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Bis(benzene-1,2-diolato-κ 2 O , O ′)bis(dimethyl sulfoxide-κ O )titanium(IV), [Ti(C 6 H 4 O 2 ) 2 (C 2 H 6 OS) 2 ], crystallizes with two crystallographically independent molecules in the space group P 2 1 / c emulating orthorhombic Pbca symmetry (β = 90.0445 (9)°]. The two molecules are related by pseudo-glide symmetry, broken by modulation of each one catecholate and dimethyl sulfoxide (DMSO) ligand. Twinning by pseudomerohedry was observed [twin ratio 0.5499 (7):0.4401 (7)]. Complex 3 was obtained by heating of diprotonated titanium tris-catecholate precursor 2 H in DMSO, by formal displacement of a catechol molecule by two DMSO molecules. Complex 3 is just the second heteroleptic, mono-nuclear, neutral bis-catecholate complex with TiO 6 metal coordination, the only other one being its bis-DMF analogue 6 . The two molecules of 3 exhibit a distorted octahedral geometry. The geometry and distortions from ideal symmetry of 3 are discussed and compared to 6 and to cationic tris-catecholate titanium complexes.
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Iridium Complexes of a Bis( N -pyrrolyl)boryl/Bis(phosphine) PBP Pincer Ligand
- Award ID(s):
- 2102324
- PAR ID:
- 10559276
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- Inorganic Chemistry
- Volume:
- 63
- Issue:
- 51
- ISSN:
- 0020-1669
- Format(s):
- Medium: X Size: p. 24133-24140
- Size(s):
- p. 24133-24140
- Sponsoring Org:
- National Science Foundation
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