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Charge complexes

Photoinduced copolymerization of donor-acceptor monomer pairs (Scheme 1) can be either self initiated by excitation of the charge transfer complex (charge transfer initiation) or by polymerization of the charge transfer complex/monomer equilibrium... [Pg.122]

The kinetics of base hydrolysis of several complexes of the type [Co(NH3)3L3] have been examined in order to see whether the mechanism for these uncharged complexes is the same as that operating for base hydrolysis of the standard cationic complexes (75). A comparison of kinetic parameters - a small selection is given in Table II (76,77) - suggests that all cobalt(III)-nitro-amine complexes, charged and uncharged, undergo base hydrolysis by the SnICB (Dch) mechanism. [Pg.80]

The technique, although attractive, is experimentally rather complex charging problems can frequently occur, leading to the observation of elevated apparent binding energies, and interpretational difficulties exist. Thus, the X-PES of palladium(II) sulfoxide complexes are difficult to interpret unambiguously as the oxygen Is peak is nearly... [Pg.143]

Fig. 5. Ten types of different structures identified by X-ray diffraction, where the abbreviated N-0 is used to express each bridging amidate ligand and X denotes axial donors such as OH2, N03, N02 (nitro), Cl, and Br. For the compounds involving axial ligands (X), the total complex charge is given assuming that X is a monoanion. Note that, in some cases, amine ligand in cis-Pt(NH3)2 will be replaced with other ligands, such as in Pt(en), cis-Pt(NH3)Cl, cis-PtCl2, and Pt(bpy). Fig. 5. Ten types of different structures identified by X-ray diffraction, where the abbreviated N-0 is used to express each bridging amidate ligand and X denotes axial donors such as OH2, N03, N02 (nitro), Cl, and Br. For the compounds involving axial ligands (X), the total complex charge is given assuming that X is a monoanion. Note that, in some cases, amine ligand in cis-Pt(NH3)2 will be replaced with other ligands, such as in Pt(en), cis-Pt(NH3)Cl, cis-PtCl2, and Pt(bpy).
A number of experimental in vivo gene therapy trials on animals using PAMAM dendrimers are in their preliminary stages. Numerous in vivo experiments are currently being conducted in order to optimize the dendrimer generation, concentration, and complex charge ratio to obtain optimal transfection efficiency. [Pg.456]

Boron complex (charge control agent) 2 Quinacridone master batch (pigment) 12... [Pg.56]

As with carbonyl coordination, the degree of backbonding in the linear mode of coordination is influenced by the complex charge, metal oxidation state and nature of the ancillary ligands. An example of how both the oxidation state and the relative d orbital energies influence vN0 is shown dramatically in the pentacyanonitrosyl systems M(NO)(CN) " (z = 2, M = Fe,... [Pg.146]

We see that for the (alkali metal + oxygen macrocycle) complexes, charge and relative size of the ion play an important part in determining the stability of the complex. However, for the (transition metal + aza- or thia-substituted macrocycle) complexes, the nature of the bonding seems to be the important effect. Sten Ahrland16 has used a classification scheme for metal ion acceptors that helps us understand this difference. He designates the metal ion as either hard or soft. The characteristics that determine the assignment are as follows. [Pg.204]

Anionic surfactants complexation, charge neutralization, aggregation, precipitation, structure formation... [Pg.171]

Polyanions complexation, charge neutralization colloidal aggregates stable turbid dispersions flocculated precipitates coherent gels... [Pg.171]

Figure 6.24 VIP plot for various descriptors in a PLS model for the hydrocyanation of pentenenitrile in the presence of Ni-biphosphine/biphosphite complexes. Charge descriptors refer to the Mulliken charge calculated at the ligating atoms. A bind is the energy difference between the free ligand and the metal complex, and can be related to the... Figure 6.24 VIP plot for various descriptors in a PLS model for the hydrocyanation of pentenenitrile in the presence of Ni-biphosphine/biphosphite complexes. Charge descriptors refer to the Mulliken charge calculated at the ligating atoms. A bind is the energy difference between the free ligand and the metal complex, and can be related to the...
Cation anion ratio in complex Charge on metal ion Charge on ligand pKo Concentration of complex at / = 0 (xlO4 mol nT1) Extent of complexation at 2.6 mol m-3 of complex formation at / = 0... [Pg.243]

