Low-Valent Iron(I) Amido Olefin Complexes as Promotors for Dehydrogenation Reactions

Lichtenberg C, Viciu L, Adelhardt M, Sutter J, Meyer K, De Bruin B, Gruetzmacher H (2015)


Publication Status: Published

Publication Type: Journal article

Publication year: 2015

Journal

Publisher: Wiley-VCH Verlag

Book Volume: 54

Pages Range: 5766-5771

DOI: 10.1002/anie.201411365

Abstract

Fe-I compounds including hydrogenases show remarkable properties and reactivities. Several iron(I) complexes have been established in stoichiometric reactions as model compounds for N-2 or CO2 activation. The development of well-defined iron(I) complexes for catalytic transformations remains a challenge. The few examples include cross-coupling reactions, hydrogenations of terminal olefins, and azide functionalizations. Here the syntheses and properties of bimetallic complexes [MFeI(trop(2)dae)(solv)] (M= Na, solv= 3thf; M= Li, solv= 2Et(2)O; trop= 5H-dibenzo[a, d] cyclo-hepten-5-yl, dae=(N-CH2-CH2-N) with a d(7) Fe low-spin valence-electron configuration are reported. Both compounds promote the dehydrogenation of N, N-dimethylaminoborane, and the former is a precatalyst for the dehydrogenative alcoholysis of silanes. No indications for heterogeneous catalyses were found. High activities and complete conversions were observed particularly with [NaFeI(trop(2)dae)(thf)(3)].

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APA:

Lichtenberg, C., Viciu, L., Adelhardt, M., Sutter, J., Meyer, K., De Bruin, B., & Gruetzmacher, H. (2015). Low-Valent Iron(I) Amido Olefin Complexes as Promotors for Dehydrogenation Reactions. Angewandte Chemie International Edition, 54, 5766-5771. https://dx.doi.org/10.1002/anie.201411365

MLA:

Lichtenberg, Crispin, et al. "Low-Valent Iron(I) Amido Olefin Complexes as Promotors for Dehydrogenation Reactions." Angewandte Chemie International Edition 54 (2015): 5766-5771.

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