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Bonds forming strong

The properties of copper(Il) are quite different. Ligands that form strong coordinate bonds bind copper(Il) readily to form complexes in which the copper has coordination numbers of 4 or 6, such as tetraammine copper(Tl) [16828-95-8] [Cu(NH3)4], and hexaaquacopper(Il) [14946-74-8] [Cu(H,0),p+ ( see Coordination compounds). Formation of copper(Il) complexes in aqueous solution depends on the abiUty of the ligands to compete with water for coordination sites. Most copper(Il) complexes are colored and paramagnetic as a result of the unpaired electron in the 2d orbital (see Copper... [Pg.195]

When freshly mixed, the carboxyHc acid groups convert to carboxjiates, which seems to signify chemical adhesion mainly via the calcium of the hydroxyapatite phase of tooth stmcture (32,34—39). The adhesion to dentin is reduced because there is less mineral available in this substrate, but bonding can be enhanced by the use of minerali2ing solutions (35—38). Polycarboxylate cement also adheres to stainless steel and clean alloys based on multivalent metals, but not to dental porcelain, resin-based materials, or gold alloys (28,40). It has been shown that basic calcium phosphate powders, eg, tetracalcium phosphate [1306-01-0], Ca4(P0 20, can be substituted for 2inc oxide to form strong, hydrolytically stable cements from aqueous solution of polyacids (41,42). [Pg.473]

Halobutyl Cures. Halogenated butyls cure faster in sulfur-accelerator systems than butyl bromobutyl is generally faster than chlorobutyl. Zinc oxide-based cure systems result in C—C bonds formed by alkylation through dehydrohalogenation of the halobutyl to form a zinc chloride catalyst (94,95). Cure rate is increased by stearic acid, but there is a competitive reaction of substitution at the halogen site. Because of this, stearic acid can reduce the overall state of cure (number of cross-links). Water is a strong retarder because it forms complexes with the reactive intermediates. Amine cure may be represented as follows ... [Pg.486]

The cellulose molecule is rigid and forms strong hydrogen bonds with adjacent molecules. It is thus insoluble and decomposes before softening on heating. Partial replacement of hydroxyl groups by acetyl groups has a number of effects ... [Pg.623]

The outer surfaces of these plasma polymers are terminated with hydroxyl groups and have high surface energies. They are readily wet by adhesives and form strong and durable adhesive bonds [51]. [Pg.445]

The simulated free surface of liquid water is relatively stable for several nanoseconds [68-72] because of the strong hydrogen bonds formed by liquid water. The density decrease near the interface is smooth it is possible to describe it by a hyperbolic tangent function [70]. The width of the interface, measured by the distance between the positions where the density equals 90% and 10% of the bulk density, is about 5 A at room temperature [70,71]. The left side of Fig. 3 shows a typical density profile of the free interface for the TIP4P water model [73]. [Pg.355]

As pointed out in the introduction, if one of the substituents on the nitrogen atom is a hydrogen atom, tautomeric equilibrium between enamino and imino forms strongly favors the latter form 18,140,141). According to physiochemical measurements, the occurrence of simply substituted /1 -pyrrolines and zl -piperideines is very improbable. The formulation of this type of compound with a double bond in the position (used mainly by early authors) was of formal meaning only, having no experimental evidence (142-144). [Pg.265]

Chymotrypsin shows a strong preference for hydrolyzing peptide bonds formed by the carboxyl groups of the aromatic amino acids, phenylalanine, tyrosine, and tryptophan. Flowever, over time chymotrypsin also hydrolyzes amide bonds involving amino acids other than Phe, Tyr, or Trp. Peptide bonds having leucine-donated carboxyls become particularly susceptible. Thus, the specificity... [Pg.134]

Compared to later elements in their respective transition series, scandium, yttrium and lanthanum have rather poorly developed coordination chemistries and form weaker coordinate bonds, lanthanum generally being even less inclined to form strong coordinate bonds than scandium. This is reflected in the stability constants of a number of relevant 1 1 metal-edta complexes ... [Pg.950]

Experimental reactivity patterns are based on solution behavior which are influenced by interactions between solvent and reacting molecules (especially ions). Compare electrostatic potential maps of 2-methyl-2-propyl cation and dimethylhydroxy cation. Identify sites that might form strong hydrogen bonds with water. Which ion will be better stabilized by its interaction with water ... [Pg.137]

Non-epitaxial electrodeposition occurs when the substrate is a semiconductor. The metallic deposit cannot form strong bonds with the substrate lattice, and the stability conferred by co-ordination across the interface would be much less than that lost by straining the lattices. The case is the converse of the metal-metal interface the stable arrangement is that in which each lattice maintains its equilibrium spacing, and there is consequently no epitaxy. The bonding between the met lic lattice of the electrodeposit and the ionic or covalent lattice of the substrate arises only from secondary or van der Waals forces. The force of adhesion is not more than a tenth of that to a metal substrate, and may be much less. [Pg.357]

The standard polymers used for rubber linings consist of materials that are cross-linkable macromolecules which, on mixing with suitable reactants that form strong chemical bonds, change from a soft deformable substance into an elastic material. These polymers include natural rubber and its corresponding synthetic, c/s-polyisoprene, styrene-butadiene rubber, polychloroprene, butyl rubber, halogenated butyl rubbers, acrylonitrile-... [Pg.938]

Show how uracil can form strong hydrogen bonds to adenine. [Pg.1109]

A negative value of AH. Exothermic reactions (AH < O) tend to be spontaneous, inasmuch as they contribute to a negative value of AG. On the molecular level, this means that there will be a tendency to form strong bonds at the expense of weak ones. [Pg.459]


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See also in sourсe #XX -- [ Pg.41 ]




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Bond-forming

Strong form

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