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Spacer Substituent Effects

Another important effect associated with the introduction of lateral substituents in the spacer is the creation of chiral groups along [Pg.46]


Structures have been determined for [Fe(gmi)3](BF4)2 (gmi = MeN=CHCF[=NMe), the iron(II) tris-diazabutadiene-cage complex of (79) generated from cyclohexanedione rather than from biacetyl, and [Fe(apmi)3][Fe(CN)5(N0)] 4F[20, where apmi is the Schiff base from 2-acetylpyridine and methylamine. Rate constants for mer fac isomerization of [Fe(apmi)3] " were estimated indirectly from base hydrolysis kinetics, studied for this and other Schiff base complexes in methanol-water mixtures. The attenuation by the —CH2— spacer of substituent effects on rate constants for base hydrolysis of complexes [Fe(sb)3] has been assessed for pairs of Schiff base complexes derived from substituted benzylamines and their aniline analogues. It is generally believed that iron(II) Schiff base complexes are formed by a template mechanism on the Fe " ", but isolation of a precursor in which two molecules of Schiff base and one molecule of 2-acetylpyridine are coordinated to Fe + suggests that Schiff base formation in the presence of this ion probably occurs by attack of the amine at coordinated, and thereby activated, ketone rather than by a true template reaction. ... [Pg.442]

By increasing the size of the substituents, i.e., di-fert-butylphenyl groups, the porphyrin core can be separated and electronically decoupled from the substrate (Fig. 7,14). These spacer groups effectively act as legs which physically separate the porphyrin central ring from the substrate. The rotation... [Pg.215]

The effect of lateral methyl groups in the spacer on the phase behavior has been studied in several polybibenzoates [18,19] derived from poly(tetramethy]ene p,p bibenzoate), P4MB. The branched polymers display transition temperatures significantly lower than P4MB. Moreover, the substituents have a clear effect on the kind of mesophase formed. Thus, P4MB displays a smectic A mesophase, while the lateral methyl groups... [Pg.387]


See other pages where Spacer Substituent Effects is mentioned: [Pg.46]    [Pg.2054]    [Pg.2108]    [Pg.46]    [Pg.2054]    [Pg.2108]    [Pg.166]    [Pg.5]    [Pg.62]    [Pg.458]    [Pg.748]    [Pg.227]    [Pg.386]    [Pg.62]    [Pg.715]    [Pg.70]    [Pg.340]    [Pg.275]    [Pg.172]    [Pg.167]    [Pg.147]    [Pg.104]    [Pg.170]    [Pg.240]    [Pg.601]    [Pg.673]    [Pg.107]    [Pg.391]    [Pg.104]    [Pg.275]    [Pg.126]    [Pg.1564]    [Pg.505]    [Pg.120]    [Pg.211]    [Pg.271]    [Pg.221]    [Pg.280]    [Pg.410]    [Pg.413]    [Pg.50]    [Pg.500]    [Pg.77]    [Pg.191]    [Pg.103]    [Pg.105]    [Pg.128]    [Pg.128]   


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