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Reactivity functionalized

Let us now turn our attention to understanding the nature of the interactions giving rise to the adhesion of particles to surfaces. First, one should recognize that most particles commonly encountered have been exposed to ambient conditions for lengthy times. As a result, any functionally reactive groups on the particles... [Pg.160]

Scheme 1.1 How organic templates control porosity of materials (and consequences from a functional, reactivity viewpoint). Scheme 1.1 How organic templates control porosity of materials (and consequences from a functional, reactivity viewpoint).
Chlorotetrolic esters are small, highly functionalized, reactive molecules of particular interest is the possibility of using them as reagents for chemical modification of biological macromolecules. Different protein nucleophiles react under mild conditions with methyl 4-chloro-2-butynoate by addition across the triple bond and/or substitution of chlorine while the triple bond and the ester group are involved in the reaction of chlorotetrolic... [Pg.26]

It might be instructive to consider the functional, reactive groups (in a molecule) which undergo metabolic changes, no matter whether these be oxidation, conjugation, or some other chemical change, without regard... [Pg.244]

The succes of a research work depends fundamentally on the method used, once the approach to the problem has been decided. Considering this last point first, one must say that an oversimplification has been made in the theoretical treatment of the nucleic acids. The theoretical approach has consisted of investigating their basic components. One could say that this choice is obvious, but even so one must keep in mind that the functional reactivity of the different nucleic acids seems to depend on the molecular weight, and on the substitution of ribose by deoxyribose and thymine by uracil. [Pg.44]

We must be aware of the large amount of research still to be performed since the fluorinated groups modify the functions-reactivity and cannot be used for certain syntheses. [Pg.164]

Diluents will also affect the performance properties of the adhesive. Diluents generally lower the degree of crosslinking and degrade the physical properties of the cured epoxy. This reduction in crosslink density increases the resiliency of the adhesive, but it also reduces tensile strength as well as heat and chemical resistance. These effects are more pronounced at elevated temperatures than at room temperature. The degree of these effects will depend on whether the diluent has epoxy functionality (reactive diluents) or whether the diluent is incapable of reacting with the epoxy system (nonreactive diluents). [Pg.117]

Skin. Most epoxy resins are not acutely irritating to the skin. However, they are capable of causing skin sensitization. Susceptibility to skin irritation and sensitization varies from person to person. The epoxy resins are considered to be milder skin sensitizers than amine-type curing agents or epoxy functional reactive diluents. [Pg.415]

Chlorotetrolic esters are small, highly functionalized, reactive molecules of particular interest is the possibility of using them as reagents for chemical modification of biological macromolecules. Different protein... [Pg.50]

The method of Fastrez [12] It considers the reaction of two symmetrical, bifunctional monomers (A-A and B-B with A functions reactive toward B) which are added to an extremely large volume of solvent at a constant rate. The theoretical yield of the reaction is calculated — on the assumption that the probability of the formation of a macrocycle is not dependent on its size, i.e., with neglect of the entropic term — by setting up differential equations for the rate of formation of the different possible products (Fig. 1). [Pg.12]

Aqueous solutions can also by microencapsulated in high concentration [6]. To prepare the reverse phase W/0 (Water-in-Oil) emulsions care must be taken to select monomers that will remain in the dispersed water droplets during the emulsion stage. If the monomers diffuse from suspended droplets into the continuous phase polymerization will happen throughout the emulsion and not at the interface as intended. No microcapsules will be formed. This problem has been addressed utilizing carboxy-functional polymers to associate with amine functional reactive monomers dissolved into the water droplets [7]. Shellwalls are formed at the W/0 interface by addition of the oil-soluble monomers to the continuous oil phase. Without the carboxy-functional protective polymers amine monomers would have partitioned out of dispersed water droplets and into the oil phase. Microcapsules would not have been produced. [Pg.273]

Special Properties Easy formulation and application will exhaust to many fabrics contains both sllanol and organo-functional reactivity... [Pg.269]

Physically persistent stabilizers classified as functionalized oligomers or polymers can be synthesized by polyreactions of functionalized monomers and/or by polymer analogous reactions exploiting the reactivity of functionalized reactive low molecular weight compounds with polymeric substrates. For a detailed classification of synthetical approaches, the classification principle used in Houben-Weyl [42] was adopted. The nomenclature of functionalized polymers is based on the monomer s unit principle. Abbreviations of conventional polymers are used as recommended by [1, 2]. [Pg.79]

