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Light-induced

The themial light induces transitions from a b and from b ain proportion to the iiumber of photons present. The iiumber of transitions per second induced by absorption is... [Pg.223]

Kothe G, Weber S, BittI R, Ohmes E, Thurnauer M and Norris J 1991 Transient EPR of light-induced radical pairs in plant photosystem I observation of quantum beats Chem. Rhys. Lett. 186 474-80... [Pg.1588]

Department of Physical Chemistry and the Parkas Center for Light Induced Processes, Hebrew University of Jerusalem, Jerusalem, Israel... [Pg.327]

We thank Professor S. Shaik, Professor B. Dick, Professor L, S. Cederbaum, and Dr. W. Fuss for many enlightening discussions and suggestions, This research was supported by The Israel Science Foundation founded by The Israel Academy of Sciences and Humanities and partially by The VolkswagenStiftung. The Farkas Center for Light Induced Processes is supported by the Minerva Gesellschaft mbH,... [Pg.394]

From the colorless state it can be switched with light of short wavelength (A = 380 nm) via an electrocycHc ring opening and cis/trans rotation of one half of the molecule into a state with violet/purple color. The reverse reaction is effected by visible light (A = 580 nm). Since the system is metastable, one of the two reaction directions is matched by a rival thermal reaction, the thermoreversion. This progresses, however, in the case of benzospiropyran, at room temperature by a factor of 10 slower than the light-induced reaction. [Pg.151]

Water-soluble sdanols such as (1) were found to undergo successive oxidative demethylations with tropospheric ultraviolet irradiation in the presence of suitable chromophores, such as nitrogen oxides (516). The water-soluble methylated sdicones did not promote diatom (Nap cu/apelliculosd) growth but the demethylated photo products did. The sequence of sod-induced degradation of sdicones to water-soluble species such as (1), followed by light-induced conversion to sdicate, suggests a pathway, conceptually at least, for the mineralization of sdicones. [Pg.61]

Apart from the nuclear bromination observed (Section 2.15.13.1) in the attempted radical bromination of a side-chain methyl group leading to (396), which may or may not have involved radical intermediates, the only other reaction of interest in this section is a light-induced reduction of certain hydroxypyrido[3,4-f)]pyrazines or their 0x0 tautomers analogous to that well-known in the pteridine field (63JCS5156). Related one-electron reduction products of laser photolysis experiments with 1 -deazaflavins have been described (79MI21502). [Pg.254]

The light-induced rearrangement of 2-phenyl- to 3-phenyl-thiophene may occur by a similar mechanism an equilibrium between the bicyclic intermediate (26) and the cyclopro-penylthioaldehyde (27) has been suggested (Scheme 2). The formation of IV-substituted pyrroles on irradiation of either furans or thiophenes in the presence of a primary amine supports this suggestion (Scheme 3). Irradiation of 2-phenylselenophene yields, in addition to 3-phenylselenophene, the enyne PhC=C—CH=CH2 and selenium. Photolysis of 2-phenyltellurophene furnishes solely the enyne and tellurium (76JOM(108)183). [Pg.42]

FIGURE 22.21 The mechanism of photophosphorylation. Photosynthetic electron transport establishes a proton gradient that is tapped by the CFiCFo ATP synthase to drive ATP synthesis. Critical to this mechanism is the fact that the membrane-bound components of light-induced electron transport and ATP synthesis are asymmetrical with respect to the thylakoid membrane so that vectorial discharge and uptake of ensue, generating the proton-motive force. [Pg.729]

FIGURE 22.27 Light-induced pH changes in chloroplast compartments. Illumination of chloroplasts leads to proton pumping and pH changes in the chloroplast, such that the pH within the thylakoid space falls and the pH of the stroma rises. These pH changes modulate the activity of key Calvin cycle enzymes. [Pg.736]

As discussed in Section 22.7, illumination of chloroplasts leads to light-driven pumping of protons into the thylakoid lumen, which causes pH changes in both the stroma and the thylakoid lumen (Figure 22.27). The stromal pH rises, typically to pH 8. Because rubisco and rubisco activase are more active at pH 8, COg fixation is activated as stromal pH rises. Fructose-1,6-bisphosphatase, ribulose-5-phosphate kinase, and glyceraldehyde-3-phosphate dehydrogenase all have alkaline pH optima. Thus, their activities increase as a result of the light-induced pH increase in the stroma. [Pg.736]

Light-Induced Mg" Efflux from Thylakoid Vesicles... [Pg.736]

What is the for the light-generated primary oxidant of photosystem II if the light-induced oxidation of water (which leads to Og evolution) proceeds with a AG° of —25 kj/mol ... [Pg.740]

Model compounds in the study of repair of UV-light-induced DNA lesions 98EJ01245. [Pg.225]

The prototype of the antihistamines based on benzhydrol, diphenhydramine (3), is familiar to many today under the trade name Benadryl . Light-induced bromination of diphenylmethane affords benzhydryl bromide (2). This is then allowed to react with dimethylaminoethanol to give the desired ether. Although no mechanistic studies have been reported, it is not unlikely that I he bromine undergoes SNi solvolysis in the reaction medium the carbonitjm ion then simply picks up the alcohol. It might be noted in passing that the theophyline salt of 4 is familiar to many Iravelers as a motion sickness remedy under the trade name Oram amine . [Pg.41]


