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A Mononuclear and High-Spin Tetrahedral Ti(II) Complex
[Image: see text] A high-spin, mononuclear Ti(II) complex, [(Tp(tBu,Me))TiCl] [Tp(tBu,Me–) = hydridotris(3-tert-butyl-5-methylpyrazol-1-yl)borate], confined to a tetrahedral ligand-field environment, has been prepared by reduction of the precursor [(Tp(tBu,Me))TiCl(2)] with KC(8). Complex [(Tp(tBu,M...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7928263/ https://www.ncbi.nlm.nih.gov/pubmed/33258366 http://dx.doi.org/10.1021/acs.inorgchem.0c02586 |
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author | Reinholdt, Anders Pividori, Daniel Laughlin, Alexander L. DiMucci, Ida M. MacMillan, Samantha N. Jafari, Mehrafshan G. Gau, Michael R. Carroll, Patrick J. Krzystek, J. Ozarowski, Andrew Telser, Joshua Lancaster, Kyle M. Meyer, Karsten Mindiola, Daniel J. |
author_facet | Reinholdt, Anders Pividori, Daniel Laughlin, Alexander L. DiMucci, Ida M. MacMillan, Samantha N. Jafari, Mehrafshan G. Gau, Michael R. Carroll, Patrick J. Krzystek, J. Ozarowski, Andrew Telser, Joshua Lancaster, Kyle M. Meyer, Karsten Mindiola, Daniel J. |
author_sort | Reinholdt, Anders |
collection | PubMed |
description | [Image: see text] A high-spin, mononuclear Ti(II) complex, [(Tp(tBu,Me))TiCl] [Tp(tBu,Me–) = hydridotris(3-tert-butyl-5-methylpyrazol-1-yl)borate], confined to a tetrahedral ligand-field environment, has been prepared by reduction of the precursor [(Tp(tBu,Me))TiCl(2)] with KC(8). Complex [(Tp(tBu,Me))TiCl] has a (3)A(2) ground state (assuming C(3v) symmetry based on structural studies), established via a combination of high-frequency and -field electron paramagnetic resonance (HFEPR) spectroscopy, solution and solid-state magnetic studies, Ti K-edge X-ray absorption spectroscopy (XAS), and both density functional theory and ab initio (complete-active-space self-consistent-field, CASSCF) calculations. The formally and physically defined Ti(II) complex readily binds tetrahydrofuran (THF) to form the paramagnetic adduct [(Tp(tBu,Me))TiCl(THF)], which is impervious to N(2) binding. However, in the absence of THF, the Ti(II) complex captures N(2) to produce the diamagnetic complex [(Tp(tBu,Me))TiCl](2)(η(1),η(1);μ(2)-N(2)), with a linear Ti=N=N=Ti topology, established by single-crystal X-ray diffraction. The N(2) complex was characterized using XAS as well as IR and Raman spectroscopies, thus establishing this complex to possess two Ti(III) centers covalently bridged by an N(2)(2–) unit. A π acid such as CNAd (Ad = 1-adamantyl) coordinates to [(Tp(tBu,Me))TiCl] without inducing spin pairing of the d electrons, thereby forming a unique high-spin and five-coordinate Ti(II) complex, namely, [(Tp(tBu,Me))TiCl(CNAd)]. The reducing power of the coordinatively unsaturated Ti(II)-containing [(Τp(tBu,Me))TiCl] species, quantified by electrochemistry, provides access to a family of mononuclear Ti(IV) complexes of the type [(Tp(tBu,Me))Ti=E(Cl)] (with E(2–) = NSiMe(3), N(2)CPh(2), O, and NH) by virtue of atom- or group-transfer reactions using various small molecules such as N(3)SiMe(3), N(2)CPh(2), N(2)O, and the bicyclic amine 2,3:5,6-dibenzo-7-azabicyclo[2.2.1]hepta-2,5-diene. |
format | Online Article Text |
