99315-94-3

Upstream product

• 4097-89-6 2,2',2''-triaminotriethylamine 
• 90-02-8 salicylaldehyde 
• 1129-30-2 2,6-Diacetylpyridine 

Downstream Products

• 61007-89-4 1:1 manganese(III) complex of N,N',N''-tris[salicylideneaminoethyl]amine 
• 212757-76-1 Al⁽³⁺⁾*CH₃^(1-)*N(HOC₆H₄CHNCH₂CH₂)(OC₆H₄CHNCH₂CH₂)2^(2-)=N(HOC₆H₄CHNCH₂CH₂)(OC₆H₄CHNCH₂CH₂)2Al(CH₃) 
• 142066-86-2 tris(((2-hydroxybenzyl)amino)ethyl)amine 

Relevant academic research and scientific papers

Synthesis, spectral characterization, and luminescence properties of a cup-like ligand and its magnesium(II) complex

A new tripodal ligand, N,N,N-tri(salicylaldehyde)triaminotriethylamine (1) has been synthesized and characterized by elemental analysis, IR and UV spectroscopy, MS, and X-ray crystallography. X-ray diffraction analysis reveals that the three chains of the

Evaluation of trimetallic Ru(II)- and Os(II)-Arene complexes as potential anticancer agents

Schiff-base ligands, tris-2-(salicylaldimine ethyl)amine and tris-2-(2-pyridylimine ethyl)amine (1 and 2) were prepared and complexed to Ru(II) and Os(II) entities to form new trimetallic complexes (3-10). The complexes are air- and moisture-stable and ha

Attemted Functionalisation of a Mononuclear Barium Complex of a 24-Membered Bibracchial Tetraimine Schiff-base Macrocycle derived from Tris(2-aminoethyl)amine using Salicylaldehyde

Functionalisation of a mononuclear barium complex of a 24-membered bibracchial tetraimine Shiff-base macrocycle (L1) derived from the barium-templated cyclocondensation of 2,6-diacetylpyridine and tris(2-aminoethyl)amine was attempted using salicylaldehyde.The reaction leads to the isolation of the tripodal ligand trisamine (L2) and the complex BaL22(CLO4)2.The crystal structures of the parent macrocyclic complex, 1>2(2-) 1/c (no. 14), a = 11.755(7), b = 21.733(17), c = 15.621(15) Angstroem, β = 90.50(7) deg, Z = 4>, and BaL22(CLO4)2 1/c (, no. 14), a = 12.299(15), b = 9.530(15), c = 25.798(32) Angstroem, β = 108.679(9) deg, Z =2> have been determined.

Synthesis and characterization of 5- and 7-donor Schiff base ligands and spectroscopic evidence for tautomerism: A crystal structure showing tautomeric forms within one ligand

An improved method for the synthesis of fifteen Schiff base ligands, of which six are novel, are reported. Optimised yields were obtained and the ligands have been fully characterized via several analytical techniques. It was found that tautomeric forms o

Synthesis, characterization and crystal structure of CD(II) complex with potentially heptadentate Schiff base ligand

(Formula presented) The heptadentate N4O3-type Schiff base was derived from the condensation reaction of salicylaldehyde and tris(2-aminoethyl)amine. The heptadentate Schiff base ligand was characterized by elemental analysis, 1

Synthesis, characterization, and antibacterial activities of Cr(III), Co(III), Ni(II), and Mn(III) complexes of heptadentate Schiff base ligand derived from tris(2-aminoethyl)amine

This is the first study of the antibacterial activity of heptadentate Schiff base ligand (trensal) and its Cr(III), Co(III), Ni(II), and Mn(III) complexes that have been synthesized from the heptadentate Schiff base ligand derived from salicylaldehyde and

A cap-type Schiff base acting as a fluorescence sensor for zinc(ii) and a colorimetric sensor for iron(ii), copper(ii), and zinc(ii) in aqueous media

A simple and low cost chemosensor is described. This sensor could simultaneously detect three biologically important metal ions through fluorogenic (Zn2+) and chromogenic (Fe2+, Cu2+, and Zn2+) methods in aqueou

Encapsulating ruthenium and osmium with tris(2-aminoethyl)amine based tripodal ligands

The reaction of a series of tripodal ligands, H3L1,2 and L3-6, with [M(PPh3)2Cl2] (M = Ru, Os) affords a family of coordination cage compounds of the type [M IIIL1,2]

Benign routes for the syntheses of polydentate Schiff base and their lanthanide complexes

Tris-imine septadentate Schiff base ligand has conveniently made in high yield (～95% or more), when tris(2-aminoethyl)araine condensed with salicylaldehyde using 1:3 molar ratio under solvent free conditions. Lanthanide complexes have also synthesised by

Prochelators triggered by hydrogen peroxide provide hexadentate iron coordination to impede oxidative stress

Prochelators are agents that have little affinity for metal ions until they undergo a chemical conversion. Three new aryl boronate prochelators are presented that are responsive to hydrogen peroxide to provide hexadentate ligands for chelating metal ions.