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Metallaboratrane Facilitated E‒H Bond Activation and Hydrogenation Catalysis

Citation

Fong, Henry (2015) Metallaboratrane Facilitated E‒H Bond Activation and Hydrogenation Catalysis. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/Z9TX3C9P. http://resolver.caltech.edu/CaltechTHESIS:12152014-181907516

Abstract

The E‒H bond activation chemistry of tris-phosophino-iron and -cobalt metallaboratranes is discussed. The ferraboratrane complex (TPB)Fe(N2) heterolytically activates H‒H and the C‒H bonds of formaldehyde and arylacetylenes across an Fe‒B bond. In particular, H‒H bond cleavage at (TPB)Fe(N2) is reversible and affords the iron-hydride-borohydride complex (TPB)(μ‒H)Fe(L)(H) (L = H2, N2). (TPB)(μ‒H)Fe(L)(H) and (TPB)Fe(N2) are competent olefin and arylacetylene hydrogenation catalysts. Stoichiometric studies indicate that the B‒H unit is capable of acting as a hydride shuttle in the hydrogenation of olefin and arylacetylene substrates. The heterolytic cleavage of H2 by the (TPB)Fe system is distinct from the previously reported (TPB)Co(H2) complex, where H2 coordinates as a non-classical H2 adduct based on X-ray, spectroscopic, and reactivity data. The non-classical H2 ligand in (TPB)Co(H2) is confirmed in this work by single crystal neutron diffraction, which unequivocally shows an intact H‒H bond of 0.83 Å in the solid state. The neutron structure also shows that the H2 ligand is localized at two orientations on cobalt trans to the boron. This localization in the solid state contrasts with the results from ENDOR spectroscopy that show that the H2 ligand freely rotates about the Co‒H2 axis in frozen solution. Finally, the (TPB)Fe system, as well as related tris-phosphino-iron complexes that contain a different apical ligand unit (Si, PhB, C, and N) in place of the boron in (TPB)Fe, were studied for CO2 hydrogenation chemistry. The (TPB)Fe system is not catalytically competent, while the silicon, borate, carbon variants, (SiPR3)Fe, (PhBPiPr3)Fe, and (CPiPr3)Fe, respectively, are catalysts for the hydrogenation of CO2 to formate and methylformate. The hydricity of the CO2 reactive species in the silatrane system (SiPiPr3)Fe(N2)(H) has been experimentally estimated.

Item Type:Thesis (Dissertation (Ph.D.))
Subject Keywords:Metallaboratrane; hydrogenation catalysis; inorganic chemistry; carbon dioxide
Degree Grantor:California Institute of Technology
Division:Chemistry and Chemical Engineering
Major Option:Chemistry
Thesis Availability:Public (worldwide access)
Research Advisor(s):
  • Peters, Jonas C.
Group:Joint Center for Artificial Photosynthesis
Thesis Committee:
  • Agapie, Theodor (chair)
  • Gray, Harry B.
  • Reisman, Sarah E.
  • Peters, Jonas C.
Defense Date:5 December 2014
Record Number:CaltechTHESIS:12152014-181907516
Persistent URL:http://resolver.caltech.edu/CaltechTHESIS:12152014-181907516
DOI:10.7907/Z9TX3C9P
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1021/om400281vDOIArticle adapted for ch. 2
http://dx.doi.org/10.1021/ja508117hDOIArticle adapted for ch. 3
http://dx.doi.org/10.1021/ic502508pDOIArticle adapted for ch. 4
Default Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:8746
Collection:CaltechTHESIS
Deposited By: Henry Fong
Deposited On:19 Dec 2014 19:20
Last Modified:30 Aug 2018 18:01

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