id | pubmed-7928263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79282632021-03-04 A Mononuclear and High-Spin Tetrahedral Ti(II) Complex Reinholdt, Anders Pividori, Daniel Laughlin, Alexander L. DiMucci, Ida M. MacMillan, Samantha N. Jafari, Mehrafshan G. Gau, Michael R. Carroll, Patrick J. Krzystek, J. Ozarowski, Andrew Telser, Joshua Lancaster, Kyle M. Meyer, Karsten Mindiola, Daniel J. Inorg Chem [Image: see text] A high-spin, mononuclear Ti(II) complex, [(Tp(tBu,Me))TiCl] [Tp(tBu,Me–) = hydridotris(3-tert-butyl-5-methylpyrazol-1-yl)borate], confined to a tetrahedral ligand-field environment, has been prepared by reduction of the precursor [(Tp(tBu,Me))TiCl(2)] with KC(8). Complex [(Tp(tBu,Me))TiCl] has a (3)A(2) ground state (assuming C(3v) symmetry based on structural studies), established via a combination of high-frequency and -field electron paramagnetic resonance (HFEPR) spectroscopy, solution and solid-state magnetic studies, Ti K-edge X-ray absorption spectroscopy (XAS), and both density functional theory and ab initio (complete-active-space self-consistent-field, CASSCF) calculations. The formally and physically defined Ti(II) complex readily binds tetrahydrofuran (THF) to form the paramagnetic adduct [(Tp(tBu,Me))TiCl(THF)], which is impervious to N(2) binding. However, in the absence of THF, the Ti(II) complex captures N(2) to produce the diamagnetic complex [(Tp(tBu,Me))TiCl](2)(η(1),η(1);μ(2)-N(2)), with a linear Ti=N=N=Ti topology, established by single-crystal X-ray diffraction. The N(2) complex was characterized using XAS as well as IR and Raman spectroscopies, thus establishing this complex to possess two Ti(III) centers covalently bridged by an N(2)(2–) unit. A π acid such as CNAd (Ad = 1-adamantyl) coordinates to [(Tp(tBu,Me))TiCl] without inducing spin pairing of the d electrons, thereby forming a unique high-spin and five-coordinate Ti(II) complex, namely, [(Tp(tBu,Me))TiCl(CNAd)]. The reducing power of the coordinatively unsaturated Ti(II)-containing [(Τp(tBu,Me))TiCl] species, quantified by electrochemistry, provides access to a family of mononuclear Ti(IV) complexes of the type [(Tp(tBu,Me))Ti=E(Cl)] (with E(2–) = NSiMe(3), N(2)CPh(2), O, and NH) by virtue of atom- or group-transfer reactions using various small molecules such as N(3)SiMe(3), N(2)CPh(2), N(2)O, and the bicyclic amine 2,3:5,6-dibenzo-7-azabicyclo[2.2.1]hepta-2,5-diene. American Chemical Society 2020-12-01 2020-12-21 /pmc/articles/PMC7928263/ /pubmed/33258366 http://dx.doi.org/10.1021/acs.inorgchem.0c02586 Text en © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Reinholdt, Anders Pividori, Daniel Laughlin, Alexander L. DiMucci, Ida M. MacMillan, Samantha N. Jafari, Mehrafshan G. Gau, Michael R. Carroll, Patrick J. Krzystek, J. Ozarowski, Andrew Telser, Joshua Lancaster, Kyle M. Meyer, Karsten Mindiola, Daniel J. A Mononuclear and High-Spin Tetrahedral Ti(II) Complex |
title | A Mononuclear and High-Spin Tetrahedral Ti(II) Complex |
title_full | A Mononuclear and High-Spin Tetrahedral Ti(II) Complex |
title_fullStr | A Mononuclear and High-Spin Tetrahedral Ti(II) Complex |
title_full_unstemmed | A Mononuclear and High-Spin Tetrahedral Ti(II) Complex |
title_short | A Mononuclear and High-Spin Tetrahedral Ti(II) Complex |
title_sort | mononuclear and high-spin tetrahedral ti(ii) complex |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7928263/ https://www.ncbi.nlm.nih.gov/pubmed/33258366 http://dx.doi.org/10.1021/acs.inorgchem.0c02586 |
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