. A.; Miller, A. J. M.; Hillhouse, G. L.; Cundari, T. R. J. Am. Chem. Soc., 2011, 133, 771.
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Ni(II)-Carbene-Bridged Dimers
Laskowski, C. A.; Hillhouse, G. L. Chem. Sci., 2010, 2, 321.
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Ni(III)-Imido Complex
• A terminal Ni(III)-imido should be exceptionally reactive and therefore unstable.
Iluc, V. M.; Miller, A. J. M.; Anderson, J. S.; Monreal, M. J.; Mehn, M. P.; Hillhouse, G. L. J. Am. Chem. Soc., 2011, 133, 13055.
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Bis-NHC-Ni Complexes
Harrold, N. D.; Hillhouse, G. L. Chem. Sci., 2013, 4, 4011.
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Bis-NHC-Ni Complexes
Harrold, N. D.; Hillhouse, G. L. Chem. Sci., 2013, 4, 4011.
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Towards NHC-Ni(I) Alkyl Complexes
Laskowski, C. A.; Bungum, D. J.; Baldwin, S. M.; Del Ciello, S. A.; Illuc, V. M.; Hillhouse, G. L. J. Am. Chem. Soc., 2013, 135, 18272.
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3-Coordinate Ni(II) Carbenes
Iluc, V. M.; Hillhouse, G. L. J. Am. Chem. Soc., 2014, 136, 6479.
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Isocyano Ligands and Cu(I)
Fox, B. J.; Sun, Q. Y.; DiPasquale, A. G.; Fox, A. R.; Rheingold, A. L.; Figueroa, J. S. Inorg. Chem., 2009, 131, 11318.
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Isocyano Ligands with Ni(0)
Fox, B. J.; Millard, M. D.; DiPasquale, A. G.; Rheingold, A. L.; Figueroa, J. S. Angew. Chem., Int. Ed., 2009, 48, 3473.Emerich, B. M.; Moore, C. E.; Fox, B. J.; Rheingold, A. L.; Figueroa, J. S. Organometallics, 2011, 30, 2598.
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2-Coordinate Pd(0) with Isocyano Ligands
Labios, L. A.; Millard, M. D.; Rheingold, A. L.; Figueroa, J. S. J. Am. Chem. Soc., 2009, 131, 11318.
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Ligand C−H Amination with Fe(II)
• Replacing Fe(II) with Zn(II) shuts down the reaction.
King, E. R.; Betley, T. A. Inorg. Chem., 2009, 48, 2361.
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Complexes of Dipyrromethane
King, E. R.; Betley, T. A. J. Am. Chem. Soc., 2009, 131, 14379.
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Complexes of Dipyrromethane
King, E. R.; Hennessy, E. T.; Betley, T. A. J. Am. Chem. Soc., 2011, 133, 4917.
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Complexes of Dipyrromethane
• The reaction of 1 with adamantyl amine in toluene gives 6.7 turnover (amine 95%, imine 2.8%,
adamantylamine 1.8%).
• Product inhibited by anything that outcompetes azide for chelation.
• KIE is consistent with H abstraction being the RDS.
King, E. R.; Hennessy, E. T.; Betley, T. A. J. Am. Chem. Soc., 2011, 133, 4917.
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Complexes of Dipyrromethane
King, E. R.; Hennessy, E. T.; Betley, T. A. J. Am. Chem. Soc., 2011, 133, 4917.
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Electronic Perturbation of Ligands
Scharf, A. B.; Betley, T. A. Inorg. Chem., 2011, 50, 6837.
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Co(III) Complexes of Dipyrromethane
King, E. R.; Sazama, G. T.; Betley, T. A. J. Am. Chem. Soc., 2012, 134, 17858.
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Intramolecular Cyclization of Alkyl Azides
• Based on the previous results, the group next wanted to explore the substrate scope of their
nitrene insertion into aliphatic C−H bonds.
Hennessy, E. T.; Betley, T. A. Science, 2013, 340, 591.
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Intramolecular Cyclization of Alkyl Azides
Hennessy, E. T.; Betley, T. A. Science, 2013, 340, 591.
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Intramolecular Cyclization of Alkyl Azides
Hennessy, E. T.; Betley, T. A. Science, 2013, 340, 591.
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Intramolecular Cyclization of Alkyl Azides
• As the substrates become more complex, so too are the product(s).
Hennessy, E. T.; Betley, T. A. Science, 2013, 340, 591.
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Intramolecular Cyclization of Alkyl Azides
Hennessy, E. T.; Betley, T. A. Science, 2013, 340, 591.
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Thank you for your attention!
http://www.phdcomics.com/comics.php?f=1768, Accessed 01/14/2015.