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Nitrogen donor properties

Pyridyl functionalized tris(pyrazolyl)borate ligands show some interesting properties including the formation of polynuclear zinc complexes.23,1 Some of these contain extensive H bonding and have potential as models for multinuclear zinc enzymes such as phospholipase C or PI nuclease.235 A bis-ligand complex of the hydrotris(5-methyl-3-(3-pyridyl)pyrazolyl)borate ligand (23) shows octahedral coordination of all six pyrazole nitrogen donors despite the steric bulk. [Pg.1163]

The coordinating properties of a zinc 2,2 -bipyridyl unit with adenosine 5 -triphosphate and cytidine 5 -triphosphate were studied in aqueous solution. The binding of zinc to both phosphate and ATP nitrogen donor was observed with the potential for displacement of the ATP nitrogen donor by hydroxide.426 The interaction of zinc with the phosphate groups in a platinum(II) bound 2 -deoxyguanosine 5 -monophosphate has been studied in aqueous solution, with little difference noted in the coordinating properties of the phosphate residue or backbone relative to the free nucleobase.427... [Pg.1181]

The N-doped carbons with a nanotube backbone combine a moderate presence of micropores with the extraordinary effect of nitrogen that gives pseudocapacitance phenomena. The capacitance of the PAN/CNts composite (ca. 100 F/g) definitively exceeds the capacitance of the single components (5-20 F/g). The nitrogen functionalities, with electron donor properties, incorporated into the graphene rings have a great importance in the exceptional capacitance behavior. [Pg.42]

There have been many studies on the formation of hydrogen bonds between alcohols and a wide range of bases. If the bases are of similar type (for example, all nitrogen donor atoms in amines), there is also frequently a rather good correlation between the shift of the O-H stretching band and other properties. For example, stretching frequency shifts of the OH bonds in alcohols have been correlated... [Pg.201]

The bonding mode is dependent on the nature of the metal centre as well as the steric or electronic properties of the imido substituent. For example, the M(CO)5 unit in the (AO-trigonal complex [W(CO)5 S(NMe)2 ] undergoes a 1,3-shift between the two nitrogen donors, whereas the tert-butyl forms a N,N -chelated [W(CO)4 S(NtBu)2 ] complex, as is also observed with main-group metal halides, e.g., [SnCl4 E(NtBu)2 ] (E=S, Se).153... [Pg.247]

The tendency for the fragmentation initiation with the radical site is parallel to the donor properties of this site. The most spectacular examples involve the processes triggered by the removal of a nitrogen n-electron. Halogens are the least active in these reactions. [Pg.149]

Yang JS, Hwang CY, Hsieh CC et al (2004) Spectroscopic correlations between supermolecules and molecules. Anatomy of the ion-modulated electronic properties of the nitrogen donor in monoazacrown-derived intrinsic fluoroionophores. J Org Chem 69 719-726... [Pg.98]

As with any metalloprotein, the chemical and physical properties of the metal ion in cytochromes are determined by the both the primary and secondary coordination spheres (58-60). The primary coordination sphere has two components, the heme macrocycle and the axial ligands, which directly affect the bound metal ion. The pyrrole nitrogen donors of the heme macrocycle that are influenced by the substitutents on the heme periphery establish the base heme properties. These properties are directly modulated by the number and type of axial ligands derived from the protein amino acids. Typical heme proteins utilize histidine, methionine, tyrosinate, and cysteinate ligands to affect five or six coordination at the metal center. [Pg.413]


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See also in sourсe #XX -- [ Pg.313 ]




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