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Effective coupling

IVR in tlie example of the CH clnomophore in CHF is thus at the origin of a redistribution process which is, despite its coherent nature, of a statistical character. In CHD, the dynamics after excitation of the stretching manifold reveals a less complete redistribution process in the same time interval [97]. The reason for this is a smaller effective coupling constant between the Fenni modes of CHD (by a factor of four) when... [Pg.1072]

TOF mass spectrometers are very robust and usable with a wide variety of ion sources and inlet systems. Having only simple electrostatic and no magnetic fields, their construction, maintenance, and calibration are usually straightforward. There is no upper theoretical mass limitation all ions can be made to proceed from source to detector. In practice, there is a mass limitation in that it becomes increasingly difficult to discriminate between times of arrival at the detector as the m/z value becomes large. This effect, coupled with the spread in arrival times for any one m/z value, means that discrimination between unit masses becomes difficult at about m/z 3000. At m/z 50,000, overlap of 50 mass units is more typical i.e., mass accuracy is no better than about 50-100 mass... [Pg.191]

Nonlinear refraction phenomena, involving high iatensity femtosecond pulses of light traveling in a rod of Tfsapphire, represent one of the most important commercial exploitations of third-order optical nonlinearity. This is the realization of mode-locking ia femtosecond Tfsapphire lasers (qv). High intensity femtosecond pulses are focused on an output port by the third-order Kerr effect while the lower intensity continuous wave (CW) beam remains unfocused and thus is not effectively coupled out of the laser. [Pg.138]

Midazolam and diazepam decrease arterial pressure without a change ia heart rate. Like thiopeatoae, midazolam is a respiratory depressant. Advantages of midazolam are its amnestic effect, coupled with less postoperative depression (102). A reversal agent for the benzodiazepiaes has also become available. Flumazenil [78755-81-4] C25H24FN2O2, (5) displaces the beazodiazepiaes from their receptor but has Httie demoastrable activity of its owa (103,104). [Pg.410]

The unusual conditions needed to produce an a2o dye, namely, strong acid plus nitrous acid for dia2oti2ation, the low temperatures necessary for the unstable dia2onium salt to exist, and the presence of electron-rich amino or hydroxy compounds to effect coupling, means that a2o dyes have no natural counterparts. [Pg.274]

Salt flux across a membrane is due to effects coupled to water transport, usually negligible, and diffusion across the membrane. Eq. (22-60) describes the basic diffusion equation for solute passage. It is independent of pressure, so as AP — AH 0, rejection 0. This important factor is due to the kinetic nature of the separation. Salt passage through the membrane is concentration dependent. Water passage is dependent on P — H. Therefore, when the membrane is operating near the osmotic pressure of the feed, the salt passage is not diluted by much permeate water. [Pg.2035]

Mechanistic studies to identify how endocrine disrupting chemicals interact with hormone systems are required. Although population effects coupled with biomarkers of exposure are strongly suggestive of endocrine disruption, the effect could be secondary to metabolic toxicity. Establishing mechanisms may avoid the need to make decisions on a weight of evidence approach alone. [Pg.60]

Should it be capable of reacting with both phases, there is nothing to preclude a functional homopolymer from being an effective coupling agent. For example. [Pg.413]

J. C. Giddings, Plate height of nonuniform cliromatographic columns. Gas compression effects, coupled columns and analogous systems . Anal. Chem. 35 353-356 (1963). [Pg.169]

Acid-base effect—coupling agents alter acidity of substrate surface. [Pg.796]

Energy from the heel strike is free —it would otherwise be dissipated as heat. The heel-strike generator effectively couples the compression of the heel to the deformation of an array of multi-... [Pg.290]

Another excellent catalyst for coupling is a mixture of CuBr-S(CH3)2, LiBr, and LiSPh. This catalyst can effect coupling of a wide variety of Grignard reagents with tosylates and mesylates and is superior to Li2CuCl4 in coupling with secondary sulfonates.64... [Pg.691]

There are a number of procedures for coupling of terminal alkynes with halides and sulfonates, a reaction that is known as the Sonogashira reaction.161 A combination of Pd(PPh3)4 and Cu(I) effects coupling of terminal alkynes with vinyl or aryl halides.162 The reaction can be carried out directly with the alkyne, using amines for deprotonation. The alkyne is presumably converted to the copper acetylide, and the halide reacts with Pd(0) by oxidative addition. Transfer of the acetylide group to Pd results in reductive elimination and formation of the observed product. [Pg.726]

