Search results for "Diamine"

CCDC 917250: Experimental Crystal Structure Determination

2013

Related Article: A.B.Djamaa,M.Clemente-Leon,E.Coronado,M.Lopez-Jorda|2013|Polyhedron|64|142|doi:10.1016/j.poly.2013.03.015

CCDC 984093: Experimental Crystal Structure Determination

2014

Related Article: Pallab Bhowmik, Saptarshi Biswas, Shouvik Chattopadhyay, Carmen Diaz, Carlos J. Gómez-García, Ashutosh Ghosh|2014|Dalton Trans.|43|12414|doi:10.1039/C4DT00328D

1967

Optically active polyamides with regular structural sequences have been prepared from L-lysine and adipic acid. A novel optically active symmetrical diamine, N.N'-bis(L-5-amino-5-carboxyl-amyl)adipamide, was obtained by treating L-lysine with adipyl chloride in the presence of copper(II) ions. The interfacial polycondensation of this diamine with adipyl chloride afforded a regular polymer, while the polycondensation of L-lysine with adipyl chloride gave an irregular polymer of the same analytical composition. The melting points, optical rotations and the optical rotatory dispersions of these polymers were investigated. Optisch aktive Polyamide mit regelmasiger Struktur wurden aus L-Lysin un…

Stability−Charge and Stability−Structure Relationships in the Binding of Dicarboxylic Ligands by Open-Chain Polyammonium Cations

2000

The stability of complexes formed by 5 dicarboxylic ligands with 11 open-chain polyammonium cations (40 systems) was studied potentiometrically, in aqueous solution, at 25 °C. In all the systems ALHr species (A = amine, L = dicarboxylic ligand, r = 1 ... n; diamines n = 3, triamines n = 4, tetraamines n = 4 or 5) were found. Formation constants for the various complexes studied in this work, together with data for the analogous systems previously studied (20 systems), were examined as a function of charges involved in the formation reaction and of the structure of both the dicarboxylic ligand and the polyammonium cation. Structure generally has little effect on stability, while charges play…

An ionene with spirane structure (spiroionene)

1990

The secondary diamine 1,3,5,7-tetrahydro[1,2c:4,5c'] benzodipyrrole (3) and 1,2,4,5-tetrabromomethylbenzene (1) form a polymeric ionene with spirane structure through a repetitive alkylation reaction. The structure of the product could be proven by13C-NMR spectroscopy by comparison with suitable reference compounds. Solutions in aqueous methanol exhibit a typical polyelectrolyte effect. Variation of the counterions produces sufficient solubility in organic solvents. From the crystal structure of a similar model compound one can conclude that the synthesized polymer has a rod-like shape.

ChemInform Abstract: 1-Alkyl- and Azeto[1,2-a][1,5]benzodiazepine Derivatives in the Reaction of o-Phenylenediamine with 3-(Dimethylamino)propiopheno…

2001

The reaction of o-phenylenediamine (4) with one, two or three equivalents of p-substituted 3-dimethylaminopropiophenone hydrochlorides 5a−e was studied. 4-Aryl-2,3-dihydro-1H-1,5-benzodiazepine derivatives 6a−e were obtained in good yields, along with the 1:2-adducts 7c−e and the unexpected 1:3-adducts rac-8c−e. The type of adduct formed is determined by the molar ratio of the reactants 4 and 5 and by the nature of the substituent in the para position of the propiophenone 5.

Novel diamine-bis(phenolate) Ti(IV) complexes – tuning the complex structure to control catalytic properties in α-olefin polymerization

2016

Abstract Four monomeric titanium(IV) dichloride complexes of amine-bis(phenolate) ligands having an extra donor arm (2a–2d) and one oxo-bridged complex 3 were successfully synthesized in the reaction of TiCl4 with a sodium salt of the appropriate ligand, and they were characterized by 1H NMR spectroscopy. The ligands had either a dimethylamino side‐arm donor and t-Bu substituents on both (1a) and one (1d) phenolate rings or a diisopropylamino side-arm donor and t-Bu (1b) and t-Bu along with OMe (1c) phenolate substituents. All complexes upon activation with [Ph3CB(C6F5)4] and MAO were used to catalyze polymerization of 1-octene (in liquid monomer) into poly(1-octene). Their activities as we…

Effect of ethylenediamine on the anodic stripping voltammetric determination of heavy metals in the presence of humic acid

1994

Ligand competition coupled with differential pulse anodic stripping voltammetry has been investigated for the determination of copper, lead and cadmium. Ethylenediamine displaces humic acid in its metal complexes forming kinetically labile compounds. It also eliminates interferences associated with the oxidation of copper. This enhances the sensitivity of the determination of the metals over a wide range of humic acid concentration (up to 30 mg/l). The procedure has been applied to the determination of heavy metals in a real water sample.

Studien zum Vorgang der Wasserstoffübertragung, 45. Elektroreduktion aromatischer Carbonsäureester

1977

Bei der Elektroreduktion der Benzoesaureester 1 in Alkoholen an einer Quecksilberkathode mit quartare Ammoniumleitsalzen entsteht ein Gemisch von partiell kernhydrierten Reaktionsprodukten und Benzylalkohol (Tabelle 3). Elektroreduziert man jedoch in Gegenwart von Essigsaure, so wird die Kernhydrierung vollstandig unterdruckt und es entstehen ca. 70% Benzylalkohol (3) neben ca. 30% 1,2-Diphenylethylenglykol (9) als Hydrodimerem (Tabelle 4). Benzoesaure-phenylester (2h) wird nahezu ausschlieslich zu Benzylalkohol (3) elektroreduziert; Substituenten an der Benzoesaure (Verbindungen 2a-i) verandern diesen Reaktionsablauf nicht, wenn in Gegenwart von Essigsaure gearbeitet wird (Tabelle 8).Gleic…

Helicate Extension as a Route to Molecular Wires

2008

We describe the preparation of a helicate containing four closely spaced, linearly arrayed copper(I) ions. This product may be prepared either directly by mixing copper(I) with a set of precursor amine and aldehyde subcomponents, or indirectly through the dimerization of a dicopper(I) helicate upon addition of 1,2-phenylenediamine. A notable feature of this helicate is that its length is not limited by the lengths of its precursor subcomponents: each of the two ligands wrapped around the four copper(I) centers contains one diamine, two dialdehyde, and two monoamine residues. This work thus paves the way for the preparation of longer oligo- and polymeric structures. DFT calculations and elec…