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Phenols mononuclear

T o stabilize polypropylene against oxidation by atmospheric oxygen, phenolic mononuclear and polynuclear antioxidants containing one hydroxyl group on the aromatic nucleus are used successfully. Thus far the behavior of antioxidants having the structure of polyhydric phenols has not been studied extensively for stabilizing polyolefins. We have systematically observed the properties of dihydric mononuclear phenols with the structure of pyrocatechol and hydroquinone in isotactic poly-... [Pg.184]

The composition of coal tar varies with the carbonization method but consists, largely, of mononuclear and polynuclear aromatic compounds and their derivatives. Coke oven tars are relatively low in aliphatic and phenolic content while low-temperature tars have much higher contents of both. [Pg.103]

N40 donor set ligands with pyridyl and phenolic arms form mononuclear complexes with approximately trigonal-bipyramidal coordination geometries.888... [Pg.1227]

In the last few years McCleverty, Ward, and co-workers have reported the NIR electrochromic behavior of a series of mononuclear and dinuclear complexes containing the oxo-Mo(iv) v core unit [Mo(Tp )(0)Cl(OAr)], where Ar denotes a phenyl or naphthyl ring system [Tp = hydro-hydrotris(3,5-dimethylpyrazolyl)borate].184-189 Mononuclear complexes of this type undergo reversible MoIV/Mov and Mov/MoVI redox processes with all three oxidation states accessible at modest potentials. Whilst reduction to the MoIV state results in unremarkable changes in the electronic spectrum, oxidation to MoVI results in the appearance of a low-energy phenolate- (or naphtholate)-to-MoVI LMCT process.184,185... [Pg.598]

Another example of heterogeneous catalysis by oxo-ions is the one-step oxidation of benzene to phenol with nitrous oxide, N2O. Fe/MFI catalysts have, again been found to be very active. This catalysis was discovered by Iwamoto and has been extensively studied by the group of G. Panov in Novosibirsk. " Preparations of Fe/MFI which appear highly active for this reaction display poor activity for NOj reduction and those which are optimum for that process, are poor for benzene oxidation. This shows that different sites are used. Work by Jia et al. revealed that the active sites for benzene oxidation appear to be Fe-oxo-ions containing only one Fe ion. This does not necessarily mean that the sites are mononuclear. A recent work by Zhu et al. has rather suggested that the site consists of one Fe and one Al + ion, the latter ion having left the zeolite framework. ... [Pg.149]

It has been shown that mononuclear cobalt superoxo complexes react with 2,4,6-tri-t-butyl-phenol. The anion [Co(CN)5(02)]3 acts as a base in the oxidation of the phenol. The neutral complex Co(salptr)(Oz) forms a peroxy adduct with 2,4,6-tri-t-butylphenol. An X-ray study on this adduct has revealed the structure shown in (10).m... [Pg.329]

Holmes, S. and CJ. Carrano. 1991. Models for the binding site in bromoperoxidase Mononuclear vanadium(V) phenolate complexes of the hydridotris(3,5-dimethylpyra-zolyl)borate ligand. Inorg. Chem. 30 1231-1235. [Pg.170]

The use of unsubstituted or 4-methyl phenols resulted in the formation of cluster compounds [58]. However, 2,6-di(fcrt-butyl) substituted aryloxide ligands allowed the isolation of mononuclear 3-coordinate homoleptie complexes of the lanthanide elements, the coordination mode of which was first demonstrated with the N(SiMe3)2 ligand [59], The 2,6-substitution pattern is very effective because the alkyl groups are directed towards the metal center and impose a steric coordination number onto the metal which is comparable to the Cp ligand (Cp 2.49 OC6H3rBu2-2,6 2.41) [60],... [Pg.164]

The reaction product of ytterbium metal with benzophenone in a 1 1 molar ratio could be determined by an X-ray structure [278]. The benzophenone dianion unsymmetrically bridges the ytterbium atoms in the HMPA solvate [Yb(OCPh2)2(HMPA)2]2. The aryl oxygen forms a Yb-O bond with a typical terminal bond length (Table 18), but also donates to the other ytterbium. A Yb-C a-bond involving the a-C-atom (2.59(5) A) balances the charge at Yb (II). Reaction of the dianionic complex with four equivalents of phenol HOC6H3tBu2-2,6-Me-4 afforded the mononuclear aryloxide complex Yb(OAr)2(HMPA)2 (Sect. 4.2) [72],... [Pg.222]

However, treatment of the analogous samarium benzophenone dianion with the phenol resulted in oxidation to a mononuclear mixed aryloxide/enolate Sm(III)-complex, Sm[OC=(C6H6XPh)]2(OAr)(HMPA)2, where protonation occured at the aromatic rings (Fig. 36A) [279]. The ligands are arranged in... [Pg.222]

The effective but volatile 2,6-di-ferf.butyl-4-methyIphenol (11) was replaced for most applications by various mononuclear (12), binuclear (13), trinuclear (14) and tet-ranuclear phenols (15, 16). Recently, synthetic DL-a-tocopherol (17) was introduced for effective melt stabilization of PO. This antioxidant may be listed among the stabilizers generally recognised as safe (GRAS). [Pg.56]

B. Optical features of structurally defined mononuclear copper(II) phenolate complexes Complex Cu+2 Geometry CT(nm)a d-d(Alna,)(nm)a Ref. [Pg.41]


See other pages where Phenols mononuclear is mentioned: [Pg.346]    [Pg.91]    [Pg.61]    [Pg.778]    [Pg.801]    [Pg.826]    [Pg.598]    [Pg.52]    [Pg.435]    [Pg.315]    [Pg.189]    [Pg.183]    [Pg.189]    [Pg.194]    [Pg.192]    [Pg.625]    [Pg.121]    [Pg.121]    [Pg.167]    [Pg.337]    [Pg.423]    [Pg.211]    [Pg.346]    [Pg.59]    [Pg.39]    [Pg.114]    [Pg.82]    [Pg.235]    [Pg.199]    [Pg.134]    [Pg.56]    [Pg.439]    [Pg.467]    [Pg.153]    [Pg.81]    [Pg.184]    [Pg.144]    [Pg.436]   
See also in sourсe #XX -- [ Pg.540 ]




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