162463-15-2

Upstream product

• 122-78-1 phenylacetaldehyde 
• 4704-99-8 α,α,α-tris(hydroxymethyl)toluene 
• 162463-14-1 α,α,α-tris<(4-tolylsulfonyl)methyl>toluene 

Downstream Products

• 866775-55-5 α,α,α-tris[((triphenylphosphoranylidene)amino)methyl]toluene 
• 866775-56-6 α,α,α-tris[((tricyclopentylphosphoranylidene)amino)methyl]toluene 
• 162463-16-3 α,α,α-tris(aminomethyl)toluene 

Relevant academic research and scientific papers

New polypodal polycarboxylic ligands - Complexation of rare-earth ions in aqueous solution

The complexation ability of new polypodal carboxylic ligands prepared from 2,2-bis(hydroxymethyl)-1-alkanols was investigated in aqueous solution with Y3+ and various lanthanide ions (La3+, Sm3+, Eu3+, Gd3+, Tb3+, Dy3+). The values of the stability constants for ML complexes are of the order of 104 for the hexadentate trioxypropionates, 107 for the hexadentate trioxyacetates and 1014 for the nonadentate triaminohexaacetates. In these systems, the nitrogens of the amino groups seem to be better chelating atoms than the oxygens of the ether groups. The hydration numbers of dysprosium(III) complexes have been determined from the DyIII-induced 17O NMR water shifts.

A new tripodal ligand system based on the iminophosphorane functional group. Part 1: Synthesis and characterization

Two tripodal alcohols, viz., 1,1,1-tris(hydroxymethyl)ethane and α,α,α-tris(hydroxymethyl)toluene were converted by an efficient multi-step pathway involving azide formation into the corresponding tris(iminophosphorane) scaffolds bearing cyclopentyl (Cp)

Tripodal Triamidostannates as Building Blocks in the Generation of Sn-M-Bonded Heterobimetallics (M = Fe, Ru)

By in situ lithiation of the trifunctional amines H3CC(CH2NHSiMe3)3, PhC(CH2NHSiMe3)3 and HC3 and subsequent reaction with SnCl2 the corresponding triamidostannates were obtained.These were coupled with CpM(CO)2Cl (M = Fe, Ru) to yield t