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A donors

Figure A3.10.23 Schematic diagram of molecular CO chemisorption on a metal surface. The model is based on a donor-acceptor scheme where the CO 5 a FIOMO donates charge to surface unoccupied states and the surface back-donates charge to the CO 2 71 LUMO [58]. Figure A3.10.23 Schematic diagram of molecular CO chemisorption on a metal surface. The model is based on a donor-acceptor scheme where the CO 5 a FIOMO donates charge to surface unoccupied states and the surface back-donates charge to the CO 2 71 LUMO [58].
A gap level is called an acceptor level if tlie defect is neutral when tlie state is empty (no electron). It is called a donor level if tlie defect is neutral when tlie state is occupied (one electron). The foniier is often labelled (0 / -) and tlie latter (-t / 0), where tlie first (second) sign refers to tlie charge of tlie defect when no electron (one electron) is present. Double or triple acceptor and donor levels are similarly labelled. [Pg.2884]

The K factors in (C3.4.1) represent another very important facet of tire energy transfer [4, H]. These factors depend on tire orientations of tire donor and acceptor. For certain orientations tliey can reduce tire rate of energy transfer to zero—for otliers tliey effect an enhancement of tire energy transfer to its maximum possible rate. Figure C3.4.1 exhibits tire angles which define tire mutual orientation of a donor and acceptor pair in tenns of Arose angles the orientation factors and are given by [6, 7]... [Pg.3019]

Figure C3.4.2. Schematic presentation of energy transfer between (a) two donor molecules and six acceptor molecules and (b) a general case of energy transfer involving a pool of A donor molecules and a pool of M acceptor molecules. Figure C3.4.2. Schematic presentation of energy transfer between (a) two donor molecules and six acceptor molecules and (b) a general case of energy transfer involving a pool of A donor molecules and a pool of M acceptor molecules.
Let us consider tire case of a donor-acceptor pair where tire acceptor, after capturing excitation from tire donor, can emit a photon of fluorescence. If tire excitation light is linearly polarized, tire acceptor emission generally has a different polarization. Common quantitative expressions of tliis effect are tire anisotropy of fluorescence, r, or tire degree of polarization,... [Pg.3021]

In this molecule, the aluminium receives a pair of electrons from the nitrogen atom. The nitrogen atom is referred to as a donor atom and the aluminium as an acceptor atom. Once the bond is formed it is identical to the covalent bond of previous examples it differs... [Pg.41]

Boron achieves a covalency of three by sharing its three outer electrons, for example BFj (p. 153). By accepting an electron pair from a donor molecule or ion, boron can achieve a noble gas configuration whilst increasing its covalency to four, for example H3N->BCl3. K BF4. This is the maximum for boron and the second quantum level is now complete these 4-coordinate species are tetrahedral (p. 38). [Pg.140]

Borane does not exist as such, but a donor molecule can break up diborane and form an adduct, thus ... [Pg.146]

Ammonia as a donor molecule. Because of the presence of the lone pair of electrons on the nitrogen atom, ammonia can behave as an electron pair donor. For example, ammonia abstracts a proton from a water molecule producing the tetrahedral ammonium, NH4, ion and forms the compounds HjN- AlClj and HjN- BClj. [Pg.217]

Finally, the solvent also interacts with sites of the Lewis acid and the Lewis base that are not directly involved in mutual coordination, thereby altering the electronic properties of the complex. For example, delocalisation of charges into the surrounding solvent molecules causes ions in solution to be softer than in the gas phase . Again, water is particularly effective since it can act as an efficient electron pair acceptor as well as a donor. [Pg.31]

An alternative drivirg force could involve a donor - acceptor interaction. The electron-poor pyridine ring that is coordinated to the copper cation can act as electron acceptor with respect to the aromatic ring of the -amino acid. The fact that donating substituents on the amino acid increase the efficiency... [Pg.99]

O The change of a donor reagent into an acceptor reagent and vice versa is called um-polung" (=dipole inversion). [Pg.1]

The cyclization reactions discussed here either involve the intramolecular reaction of a donor group D with an acceptor group A or a cyclizing dimerization of two molecules with two terminal acceptors and two donors. A polymerization reaction will always compete with cyclization. For macrolides see p. 146 and p. 319 — 329. [Pg.246]

The basic steps of gene cloning first involve cutting a precise DNA segment (gene) from a donor source DNA by use of a restriction enzyme (Figure 45.2). At the same time, a small looped... [Pg.328]

Blood components are also collected through apheresis. In apheresis, advanced blood cell separators are used to collect one or more specific blood components from a donor. The cell separators collect blood iato a separation chamber, isolate the desired blood components, and return the blood components not needed to the donor. This procedure is performed on-line within one sterile disposable tubiag set. The two principal components collected through apheresis are plasma and siagle-donor platelets (SDP). [Pg.520]

Fig. 1. (a) Silicon (valence = 4) crystal lattice shown in two dimensions with no broken bonds, T = 0 K (b) siUcon crystal lattice with a broken bond (c) sibcon crystal lattice with a siUcon atom displaced by a donor dopant, ie, -doped (valence = 5) and (d) siUcon crystal lattice with a siUcon atom displaced... [Pg.467]

The variations in D and D and the much larger value for In show the limitations of a simple hydrogen atom model. Other elements, particularly transition metals, tend to introduce several deep levels in the energy gap. For example, gold introduces a donor level 0.54 eV below D and an acceptor level 0.35 eV above D in siHcon. Because such impurities are effective aids to the recombination of electrons and holes, they limit carrier lifetime. [Pg.345]

