Chemical and Biochemical Functionalization

The chemical modification of CNTs can be endohedral (inside the cavity of the tube) or exohedral [42]. There are some examples in the literature that have demonstrated the filling of CNTs with fullerenes, biomolecules (proteins, DNA), metals and oxides that have been driven inside by capillary pressure [39, 42, 72-78]. However, in this section we will focus on exohedral functionalization, taking place just at the external walls of the tubes. Both covalent (chemical-bond formation) and noncovalent (physiadsorption) functionlizations can be carried out. In the following 

For electrochemical devices, such functionalization schemes can be performed either before or after the CNTs are assembled on the electrodes. 

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As noted above, one of the most important attributes of a nanombe is that it has distinct inner and outer surfaces that can be differentially chemical and biochemically functionalized. The template method provides a particularly easy route to accomplish this differential functionalization. The details of nanombe modifications using differential silane chemistry on nanombes are available elsewhere [4]. In the following paragraphs, we briefly describe the results of differential-functionalized nanombes and their applications in highly selective chemical and biochemical extractions [2,4]. 

A considerable improvement over purely graph-based approaches is the analysis of metabolic networks in terms of their stoichiometric matrix. Stoichiometric analysis has a long history in chemical and biochemical sciences [59 62], considerably pre-dating the recent interest in the topology of large-scale cellular networks. In particular, the stoichiometry of a metabolic network is often available, even when detailed information about kinetic parameters or rate equations is lacking. Exploiting the flux balance equation, stoichiometric analysis makes explicit use of the specific structural properties of metabolic networks and allows us to put constraints on the functional capabilities of metabolic networks [61,63 69]. 

The terminology nucleotide or nucleoside immediately directs our thoughts towards nucleic acids. Remarkably, nucleosides and nucleotides play other roles in biochemical reactions that are no less important than their function as part of nucleic acids. We also encounter more stmctural diversity. It is rare that the chemical and biochemical reactivities of these derivatives relate specihcally to the base plus sugar part of the structure, and usually reside elsewhere in the molecule. Almost certainly, it is this base plus sugar part of the structure that provides a recognition... 

Today, well over 100 biological parameters of mammals are known to be linearly related to body weight and highly predictable on an mterspecies basis (Davidson et al. 1986, Voisin et al. 1990, Calabrese et al. 1992). The allometric equation has traditionally been used for extrapolation of experimental data concerning physiological and biochemical functions from one mammalian species to another. In addition, the allometric equation has also been used extensively as the basis for extrapolation, or scaling, of e.g., a NOAEL derived for a chemical from studies in experimental animals to an equivalent human NOAEL, i.e., a correction for differences in body size between humans and experimental animals. 

Biological interactions between molecules are stereo-specific the fit in such interactions must be stereo-chemically correct. The three-dimensional structure of biomolecules large and small—the combination of configuration and conformation—is of the utmost importance in their biological interactions reactant with enzyme, hormone with its receptor on a cell surface, antigen with its specific antibody, for example (Fig. 1-22). The study of biomolecular stereochemistry with precise physical methods is an important part of modem research on cell structure and biochemical function. 

Carbonyl compounds comprise a large and important class of organic substances, and the chemistry of this functional group is essential to the understanding of many chemical and biochemical processes.1 In this chapter we use a few fundamental ideas of mechanism to correlate reactions of various carbonyl functional groups. We shall touch briefly on the closely related chemistry of carbon-nitrogen double bonds. 

More recently, Porta and co-workers [6] applied similar considerations of the polar effects to a new one-pot multicomponent process for the addition of nucleophilic radicals to aldimines, generated in situ in the presence of Ti(IV). In analogy with the Minisci reaction, Ti(IV), which acts as a Lewis acid, coordinates the nitrogen of the imine, strongly increasing the electron-deficient character of the carbon in the a-posilion and thus the reactivity of the imine toward nucleophilic radicals. This reaction, as well as the Minisci one, represents a useful route for the synthesis of a variety of poly-functionalized derivatives of chemical and biochemical relevance. 

Because sedimentary carbonates represent primarily chemical and biochemical precipitates from seawater, and because they make up 20% of the common sedimentary rock record, these rock types have been particularly good sources of chemical and mineralogical data for interpretation of the secular and cyclic evolution of the Earth s surface environment. This carbonate rock record as a function of geological age is now explored as are age trends in other rock types and sediment properties. With this information as background material, we can then discuss what these relationships tell us about the history of carbonates and the exogenic system throughout geologic dme. 

As discussed in the introduction, a major motivation for the development of methods to controllably functionalize silicon surfaces is the opportunity to create novel hybrid organic/silicon devices. By integrating organic molecules with silicon substrates it should be possible to expand the functionality of conventional microelectronic devices. Possibilities include high-density molecular memory and logic as well as chemical and biochemical sensors. Realization of these opportunities requires not only the development of the attachment chemistries, as discussed in the previous sections, but also detailed studies of the electronic properties of the resulting surfaces. 

In spite of all these changes in this book, the term Chemical Industry will often be used in its broadest possible context, covering the pharmaceutical business, even if not specifically stated in parts of the text The content will therefore be of relevance to all those professionals who are already working, or new recmits about to start, in the R D function of any company which uses both chemical and biochemical processes to invent and produce products or services for commercial gain. This will... 

Preceding chapters have described the detailed operating principles of acoustic wave (AW) devices and how these devices can function as sensors of various physicochemical phenomena in surrounding media. This chapter describes die extension of these capabilities to the detection and quantitation of chemical and biochemical species. An introduction to the fundamental background of various important physical and chemical interactions is presented for those not especially familiar with these topics. 

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