Carbonyltungsten(0) complexes of acryloylferrocene: Synthesis and characterization

Date

2006-07-15

Author

Boga, Dilek Ayse
Özkar, Saim

Metadata

Show full item record

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

Item Usage Stats

192
views

0
downloads

Photolysis of hexacarbonyltungsten(0) in the presence of acryloylferrocene in n-hexane solution at 10 C yields pentacarbonyl(eta(2)-acryloylferrocene)tungsten(0) (1) as the only photo-substitution product, different from the general reaction pattern observed for the Group 6 metal carbonyls with other olefins. W(CO)5(eta(2)-acryloylferrocene) (1) decomposes in solution to the parent hexacarbonyltungsten(0) and free acryloylferrocene. Trimethylphosphite was introduced as ligand into the molecule to increase the stability. The photolysis of pentacarbonyl(trimethylphosphite)tungsten(0) in the presence of acryloylferrocene in n-hexane solution at 10 degrees C yields only Cis-W(CO)(4)[P(OCH3)(3)](eta(2)-acryloylferrocene) (2) as the monosubstitution product. Both eta(2)-acryloylferrocene complexes (1 and 2) could be isolated and characterized by MS, IR and NMR spectroscopy. The trimethylphosphite complex (2) is found to be even less stable than W(CO)(5)( eta(2)-acryloylferrocene) (1).

Subject Keywords

Physical and Theoretical Chemistry, Inorganic Chemistry, Organic Chemistry, Materials Chemistry, Biochemistry

URI

https://hdl.handle.net/11511/46256

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY

DOI

https://doi.org/10.1016/j.jorganchem.2006.04.003

Collections

Department of Chemistry, Article

Suggestions

OpenMETU
Core

Pentacarbonyl(eta(2)-vinylferrocene)metal(0) complexes of Group 6 elements: synthesis and characterization Özkar, Saim; Demir, N (Elsevier BV, 2003-12-15) Photolysis of hexacarbonylmetal(0) complexes of the Group 6 elements in the presence of vinylferrocene in an n-hexane solution at -15 degreesC yields pentacarbonyl (eta(2)-vinylferrocene)metal(0) complexes as the sole photo-substitution product, different from the general reaction pattern observed for the same Group 6 metal carbonyls with other olefins. M(CO)(5)(eta(2)-vinylferrocene) complexes (M = Cr, Mo, W) could be isolated from the solution and characterized by using spectroscopic techniques. The compl...
Aminophosphine-palladium(II) complexes: Synthsesis, structure and applications in Suzuki and Heck cross-coupling reactions AYDEMİR, MURAT; BAYSAL, AKIN; ŞAHİN, Ertan; Gumgum, Bahattin; Özkar, Saim (Elsevier BV, 2011-11-30) Reaction of furfurylamine with 1 or 2 equivalents of PPh2Cl in the presence of Et3N, proceeds under anaerobic conditions in thf to give furfuryl-2-(N-diphenylphosphino)amine, Ph2PNHCH2-C4H3O, 1 and furfuryl-2-(N,N-bis(diphenylphosphino)amine), (Ph2P)(2)NCH2-C4H3O, 2, respectively. The reactions of 1 and 2 with MCl2(cod) (M = Pd, Pt; cod = 1,5-cyclooctadiene) or Pt(CH3)(2)(cod) yield complexes [M(Ph2PNHCH2-C4H3O)(2)Cl-2] (M= Pd 1a, Pt 1b), [Pt(Ph2PNHCH2-C4H3O)(2)(CH3)(2)] (1c), and [M((Ph2P)(2) NCH2-C4H3O)Cl...
Organosilanols as Catalysts in Asymmetric Aryl Transfer Reactions Özçubukçu, Salih; BOLM, Carsten (American Chemical Society (ACS), 2005-03-01) Various ferrocene-based organosilanols have been synthesized in four steps starting from achiral ferrocene carboxylic acid. Applying these novel planar-chiral ferrocenes as catalysts in asymmetric phenyl transfer reactions to substituted benzaldehydes afforded products with high enantiomeric excesses. The best result (91% ee) was achieved in the addition to p-chlorobenzaldehyde with organosilanol 2b, which has a tert-butyl substituent on the oxazoline ring and an isopropyl group on the silanol fragment.
Electronic absorption and MCD spectra for octacyanometallate complexes M(CN)(8)(n-), M = Mo(IV), W(IV), n=4 and Mo(V), W(V), n=3 Isci, H; Mason, WR (Elsevier BV, 2004-11-15) Electronic absorption and 8.0 T magnetic circular dichroism (MCD) spectra are reported for M(CN)(8)(4-), M = Mo(IV) and W(IV), in aqueous solution and M(CN)(8)(3-), M = Mo(V) and W(V), in acetonitrile solutions. In addition some absorption and MCD spectra are reported for the M(CN), 3- ions embedded in thin poly methyl methacrylate (PMMA) plastic films at temperatures from 295 to 10 K. The temperature dependence of the MCD spectra confirms the presence of C terms. The solution and PMMA spectra for the both ...
Benzaldehyde lyase-catalyzed enantioselective carboligation of aromatic aldehydes with mono- and dimethoxy acetaldehyde Demir, Ayhan Sıtkı; Sesenoglu, O; Dunkelmann, P; Muller, M (American Chemical Society (ACS), 2003-06-12) Benzaldehyde lyase from the Pseudomonas fluorescens catalyzes the reaction of aromatic aldehydes with methoxy and dimethoxy acetaldehyde and furnishes (R)-2-hydroxy-3-methoxy-1-arylpropan-1-one and (R)-2-hydroxy-3,3-dimethoxy-1-arylpropan-1-one in high yields and enantiomeric excess via acyloin linkage. Aromatic aldehydes and benzoins are converted into enamine-carbanion-like intermediates prior to carboligation.

Citation Formats

D. A. Boga and S. Özkar, “Carbonyltungsten(0) complexes of acryloylferrocene: Synthesis and characterization,” JOURNAL OF ORGANOMETALLIC CHEMISTRY, pp. 3293–3297, 2006, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/46256.