scholarly journals Synthesis and Characterization of Chloridobis(dimethylglyoximato)4-(2-ferrocenylvinyl)pyridinecobalt(III): A New Heterobinuclear Cobaloxime

2016 ◽  
Vol 2016 ◽  
pp. 1-5 ◽  
Author(s):  
Sebastián Pizarro ◽  
Guillermo Saá ◽  
Francisco Gajardo ◽  
Alvaro Delgadillo

The synthesis of a new heterobinuclear cobaloxime with 4-(2-ferrocenylvinyl)pyridine, fcvpy, is reported. The complex [CoCl(dmgH)2(fcvpy)], where dmgH2is dimethylglyoxime and dmgH is dimethylglyoximato, has been characterized by1H-NMR, UV-Vis, cyclic voltammetry, and elemental analysis. The cyclic voltammogram of this complex shows a fc/fc+reversible wave at +0.58 V versus Ag/AgCl, one irreversible wave,Epc= −0.54 V versus Ag/AgCl, assigned to the reduction of Co(III) to Co(II), and two quasireversible processes at −1.02 V and −1.10 V versus Ag/AgCl associated with the reduction of Co(II). The complex showed ferrocene-ligand charge transfer bands at 334 nm and 505 nm. TDDFT/B3LYP/6-31G(d) calculations support this assignation.

2011 ◽  
Vol 335-336 ◽  
pp. 989-993
Author(s):  
Mi Ouyang ◽  
Zhen Wei Yu ◽  
Yi Xu ◽  
Yu Jian Zhang ◽  
Cheng Zhang

Copolymers based on 1, 4-diethoxybenzene (DEB) and 3, 4-ethylenedioxythiophene (EDOT) were electrochemically synthesized and characterized. The structures of the copolymers were established by 1H NMR and FT-IR spectroscopy. The results indicated the final product was a copolymer instead of a blend or a composite. The physical properties were systematically investigated by cyclic voltammetry, UV-vis absorption and fluorescence. The PL maximum of copolymers presented obviously red-shift to long wavelength as the feed ratio of EDOT in monomer mixture increased.


2012 ◽  
Vol 476-478 ◽  
pp. 1322-1326
Author(s):  
Xiao Yu Jiang ◽  
Jin Chen ◽  
Wen Zhe Chen

Nanoscale lanthanum cobaltite with perovskite-type was successfully synthesized by microwave irradiation directly and was characterized by XRD, SEM, XPS and BET analysis. The results show that the size of particle was 18 nm averagely, the surface area to be 31.0 m2 g−1. The electrochemical properties were studied by cyclic voltammetry and steady state polarization. The cyclic voltammogram between 0 and 0.55 V exhibited two pairs of redox peaks prior to the onset of O2 evolution in 1 mol dm−3 KOH. The Tafel slope and the reaction order with respect to concentration of OH− were found to be 60 mV decade−1 and ca. 1, respectively.


1986 ◽  
Vol 64 (4) ◽  
pp. 751-759 ◽  
Author(s):  
Daniel Cozak ◽  
Abdelhakim Mardhy ◽  
André Morneau

The reaction of CpTi(CO)2 (1), Cp2TiCl (2), and Cp2TiCl2 (3) (Cp = η5-C5H5) with purine (PuH) and adenine (AdH) in organic solvents is described. The compound 1 reacts with both molecules in an oxidative fashion giving Cp2Ti(C5H3N4)(C5H4N4) (4) and (Cp2Ti)2(C5H3N5) (5) with concomitant liberation of molecular carbon monoxide and hydrogen (4:1) following a first order rate law in metal complex. The compound 2 forms an adduct compound Cp2TiCl(C5H4N4) (6) with PuH. Monosubstituted derivatives Cp2TiCl(C5H3N4) (7) and Cp2TiCl(C5H4N5) (8) are formed from the reaction of the deprotonated bases with 3. In addition to the usual elemental analysis, the characteristic ir, 1H nmr, epr, and ms results are given for the new compounds.


