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The Coordination Chemistry of “[BP_3]NiX” Platforms: Targeting Low-Valent Nickel Sources as Promising Candidates to L_3Ni=E and L_3Ni≡E Linkages

MacBeth, Cora E. and Thomas, J. Christopher and Betley, Theodore A. and Peters, Jonas C. (2004) The Coordination Chemistry of “[BP_3]NiX” Platforms: Targeting Low-Valent Nickel Sources as Promising Candidates to L_3Ni=E and L_3Ni≡E Linkages. Inorganic Chemistry, 43 (15). pp. 4645-4662. ISSN 0020-1669. doi:10.1021/ic049936p. https://resolver.caltech.edu/CaltechAUTHORS:20140804-151216151

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Abstract

A series of divalent, monovalent, and zerovalent nickel complexes supported by the electron-releasing, monoanionic tris(phosphino)borate ligands [PhBP_3] and [PhBP^(iPr)_3] ([PhBP_3] = [PhB(CH_2PPh_2)_3]-, [PhBP^(iPr)_3] = [PhB(CH_2PiPr_2)_3]-) have been synthesized to explore fundamental aspects of their coordination chemistry. The pseudotetrahedral, divalent halide complexes [PhBP_3]NiCl (1), [PhBP_3]NiI (2), and [PhBP^(iPr)_3]NiCl (3) were prepared by the metalation of [PhBP_3]Tl or [PhBP^(iPr)_3]Tl with (Ph_3P)_2NiCl_2, NiI_2, and (DME)NiCl_2 (DME = 1,2-dimethoxyethane), respectively. Complex 1 is a versatile precursor to a series of complexes accessible via substitution reactions including [PhBP_3]Ni(N_3) (4), [PhBP_3]Ni(OSiPh_3) (5), [PhBP_3]Ni(O-p-tBu-Ph) (6), and [PhBP_3]Ni(S-p-tBu-Ph) (7). Complexes 2−5 and 7 have been characterized by X-ray diffraction (XRD) and are pseudotetrahedral monomers in the solid state. Complex 1 reacts readily with oxygen to form the four-electron-oxidation product, {[PhB(CH_2P(O)Ph_2)_2(CH_2PPh_2)]NiCl} (8A or 8B), which features a solid-state structure that is dependent on its method of crystallization. Chemical reduction of 1 using Na/Hg or other potential 1-electron reductants generates a product that arises from partial ligand degradation, [PhBP_3]Ni(η^2-CH_2PPh_2) (9). The more sterically hindered chloride 3 reacts with Li(dbabh) (Hdbabh = 2,3:5,6-dibenzo-7-azabicyclo[2.2.1]hepta-2,5-diene) to provide the three-coordinate complex [κ^2-PhBP^(iPr)_3]Ni(dbabh) (11), also characterized by XRD. Chemical reduction of complex 1 in the presence of L-type donors produces the tetrahedral Ni(I) complexes [PhBP_3]Ni(PPh_3) (12) and [PhBP3]Ni(CNtBu) (13). Reduction of 3 following the addition of PMe_3 or tert-butyl isocyanide affords the Ni(I) complexes [PhBP^(iPr)_3]Ni(PMe_3) (14) and [PhBP^(iPr)_3]Ni(CN^tBu) (15), respectively. The reactivity of these [PhBP_3]Ni^IL and [PhBP^(iPr)_3]NiI^L complexes with respect to oxidative group transfer reactions from organic azides and diazoalkanes is discussed. The zerovalent nitrosyl complex [PhBP_3]Ni(NO) (16) is prepared by the reaction of 1 with excess NO or by treating 12 with stoichiometric NO. The anionic Ni(0) complexes [[κ^2-PhBP_3]Ni(CO)_2][^nBu_4N] (17) and [[κ^2-PhBP^(iPr)_3]Ni(CO)_2][ASN] (18) (ASN = 5-azoniaspiro[4.4]nonane) have been prepared by reacting [PhBP_3]Tl or [PhBP^(iPr)_3]Tl with (Ph_3P)_2Ni(CO)_2 in the presence of R_4NBr. The photolysis of 17 appears to generate a new species consistent with a zerovalent monocarbonyl complex which we tentatively assign as {[PhBP_3]Ni(CO)}{^nBu_4N}, although complete characterization of this complex has been difficult. Finally, theoretical DFT calculations are presented for the hypothetical low spin complexes [PhBP_3]Ni(N^tBu), [PhBP^(iPr)_3]Ni(N^tBu), [PhBP^(iPr)_3]Ni(NMe), and [PhBP^(iPr)_3]Ni(N) to consider what role electronic structure factors might play with respect to the relative stability of these species.


Item Type:Article
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http://pubs.acs.org/doi/abs/10.1021/ic049936pPublisherArticle
http://dx.doi.org/10.1021/ic049936pDOIArticle
http://pubs.acs.org/doi/suppl/10.1021/ic049936p/suppl_file/ic049936psi20040115_124544.pdfPublisherSupporting Information
http://pubs.acs.org/doi/suppl/10.1021/ic049936p/suppl_file/ic049936psi20040115_124736.cifPublisherSupporting Information
ORCID:
AuthorORCID
Peters, Jonas C.0000-0002-6610-4414
Additional Information:© 2004 American Chemical Society. Received January 15, 2004. Publication Date (Web): June 25, 2004. We acknowledge the DOE (PECASE) and the NSF (CHE-0132216) for financial support of this work. Larry Henling, Smith Nielsen, and Eric Peters provided technical assistance. We are grateful to Professors Peter T. Wolczanski and Daniel Rabinovich for providing insightful discussions. We also thank Professor Clifford Kubiak for disclosing results prior to publication. The Beckman Institute Senior Research Fellows Program (CEM), the Moore Foundation (J.C.T.), the NSF (J.C.T.), and the DOD (T.A.B.) are each acknowledged for fellowship support.
Funders:
Funding AgencyGrant Number
Department of Energy (DOE)UNSPECIFIED
NSFCHE-0132216
Beckman Institute Senior Research Fellows Program (CEM)UNSPECIFIED
Gordon and Betty Moore FoundationUNSPECIFIED
Department of DefenseUNSPECIFIED
Issue or Number:15
DOI:10.1021/ic049936p
Record Number:CaltechAUTHORS:20140804-151216151
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20140804-151216151
Official Citation:The Coordination Chemistry of “[BP3]NiX” Platforms:  Targeting Low-Valent Nickel Sources as Promising Candidates to L3NiE and L3Ni⋮E Linkages Cora E. MacBeth,J. Christopher Thomas,Theodore A. Betley, and, and Jonas C. Peters Inorganic Chemistry 2004 43 (15), 4645-4662
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:47932
Collection:CaltechAUTHORS
Deposited By: Ruth Sustaita
Deposited On:04 Aug 2014 22:49
Last Modified:10 Nov 2021 17:51

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