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Dendritic negative

Coin and Button Cell Commercial Systems. Initial commercialization of rechargeable lithium technology has been through the introduction of coin or button cells. The eadiest of these systems was the Li—C system commercialized by Matsushita Electric Industries (MEI) in 1985 (26,27). The negative electrode consists of a lithium alloy and the positive electrode consists of activated carbon [7440-44-0J, carbon black, and binder. The discharge curve is not flat, but rather slopes from about 3 V to 1.5 V in a manner similar to a capacitor. Use of lithium alloy circumvents problems with cycle life, dendrite formation, and safety. However, the system suffers from generally low energy density. [Pg.583]

On the other hand, Xiao et al. [215] reported that smooth, dense, and erystalline PbTe films with nearly stoichiometric composition could be obtained by an optimized electrodeposition process from highly acidic (pH 0) tellurite solutions of uncomplexed Pb(II), on Au-coated silicon wafers. The results from electroanalyti-cal studies on Te, Pb, and PbTe deposition with a Pt rde at various temperatures and solution compositions supported the induced co-deposition scheme. The microstructure and preferred orientation of PbTe films was found to change significantly with the deposition potential and electrolyte concentration. At -0.12 V vs. Ag/AgCl(sat. KCl), the film was granular and oriented preferentially in the [100] direction. At potentials more negative than -0.15 V, the film was dendritic and oriented preferentially in the [211] direction (Pig. 3.13). [Pg.127]

Van Koten et al. reported on a negative dendritic effect in the Kharasch addition reaction. [3 9,40] A fast deactivation for the carbosilane dendrimer supported NCN pincer catalyst (Figures 4.28 and 4.29) was observed by comparison with a mononuclear analogue. This deactivation is expected to be caused by irreversible formation of inactive Ni(III) sites on the periphery of these dendrimers. [Pg.92]

The postsynaptic receptors on any given neuron receive information from transmitters released from another neuron. Typically, postsynaptic receptors are located on dendrites or cell bodies of neurons, but may also occur on axons or nerve terminals in the latter case, an axoaxonic synaptic relationship may cause increases or decreases in transmitter release. In contrast, autoreceptors are found on certain neurons and respond to transmitter molecules released from the same neuron. Autoreceptors may be widely distributed on the surface of the neuron. At the nerve terminal, they respond to transmitter molecules released into the synaptic cleft on the cell body, they may respond to transmitter molecules released by dendrites. Functionally, most autoreceptors appear to decrease further transmitter release in a kind of negative feedback loop. Autoreceptors have been identified for all the catecholamines, as well as for several other neurotransmitters. a2-adrenergic receptors are often found on noradrenergic nerve terminals of postganglionic sympathetic nerves, as well as on noradrenergic neurons in the CNS [36], and activation of these receptors decreases further norepinephrine release. Dopamine autoreceptors,... [Pg.218]

Fluorescence lifetime measurements on the aggregate have shown that the rate constant of the intermolecular energy transfer from the zinc porphyrin unit to the free-base porphyrin unit has been evaluated to be 3.0 x 109 s-1. This value is reasonable from a model in which dendritic donor 6b and acceptor 5a contact each other directly at their exterior surfaces (Scheme 2). Therefore, electrostatic assembly of positively and negatively charged dendrimers provides a promising supramolecular approach to construct photofunctional materials with nanometric precision. [Pg.436]

Figure 6 Immunopotentiating reconstituted influenza virosomes (IRIV) adjuvant effects in the induction of tumor associated antigen-specific cytotoxic T cell. CD14-negative cells from a healthy donor peripheral blood mononuclear cells were cocultured with autologous immature dendritic cells (iDC) in the presence of Melan-A/Mart-l27-35, alone (A) or supplemented with either control liposomes (B) or IRIV (1 50, C). On day 7, culture cells were restimulated with Melan-A/MART-127-35 pulsed iDC and cultured for six further days [see Materials and Methods ]. On day 7 after restimulation cells were stained with fluorescein isothiocyanate-conjugated anti-CD8 and phosphatidylethanolamine-conjugated HL A-A0201 /Melan-A/MART -127-3 5 tetramers. Source From Ref. 6. Figure 6 Immunopotentiating reconstituted influenza virosomes (IRIV) adjuvant effects in the induction of tumor associated antigen-specific cytotoxic T cell. CD14-negative cells from a healthy donor peripheral blood mononuclear cells were cocultured with autologous immature dendritic cells (iDC) in the presence of Melan-A/Mart-l27-35, alone (A) or supplemented with either control liposomes (B) or IRIV (1 50, C). On day 7, culture cells were restimulated with Melan-A/MART-127-35 pulsed iDC and cultured for six further days [see Materials and Methods ]. On day 7 after restimulation cells were stained with fluorescein isothiocyanate-conjugated anti-CD8 and phosphatidylethanolamine-conjugated HL A-A0201 /Melan-A/MART -127-3 5 tetramers. Source From Ref. 6.
Generally these globular dendritic architectures offer several advantages over other kinds of organic polymers, such as the full exposure of the catalytic centers to the environment. In contrast to linear or cross-Hnked polymeric supports, which can partially hide catalytic centers, the functional groups are located on the surface of the dendritic nanoparticle and diffusional Hmitations are less relevant Furthermore the close proximity of the catalytic centers on the surface of the dendritic polymer can enhance the catalytic activity by multiple complexation or even cooperativity. This behavior is described as positive dendritic effect. However, in some cases a negative dendritic effect was observed, which is caused by an undesired interaction or electron transfer between the neighboring catalytic centers on the surface of the dendrimer [70]. [Pg.332]

Pincer ligand Carbosilane Den- Ni Kharasch reaction 0.03 mol% 1-79 Ultrafiltration Negative dendritic 68, 70,... [Pg.337]

PPh2 Carbosilane Pd Hydrovinylation 0.01-0.05 mol% 68-99.9 Continuous mem- Negative dendritic 27... [Pg.337]

Already at an early stage in the research with dendritic catalysis, these novel systems were proposed to form a promising class of recyclable catalysts. Furthermore, new, interesting properties were proposed to arise by catalyst attachment to these large, structurally well-defined polymers. In the previous section we summarized the results obtained so far in the recycling of dendritic catalysts, and here we describe some of the dendritic effects observed in catalysis. Both negative and positive effects are discussed, in an attempt to provide a balanced view of the current state of affairs. [Pg.133]


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See also in sourсe #XX -- [ Pg.332 , Pg.334 ]




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