2001 ◽  
Vol 05 (04) ◽  
pp. 367-375 ◽  
Author(s):  
S. ZEKİ YILDIZ ◽  
HALTİ KANTEKİN ◽  
YAŞAR GÖK

New metal-free 5 and metallophthalocyanines 6-11( M = Cu , Ni , Co , Pb , Zn ) fused in peripheral positions with four 24-membered tetraoxatetraaza macrocycles were prepared by cyclotetramerization of 24,25-dicyano-4,10,13,17-tetra(toluene-p-sulfonyl)-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22-didicontinehydrobenzo[y][3,9,12,18]tetraaza[1,7,16,22]tetraoxatetradicontine in the presence of the corresponding metal salt or a strong organic base. While the N-tosylated derivatives of the phthalocyanines are soluble in common organic solvents, the detosylated derivative of copper phthalocyaninate is soluble in water. The aggregation properties of the phthalocyanines were also investigated as a function of concentration, solvent and oxidative medium. The new compounds are characterized by a combination of elemental analysis and 1 H NMR, 13 C NMR, IR, UV-vis and MS spectral data.


2006 ◽  
Vol 60 (2) ◽  
Author(s):  
Y. Xuwu ◽  
S. Wujuan ◽  
K. Congyu ◽  
Z. Li ◽  
Z. Hangguo ◽  
...  

AbstractSeven rare-earth complexes with salicylic acid RE(HSal)3·nH2O (HSal = C7H5O3; RE = La-Sm, n = 2; RE = Eu, Gd, n = 1) were synthesized and characterized by elemental analysis, the IR spectrum, and cyclic voltammetry. The constant-volume combustion energies of complexes, Δc U, were determined by a precise rotating-bomb calorimeter at 298.15 K. Their standard molar enthalpies of combustion, Δc H mo, and standard molar enthalpies of formation, Δf H mo, were calculated.


2001 ◽  
Vol 05 (10) ◽  
pp. 717-720 ◽  
Author(s):  
M. S. AǦIRTAŞ ◽  
Ö. BEKAROǦLU

The synthesis of new metal-free and zinc(II), cobalt(II) phthalocyanines substituted with four 4-(2-N'-cyanoethyl)aminoethylsulfanyl groups is described. The new compounds have been characterized by elemental analysis and IR, 1 H NMR and UV-vis spectroscopy.


1999 ◽  
pp. 1749-1750 ◽  
Author(s):  
Kevin D. Ley ◽  
Yiting Li ◽  
Jodie V. Johnson ◽  
David H. Powell ◽  
Kirk S. Schanze

2013 ◽  
Vol 781-784 ◽  
pp. 1003-1006
Author(s):  
He Ping Yan ◽  
Gui Ping Ouyang

Four compounds of 7-(3- (substituted-phenoxy) propoxy) quinazoline compounds, including 7-(3-(2,4-dichlorophenoxy) propoxy)-N-(3-chlorophenyl)-6-methoxyquinazolin-4-amine, 7-(3-(2-chlo-rophenoxy) propoxy)-N-(3-chlorophenyl)-6-methoxyquinazolin-4-amine, 7-(3-(4-chlorophenoxy) prop-oxy)-N-(3-chlorophenyl)-6-methoxyquinazolin-4-amine, 7-(3-(naphthalen-3-yloxy) propoxy)-N-(3-chl-orophenyl)-6-methoxyquinazolin-4-amine, were synthesized fromN-(5-(3-chloropropoxy)-2-cyano-4-methoxyphen-yl)-N, N-dimethylformamidine by cyclization,etheration, in the yield of 45.9%50.6%56.34% and 80.6% respectively. Their structures were characterized by IR,1H NMR,13C NMR, MS and elemental analysis.


2011 ◽  
Vol 277 ◽  
pp. 112-119 ◽  
Author(s):  
Mochamad Chalid

As diols, N,N'-1,2-ethanediylbis-(4-hydroxy-pentanamide) (1) and 4-hydroxy-N-(2-hydroxyethyl)-pentanamide (2)) are versatile precursors for the manufacture of bio-polymers. Polymer design, by exploiting the variation in structure of both diol and di-isocyanate monomers, such as backbone structure and presence of functional groups, appears to be a promising biopolymer engineering pathway to synthesize polyurethanes. Both diols (1) and (2) were then polymerized by reaction with aliphatic and aromatic di-isocyanates at 140 °C in (N,N-dimethylacetamide (DMA) solvents using triethylamine (TEA) catalysts, to obtain novel polyurethanes. The products were characterized by FTIR, 1H-NMR, 13C-NMR, and Elemental Analysis. This working has created a new chance to synthesis bio-polyurethanes based on levulinic acid, as one of biomass compounds


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