Bond, directiveness chemical

Direct bonding. Direct-chemical bonding occurs when functional groups of a polymer react directly with functional groups of a sub-strate. Strong covalent bonds can thus be formed between the functional groups of a polymer adhesive and those of a substrate such as aplastic-... 

The tutorial in Section 10.3.1.8 presents some of the various ways the information in the Biochemical Pathways database can be retrieved. In this tutorial the importance of searching for the reaction center, the atoms and bonds directly involved in the bond rearrangement scheme, is emphasized, It is a prerequisite for getting a deeper understanding of chemical reactions. 

In this chapter we examine in turn the properties of alkyl and aryl-thiazoles that do not possess functional groups bonded directly to the thiazole ring. The general trends are underlined, and the applications of certains thiazole compounds in such areas as polymers, flavorings, and pharmacological and agricultural chemicals are discussed. 

Bioglasses are surface-active ceramics that can induce a direct chemical bond between an implant and the surrounding tissue. One example is 45S5 bioglass, which consists of 45% Si02, 6% 4.5% CaO, and 24.5% Na20. The various calcium phosphates have exceUent compatibUity with bone and... 

Chemical covalent bonding. The formation of covalent chemical bonds between elements at an interface may be an important factor. Such direct chemical bonding would greatly enhance interfacial adhesion, but specific chemical functional groups are required for the reactions to occur. 

Ketones may be prepared from 5a- and 5/5-saturated-3-ketones, A -3-ketones, A -3-ketones and 5a-A -3-ketones. At one time it was the only direct chemical alternative to microbiological methods for the preparation of the prednisone type of corticoids. A -Double bond formation is not observed, although A -trienones can be prepared from A -3-ketones. In common with DDQ, selenium dioxide is not normally useful for the preparation of A -3-ketones from 5a-3-ketones or A -3-ketones from 5j5-3-ketones. 

The chemical modification techniques refer to the treatments used to modify the chemical compositions of polymer surfaces. Those can also be divided into two categories modification by direct chemical reaction with a given solution (wet treatment) and modification by covalent bonding of suitable macromolecular chains to the polymer surface (grafting). Among these techniques, surface grafting has been widely used to modify the surface of PDMS. 

Chen et al. utUized a direct chemical reaction with a given solution (wet treatment) to modify the surface of the silicone rubber. The presence of a layer of PEO on a biomaterial surface is accompanied by reductions in protein adsorption, and cell and bacterial adhesion. In order to obtain a PEO layer on top of the silicone rabber surface, the surface was firstly modihed by incorporating an Si-H bond using (MeHSiO) , and followed by PEO grafting to the surface using a platinum-catalyzed hydrosilylation reaction. These PEO-modified surfaces were demonstrated by fibrinogen adsorption both from buffer and plasma, as well as albumin adsorption from buffer. Reductions in protein adsorption of as much as 90% were noted on these surfaces. 

Cement formation requires a continuous structure to be formed in situ from a large number of nuclei. Moreover, this structure must be maintained despite changes in the character of the bonds. These criteria are, obviously, more easily satisfied by a flexible random structure than by one which is highly-ordered and rigid. Crystallinity implies well-satisfied and rigidly-directed chemical bonds, exact stoichiometry and a highly ordered structure. So unless crystal growth is very slow a continuous molecular structure cannot be formed. 

Isomer shift and quadmpole splitting of salts, [Ru(C5H5)X] Y (X = Cl, Br Y = PFg and X = I, Y = I3) are larger compared to those of ruthenocene. This indicates direct chemical bonding between Ru and Cl, Br and I and that the Ru ion in each salt is in an oxidation state higher than Ru(II) in ruthenocene... 

In cases of complexes bearing an exocyclic double bond directly coordinated to the metal center, the carbons of the double bond usually exhibit coupling with NMR-active metal centers and/or auxiliary ligands.6 14 18 19 The chemical shifts of the quaternary carbon atom vary from 66.976 to 82.2818 ppm, while the methylene group gives rise to signals at 29.16,14 41.91,6 or 51.3418 ppm in the 13C 1H NMR spectra. As one can see, the chemical shift variation is relatively broad and significantly affected by the nature of the metal center. 

The nature of intermolecular force is essentially no different from that which participates in the chemical bond or chemical reaction. The factor which determines the stable shape of a molecule, the influence on the reaction of an atom or group which does not take any direct part in the reaction, and various other sterically controlling factors might also be comprehended by a consideration based on the same theoretical foundation. 

Hench, L.L. and Paschall H.A. (1973) Direct chemical bond of bioactive glass-ceramic materials to bone and muscle. Journal of Biomedical Materials Research Symposium, 4, 25. 

Because visible light is not energetic enough to break chemical bonds, direct production of free radicals by the photoinitiator does not occur. Instead when cationic initiation is needed, as for reaction with epoxies, DIBF is used in conjunction with an iodonium compound such as 4-octyloxyphenyl-phenyliodonium hexaf luoroantimonate (OPPI). It has been proposed that when irradiated, DIBF and OPPI interact to form a cationic species. 

Another approach to explain tubule formation was taken by Lubensky and Prost as part of a general theoretical study of the relationship between orientational order and vesicle shape.173 These authors note that a membrane in an Lp/ phase has orientational order within the membrane which is lacking in the La phase. The clearest source of orientational order is the tilt of the molecules with respect to the local membrane normal The molecules select a particular tilt direction, and hence the local elastic properties of the membrane become anisotropic. A membrane might also have other types of orientational order. For example, if it is in a hexatic phase, it has order in the orientations of the intermolecular bonds (not chemical bonds but lines indicating the directions from one molecule to its nearest neighbors in the membrane). 

Chemical modification of wood surfaces can be employed in order to provide active sites to allow for self-bonding directly, or to allow for covalent bonding between wood... 

Reactions in monolayers (38b) also provide direct chemical evidence for the dependence of molecular orientation on the surface area. The rates of oxidation and halogenation of double bonds midway along the carbon chain of oleic acid, the rate of lactoniza-... 

What makes FHF an attractive species to investigate by nmr spectroscopy is that it consists of three nuceli each with spin 1/2 bonded directly. Also, the proton of the strong hydrogen bond should have an unusual chemical shift. Early work failed to detect the expected F doublet and H triplets (e.g. Soriano et al., 1969), and it was not until the importance of the solvent was appreciated that coupling was observed (Fujiwara and Martin, 1971, 1974a,b). Suitable media were found to be the dipolar aprotic solvents acetonitrile, nitromethane and dimethylformamide. 

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