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Organic functionalization for

Germanium surface passivation by chloride termination inhibits oxide formation and maintains a well-ordered surface. The chloride-terminated surface can also be used as a reactive precursor for wet organic functionalization. For example, Cullen et al. [105] first demonstrated the reaction of a chloride-terminated Ge(lll) surface with ethyl Grignard as a means of ethylation for use in surface stabilization. The chlorination was performed by a mixture of Cl2 and HC1 gas with N2 above atmospheric pressures [105]. Although this resulted in approximately a one-to-one ratio of adsorbed chlorine atoms with Ge surface atoms, the high pressures resulted in severe etching of the substrate [105]. [Pg.337]

Nature, or Qod, if you will, has set laws by which physical organisms function for the benefit of the individual and the species. If the organism is nonfunctional, natural law decrees it must be eliminated. But Reagan has outlawed Nature, or God. [Pg.101]

These examples show that colloidal systems produced by the sol-gel process can be surface modifed by organics and to obtain a new type precursors with organic functions for further processing. [Pg.185]

To use direct dynamics for the study of non-adiabatic systems it is necessary to be able to efficiently and accurately calculate electronic wave functions for excited states. In recent years, density functional theory (DFT) has been gaining ground over traditional Hartree-Fock based SCF calculations for the treatment of the ground state of large molecules. Recent advances mean that so-called time-dependent DFT methods are now also being applied to excited states. Even so, at present, the best general methods for the treatment of the photochemistry of polyatomic organic molecules are MCSCF methods, of which the CASSCF method is particularly powerful. [Pg.299]

The graphic interface is a multitasking environment that works well. The protein and carbohydrate builders are particularly convenient to use. The small-molecule builder has a selection of common organic functional groups as well as individual atoms for organics and common heteroatoms. There are a... [Pg.345]

The value of alkyl halides as starting materials for the preparation of a variety of organic functional groups has been stressed many times In our earlier discussions we noted that aryl halides are normally much less reactive than alkyl halides m reactions that involve carbon-halogen bond cleavage In the present chapter you will see that aryl halides can exhibit their own patterns of chemical reactivity and that these reac tions are novel useful and mechanistically interesting... [Pg.971]

Quantum mechanics calculations use either of two forms of the wave function Restricted Hartree-Fock (RHF) or Unrestricted Hartree-Fock (UHF). Use the RHF wave function for singlet electronic states, such as the ground states of stable organic molecules. [Pg.37]

Selected Gravimetric Methods for the Analysis of Organic Functional Groups and Heteroatoms Based on Precipitation... [Pg.250]

Organic Analysis Several organic functional groups or heteroatoms can be determined using gravimetric precipitation methods examples are outlined in Table 8.5. Note that the procedures for the alkoxy and alkimide functional groups are examples of indirect analyses. [Pg.250]

Selected Acid-Base Titrimetric Procedures for Organic Functional Groups Based on the Production or Consumption of Acid or Base... [Pg.303]

The two most useful supplementary techniques for the light microscope are EDS and FTIR microscopy. Energy dispersed x-ray systems (EDS) and Eourier-transform infrared absorption (ETIR) are used by chemical microscopists for elemental analyses (EDS) of inorganic compounds and for organic function group analyses (ETIR) of organic compounds. Insofar as they are able to characterize a tiny sample microscopically by PLM, EDS and ETIR ensure rapid and dependable identification when appHed by a trained chemical microscopist. [Pg.334]

Fig. 6. Band edge positions of several semiconductors ia contact with an aqueous electrolyte at pH 1 ia relation to the redox (electrode) potential regions (vs the standard hydrogen electrode) for the oxidation of organic functional groups (26,27). Fig. 6. Band edge positions of several semiconductors ia contact with an aqueous electrolyte at pH 1 ia relation to the redox (electrode) potential regions (vs the standard hydrogen electrode) for the oxidation of organic functional groups (26,27).
Organic titanates perform three important functions for a variety of iadustrial appHcations. These are (/) catalysis, especially polyesterification and olefin polymerization (2) polymer cross-linking to enhance performance properties and (J) Surface modification for adhesion, lubricity, or pigment dispersion. [Pg.161]

There should be an organization chart for the company showing individual functions and to whom they are responsible. Job descriptions should clearly indicate responsibilities for quality. The assessor should read the job description of the quality assurance/improvement coordinator as well as of a few managers and supervisors to establish the answer to the question. [Pg.191]

B. Empirical electronegativities for some organic functional groups ... [Pg.17]

Table 1.7. Bond and Group Dipoles for Some Organic Functional Groups"... Table 1.7. Bond and Group Dipoles for Some Organic Functional Groups"...

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