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53) Functional Group Tolerance and Substrate Scope in Bis(imino)pyridine Iron Catalyzed Alkene Hydrogenation
Trovitch, R. J.; Lobkovsky, E.; Bill, E.; Chirik, P. Organometallics. 2008, 1470-1478.
50) Synthesis of Bis(imino)pyridine Iron Di- and Monoalkyl Complexes: Stability Differences between FeCH2SiMe3 and FeCH2CMe3 Derivatives
Fernández, I.; Trovitch, R.J.; Lobkovsky, E.; Chrik, P. Organometallics, 2008, 27, 109-118.
49) Neutral –ligand complexes of bis(imino)pyridine iron: Synthesis, structure and spectroscopy.
Bart, S. C.; Lobkovsky, E.; Bill, E.; Weighardt, K.; Chirik, P. J. Inorg. Chem. 2007, 46, 7055-7063.
46) Iron Diazoalkane Chemistry: N-N Bond Hydrogenation and Intramolecular C-H Activation. 
Bart, S. C.; Bowman, A. C.; Lobkovsky, E.; Chirik, P. J. J. Am. Chem. Soc. 2007, 129, 7212-7213.
38) An FeVI Nitride: There Is Plenty of Room at the Top! 
Chirik, P. J.Angew. Chem. Int. Ed. 2006, 45, 6956.
37) Electronic Structure of Bis(imino)pyridine Iron Dichloride, Monochloride, and Neutral Ligand Complexes: A Combined Structural, Spectroscopic, and Computational Study. 
Bart, S. C.; Chlopek, K.; Bill, E.; Bouwkamp, M. W.; Lobkovsky, E.; Neese, F.; Wieghardt, K.; Chirik, P. J.J. Am. Chem. Soc. 2006, 128, 13901.
36) Iron-Catalyzed [2 + 2] Cycloaddition of ,-Dienes: The Importance of Redox-Active Supporting Ligands. 
Bouwkamp, M. W.; Bowman, A. C.; Lobkovsky, E.; Chirik, P. J. J. Am. Chem. Soc. 2006, 128, 13340.
35) Bis(diisopropylphosphino)pyridine Iron Dicarbonyl, Dihydride, and Silyl Hydride Complexes. 
Trovitch, R; Lobkovsky, E.; Chirik, P. J. Inorganic Chemistry. 2006, 45, 7252.
34) Arene Coordination in Bis(imino)pyridine Iron Complexes: Identification of Catalyst Deactivation Pathways in Iron-Catalyzed Hydrogenation and Hydrosilation. 
Archer, A. M.; Bouwkamp, M. W.; Cortez, M.P.; Lobkovsky, E.; Chirik, P. J. Organometallics. 2006, 25, 4269.
30) The Synthesis and Hydrogenation of Bis(imino)pyridine Iron Imides 
Bart, S. C.; Lobkovsky, E.; Bill, E.; Chirik, P. J. J. Am. Chem. Soc. 2006, 128, 5302.
26) Bis(imino)pyridine Ligand Deprotonation Promoted by a Transient Iron Amide 
Bouwkamp, M. W.; Lobkovsky, E.; Chirik, P. J. Inorg. Chem., 45, 2.
24) Low-Valent a-Diimine Iron Complexes for Catalytic Olefin Hydrogenation 
Bart, S. C.; Hawrelak, E. J.; Lobkovsky, E.; Chirik, P. J. Organometallics 2005, 24, 5518.
20) Bis(imino)pyridine Iron(II) Alkyl Cations for Olefin Polymerization 
Bouwkamp, M. W.; Lobkovsky, E.; Chirik, P. J. J. Am. Chem. Soc. 2005, 127, 9660.
19) Square Planar Bis(imino)pyridine Iron Halide and Alkyl Complexes 
Bouwkamp, M. W.; Bart, S. C.; Hawrelak, E. J.; Trovitch, R. J.; Lobkovsky, E.; Chirik, P. J. Chem. Commun. 2005, 3406.
17) Square Planar vs Tetrahedral Geometry in Four Coordinate Iron(II) Complexes 
Hawrelak, E. J.; Bernskoetter, W. H.; Lobkovsky, E.; Yee, G. T.; Bill, E.; Chirik, P. J. Inorg. Chem. 2005, 44, 3103.
12) Preparation and Molecular and Electronic Structures of Iron(0) Dinitrogen and Silane Complexes and Their Application to Catalytic Hydrogenation and Hydrosilation 
Bart, S. C.; Lobkovsky, E.; Chirik, P. J. J. Am. Chem. Soc. 2004 126, 13794.
11) Synthesis and Characterization of Zirconium and Iron Complexes Containing Substituted Indenyl Ligands: Evaluation of Steric and Electronic Parameters 
Bradley, C. A.; Flores-Torres, S.; Lobkovsky, E.; Abruna, H. D.; Chirik, P. J. Organometallics 2004, 23, 5332.
7) Synthesis, Reactivity, and Solid State Structures of Four-coordinate Iron(II) and Manganese(II) Alkyl Complexes 
Bart, S.C.; Hawrelak, E.J.; Schmisseur, A.K.; Lobkovsky, E.; Chirik, P.J. Organometallics 2004, 23, 237.http://pubs.acs.org/cgi-bin/abstract.cgi/orgnd7/asap/abs/om701091z.htmlhttp://pubs.acs.org/cgi-bin/abstract.cgi/orgnd7/asap/abs/om700913g.htmlhttp://pubs.acs.org/cgi-bin/article.cgi/inocaj/2007/46/i17/pdf/ic700869h.pdfhttp://dx.doi.org/10.1021/ja070056uhttp://dx.doi.org/10.1002/anie.200603056http://dx.doi.org/10.1021/ja064557bhttp://dx.doi.org/10.1021/ja064557bhttp://dx.doi.org/10.1021/ja064711uhttp://dx.doi.org/10.1021/ja064711uhttp://dx.doi.org/10.1021/ic0608647http://dx.doi.org/10.1021/om060441chttp://dx.doi.org/10.1021/om060441chttp://dx.doi.org/10.1021/ja057165yhttp://dx.doi.org/10.1021/ic051839ohttp://dx.doi.org/10.1021/om050625bhttp://dx.doi.org/10.1021/ja0524447http://dx.doi.org/10.1039/b504063ahttp://dx.doi.org/10.1039/b504063ahttp://dx.doi.org/10.1021/ic048202+http://dx.doi.org/10.1021/ic048202+http://dx.doi.org/10.1021/ja046753thttp://dx.doi.org/10.1021/om0495675http://dx.doi.org/10.1021/om0495675http://dx.doi.org/10.1021/om034188hhttp://dx.doi.org/10.1021/om034188hhttp://livepage.apple.com/shapeimage_7_link_0shapeimage_7_link_1shapeimage_7_link_2shapeimage_7_link_3shapeimage_7_link_4shapeimage_7_link_5shapeimage_7_link_6shapeimage_7_link_7shapeimage_7_link_8shapeimage_7_link_9shapeimage_7_link_10shapeimage_7_link_11shapeimage_7_link_12shapeimage_7_link_13shapeimage_7_link_14shapeimage_7_link_15shapeimage_7_link_16shapeimage_7_link_17shapeimage_7_link_18shapeimage_7_link_19shapeimage_7_link_20shapeimage_7_link_21shapeimage_7_link_22shapeimage_7_link_23shapeimage_7_link_24
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