See other pages where Light-induced is mentioned: [Pg.1978]    [Pg.2493]    [Pg.2496]    [Pg.348]    [Pg.209]    [Pg.314]    [Pg.143]    [Pg.389]    [Pg.428]    [Pg.429]    [Pg.429]    [Pg.431]    [Pg.432]    [Pg.433]    [Pg.61]    [Pg.103]    [Pg.420]    [Pg.474]    [Pg.481]    [Pg.429]    [Pg.433]    [Pg.220]    [Pg.13]    [Pg.309]    [Pg.721]    [Pg.722]    [Pg.736]    [Pg.736]    [Pg.736]    [Pg.737]    [Pg.10]    [Pg.185]    [Pg.317]   
See also in sourсe #XX -- [ Pg.107 , Pg.108 , Pg.109 , Pg.110 , Pg.111 , Pg.112 , Pg.113 , Pg.114 , Pg.115 , Pg.116 , Pg.117 , Pg.118 , Pg.119 , Pg.120 , Pg.121 ]

See also in sourсe #XX -- [ Pg.398 ]




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AMORPHOUS AZOBENZENE POLYMERS FOR LIGHT-INDUCED SURFACE PATTERNING

Anisotropy collision-induced light scattering

Atom light induced

Beam induced light emission

Biosynthesis light-induced regulation

Birefringence light-induced

Charge light-induced

Chemistry of Light-Induced Degradation

Chromophores light-induced molecular response

Collision-induced light scattering solids

Coupled light-induced electron transport

Cross-linking light-induced degradation

Current light-induced

Defects light induced

Degradation light-induced

Depolarization collision-induced light scattering

Description of photo-induced light scattering in sbn

Diffusion light-induced

Dimerization, ultraviolet light-induced

Dissociation light-induced water

Dual light-induced

Electric field induced light scattering

Electron light-induced defect

Electron transfer light induced

Ethane light-induced formation

Ethylene, light-induced formation

Gases, collision-induced light scattering

Helium collision-induced light scattering

Hydrolysis light-induced

Inhibition of light-induced yellowing

Isomerization, light-induced

Laser light-induced excited spin-state trapping

Latent light induced activation

Ligand driven light induced spin change

Ligand driven light induced spin change LD-LISC)

Light changes induced

Light fluorescence, collision-induced

Light induced activation irradiation

Light induced electron spin resonance

Light induced electron-transfer reactions

Light induced emission

Light induced functions

Light induced potentials

Light induced thermal hysteresis

Light scattering theory, interaction-induced

Light scattering, collision-induced

Light-Induced Chemical Reactions

Light-Induced Depoling

Light-Induced Effects on Photocurrent Transients

Light-Induced Electron-Spin Resonance Detection of the Charge Transfer Process

Light-Induced Excited State Spin Trapping in Iron(ll) Compounds

Light-Induced Metal Deposition

Light-Induced-Excited-Spin-State-Trapping

Light-Induced-Excited-Spin-State-Trapping LIESST)

Light-induced ESR

Light-induced Energy Transfer in Model Systems

Light-induced Shape Transitions of Giant

Light-induced Shape Transitions of Giant Vesicles

Light-induced activation

Light-induced aging

Light-induced biological processes

Light-induced brushes

Light-induced chain cross-linking

Light-induced changes, reversal

Light-induced charge separation

Light-induced charge separation photovoltaics

Light-induced chemical alterations

Light-induced collisional energy

Light-induced collisional energy transfer

Light-induced conversion

Light-induced crystal oscillation

Light-induced current response

Light-induced decomposition

Light-induced defects metastability

Light-induced defects temperature dependence

Light-induced degradation mechanisms

Light-induced displacement currents

Light-induced dissociation

Light-induced dissolution of hematite

Light-induced drift

Light-induced effects

Light-induced electron resonance (LESR

Light-induced electron spin resonance LESR)

Light-induced energy transfer

Light-induced excited spin state

Light-induced excited-spin-state-transition

Light-induced excited-spin-state-transition LIESST) effect

Light-induced fluorescence

Light-induced metastable changes

Light-induced phase transitions

Light-induced polymerization

Light-induced processes

Light-induced proton-pump

Light-induced rapid charge separation

Light-induced reactions

Light-induced repair

Light-induced sterilization

Light-induced structural change

Light-induced transfer reaction, reversible

Light-induced transformation

Light-induced transients

Light-induced volatiles release

Light-induced yellowing

Light-induced yellowing effect

Light-induced yellowing of wood-containing

Light-induced yellowing of wood-containing papers

Light-induced yellowing problem

Liquids collision-induced light scattering

Mass light-induced

Metastable light-induced effects

Micelle light induced electron transfer

Mutation, light-induced

Olefin light-induced

Optical light-induced

Oxidation light induced

Pair polarizabilities collision-induced light scattering

Photo-induced light scattering

Photo-oxidation light-induced degradation

Photocatalysis visible light-induced

Photocurrent, light induced

Photodiodes, light-induced electron

Photolysis light-induced degradation

Picosecond Light-induced Processes

Polarizabilities collision-induced light scattering

Polarized light induced dichroism

Polymer Photovoltaics (Light-Induced Charge Separation)

Polymer light-induced mass transport

Porphyrin light-induced charge separation

Raman spectroscopy collision-induced light scattering

Reaction light-induced, ultrafast

Reactive collision-induced light

Redox process light-induced

Role in light-induced yellowing

Second light-induced generation

Sensitized light-induced degradations

Shape light-induced

Shuttle light-induced

Solar cells light induced degradation,

Spectral moments, collision-induced light

Spectral moments, collision-induced light scattering

Staebler-Wronski effect light-induced defects

Stress light-induced formation

Taste light-induced

Temperature collision-induced light scattering

The Effect of Light Photochemically Induced Reductive Elimination

The Light-Induced Transformation

Transcription of genetic information light-induced

UV LIGHT INDUCED REACTIONS IN POLYMERS

Ultraviolet light apoptosis induced

Ultraviolet light cancer induced

Ultraviolet light lesions induced

Ultraviolet light mutagenesis induced

Visible light induced arylation

Wood-containing papers, light-induced

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