Alkyl substituents on boron in 9-BBN derivatives can be coupled with either vinyl or aryl halides through Pd catalysts.22413 This is an especially interesting reaction because of its ability to effect coupling of saturated alkyl groups. Palladium-catalyzed couplings of alkyl groups by most other methods often fail because of the tendency for (3-elimination... [Pg.742]

Nickel carbonyl effects coupling of allylic halides when the reaction is carried out in very polar solvents such as DMF or DMSO. This coupling reaction has been used intramolecularly to bring about cyclization of to-allylic halides and was found useful in the preparation of large rings. [Pg.755]

Nickel carbonyl is an extremely toxic substance, but a number of other nickel reagents with generally similar reactivity can be used in its place. The Ni(0) complex of 1,5-cyclooctadiene, Ni(COD)2, can effect coupling of allylic, alkenyl, and aryl halides. [Pg.755]

Another family of coupling reagents frequently used with the Fmoc method is related to A-hydroxybenzotriazole and A-hydroxy 7-azabenzotriazole but also incorporates phosphonium or amidinium groups. The latter can exist in either the O-(uronium) or A-(guanidinium) forms.48 Both can effect coupling. The former are more reactive but isomerize to the latter. Which form is present depends on the protocol of preparation, including the amine used and the time before addition of the carboxylic acid 49 The... [Pg.1248]

Local p, G, X effects and channel size effects Coupled p-G-X effects Boiling length effects... [Pg.334]

We can expect to see future research directed at QM/MM and ab initio simulation methods to handle these electronic structure effects coupled with path integral or approximate quantum free energy methods to treat nuclear quantum effects. These topics are broadly reviewed in [32], Nuclear quantum effects for the proton in water have already received some attention [30, 76, 77]. Utilizing the various methods briefly described above (and other related approaches), free energy calculations have been performed for a wide range of problems involving proton motion [30, 67-69, 71, 72, 78-80]. [Pg.417]

However, Gi2 is unlikely to be the only G protein that couples 8 receptors to adenylyl cyclase since the cloned 8 receptor expressed in HEK 293 cells effectively couples to adenylyl cyclase via a pertussis toxin sensitive G protein [74], yet these cells lack immunologically detectable Gi2 and G0 [78] suggesting that either Gix or Gi3 in these cells couples the 8 receptor to adenylyl cyclase. Prather et al. [69] and Law and Reisine [73] have reported that 8 receptors can associate with Gix and Gi3. Furthermore, Sanchez-Blazquez et al. [68] have reported that antisense against Gi3 mRNA administered to the nervous system blocked 8 agonist-induced analgesia. [Pg.469]


See other pages where Effective coupling is mentioned: [Pg.252]    [Pg.118]    [Pg.73]    [Pg.400]    [Pg.273]    [Pg.263]    [Pg.403]    [Pg.412]    [Pg.426]    [Pg.389]    [Pg.739]    [Pg.374]    [Pg.47]    [Pg.215]    [Pg.74]    [Pg.5]    [Pg.705]    [Pg.1251]    [Pg.262]    [Pg.110]    [Pg.116]    [Pg.119]    [Pg.45]    [Pg.68]    [Pg.505]    [Pg.284]    [Pg.66]    [Pg.99]    [Pg.265]    [Pg.87]    [Pg.105]   


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Acid-base-coupled temperature effect

Anharmonic coupling rotational level effects

Anharmonic coupling theory effect

Approach to Cooperative Jahn-Teller Effect in Crystals with Strong Intra-site Vibronic Coupling

Bonding, relativistic effects Coupled cluster method

Brueckner coupled-cluster effect

Carbenes, coupling electronic effects

Carbon-proton coupling constants solvent effects

Common Additives in Palladium-Catalyzed Cross-Coupling Reactions - Effect on (Pre)catalyst and Active Catalytic Species

