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1,1,4,7,7-pentamethyldiethylenetriamine PMDT

A similar example is given by Whitney et al. [420] who have shown that addition of 1,1,4,7,7-pentamethyldiethylenetriamine (PMDT) even produces sufficiently conductive solutions of Hthium salts in toluene, in which the lithium salts are scarcely soluble. [Pg.593]

The dimethylaurate(I) anion was more readily isolated (9) when the lithium ion was complexed with pentamethyldiethylenetriamine (PMDT) [Eq. (2)]. The greater thermal stability of these complexes compared with their phosphine analogs was explained in terms of less-ready ligand dissociation and complexation of the lithium ion, preventing its attack at the gold center. [Pg.41]

N,N, N",N"-Pentamethyldiethylenetriamine CAS 3030-47-5 EINECS/ELINCS 221-201-1 Synonyms Bis-[2-(dimethylamino)ethyl] methylamine N-(2-Dimethylaminoethyl)-N,N, N -trimethyl-ethane-1,2-diamine Pentamethyidiethylenetriamine N,N,N, N, N"-Pentamethyldiethylenetriamine PMDT Classification Nonaromatic amine Empirical C9H23N3 Formula [(CH3)2NCH2CH2]2NCH3 Properties Colorless to pale yel. liq. strong ammoniacal odor sol. in water, phosphoric acid, ethylene glycol, most aq. acids and bases m.w. 173.30 dens. 0.830 m.p. < 20 C b.p. 198 C flash pt. 53 C ref. index 1.4420 (20 C)... [Pg.3240]

Crassous et al.177) studied the polymerization of ethylene using n-butyllithium in conjunction with the tertiary diamines TMEDA, TEEDA (tetraethylethylenedi-amine) and PMDT (pentamethyldiethylenetriamine). In contrast to the situation with TMEDA the rate of polymerization was found to show a first order dependence upon the complexed chain end concentration. Steric hindrance seems to prevent the dimerization of the chain ends. Examination of the n-BuLi. TEEDA complex by -NMR shows that the displacement to high field of the protons a to the lithium induced by complexation is much smaller with TEEDA than with TMEDA or PMDT. With [TEEDA] < [RLi] time-averaged signals were obtained showing that the exchange process... [Pg.37]

TMED tetramethylethylenediamine PMDT pentamethyldiethylenetriamine iso-HMTT tris- (0-dimethylaminoethyl) amine HMTP heptamethyltetraethylenepentamine OMPH octamethylpentaethylenehexamine Two examples of chelated organosodium compounds are shown in Figure 1. [Pg.210]

PMA. See Polymaleic acid Propylene glycol methyl ether acetate PMAA. See Polymethacrylic acid PMAA, sodium salt. See Sodium polymethacrylate PM acetate. See Propylene glycol methyl ether acetate PMDT. See N,N, N",N"-Pentamethyldiethylenetriamine PMM PMMA. See Polymethyl methacrylate PnB. See Butoxypropanol PO-dimsthylsiloxane-PO block copolymer CAS 161755-53-9... [Pg.2344]


See other pages where 1,1,4,7,7-pentamethyldiethylenetriamine PMDT is mentioned: [Pg.603]    [Pg.206]    [Pg.271]    [Pg.14]    [Pg.271]    [Pg.540]    [Pg.3391]    [Pg.603]    [Pg.174]   
See also in sourсe #XX -- [ Pg.593 ]




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PMDT

Pentamethyldiethylenetriamine

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