Advancing frontiers in reactive and selective iridium c-h borylation catalysis and targeted silsesquioxane synthesis
The studies in this dissertation are aimed at uncovering reactive and selective Ir-catalyzed C-H borylation (CHB) catalysts. Due to the high versatility of organoboron species, green methodology to produce the C-B bond is poised to support a myriad of subsequent transformations. These transformations include Suzuki couplings, aminations, oxidations, halogenations, cyanations, and trifluoromethylations.Typical iridium catalyzed CHBs proceed through an iridium trisboryl with a bidentate ligand such as bipyridine or 1,10-phenanthroline. The selectivity of these standard catalysts is generally driven by sterics; however, many methods of overcoming the steric bias have been developed in the two decades since the first thermal catalytic C-H activation borylation. These methods include both inner- and outer-sphere directed mechanisms. Outer-sphere directed borylations have been accomplished by leveraging hydrogen bonding, Lewis acid-base, and ion-pairing as directing elements. In general this reactivity is activated by precise design of the bidentate ligand framework.Herein is reported a subtle electrostatic interaction to direct ortho-borylation of phenols by simply switching boron source from the common B2pin2 (pin = pinacolate) to B2eg2 (eg = ethyleneglycolate). This electrostatic interaction was revealed by a careful computational analysis of key C-H activation transition states. Understanding gained by the computational studies led to the redesign of the boron source which enabled by selectivities of > 99% ortho borylation. This methodology was extended to the highly selective ortho-borylation of anilines, and the underlying mechanism has been interrogated.Currently, iridium based catalysts have been generated to borylate ortho, meta, and even para to a variety of classes of substrates; however, control of selectivity can breakdown in many fluorinated arenes without a directing group. These substrates are challenging because the fluoro moiety being similar in size to a hydrogen offers little in the way of steric bias. While working to overcome these challenges, a serendipitously discovered hydrazone based ligand was discovered. Exploration of the catalysts generated by this ligand revealed not only impressive activity rivaling dtbpy but also incredible selectivity for meta to a fluoro group.In general iridium CHB catalysts selectively activate sp2 C-H bonds leaving all sp3 C-H bonds intact; however, a method to turn on sp3 C-H activation would be desirable. It was reasoned that a directing group able to increase the effective concentration of the iridium catalyst near a C(sp3)-H bond may enable this transformation. Indeed, it was discovered that catalysts able to accept amide directing groups were able to selectively borylate compounds with amide N-methyl substituents.
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- In Collections
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Electronic Theses & Dissertations
- Copyright Status
- Attribution-NonCommercial-ShareAlike 4.0 International
- Material Type
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Theses
- Authors
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Dannatt, Jonathan E.
- Thesis Advisors
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Maleczka, Robert E.
- Committee Members
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Borhan, Babak
Smith, Milton R.
Wulff, William D.
- Date Published
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2019
- Program of Study
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Chemistry - Doctor of Philosophy
- Degree Level
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Doctoral
- Language
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English
- Pages
- xix, 501 pages
- ISBN
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9781085673259
1085673251
- Permalink
- https://doi.org/doi:10.25335/hv2a-8r78