Zagury, D., Bernard, J., Thiemess, N., Feldman, M. and Berke, G. (1975). Isolation and characterisation of individual functionally reactive cytotoxic T-lymphocytes. Conjugation, killing and recycling at the single cell level. Eur. J. Immunol. 5, 812-818. [Pg.32]

From the Fukui function and hardness to the complete set of shape function reactivity descriptors... [Pg.10]

Some textbooks on physical chemistry treat some of the aspects discussed here, e.g., Chang (see Chapter 1). Most texts on biochemistry give much information on protein structure, function, reactivity, and other properties. For food scientists the following introduction can be recommended ... [Pg.267]

Interface control at the molecular level is important for the development of molecular electronic junctions [1,2] with potential impact in the fields of molecular memories, photovoltaic conversion and biochemical sensing. In order to achieve homogeneous and reliable long term electrical properties, the design of robust interfaces requires the selection of molecules bearing a chemical functionality reactive towards a solid surface, usually a metal (e.g., gold) or a semiconductor (e.g., hydrogen-passivated crystalline silicon). However, these materials may not be ideal substrates because thiol chemistry produces weak Au-S bonds (167 kJ/mol), while the unreacted Si-H interface bonds at Si(lll) H surfaces are prone to partial oxidation [3],... [Pg.90]


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Carbocations reactive intermediate functions

Carbyne, reactive function

Chemical reactivity Fukui functions

Chemical reactivity and the shape function

Chemical reactivity density functional theory

Chemical reactivity energy function

Chemical reactivity functional groups

Compatibility functional groups, reactivity

Conceptual density functional theory chemical reactivity

Condensation polymerization reactive functional groups

Constitutional Factors Affecting the Reactivity of Functional Groups

Density functional theory chemical reactivity index

Density functional theory reactivity indices

Density functionals reactivity

Direct Oxidative Addition of Reactive Zinc to Functionalized Alkyl, Aryl, and Vinyl Halides

Distribution function reactivity

Equal reactivity of functional groups

Fukui function local reactivity index

Fukui function reactivity descriptor

Function and Reactivity

Functional cross-reactivity

Functional group activation reactive intermediates

Functional group reactivity

Functional group reactivity Polymer substrate

Functional group, reactivity with

Functional groups and reactivity

Functional groups centers of reactivity

Functional groups, concept equal reactivity

Functional groups, organic reactivity

Functional groups, reactive

Functional reactive polyesters

Functionalized Grignard reagents reactivity

Functionalized polyesters cross reactivity

Functionalized polymers, reactive homopolymers

Introduction of Non-functional Alkyl and Reactive Allyl Groups

Phase separation functional/reactive

Polymers with reactive functional groups

Polymers with reactive functional groups anionic polymerization

Polymers, functional oxazoline reactive groups

Polystyrene, reactive functional

Polystyrene, reactive functional groups

Properties and Reactivities of Common Functional Groups

Reactive Functionally Terminated Siloxane Oligomers

Reactive Polymers Having MAn Functionality

Reactive Polymers with Carboxylic Acid Functionality

Reactive flux correlation function

Reactive functionalized polymers

Reactive liquid polymers higher functionality

Reactive oxirane functions

Reactive processing chain functionalization

Reactivity and Product Determination as a Function of Conformation

Reactivity and Selectivity in Transition Metal-Catalyzed, Nondirected Arene Functionalizations

Reactivity as a function of the

Reactivity of 1-Functionalized-l-Metallo. Small Ring Compounds

Reactivity of functional groups

Reactivity space function

Selected Ferrocene Derivatives with Reactive Functional Substituents

Shape function chemical reactivity

Side chain functional substituents, reactivity

Silanol functional groups, reactive

Spin-polarized density functional theory chemical reactivity

Stability functional groups* reactivity

Step polymerization functional group reactivity

Structure-reactivity relationships functional group effects

Surface reactive functionalities

Thiol-reactive functions

Topic 1.5. Application of Density Functional Theory to Chemical Properties and Reactivity

Unequal Reactivity of Functional Groups

Unequal functional group reactivity

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