These and undoubtedly several other reactions occur during the smelting of the very complex charge placed in the furnace. As indicated by the preceding reactions, elemental lead may be liberated as a product of five (or more) separate reactions. The lead so produced is drained from the furnace and is then ready for purification. The chief impurities present in the crude product (known as lead bullion) are Cu, Ag, Au, As, Sb, and Bi. [Pg.560]


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See also in sourсe #XX -- [ Pg.262 ]

See also in sourсe #XX -- [ Pg.91 ]

See also in sourсe #XX -- [ Pg.72 ]




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1.3.5- Trinitrobenzene, charge-transfer complexes

Activated complex charge development

Anilines charge-transfer complexes

Arenes charge-transfer complexes

Aromatic charge transfer complexes

Aromatic substitution reactions, role charge-transfer complexes

Atomic complexities singly charged ions

Azines charge-transfer complexes

Azulenes charge transfer complexes

Benzene-iodine complex, charge-transfer

Benzene-iodine complex, charge-transfer reaction

Binuclear complex charge transfer spectra

Block Copolymers from charge transfer complexes

Bromine-olefin charge transfer complexes as essential intermediates in bromination

Carbene complexes charge distributions

Carbon dioxide Charge-transfer complexes

Carbyne complexes charge

Charge Complex Formation

Charge amphoteric surface with complexation

Charge balances, triple-layer model surface complexes

Charge complexation model

Charge distribution chromium complexes

Charge distribution complex

Charge distribution multisite complexation

Charge distribution, alkali metal complexes

Charge donor-acceptor complexes

Charge inner-sphere complex

Charge metal complex

Charge outer-sphere complex

Charge transfer and other donor---acceptor PLC complexes

Charge transfer complex (CTC

Charge transfer complex electric conductivity

Charge transfer complex matrix

Charge transfer complex mechanical properties

Charge transfer complex, solid state

Charge transfer complexes between

Charge transfer complexes constants

Charge transfer complexes from electrophilic

Charge transfer complexes group

Charge transfer complexes luminescent spectra

Charge transfer complexes monomers

Charge transfer complexes olefins

Charge transfer complexes polymerization

Charge transfer complexes spectra

Charge transfer complexes spectra! features

Charge transfer complexes theory

Charge transfer complexes thermodynamics

Charge transfer complexes viologens

Charge transfer complexes with fullerenes

Charge transfer complexes with halogens

Charge transfer complexes, biological

Charge transfer complexes, biological electron donor-acceptor

Charge transfer complexes, biological examples

Charge transfer complexes, biological stability

Charge transfer complexes, biological systems

Charge transfer complexes, titration

Charge transfer dithiolene-diimine complexes

Charge transfer dithiolene-donor complexes

Charge transfer gold complexes

Charge transfer in endohedral complexes

Charge transfer iron complexes

Charge transfer ruthenium complexes

Charge transfer transitions cobalt complexes

Charge transfer transitions complexes

Charge transfer, bonding complexes

Charge transfer, metal-carbonyl complexes

Charge transfer, radical complex

Charge-Compensated Complexes

Charge-Transfer Complexes of Polyalkylated Ferrocenes

Charge-Transfer Excited States of Transition Metal Complexes

Charge-separated activated complexes

Charge-transfer (CT) complexes

Charge-transfer absorption band complexes

Charge-transfer complex 424 Subject

Charge-transfer complex comonomers

Charge-transfer complex formation and

Charge-transfer complex of TTF

Charge-transfer complex participation

Charge-transfer complex, photoluminescence

Charge-transfer complexes and radical ion salts

Charge-transfer complexes chlorination

Charge-transfer complexes from

Charge-transfer complexes from tetracyanobenzenes

Charge-transfer complexes from tetracyanoethylene

Charge-transfer complexes from tetracyanoquinodimethane

Charge-transfer complexes of ferrocene

Charge-transfer complexes of halogens

Charge-transfer complexes polyimides

Charge-transfer complexes polymer-oxygen

Charge-transfer complexes polystyrene

Charge-transfer complexes pyridine-halogen

