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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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.
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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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