Addition compounds form with those organics that contain a donor atom, eg, ketonic oxygen, nitrogen, and sulfur. Thus, adducts form with amides, amines, and A/-heterocycles, as well as acid chlorides and ethers. Addition compounds also form with a number of inorganic compounds, eg, POCl (6,120). In many cases, the addition compounds are dimeric, eg, with ethyl acetate, in titanium tetrachloride-rich systems. By using ammonia, a series of amidodichlorides, Ti(NH2) Cl4, is formed (133). [Pg.131]

For membrane transport experiments, the relevant membrane is sandwiched between two solutions a donor typicaUy at constant dmg concentration, C = Cg, and a receiver at zero concentration, C = 0. The dmg concentration in the receiver is monitored as a function of time and the cumulative amount transported, has a linear asymptote with time where M is the area,/ is the steady-state flux, /is the time, and / is the time lag. [Pg.224]

Acetylene is oxidized to ketene by hot air (24JCS(125)1534). Oxirene is probably not involved since molecular oxygen is not a donor of singlet oxygen atoms (see the remarks on this point in (64JA4866)). [Pg.124]

Depending on its rank, coal can be dissolved in as little as one minute in the temperature range of 623 to 723 K (662 to S42°F) in suitable solvents, which are assumed to promote thermal cracking of the coal into smaller, more readily dissolved fragments. These fragments may be stabilized through reactions with one another or with hydrogen supplied either by a donor solvent or from a gas phase. [Pg.2373]

The results obtained show, that absolute meanings of elemental concentrations in the nails of each human are individual. The change of the elemental content with time in nails of a donor is individually dominated. These data allow drawing a conclusion, that the application of nails in non-invasive diagnostic is correct. [Pg.430]


See other pages where A donors is mentioned: [Pg.170]    [Pg.894]    [Pg.100]    [Pg.100]    [Pg.101]    [Pg.78]    [Pg.211]    [Pg.192]    [Pg.521]    [Pg.522]    [Pg.90]    [Pg.386]    [Pg.346]    [Pg.295]    [Pg.298]    [Pg.435]    [Pg.50]    [Pg.181]    [Pg.183]    [Pg.378]    [Pg.48]    [Pg.329]    [Pg.329]    [Pg.330]    [Pg.287]    [Pg.384]    [Pg.421]    [Pg.138]    [Pg.285]   
See also in sourсe #XX -- [ Pg.536 ]




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A Detailed Look at the Hydrogen Bond Donor Features of HFIP

A donor strength

Acids as proton donors

Alcohols as hydrogen donors

Aldehydes as Michael Donors

Alkyl benzenes react at the ortho and para positions a donor substituents

Anhydro Sugars as Glycosyl Donors

Anhydro sugars as electrophilic donors

Anions as Electron Donors in Charge-Transfer Salts

Applications as glycosyl donors

As a 71 Donor

As a 71 Donor

As a n Donor

As electron donor

As(O)-Donor Ligands

As-donor Ligands

Betaine, as methyl donor

Bonds as Electron Donors

Bonds as Electron Donors or Acceptors

Bronsted Acid as a Proton Donor

Bronsted-Lowry acid A proton donor

Cation-Radicals as Acceptors or Donors of Hydrogen Atoms

Chiral Squaramides as Hydrogen-Bond Donor Catalysts

Complexes Containing a -Donor Ligands

Dicyanomethylenephenoxazines and dicyanoiminophenoxazines as novel donor-acceptor systems

Disubstituted-1,2,3-Triazoles as Monodentate N-Donor Ligands

Donor angle of incidence to a-synthons

Formates as hydrogen donor

Formation of a donor-acceptor complex

Free Sugars as Glycosyl Donors

Glucosyl Phosphate as Glycosyl Donor

Glycals as glycosyl donor

Glycosides as glycosyl donors

Glycosyl donors with a C-2 heteroatom

Group 1 Complexes of P- and As-Donor

Group 1 Complexes of P- and As-Donor Ligands

Hydrogen Evaluation Involving Ligands as Proton Donors

Isopropenyl glycosides as glycosyl donors

Ketones as Michael Donors

Metal Complexes as Donor Groups

Monomers as electron donors

N-, NO-, As-, and P-Donor Ligands

NO Donors as Antiplatelet Agents

Nitrous Oxide as an Oxygen Donor in Oxidation Chemistry and Catalysis

Oligo-Phenylene Vinylene A Model System for Donor-Acceptor Interactions

Other ligands containing sulfur as donor atom

P- and As-Donor Ligands

Pentenyl Glycosides as Glycosyl Donors

Phenothiazine as donor

Phosphites, as glycosyl donors

Polymers as Photoexcited Donors

Rich Compounds as Electron Donors

Role of Phenol as Hydrogen Donor

Role of Urea and Thiourea as Hydrogen Donors

Ru(II) complexes with -P, -As and -Sb Donors

Ru(III) Complexes with -P, -As, -Sb and -S Donors

Selenoglycosides as glycosyl donors

Sensors based on a single sample-donor stream

Silanes as hydride donors

Stereoelectronic Effects with Donor and Acceptor Separated by a Vinyl Bridge

Stereoelectronic chameleons donors masquerading as acceptors

Structural Effects Derived from M-OH2 Acting as an Intramolecular H-Bond Donor to a Bound Phosphate Ester

Sucrose as glucosyl donor

The Complexes as Particle Donors

Thioglycosides as Glycosyl Donors in Oligosaccharide Synthesis

Thioglycosides, as glycosyl donors

Thiols as hydrogen donors

Transition metal clusters as four-electron donor

Use of anomeric acetates as glycosyl donors

Use of glycals as direct glycosyl donors haloglycosylation

Use of vinyl glycosides as glycosyl donors

Water as H-donor

Water as electron donor

Water as hydrogen-bond donor

Which B is a n-Pair Donor

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