Charge-transfer complexes reversible ionization

Charge-transfer complexes solvent photochemistry

Charge-transfer complexes tetrahydrofurane

Charge-transfer complexes triplet excitons

Charge-transfer complexes with other organic systems

Charge-transfer complexes with various organic

Charge-transfer complexes with various organic acceptors

Charge-transfer complexes, formation

Charge-transfer complexes, in organic

Charge-transfer complexes, work term

Charge-transfer complexes/interaction

Charge-transfer complexing

Charge-transfer complexing lone pair

Charge-transfer complexities

Charge-transfer donor-acceptor complexes

Charge-transfer oxygen-polystyrene complexes

Charge-transfer transitions metal-carbonyl complexes

Charged complex species

Charged complexes

Chromium complexes charge-transfer transitions

Cobalt complex charge-transfer process

Cobalt complexes, absorption charge transfer transitions

Colours charge transfer complexes

Complex charge-transfer

Complex impedance spectroscopy charge transfer kinetics

Complexation charge-transfer

Complexes, alkyne-metal charge transfer

Conductivity charge-transfer complex-based

Contact charge transfer complexes

Copper charge-transfer complexes

Donor-acceptor complex Charge-transfer complexes

Electron Affinities and Charge Transfer Complex Energies

Electron Affinities of Charge Transfer Complex Acceptors

Electron paramagnetic resonance charge-transfer complex

Encounter complex charge-transfer interactions

Exciplexes, Electron Donor-Acceptor Complexes, and Related Charge-transfer Phenomena

Excited radical, charge transfer complex

Ferrocene charge transfer complexes

General Spectral Features of Charge Transfer Complexes

Ground-state charge-transfer complexes

Group 17 elements charge-transfer complexes

Halide complexes charge transfer spectra

Halogens charge-transfer complexes

Host-guest complexes calixarenes. Charged

Hydrogen Bonding and Charge-Transfer Complexing

INDEX charge-transfer complexes

Impurity charge-transfer complexes

Initiation charge-transfer complexes

Inner-sphere complex surface charge

Intraligand charge transfer complexes

Intramolecular charge-transfer complexes

Iodine charge-transfer complexes

Iodine-containing charge transfer complexes

Iron -1,10-phenanthroline complex charge transfer

Iron complexes charge transfer transitions

Irradiation of Charge-Transfer Complexes

Langmuir-Blodgett films charge-transfer complexes

Ligand-metal charge transfer complexes

Ligand-to-metal charge transfer d complexes

Metal complexes charges, coordination

Metal complexes having charge

Methyl complexes, charge transfer spectra

Models charge distribution multisite complexation

Mulliken charge-transfer complex

Mulliken relationship charge-transfer complex absorption

Octahedral complexes charge transfer absorption

Oppositely charged polyelectrolytes, complex

Oppositely charged polyelectrolytes, complex formation

Outer-sphere complex surface charge density

Oxygen charge-transfer complexes with

Oxygen with poly charge-transfer complexes

Paraquat charge-transfer complexes

Penultimate Effects and Charge-Transfer Complexes

Phenol complex with iron, charge transfer

Phenothiazines charge-transfer complexes

Photochemical mechanism, charge complexes

Poly charge-transfer complexes

Polyene charge transfer complexes between

Ruthenium complex charge-transfer process

Ruthenium complexes charge transfer transitions

Solutions and charge-transfer complexes

Spectra of charge transfer complexes

Square-planar complexes charge transfer

Strong charge-transfer complexes

Structural Alignment in Charge Transfer Complexes

Sulfur complexes, charge-transfer bands

Supramolecular Charge Transfer Complexes

Surface charge complexation model

Surface charge complexes

Surface charge density inner-sphere complex

TPD complexes charge transport of molecular glasses, hole

Tetracyanoethene, charge-transfer complex

Theory of Charge Transfer Complexes

Thermodynamics of Charge Transfer Complexes

Titanium complexes charge-transfer spectra

Transition metal complexes charge distribution

Transition metal complexes charge-transfer transitions

Transition state, charge separation complex

Weak charge-transfer complex crystals

Wheland complexes charge distribution

Zeolites charge-transfer complex with oxygen

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