Conjugation, effect Coupling constant

Cotton effects exciton coupled

Coupled Transport Effects

Coupled cluster formalisms effective operators

Coupled effect

Coupled homogeneous electrode reactions measurements, effects

Coupled iron oxidation—reduction, effects

Coupled mode equations polarization effects

Coupled oxidation steric effects

Coupled-cluster effect

Coupled-cluster effective, similarity-transformed

Coupling 3/, orbital effects

Coupling constant effect of hybridization on, 136

Coupling constant second-order effects

Coupling constants exchange, effect

Coupling constants factors effecting

Coupling dynamic effects

Coupling effects

Coupling effects, vibronic

Coupling image effects

Coupling modifiers, effects

Couplings, short relaxation times effects

Cross coupling reactions steric effect

Cross coupling reactions substituent effect study

Cross-coupling reactions copper effect

Diazo coupling steric effects

Direct molecular dynamics vibronic coupling, adiabatic effects

Effect galvanic coupling

Effect of Chemical Shifts and Spin Coupling

Effect of Molecule Chirality on Coupling

Effect of Non-Adiabatic Coupling on Vibrational Energy Transfer

Effect of Strong Coupling

Effect of coupling

Effect of magnetic coupling

Effect of spin-orbit coupling

Effective Coupling Coefficient

Effective Electronic Coupling in Duplexes with Separated Donor and Acceptor Sites

Effective core potentials coupled-cluster

Effective core potentials coupled-cluster spin-orbit effects

Effective core potentials coupled-cluster theory

Effective coupling factor

Effective coupling function

Effective coupling function calculation

Effective coupling function propagator

Effective coupling function scaling

Effective coupling function systems

Effective coupling tensor

Effective dipolar coupling

Effective tunneling coupling

Effective tunneling coupling calculations

Electronic coupling metal-dependent effects

Electronic coupling, electron-transfer reactions, nonadiabatic solvent effects

Enzymatically coupled field effect transistor

Examples of Silane Coupling Agent Effects in Filled Polymers

Exchange reactions, effect coupling constants

FACTORS THAT INFLUENCE THE SIGN AND MAGNITUDE OF SECOND-ORDER (STRONG) COUPLING EFFECTS

Hartmann-Hahn transfer effective coupling tensors

Inductively coupled plasma memory effects

Interference Effects in TB Coupling

Intermediate coupling effects

Intermolecular coupling effects

Ionization potentials, spin-orbit coupling effects

Isotope effects on couplings

Jahn-Teller effect higher order coupling

Jahn-Teller effect spin-orbit coupling

Jahn-Teller effect vibronic coupling

Jahn-Teller effect, linear vibronic coupling

Kirkendall effect couples

Ligand effects Stille coupling

Ligand effects Suzuki coupling reactions

Linear Magnetoelectric Coupling and Ferroelectricity Induced by Flexomagnetic Effect in Ferroics

Magnetic coupling effective

Multiple-pulse sequence effective coupling tensor

Non-adiabatic coupling Geometric phase effect

Non-adiabatic coupling geometric phase effect, two-dimensional

Nonadiabatic coupling effects

Nonadiabatic effects coupling terms

Nonadiabatic solvent effects, electron-transfer electronic coupling

Nuclear Overhauser effect spectroscopy coupling constant determination

Nuclear dynamics nonadiabatic coupling effects

Nuclear magnetic resonance coupling constant isotope effects

Nuclear magnetic resonance coupling effect

Optimized-orbital coupled-cluster effect

Phosphonium coupling base effect

Phosphonium coupling solvent effect

Phosphorylation, coupled effect

Protecting Groups Effects on Reactivity, Glycosylation Stereoselectivity, and Coupling Efficiency

Renner-Teller effect generalized coupling

Renner-Teller effect order coupling

Residual Coupling Effects due to Quadrupolar Nuclei in MAS Spectra

Rotational constants nuclear quadrupole coupling effect

Scalar coupling effects

Second-order coupling effects, carbonyl

Silane coupling effect

Singular and Coupled Stress Effects

Slanting Multiplets and Second-Order (Strong Coupling) Effects

Solution NMR JHD Coupling and Isotope Effects

Solvent effect on coupling constants

Solvent effects electronic coupling

Some spin-coupling effects (first-order)

Some spin-coupling effects (second-order)

Spin-Orbit Coupling and Relativistic Effective Potentials—Applications

Spin-orbit coupling Renner-Teller effect

Spin-orbit coupling effective Hamiltonians

Spin-orbit coupling effects

Spin-orbit coupling multi-state effects

Steel galvanic coupling, effects

Steric effects diazonium coupling

Stille coupling copper effect

Strong coupling effects

Structure determination coupling constants, effects

Substituent effects cross-coupling

THE COUPLING EFFECT

Thermo-mechanical coupling temperature effects

Torsion-coupling effect

Trans effect coupling constants

Tunnel effect theory vibrational mode coupling

With effects, coupling pesticide

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