Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
Thermal catalytic hydrosilylation of conjugated dienes with triethylsilane in the presence of tricarbonyl(o-xylene)metal (metal = Cr, Mo, W) complexes
Date
2001-11-01
Author
Kayran, C
Rouzi, P
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
239
views
0
downloads
Cite This
The thermal catalytic hydrosilylation of 1,3-butadiene (1), trans-2-methyl-1, 3-pentadiene (2), 2,3-dimethyl-1,3-butadiene (3), and isoprene (4), with triethylsilane were studied in the presence of M(CO)(3) (o-xylene) (M = Cr, Mo, W) complexes in polar and nonpolar solvents such as tetrahydrofuran, hexane and toluene. Mo(CO)(3) (o-xylene) was found to be the only active catalyst for the hydrosilylation of 3 with triethylsilane, which gave 1-triethylsilyl-2,3-dimethyl-2-butene (3a), as hydrosilylated product in tetrahydrofuran. The product was identified by means of H-1 and C-13-NMR and GLC. The same catalyst, Mo(CO)(3) (o-xylene), decomposed to MO(CO)(6) without giving hydrosilylated products of 1, 2 and 4 in tetrahydrofuran. M(CO)(3) (o-xylene) (M = Cr, Mo, W) complexes were found to be stable for about 6 h in hexane and toluene, and showed no catalytic activity for the hydrosilylation of 1, 2, 3 and 4.
Subject Keywords
General Chemistry
URI
https://hdl.handle.net/11511/64840
Journal
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES
DOI
https://doi.org/10.1515/znb-2001-1107
Collections
Department of Chemistry, Article
Suggestions
OpenMETU
Core
Experimental investigation of drag reduction effects of polymer additives on turbulent pipe flow using ultrasound Doppler velocimetry
Zeybek Vural, Serife; Bayram, Göknur; Uludağ, Yusuf (The Scientific and Technological Research Council of Turkey, 2014-01-01)
Drag reduction in fully developed turbulent pipe flow with 4 concentrations (200 to 500 wppm or mg/kg) of low molecular weight sodium carboxymethylcellulose (CMC) in aqueous solutions was investigated experimentally. Drag reduction was determined by pressure drop measurements. Maximum drag reduction achieved was 22% using 500 wppm CMC solution. To observe the impact of the presence of CMC on the flow, ultrasound Doppler velocimetry (UDV) was employed to monitor the instantaneous velocity distributions. Expe...
ANODIC POTENTIAL HOMO ENERGY RELATIONS OF FLUORENE DERIVATIVES
SEN, S; CELEBI, N; TURKER, L; Önal, Ahmet Muhtar (Wiley, 1993-09-01)
Anodic oxidation peak potentials (E(p,a)) of some fluorene derivatives were measured on a Pt-degrees electrode versus Ag-degrees/Ag+ in acetonitrile-TBAFB by cyclic voltammetry. The highest occupied molecular orbital (HOMO) energies of the compounds were calculated within the Huckel molecular orbital (HMO) framework. The measured E(p,a) values were correlated to theoretical HOMO energies with a linear regression model.
Voltammetric methods of reboxetine analysis and the mechanism of its electrode reactions
Altunöz Erdoğan, Deniz; Erk, Nevin; Kilic, Esma (Walter de Gruyter GmbH, 2013-05-01)
Reboxetine (RBX) electrochemical redox behavior at hanging mercury drop (HMDE) and glassy carbon electrodes (GCE) was studied in various pH Britton-Robinson universal buffers using cyclic voltammetry and square-wave voltammetry. RBX was reduced at the HMDE and oxidized at the GCE with reversible adsorption controlled and irreversible diffusion controlled processes respectively. The anodic peak is due to the amine and the cathodic peak may correspond to oxygen protonation. An oxidation reaction mechanism is ...
Economic synthesis of quinaldinium fluorochromate(VI), (QnFC), and solvent-free periodic acid oxidation of alcohols catalyzed by QnFC
Özdemir, Melek (The Scientific and Technological Research Council of Turkey, 2014-01-01)
A 1: 1: 1 stoichiometric reaction between CrO3, aqueous HF, and quinaldine affords orange crystalline quinaldinium fluorochromate(VI) (QnFC) (C10H9NH[CrO3F]) in 99.4% isolated yield. A highly efficient, simple, chemoselective, and environmentally benign procedure for QnFC (3 mol%) catalyzed oxidation of primary and secondary alcohols to aldehydes and ketones using 1.1 equiv of H5IO6 under solvent-free conditions is described.
Atom transfer rearrangement radical polymerization of diammine-bis(2,4,6-trihalophenolato)copper(II) complexes in the solid state
Goekagac, Guelsuen; Sonsuz, Muammer; Sen, Fatih; Kisakuerek, Duygu (Walter de Gruyter GmbH, 2006-10-01)
The synthesis of the poly(dichloro- or dibromophenylene oxide)s was achieved by the thermal decomposition of diammine-bis(2,4,6-trihalophenolato)copper(II) complexes in the solid state by atom transfer rearrangement radical polymerization. The thermal decomposition was performed either at different temperature ranges, 110-250 degrees C, for 3 h, or at the maximum conversion temperature for different time intervals, 3-48 h. Maximum yields of polymers were obtained at 190 degrees C and 3 h. The polymers were ...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
C. Kayran and P. Rouzi, “Thermal catalytic hydrosilylation of conjugated dienes with triethylsilane in the presence of tricarbonyl(o-xylene)metal (metal = Cr, Mo, W) complexes,”
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES
, pp. 1138–1142, 2001, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/64840.