Formate complexes of tri- and tetravalent titanium supported by a tris(phenolato)amine ligand. Issue 37 (7th September 2022)
- Record Type:
- Journal Article
- Title:
- Formate complexes of tri- and tetravalent titanium supported by a tris(phenolato)amine ligand. Issue 37 (7th September 2022)
- Main Title:
- Formate complexes of tri- and tetravalent titanium supported by a tris(phenolato)amine ligand
- Authors:
- Okumura, Akira
Ghana, Priyabrata
Fink, Fabian
Schmidt, Regina
Hoffmann, Alexander
Spaniol, Thomas P.
Herres-Pawlis, Sonja
Okuda, Jun - Abstract:
- Abstract : Titanium(iii ) and titanium(iv ) formate complexes supported by the sterically encumbering tris(phenolato)amine ligand (H3 (O3 N) = tris(4, 6-di- tert -butyl-2-hydroxybenzyl)amine) are described. Abstract : Titanium(iii ) and titanium(iv ) formate complexes supported by the sterically encumbering tris(phenolato)amine ligand (H3 (O3 N) = tris(4, 6-di- tert -butyl-2-hydroxybenzyl)amine) are described. Salt metathesis of the chlorido precursor [(O3 N)TiCl] (1-Cl ) with sodium formate in a 2 : 1 ratio in THF gave a dimer of sodium dititanium triformate units with 12-membered ring [Na{(O3 N)Ti}2 (μ-OCHO-η O :η O ′)3 ]2 (3-Na ) when crystallized from acetonitrile. Complex 3-Na was also prepared by reacting the previously reported terminal formate complex [(O3 N)Ti(OCHO)] (2 ) with excess sodium formate. Salt metathesis of 1-Cl with potassium formate gave a tetratitanium cluster of the composition [K3 {(O3 N)Ti}4 (OCHO)7 ] (3-K ) which can be also obtained by treating 2 with potassium formate. In 3-K both Ti and K centers are six-coordinate. The titanium(iii ) complexes [(O3 N)Ti(L)] (4-L, L = THF, THP, Et2 O) and solvent free dimeric [(O3 N)Ti]2 (5 ) were synthesized by reduction of 1-Cl with sodium sand or magnesium in THF, THP, Et2 O, and n -pentane, respectively. The tert -butyl formate adduct of titanium(iii )-[(O3 N)Ti( t BuOCHO)] (6 ) was isolated by reacting 4-L or 5 with tert -butyl formate. Complex 6 is thermolabile and slowly decomposed in solution to produceAbstract : Titanium(iii ) and titanium(iv ) formate complexes supported by the sterically encumbering tris(phenolato)amine ligand (H3 (O3 N) = tris(4, 6-di- tert -butyl-2-hydroxybenzyl)amine) are described. Abstract : Titanium(iii ) and titanium(iv ) formate complexes supported by the sterically encumbering tris(phenolato)amine ligand (H3 (O3 N) = tris(4, 6-di- tert -butyl-2-hydroxybenzyl)amine) are described. Salt metathesis of the chlorido precursor [(O3 N)TiCl] (1-Cl ) with sodium formate in a 2 : 1 ratio in THF gave a dimer of sodium dititanium triformate units with 12-membered ring [Na{(O3 N)Ti}2 (μ-OCHO-η O :η O ′)3 ]2 (3-Na ) when crystallized from acetonitrile. Complex 3-Na was also prepared by reacting the previously reported terminal formate complex [(O3 N)Ti(OCHO)] (2 ) with excess sodium formate. Salt metathesis of 1-Cl with potassium formate gave a tetratitanium cluster of the composition [K3 {(O3 N)Ti}4 (OCHO)7 ] (3-K ) which can be also obtained by treating 2 with potassium formate. In 3-K both Ti and K centers are six-coordinate. The titanium(iii ) complexes [(O3 N)Ti(L)] (4-L, L = THF, THP, Et2 O) and solvent free dimeric [(O3 N)Ti]2 (5 ) were synthesized by reduction of 1-Cl with sodium sand or magnesium in THF, THP, Et2 O, and n -pentane, respectively. The tert -butyl formate adduct of titanium(iii )-[(O3 N)Ti( t BuOCHO)] (6 ) was isolated by reacting 4-L or 5 with tert -butyl formate. Complex 6 is thermolabile and slowly decomposed in solution to produce a formate-bridged mixed-valence titanium(iii )/titanium(iv ) complex [{(O3 N)Ti}2 (μ-OCHO-η O :η O ′)] (7 ) which further decomposed to a mixture containing 2, [(O3 N)Ti(OH)] and [(O3 N)Ti–O–Ti(O3 N)]. All new complexes were isolated in moderate to good yields and fully characterized by elemental analysis, 1 H and 13 C NMR spectroscopy, and single crystal X-ray diffraction analysis. For the titanium(iii ) complexes solution magnetic moments were measured by the Evans method and EPR spectra recorded as toluene glass at 77 K. … (more)
- Is Part Of:
- Dalton transactions. Volume 51:Issue 37(2022)
- Journal:
- Dalton transactions
- Issue:
- Volume 51:Issue 37(2022)
- Issue Display:
- Volume 51, Issue 37 (2022)
- Year:
- 2022
- Volume:
- 51
- Issue:
- 37
- Issue Sort Value:
- 2022-0051-0037-0000
- Page Start:
- 14345
- Page End:
- 14351
- Publication Date:
- 2022-09-07
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2dt01739c ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 23863.xml