Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sodium tetramer

In this paper, we investigate the possibilities offered by widely used DFT methods. We have chosen test cases in three different, difficult classes of problems (1) the linear and nonlinear polarizabilities of metal clusters, (2) the polarizabilities of novel compounds, and (3) the interaction-induced polarizability in weakly bonded systems. In particular, the three test cases are the sodium tetramer, a particularly soft molecule, the new compound HXel, and the interaction polarizability of two water molecules in the dimer (H20)2. [Pg.96]

We have used the data in Table 1 to calculate distance/proximity and similarities for the ab initio and DFT theoretical descriptions (TD) of the electric (hyper) polarizability of the sodium tetramer. We have a total of nine independent Cartesian components so we have in our hands a 9D problem. The similarities between the... [Pg.105]

Fig. 5 Minimum spanning tree (MST) for the theoretical descriptions of the sodium tetramer and subsequent clustering with a distance threshold D-y = 0.4. Fig. 5 Minimum spanning tree (MST) for the theoretical descriptions of the sodium tetramer and subsequent clustering with a distance threshold D-y = 0.4.
We have investigated and closely analyzed the predictive capability of DPT methods in the calculation of electric polarizabilities and hyperpolarizabilities for three difficult cases the sodium tetramer, the new compound HXel, and the interaction (hyper)polarizability of the two moieties in the weakly bonded water dimer. In the first two cases we have shown that the ab initio and DPT methods offer a quite different picture of the electric polarizability and hyperpolarizability. In the case of (H20)2 we are led to two drastically divergent pictures as the two classes of methods clearly differ even in the sign of the interaction-induced mean polarizability and h3q)erpolarizability. [Pg.125]

These reactions are usehil for the preparation of homogeneous difunctional initiators from a-methylstyrene in polar solvents such as tetrahydrofuran. Because of the low ceiling temperature of a-methylstyrene (T = 61° C) (26), dimers or tetramers can be formed depending on the alkaU metal system, temperature, and concentration. Thus the reduction of a-methylstyrene by sodium potassium alloy produces the dimeric dianionic initiators in THF (27), while the reduction with sodium metal forms the tetrameric dianions as the main products (28). The stmctures of the dimer and tetramer correspond to initial tail-to-tail addition to form the most stable dianion as shown in equations 6 and 7 (28). [Pg.237]

Detergent All late. In the 1940s, sodium dodecylben2ene sulfonate [25155-30-0] (DDES) produced by the alkylation of ben2ene with propylene tetramer followed by sulfonation with oleum [8014-95-7] (H2SO4 mixture with sulfur trioxide) or sulfur trioxide and then neutrali2ation... [Pg.51]

The half-sandwich and sandwich complexes of phospholides and phosphole tetramer are known even for the nontransition metals. The half-sandwich arrangement was studied for lithium tetramethylphospholide [89AG(E)1367] and sodium derivative 127 generated from the phospholide tetramer and sodium in the presence of 1,2-dimethoxyethane [94JA3306 96AG(E)1125]. Potassium and 1,2-dimethoxyethane in THE in these conditions give a full dianionic sandwich 128. [Pg.139]

Coscoy, S., Lingueglia, E., Lazdunski, M., and Barbry, P. (1998) The Phe-Met-Arg-Phe-amide-activated sodium channel is a tetramer./. Biol. Chem. 273, 8317. [Pg.1056]

The precipitated silica (J. Crosfield Sons) was heated in vacuo at 120° for 24h. before use. Two grades of surface areas 186 and 227 m g l (BET,N2), were used during this project. Random copolymers, poly(methyl methacrylates) and polystyrene PS I were prepared by radical polymerization block polymers and the other polystyrenes were made by anionic polymerization with either sodium naphthalene or sodium a methylstyrene tetramer as initiator. The polymer compositions and molecular weights are given in Table I. [Pg.298]

