نتایج جستجو برای: triethyl orthoesters
تعداد نتایج: 511 فیلتر نتایج به سال:
In the crystal structure of the title compound, C(14)H(11)NO(3), isolated from the reaction of 2-bromo-1-phenyl-ethanone and pyridine-4-carboxylic acid using triethyl-amine as a base to deprotonate the organic acid, the mol-ecular packing is stabilized by C-H⋯π inter-actions involving the phenyl and pyridine rings. The C-C-O-C torsion angle for the linkage between the two carbonyl groups is -80...
A simple, rapid and precise reverse phase high performance liquid chromatography method was developed for the analysis of Almotriptan. Chromatographic separation of Almotriptan was performed by using a kromosil C18 column (250 x 4.6mm, 5 μm) as stationary phase with a mobile phase comprising of 1% Triethyl amine : acetonitrile:methanol: 05:55:40 (v/v) at a flow rate of 1.0ml/min and UV detectio...
The title fluoridogermanate, {[Cd(2)(C(6)H(18)N(4))(3)][GeF(6)]}(n), was synthesized hydro-thermally. The crystal structure comprises undulated cationic [Cd(2)(TETA)(3)](4+) chains (TETA is triethyl-ene-tetra-mine) propagating parallel to [101]. The central Cd(II) atom is six-coordinated in a CdN(6) set by three TETA ligands. The isolated [GeF(6)](2-) units, serving as counter-anions, occupy th...
Equilibrium constants have been determined for the formation of 15 different zirconocene monomethyl monochloro complexes from the respective dichloride complexes and AI2 (CH3)6' The results indicate that the tendency of a particular zirconocene complex to exchange a chloride against a methyl ligand is a measure for the electron deficiency at its Zr center. The results indicate particularly low ...
In the crystal structure of the title compound, C(6)H(16)N(+)·C(20)H(12)O(4)P(-), an N-H⋯O inter-action links the cation to the anion. The N atom in the triethyl-ammonium cation exhibits a trigonal-bipyramidal coordination geometry and forms an N-H⋯O inter-action with one phosphate O atom of the 1,1'-binaphthyl-2,2'-diyl phosphate ligand. A bifurcated C-H⋯O inter-action with the other phosphate...
The title compound, C(14)H(11)ClN(2)O(3)S, with fused thiophene and pyran rings, was synthesized via the condensation of dihydro-thio-phen-3(2H)-one 1,1-dioxide and 2-(3-chloro-benz-yl-idene)malononitrile catalysed by triethyl-amine in ethanol. The thio-phene ring adopts an envelope conformation and the pyran ring is planar (r.m.s. deviation = 0.0067 Å). The dihedral angle between the pyran and...
The title compound, 2[Ce(C(51)H(75)N(4)O(3))]·C(4)H(10)O, was obtained in high yield (92%) by reduction of (TRENDSAL)Ce(IV)Cl [TRENDSAL is N,N',N''-tris-(3,5-di-tert-butyl-salicyl-ide-natoamino)-triethyl-amine] with potassium in THF. The bulky tripodal TRENDSAL ligand effectively encapsulates the central Ce(III) cation with a Ce-N(imine) distance of 2.860 (2) Å and an average C-N(amine) distanc...
A series of quinoline based imidazolium salts were prepared and characterised as nucleophilic heterocyclic carbene (NHC) ligand precursors. The symmetrically saturated imidazolium salt prepared by ring closure of achiral tetradentate diquinolyl-diamine with triethyl orthoformate is a tridentate ligand and can function as pincer ligand while the two asymmetric imidazolium salts are bidentate and...
The potential tridentate Schiff base ligand 2-[1-(2-pyridyl-methyl-imino)eth-yl]pyrrole (HL) was synthesized from the condensation of 2-acetyl-pyrrole with 2-amino-methyl-pyridine. The title compound, [Cu(C(12)H(12)N(3))Cl], was synthesized from HL and copper(II) chloride using triethyl-amine as a base to deprotonate the pyrrole NH group. The title compound is a monomer and the central copper(I...
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