Structural characterization and electrochemical properties of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone.
Mehmet Tümer, Mehmet Aslantaş, Ertan Sahin, Nihal Deligönül
Index: Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 70(3) , 477-81, (2008)
Full Text: HTML
Abstract
Crystals of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone (TTBDQ) in the reaction mixture DCM/MeOH (1:1, v/v) were obtained as a result of CC coupling reaction of the sterically hindered phenol (2,6-di-tert-butylphenol, DTBP) using the binuclear Co(II) complexes. The oxidation product (TTBDQ), C(28)H(40)O(2), crystallizes in the space group P1 with one-half molecule in the asymmetric unit and the other half generated by an inversion centre. The diphenoquinone moiety is planar within +/-0.016(3)A. The crystal structure is stabilized by intramolecular C-H...O hydrogen bonds. The spectroscopic and electrochemical properties of the TTBDQ also have been studied.
Related Compounds
Related Articles:
2005-11-17
[J. Med. Chem. 48 , 7234-42, (2005)]
2009-04-15
[Bioorg. Med. Chem. 17 , 3207-11, (2009)]
Antioxidant activity of propofol and related monomeric and dimeric compounds.
2005-03-01
[Chem. Pharm. Bull. 53(3) , 344-6, (2005)]
2003-03-01
[Eur. J. Anaesthesiol. 20(3) , 220-4, (2003)]
1996-02-01
[Dokl. Akad. Nauk. 346(5) , 705-7, (1996)]