In erythrocytes and most other cells, the major structural link of plasma membranes to the cytoskeleton is mediated by interactions between ankyrin and various integral membrane proteins, including Cf/HCOj antiporters, sodium ion pumps and voltage-dependent sodium ion channels. Ankyrin also binds to the =100 nm, rod-shaped, antiparallel a(3 heterodimers of spectrin and thus secures the cytoskeleton to the plasma membrane. Spectrin dimers self-associate to form tetramers and further to form a polygonal network parallel to the plasma membrane (Fig. 2-9D). Neurons contain both spectrin I, also termed erythroid spectrin, and spectrin II, also termed fodrin. Spectrin II is found throughout neurons, including axons, and binds to microtubules, whereas spectrin I occurs only in the soma and dendrites. [Pg.29]

The reaction of the phosphole tetramer (PC4-2-Ph-3,4-Me2)4 (71) with either sodium or potassium yields the complexes 72 and 73, respectively (Scheme 6) (26). [Pg.98]

The sodium atoms are both bound rf to one phospholide ring and 171 to the phosphorus atom of the other phospholide ring of the dianion. Each Na atom is further coordinated by one of the phosphole phosphorus atoms and two oxygen atoms of the DME coligand. The potassium complex is quite different reduction of the phosphole tetramer with 4 equiv of potassium yields a tetraanion, which, after crystallization from DME containing 18-crown-6, gives the solvent sepa-... [Pg.98]

Oligomeric deoxyguanosines 69 all assemble into columns in water.93 Using SANS, the average length of the columns (DP) of freshly prepared samples was determined to be around 6 nm at a concentration of 1% in D2O.88 Increase of the temperature resulted in the loss of the cylindrical aggregates. When the sodium salt was used, subsequent cooling did not result in the reformation of the cylindrical polymers. In contrast, the potassium salt did allow for reversible self-assembly. The addition of extra potassium salt even increased the DP. It binds to the inner carbonyls of the G-tetramer and stabilizes the tetramer 94... [Pg.412]

Cyclic polymers form nearly 50 per cent of the product while the tetramer, octamethylcyclotera siloxane (I) constitutes the main cyclic compound. Now the polymerisation of the tetramer is done by heating at 150-200°C with a trace of sodium hydroxide and a very small amount of non-functional material so as to control the Molecular weight. The products obtained is a highly viscous gum having no elastic properties. [Pg.207]

Arylalkenes can undergo various reactions when treated with sodium, since compounds such as a-methylstyrene are both olefins with allylic hydrogens and styrenes, both of which are reactive. The reaction of a-methylstyrene with sodium has been reported by Bergmann et al. (6i) to yield tetramers. More recent work by Kolobielski and Pines (56) has shown that dimers and products derived from dimers are formed when this compound is heated with a sodium-benzyl-sodium catalyst. Some of the major products were cumene (VII), p-terphenyl (VIII), and 1-methyl-1,3-diphenyl-cyclopentane (IX). [Pg.144]

Originality The use of sodium sulfite as an agent to lower tetramer formation in... [Pg.215]

The current application has determined that tetramer formation can be minimized using amounts low in sodium sulfite as a reaction catalyst. [Pg.215]


See other pages where Sodium tetramer is mentioned: [Pg.994]    [Pg.247]    [Pg.95]    [Pg.102]    [Pg.103]    [Pg.106]    [Pg.994]    [Pg.247]    [Pg.95]    [Pg.102]    [Pg.103]    [Pg.106]    [Pg.428]    [Pg.92]    [Pg.516]    [Pg.162]    [Pg.562]    [Pg.97]    [Pg.123]    [Pg.216]    [Pg.65]    [Pg.69]    [Pg.188]    [Pg.257]    [Pg.46]    [Pg.183]    [Pg.248]    [Pg.412]    [Pg.302]    [Pg.394]    [Pg.54]    [Pg.387]    [Pg.459]    [Pg.221]    [Pg.160]    [Pg.227]    [Pg.215]    [Pg.130]    [Pg.138]   
See also in sourсe #XX -- [ Pg.102 ]




SEARCH



Tetramer

Tetramers

© 2024 chempedia.info