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Meso-2,3-Diaminobutane

Five-membered chelate ring of meso-2,3-diaminobutane is puckered with one methyl group equatorial and one axial. [Pg.415]

Table 1. Formation constants of some metal complexes with RS-diaminobutane (meso-DAB) and RR/SS-diaminobutane (rac-DAB) and the corresponding tetraacetic acids (DABTA)... Table 1. Formation constants of some metal complexes with RS-diaminobutane (meso-DAB) and RR/SS-diaminobutane (rac-DAB) and the corresponding tetraacetic acids (DABTA)...
Another example studied is the isomers of the complex derived from racemic and meso forms of 2,3-diaminobutane. The complex is depicted below. With the racemic addition of Eu[(+)fpc]3 gives the two sets of resonances due to R,R- and 5,5-diastereomers. With meso form, a doubling of each spectral peak was observed. The doubling is due to the presence of a meso plane in the molecule which makes each half of the molecule enantiotropic. [Pg.813]

The synthesis and reactivities of substituted aliphatic bidentate complexes are similar to the reactions of analogous ethylenediamine complexes. Basolo and co-workers prepared619 and studied the rates of chloride aquation555 of a variety of trails-[Rh(N N)2 Cl2 ]+ complexes (NN = meso-bn, where bn = 2,3-diaminobutane (+)-bn, and tetrameen—both cis and trans isomers) the rate of chloride release is not dramatically dependent on the nature of the aliphatic amine ligand. [Pg.979]

Diaminobutane, CH3.CH(NH2)XH(NH2).CH3 forms many salts which are unstable on heating exists as meso form, bp 59-60° at 60mm Hg, and as ragem form, bp 57-58° at 60mm Hg (Ref 4)... [Pg.28]

Tertiary Amines. The photolysis of trlethylamine has been studied by Pfordte and Leuschner (212) and by Allan and Swan (218). They identified the dehydrodimer N,N,N, N -tetraethyl-2, 3-diaminobutane (meso and racemic) and tetraethylhydrazine as well as N,N -diethyl-2,3-diaminobutane (218). [Pg.107]


See other pages where Meso-2,3-Diaminobutane is mentioned: [Pg.6]    [Pg.11]    [Pg.6]    [Pg.128]    [Pg.44]    [Pg.63]   
See also in sourсe #XX -- [ Pg.359 , Pg.438 ]




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