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By Alberto D'Amore, A. K. Haghi, Gennady Efremovich Zaikov

The box of bioscience methodologies in actual chemistry stands on the intersection of the facility and generality of classical and quantum physics with the minute molecular complexity of chemistry and biology. This publication presents an program of actual ideas in explaining and rationalizing chemical and organic phenomena. It doesn't persist with the classical issues which are conventionally regarded as a part of actual chemistry; as an alternative it provides ideas deciphered from a latest viewpoint, that's the power of this e-book.

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The creation of mesopores in zeolite particles to increase accessibility to internal surface has been the subject of many studies (mesopore – modified zeolites). It is known that postsynthesis hydrothermal dealumination and other chemical treatments form defect domains of 5 – 50 nm (which are attributed to mesopores) in faujasites, mainly zeolite Y [48]. The low activity of these zeolite catalysts is connected with their highly hydrophility as result of low silicon to aluminum ration. The deactivation by sorption of polar products and solvent on pores of zeolite still remained a serious issue for oxidation of alkanes (with low polarity).

The products were formed with auto acceleration period longer than in the case of the H2O additives – free process. The reaction rates (as well as in the absence of the H2O additives [22]) rapidly becomes equal to w = wlim = wmax (w0). Under these steady – state reaction conditions the changes in oxidation rates in the both cases were due to the changes in PEH or P (AC+MPC) accumulations. The increase in w0 at catalysis by complexes (Fe(II)(acac)2)n(Me4NBr)m in the presence of the H2O is observed (as compared with catalysis by Fe(II) (acac)2, and catalysis by complexes (Fe(II)(acac)2)n(Me4NBr)m without H2O [93]).

The formation of complexes Ni(L1)2 with L2=18C6 or R4NBr was also proved by spectrophotometry under analysis of UV spectra of absorption of Ni(L1)2 and R4NBr (18C6) mixtures solutions. At that L2 coordinate with metal ion with preservation of ligand L1 in internal coordination sphere of complex [90, 92]. Under formation of complexes of Ni(L1)2 with L2 in spite of axial coordination by the fifth coordination place of nickel (II) ion the outer sphere coordination of L2 (H–bonding) with acetylacetonate-ion is also possible.

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